Monday, April 29, 2013

The IPKat: The rise of patent monetization entities Part Three ...

In Part Two of this series of Katposts, we looked at the diffusion of patent assertion entities in England and Wales, where data show that only 6% of patent cases involve a PAE (in the US, instead, PAEs filed 56% of patent lawsuits in 2012 - see Part One). In the absence of detailed data on the rise of patent assertion entities in other EU countries, this Kat decided to take an indirect approach to the issue, looking at similarities or differences in (1) the usage of patents and (2) the legal framework in the UK and the rest of the EU.

On the first aspect, the PatVal-EU study provides some useful evidence on 'unused blocking patents', a concept that refers to patents which are neither used internally by the right owner, nor licensed. Their most frequent use is strategic blocking, which aims to prevent competitors from using the patented innovations. It is therefore probable that PAEs may assert patents falling within this category. A look at the findings of the PatVal-EU study shows that, in respect to about 9000 patents with priority date in 1993-1997 (located in France, Germany, Italy, Netherlands, Spain and UK), the share of unused blocking patents is between 12,6 and 23% [these data, coupled with similar data on unused sleeping patents, brought concerns about low patent valorization in the EU: the Commission, here and here, suggested that the development of patent funds and pools may increase valorization, but noted that their activities could lead to anti-competitive and hold-up practices, unless they were committed to non exclusive licensing, based on reasonable remuneration - similar private-public funds are starting to appear in Korea (Intellectual Discovery Fund), France (Brevets) and Japan (Innovation Network Corp.), as reported by Reuters here]. The highest percentage of unused blocking patents is found in the UK, which suggests that the number of PAE cases in the UK and in other EU countries should be comparable, unless the former has a peculiar legal framework which discourages PAEs from filing lawsuits at the PHC.

This finding is corroborated by a research conducted by S. Fusco, who found that the number of known PAE cases in Italy and Germany is particularly low. According to her paper, in the period 2000-2012, only five lawsuits involved a patent assertion entity in Italy (out of about 1,000 patent cases); in Germany, again, Fusco was only able to gather evidence of five PAE cases (out of about 8,000 patent cases) in the same span of time (although these data were collected through indirect evidence). A study that examined the activity of patent assertion entities in the German patent market also confirmed these data: T. Fischer and J. Henkel found that PAEs are not particularly active in the market for technology, a conclusion which falls in line with the UK data (particularly, with the low activity in patent filing and litigation). The researchers were able to identify only 107 patent transfers to known PAEs in Germany, while similar entities acquired 458 patents in the US [the data, however, also suggest that the entities operating in the EU differ from those active in the US and vice versa: of all the PAEs listed in the study, only Intergraph and Rambus had engaged in patent transfers in both markets]. Although there may not be an exact correspondence between patent transfers and litigation, this study certainly suggests that PAEs' activity in Germany remains low, as highlighted in Fusco's work.

Since (1) patent usage (and market) looks uniform, attention should be devoted to (2) the differences in the legal framework of patent litigation around Europe. If one or more of the elements that are commonly regarded as safeguards against the spread of PAE litigation cannot be found in one or more of the EU member states, it could mean that the reassuring data on PAE cases in England and Wales cannot be extended to other countries. Before digging deeper, however, it may be useful to list these 'safeguards'. According to several studies (for example, here and here), these elements comprise:
(a) strict rules on the patentability of software and business method;
(b) fragmented enforceability, which increases the costs and complexity of litigation (and the likelihood of inconsistent decisions);
(c) unavailability of contingency fees;
(d) low litigation costs and damage awards in comparison to the US [similarly, low damage awards appear to be a factor in limiting PAE litigation in India - thanks Rahul!];
(e) implementation of the 'loser pays' rule.
Although they may be interpreted in slightly different ways, these safeguards appear to be present all over the EU. However, the major threat comes from the fragmented enforceability, which brings with it the risk of conflicting decisions. This certainly increases the litigation's complexity, but also allows a patent assertion entity to exploit the inconsistencies to identify the most PAE-friendly courts (look here for a comparison between UK, Germany, France and Netherlands). A prime example of this risk may be found in the different attitude of the courts on the issuance of injunctions in PAE cases. Sir Robin Jacob, at the 2008 GRUR Meeting in Stuttgart, offered a humorous perspective on the issue, discussing the different approach of UK and German courts:
[I]t comes out of a little discussion I had with a prominent German lawyer. He said to me: "for us, there is no problem." "Why?" I said. "Because if a valid patent is infringed, there will be an injunction." "Suppose", I asked, "the patent was for a life saving drug and the patentee had not enough product to supply the market. Would a German court really stop the supply of an infringer?s product?" "Well", he said, conceding the point: "Maybe not. But it would have to be a very extreme case."
In Germany, an injunction is usually granted if there is a finding or likelihood of infringement, and its use as an incentive to force settlement is openly acknowledged. In the PAE case IPCom v HTC, a German judge held that:
The Chamber does assume in principle that the enforcement of a cease-and-desist claim can be disproportionate since rights arising from a patent are not granted without limits (Art. 14 (2) of the Basic Law, ? 242 of the German Civil Code). However, since the legislator does not make the cease-and-desist claim subject to any general prohibition on commensurability (not so: ? 140a (4), ? 140b (4), ? 140c (2), ? 140d (2) of the Patent Act) and the cease-and-desist claim secures the exclusivity right protected under constitutional law, the scope of the disproportionality defense remains restricted to atypical exceptional cases which could not be foreseen by the legislator. The fact that the patent licensing entity is attempting to enforce a cease-and-desist claim in order to urge infringing parties to pay for a license does not, in the view of the Chamber, constitute such an exception but rather is an inherent part of the patent system as part of the applicable legal and economic system, especially since a patent licensing entity will usually be urged to take such action with respect to existing license agreements.
The German approach seems at odds with the one taken by the PHC. Again, Sir Robin Jacob explained that judges in England and Wales are prepared to grant injunctions, but maintain a degree of discretion in relation to the relief, which they exercise taking into account the plaintiff's interest and previous conduct. He noted that UK courts reject absolutism and affirm the right to refuse an injunction when damages appear to be an adequate remedy. Reciting Seager v Copydex and Banks v EMI Songs, the former judge stated that 'where an inventor wanted to sell his idea for money, money is what he got'. A similar approach is adopted by courts in the Netherlands, which generally also exhibit a more sensitive attitude, than German courts, towards foreign judgments (head here and here for some food for thought on the topic). The practical consequence is that some companies are moving away from Germany, to relocate their headquarters in the Netherlands, citing legal concerns as the main reason for the relocation (Microsoft is probably the most prominent example - test your German here). The recent judgment of the CJEU in Case C?616/10, Solvay SA v Honeywell et al.?(IPKat comments here), stirred things up, as it recognized the possibility of granting pan-European injunctions, if there is 'a real connecting link between the subject-matter of the provisional measures sought and the territorial jurisdiction of the Member State of the court seised' (a paper just published offers a perspective on the case). The Court did not move away from its previous ruling in Case C-4/03, Gesellschaft f?r Antriebstechnik mbH & Co. v Lamellen und Kupplungsbau Beteiligungs, which taught that a national court may assess infringement (or non-infringement) beyond national boundaries, but cannot rule on the validity of the patent at issue, as the courts of the member state where the patent was registered have exclusive jurisdiction on questions of validity, pursuant to the mandatory rule of Article 22(4) of Regulation 44/2001 (Article 16(4) of the Brussels Convention). Instead, the judges recognized that a pan-European interim injunction is permitted, if it does not lead to a final decision on the patent's validity:
According to the referring court, the court before which the interim proceedings have been brought does not make a final decision on the validity of the patent invoked but makes an assessment as to how the court having jurisdiction under Article 22(4) of the regulation would rule in that regard, and will refuse to adopt the provisional measure sought if it considers that there is a reasonable, non-negligible possibility that the patent invoked would be declared invalid by the competent court. In those circumstances, it is apparent that there is no risk of conflicting decisions ..., since the provisional decision taken by the court before which the interim proceedings have been brought will not in any way prejudice the decision to be taken on the substance by the court having jurisdiction under Article 22(4) of Regulation No 44/2001.
Further, the Court ruled that Article 6(1) of Regulation 44/2001 may be applied in cases where two or more companies from different Member States, in proceedings pending before a court of one of those Member States, 'are each separately accused of committing an infringement of the same national part of a European patent which is in force in yet another Member State by virtue of their performance of reserved actions with regard to the same product'. In Actavis Group HF v Eli Lilly & Company, the High Court for England and Wales accepted to hear foreign patent claims (if no question of validity is involved), declining arguments pointing to the forum non conveniens (and the AdvoKat commented it here).

It is difficult to predict whether these recent development may fuel or hinder the rise of patent assertion entities in the EU. The prospect of obtaining a pan-European injunction could potentially help the spread of PAE cases, while pan-European infringement proceedings might reduce fragmentation, inconsistency and litigation costs. This Kat, however, does not think that these elements could cause a sudden surge in PAE litigation: on one side, the judges' attitude towards the issuance of injunctions in PAE cases has so far been cautious; on the other, fragmentation could be restored, and usually will, through an invalidity claim.

The same concerns expressed above accompanied the Unified Patent Court Agreement (UPC), which many studies depicted as a test for the EU patent litigation system's resistance to the diffusion of PAEs. In particular, commentators (European Scrutiny Committee report here) pointed to bifurcation, forum shopping (and pro-patentee attitude, determined by competition between local divisions - see a recap of issues here) and pan-European injunctions as the main issues that might transform the EU into a 'trolls' paradise'. Professor Harhoff?however stated that the UPC is designed with an emphasis on revocation, low costs and cautious use of injunctions, elements which should be adequate to counter 'trolling' activities. Certainly, that seems to be one of the aims of the UPC, as a recital states: '[w]ishing to improve the enforcement of patents and the defence against unfounded claims and patents which should be revoked and to enhance legal certainty by setting up a Unified Patent Court for litigation relating to the infringement and validity of patents'.

Of relevance to assess potential effects on PAE lawsuits are, inter alia, the following provisions:

* Article 19: the establishment of a training framework for the judges should ensure, or at least contribute to, the uniformity of judicial decisions among the different divisions (as expressly stated by the provision itself: 'Regular meetings shall be organised between all judges of the Court in order to discuss developments in patent law and to ensure the consistency of the Court's case law');
*?Article 33(1)(b): allowing the plaintiff to bring an action under Article 32(1)(a), (c), (f) and (g) against multiple defendants 'only where the defendants have a commercial relationship and where the action relates to the same alleged infringement' should prevent the EU from suffering from one of the issues that plagued US litigation before the America Invents Act, which introduced stricter joinder rules;
*?Article 33(3): bifurcation may be feared by many, but the real effects of the provision remain to be discovered, as two out of three options allow the case to proceed safely united. The risk, here, is that judges across the different divisions may adopt different practices with regard to bifurcation, effectively creating a pro-patentee enclave [shall we call it Eastern District for Europe, perhaps?];
*?Article 33(10): as evidenced by the study cited in Part One of this post, information asymmetry may play a key role in favouring PAE litigation [Merpel cannot make up her mind on whether the adoption of a fair play rule in patent litigation - or in any fields of litigation - would be beneficial or deadly];
*?Article 42: principles of proportionality and fairness, albeit theoretical premises which might be disregarded, certainly point the system in the right direction, as far as PAE (or any type of) litigation is concerned (e.g. they may influence the judges' decisions on bifurcation, when a patent assertion entity is concerned, concentrating litigation to avoid unfair use of the temporal discrepancy between the judgments of infringement and validity);
*?Article 62: discretionary grant of provisional injunctions challenges the courts with the task of defining clear and consistent standards, giving actual shape to the elements indicated in Article 62(2) (interests of the parties and potential harm from granting or refusal). Once again, as with bifurcation, uniformity appears to be the key to a PAE-proof system;
*?Article 63: similarly, allowing discretionary grant of permanent injunctions could lead courts to take a UK-inspired approach, limiting the award of permanent injunctions in PAE cases (again, uniformity is the issue here);
*?Article 69: the adoption of the 'loser pays' rule is likely to be a disincentive for exploratory lawsuits and is commonly thought to be a powerful antidote to PAE litigation.

On a train to Milan, the

Kat saw something familiar...

To this Kat, the risk that the UPC Agreement may provide fertile ground for PAE cases does not appear significantly higher than that embedded in the current situation. The system, however, seems characterized by a degree of fragmentation, and perhaps incoherency [as shown by readers' comments to a recent IPKat post], which makes it hard to foresee how judges are going to apply the provisions of the Agreement. Usually, trolling activity thrives in situations where complexity and confusion rule. Thus, the challenge that awaits judges, practitioners and scholars is to shed light on the obscure issues and to ensure that the divisions' decisions will be consistent and uniform [Merpel adds that a good starting point would be to address some of the Max Planck's criticisms, examined by the AmeriKat here].

The analysis conducted so far, in Parts Two and Three, showed that (1) England and Wales enjoy a relatively PAE-adverse environment, (2) PAE litigation in other EU member states is equally constricted, although there is some inconsistency with respect to the use of injunctions, (3) the trend towards pan-European litigation should not significantly alter the current situation, and (4) the UPC Agreement contains potentially dangerous provisions, whose effects can [should, says Merpel] be contrasted by an effort to achieve consistency and to establish clear and shared standards for issuing injunctive remedies and dealing with bifurcation.

There is still one issue which is worth mentioning, as it gives a preview of possible developments of PAE litigation in Europe. As highlighted at the beginning of Part Two, the expression 'patent assertion entity' commonly refers to a company who manages a portfolio of patents for the primary aim of assertion and litigation, without practising the invention. Recently, however, primary companies in the ICT sector started using PAEs (already existent or created ad hoc) to assert patents against each other, in an effort to gain a competitive advantage and to hold up competitors, relying on the ever growing phenomenon of patent thickets ('a dense web of overlapping intellectual property rights that a company must hack its way through in order to actually commercialize new technology' according to Shapiro, more here). In June 2012, for example, Google filed a complaint with the EU Commission, alleging that Microsoft and Nokia 'are colluding to raise the costs of mobile devices for consumers, creating patent trolls that sidestep promises both companies have made' (Guardian article here). The giant search-engine company demanded that the competitors be held accountable and invited the Commission to look into these practices. Further, intense litigation in the EU (and US) is currently surrounding standard essential patents and FRAND licensing (examples: Germany here and UK here).

It seems that, if the EU has been relatively immune from traditional patent trolling, a new wave of better looking, well dressed, yet secretly malicious PAEs is appearing on the horizon. A similar development would not only shake the safeguards that protected the EU from traditional PAE litigation, but would ultimately challenge the patent system itself, shifting the focus from protection of research and innovation, to strategic use of patents to alter competition on the merits. Thus closely observing and studying old and new PAEs, even if the phenomenon appears to be minor in the EU, might be a very wise thing to do.

Source: http://ipkitten.blogspot.com/2013/04/the-rise-of-patent-monetization_5980.html

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Tuesday, April 23, 2013

Dancer who lost foot in Boston bombing vows to take to the floor again

A week ago, Adrianne Haslet and her husband, Adam Davis, were watching the Boston Marathon from the sidelines. Then the bombs went off.

Davis, a U.S. airman, had just returned from Afghanistan.

"We sat up and I said, 'Wait, my foot hurts.' And then he held up my foot and we both just screamed bloody murder," she told ABC News today during a phone call from Boston Medical Center. "I didn't feel heat from it. I just felt air and then I fell to the ground."

The blast had torn off the dancer's left foot - a devastating loss for the ballroom dance instructor at Boston's Arthur Murray Studios. The bombings killed three people, including an 8-year-old boy, and injured at least 200 people.

Haslet, who appeared on the cover of the Boston Herald this morning, said she had not lost her spirit.

"I absolutely want to dance again," she said.

Dr. Linda Arslanian, a physical therapist at Boston's Brigham and Women's Hospital, said Haslett likely would dance again thanks to the advancement of prosthetic technology.

"If they were walking before they had their amputation, we can have them walk again," she said. "Much depends on the level of their amputation and all of it depends on what their goals and objectives are."

CLICK: Breakthroughs Will Benefit Boston Bombing Amputees

"If they want a vigorous life, we can give them a prosthesis that will allow huge amounts of versatility in their demands," Arslanian said. She did not treat Haslet.

Last year, ABC News interviewed Aimee Mullins, a model and athlete, who'd been born without shin bones and had to have legs amputated at the knee when she was a year old. With the aid of prosthetic legs, she became the first amputee to compete on an NCAA track team and competed in the 1996 Paralympics in Atlanta.

Haslet today said she was determined, like the rest of the city, to get back on her feet again.

"I just want people to know that you can come out of a situation that might seem like the end of the world and come out stronger," she said.

Also Read

Source: http://news.yahoo.com/blogs/abc-blogs/dancer-lost-foot-boston-marathon-bombing-vows-floor-021109058--abc-news-topstories.html

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Antibody transforms stem cells directly into brain cells

Apr. 22, 2013 ? In a serendipitous discovery, scientists at The Scripps Research Institute (TSRI) have found a way to turn bone marrow stem cells directly into brain cells.

Current techniques for turning patients' marrow cells into cells of some other desired type are relatively cumbersome, risky and effectively confined to the lab dish. The new finding points to the possibility of simpler and safer techniques. Cell therapies derived from patients' own cells are widely expected to be useful in treating spinal cord injuries, strokes and other conditions throughout the body, with little or no risk of immune rejection.

"These results highlight the potential of antibodies as versatile manipulators of cellular functions," said Richard A. Lerner, the Lita Annenberg Hazen Professor of Immunochemistry and institute professor in the Department of Cell and Molecular Biology at TSRI, and principal investigator for the new study. "This is a far cry from the way antibodies used to be thought of -- as molecules that were selected simply for binding and not function."

The researchers discovered the method, reported in the online Early Edition of the Proceedings of the National Academy of Sciences the week of April 22, 2013, while looking for lab-grown antibodies that can activate a growth-stimulating receptor on marrow cells. One antibody turned out to activate the receptor in a way that induces marrow stem cells -- which normally develop into white blood cells -- to become neural progenitor cells, a type of almost-mature brain cell.

Nature's Toolkit

Natural antibodies are large, Y-shaped proteins produced by immune cells. Collectively, they are diverse enough to recognize about 100 billion distinct shapes on viruses, bacteria and other targets. Since the 1980s, molecular biologists have known how to produce antibodies in cell cultures in the laboratory. That has allowed them to start using this vast, target-gripping toolkit to make scientific probes, as well as diagnostics and therapies for cancer, arthritis, transplant rejection, viral infections and other diseases.

In the late 1980s, Lerner and his TSRI colleagues helped invent the first techniques for generating large "libraries" of distinct antibodies and swiftly determining which of these could bind to a desired target. The anti-inflammatory antibody Humira?, now one of the world's top-selling drugs, was discovered with the benefit of this technology.

Last year, in a study spearheaded by TSRI Research Associate Hongkai Zhang, Lerner's laboratory devised a new antibody-discovery technique -- in which antibodies are produced in mammalian cells along with receptors or other target molecules of interest. The technique enables researchers to determine rapidly not just which antibodies in a library bind to a given receptor, for example, but also which ones activate the receptor and thereby alter cell function.

Lab Dish in a Cell

For the new study, Lerner laboratory Research Associate Jia Xie and colleagues modified the new technique so that antibody proteins produced in a given cell are physically anchored to the cell's outer membrane, near its target receptors. "Confining an antibody's activity to the cell in which it is produced effectively allows us to use larger antibody libraries and to screen these antibodies more quickly for a specific activity," said Xie. With the improved technique, scientists can sift through a library of tens of millions of antibodies in a few days.

In an early test, Xie used the new method to screen for antibodies that could activate the GCSF receptor, a growth-factor receptor found on bone marrow cells and other cell types. GCSF-mimicking drugs were among the first biotech bestsellers because of their ability to stimulate white blood cell growth -- which counteracts the marrow-suppressing side effect of cancer chemotherapy.

The team soon isolated one antibody type or "clone" that could activate the GCSF receptor and stimulate growth in test cells. The researchers then tested an unanchored, soluble version of this antibody on cultures of bone marrow stem cells from human volunteers. Whereas the GCSF protein, as expected, stimulated such stem cells to proliferate and start maturing towards adult white blood cells, the GCSF-mimicking antibody had a markedly different effect.

"The cells proliferated, but also started becoming long and thin and attaching to the bottom of the dish," remembered Xie.

To Lerner, the cells were reminiscent of neural progenitor cells -- which further tests for neural cell markers confirmed they were.

A New Direction

Changing cells of marrow lineage into cells of neural lineage -- a direct identity switch termed "transdifferentiation" -- just by activating a single receptor is a noteworthy achievement. Scientists do have methods for turning marrow stem cells into other adult cell types, but these methods typically require a radical and risky deprogramming of marrow cells to an embryonic-like stem-cell state, followed by a complex series of molecular nudges toward a given adult cell fate. Relatively few laboratories have reported direct transdifferentiation techniques.

"As far as I know, no one has ever achieved transdifferentiation by using a single protein -- a protein that potentially could be used as a therapeutic," said Lerner.

Current cell-therapy methods typically assume that a patient's cells will be harvested, then reprogrammed and multiplied in a lab dish before being re-introduced into the patient. In principle, according to Lerner, an antibody such as the one they have discovered could be injected directly into the bloodstream of a sick patient. From the bloodstream it would find its way to the marrow, and, for example, convert some marrow stem cells into neural progenitor cells. "Those neural progenitors would infiltrate the brain, find areas of damage and help repair them," he said.

While the researchers still aren't sure why the new antibody has such an odd effect on the GCSF receptor, they suspect it binds the receptor for longer than the natural GCSF protein can achieve, and this lengthier interaction alters the receptor's signaling pattern. Drug-development researchers are increasingly recognizing that subtle differences in the way a cell-surface receptor is bound and activated can result in very different biological effects. That adds complexity to their task, but in principle expands the scope of what they can achieve. "If you can use the same receptor in different ways, then the potential of the genome is bigger," said Lerner.

In addition to Lerner and Xie, contributors to the study, "Autocrine Signaling Based Selection of Combinatorial Antibodies That Transdifferentiate Human Stem Cells," were Hongkai Zhang of the Lerner Laboratory, and Kyungmoo Yea of The Scripps Korea Antibody Institute, Chuncheon-si, Korea.

Funding for the study was provided by The Scripps Korea Antibody Institute and Hongye Innovative Antibody Technologies (HIAT).

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Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_science/~3/4sCqbLxIxUg/130422154756.htm

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Monday, April 22, 2013

FAA furloughs kick in, some flight delays appear

Commercial airline flights moved smoothly throughout most of the country on Sunday, the first day air traffic controllers were subject to furloughs resulting from government spending cuts, though some delays appeared in the late evening in and around New York. And even though the nightmarish flight delays and cancellations that the airline industry predicted would result from the furloughs did not materialize yet, the real test will come Monday, when traffic ramps up.

Information from the FAA and others showed that flying Sunday was largely uneventful, with most flights on time. There were delays in parts of Florida, but those were caused by thunderstorms.

Mark Duell at the flight tracking website FlightAware said that John F. Kennedy and LaGuardia airports in New York indicated delays due to lower staffing starting late Sunday evening. JFK averaged 70-minute delays for inbound flights, but no detectable departure delays. LaGuardia averaged 74-minute delays for inbound flights, and departure delays of 37 minutes.

The FAA website said that flights from Philadelphia and Orlando, Fla., into John F. Kennedy, LaGuardia and Westchester County airports were delayed due to staffing issues.

The trade group Airlines for America, which represents the airlines and had predicted a big traffic snarl, said Sunday evening that it was "not seeing a significant impact at this point." A spokeswoman said the group would continue to monitor the situation, and urged flyers to stay in contact with their airlines.

Delays were also affecting travelers in Los Angeles. The FAA said late Sunday night that staffing cuts were causing delays averaging more than three hours for flights arriving at Los Angeles International Airport. The agency did not say how many flights were affected.

Airport spokesman Marshall Lowe said about 70 flights had delays of about an hour or more Sunday, but he could not say what role the staffing cuts played in the delays.

The FAA said that "relatively good weather" and light traffic, which is typical of Sundays, helped keep delays in check. The agency said it would be working with airlines "to minimize the delay impacts of lower staffing" as the busy summer travel season approaches.

Government budget cuts that kicked in last month are forcing the FAA and other agencies to cut their spending. FAA officials have said they have no choice but to furlough all 47,000 agency employees, including nearly 15,000 controllers. Each employee will lose one day of work every other week. The FAA has said that planes will have to take off and land less frequently, so as not to overload the remaining controllers on duty.

Friday, airline trade groups and the country's biggest pilots union sued the FAA to try to stop the furloughs. They predicted that the furloughs would delay or cancel flights for as many as one out of every three airline passengers across the country. Airlines have also directed their customers to tell the FAA to find other ways to cut costs.

Source: http://news.yahoo.com/faa-furloughs-kick-flight-delays-appear-000550777--finance.html

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Big scramble seen in open Senate seat in Georgia (The Arizona Republic)

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Sunday, April 21, 2013

Boston's Ortiz set to return from 8-month layoff

BOSTON (AP) ? David Ortiz is set to make his return for the Boston Red Sox following an eight-month layoff.

Ortiz was in the batting order to hit cleanup and be the designated hitter in Saturday's game against the Kansas City Royals.

The 37-year-old was activated from the disabled list Friday. Ortiz injured his right Achilles tendon running the bases on July 17 and appeared just once in Boston's final 72 games, going 2 for 3 against the Royals on Aug. 24.

Ortiz was bothered by inflammation in both heels during spring training, and he went 4 for 18 (.222) with a home run during a six-game injury rehabilitation assignment with Triple-A Pawtucket from April 11-18.

Source: http://news.yahoo.com/bostons-ortiz-set-return-8-month-layoff-154246192--mlb.html

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Saturday, April 20, 2013

Penn receives prestigious national award for breakthrough in gene therapy

Penn receives prestigious national award for breakthrough in gene therapy [ Back to EurekAlert! ] Public release date: 19-Apr-2013
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Contact: Katie Delach
katie.delach@uphs.upenn.edu
215-349-5964
University of Pennsylvania School of Medicine

Award recognizes improvements in human health and efforts to alleviate suffering from disease

PHILADELPHIA A gene therapy study focused on finding a cure for a rare congenital blinding disease has been recognized as one of the ten most outstanding clinical research projects of the year by the Clinical Research Forum (CRF). The study, led by Jean Bennett, MD, Phd, F.M. Kirby professor of Ophthalmology at the University of Pennsylvania School of Medicine, and carried out in collaboration with Penn Medicine's Albert M. Maguire, MD, and Katherine A. High, MD at The Children's Hospital of Philadelphia (CHOP), has been presented with the Distinguished Clinical Research Achievement Award, the second highest given in the CRF's Annual Top 10 Clinical Research Achievement Awards. CRF award winners are cited as the most compelling examples of scientific innovation that results from the nation's investment in clinical research that can benefit human health and welfare.

The results of the most recent phase of the study for Leber's Congenital Amaurosis (LCA) at CHOP have led to the first Phase 3 gene therapy study in the United States and the first Phase 3 gene therapy study in the world for a non-lethal disorder. The team of researchers hopes that the studies could lead to the first approved gene therapy product in the United States.

"The data from our study has already been used to develop additional clinical trials for other blinding diseases," said Bennett. "There are two things that I think are really going to be important from this work: one, that we'll move forward with this particular disease and get approval for the drug that we've been developing, and two, that this could ultimately lead to approved treatments for other currently untreatable conditions."

Published in 2012, the winning studies are the latest in a long tradition of notable health advances that have occurred through clinical research such as eliminating polio, reducing the mortality of AIDS, and improving cancer survival rates that were propelled by combined investment in basic science and clinical research.

"These patients, once rendered blind by LCA, have had their lives transformed and their vision restored by this team's efforts to further gene therapy research," said Joan O'Brien, MD, chair of the department of Ophthalmology at the Scheie Eye Institute at Penn Medicine. "The groundbreaking work sets the stage for the treatment of numerous other blinding conditions, but is also a shining example of what scientists with NIH resources can accomplish for the betterment of humanity."

###

The Clinical Research Forum is an organization comprised of the nation's most prestigious and acclaimed academic medical centers and healthcare systems whose goal is to sustain and expand a cadre of talented, well-trained clinical investigators at all stage of career development, and support nurturing environments and comprehensive research capabilities within academic institutions. Its mission is to provide leadership to the national clinical and translational research enterprise and promote understanding and support for clinical research and its impact on health.

Penn Medicine is one of the world's leading academic medical centers, dedicated to the related missions of medical education, biomedical research, and excellence in patient care. Penn Medicine consists of the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania (founded in 1765 as the nation's first medical school) and the University of Pennsylvania Health System, which together form a $4.3 billion enterprise.

The Perelman School of Medicine has been ranked among the top five medical schools in the United States for the past 16 years, according to U.S. News & World Report's survey of research-oriented medical schools. The School is consistently among the nation's top recipients of funding from the National Institutes of Health, with $398 million awarded in the 2012 fiscal year.

The University of Pennsylvania Health System's patient care facilities include: The Hospital of the University of Pennsylvania -- recognized as one of the nation's top "Honor Roll" hospitals by U.S. News & World Report; Penn Presbyterian Medical Center; and Pennsylvania Hospital -- the nation's first hospital, founded in 1751. Penn Medicine also includes additional patient care facilities and services throughout the Philadelphia region.

Penn Medicine is committed to improving lives and health through a variety of community-based programs and activities. In fiscal year 2012, Penn Medicine provided $827 million to benefit our community.


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Penn receives prestigious national award for breakthrough in gene therapy [ Back to EurekAlert! ] Public release date: 19-Apr-2013
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Contact: Katie Delach
katie.delach@uphs.upenn.edu
215-349-5964
University of Pennsylvania School of Medicine

Award recognizes improvements in human health and efforts to alleviate suffering from disease

PHILADELPHIA A gene therapy study focused on finding a cure for a rare congenital blinding disease has been recognized as one of the ten most outstanding clinical research projects of the year by the Clinical Research Forum (CRF). The study, led by Jean Bennett, MD, Phd, F.M. Kirby professor of Ophthalmology at the University of Pennsylvania School of Medicine, and carried out in collaboration with Penn Medicine's Albert M. Maguire, MD, and Katherine A. High, MD at The Children's Hospital of Philadelphia (CHOP), has been presented with the Distinguished Clinical Research Achievement Award, the second highest given in the CRF's Annual Top 10 Clinical Research Achievement Awards. CRF award winners are cited as the most compelling examples of scientific innovation that results from the nation's investment in clinical research that can benefit human health and welfare.

The results of the most recent phase of the study for Leber's Congenital Amaurosis (LCA) at CHOP have led to the first Phase 3 gene therapy study in the United States and the first Phase 3 gene therapy study in the world for a non-lethal disorder. The team of researchers hopes that the studies could lead to the first approved gene therapy product in the United States.

"The data from our study has already been used to develop additional clinical trials for other blinding diseases," said Bennett. "There are two things that I think are really going to be important from this work: one, that we'll move forward with this particular disease and get approval for the drug that we've been developing, and two, that this could ultimately lead to approved treatments for other currently untreatable conditions."

Published in 2012, the winning studies are the latest in a long tradition of notable health advances that have occurred through clinical research such as eliminating polio, reducing the mortality of AIDS, and improving cancer survival rates that were propelled by combined investment in basic science and clinical research.

"These patients, once rendered blind by LCA, have had their lives transformed and their vision restored by this team's efforts to further gene therapy research," said Joan O'Brien, MD, chair of the department of Ophthalmology at the Scheie Eye Institute at Penn Medicine. "The groundbreaking work sets the stage for the treatment of numerous other blinding conditions, but is also a shining example of what scientists with NIH resources can accomplish for the betterment of humanity."

###

The Clinical Research Forum is an organization comprised of the nation's most prestigious and acclaimed academic medical centers and healthcare systems whose goal is to sustain and expand a cadre of talented, well-trained clinical investigators at all stage of career development, and support nurturing environments and comprehensive research capabilities within academic institutions. Its mission is to provide leadership to the national clinical and translational research enterprise and promote understanding and support for clinical research and its impact on health.

Penn Medicine is one of the world's leading academic medical centers, dedicated to the related missions of medical education, biomedical research, and excellence in patient care. Penn Medicine consists of the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania (founded in 1765 as the nation's first medical school) and the University of Pennsylvania Health System, which together form a $4.3 billion enterprise.

The Perelman School of Medicine has been ranked among the top five medical schools in the United States for the past 16 years, according to U.S. News & World Report's survey of research-oriented medical schools. The School is consistently among the nation's top recipients of funding from the National Institutes of Health, with $398 million awarded in the 2012 fiscal year.

The University of Pennsylvania Health System's patient care facilities include: The Hospital of the University of Pennsylvania -- recognized as one of the nation's top "Honor Roll" hospitals by U.S. News & World Report; Penn Presbyterian Medical Center; and Pennsylvania Hospital -- the nation's first hospital, founded in 1751. Penn Medicine also includes additional patient care facilities and services throughout the Philadelphia region.

Penn Medicine is committed to improving lives and health through a variety of community-based programs and activities. In fiscal year 2012, Penn Medicine provided $827 million to benefit our community.


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AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.


Source: http://www.eurekalert.org/pub_releases/2013-04/uops-prp041913.php

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Friday, April 19, 2013

Scientists produce best image yet of atoms moving in real time

Apr. 17, 2013 ? Call it the ultimate nature documentary. Scientists at the University of Toronto have recorded atomic motions in real time, offering a glimpse into the very essence of chemistry and biology at the atomic level.

Their recording is a direct observation of a transition state in which atoms undergo chemical transformation into new structures with new properties -- in this case the transfer of charge leading to metallic behaviour in organic molecules. It is described in a study reported in the April 18 issue of Nature.

"It's the first look at how chemistry and biology involve just a few key motions for even the most complex systems," says U of T chemistry and physics professor R. J. Dwayne Miller, principal investigator of the study. "There is an enormous reduction in complexity at the defining point, the transition state region, which makes chemical processes transferrable from one type of molecule to another. This is how new drugs or materials are made."

Miller, who holds a joint appointment as director of the Max Planck Research Group for Structural Dynamics at the Centre for Free Electron Laser Science, conducted the research with colleagues from institutions in Germany and Japan. He says nature uses this reduction principle at transition states to breathe life into otherwise inanimate matter.

"Imagine the complexity of all the enormous number of possible arrangements of atoms in DNA or any other biologically active molecule. It always does the same thing to drive a biological function. We can now see how all these possible motions become coerced along a particular pathway by a dominant player."

To help illuminate what's going on here, Miller explains that with two atoms there is only one possible coordinate or dimension for following the chemical pathway. With three atoms, two dimensions are now needed. However, with a complex molecule, it would be expected that hundreds or even thousands of dimensions would be required to map all possible trajectories of the atoms.

"In this case, chemistry would be a completely new problem for every molecule," says Miller. "But somehow there is an enormous reduction in dimensions to just a few motions, and we are now able to see exactly how this works at the atomic level of detail."

The result builds on a milestone Miller and some former graduate students first reached a decade ago.

"One of the longstanding dream experiments is to directly observe atomic motions during the defining moments that lead to structure change, and we were able to watch simple phase transitions at the atomic level back in 2003," says Miller. "This led to a new understanding that now allows for minimally invasive laser surgery. It's a testimony to the importance of basic science and never knowing where new understandings will lead."

"The first atomic movies were very grainy, much like the first motion pictures," says Miller. "The new movies are so clear one could dare say they are becoming beautiful to behold, especially when you remember you are looking at atoms moving on the fly. We've captured them at an incredibly fast rate of less than 1 millionth of a millionth of a second per frame."

The breakthrough was based on the development of ultra-bright electron sources that dates back to the 2003 work.

"Other researchers use x-rays to capture atomic motions, so no one thought we could ever develop a bright enough source based on electrons as they undergo electron-electron repulsion and would blow up without being able to capture an image on the incredibly short time scale required," says Miller. "We found a way to coerce the electrons into an ultra-short pulse sufficiently bright to literally light up atomic motions as they occur."

"Electrons interact with atoms 1 million times stronger than x-rays and can be produced with a table-top instrument to efficiently produce enormous, effective brightness for viewing atomic motions."

Funding for this research was provided by the Natural Sciences and Engineering Research Council of Canada and the Canada Foundation for Innovation. Additional support was provided by the Max Planck Society in Germany, a Grant-in-Aid for Scientific Research on Innovative Areas and the G-COE program for the field of Chemistry from The Ministry of Education, Culture, Sports, Science and Technology in Japan, and by Creative Scientific Research from The Japan Society for the Promotion of Science.

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The above story is reprinted from materials provided by University of Toronto, via EurekAlert!, a service of AAAS.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. Meng Gao, Cheng Lu, Hubert Jean-Ruel, Lai Chung Liu, Alexander Marx, Ken Onda, Shin-ya Koshihara, Yoshiaki Nakano, Xiangfeng Shao, Takaaki Hiramatsu, Gunzi Saito, Hideki Yamochi, Ryan R. Cooney, Gustavo Moriena, Germ?n Sciaini, R. J. Dwayne Miller. Mapping molecular motions leading to charge delocalization with ultrabright electrons. Nature, 2013; 496 (7445): 343 DOI: 10.1038/nature12044

Note: If no author is given, the source is cited instead.

Disclaimer: Views expressed in this article do not necessarily reflect those of ScienceDaily or its staff.

Source: http://feeds.sciencedaily.com/~r/sciencedaily/matter_energy/physics/~3/GyyPkKDFz-0/130417131907.htm

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Thursday, April 18, 2013

Officials: 2nd suspicious letter intercepted

(AP) ? Law enforcement officials say a second suspicious letter that has been received in Washington was actually directed to the White House, not the Senate.

Two officials told The Associated Press on Wednesday that the letter was being treated in the same manner as a separate one sent to Mississippi Sen. Roger Wicker and was undergoing field tests.

The officials spoke on the condition of anonymity because the investigation is ongoing.

The U.S. Secret Service said it intercepted a letter addressed to President Barack Obama that contained a "suspicious substance."

The letter to Wicker, a Republican, was intercepted at a Senate mail facility just outside Washington and has tested positive for ricin. Sen. Claire McCaskill has said authorities have a suspect in mind in that case, though no one has been charged.

Associated Press

Source: http://hosted2.ap.org/APDEFAULT/89ae8247abe8493fae24405546e9a1aa/Article_2013-04-17-Senator-Ricin-Second%20Letter/id-0f8766346114498ba133f025c5515e31

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Wednesday, April 17, 2013

Daughter tells Philadelphia abortion doctor trial about mom's final hours

By Dave Warner

PHILADELPHIA (Reuters) - The daughter of a woman who died after an abortion at a Philadelphia clinic testified on Tuesday at the murder trial of the clinic's owner about the final hours of her mother's life.

Karnamaya Mongar, 41, died on November 20, 2009, after undergoing the procedure at the Women's Medical Society in West Philadelphia. Kermit Gosnell, 72, the physician who owned the clinic, is charged with murder in the deaths of Mongar and seven infants.

Gosnell is accused of severing infants' spinal cords after they lived through abortion procedures. He faces the death penalty if convicted.

"My mom was complaining it was hurting, so they gave her an IV," said Yashodo Gurung, 26, of Woodbridge, Virginia, as she testified about her mother's experience at the clinic.

Gurung, a native of Bhutan who spent much of her life in Nepal, testified through an interpreter at the trial in Common Pleas Court.

"I remember they gave her pills two or three times," she said, "but I forget how many times they put something in the IV."

An ambulance took her mother to a nearby hospital, where she and other family members anxiously waited overnight, she said.

She testified that the next morning doctors told her, "We tried our best, but your mom's heart stopped working."

Prosecutors have said Mongar died of an overdose of anesthetics prescribed by Gosnell.

Gosnell has been in jail since he was charged in January 2011 after a grand jury probe. He is on trial on 26 charges, including the eight counts of murder.

The case has rekindled the debate in the United States about late-term abortions. Under Pennsylvania law, abortions can be performed up to 24 weeks.

A friend of Mongar's family, Damber Ghalley, said he spoke to Gosnell the morning she died. He testified that Gosnell told him "the procedure was done fine. I did not do anything wrong."

Also on Tuesday, a registered nurse from the city's Department of Public Health, Lorraine Matijkiw, testified about what she found at the clinic during inspections in 2008 and 2009.

The grand jury report that led to the murder charges against Gosnell was highly critical of unsanitary conditions it said existed in the clinic.

"When I walked in the lobby, it was really filthy," Matijkiw testified. "It smelled of urine. I did not see any cats, but I could smell cats," said Matijkiw, who was inspecting the clinic as part of a program for doctors to provide vaccinations to children.

"There was spilled junk all over," she said. "I saw things that were not right. They were not clean."

(Editing by Ellen Wulfhorst)

Source: http://news.yahoo.com/daughter-tells-philadelphia-abortion-doctor-trial-moms-final-235918851.html

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Security beefed up worldwide after Boston blasts

LOS ANGELES (AP) ? Police in Los Angeles, New York City, London, Washington and other cities worldwide stepped up security Monday following explosions at the Boston Marathon.

In Los Angeles, the Sheriff's Department activated its emergency operations center and increased patrols at transit hubs, schools and county buildings, while in New York, critical response teams were deployed citywide and officials stepped up security at hotels and other prominent locations.

California emergency management officials activated their statewide threat assessment system, which was established after the Sept. 11, 2001, World Trade Center attacks. And officials in multiple cities and counties throughout the state were reviewing information from federal authorities for possible threats.

Meanwhile, police in Washington, San Diego, Las Vegas, Detroit and Atlanta were monitoring events closely and assessing potential increases in security measures.

At the White House, the Secret Service quickly expanded its security perimeter, shutting down Pennsylvania Avenue and cordoning off the area with yellow police tape. Several Secret Service patrol cars blocked off entry points to the road, though the White House was not on lockdown and tourists and other onlookers were still allowed in the park across the street.

Agencies were also stepping up their social media response, telling the public via Twitter and Facebook to report suspicious activity to the police.

In Seattle, police increased patrols in neighborhoods and around government buildings and other facilities. In Colorado a statewide alert was sent out advising law enforcement agencies to look out for suspicious activities.

Police at three major Los Angeles area airports, including Los Angeles International, were in a "heightened state of vigilance," with increased patrols, said Chief of Airport Police Patrick Gannon.

"We have no indications that suggest there's a nexus from Boston to the Los Angeles airport, but in an overabundance of caution, we have heightened our patrols," Gannon said.

At the Port of Los Angeles and Long Beach, police increased security procedures by doing critical site checks of property around the port complex as well as coordinating with multiple local and federal law enforcement officers.

The explosions also spurred a review of security at upcoming sporting events. British police said they were re-examining plans for Sunday's London Marathon ? the next major international marathon.

The San Francisco Police Department was also rethinking security for the upcoming San Francisco Marathon in June and the Bay to Breakers race in May. In Indianapolis, authorities were reviewing security for next month's 500 Festival Mini-Marathon, while in Nashville, increased security precautions were being considered for the Country Music Marathon on April 27. Stepped up security was also put in place for this weekend's marathon in Lansing, Mich.

Security was heightened for a number of sporting events Monday night, including the Dodgers-Padres game in Los Angeles and the Nationals-Marlins game in Miami. But Major League Baseball said no changes were planned to ceremonies at ballparks around the country to commemorate Jackie Robinson Day, though several teams informed the league they planned moments of silence.

In Miami, a police officer with a dog patrolled near a ballpark entrance ? an unusual sight at the venue ? two hours before the game. In Tennessee, hockey fans watching the Nashville Predators play the Vancouver Canucks were seeing "more visible presence around the building," team spokesman Kevin Wilson said.

___

Associated Press writers Colleen Long in New York, Brett Zongker in Washington, Gregory Katz in London, Juliet Williams in Sacramento, Elliot Spagat in San Diego, Jason Dearen in San Francisco contributed to this report

Source: http://news.yahoo.com/security-beefed-worldwide-boston-blasts-203546055--spt.html

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Monday, April 15, 2013

93% Room 237

All Critics (100) | Top Critics (25) | Fresh (94) | Rotten (7) | DVD (1)

The results can range from enlightening - Kubrick did like to mess with things - to embarrassing. But it's never dull. "Room 237" shines.

You don't have to buy any of the nutty theories in Room 237 to appreciate what director Rodney Ascher has accomplished.

It's nuts, in the best possible way.

Their imaginings are not far removed from the deconstuctionist gobbledygook that has hammerlocked academic film and literary scholarship. But here at least the gobbledygook is entertaining.

[It] may be the surpassingly eccentric-and enormously entertaining-film that Kubrick deserves.

"Room 237" is an act of uncommon devotion to cinema, embracing the notion that movies are best defined by what happens to us as we watch them - how our own beliefs and experiences dictate our interpretation of what we've seen and heard.

As fascinating as it is frustrating

It is nice to see a doc that makes you smile instead of making you angry. Anyone who is a fan of Stanley Kubrick will eat this up.

Powered by a deep and abiding affection for both The Shining and Kubrick in general, Room 237 is an amuse-bouche of remix culture.

Room 237 is an extended riff of the "Paul is dead" variety. But, you know what? Sometimes a guy moving a table in the background is just a guy moving a table in the background.

A diverting excursion for lovers of Kubrick's films...even if, at over a hundred minutes, it does go on a bit long.

A fascinating doc that will get both film geeks and conspiracy theorists alike drooling, it all but guarantees you'll never watch The Shining quite the same way again.

Confounding, eye-opening, and often hilarious.

I suspect that Ascher's intention was to dynamize an academic exercise, but these constant, sundry inserts render the tone as corny and glib as a VH1 special.

The thrill's in the thinking about little pieces of cinematic language as words contributing to a two-hour essay.

Would it be hypocritical to say that I loved "Room 237," even thought I felt like 75 percent of what was said in it was completely hooey?

a journey down a rabbit hole worth taking, as the film immerses us in alternately fascinating, compelling, absurd, and frightening theories about what, exactly, The Shining is (or might be) about

No quotes approved yet for Room 237. Logged in users can submit quotes.

Source: http://www.rottentomatoes.com/m/room_237_2012/

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Police: 3 found shot to death inside Kansas home

TOPEKA, Kan. (AP) ? Police say three people have been found shot to death inside a home in Topeka, Kan.

Topeka police Lt. Scott Gilchrist says officers and emergency medical responders arrived after getting a 911 call around 9:15 p.m. CDT Friday from a woman at the home reporting that several people had been shot. He declined to give any identifying information about the three people who were found dead, including whether they lived in the house.

Gilchrist tells the Topeka Capital-Journal (http://bit.ly/10Sm6CZ ) that police were searching for a person of interest. He says the person isn't believed to be a threat to the general public.

The city of Topeka had recorded only two homicides this year prior to Friday, the newspaper reported.

___

Information from: The Topeka (Kan.) Capital-Journal, http://www.cjonline.com

Source: http://news.yahoo.com/police-3-found-shot-death-inside-kansas-home-103339862.html

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Sunday, April 14, 2013

Woods story, predictably, dominates CBS broadcast

Spectators walk past a leader board displaying Tiger Woods' two first two rounds scores before the third round of the Masters golf tournament Saturday, April 13, 2013, in Augusta, Ga. The score board reflects the 2-stroke penalty assessed to Woods for a drop in 2nd round of the Masters. (AP Photo/Matt Slocum)

Spectators walk past a leader board displaying Tiger Woods' two first two rounds scores before the third round of the Masters golf tournament Saturday, April 13, 2013, in Augusta, Ga. The score board reflects the 2-stroke penalty assessed to Woods for a drop in 2nd round of the Masters. (AP Photo/Matt Slocum)

CBS announcer Jim Nantz led off the network's Masters coverage Saturday by describing what Tiger Woods did the day before on the 15th hole as an "innocent" and "absent-minded" mistake.

CBS devoted the first 12 minutes of its broadcast from the Masters entirely to Woods, who was given a two-stroke penalty earlier in the day for a bad drop that led to his signing an incorrect scorecard after his second round.

Woods' shot on the 15th hole of the second round hit the flag stick and bounced back into the water. He took his penalty drop 2 yards behind where he hit the original shot, a rules violation.

Woods was tied for 17th when the third-round broadcast started at 3 p.m. EDT, five shots off the lead. His story dominated the early coverage, and CBS didn't mention another player until 3:12 p.m., when it showed the leaderboard for the first time.

"A day of high drama at Augusta National Golf Club before a single shot was struck." was how Nantz described the scene.

The broadcast started with a live shot of Woods at the sixth hole and being applauded by the gallery.

From there, the network displayed the ruling that cost Woods two strokes but allowed him to remain in the tournament. It broke down what his three options were after his shot on the 15th hole on Friday ended up in the water, then aired a lengthy interview by Nantz of Fred Ridley, chairman of the Masters' competition committees.

Augusta National said it was Nantz who alerted Masters officials Friday that Woods' post-rounds comments were causing some doubts, leading to another review.

Woods had said after his round, "I went back to where I played it from, but went two yards further back and I tried to take two yards off the shot of what I felt I hit. And that should land me short of the flag and not have it either hit the flag or skip over the back. I felt that was going to be the right decision to take off four (yards) right there. And I did. It worked out perfectly."

"It was an innocent mistake," Nantz said, referring to Woods' actions.

Once CBS got through the initial wave of Woods coverage, it was largely business-as-usual, with cameras trained on an array of players over roughly the next 35 minutes. Then CBS again revisited the Woods matter, with analyst Nick Faldo ? a three-time Masters champion ? saying the way Friday's events transpired ultimately saved Woods.

Augusta National reviewed the matter Friday even before Woods' second round was complete and found no breach of rules. But when Woods said after the round that he chose to play his drop slightly farther back from where he played his original shot, Augusta National decided to review the matter once again.

"If this had all happened later at night, if somebody had called in late at night and then had gone back and reviewed everything, then in fact Tiger would be disqualified," Faldo said. "He would have signed for the wrong score. In a way, that helped him. They reviewed the situation, they decided from what they saw there was no infringement, but it was only after Tiger then said, 'Hey, I intentionally came back a couple of yards.'"

Faldo said he was surprised Woods did not know the rule, but added that he gave the world's No. 1 player "the benefit of doubt."

Earlier in the day, the Golf Channel's Brandel Chamblee said:

"The integrity of this sport is bigger than the desire to see Tiger Woods play golf today," Chamblee said. "I want to see Tiger Woods play golf. I have never seen anybody play golf like him. I want to see him make a run at Jack Nicklaus' majors record. I want to see that. But I don't want to see it this week; I don't want to see it under these circumstances. The right thing to do here, for Tiger and for the game, is for Tiger to disqualify himself."

Faldo agreed with Chamblee and didn't back down during the CBS broadcast.

"There was absolutely no intention to try to drop that as close to the divot, absolutely none at all," Faldo said. "So, in black and white, and that is the greatest thing about our game, our rules are very much black and white. You know, that's a breach of the rules. Simple as that."

Later in the telecast, Faldo's tone seemed more conciliatory.

Faldo reiterated that in his era, he thought most players ? when presented with a situation like the one Woods was in ? would either be disqualified or withdraw. But he stopped short of calling again for that to happen.

"We're in a new era now under new rules and even if they bring some controversy, Tiger is playing rightly under the new rules," Faldo said. "And myself and some of my old pros, we have to accept that now."

Associated Press

Source: http://hosted2.ap.org/APDEFAULT/347875155d53465d95cec892aeb06419/Article_2013-04-13-GLF-Masters-Woods-CBS/id-8a8e4e77bcb14af6b722ad1b301c5d2d

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Martha Stewart ruling: What it means for Macy's

Martha Stewart's lawyers tried to get the lawsuit thrown out, but today's ruling says no: Macy's case against Martha Stewart will proceed.

By Anne D'Innocenzio,?Associated Press / April 11, 2013

Martha Stewart departs the New York state Supreme Court after testifying, March 5. Macy's claims that Martha Stewart violated her exclusive contract with them when her company designed products for JC Penney. Ms. Stewart's attorneys tried to get the case dismissed, but today's ruling says that the case will move forward.

Lucas Jackson / Reuters / File

Enlarge

A New York State Supreme Court judge has rejected a motion by Martha Stewart Living Omnimedia lawyers to dismiss Macy's claim that the New York-based merchandising and media company violated its pact when it developed certain products for competitor J.C. Penney even though they don't carry the home designer's name.

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Lawyers for Martha Stewart argued Thursday that the exclusive contract with Macy's in certain products like bedding and bath items did not give exclusivity on design work. But Judge Jeffrey Oing ruled that Macy's has provided sufficient evidence that the contract does cover exclusivity in designs even if the items don't carry the Martha Stewart name.

Judge Oing cautioned that his decision not to dismiss the claim doesn't mean Macy's will win the lawsuit against Martha Stewart Living. The suit charges that Martha Stewart breached a long-standing contract with Macy's when it signed a deal with Penney in December 2011 to open Martha Stewart mini-shops.

Separately, Macy's has sued Penney for having no regard for the contract with the home maven and that it set out to steal the business. But Oing's decision could influence whether Penney can go ahead and sell products designed by Martha Stewart that bear the name JCP Everyday.

Those products, which were expected to be shipped to stores this spring and housed in Penney's overhauled home area, are now in limbo. Judge Oing is expected to rule Friday whether to temporarily stop Penney from selling those products.

A move to block Penney from selling the goods in the exclusive categories could be a financial blow to Penney just as the company finished a year of disastrous results that led to the ousting of its CEO, Ron Johnson. Johnson, who had been on the job for 17 months, had spearheaded a major overhaul of the company that failed to resonate with shoppers. Deborah Weinswig, an analyst at Citi Research estimated in a report earlier this week that Penney could take a hit of as much as $100 million on the JCP Everyday products.

"When given the opportunity to present our case, (Martha Stewart Living) lawyers will show that ... (the company) is a design house committed to designing beautiful, high-quality products and that our contract with Macy's permits us to license our designs to all retailers so that consumers can buy them wherever they shop," according to a statement issued Thursday by Martha Stewart Living.

Meanwhile, Judge Oing dismissed Macy's claims that Penney intentionally interfered with its contract with Martha Stewart. He also dismissed Macy's claim that Martha Stewart violated its licensing contract when it shared the contract with Penney.

Last July, Macy's won a preliminary injunction against Martha Stewart Living that prevented it from selling Martha Stewart branded houseware and other exclusive products at Penney. In August, the judge granted permission for Penney to open Martha Stewart mini-shops as long as the items covered by the exclusive contract with Macy's were not sold in them.

The stakes are high for all three companies, but particularly for Penney. The struggling department store chain is counting on the overhauled home department to help recover from a year of mounting losses and deep sales drops. Martha Stewart shops were expected to anchor the area.

Penney is going ahead with opening shops filled with goods labeled Martha Celebrations, featuring stationery and paper products for parties. Those items are not covered by the Macy's contract.

Source: http://rss.csmonitor.com/~r/feeds/csm/~3/eKbti09AgDY/Martha-Stewart-ruling-What-it-means-for-Macy-s

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