Genetic Testing, Personalized Medicine, Stem Cell

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Genetic Testing, Personalized Medicine, Stem Cell

Post  nikki6278 on Wed Aug 25, 2010 11:36 am

Obama to appeal stemcell research ruling

WASHINGTON — The US Justice Department said Tuesday it will appeal a judge's decision to block federal funding for stemcell research, risking an election year fight over hot button issues of science and religion.

snip
"The president said very plainly that this is important, life-saving research," White House spokesman Bill Burton told reporters earlier. "We're reviewing all possibilities."

"We're reviewing it so we can keep this important, potentially life-saving research moving forward in the most ethical way possible," he said.

President Barack Obama authorized the renewal of federal funding in March 2009, reversing a ban imposed by his predecessor George W. Bush in 2001 on moral and religious grounds.

In lifting the ban, Obama rejected what he said was a "false choice" between sound science and moral values.

But in his ruling Monday, Lambert sided with a group that includes several Christian organizations who argued that federal funding would go for research that involved destroying human embryos, which it argued violated a 1996 law.

Scientists, who had lauded the easing of Bush-era restrictions, saw the latest turn as a dismaying setback for research that is believed to hold great potential for treatment of diseases like diabetes, Alzheimers and Parkinson's.
http://www.google.com/hostednews/afp/article/ALeqM5gMTWIlIUUtm7PTSV5kOXsRlno12g

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Re: Genetic Testing, Personalized Medicine, Stem Cell

Post  nikki6278 on Wed Aug 25, 2010 11:39 am

Plaintiffs in stem cell lawsuit made news for other issues

Dr. James L. Sherley and Theresa Deisher, the plaintiffs in the civil lawsuit that threatens to end federal funding for research on human embryonic stem cells, are perhaps better known for their extracurricular activities than for their scientific feats.

Sherley, an African American, is a former MIT researcher who claimed racism when he was denied tenure, then garnered headlines when he went on a 12-day hunger strike in 2007 to protest the decision. Now employed by the Boston Biomedical Research Institute in Watertown, Mass., he writes frequent letters to Boston newspapers protesting articles or commentary he views as pro- abortion.

Deisher, founder of AVM Biotechnology in Seattle, is a frequent speaker warning against the use of embryonic cells to produce vaccines and other medical products. The company name — AVM, as in "Ave Maria" — reflects the struggling firm's efforts to provide products that don't rely on embryonic or fetal cells for their production.

snip
In declarations they submitted with the lawsuit, the two claimed that awarding federal funds for research on embryonic stem cells necessarily restricted the amount of funds available for their research on so-called induced pluripotent stem cells — that is, adult cells that can be rewound to an almost embryonic state.

Sherley, the son of a Baptist minister, received Ph.D. and M.D. degrees from Johns Hopkins University in 1988, then did postdoctoral studies at Princeton University. He was on the staff of the Fox Chase Cancer Center in Philadelphia for seven years before joining MIT in 1998.

snip
Deisher received her doctorate in molecular and cellular physiology from Stanford University 17 years ago, then took a series of positions at Repligen Corp. in Cambridge, Mass., ZymoGenetics Inc. in Seattle and Immunex Corp., also in Seattle. When Immunex was purchased by Amgen, she became principal scientist at the company, according to her AVM biography. She was vice president of research and development for CellCyte Genetics Corp. in Seattle before leaving in 2007 to found AVM. Her biography says she has 23 patents.
http://www.latimes.com/news/science/la-sci-stem-cells-plaintiffs-20100825,0,7279207.story



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Re: Genetic Testing, Personalized Medicine, Stem Cell

Post  nikki6278 on Wed Aug 25, 2010 11:45 am

Sounds like the Catholics are behind the stem cell issue. check out AVM

Advisors
http://www.avmbiotech.com/advisors.html

Thomas J. Van Gilder, MD, JD, MPH
snip
He spent over nine years in the U.S. Public Health Service at the Centers for Disease Control and Prevention, and obtained a Masters in Public Health from the Harvard School of Public Health. Dr. Van Gilder is also an attorney specializing in intellectual property.

David Spellman, JD
Mr. Spellman is a shareholder with Lane Powell’s Intellectual Property Litigation Group. Mr. Spellman graduated with honors from Georgetown University Law Center in 1985

Debra Vinnedge
Ms. Vinnedge is the Founder and Executive Director of Children of God for Life, a pro-life outreach source championing the campaign for ethical vaccines. Ms. Vinnedge is a nationally recognized author and speaker and has provided written testimony for the Embryonic Stem Cell Research (ESCR) Congressional hearings. She has appeared on both local and national television programs, including Fox News Channel’s Hannity and Colmes, a nationally syndicated program focusing on current events and issues. She has been a guest speaker on several national radio broadcasts, including USA Radio, EWTN and Human Life International. Her work has been publicized in Our Sunday Visitor, New Covenant Magazine, American Life League’s Celebrate Life, the National Catholic Register, Human Life International Reports and numerous diocesan newsletters and periodicals. Ms. Vinnedge resides in Murfreesboro, TN and is an active member of St. Rose of Lima Catholic Church where she promotes and defends Respect Life issues. She has been married 33 years and has 2 children and 6 grandchildren.


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Re: Genetic Testing, Personalized Medicine, Stem Cell

Post  seeker401 on Wed Aug 25, 2010 11:59 am

nikki6278 wrote:Sounds like the Catholics are behind the stem cell issue. check out AVM

Advisors
http://www.avmbiotech.com/advisors.html

Thomas J. Van Gilder, MD, JD, MPH
snip
He spent over nine years in the U.S. Public Health Service at the Centers for Disease Control and Prevention, and obtained a Masters in Public Health from the Harvard School of Public Health. Dr. Van Gilder is also an attorney specializing in intellectual property.

David Spellman, JD
Mr. Spellman is a shareholder with Lane Powell’s Intellectual Property Litigation Group. Mr. Spellman graduated with honors from Georgetown University Law Center in 1985

Debra Vinnedge
Ms. Vinnedge is the Founder and Executive Director of Children of God for Life, a pro-life outreach source championing the campaign for ethical vaccines. Ms. Vinnedge is a nationally recognized author and speaker and has provided written testimony for the Embryonic Stem Cell Research (ESCR) Congressional hearings. She has appeared on both local and national television programs, including Fox News Channel’s Hannity and Colmes, a nationally syndicated program focusing on current events and issues. She has been a guest speaker on several national radio broadcasts, including USA Radio, EWTN and Human Life International. Her work has been publicized in Our Sunday Visitor, New Covenant Magazine, American Life League’s Celebrate Life, the National Catholic Register, Human Life International Reports and numerous diocesan newsletters and periodicals. Ms. Vinnedge resides in Murfreesboro, TN and is an active member of St. Rose of Lima Catholic Church where she promotes and defends Respect Life issues. She has been married 33 years and has 2 children and 6 grandchildren.


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Re: Genetic Testing, Personalized Medicine, Stem Cell

Post  seeker401 on Wed Aug 25, 2010 12:00 pm

catholics organising a divide and conquer issue??..you sure nikki? Smile /insert sarcasm Smile

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Re: Genetic Testing, Personalized Medicine, Stem Cell

Post  nikki6278 on Wed Aug 25, 2010 12:02 pm

I wonder if the stem cell ruling will help these companies? and Genetic Testing? Timing?

N.J.'s Medco Research will study personalized medicine approach to treating mental illness
Tuesday, August 24, 2010

Medco Research Institute and SureGene said they have entered into a research collaboration to evaluate whether variation in genetic biomarkers can predict how patients will respond to widely prescribed antipsychotic drugs.

The results of the research could provide evidence that would help develop genetic tests to help doctors make more precise prescribing decisions, which would lead to better outcomes, compliance and safety for patients with mental illnesses.
http://www.nj.com/business/index.ssf/2010/08/njs_medco_research_will_study.html


Roche to Buy BioImagene, U.S. Diagnostics Firm
ZURICH—Roche Holding AG on Monday said it will buy closely held BioImagene Inc. for $100 million, helping the Swiss drug company to extend its diagnostics business.

As part of the deal, Roche's unit Ventana Medical System Inc. will acquire 100% of the California-based company, which specializes in tissue-based cancer diagnostics and research.
http://online.wsj.com/article/SB10001424052748703846604575447502864400076.html


BioFortis and Catholic Health Initiatives' Center for Translational Research Announce Biorepository Information Technology Strategic Partnership to Drive Progress in Personalized Medicine
Catholic Health Initiatives' (CHI) Institute for Research and Innovation's Center for Translational Research and BioFortis, Inc. have announced a joint strategic partnership to focus on CHI's vision in personalized healthcare initiatives for community hospitals across their system.

CHI's Center for Translational Research (CTR) is a clinical R&D and molecular diagnostics laboratory that supports the progressive advancement, commercialization, and integration of personalized medicine in CHI's community-based healthcare system. After an in-depth evaluation of existing software solutions on the market, CTR executives concluded that BioFortis' Labmatrix™ would best meet the innovative informatics needs in the areas of workflow-driven protocols, specimen biobanking, next generation diagnostics, biomarker discovery, and translational research.
http://www.prnewswire.com/news-releases/biofortis-and-catholic-health-initiatives-center-for-translational-research-announce-biorepository-information-technology-strategic-partnership-to-drive-progress-in-personalized-medicine-101404004.html

and found this:
2010 National Summit on Personalized Health Care Will Focus on Development of Core Transformative Roadmap
The third annual event will be held October 3-5, 2010, at Stein Eriksen Lodge in Deer Valley, Utah

Participants will collaborate in creating a core roadmap to accelerate, align and coordinate industrywide efforts in delivering the vision of personalized health care

snip
The 2009 Summit announced the creation of the Forum on Personalized Health Care (PHC), and announced the formation of its world-class Board of Directors, including: Clayton Christensen, prominent author and strategy professor at Harvard Business School; Leroy (Lee) Hood, CEO of the Institute for Systems Biology; Michael O. Leavitt, chairman Leavitt Partners (former Utah Governor and HHS Secretary); Clay Marsh, executive director of the Center for Personalized Medicine at Ohio State University; Ralph Snyderman, chairman of Proventys and chancellor emeritus at Duke University; and Kimball Thomson, executive director of the Forum on Personalized Health Care.
http://www.marketwatch.com/story/2010-national-summit-on-personalized-health-care-will-focus-on-development-of-core-transformative-roadmap-2010-08-23?reflink=MW_news_stmp









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Personalized approach tailors therapy based on genes, metabolism, environment

Post  ianadds on Wed Aug 25, 2010 12:03 pm

Personalized approach tailors therapy based on genes, metabolism, environment
http://www.signonsandiego.com/news/2010/aug/24/evidence-based-medicine-move-over/
A little background information for us non-bio majors..
“Personalized medicine” is the mantra of modern medical science, a popular phrase coined to describe an impending world in which patients are treated based upon their individual genetic makeup.


Q: The promise of personalized medicine is huge, but we’re clearly not there yet. Is it a question of science or something else?

A: We are only beginning to scratch the surface on personalized medicine because the technology for evaluating or stratifying individuals is expensive and not well-developed. The amount of information that will be collected and analyzed is enormous compared with our current capabilities. Deciphering a person’s genes is only a small part of the puzzle. Genes are important and will provide valuable clues to disease susceptibility in some cases, but there are many other ingredients in the mix, including the environment, the proteins expressed, how DNA is modified in cells, how metabolic pathways are altered. Many of these seem to be independent of our genes. Also, some genes are important only in specific subpopulations of people, such as Asians or people of Western European descent. A separate complete analysis of each group is needed before we truly understand the importance of a gene in a single person.


Q: There’s talk of $1,000 personal genome sequencing in three to five years. If that happens, how will that change things?

A: This information will undoubtedly have an impact on how we make decisions on health care and also how we can prevent disease. But remember, genes are only part of the picture. In some cases, such as with drug metabolism, understanding the genes might be sufficient to make informed decisions on which type of medicine to use or avoid. Complex human diseases are probably going to require considerably more information than the gene sequences to have a quantum leap in managing health and preventing disease.
I can see why that you started this thread..mucho bucks are on the line..

Q: Five years from now, do you think we’ll still be asking and answering the same questions?

A: We will certainly understand more about our genes and how they interact with the environment. Certain risk factors, either environmental or genetic, will gradually emerge as important in health and disease. These advances will likely be incremental in the short run. The timeline for true breakthroughs will probably be measured in decades rather than years.
I am on it.. Very Happy

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Re: Genetic Testing, Personalized Medicine, Stem Cell

Post  isabel on Wed Aug 25, 2010 1:07 pm

probably old news but still on and interesting
wife of g oogle company
23AndMe
http://en.wikipedia.org/wiki/23andMe

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Re: Genetic Testing, Personalized Medicine, Stem Cell

Post  seeker401 on Wed Aug 25, 2010 2:30 pm

with genome..you really are letting the genie out of the bottle..i can see euthanasia issues based on your genome..less care based on your genome etc

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Storing infant DNA

Post  nikki6278 on Thu Aug 26, 2010 10:44 pm

Citing privacy concerns, Michigan hospitals will start asking parents to store newborn blood spots

Starting Oct. 1, staff at Michigan hospitals must ask parents for written permission to store blood spots for research leftover after their newborn has been tested for life-threatening conditions.

Parents can decline, and the dried spots will be destroyed

snip
The change also allows grown children to later ask that their blood spots be destroyed.

"We're trying to be more transparent," said Janet Olszewski, director of the Michigan Department of Community Health. "You'll be asked upfront. We want people to understand that it is stored."

snip
Scientists have come to regard the stored blood spots as a gold mine for research, but there are indications the move toward transparency could reduce that treasure trove.

snip
Michigan has screened newborns for rare but serious genetics conditions since the 1970s, and was storing blood spots for almost 22 years before a change in state law in 2000 that allowed the genetic material to be stored indefinitely.

http://www.mlive.com/news/grand-rapids/index.ssf/2010/08/citing_privacy_concerns_michig.html

how old are you? Is your blood stored? I bet they have blood stores on most of us....all of the sudden they are claiming transparency? BS..something is up.

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Re: Genetic Testing, Personalized Medicine, Stem Cell

Post  isabel on Fri Aug 27, 2010 12:18 am

I THOUGH SOMETHING WAS UP AFTER 9-11 at nurse broke up this news about so many plp give blood after and was storage on at different method
my 2 cents of conspiracy was why the mason temples are next to the red cross
http://memes.org/illuminati-controlled-red-cross-conspiracy
The government is harvesting samples of DNA from every newborn child in the country
http://info-wars.org/2010/02/08/newborns%E2%80%99-dna-routinely-harvested-for-government-bio-banks/

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Re: Genetic Testing, Personalized Medicine, Stem Cell

Post  seeker401 on Fri Aug 27, 2010 9:41 am

jesus h christ isabel..and nikki..blood spots wtf..this world is crazy

The Red Cross has a long history of thieving and stealing cash donations intended for disaster relief. Even as far back as the Korean War the Red Cross was plundering soldiers' mail and care packages. Some veterans have informed us that they would buy cigarettes from the Red Cross and find a twenty dollar bill or a note from a soldier's mother tucked into the pack.

More recent examples are plentiful. Families of September 11th victims were prevented from receiving half of the donations sent by well meaning citizens to the Red Cross for their aid. The recent Tsunami also was a great money-making opportunity for the Red Cross, which was very clear in its calls for donations of only cash, which would be much easier for the organization to funnel and launder and steal. Only recently have tsunami survivors begun to see a dime of the money collected on their behalf by the Red Cross.

The Red Cross is very adept at stealing money and looting mail. They have been caught innumerable times, but always allowed to get away with their schemes because the organisation is so tightly linked to the establishment. Libby Dole, wife of Senator and powerbroker Bob Dole, was for a long time the head of the outfit. It is an organization by and for the elite insiders designed to gather intelligence and steal from those who need aid.

The International Organization of the Red Cross is a secret intelligence agency that has acted as an arm of the British Intelligence Services since its inception.

If you want to help survivors of Katrina, do a little research and find organizations that you can trust or better yet, use available resources and work together with neighbors.

Red Cross Pocketed Half Of 9/11 Donations

CNN | January 3 2005

WASHINGTON (CNN) -- Charities swung into action after the September 11 terrorist attacks, raising more than $1 billion. But questions are being raised about where and how and how much of that money is being distributed. Bearing the brunt Tuesday during a hearing of the House Energy and Commerce Committee's oversight panel was outgoing Red Cross President Dr. Bernadine Healy.

The Red Cross has raised more than $564 million for the Liberty Fund, which was set up in response to the attacks on the World Trade Center and the Pentagon. While the agency states on its Web site that it is spending more than any other relief agency responding to the terrorist attacks, it has distributed only $154 million.

Healy was hammered by one New York official for the Red Cross' decision to put aside nearly half of the money raised for future needs that may include terrorist attacks. "I see the Red Cross, which has raised hundreds of millions of dollars that was intended by the donating public to be used for the victims of September 11 -- I see those funds being sequestered into long-term plans for an organization," testified New York Attorney General Eliot Spitzer.

Healy later told CNN the Red Cross was a service organization and that previous donations had prepared the agency to deal with September 11. "We had planned for a weapon of mass destruction attack," she said. "We knew our obligations under the congressional charter. We knew it involved victim assistance and sheltering. We knew that it involved with dealing with rescue workers. We knew that it involved blood." She also noted that some of the new funding went toward helping communities learn how to deal with other threats such as anthrax.

The hearing was contentious, with panel members trying to get at the issue of donor intent and whether the Red Cross misled donors. "What's at issue here is that a special fund was established for these families. It was specially funded for this event, September 11," said Rep. Billy Tauzin, R-Louisiana. "And it is being closed now because we are told enough money's been raised in it, but we're also being told, by the way, we're going to give two-thirds of it away to other Red Cross needs." The subcommittee asked Healy and her agency to provide the exact language of all of its television and newspaper appeals for donations. Healy said what the agency has learned is it needs to explain to the public the mission of the Red Cross. "Don't confuse us with the 9/11 Fund in New York. Don't confuse us with Habitat for Humanity. Don't confuse us with the scholarship in New York for the victims. We have to get that out," she said.

Controversy over the Liberty Fund was one reason Healy decided to resign at year's end. But she defended the agency's decision of how to use the money. "The Liberty Fund is a war fund. It has evolved into a war fund," she said. "We must have blood readiness. We must have the ability to help our troops if we go into a ground war. We must have the ability to help the victims of tomorrow."

A widow who lost her husband in the World Trade Center attack also complained to the panel that what money was available from various charities was tied up in red tape and confusion. "Why then haven't these charities been able to get together and agree on one uniform application? Why haven't they been able to get together and develop a quicker way for families to receive these funds?" asked Elizabeth McLaughlin of Pelham, New York. "We all have the missing persons reports, death certificates, and any other proof needed to avoid fraud. But the charities are not sharing these documents and information with each other," she testified in tears. She told the panel that she had to construct an 18-page spreadsheet to try to keep track of all the requirements of various aid groups. McLaughlin received a $27,000 check from the Red Cross, but fears she may still lose her house without additional aid.

The Red Cross said it has helped 25,000 families with food and temporary shelter, counseling and cash assistance.

[According to Bush, cash is all they want you to donate... see bottom of page to learn what agency is now going to oversee your charity money]

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Jackson Lab

Post  nikki6278 on Mon Sep 13, 2010 11:13 am

Gene testing to predict athlete’s injuries could be part of Jackson Lab project

AVE MARIA — Some genetic tests could become best-sellers among an unlikely alliance of overbearing mothers and athletic trainers.

Some direct-to-consumer genetic tests that indicate an athlete’s predisposition to concussions from playing football or to an ACL tear from sliding into home plate could be marketed someday from a Collier County address. A specialized training center could operate next door for athletes to follow a tailored exercise program based on their injury propensity after a genetic work-up.

That is former NFL player James Kovach’s plan with his start-up company, Athleticode, based in California but which could have a presence in a proposed biomedical park near Ave Maria.

Athleticode is the first commercial company that the Maine-based Jackson Laboratory is bringing to the table as having an interest in the proposed biomedical park. That’s along side the University of South Florida in Tampa, Florida Gulf Coast University in Estero and Edison State College, which all have memorandums of understanding with Jackson to potentially develop programs there
http://www.naplesnews.com/news/2010/sep/12/jackson-lab-gene-test-athlete-injury-Athleticode/

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Re: Genetic Testing, Personalized Medicine, Stem Cell

Post  seeker401 on Tue Sep 14, 2010 12:21 pm

thanks nikki..so they are predicting injuries now?

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Accepting Your Genetic Destiny

Post  ianadds on Mon Sep 27, 2010 12:20 pm

Accepting Your Genetic Destiny
http://www.huffingtonpost.com/robert-tornambe-md/accepting-your-genetic-de_b_733881.html

The traits that we inherit from our parents, physical and emotional, are derived from the genetic characteristics, or DNA, from both your mother and father. Simply stated, genes carry pieces of DNA found on chromosomes, which are located in the cells of your body. Genes can be dominant or recessive. Traits from dominant genes require only one copy (or one parent) for the trait to be inherited. Traits from recessive genes are rare because you require a recessive gene from both parents for that particular trait to be passed on. For example, free floating ear lobes (check yours out in the mirror!) are derived from a dominant gene and attached earlobes, from a recessive gene. Facial dimples from smiling are derived from a dominant gene, whereas no dimples is a recessive trait. Emotional or psychological traits that we inherit from our parents usually indicate a tendency towards a certain state of mind. What we do with those tendencies determine the actual outcome, or personality. Bottom line: the genes inherited from your parents determine your particular Genetic Destiny, and define who you are!


Acceptance of your Genetic Destiny is a healthy and realistic achievement that will allow you to be more confident and satisfied. This means that you acknowledge your body type and height, the intrinsic shape of your face, and your predisposition to have wide hips like your mother and broad shoulders like your father. If you are five-foot-two, you are never going to be five-foot-ten. If you have a delicate bone structure in your face, you are never going to look like Angelina Jolie (and getting your lips plumped will not make you look more like her!).
Prepping peasants for things to come..

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