StemCells Therapy

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23-12-2011 02:33 KXAN Medical Minute — Texas Oncology www.texasoncology.com

SAN DIEGO, Feb. 2, 2012 /PRNewswire/ — Sequenom, Inc. (NASDAQ: SQNM – News), a life sciences company providing innovative genetic analysis solutions, today announced that a new publication of an independent multi-center study on Sequenom Center for Molecular Medicine's MaterniT21™ laboratory-developed test (LDT) appears today in the online issue of Genetics in Medicine

26-01-2012 09:21 Jared Taylor, editor of American Renaissance, explains the biological basis of race.

According to a study published in the online version of the journal The Oncologist, a genetic variation that increases the risk of individuals who take bisphosphonates, developing serious necrotic jaw bone lesions, has been identified by researchers at the Columbia University College of Dental Medicine. Bisphosphonates are a common class of osteoclastic inhibitors that work by attaching to …

02-11-2011 12:51 Selena shares her family’s experience with Lynch syndrome.

CAMBRIDGE, MASS.–(BUSINESS WIRE)– Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) announced today that the U.S. Food and Drug Administration (FDA) has approved KALYDECOTM (ivacaftor), the first medicine to treat the underlying cause of cystic fibrosis (CF), a rare, genetic disease. KALYDECO (kuh-LYE-deh-koh) is approved for people with CF ages 6 and older who have at least one copy of the G551D mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene

30-01-2012 09:19 Website qdragon.info Shirts and Stuff www.zazzle.com My twitter twitter.com Like Brainstorm on Facebook www.facebook.com Technology News tinyurl.com Medical News tinyurl.com Biotechnology News tinyurl.com Hosted by www.youtube.com Contributors www.youtube.com www.youtube.com RNA Video www.youtube.com

ScienceDaily (Jan. 31, 2012) — A report from investigators at the Massachusetts General Hospital (MGH) Cancer Center has defined the role of a recently identified gene abnormality in a deadly form of lung cancer.

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Public release date: 31-Jan-2012 [ | E-mail | Share ] Contact: Katie Marquedant kmarquedant@partners.org 617-726-0337 Massachusetts General Hospital A report from investigators at the Massachusetts General Hospital (MGH) Cancer Center has defined the role of a recently identified gene abnormality in a deadly form of lung cancer. Tumors driven by rearrangements in the ROS1 gene represent 1 to 2 percent of non-small-cell lung cancers (NSCLC), the leading cause of cancer death in the U.S.

11-12-2011 09:20 A decade ago, scientists announced that they had produced the first draft of the human genome, the 3.6 billion letters of our genetic code.

CAMBRIDGE, Mass.–(BUSINESS WIRE)– Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX – News) announced today that the U.S.

22-01-2012 23:39 Jan. 23 (Bloomberg) — Dana Nieder, mother of three-year-old Maya Nieder, talks with Bloomberg’s John Lauerman about her daughter’s undiagnosed genetic disorder and her struggles with medical and insurance bureaucracies for advanced testing.

Researchers at Boston University’s School of Public Health and School of Medicine found 13 new genetic areas associated with immune function and DNA repair affecting aging and the beginning of menopause, according to a press release.

Researchers at Geisinger Health System have found that genetic abnormalities may be the cause for the majority of cerebral palsy (CP) cases, a group of disorders that can involve the brain and nervous system functions, such as seeing, movement, hearing, thinking, and learning, rather than a difficult birth or other perinatal factors.

Scientists have made a major genetic breakthrough that could change the way pediatric cancers are treated in the future.

In this June 6, 2011 file photo, former Pennsylvania Sen.

( University of Helsinki ) The research group at the Institute for Molecular Medicine Finland has revealed eleven new genetic regions associated with the blood levels of the metabolites, including new loci affecting well-established risk markers for cardiovascular disease and potential biomarkers for type 2 diabetes. The findings may help in elucidating the processes leading to common diseases …

Via Scoop.it – inPharmaticsOracle Exadata gets into Personlized Medicine & Bioinformatics space dressed as Oracle® Health Sciences Omics Data Bank.    Oracle Health Sciences today announced availability of Oracle® Health Sciences Omics Data Bank, a molecular data model, which is part of Oracle Health Sciences Translational Research Center.   The new data model provides integration [...]