Related topics: cancer , brain , genes , stem cells , genetic variation
Nature Genetics
hideNature Genetics is a scientific journal concerning genetics. It is published by Nature Publishing Group, and was founded in 1992. The 2008 impact factor is 30.259. Its sister journal is Nature Reviews Genetics.
For more information about Nature Genetics, read the full article at
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News tagged with nature genetics
Gene for devastating kidney disease discovered
Dec 22, 2009 |
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(PhysOrg.com) -- Researchers from Children's Hospital Boston and Brigham and Women's Hospital have identified an important genetic cause of a devastating kidney disease that is the second leading cause of kidney failure in ...
Study unveils potential genetic links to lung disease risk
Dec 14, 2009 |
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A new study involving data from more than 20,000 individuals has uncovered several DNA sequences linked to impaired pulmonary function. The research, an analysis that combined the results of several smaller studies, provides ...
New genes for lung disease discovered
Dec 13, 2009 |
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(PhysOrg.com) -- Scientists have discovered five genetic variants that are associated with the health of the human lung. The research by an international consortium of 96 scientists from 63 centres in Europe and Australia ...
Gene mismatch influences success of bone marrow transplants
Nov 22, 2009 |
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A commonly inherited gene deletion can increase the likelihood of immune complications following bone marrow transplantation, an international team of researchers reports in the November 22 advance online issue of Nature Ge ...
Researchers Identify Gene Mutations Underlying Risk for Most Common Form of Parkinson's Disease
Nov 17, 2009 |
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(PhysOrg.com) -- Two genes containing mutations known to cause rare familial forms of parkinsonism are also associated with the more common, sporadic form of the disease where there is no family history, researchers have ...
For the first time, scientists discover causative gene of a rare disorder by exome sequencing
Nov 17, 2009 |
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(PhysOrg.com) -- UW researchers have successfully used a method called exome sequencing to quickly discover a previously unknown gene responsible for a rare disorder. The finding demonstrates the usefulness ...
Largest gene study of childhood IBD identifies 5 new genes
Nov 15, 2009 |
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In the largest, most comprehensive genetic analysis of childhood-onset inflammatory bowel disease (IBD), an international research team has identified five new gene regions, including one involved in a biological pathway ...
Deepening the search for clues to rheumatoid arthritis
Nov 09, 2009 |
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(PhysOrg.com) -- The gnawing pain of rheumatoid arthritis is a signal that the body’s immune system has hit the wrong target: its own cartilage and bone.
Developmental delay could stem from nicotinic receptor deletion
Nov 08, 2009 |
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The loss of a gene through deletion of genetic material on chromosome 15 is associated with significant abnormalities in learning and behavior, said a consortium of researchers led by Baylor College of Medicine in a report ...
Cucumber genome published
Nov 02, 2009 |
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The genome of the cucumber has been sequenced by an international consortium lead by Chinese and U.S. institutions. The annotated genome is published online Nov. 1 by the journal Nature Genetics.
The entwined destinies of mankind and leprosy bacteria
Nov 02, 2009 |
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Leprosy still affects hundreds of thousands of people today throughout the entire world. An international team headed by EPFL professor Stewart Cole has traced the history of the disease from ancient Egypt to today and in ...
Testicular tumors may explain why some diseases are more common in children of older fathers
Oct 25, 2009 |
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A rare form of testicular tumour has provided scientists with new insights into how genetic changes (mutations) arise in our children. The research, funded by the Wellcome Trust and the Danish Cancer Society, could explain ...
Rare mutation dramatically increasing schizophrenia risk
Oct 25, 2009 |
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An international team of researchers led by geneticist Jonathan Sebat, Ph.D., of Cold Spring Harbor Laboratory (CSHL), has identified a mutation on human chromosome 16 that substantially increases risk for schizophrenia.
New chromosomal abnormality identified in leukemia associated with Down syndrome
Oct 18, 2009 |
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Researchers identified a new chromosomal abnormality in acute lymphoblastic leukemia (ALL) that appears to work in concert with another mutation to give rise to cancer. This latest anomaly is particularly common in children ...
Loss of Tumor-Suppressor and DNA-Maintenance Proteins Causes Tissue Demise, Study Finds
Oct 15, 2009 |
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(PhysOrg.com) -- A study published in the October issue of Nature Genetics demonstrates that loss of the tumor-suppressor protein p53, coupled with elimination of the DNA-maintenance protein ATR, severely disrup ...
