Researchers link cancer to failures in chromosome protection for the first time
A study published today in the journal Nature Genetics explores a new mechanism that may contribute to the development of several tumours, including Chronic Lymphocytic Leukaemia, a type of cancer that affects more than a ...
Genetics
Mar 19, 2013 |
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New clues in hunt for heredity in type 2 diabetes
Type 2 diabetes has strong hereditary tendencies and the genes we are born with cannot be changed. However, new research from Lund University in Sweden shows that we can modify the function of the genes through the epigenetic ...
Genetics
Mar 19, 2013 |
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Researchers create map of 'shortcuts' between all human genes
Some diseases are caused by single gene mutations. Current techniques for identifying the disease-causing gene in a patient produce hundreds of potential gene candidates, making it difficult for scientists to pinpoint the ...
Genetics
Mar 18, 2013 |
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New database to speed genetic discoveries
A new online database combining symptoms, family history and genetic sequencing information is speeding the search for diseases caused by a single rogue gene. As described in an article in the May issue of Human Mutation, the da ...
Genetics
Mar 18, 2013 |
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Two new genes linked to amyotrophic lateral sclerosis and related disorders
(Medical Xpress)—A study led by St. Jude Children's Research Hospital has discovered mutations in two genes that lead to the death of nerve cells in amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, ...
Genetics
Mar 18, 2013 |
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Not dead yet: Junk DNA is back
A controversy at last: most of our DNA is junk, no it isn't, yes it is. Actually, I think it is – up to 90% really is junk.
Genetics
Mar 15, 2013 |
4.5 / 5 (4) |
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New structural insight into neurodegenerative disease
A research team from the Korea Advanced Institute of Science and Technology (KAIST) released their results on the structure and molecular details of the neurodegenerative disease-associated protein Ataxin-1. ...
Genetics
Mar 14, 2013 |
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Novel treatment approach for bladder pain using a herpes simplex virus vector reported
Severe chronic pain associated with conditions such as bladder pain syndrome/interstitial cystitis often require the use of opioid medication, with the risk of dependency and serious adverse reactions. An ...
Genetics
Mar 14, 2013 |
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Study identifies multiple genetic factors impacting development of nearsightedness
In the largest ever genome-wide association study on myopia, 23andMe, the leading personal genetics company, identified 20 new genetic associations for myopia, or nearsightedness. The company also replicated two known associations ...
Genetics
Mar 14, 2013 |
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Education resource focuses on teaching population genetics using current research
Genetics and life sciences instructors, who teach undergraduate students about population and evolutionary genetics, have a new teaching resource: the March 2013 Primer in the Genetics Society of America's journal Genetics uses c ...
Genetics
Mar 13, 2013 |
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Havoc in biology's most-used human cell line: Genome of HeLa cells sequenced for the first time
HeLa cells are the world's most commonly used human cell lines, and have served as a standard for understanding many fundamental biological processes. In a study published today in G3: Genes, Genomes and Ge ...
Genetics
Mar 12, 2013 |
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Epigenetics mechanism may help explain effects of mom's nutrition on her children's health
Pioneering studies by U. S. Department of Agriculture-funded research molecular geneticist Robert A. Waterland are helping explain how the foods that soon-to-be-moms eat in the days and weeks around the time of conception—or ...
Genetics
Mar 11, 2013 |
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Secrets of a t-haplotype gene revealed: Decade-long hunt turns up key gene involved in early mammalian development
The t haplotype in mice—a block of linked genes occupying the proximal half of mouse chromosome 17—is one of the best-studied examples of a selfish genetic element. Through an elaborate sperm-poisoning ...
Genetics
Mar 08, 2013 |
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Persistence pays off in solving hemophilia mystery, showing curiosity drives discovery
An Australian researcher has found the third and final missing piece in the genetic puzzle of an unusual form of hemophilia, more than 20 year after he discovered the first two pieces.
Genetics
Mar 07, 2013 |
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Genomic screening for improved public health
In ten years time, routine preventive health care for adults may include genetic testing alongside the now familiar tests for cholesterol levels, mammography and colonoscopy. As genomic testing prepares to enter the realm ...
Genetics
Mar 07, 2013 |
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