News tagged with genetic causes
Related topics: genes , genetic variation , genetic mutations , intellectual disability
Genetic test developed for those at-risk for Autism Spectrum Disorder: Accuracy to be studied
(Medical Xpress)—A team of Australian researchers, led by University of Melbourne has developed a genetic test that is able to predict the risk of developing Autism Spectrum Disorder, ASD.
Autism spectrum disorders
Sep 12, 2012 |
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Breast cancer risks acquired in pregnancy may pass to next three generations
Chemicals or foods that raise estrogen levels during pregnancy may increase cancer risk in daughters, granddaughters, and even great-granddaughters, according to scientists from Virginia Tech and Georgetown University.
Cancer
Sep 11, 2012 |
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First evidence for genetic cause for Barrett's oesophagus found
Genetic variations that are linked with the onset of Barrett's oesophagus (BE), a pre-cancerous condition of the lower end of the gullet, have been identified for the first time. The discovery of variations in regions on ...
Genetics
Sep 09, 2012 |
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Genetic discovery for hereditary spastic ataxia—rare disease in Newfoundland
Researchers from the Guy Rouleau Laboratory affiliated with the CHUM Research Centre and the CHU–Sainte-Justine Research Centre have discovered the genetic cause of a rare disease reported only in patients originating from ...
Genetics
Sep 06, 2012 |
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ENCODE project: Researchers unlock disease information hidden in genome's control circuitry
Researchers at the University of Washington have determined that the majority of genetic changes associated with more than 400 common diseases and clinical traits affect the genome's regulatory circuitry. ...
Genetics
Sep 05, 2012 |
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A new light shed on genetic regulation's role in the predisposition to common diseases
An international team of researchers from King's College, Oxford University, Wellcome Trust Sanger Institute and Faculty of Medicine of University of Geneva, has discovered several thousands new genetic variants impacting ...
Genetics
Sep 02, 2012 |
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Researchers solve mystery surrounding the death of two sisters nearly 50 years ago
Researchers at Mount Sinai School of Medicine have identified the genetic cause of a rare and fatal bone disease by studying frozen skin cells that were taken from a child with the condition almost fifty years ago. Their ...
Genetics
Aug 29, 2012 |
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Scientists identify new gene that influences survival in amyotrophic lateral sclerosis
A team of scientists, including faculty at the University of Massachusetts Medical School (UMMS), have discovered a gene that influences survival time in amyotrophic lateral sclerosis (ALS, also known as Lou Gehrig's disease). ...
Genetics
Aug 26, 2012 |
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Fragile X and Down syndromes share signalling pathway for intellectual disability
Intellectual disability due to Fragile X and Down syndromes involves similar molecular pathways report researchers in The EMBO Journal. The two disorders share disturbances in the molecular events that regula ...
Genetics
Aug 03, 2012 |
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Researchers find new gene mutation associated with congenital myopathy
University of Michigan researchers have discovered a new cause of congenital myopathy: a mutation in a previously uncharacterized gene, according to research published this month in the American Journal of Human Genetics.
Genetics
Jul 25, 2012 |
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Cystic fibrosis makes airways more acidic, reduces bacterial killing
The human airway is a pretty inhospitable place for microbes. There are numerous immune defense mechanisms poised to kill or remove inhaled bacteria before they can cause problems. But cystic fibrosis (CF) disrupts these ...
Medical research
Jul 04, 2012 |
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New mouse model helps explain gene discovery in congenital heart disease
Scientists now have clues to how a gene mutation discovered in families affected with congenital heart disease leads to underdevelopment of the walls that separate the heart into four chambers. A Nationwide Children's Hospital ...
Genetics
Jun 26, 2012 |
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Researchers, with stem cells, advance understanding of spinal muscular atrophy
Cedars-Sinai's Regenerative Medicine Institute has pioneered research on how motor-neuron cell-death occurs in patients with spinal muscular atrophy, offering an important clue in identifying potential medicines to treat ...
Medical research
Jun 20, 2012 |
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A study shows that 'mosaicism' is gaining ground in cancer research
A study recently published in Nature Genetics provides new evidence that the genetic makeup of the embryo may cause the appearance of tumors in adult life. These results bear out the growing theory that some tumors may ha ...
Cancer
Jun 12, 2012 |
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Scientists find new genetic path to deadly diarrheal disease
Scientists have found new genetic information that shows how harmful bacteria cause the acute diarrheal disease shigellosis, which kills more than a million people worldwide each year.
Diseases, Conditions, Syndromes
Jun 11, 2012 |
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