News tagged with gene family


Gene discoveries give hope against 'Brittle bone' disease

(HealthDay)—Mutations in a gene involved in bone development appear to cause certain severe forms of bone loss, a finding that could lead to new therapies for the common bone-thinning disorder osteoporosis, ...

Genetics created May 08, 2013 | popularity 5 / 5 (2) | comments 0

Family history of Alzheimer's associated with abnormal brain pathology

Close family members of people with Alzheimer's disease are more than twice as likely as those without a family history to develop silent buildup of brain plaques associated with Alzheimer's disease, according to researchers ...

Alzheimer's disease & dementia created Apr 17, 2013 | popularity 5 / 5 (1) | comments 0 | with audio podcast

Nearly half of breast cancer patients at risk of having BRCA mutations not sent for genetic testing

Only 53 percent of newly diagnosed breast cancer patients who were at high risk of carrying a BRCA 1 or BRCA 2 mutation – based on age, diagnosis, and family history of breast or ovarian cancer – reported that their doctors ...

Cancer created Apr 08, 2013 | popularity not rated yet | comments 0

Australia-led study in epilepsy breakthrough

An Australia-led study has identified a gene associated with a common form of epilepsy which could lead to earlier diagnosis, a researcher said Tuesday.

Genetics created Apr 02, 2013 | popularity 3 / 5 (1) | comments 0

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 created Mar 18, 2013 | popularity not rated yet | comments 0

Whole-exome sequencing identifies inherited mutations in autism

While autism clearly runs in some families, few inherited genetic causes have been found. A major reason is that these causes are so varied that it's hard to find enough people with a given mutation to establish a clear pattern. ...

Autism spectrum disorders created Jan 23, 2013 | popularity not rated yet | comments 0 | with audio podcast

Rare genetic faults identified in families with bowel cancer

(Medical Xpress)—Rare DNA faults in two genes have been strongly linked to bowel cancer by Oxford University researchers, who sequenced the genomes of people from families with a strong history of developing ...

Cancer created Dec 24, 2012 | popularity not rated yet | comments 0 | with audio podcast

Patients with family history of colorectal cancer may be at risk for aggressive form of the disease

BOSTON—When people with a family history of colorectal cancer develop the disease, their tumors often carry a molecular sign that the cancer could be life-threatening and may require aggressive treatment, Dana-Farber Cancer ...

Cancer created Dec 12, 2012 | popularity not rated yet | comments 0

'Smart' genes put us at risk of mental illness

(Medical Xpress)—Humans may be endowed with the ability to perform complex forms of learning, attention and function but the evolutionary process that led to this has put us at risk of mental illness.

Neuroscience created Dec 05, 2012 | popularity 5 / 5 (1) | comments 0 | with audio podcast

Researchers discover how the deadly malaria parasite evades the immune system, make progress toward developing a cure

(Medical Xpress)—More than a million people die each year of malaria caused by different strains of the Plasmodium parasite transmitted by the Anopheles mosquito. The medical world has yet to find an effective ...

Medical research created Dec 03, 2012 | popularity 5 / 5 (1) | comments 0 | with audio podcast

Most women who have double mastectomy don't need it, study finds

About 70 percent of women who have both breasts removed following a breast cancer diagnosis do so despite a very low risk of facing cancer in the healthy breast, new research from the University of Michigan Comprehensive ...

Cancer created Nov 27, 2012 | popularity not rated yet | comments 0

Exome sequencing: Potential diagnostic assay for unexplained intellectual disability

Research findings confirming that de novo mutations represent a major cause of previously unexplained intellectual disability were presented on Nov. 8 at the American Society of Human Genetics 2012 meeting in San Francisco.

Genetics created Nov 08, 2012 | popularity 5 / 5 (1) | comments 0

Cancer gene family member functions key to cell adhesion and migration

The WTX gene is mutated in approximately 30 percent of Wilms tumors, a pediatric kidney cancer. Like many genes, WTX is part of a family. In this case, WTX has two related siblings, FAM123A and FAM123C. While ...

Cancer created Aug 30, 2012 | popularity not rated yet | comments 0 | with audio podcast

Fainting: All in the family?

Fainting has a strong genetic predisposition, according to new research published in the August 7, 2012, print issue of Neurology, the medical journal of the American Academy of Neurology. Fainting, also called vasovagal syncop ...

Neuroscience created Aug 06, 2012 | popularity not rated yet | comments 0

Mice have distinct subsystem to handle smell associated with fear

A new study finds that mice have a distinct neural subsystem that links the nose to the brain and is associated with instinctually important smells such as those emitted by predators. That insight, published ...

Neuroscience created Jul 23, 2012 | popularity not rated yet | comments 0 | with audio podcast