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Chromosome 11 News and Research RSS Feed - Chromosome 11 News and Research

Humans normally have 46 chromosomes in each cell, divided into 23 pairs. Two copies of chromosome 11, one copy inherited from each parent, form one of the pairs. Chromosome 11 spans about 134 million DNA building blocks (base pairs) and represents between 4 percent and 4.5 percent of the total DNA in cells.

Identifying genes on each chromosome is an active area of genetic research. Because researchers use different approaches to predict the number of genes on each chromosome, the estimated number of genes varies. Chromosome 11 likely contains about 1,500 genes. More than 150 of these genes provide instructions for making olfactory receptors, which are proteins that are used to detect different smells.

Genes on chromosome 11 are among the estimated 20,000 to 25,000 total genes in the human genome.

Two more genetic risk factors for Alzheimer's disease discovered

7. September 2009 04:05
An international team of scientists has identified two more genetic risk factors for Alzheimer's disease. The findings are reported in the online edition of the journal Nature Genetics. [More]

New insight into human ciliopathy

4. August 2009 19:50
In the September 1st issue of G&D, Dr. Karen Oegema (UCSD) and colleagues identify the molecular basis of the lethal developmental disorder, hydrolethalus syndrome, and reveal that hydrolethalus syndrome actually belongs to the emerging class of human ciliopathy diseases. [More]

Discovery of gene variant associated with increased risk of atopic dermatitis

6. April 2009 22:18
Scientists of the Max Delbrück Center for Molecular Medicine (MDC) Berlin-Buch and Charité - University Medical School, Berlin, Germany, in collaboration with researchers from the Klinikum rechts der Isar of Technical University Munich and Christian Albrecht University, Kiel, have identified a gene variant on chromosome 11 that is associated with an increased risk of atopic dermatitis. [More]

Scientists pinpoint two new risk factors for Wilms tumour

1. December 2008 17:26
Scientists at The Institute of Cancer Research have made significant progress in pinpointing two new risk factors associated with the most common childhood kidney cancer, known as Wilms tumour. [More]

Posted in: Medical Research News

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Newly discovered mechanism can explain the Beckwith-Wiedemann syndrome

26. October 2008 17:39
Researchers from Uppsala University have discovered a mechanism that silences several genes in a chromosome domain. The findings, published in today's on-line issue of Molecular Cell, have implications in understanding the human disorder Beckwith-Wiedemann syndrome. [More]

Posted in: Medical Condition News

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Low levels of 'brain derived neurotrophic factor' may lead to obesity

28. August 2008 18:07
A brain chemical that plays a role in long term memory also appears to be involved in regulating how much people eat and their likelihood of becoming obese, according to a National Institutes of Health study of a rare genetic condition. [More]

deCODE discovers novel genetic links between pigmentation traits and risk of skin cancer

19. May 2008 01:18
In two papers published today, deCODE scientists and academic colleagues from Europe and the U.S. expand upon the company's recent findings in the genetics of pigmentation traits in people of European descent, and demonstrate that certain of these common variants also confer risk of two types of skin cancer. [More]

Posted in: Medical Research News

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Discovery of small molecule that disrupts Ewing's sarcoma oncogene

13. April 2008 22:28
Researchers at Georgetown University Medical Center have found a small molecule they say can block the action of the oncogene that causes Ewing's sarcoma, a rare cancer found in children and young adults. [More]

New research may lead to future gene therapies for patients with sickle cell anemia and beta-thalassemia

7. August 2007 07:15
Virginia Commonwealth University researchers studying hemoglobin genes, mutations of which play a role in genetic blood disorders like sickle cell anemia and beta-thalassemia, have identified two proteins that are responsible for regulating overlapping groups of genes during the development of red blood cells. [More]

Common DNA variations underlie susceptibility to fever after smallpox vaccination

19. June 2007 06:58
Their finding is the first to link individual differences written into the genetic code with a vaccine-related complication, albeit a mild one. [More]

Genetic factors linked to adverse events related to smallpox vaccination

17. June 2007 22:50
The study, published in the July 15th issue of The Journal of Infectious Diseases, now available online, may have implications for predicting adverse events from other live vaccines. . [More]

Posted in: Drug Trial News

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Researchers identify genetic markers associated with breast cancer tumor grade and lymph node metastases

16. May 2007 12:50
Researchers have identified genetic markers on several chromosomes in the tissue surrounding tumor cells that are associated with breast cancer tumor grade and the presence of lymph node metastases, according to a study in the May 16 issue of JAMA. [More]

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Genetic component to autism

10. May 2007 13:06
Using an innovative statistical approach, a research team from Washington University School of Medicine in St. Louis and the University of California, Los Angeles, has identified two regions of DNA linked to autism. [More]

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There may be a real code to chromosomal organization

4. May 2007 09:22
The identification of a cluster of essential genes on mouse chromosome 11 as well as similar clusters on the chromosomes of other organisms , including humans , buttresses the argument that there may be rules as to how genes are structured or laid out on chromosomes, said the Baylor College of Medicine senior author of a report that appears online in the Public Library of Science Genetics, an open-access publication. [More]

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Ten genetic variants associated with type 2 diabetes

27. April 2007 22:09
Ten genetic variants associated with type 2 diabetes, a disease which impacts more than 170 million people worldwide, have been identified or confirmed by a U.S.-Finnish team led by scientists at the University of Michigan School of Public Health. [More]

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