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Mutation in deafness gene can help heal wounds and prevent infection
May 08, 2006
A mutation in a gene commonly associated with deafness can play an important part in improving wound healing, a scientist told the annual conference of the European Society of Human Genetics in Amsterdam, The Netherlands, today (Monday 8 May 2006). Dr. Stella Man, from the Institute of Cell and Molecular Sciences, Queen Mary's University, London, UK, said that the discovery may have implications for the treatment of a wide range of wounds, including post-surgery. Dr. Man and her team, led by Professor David Kelsell, were studying the association between a mutation of a gene (GJB2) which produces a protein called Cx26 which is the most common cause of genetic deafness. Professor Kelsell was the first to describe the link between Cx26 mutations and deafness in 1997. "Since many people carry this mutation", Dr. Man said, "and people who have just one such mutation are not deaf, we felt that there might be some evolutionary advantage to it, so we decided to investigate how the mutation affected the ability of cells to communicate with each other in the epidermis where Cx26 is also expressed."
The cells within tissues such as skin need to be able to communicate with each other in order to retain their correct characteristics and allow the tissue to grow and repair itself. One way that cells communicate is through the regulated opening and closing of channels called gap junctions that link cells together. The main components of these channels are proteins called connexins, of which Cx26 is one.
"When we looked at the function of Cx26 in a laboratory skin model", said Dr. Man, "we found that it was directly associated with wound healing and bacterial invasion. We concluded that there is a definite advantage to carrying a mutation in this protein."
If a drug that temporarily knocks out Cx26 protein can be successfully delivered to the wound, healing could be improved. Such a drug could be useful in a wide range of epidermal wounds, she said. The scientists now intend to test the effect of Cx26 mutation in other epithelial cell types, such as the gut, where defence against infection is also important.
"It is interesting to speculate that Cx26 deafness mutations have been selected over the evolutionary process due to their beneficial effects on wound healing," said Dr. Man.
European Society of Human Genetics
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Gene: Gene. History of genetics, Mendelian inheritance, Gene expression, Genetic code, Mutation, Gene targeting, The Selfish Gene, Copy number variation, ... Gene- centered view of evolution
by Frederic P. Miller (Editor), Agnes F. Vandome (Editor), John McBrewster (Editor)
Gene. History of genetics, Mendelian inheritance, Gene expression, Genetic code, Mutation, Gene targeting, The Selfish Gene, Copy number variation, DNA, Epigenetics, Gene- centered view of evolution, Gene therapy, Genetic algorithm, Genetics, Genome, Genomics, List of human genes, Meme, Pseudogene, Predictive medicine
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ABC News Nightline Confronting a Genetic Legacy
Imagine you were told that you carry a gene that makes it all but certain you will one day get breast cancer, ovarian cancer or both. What would you do? Jessica Queller, a 35-year-old writer for the hit series "Gilmore Girls," has had to answer that question. In 2004, she found out that she carries the BRCA1 gene mutation, or, the breast cancer gene. According to one study, possessing that gene means she has an 85 percent chance of developing breast cancer before the age of 70 and a 50 percent chance of developing it before the age of 50. Queller took the test because her mother had recently died of ovarian cancer, and several years earlier had fought and beaten breast cancer. Queller now knows what her mother never did, and now she is left in a place where modern science has told her...
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Mutation linked to some cases of Parkinson's: identifying gene raises ethical questions about its use in testing, given the lack of preventive therapy.(Neuropsychiatric ... An article from: Clinical Psychiatry News
by Christine Kilgore (Author)
This digital document is an article from Clinical Psychiatry News, published by International Medical News Group on April 1, 2005. The length of the article is 933 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.
Citation Details Title: Mutation linked to some cases of Parkinson's: identifying gene raises ethical questions about its use in testing, given the lack of preventive therapy.(Neuropsychiatric Medicine) Author: Christine Kilgore Publication: Clinical Psychiatry News (Magazine/Journal) Date: April 1, 2005 Publisher: International Medical News Group Volume: 33 Issue: 4 Page:...
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Limited Family Structure and BRCA Gene Mutation Status in Single Cases of Breast Cancer / Identifying Widely Covered Drugs and Drug Coverage Variation Among Medicare Part D Formularies (JAMA: The Journal of the American Medical Association, Volume 297, Number 23, June 20, 2007)
by J. N. Weitzel (Author)
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MRI best for carriers of BRCA gene mutations: study shows MRI detects more breast cancers in this population than do ultrasound or mammography.(Women's ... An article from: Family Practice News
by Betsy Bates (Author)
This digital document is an article from Family Practice News, published by International Medical News Group on December 1, 2004. The length of the article is 979 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.
Citation Details Title: MRI best for carriers of BRCA gene mutations: study shows MRI detects more breast cancers in this population than do ultrasound or mammography.(Women's Health)(Magnetic resonance imaging) Author: Betsy Bates Publication: Family Practice News (Magazine/Journal) Date: December 1, 2004 Publisher: International Medical News Group Volume: 34 Issue: 23 Page:...
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Mouse lymphoma thymidine kinase gene mutation assay: Meeting of the International Workshop on Genotoxicity Testing, San Francisco, 2005, recommendations ... Toxicology and Environmental Mutagenesis]
by M.M. Moore (Author), M. Honma (Author), J. Clements (Author), G. Bolcsfoldi (Author)
This digital document is a journal article from Mut.Res.-Genetic Toxicology and Environmental Mutagenesis, published by Elsevier in 2007. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description: The Mouse Lymphoma Assay (MLA) Workgroup of the International Workshop on Genotoxicity Testing (IWGT), comprised of experts from Japan, Europe and the United States, met on September 9, 2005, in San Francisco, CA, USA. This meeting of the MLA Workgroup was devoted to reaching a consensus on issues involved with 24-h treatment. Recommendations were made concerning the acceptable values for the negative/solvent control (mutant frequency, cloning efficiency and suspension growth)...
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American Cancer Society Film: Time is Life (1949) [DVD]
Time is Life highlights the importance of time in combating the second highest cause of death in the world, cancer. The film also underscores the efforts of the American Cancer Society towards the alleviation, if not elimination, of cancer in the American society. The film starts with Mary Bronson being stressed out with the possibility of having a cancer. Cancer is not given proper attention by the public so it causes insurmountable effects on people in the society. Cancer chooses no one. In addition, the film gives conveying figures on cancer fatalities in the United States saying that one in every eight American has cancer. The film has also mentioned that cancer has killed more Americans than the slaughter at the Pearl Harbor and Tokyo Bay during World War Two. The film also dispels...
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Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African Brazilians.: An article from: Human Biology
by C.A. Oliveira (Author), F. Alexandrino (Author), K. Abe-Sandes (Author), W.A. Silva (Author), A.T. Maciel-Guerra (Author), L.A. Magna (Author), E.L. Sartorato (Author)
This digital document is an article from Human Biology, published by Wayne State University Press on April 1, 2004. The length of the article is 1423 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.
From the author: KEY WORDS: GJB2, BRAZILIAN POPULATION, CONGENITAL DEAFNESS
Citation Details Title: Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African Brazilians. Author: C.A. Oliveira Publication: Human Biology (Refereed) Date: April 1, 2004 Publisher: Wayne State University Press Volume: 76 Issue: 2 Page: 313(4)
Distributed by...
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Screening of APOB gene mutations in subjects with clinical diagnosis of familial hypercholesterolemia.: An article from: Human Biology
by Erardo Merino-Ibarra (Author), Sergio Castillo (Author), Pilar Mozas (Author), Ana Cenarro (Author), Esperanza Martorell (Author), Jose Luis Diaz (Author), Manuel Suarez-Tembra (Author), Rodrigo Alonso (Author), Fernando Civeira (Author), Pedro Mata (Author), Miguel Pocovi (Author)
This digital document is an article from Human Biology, published by Thomson Gale on October 1, 2005. The length of the article is 4221 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.
From the author: KEY WORDS: FAMILIAL DEFECTIVE APOB, AUTOSOMAL DOMINANT MONOGENIC HYPERCHOLESTEROLEMIA (ADMH), HYPERCHOLESTEROLEMIA, APOB, LDLR, R3500Q MUTATION, T3552T MUTATION, SSCP (SINGLE-STRAND CONFORMATION POLYMORPHISM) ANALYSIS, SPAIN.
Citation Details Title: Screening of APOB gene mutations in subjects with clinical diagnosis of familial hypercholesterolemia. Author: Erardo...
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657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population.(Author Abstract): An article from: Human Biology
by Mustafa Tekin (Author), Duygu Akcayoz (Author), Canan Ucar (Author), Huseyin Gulen (Author), Nejat Akar (Author)
This digital document is an article from Human Biology, published by Thomson Gale on June 1, 2005. The length of the article is 1366 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.
From the author: KEY WORDS: FOUNDER EFFECT, NIJMEGEN BREAKAGE SYNDROME, NBS1, SLAVS, TURKS.
Citation Details Title: 657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population.(Author Abstract) Author: Mustafa Tekin Publication: Human Biology (Magazine/Journal) Date: June 1, 2005 Publisher: Thomson Gale Volume: 77 Issue: 3 Page: 393(5)
Article Type: Author...
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