نتایج جستجو برای: msh2

تعداد نتایج: 1696  

Journal: :Journal of clinical pathology 2011
Emma Barrow D Gareth Evans Ray McMahon James Hill Richard Byers

AIMS Lynch Syndrome is caused by mutations in DNA mismatch repair (MMR) genes. Mutation carrier identification is facilitated by immunohistochemical detection of the MMR proteins MHL1 and MSH2 in tumour tissue and is desirable as colonoscopic screening reduces mortality. However, protein detection by conventional immunohistochemistry (IHC) is subjective, and quantitative techniques are required...

Journal: :Stroke 2017
Robert Shenkar Changbin Shi Cecilia Austin Thomas Moore Rhonda Lightle Ying Cao Lingjiao Zhang Meijing Wu Hussein A Zeineddine Romuald Girard David A McDonald Autumn Rorrer Carol Gallione Peter Pytel James K Liao Douglas A Marchuk Issam A Awad

BACKGROUND AND PURPOSE We sought to compare the effect of chronic treatment with commonly tolerated doses of Fasudil, a specific RhoA kinase (ROCK) inhibitor, and simvastatin (with pleiotropic effects including ROCK inhibition) on cerebral cavernous malformation (CCM) genesis and maturation in 2 models that recapitulate the human disease. METHODS Two heterozygous murine models, Ccm1+/-Msh2-/-...

ژورنال: :پژوهنده 0
دکتر مهسا مولایی mahsa molaei department of pathology, research institute for gastroenterology and liver disease, shahid beheshti university, m.c., tehran, iran.تهران، اوین، بیمارستان طالقانی، طبقه هفتم، مرکز تحقیقات بیماریهای گوارش و کبد دکتر مهدی یداله زاده mahdi yadollahzadeh دکتر رضا مشایخی reza mashayekhi شهره الماسی shohreh almasi دکتر سیدرضا فاطمی seyed reza fatemi دکتر محمدرضا زالی mohammad reza zali

سابقه و هدف: بیشتر سرطانهای کولون از پولیپ های خوش خیم منشاء می گیرند. با پیشرفت آهسته و مرحله به مرحله بافت شناسی پولیپ های آدنوماتوز و آدنوم serrated به آدنوکارسینوم و سرطان بدخیم تبدیل می شوند. تغییرات ژنتیکی و اپی ژنتیک با مراحل خاصی از پیشرفت پولیپ به آدنوکارسینوم و نیز تغییرات بافت شناسی در سرطان کولون ارتباط دارد. در این مطالعه، با استفاده از رنگ آمیزی immunohistochemistry (ihc) در پولیپ...

Journal: :Journal of medical genetics 1999
N J Froggatt J Green C Brassett D G Evans D T Bishop R Kolodner E R Maher

The frequency, origin, and phenotypic expression of a germline MSH2 gene mutation previously identified in seven kindreds with hereditary non-polyposis cancer syndrome (HNPCC) was investigated. The mutation (A-->T at nt943+3) disrupts the 3' splice site of exon 5 leading to the deletion of this exon from MSH2 mRNA and represents the only frequent MSH2 mutation so far reported. Although this mut...

Journal: :Current Biology 1996
Ingram Iaccarino Fabio Palombo James Drummond Nicholas F. Totty J.Justin Hsuan Paul Modrich Josef Jiricny

The process of post-replicative DNA-mismatch repair seems to be highly evolutionarily conserved. In Escherichia coli, DNA mismatches are recognized by the MutS protein. Homologues of the E. coli mutS and mutL mismatch-repair genes have been identified in other prokaryotes, as well as in yeast and mammals. Recombinant Saccharomyces cerevisiae MSH2 (MSH for MutS homologue) and human hMSH2 protein...

Journal: :Nucleic Acids Research 2005
Sreeparna Banerjee Hernan Flores-Rozas

Cadmium (Cd2+) is a known carcinogen that inactivates the DNA mismatch repair (MMR) pathway. In this study, we have tested the effect of Cd2+ exposure on the enzymatic activity of the mismatch binding complex MSH2-MSH6. Our results indicate that Cd2+ is highly inhibitory to the ATP binding and hydrolysis activities of MSH2-MSH6, and less inhibitory to its DNA mismatch binding activity. The inhi...

Journal: :Genetics 1999
M Vedel A Nicolas

We have examined meiotic recombination at the CYS3 locus. Genetic analysis indicates that CYS3 is a hotspot of meiotic gene conversion, with a putative 5'-3' polarity gradient of conversion frequencies. This gradient is relieved in the presence of msh2 and pms1 mutations, indicating an involvement of mismatch repair functions in meiotic recombination. To investigate the role of mismatch repair ...

Journal: :Journal of experimental botany 2011
Luciana D Lario Elena Ramirez-Parra Crisanto Gutierrez Paula Casati Claudia P Spampinato

Deleterious effects of UV-B radiation on DNA include the formation of cyclobutane pyrimidine dimers (CPDs) and pyrimidine (6-4) pyrimidone photoproducts (6-4PPs). These lesions must be repaired to maintain the integrity of DNA and provide genetic stability. Of the several repair systems involved in the recognition and removal of UV-B-induced lesions in DNA, the focus in the present study was on...

2017
Junxiao Zhang Xiaoyan Wang Richarda M de Voer Jayne Y. Hehir-Kwa Eveline J Kamping Robbert D.A. Weren Marcel Nelen Alexander Hoischen Marjolijn J.L. Ligtenberg Nicoline Hoogerbrugge Xiangling Yang Zihuan Yang Xinjuan Fan Lei Wang Huanliang Liu Jianping Wang Roland P. Kuiper Ad Geurts van Kessel

The currently known Mendelian colorectal cancer (CRC) predisposition syndromes account for ~5-10% of all CRC cases, and are caused by inherited germline mutations in single CRC predisposing genes. Using molecular inversion probes (MIPs), we designed a targeted next-generation sequencing panel to identify mutations in seven CRC predisposing genes: APC, MLH1, MSH2, MSH6, PMS2, MUTYH and NTHL1. Fr...

Journal: :The Journal of Experimental Medicine 2004
Stella A. Martomo William W. Yang Patricia J. Gearhart

Somatic hypermutation is initiated by activation-induced cytidine deaminase (AID), and occurs in several kilobases of DNA around rearranged immunoglobulin variable (V) genes and switch (S) sites before constant genes. AID deaminates cytosine to uracil, which can produce mutations of C:G nucleotide pairs, and the mismatch repair protein Msh2 participates in generating substitutions of downstream...

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