نتایج جستجو برای: mlh3

تعداد نتایج: 113  

Journal: :Cancer research 2006
Nicholas P Taylor Matthew A Powell Randall K Gibb Janet S Rader Phyllis C Huettner Stephen N Thibodeau David G Mutch Paul J Goodfellow

MLH3 is a recently described member of the DNA mismatch repair gene family. Based on its interaction with the MutL homologue MLH1, it was postulated that MLH3 might play a role in tumorigenesis. Germ line and somatic mutations in MLH3 have been identified in a small fraction of colorectal cancers, but the role of MLH3 in colorectal cancer tumorigenesis remains controversial. We investigated MLH...

2014
Lennart M. Roesner Christian Mielke Silke Faehnrich Yvonne Merkhoffer Kurt E. J. Dittmar Hans G. Drexler Wilhelm G. Dirks

Mutations in human DNA mismatch repair (MMR) genes are commonly associated with hereditary nonpolyposis colorectal cancer (HNPCC). MLH1 protein heterodimerizes with PMS2, PMS1, and MLH3 to form MutLα, MutLβ, and MutLγ, respectively. We reported recently stable expression of GFP-linked MLH3 in human cell lines. Monitoring these cell lines during the cell cycle using live cell imaging combined wi...

Journal: :DNA repair 2006
Ziqiang Li Jonathan U Peled Chunfang Zhao Anton Svetlanov Diana Ronai Paula E Cohen Matthew D Scharff

Somatic hypermutation (SHM) and class switch recombination (CSR) allow B cells to make high affinity antibodies of various isotypes. Both processes are initiated by activation-induced cytidine deaminase (AID) to generate dG:dU mismatches in the immunoglobulin genes that are resolved differently in SHM and CSR to introduce point mutations and recombination, respectively. The MutL homolog MLH3 ha...

2017
Juan Du Maofeng Zhong Dong Liu Shufang Liang Xiaolin Liu Binbin Cheng Yani Zhang Zifei Yin Yuan Wang Changquan Ling

Traditional Chinese medicine formulates treatment according to body constitution (BC) differentiation. Different constitutions have specific metabolic characteristics and different susceptibility to certain diseases. This study aimed to assess the characteristic genes of gan-shen Yin deficiency constitution in different diseases. Fifty primary liver cancer (PLC) patients, 94 hypertension (HBP) ...

جهانی نژآد, طاهره, زعیمی, محمدعلی, شیخها, محمد حسن, پاشایی فر, حسین, کلانتر, سید مهدی ,

Introduction: Infertility is described as the inability to get pregnant after one year of unprotected intercourse. About half of infertility cases are because of male factors. Idiopathic azoospermia or severe oligozoospermia caused by genetic alterations is a significant part of male infertility. A key step of spermatogenesis is crossover events during meiotic reciprocal recombination. MLH3 pro...

Ghasemi N Jahaninejad T Kalantar SM Pashaiefar H Sheikhha MH,

Background: Infertility is increasingly recognized as a major health problem. Meiotic genes are very important candidates for genes contributing to female and male infertility. Mammalian MutL homologues have dual roles in DNA mismatch repair (MMR) after replication errors and meiotic reciprocal recombination. There are four MutL homologues in eukaryotes that mutations of three of them (Mlh1, Ml...

2013
Hossein Pashaiefar Mohammad Hasan Sheikhha Seyyed Mehdi Kalantar Tahereh Jahaninejad Mohammad Ali Zaimy Nasrin Ghasemi

BACKGROUND Meiotic genes are very important candidates for genes contributing to female and male infertility. Mammalian MutL homologues have dual roles in DNA mismatch repair (MMR) after replication errors and meiotic reciprocal recombination. The MutL homologs, MLH1 and MLH3, are crucial for meiotic reciprocal recombination and human fertility. In this study the functional polymorphisms of MLH...

Journal: :The Journal of Cell Biology 2005
Nadine K. Kolas Anton Svetlanov Michelle L. Lenzi Frank P. Macaluso Steven M. Lipkin R. Michael Liskay John Greally Winfried Edelmann Paula E. Cohen

Mammalian MutL homologues function in DNA mismatch repair (MMR) after replication errors and in meiotic recombination. Both functions are initiated by a heterodimer of MutS homologues specific to either MMR (MSH2-MSH3 or MSH2-MSH6) or crossing over (MSH4-MSH5). Mutations of three of the four MutL homologues (Mlh1, Mlh3, and Pms2) result in meiotic defects. We show herein that two distinct compl...

2013
Ricardo Mouro Pinto Ella Dragileva Andrew Kirby Alejandro Lloret Edith Lopez Jason St. Claire Gagan B. Panigrahi Caixia Hou Kim Holloway Tammy Gillis Jolene R. Guide Paula E. Cohen Guo-Min Li Christopher E. Pearson Mark J. Daly Vanessa C. Wheeler

The Huntington's disease gene (HTT) CAG repeat mutation undergoes somatic expansion that correlates with pathogenesis. Modifiers of somatic expansion may therefore provide routes for therapies targeting the underlying mutation, an approach that is likely applicable to other trinucleotide repeat diseases. Huntington's disease Hdh(Q111) mice exhibit higher levels of somatic HTT CAG expansion on a...

ژورنال: :مجله دانشگاه علوم پزشکی شهید صدوقی یزد 0
حسین پاشایی فر h pashaiefar محمد حسن شیخها mh sheikhha سید مهدی کلانتر m kalantar طاهره جهانی نژآد t jahaninejad محمدعلی زعیمی ma zaimy

مقدمه: حدود نیمی از موارد ناباروری زوجین به علت عوامل مردانه است. آزواسپرمی یا الیگواسپرمی شدید و بدون علت که در نتیجه تغییرات ژنتیکی حاصل می شود، بخش مهمی از ناباروری مردان را تشکیل می دهد. یک مرحله مهم در فرآیند اسپرماتوژنزیس وقایع کراسینگ اور در حین نوترکیبی هومولوگ در تقسیم میوز است. پروتئین mlh3 نقش اساسی در فرآیند نوترکیبی و اسپرماتوژنزیس دارد. این مطالعه به بررسی رابطه یک پلی مورفیسم عمل...

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