نتایج جستجو برای: ژن pms2

تعداد نتایج: 16271  

2010
Bente A Talseth-Palmer Mary McPhillips Claire Groombridge Allan Spigelman Rodney J Scott

BACKGROUND Approximately 10% of Lynch syndrome families have a mutation in MSH6 and fewer families have a mutation in PMS2. It is assumed that the cancer incidence is the same in families with mutations in MSH6 as in families with mutations in MLH1/MSH2 but that the disease tends to occur later in life, little is known about families with PMS2 mutations. This study reports on our findings on mu...

2016
Kokichi Sugano Takeshi Nakajima Shigeki Sekine Hirokazu Taniguchi Shinya Saito Masahiro Takahashi Mineko Ushiama Hiromi Sakamoto Teruhiko Yoshida

Germline PMS2 gene mutations were detected by RT-PCR/direct sequencing of total RNA extracted from puromycin-treated peripheral blood lymphocytes (PBL) and multiplex ligation-dependent probe amplification (MLPA) analyses of Japanese patients with colorectal cancer (CRC) fulfilling either the revised Bethesda Guidelines or being an age at disease onset of younger than 70 years, and screened by m...

2012
Guixiang Ji Yan Long Yong Zhou Cong Huang Aihua Gu Xinru Wang

BACKGROUND The mismatch repair (MMR) pathway plays an important role in the maintenance of the genome integrity, meiotic recombination and gametogenesis. This study investigated whether genetic variations in MMR genes are associated with an increased risk of sperm DNA damage and male infertility. METHODS We selected and genotyped 21 tagging single nucleotide polymorphisms (SNPs) in five MMR g...

Journal: :Carcinogenesis 2000
S E Andrew X S Xu A Baross-Francis L Narayanan K Milhausen R M Liskay F R Jirik P M Glazer

DNA mismatch repair (MMR) deficiency leads to an increased mutation frequency and a predisposition to neoplasia. 'Knockout' mice deficient in the MMR proteins Msh2 and Pms2 crossed with mutation detection reporter (supF, lacI and cII) transgenic mice have been used to facilitate a comparison of the changes in mutation frequency and spectra. We find that the mutation frequency was consistently h...

2012
E Edwards M Bowman M Walsh J Kirk

Lynch syndrome is an autosomal dominant cancer predisposition syndrome which is caused by a germline mutation in one of four genes, MLH1, MSH2, MSH6 or PMS2. Individuals with a germline mutation in one of these genes are at increased lifetime risk of colon, endometrial, ovarian, small intestine, renal pelvis and ureter. Less commonly patients may develop biliary tract cancers, gastric and pancr...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2005
Sharlene Gill Noralane M Lindor Lawrence J Burgart Regenia Smalley Olga Leontovich Amy J French Richard M Goldberg Daniel J Sargent Jeremy R Jass John L Hopper Mark A Jenkins Joanne Young Melissa A Barker Michael D Walsh Andrew R Ruszkiewicz Stephen N Thibodeau

PURPOSE Most colorectal cancers that have high levels of microsatellite instability (MSI-H) show loss of immunohistochemical expression of proteins that participate in the DNA mismatch repair process, most often involving MLH1 and MSH2. Less commonly, a third DNA mismatch repair protein, MSH6, may also be lost as the primary event. Rarely, tumors with MSI-H show normal expression of these three...

Journal: :BMJ open 2016
Christophe Rosty Mark Clendenning Michael D Walsh Stine V Eriksen Melissa C Southey Ingrid M Winship Finlay A Macrae Alex Boussioutas Nicola K Poplawski Susan Parry Julie Arnold Joanne P Young Graham Casey Robert W Haile Steven Gallinger Loïc Le Marchand Polly A Newcomb John D Potter Melissa DeRycke Noralane M Lindor Stephen N Thibodeau John A Baron Aung Ko Win John L Hopper Mark A Jenkins Daniel D Buchanan

OBJECTIVES Immunohistochemistry for DNA mismatch repair proteins is used to screen for Lynch syndrome in individuals with colorectal carcinoma (CRC). Although solitary loss of PMS2 expression is indicative of carrying a germline mutation in PMS2, previous studies reported MLH1 mutation in some cases. We determined the prevalence of MLH1 germline mutations in a large cohort of individuals with a...

Journal: :Cancer research 2005
Peng-Chieh Chen Sandra Dudley Wayne Hagen Diana Dizon Leslie Paxton Denise Reichow Song-Ro Yoon Kan Yang Norman Arnheim R Michael Liskay Steven M Lipkin

Germ line DNA mismatch repair mutations in MLH1 and MSH2 underlie the vast majority of hereditary non-polyposis colon cancer. Four mammalian homologues of Escherichia coli MutL heterodimerize to form three distinct complexes: MLH1/PMS2, MLH1/MLH3, and MLH1/PMS1. Although MLH1/PMS2 is generally thought to have the major MutL activity, the precise contributions of each MutL heterodimer to mismatc...

2014
Vahid Ezzatizadeh Chiranjeevi Sandi Madhavi Sandi Sara Anjomani-Virmouni Sahar Al-Mahdawi Mark A. Pook

BACKGROUND Friedreich ataxia (FRDA), the most common autosomal recessive ataxia disorder, is caused by a dynamic GAA repeat expansion mutation within intron 1 of FXN gene, resulting in down-regulation of frataxin expression. Studies of cell and mouse models have revealed a role for the mismatch repair (MMR) MutS-heterodimer complexes and the PMS2 component of the MutLα complex in the dynamics o...

2015
Shinichiro Fukuhara Inik Chang Yozo Mitsui Takeshi Chiyomaru Soichiro Yamamura Shahana Majid Sharanjot Saini Guoren Deng Ankurpreet Gill Darryn K. Wong Hiroaki Shiina Norio Nonomura Yun-Fai C. Lau Rajvir Dahiya Yuichiro Tanaka

DNA mismatch repair (MMR) enzymes act as proofreading complexes that maintains genomic integrity and MMR-deficient cells show an increased mutation rate. MMR has also been shown to influence cell signaling and the regulation of tumor development. MMR consists of various genes and includes post-meiotic segregation (PMS) 2 which is a vital component of mutL-alpha. In prostate, the functional role...

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