نتایج جستجو برای: hmlh1

تعداد نتایج: 646  

2015
Sanmitra Basu Subhadipa Majumder Ankur Bhowal Alip Ghosh Sukla Naskar Sumit Nandy Subhabrata Mukherjee Rajan Kumar Sinha Keya Basu Dilip Karmakar Soma Banerjee Sanghamitra Sengupta

Prostate cancer is one of the leading causes of mortality among aging males. There is an unmet requirement of clinically useful biomarkers for early detection of prostate cancer to reduce the liabilities of overtreatment and accompanying morbidity. The present population-based study investigates the factors disrupting expression of multiple functionally related genes of DNA mismatch repair path...

Journal: :The American journal of pathology 2003
Gyeong Hoon Kang Hyeon Joo Lee Kyu Sang Hwang Sun Lee Jae-Hoon Kim Jung-Sun Kim

Aberrant hypermethylation of promoter CpG islands is an important mechanism for the inactivation of tumor suppressor genes. CpG island hypermethylation occurs in relation to tumorigenesis or aging. Gastric cancer is one of the tumors with a high level of aberrant CpG island methylation. However, the data on the methylation status of normal gastric mucosa has been very limited. The present study...

2017
Wenting Li Ying Wang Xinzhi Fang Mei Zhou Yiqun Li Ying Dong Ruozheng Wang

BACKGROUND The aim of this study was to investigate the expression and the clinicopathologic significance of DNA methyltransferase 3B (DNMT3B), phosphatase and tensin homolog (PTEN) and human MutL homologs 1 (hMLH1) in endometrial carcinomas between Han and Uygur women in Xinjiang. MATERIAL AND METHODS The expression of DNMT3B, PTEN, and hMLH1 in endometrial carcinomas were assessed by immunohi...

Journal: :Carcinogenesis 2008
Kohzoh Imai Hiroyuki Yamamoto

DNA mismatch repair (MMR) deficiency results in a strong mutator phenotype and high-frequency microsatellite instability (MSI-H), which are the hallmarks of tumors arising within Lynch syndrome. MSI-H is characterized by length alterations within simple repeated sequences, microsatellites. Lynch syndrome is primarily due to germline mutations in one of the DNA MMR genes; mainly hMLH1 or hMSH2 a...

2007
M. Pedroni B. Roncari S. Maffei L. Losi A. Scarselli C. Di Gregorio M. Marino L. Roncucci P. Benatti G. Ponti G. Rossi M. Menigatti A. Viel M. Genuardi M. Ponz de Leon

Hereditary NonPolyposis Colorectal Cancer (Lynch syndrome) is an autosomal dominant disease caused by germline mutations in a class of genes deputed to maintain genomic integrity during cell replication, mutations result in a generalized genomic instability, particularly evident at microsatellite loci (Microsatellite Instability, MSI). MSI is present in 85-90% of colorectal cancers that occur i...

Journal: :Cancer research 2001
T Yan J E Schupp H S Hwang M W Wagner S E Berry S Strickfaden M L Veigl W D Sedwick D A Boothman T J Kinsella

Our previous data demonstrated that cells deficient in MutL homologue-1 (MLH1) expression had a reduced and shorter G(2) arrest after high-dose-rate ionizing radiation (IR), suggesting that the mismatch re pair (MMR) system mediates this cell cycle checkpoint. We confirmed this observation using two additional isogenetically matched human MLH1 (hMLH1)-deficient and -proficient human tumor cell ...

Journal: :Cancer research 2004
D Dean Potter Joseph A Murray John H Donohue Lawrence J Burgart David M Nagorney Jon A van Heerden Matthew F Plevak Alan R Zinsmeister Stephen N Thibodeau

Celiac disease is associated with an increased risk of small bowel adenocarcinoma. The aims of this study were to investigate the molecular basis, assess outcomes, and identify clinicopathologic characteristics of small bowel adenocarcinoma in celiac disease. Retrospective case control cohort study of all celiac disease patients treated at our institution for small bowel adenocarcinoma and matc...

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