نتایج جستجو برای: msh2

تعداد نتایج: 1696  

2017
Yulan Qing Stanton L Gerson

Whereas transformation events in hematopoietic malignancies may occur at different developmental stages, the initial mutation originates in hematopoietic stem cells (HSCs), creating a preleukemic stem cell (PLSC). Subsequent mutations at either stem cell or progenitor cell levels transform the PLSC into lymphoma/leukemia initiating cells (LIC). Thymic lymphomas have been thought to develop from...

Journal: :Journal of medical genetics 2001
A Wagner Y Hendriks E J Meijers-Heijboer W J de Leeuw H Morreau R Hofstra C Tops E Bik A H Bröcker-Vriends C van Der Meer D Lindhout H F Vasen M H Breuning C J Cornelisse C van Krimpen M F Niermeijer A H Zwinderman J Wijnen R Fodde

Hereditary non-polyposis colorectal cancer (HNPCC) is the most common genetic susceptibility syndrome for colorectal cancer. HNPCC is most frequently caused by germline mutations in the DNA mismatch repair (MMR) genes MSH2 and MLH1. Recently, mutations in another MMR gene, MSH6 (also known as GTBP), have also been shown to result in HNPCC. Preliminary data indicate that the phenotype related to...

Journal: :Blood 2003
Jane S Reese Lili Liu Stanton L Gerson

Mismatch repair deficiency is associated with carcinogenesis, increased spontaneous and induced mutagenesis, and resistance to methylating agents. In humans, leukemias and lymphomas arise in the background of mismatch repair deficiency, raising the possibility that hematopoiesis is abnormal as well. To address hematopoiesis in MSH2-/- mice, we collected marrow and performed serial transplantati...

Journal: :Current Biology 2002
Claudia Colussi Eleonora Parlanti Paolo Degan Gabriele Aquilina Deborah Barnes Peter Macpherson Peter Karran Marco Crescenzi Eugenia Dogliotti Margherita Bignami

Mismatch repair (MMR) corrects replication errors. It requires the MSH2, MSH6, MLH1, and PMS2 proteins which comprise the MutSalpha and MutLalpha heterodimers. Inactivation of MSH2 or MLH1 in human tumors greatly increases spontaneous mutation rates. Oxidation produces many detrimental DNA alterations against which cells deploy multiple protective strategies. The Ogg-1 DNA glycosylase initiates...

Journal: :The EMBO journal 1999
M R Ehrenstein M S Neuberger

During maturation of the immune response, IgM+ B cells switch to expression of one of the downstream isotypes (IgG, A or E). This class switching occurs by region-specific recombination within the IgH locus through an unknown mechanism. A lack of switch recombination in mice deficient in components of the DNA-dependent protein kinase (DNA-PK)-Ku complex has pointed to a role for non-homologous ...

Journal: :JAMA 2006
Judith Balmaña David H Stockwell Ewout W Steyerberg Elena M Stoffel Amie M Deffenbaugh Julia E Reid Brian Ward Thomas Scholl Brant Hendrickson John Tazelaar Lynn Anne Burbidge Sapna Syngal

CONTEXT Lynch syndrome is caused primarily by mutations in the mismatch repair genes MLH1 and MSH2. OBJECTIVES To analyze MLH1/MSH2 mutation prevalence in a large cohort of patients undergoing genetic testing and to develop a clinical model to predict the likelihood of finding a mutation in at-risk patients. DESIGN, SETTING, AND PARTICIPANTS Personal and family history were obtained for 191...

Journal: :BMB reports 2010
Young Mee Kim Chang Gyu Choe Somi Kim Cho In Ho Jung Won Young Chang Moonjae Cho

Hereditary non-polyposis colorectal cancer (HNPCC) is an autosomal dominant syndrome characterized by predisposition to early-onset cancers. HNPCC is caused by heterozygous loss-of-function mutations within the mismatch repair genes MLH1, MSH2, MSH6, PMS1, and PMS2. We genotyped the MLH1 and MSH2 genes in patients suffering from Lynch syndrome and in 11 unrelated patients who were diagnosed wit...

Journal: :The Journal of biological chemistry 2012
Victoria V Hargreaves Christopher D Putnam Richard D Kolodner

ATP binding causes the mispair-bound Msh2-Msh6 mismatch recognition complex to slide along the DNA away from the mismatch, and ATP is required for the mispair-dependent interaction between Msh2-Msh6 and Mlh1-Pms1. It has been inferred from these observations that ATP induces conformational changes in Msh2-Msh6; however, the nature of these conformational changes and their requirement in mismatc...

Journal: :Methods in molecular biology 2009
Marieke Aarts Marleen Dekker Rob Dekker Sandra de Vries Anja van der Wal Eva Wielders Hein Te Riele

Oligonucleotide-mediated gene targeting is an attractive alternative to current procedures to subtly modify the genome of mouse embryonic stem (ES) cells. However, oligonucleotide-directed substitution, insertion or deletion of a single or a few nucleotides was hampered by DNA mismatch repair (MMR). We have developed strategies to circumvent this problem based on findings that the central MMR p...

2017
Guénaëlle Levallet Fatéméh Dubois Pierre Fouret Martine Antoine Solenn Brosseau Emmanuel Bergot Michèle Beau-Faller Valérie Gounant Elisabeth Brambilla Didier Debieuvre Olivier Molinier Françoise Galateau-Sallé Julien Mazieres Elisabeth Quoix Jean-Louis Pujol Denis Moro-Sibilot Alexandra Langlais Franck Morin Virginie Westeel Gérard Zalcman

INTRODUCTION DNA repair is a double-edged sword in lung carcinogenesis. When defective, it promotes genetic instability and accumulated genetic alterations. Conversely these defects could sensitize cancer cells to therapeutic agents inducing DNA breaks. METHODS We used immunohistochemistry (IHC) to assess MSH2, XRCC5, and BRCA1 expression in 443 post-chemotherapy specimens from patients rando...

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