نتایج جستجو برای: pms2

تعداد نتایج: 505  

2013
Rong Bu Abdul K. Siraj Prashant Bavi Asim Belgaumi Wael Al-Haqawi Fouad Al-Dayel Shahab Uddin Fowzan S. Alkuraya Khawla S. Al-Kuraya

Biallelic germline mutations in the mismatch repair genes, including MLH1, MSH2, MSH6 or PMS2, lead to a recessive constitutional mismatch repair-deficiency (CMMR-D) syndrome characterized by early onset malignancies in children and young adults. Because consanguinity unmasks autosomal recessive disorders, we hypothesized that the frequency of CMMR-D is inflated in the highly consanguineous pop...

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...

2017
Wen-Chung Wang Ya-Ting Lee Yen-Chein Lai

BACKGROUND Granulosa cell tumors are rare ovarian malignancies. Their characteristics include unpredictable indolent growth with malignant potential and late recurrence. Approximately 95% are of adult type. Recent molecular studies have characterized the FOXL2 402C > G mutation in adult granulosa cell tumor. Our previous case report showed that unique FOXL2 402C > G mutation and defective DNA m...

Journal: :Genomics 1997
L R Osborne J A Herbrick T Greavette H H Heng L C Tsui S W Scherer

The human PMS2 mismatch repair gene and a family of at least 17 other related genes (named human PMSR or PMS2L genes) have been localized to human chromosome 7. Human PMS2 has been mapped previously to 7p22 and shown to be causative in hereditary nonpolyposis colon cancer (HNPCC), but the human PMS2L genes have not been positioned in the context of the physical or genetic map of chromosome 7. I...

2017
Sohail Jahid Jian Sun Ozkan Gelincik Pedro Blecua Winfried Edelmann Raju Kucherlapati Kathy Zhou Maria Jasin Zeynep H. Gümüş Steven M. Lipkin

Homologous recombination (HR) enables precise DNA repair after DNA double strand breaks (DSBs) using identical sequence templates, whereas homeologous recombination (HeR) uses only partially homologous sequences. Homeologous recombination introduces mutations through gene conversion and genomic deletions through single-strand annealing (SSA). DNA mismatch repair (MMR) inhibits HeR, but the role...

Journal: :Haematologica 2010
Katharina Wimmer Christian P Kratz

The mismatch repair (MMR) machinery contributes to genome integrity and the MLH1, MSH2, MSH6 and PMS2 genes play a crucial role in this process. MMR corrects single base-pair mismatches and small insertion-deletion loops that arise during replication. Moreover, the MMR system is involved in the cellular response to a variety of agents that damage DNA and in immunoglobulin class switch recombina...

2017
Sigurdis Haraldsdottir Thorunn Rafnar Wendy L Frankel Sylvia Einarsdottir Asgeir Sigurdsson Heather Hampel Petur Snaebjornsson Gisli Masson Daniel Weng Reynir Arngrimsson Birte Kehr Ahmet Yilmaz Stefan Haraldsson Patrick Sulem Tryggvi Stefansson Peter G Shields Fridbjorn Sigurdsson Tanios Bekaii-Saab Pall H Moller Margret Steinarsdottir Kristin Alexiusdottir Megan Hitchins Colin C Pritchard Albert de la Chapelle Jon G Jonasson Richard M Goldberg Kari Stefansson

Lynch syndrome, caused by germline mutations in the mismatch repair genes, is associated with increased cancer risk. Here using a large whole-genome sequencing data bank, cancer registry and colorectal tumour bank we determine the prevalence of Lynch syndrome, associated cancer risks and pathogenicity of several variants in the Icelandic population. We use colorectal cancer samples from 1,182 p...

Journal: :The Journal of Experimental Medicine 2008
Sophie Péron Ayse Metin Pauline Gardès Marie-Alexandra Alyanakian Eamonn Sheridan Christian Peter Kratz Alain Fischer Anne Durandy

Immunoglobulin (Ig) class switch recombination (CSR) deficiencies are rare primary immunodeficiencies characterized by the lack of switched isotype (IgG/IgA/IgE) production. In some cases, CSR deficiencies can be associated with abnormal somatic hypermutation. Analysis of CSR deficiencies has helped reveal the key functions of CSR-triggering molecules, i.e., CD40L, CD40, and effector molecules ...

Journal: :Voprosy onkologii 2021

Breast cancer (BC) is not a typical manifestation of Lynch syndrome. The existence and extent excessive breast risk in carriers pathogenic mutations the syndrome-associated genes (MLH1, MSH2, MSH6, PMS2) remains an open question. In addition, it known that some neoplasms patients with this syndrome are causally linked to hereditary mutation, arise completely independently defect gene DNA mismat...

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