نتایج جستجو برای: brca2 gene promoter

تعداد نتایج: 1174704  

ژورنال: دانشور پزشکی 2019
Behboodi, Hossein , Faghihzadeh, Soghrat , Ghafarpour, Sarah , Ghazanfari, Tooba , Vafa, Ashraf , Zamani, Mohammad Saber ,

Introduction: IFN-γ is one of the most important cytokines in the development of chronic inflammatory diseases such as asthma and COPD. The IFN-γ promoter methylation at CpG islands could be altered by various chemical and toxic substances which may have a role in the incidence of chronic pulmonary diseases and its severity. Thereby, the present study was aimed to evaluate the effect of sulfur ...

Journal: :Journal of applied genetics 2003
Bohdan Górski Tadeusz Debniak Anna Jakubowska Cezary Cybulski Tomasz Huzarski Tomasz Byrski Elzbieta Złowocka Jan Lubiński

Founder mutations can account for a large proportion of BRCA1/BRCA2 gene abnormalities in a given population. However there is still a need to study the entire gene in many families, even in countries where founder mutations have been identified. It is possible to decrease the number of cases which are studied by complex and expensive sequencing/Southern blot analyses of BRCA1/BRCA2 genes by ex...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1998
L Y Marmorstein T Ouchi S A Aaronson

Germ-line mutations in the human BRCA2 gene confer susceptibility to breast cancer. Efforts to elucidate its function have revealed a putative transcriptional activation domain and in vitro interaction with the DNA repair protein RAD51. Other studies have indicated that RAD51 physically associates with the p53 tumor suppressor protein. Here we show that the BRCA2 gene product is a 460-kDa nucle...

Ebrahim Azizi Mohsen Alipour Naser Jafargholizadeh Seyed Jalal Zargar Shahrokh Safarian Shamileh Fouladdel

The p21 belongs to the CIP/KIP family of CDK inhibitors involved in cell cycle arrest at specific stages of the cell cycle progression. DNA methylation is the best studied epigenetic mark that have been evidently associated to chromatin condensation, and repression of gene transcription. The CpG island hypermethylation in promoter region of certain genes occurs in cancer cells and affects tumor...

2010
Safinaz S Ibrahim Elsayed E Hafez Mervat M Hashishe

BACKGROUND Breast cancer is one of the most common diseases affecting women. Inherited susceptibility genes, BRCA1 and BRCA2, are considered in breast, ovarian and other common cancers etiology. BRCA1 and BRCA2 genes have been identified that confer a high degree of breast cancer risk. OBJECTIVE Our study was performed to identify germline mutations in some exons of BRCA1 and BRCA2 genes for ...

Journal: :Cancer research 1996
U Hamann C Herbold S Costa E F Solomayer M Kaufmann G Bastert H U Ulmer H Frenzel D Komitowski

Recently, the breast cancer susceptibility gene BRCA2 has been identified in chromosome 13q, a region that also contains the retinoblastoma gene RB1. To elucidate a possible role of BRCA2 and RB1 in sporadic breast tumorigenesis, allelic imbalance (AI) at 13q loci was examined in 78 primary sporadic breast tumors. AI was found in 52-63% of tumors. Nine tumors showed AI only in the BRCA2 region ...

Journal: :Cancer research 2004
Isabelle Tournier Brigitte Bressac-de Paillerets Hagay Sobol Dominique Stoppa-Lyonnet Rosette Lidereau Michel Barrois Sylvie Mazoyer Florence Coulet Agnès Hardouin Agnès Chompret Alain Lortholary Pierre Chappuis Violaine Bourdon Valérie Bonadona Christine Maugard Brigitte Gilbert Catherine Nogues Thierry Frébourg Mario Tosi

Although screening for large deletions or duplications of the BRCA1 gene is becoming a routine component of the molecular diagnosis of familial breast cancer, little is known about the occurrence of such rearrangements in the BRCA2 gene. Because of the high frequency of BRCA2 mutations in breast cancer families with at least one case of male breast cancer, we selected a cohort of 39 such famili...

Journal: :The Journal of veterinary medical science 2003
Toshina Oonuma Masami Morimatsu Kazuhiko Ochiai Bunei Syuto

Mammary tumors are common in cats. As mutations in human Brca2 confer an increased risk of breast cancer, the full-length cDNA of the feline homologue of Brca2 was sequenced to obtain a basis for studying the relationship between its function and susceptibility to mammary tumors. The feline Brca2 cDNA is 10 kb long, and encodes 3,371 amino acids. The amino acid sequence of feline Brca2 shares l...

Journal: :Cancer research 2006
Tanja Pejovic Jane E Yates Hong Y Liu Laura E Hays Yassmine Akkari Yumi Torimaru Winifred Keeble R Keaney Rathbun William H Rodgers Allen E Bale Najim Ameziane C Michael Zwaan Abdellatif Errami Philippe Thuillier Fabio Cappuccini Susan B Olson Joanna M Cain Grover C Bagby

Fanconi anemia is an inherited cancer predisposition disease characterized by cytogenetic and cellular hypersensitivity to cross-linking agents. Seeking evidence of Fanconi anemia protein dysfunction in women at risk of ovarian cancer, we screened ovarian surface epithelial cells from 25 primary cultures established from 22 patients using cross-linker hypersensitivity assays. Samples were obtai...

2012
Audrey Rouault Guillaume Banneau Gaëtan MacGrogan Natalie Jones Nabila Elarouci Emmanuelle Barouk-Simonet Laurence Venat Isabelle Coupier Eric Letouzé Aurélien de Reyniès Françoise Bonnet Richard Iggo Nicolas Sévenet Michel Longy

INTRODUCTION Germline BRCA1 or BRCA2 mutations account for 20-30% of familial clustering of breast cancer. The main indication for BRCA2 screening is currently the family history but the yield of mutations identified in patients selected this way is low. METHODS To develop more efficient approaches to screening we have compared the gene expression and genomic profiles of BRCA2-mutant breast t...

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