نتایج جستجو برای: brca1 gene

تعداد نتایج: 1145741  

Journal: :medical journal of islamic republic of iran 0
amir mehrgou department of medical genetics and molecular biology, school of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) mansoureh akouchekian department of medical genetics and molecular biology, school of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences)

many factors including genetic, environmental, and acquired are involved in breast cancer development across various societies. among all of these factors in families with a history of breast cancer throughout several generations, genetics, like predisposing genes to develop this disease, should be considered more. early detection of mutation carriers in these genes, in turn, can play an import...

Introduction: Breast cancer is the most common malignancy in women worldwide. BRCA1 is a tumor suppressor gene that is involved in DNA-damage repair. One of the significant risk factors of breast cancer is the family history. BRCA1 gene consists of 24 exons that encode a protein with 1863 amino acids. Exon 11 is the largest exons and most of the disease-linked mutations have been found in it. I...

Amir Nader Emami Razavi, and Javad Tavakkoly Bazzaz, Farzaneh Darbeheshti, Mir Saeed Yekaninejad, Pantea Izadi,

Background: Previous studies have suggested that BRCA1 dysregulation has been shown to have a role in triple-negative phenotypic manifestation. However, differences of BRCA1 expression, as a tumor suppressor gene, have rarely been investigated between luminal and triple-negative breast tumors. Therefore, the present study attempted to compare the BRCA1 expression in triple-negative with lu...

Journal: :iranian journal of cancer prevention 0
nasrollah saleh gohari dept. of genetics, kerman university of medical sciences, kerman, iran marzye mohammadi-anaie genetic laboratory, afzalipour hospital, kerman, iran behjat kalantari-khandani dept. of oncology, kerman university of medical sciences, kerman, iran

background: breast cancer is the most common malignancy in iranian women. mutations in brca1 gene is one of the important genetic predisposing factors in breast cancer. this gene is a tumor suppressor that plays an important role in regulating the functions of rad51 protein for strand invasion in homologous recombination repair. methods: the brca1 gene has amplified in the dna isolated from bre...

Journal: :journal of research in medical sciences 0
maryam sedghi elham esfandiari esmat fazel-najafabadi mansoor salehi abbas salavaty shirin fattahpour

background: th e second leading cause of cancer deaths in women is breast cancer. germline mutations in susceptibility breast cancer gene brca1 increase the lifetime risk of breast cancer. eighty-one large genomic rearrangements (lgrs) have been reported up to date in brca1 gene, and evaluation of these rearrangements helps with precise risk assessment in high-risk individuals. in this study, w...

Journal: :cell journal 0

objective: cd44+/cd24-/low breast cancer cells have tumour-initiating properties with stem cell-like features. breast cancer gene 1 (brca1) is a tumour suppressor gene that plays a crucial role in dna repair and maintenance of chromosome stability. the clinicopathological features of breast cancer in brca1 mutation carriers suggest that brca1 may function as a stem-cell regulator. materials and...

Introduction:  Breast cancer is one of the leading causes of cancer death in women. Variations in the BRCA1, BRCA2, CDH1, STK11 and TP53 genes increase the risk of developing breast cancer. In addition to specific genetic changes, environmental factors may influence an individual’s risk of developing breast cancer. Lead is one of the most dangerous chemicals in the air as well as many products,...

Journal: :medical journal of islamic republic of iran 0
vahid yassaee shahid beheshti university of medical sciences, koodakyar st., daneshjoo blvd, velenjak ave., tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) a dalton north trent molecular genetics service, sheffield children’s hospital, western bank, sheffield - s102th, ukسازمان اصلی تایید شده: 0 دانشگاه های خارج از کشور

abstract background: many disease susceptibility genes are large and consist of many exons in which point mutations are scattered throughout. scanning each exon individually represents a tedious task which can be time consuming and expensive. there has been increasing demand for rapid and accurate methods for full scanning of unknown point mutations in large multi-exon genes. gene assembling is...

Journal: : 2022

Investigating the Genetic Diversity of BRCA1 Gene in some Domestic and Wild Sheep Breeds World Drawing their Phylogenetic Structure

ژورنال: پژوهش در پزشکی 2007
محرابی, یدالله, نقوی, بهار, علوی مجد, حمید, واحدی, محسن,

Background: Microarray DNA technology has paved the way for investigators to expressed thousands of genes in a short time. Analysis of this big amount of raw data includes normalization, clustering and classification. The present study surveys the application of clustering technique in microarray DNA analysis. Materials and methods: We analyzed data of Van’t Veer et al study dealing with BRCA1...

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