About: A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene

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About: A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene Goto Sponge NotDistinct Permalink

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scientific article published in The Journal of the American Medical Association

Attributes	Values
rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1995 (uk) im Februar 1995 veröffentlichter wissenschaftlicher Artikel (de) article publié dans la revue scientifique Journal of the American Medical Association (fr) scientific article published in The Journal of the American Medical Association (en)
publication date	wds:Q56438525-8A5B422E-763B-4090-8358-AE628DF772E7
publication date	1995-02-15 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56438525-2DB59C86-BBF7-45E3-BF88-E3E5E08D3FDA
language of work or name	English
author name string	wds:Q56438525-1B1EF0E3-5480-49B9-9AD0-347C97E64E73
author name string	Donna Shattuck-Eidens
rdfs:label	A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene (en) A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene (nl)
skos:prefLabel	A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene (en) A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene (nl)
name	A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene (en) A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene (nl)
title	wds:Q56438525-36E304A2-3E05-4D0E-84B1-78B9F154C872
title	A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene (en)
page(s)	wds:Q56438525-E102318F-A5F5-47CF-B28B-27B1AC9C14F5
page(s)	535
instance of	wds:Q56438525-50C7EFB3-75DB-4F69-8AA7-39C95BFEF171
instance of	scholarly article
main subject	wds:Q56438525-51B03F9F-81FE-4D15-882C-2E8FDE7F902C wds:Q56438525-669E3CFB-FA89-4657-9F11-DEB3097014E5
main subject	ovarian neoplasm collaboration
published in	wds:Q56438525-1F238A0D-3F5B-4A88-B21F-6419C4173AD1
published in	The Journal of the American Medical Association
issue	wds:Q56438525-0F1FFDEA-A977-4749-9D31-7EB557E4B400
volume	wds:Q56438525-6896228D-3047-4A62-8180-42390CE9F1DF
issue	7
volume	273
DOI	wds:Q56438525-74BA5A6C-48CA-41FB-AAAA-EAF35F49F322
DOI	http://dx.doi.org/10.1001/JAMA.1995.03520310033026
DOI	10.1001/JAMA.1995.03520310033026
ResearchGate publication ID	wds:Q56438525-3F7F652B-77EA-4F3D-BF63-A4C98CC89133
ResearchGate publication ID	236312052
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56438525
is cites work of	Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations Detection of protein folding defects caused by BRCA1-BRCT truncation and missense mutations. Controlled trial of pretest education approaches to enhance informed decision-making for BRCA1 gene testing. A somatic BRCA1 mutation in an ovarian tumour. Functional analysis of CpG methylation in the BRCA1 promoter region Mutational screening of breast cancer susceptibility gene 1 from early onset, bi-lateral, and familial breast cancer patients in Taiwan. Localization of human BRCA1 and its loss in high-grade, non-inherited breast carcinomas Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene. Breast Cancer Information Core Association of BRCA1 with Rad51 in mitotic and meiotic cells The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds The C-terminal (BRCT) domains of BRCA1 interact in vivo with CtIP, a protein implicated in the CtBP pathway of transcriptional repression BRCA1 mutations in German breast-cancer families. BRCA1 and BRCA2: different roles in a common pathway of genome protection Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis Germline BRCA1 185delAG mutations in Jewish women with breast cancer Tumour biological features of BRCA1-induced breast and ovarian cancer BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: relationship to family history and implications for genetic testing The LIM domain protein LMO4 interacts with the cofactor CtIP and the tumor suppressor BRCA1 and inhibits BRCA1 activity Breast cancer: cause and prevention Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations Genetic predisposition to breast cancer: a surgical perspective Brca1 deficiency results in early embryonic lethality characterized by neuroepithelial abnormalities Somatic mutations in the BRCA1 gene in sporadic ovarian tumours. Combined loss of BRCA1/BRCA2 in grade 3 breast carcinomas Human ovarian cancer of the surface epithelium BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals A human BRCA1 gene knockout Multiple primary cancers as a guide to heritability A canine model of familial mammary gland neoplasia Cytoplasmic mislocalization of BRCA1 caused by cancer-associated mutations in the BRCT domain. BRCA1 and BRCA2 gene mutations and risk of breast cancer. Public health perspectives Novel consensus DNA‐binding sequence for BRCA1 protein complexes BRCA1 and BRCA2 mutations in Scotland and Northern Ireland Future possibilities in the prevention of breast cancer: intervention strategies in BRCA1 and BRCA2 mutation carriers The BOADICEA model of genetic susceptibility to breast and ovarian cancer Characterisation of the BRCT Domains of the Breast Cancer Susceptibility Gene Product BRCA1 Screening for hereditary cancer and genetic testing, epitomized by breast cancer. Novel mutations in the BRCA1 and BRCA2 genes in Iranian women with early-onset breast cancer Breast cancer in women < or = 35 years: review of 1002 cases from a single institution. Response to radiation therapy and prognosis in breast cancer patients with BRCA1 and BRCA2 mutations. Rapid detection of BRCA1 mutations by the protein truncation test Germ line mutations associated with breast cancer susceptibility BRCA1 mutations in young women with breast cancer BRCA1 mutations and other sequence variants in a population-based sample of Australian women with breast cancer BRCA1: more than a hereditary breast cancer gene? High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage Consortium BRCA1 and BRCA2 mutations in Turkish familial and non-familial ovarian cancer patients: a high incidence of mutations in non-familial cases Ovarian cysts in women receiving tamoxifen for breast cancer Managing hereditary ovarian cancer risk Screening of BRCA1 mutation using immunohistochemical staining with C-terminal and N-terminal antibodies in familial ovarian cancers. Common BRCA1 and BRCA2 mutations in breast cancer families: a meta-analysis from systematic review Genes implicated in hereditary breast cancer syndromes Breast and ovarian cancer screening practices in healthy women with a strong family history of breast or ovarian cancer. BRCA1 Testing: Genetic Counseling Protocol Development and Counseling Issues The expanding role of yeast in cancer research and diagnosis: insights into the function of the oncosuppressors p53 and BRCA1/2 Immunohistochemically detected p53 and HER-2/neu expression and nuclear DNA content in familial epithelial ovarian carcinomas

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