About: Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families

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About: Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families Goto Sponge NotDistinct Permalink

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scientific article published on 01 February 1997

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1997 (uk) im Februar 1997 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en febreru de 1997 (ast) artikull shkencor i botuar më 01 shkurt 1997 (sq) scientific article published on 01 February 1997 (en)
publication date	wds:Q73085107-6284C701-8A1D-4ECF-B19B-DE07A98EF95E
publication date	1997-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q73085107-D7A8F8AE-0821-46BF-A908-AAFBCED01BD2
language of work or name	English
exact match	wds:Q73085107-85948122-4D46-44CF-BA21-C7BB711A680C
exact match	https://scigraph.springernature.com/pub.10.1038/sj.onc.1200881
author name string	wds:Q73085107-21BD5086-56F5-4954-9C5D-55A97A0DE665 wds:Q73085107-424BE991-CB78-45FC-8F7C-F67C06767644 wds:Q73085107-C41874F1-16D5-4A5D-B68D-D6FBE3DFD4AA wds:Q73085107-DD0FDF22-FECE-474A-ADEC-B0AAA87E4B6C wds:Q73085107-FBB8BBE3-CA88-4F12-B45D-07AC59B68255 wds:Q73085107-FD67644D-EF71-4F88-8533-BD5C5F750780 wds:Q73085107-FFD43E2D-A7A7-4668-A281-0822993BA1AC
author name string	Schlag PM Bender E Rohde K Scherneck S Seitz S Kölble K Nothnagel A
rdfs:label	Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families (en) Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families (nl) Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families (sq)
skos:prefLabel	Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families (en) Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families (nl) Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families (sq)
name	Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families (en) Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families (nl) Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families (sq)
title	wds:Q73085107-53FBE244-CA4C-49A0-B12F-C32994DCFBCB
title	Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families (en)
page(s)	wds:Q73085107-DE45B1AE-EC63-4EDB-A4B6-0C3A326034D2
page(s)	741-743
instance of	wds:Q73085107-D3DABCA7-E4CA-4BA5-A13E-887E76D3BC4D
instance of	scholarly article
main subject	wds:Q73085107-440D9369-C6D4-4D7A-B3B4-2774405CCE9B
main subject	breast cancer
PubMed ID	wds:Q73085107-F6D0AC7A-8157-47F0-9B96-79207E343587
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9038382
PubMed ID	9038382
published in	wds:Q73085107-75826F96-17C2-4184-AE29-50DBE8D6D31C
published in	Oncogene
issue	wds:Q73085107-48169434-0D96-4D60-913D-8C5379A934BC
volume	wds:Q73085107-B7BB2985-1036-406B-96E3-B55C16F43E73
issue	6
volume	14
DOI	wds:Q73085107-577AC612-50F4-437E-885F-3ED3590865E8
DOI	http://dx.doi.org/10.1038/SJ.ONC.1200881
DOI	10.1038/SJ.ONC.1200881
Dimensions Publication ID	wds:Q73085107-824A42F4-3E83-4CBF-B6A2-5F1562C1C3A3
Dimensions Publication ID	1051321142
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73085107
is cites work of	DNA copy number losses in human neoplasms The genetic epidemiology of breast cancer genes Aberrant methylation of the Wnt antagonist SFRP1 in breast cancer is associated with unfavourable prognosis Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium Analysis of DLC-1 expression in human breast cancer. Molecular classification of familial non-BRCA1/BRCA2 breast cancer Differential expression assay of chromosome arm 8p genes identifies Frizzled-related (FRP1/FRZB) and Fibroblast Growth Factor Receptor 1 (FGFR1) as candidate breast cancer genes Deletion mapping and linkage analysis provide strong indication for the involvement of the human chromosome region 8p12-p22 in breast carcinogenesis Refined deletion mapping in sporadic breast cancer at chromosomal region 8p12-p21 and association with clinicopathological parameters. Defining biochemical functions for the BRCA1 tumor suppressor protein: analysis of the BRCA1 binding protein BAP1. Allelic loss of chromosomal arm 8p in breast cancer progression. Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium BRCA1 and BRCA2: 1994 and beyond Overexpression of EXTL3/EXTR1 enhances NF-kappaB activity induced by TNF-alpha Pooled analysis of loss of heterozygosity in breast cancer: a genome scan provides comparative evidence for multiple tumor suppressors and identifies novel candidate regions Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus. Epigenetic inactivation of the miR-124-1 in haematological malignancies How many more breast cancer predisposition genes are there? Risk factors for breast cancer Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. A genome wide linkage search for breast cancer susceptibility genes Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: suggestive linkage to 10q23.32-q25.3. Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22 Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility Gene expression in inherited breast cancer Inherited susceptibility to colorectal adenomas and carcinomas: Evidence for a new predisposition gene on 15q14-q22 Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma Chromosome 3p allele loss in early invasive breast cancer: detailed mapping and association with clinicopathological features. Cancer incidence in relatives of a population-based set of cases of early-onset breast cancer with a known BRCA1 and BRCA2 mutation status Assessing changes in ages at onset over successive generation: an application to breast cancer Immunohistochemical classification of non-BRCA1/2 tumors identifies different groups that demonstrate the heterogeneity of BRCAX families Genetic testing for breast cancer predisposition No germline FH mutations in familial breast cancer patients On the birth of breast cancer HLS5, a novel RBCC (ring finger, B box, coiled-coil) family member isolated from a hemopoietic lineage switch, is a candidate tumor suppressor Genetic alteration of chromosome 8 is a common feature of human mammary epithelial cell lines transformed in vitro with benzo[a]pyrene Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping Dependence receptor UNC5D mediates nerve growth factor depletion-induced neuroblastoma regression BAP1 and breast cancer risk Long noncoding RNA TSLNC8 is a tumor suppressor that inactivates the interleukin-6/STAT3 signaling pathway.

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