About: sporadic breast cancer

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About: sporadic breast cancer Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

human disease

Attributes	Values
rdf:type	Item
description	human disease (en) Krankheit (de) մարդու հիվանդություն (hy) хвороба людини (uk) مرض يصيب الإنسان (ar)
exact match	wds:Q18557808-1D0DAF38-EC02-47EC-8204-DD3A841EE4E0 wds:Q18557808-E21993ED-EAAF-4504-B3BD-2A5BD9CE6526
exact match	http://purl.obolibrary.org/obo/DOID_8029 http://identifiers.org/doid/DOID:8029
Mondo ID	wds:Q18557808-3E26C259-3AF6-49C9-9141-4C8758065622
Disease Ontology ID	wds:Q18557808-211D490A-A2F5-41C0-A8AD-194775BD641C
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0004438
Disease Ontology ID	http://purl.obolibrary.org/obo/DOID_DOID:8029
Mondo ID	MONDO_0004438
Disease Ontology ID	DOID:8029
rdfs:label	sporadic breast cancer (en)
skos:prefLabel	sporadic breast cancer (en)
name	sporadic breast cancer (en)
instance of	wds:Q18557808-F7E7DA78-9238-4734-97F0-3E5C0BDD2110
instance of	class of disease
subclass of	wds:Q18557808-C7511328-F630-4C9F-8FF4-A18D8E6C7FBA
subclass of	breast carcinoma
skos:altLabel	Sporadic Breast Cancer (en) Sporadic Breast Carcinoma (en)
NCI Thesaurus ID	wds:Q18557808-26F78AB4-A0CD-4DA4-8A00-DD10C0F572EE
UMLS CUI	wds:Q18557808-26BCCFCD-A6A0-416E-A551-693E745D377D
on focus list of Wikimedia project	wds:Q18557808-90CBA992-B636-4241-81C1-8CDFB44BE423
NCI Thesaurus ID	C7566
UMLS CUI	C1336076
on focus list of Wikimedia project	WikiProject Medicine
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q18557808
is main subject of	Genetic variants in the H2AFX promoter region are associated with risk of sporadic breast cancer in non-Hispanic white women aged <or=55 years Quantitative analysis of mitochondrial DNA 4977-bp deletion in sporadic breast cancer and benign breast diseases DNA repair polymorphisms might contribute differentially on familial and sporadic breast cancer susceptibility: a study on a Portuguese population Prevalence of BER gene polymorphisms in sporadic breast cancer Contribution of XPD (Lys751Gln) and XRCC1 (Arg399Gln) polymorphisms in familial and sporadic breast cancer predisposition and survival: an Indian report Expression of FANCD2 in sporadic breast cancer and clinicopathological analysis BRCA1 promoter methylation in sporadic breast cancer is associated with reduced BRCA1 copy number and chromosome 17 aneusomy High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization Differential Cytotoxicity, Cellular Uptake, Apoptosis and Inhibition of BRCA1 Expression of BRCA1-Defective and Sporadic Breast Cancer Cells Induced by an Anticancer Ruthenium(II)-Arene Compound, RAPTA-EA1. Methylation of the BRCA1 gene in sporadic breast cancer Regulation of BRCA1 expression and its relationship to sporadic breast cancer Aberrant methylation of the BRCA1 CpG island promoter is associated with decreased BRCA1 mRNA in sporadic breast cancer cells Decreased expression of BRCA1 accelerates growth and is often present during sporadic breast cancer progression Amplification of the BRCA2 Pathway Gene EMSY in Sporadic Breast Cancer Is Related to Negative Outcome Refined deletion mapping in sporadic breast cancer at chromosomal region 8p12-p21 and association with clinicopathological parameters. Association of estrogen receptor and glucocorticoid receptor gene polymorphisms with sporadic breast cancer Decreased expression of angiogenesis antagonist EFEMP1 in sporadic breast cancer is caused by aberrant promoter methylation and points to an impact of EFEMP1 as molecular biomarker Down-regulation of BRCA1 in human sporadic breast cancer; analysis of DNA methylation patterns of the putative promoter region Low frequency of microsatellite instability in sporadic breast cancer Copy number alterations of the H2AFX gene in sporadic breast cancer patients. Distinction between hereditary and sporadic breast cancer on the basis of clinicopathological data Loss of WIF-1 and Wnt5a expression is related to aggressiveness of sporadic breast cancer in Tunisian patients Analyses of microsatellite instability and the transforming growth factor-beta receptor type II gene mutation in sporadic breast cancer and their correlation with clinicopathological features Detailed deletion mapping in sporadic breast cancer at chromosomal region 17p13 distal to the TP53 gene: association with clinicopathological parameters. Identification of a possible somatic BRCA1 mutation affecting translation efficiency in an early-onset sporadic breast cancer patient. Germ-line BRCA1 mutations in women with sporadic breast cancer: clinical correlations Progesterone receptor B (PRB) promoter hypermethylation in sporadic breast cancer: progesterone receptor B hypermethylation in breast cancer Prognostic significance of loss of heterozygosity at loci on chromosome 17p13.3-ter in sporadic breast cancer is evidence for a putative tumour suppressor gene Systematic characterisation of GABRP expression in sporadic breast cancer and normal breast tissue Human familial and sporadic breast cancer: analysis of the coding regions of the 17 beta-hydroxysteroid dehydrogenase 2 gene (EDH17B2) using a single-strand conformation polymorphism assay A polymorphism C3435T of the MDR-1 gene associated with smoking or high body mass index increases the risk of sporadic breast cancer in women Is Mitochondrial DNA Variation Associated with Sporadic Breast Cancer Risk? Genetic expression profiles and chromosomal alterations in sporadic breast cancer in Mexican women Significant involvement of CCR2-64I and CXCL12-3a in the development of sporadic breast cancer BRCA1 and BRCA2 germline mutations in Korean patients with sporadic breast cancer Absence of mutations in the ATM gene in forty-seven cases of sporadic breast cancer Epstein-Barr virus infection and sporadic breast cancer risk: a meta-analysis Low prevalence of BRCA1 exon rearrangements in familial and young sporadic breast cancer patients BP1, an isoform of DLX4 homeoprotein, negatively regulates BRCA1 in sporadic breast cancer Hypermethylation of tumor suppressor genes BRCA1, p16 and 14-3-3sigma in serum of sporadic breast cancer patients Genomic organization of claudin-1 and its assessment in hereditary and sporadic breast cancer Suppression of ING1 expression in sporadic breast cancer Association of vitamin D receptor gene polymorphism with sporadic breast cancer in Taiwanese patients. FANCD2 associated with sporadic breast cancer risk Association of a vitamin D receptor polymorphism with sporadic breast cancer development Familial and sporadic breast cancer cases in Iceland: A comparison related to ABO blood groups and risk of bilateral breast cancer Tumour characteristics, survival and prognostic factors of hereditary breast cancer from BRCA2-, BRCA1- and non-BRCA1/2 families as compared to sporadic breast cancer cases Polymorphisms and haplotypes of the NBS1 gene are associated with risk of sporadic breast cancer in non-Hispanic white women <or=55 years. Haplotype analysis of common variants in the BRCA1 gene and risk of sporadic breast cancer Association of Rad51 polymorphism with DNA repair in BRCA1 mutation carriers and sporadic breast cancer risk A haplotype-based case-control study of BRCA1 and sporadic breast cancer risk An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found Genetic and epigenetic modification of mismatch repair genes hMSH2 and hMLH1 in sporadic breast cancer with microsatellite instability Loss of BRCA2 correlates with reduced long-term survival of sporadic breast cancer patients A somatic mutation in the 5'UTR of BRCA1 gene in sporadic breast cancer causes down-modulation of translation efficiency. Simultaneous CXCL12 and ESR1 CpG island hypermethylation correlates with poor prognosis in sporadic breast cancer Mutation analysis of BRCA1 and BRCA2 from 793 Korean patients with sporadic breast cancer Analysis of CHEK2 FHA domain in Czech patients with sporadic breast cancer revealed distinct rare genetic alterations Cloning and characterization of an interstitial deletion at chromosome 11p15 in a sporadic breast cancer Association of CTLA-4 gene polymorphisms with sporadic breast cancer in Chinese Han population Association of CTLA-4 gene polymorphisms with sporadic breast cancer risk and clinical features in Han women of northeast China. B7-H4 gene polymorphisms are associated with sporadic breast cancer in a Chinese Han population PD-1 polymorphisms are associated with sporadic breast cancer in Chinese Han population of Northeast China. HVEM gene polymorphisms are associated with sporadic breast cancer in Chinese women Sporadic breast cancer in young women: prevalence of loss of heterozygosity at p53, BRCA1 and BRCA2 The neurofibromin 1 type I isoform predominance characterises female population affected by sporadic breast cancer: preliminary data MYC overexpression and poor prognosis in sporadic breast cancer with BRCA1 deficiency EGFR mutations in exons 18-21 in sporadic breast cancer

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