Chromosome 11q22.3-q25 LOH in ovarian cancer: association with a more aggressive disease course and involved subregions

scientific article published on 01 November 1998

Chromosome 11q22.3-q25 LOH in ovarian cancer: association with a more aggressive disease course and involved subregions is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1006/GYNO.1998.5186
P698PubMed publication ID9826475

P2093author name stringWinqvist R
Kytölä S
Launonen V
Huusko P
Stenbäck F
Kauppila A
Bloigu R
Puistola U
P2860cites workA single ataxia telangiectasia gene with a product similar to PI-3 kinaseQ24323579
P433issue2
P921main subjectovarian cancerQ172341
P304page(s)299-304
P577publication date1998-11-01
P1433published inGynecologic OncologyQ5625182
P1476titleChromosome 11q22.3-q25 LOH in ovarian cancer: association with a more aggressive disease course and involved subregions
P478volume71

Reverse relations

cites work (P2860)
Q4074427417Beta-estradiol is carcinogenic in human breast epithelial cells
Q34146321A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation
Q30840095Allelotype analysis of common epithelial ovarian cancers with special reference to comparison between clear cell adenocarcinoma with other histological types
Q78878349Chromosome analysis in 31 cases of benign and malignant breast tumors: a study in Brazil
Q35792001Combined array comparative genomic hybridization and tissue microarray analysis suggest PAK1 at 11q13.5-q14 as a critical oncogene target in ovarian carcinoma
Q34984197Cytogenetics and molecular genetics of ovarian cancer
Q34595670Decreased progesterone receptor isoform expression in luteal phase fallopian tube epithelium and high-grade serous carcinoma
Q43947306Definition of three minimal deleted regions by comprehensive allelotyping and mutational screening of FHIT,p16(INK4A), and p19(ARF) genes in nasopharyngeal carcinoma
Q37038663Gene products of chromosome 11q and their association with CCND1 gene amplification and tamoxifen resistance in premenopausal breast cancer
Q78085398Germ-line TP53 mutations in Finnish cancer families exhibiting features of the Li-Fraumeni syndrome and negative for BRCA1 and BRCA2
Q34230195HEPN1, a novel gene that is frequently down-regulated in hepatocellular carcinoma, suppresses cell growth and induces apoptosis in HepG2 cells
Q43856089High-resolution genomic analysis of the 11q13 amplicon in breast cancers identifies synergy with 8p12 amplification, involving the mTOR targets S6K2 and 4EBP1.
Q73263784Loss of heterozygosity at chromosomes 3, 6, 8, 11, 16, and 17 in ovarian cancer: correlation to clinicopathological variables
Q43889975Loss of heterozygosity on chromosome 11 in esophageal squamous cell carcinomas
Q35746355Loss of heterozygosity on chromosome 11q22-23 in melanoma is associated with retention of the insertion polymorphism in the matrix metalloproteinase-1 promoter
Q34580748Neoplastic transformation of human breast epithelial cells by estrogens and chemical carcinogens
Q34207789OPCML at 11q25 is epigenetically inactivated and has tumor-suppressor function in epithelial ovarian cancer
Q34786129Somatic mutations of the PPP2R1B candidate tumor suppressor gene at chromosome 11q23 are infrequent in ovarian carcinomas
Q36161205The BCSC-1 locus at chromosome 11q23-q24 is a candidate tumor suppressor gene
Q41337851The analysis of a large Danish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 11q24.