Germline BRCA2 mutations and the risk of esophageal squamous cell carcinoma

scientific article published on 27 August 2007

Germline BRCA2 mutations and the risk of esophageal squamous cell carcinoma is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1038/SJ.ONC.1210739
P698PubMed publication ID17724471
P5875ResearchGate publication ID6116793

P50authorPaolo BoffettaQ3362604
Reza MalekzadehQ7319758
Steven A. NarodQ50384888
Farhad IslamiQ56241019
Shahryar SemnaniQ42538504
P2093author name stringLi S
Dawsey SM
Ghadirian P
Nasrollahzadeh D
Sotoudeh M
Akbari MR
Pourshams A
Aghcheli K
Amanian D
Salahi R
Shakeri R
Zandvakili I
P2860cites workInternal repeats in the BRCA2 protein sequenceQ53173241
Familial cancer of the esophagus in Iran.Q54018059
Cancer incidence in persons with Fanconi anemia.Q55036178
Fancd2 functions in a double strand break repair pathway that is distinct from non-homologous end joiningQ64388682
Homozygous germ line mutation in exon 27 of murine Brca2 disrupts the Fancd2-Brca2 pathway in the homologous recombination-mediated DNA interstrand cross-links' repair but does not affect meiosisQ64388688
A polymorphic stop codon in BRCA2Q71735471
Common genetic variants of TP53 and BRCA2 in esophageal cancer patients and healthy individuals from low and high risk areas of northern ChinaQ73204400
Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese populationQ73459790
Allelic loss on chromosome bands 13q11-q13 in esophageal squamous cell carcinomaQ74123243
Evaluation of BRCA2 in the genetic susceptibility of familial esophageal cancerQ79333462
Fanconi anemia: adult head and neck cancer and hematopoietic mosaicismQ80389229
BRCA2 associates with acetyltransferase activity when bound to P/CAFQ22008033
BRCA2 suppresses cell proliferation via stabilizing MAGE-D1Q24304364
Transcriptional activation functions in BRCA2Q24317762
Insights into DNA recombination from the structure of a RAD51-BRCA2 complexQ24319669
Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatinQ24563629
Oesophageal cancer among the Turkomans of northeast IranQ24648926
A haplotype map of the human genomeQ24679827
BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structureQ27639649
EMSY links the BRCA2 pathway to sporadic breast and ovarian cancerQ28188794
Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout miceQ28191400
The emerging genetic and molecular basis of Fanconi anaemiaQ28199075
Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1Q28201328
RAB22 and RAB163/mouse BRCA2: proteins that specifically interact with the RAD51 proteinQ28506888
Abnormal cytokinesis in cells deficient in the breast cancer susceptibility protein BRCA2Q28513645
A human BRCA2 complex containing a structural DNA binding component influences cell cycle progressionQ28590448
Prediction of deleterious human allelesQ29614367
Biallelic inactivation of BRCA2 in Fanconi anemiaQ29616130
Identification of the breast cancer susceptibility gene BRCA2Q29616290
Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2.Q34541051
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancerQ34597168
Modifiers of risk of hereditary breast and ovarian cancerQ35084790
Prostate cancer susceptibility genes: lessons learned and challenges posedQ35147120
Oesophageal Cancer Studies in the Caspian Littoral of Iran: The Caspian Cancer RegistryQ36040506
Risk factors for pancreatic cancerQ36105414
Molecular pathogenesis of Fanconi anemia: recent progressQ36403092
Epidemiologic features of upper gastrointestinal tract cancers in Northeastern IranQ36694883
Deletion of Brca2 exon 27 causes hypersensitivity to DNA crosslinks, chromosomal instability, and reduced life span in mice.Q40666357
Familial risks of esophageal cancer among the Turkmen population of the Caspian littoral of IranQ44035129
Familial history of esophageal cancerQ44369291
Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemiaQ46254589
Increased prevalence of the BRCA2 polymorphic stop codon K3326X among individuals with familial pancreatic cancerQ50156693
P433issue9
P407language of work or nameEnglishQ1860
P921main subjectesophageal squamous cell carcinomaQ108442577
P304page(s)1290-1296
P577publication date2007-08-27
P1433published inOncogeneQ1568657
P1476titleGermline BRCA2 mutations and the risk of esophageal squamous cell carcinoma
P478volume27