scholarly article | Q13442814 |
P50 | author | Paolo Boffetta | Q3362604 |
Reza Malekzadeh | Q7319758 | ||
Steven A. Narod | Q50384888 | ||
Farhad Islami | Q56241019 | ||
Shahryar Semnani | Q42538504 | ||
P2093 | author name string | Li S | |
Dawsey SM | |||
Ghadirian P | |||
Nasrollahzadeh D | |||
Sotoudeh M | |||
Akbari MR | |||
Pourshams A | |||
Aghcheli K | |||
Amanian D | |||
Salahi R | |||
Shakeri R | |||
Zandvakili I | |||
P2860 | cites work | Internal repeats in the BRCA2 protein sequence | Q53173241 |
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 joining | Q64388682 | ||
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 meiosis | Q64388688 | ||
A polymorphic stop codon in BRCA2 | Q71735471 | ||
Common genetic variants of TP53 and BRCA2 in esophageal cancer patients and healthy individuals from low and high risk areas of northern China | Q73204400 | ||
Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese population | Q73459790 | ||
Allelic loss on chromosome bands 13q11-q13 in esophageal squamous cell carcinoma | Q74123243 | ||
Evaluation of BRCA2 in the genetic susceptibility of familial esophageal cancer | Q79333462 | ||
Fanconi anemia: adult head and neck cancer and hematopoietic mosaicism | Q80389229 | ||
BRCA2 associates with acetyltransferase activity when bound to P/CAF | Q22008033 | ||
BRCA2 suppresses cell proliferation via stabilizing MAGE-D1 | Q24304364 | ||
Transcriptional activation functions in BRCA2 | Q24317762 | ||
Insights into DNA recombination from the structure of a RAD51-BRCA2 complex | Q24319669 | ||
Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin | Q24563629 | ||
Oesophageal cancer among the Turkomans of northeast Iran | Q24648926 | ||
A haplotype map of the human genome | Q24679827 | ||
BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure | Q27639649 | ||
EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer | Q28188794 | ||
Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice | Q28191400 | ||
The emerging genetic and molecular basis of Fanconi anaemia | Q28199075 | ||
Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1 | Q28201328 | ||
RAB22 and RAB163/mouse BRCA2: proteins that specifically interact with the RAD51 protein | Q28506888 | ||
Abnormal cytokinesis in cells deficient in the breast cancer susceptibility protein BRCA2 | Q28513645 | ||
A human BRCA2 complex containing a structural DNA binding component influences cell cycle progression | Q28590448 | ||
Prediction of deleterious human alleles | Q29614367 | ||
Biallelic inactivation of BRCA2 in Fanconi anemia | Q29616130 | ||
Identification of the breast cancer susceptibility gene BRCA2 | Q29616290 | ||
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 cancer | Q34597168 | ||
Modifiers of risk of hereditary breast and ovarian cancer | Q35084790 | ||
Prostate cancer susceptibility genes: lessons learned and challenges posed | Q35147120 | ||
Oesophageal Cancer Studies in the Caspian Littoral of Iran: The Caspian Cancer Registry | Q36040506 | ||
Risk factors for pancreatic cancer | Q36105414 | ||
Molecular pathogenesis of Fanconi anemia: recent progress | Q36403092 | ||
Epidemiologic features of upper gastrointestinal tract cancers in Northeastern Iran | Q36694883 | ||
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 Iran | Q44035129 | ||
Familial history of esophageal cancer | Q44369291 | ||
Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia | Q46254589 | ||
Increased prevalence of the BRCA2 polymorphic stop codon K3326X among individuals with familial pancreatic cancer | Q50156693 | ||
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | esophageal squamous cell carcinoma | Q108442577 |
P304 | page(s) | 1290-1296 | |
P577 | publication date | 2007-08-27 | |
P1433 | published in | Oncogene | Q1568657 |
P1476 | title | Germline BRCA2 mutations and the risk of esophageal squamous cell carcinoma | |
P478 | volume | 27 |