RAD51B Antibody

1. We successfully identified a common variant, rs911263, as being significantly associated with the disease status . In addition, this SNP was shown to be related to erosion, a clinical assessment of disease severity in RA (P = 2.89 x 10(-5), OR = 0.52). These findings shed light on the role of RAD51B in the onset and severity of Rheumatoid arthritis (RA). PMID: 28361912
2. hypermethylation of homologous recombination DNA repair genes including RAD51B and XRCC3 is associated with an inflamed phenotype in squamous cell cancers of the head and neck, lung and cervix. PMID: 27683114
3. our study suggested that miRNA-binding site genetic variants of RAD51B may modify the susceptibility to cervical cancer, which is important to identify individuals with differential risk for this malignancy and to improve the effectiveness of preventive intervention. PMID: 27334422
4. common variation is significantly associated with familial breast cancer risk PMID: 27149063
5. over-expression of RAD51B promoted cell proliferation, aneuploidy, and drug resistance, while RAD51B knockdown led to G1 arrest and sensitized cells to 5-fluorouracil PMID: 27651161
6. a novel germ line RAD51B nonsense mutation, and reduced expression of RAD51B in melanoma cells indicating inactivation of RAD51B PMID: 25600502
7. Mutations in epithelial ovarian cancer cases were more frequent in RAD51C (14 occurrences, 0.41%) and RAD51D (12 occurrences, 0.35%) than in RAD51B (two occurrences, 0.06%). PMID: 26261251
8. the risk of developing AMD exhibits dose dependency as well as an epistatic combined effect in rs17105278 T>C and rs4902566 C>T carriers and that the elevated risk for rs17105278 T>C carriers may be due to decreased transcription of RAD51B. PMID: 24526414
9. Relative excess risk of breast cancer due to interaction between RAD51L1 single-nucleotide polymorphism and BMI. PMID: 25255808
10. Data indicate that complement factor H (CFH) R1210C and common variants in COL8A1 and RAD51B plus six genes contribute predictive information for advanced macular degeneration (AMD) beyond macular and behavioral phenotypes. PMID: 24498017
11. It confirms that RAD51 paralog mutations confer breast and ovarian cancer predisposition and are rare events. PMID: 24139550
12. This study provides robust evidence for an association of rheumatoid arthritis susceptibility with genes involved in B cell differentiation (BACH2) and DNA repair (RAD51B). PMID: 24022229
13. SNP in RAD51B at 14q24.1 was significantly associated with male breast cancer risk PMID: 23001122
14. Single nucleotide polymorphism in RAD51L1 is associated with breast cancer. PMID: 22454379
15. our results suggest that RAD51L1 is unlikely to represent a high-penetrance breast cancer susceptibility gene. PMID: 21533530
16. Single Nucleotide Polymorphisms in RAD51L1 gene is associated with glioblastoma. PMID: 22017238
17. rs11249433 at 1p.11.2, and two highly correlated single-nucleotide polymorphisms rs999737 and rs10483813 (r(2)= 0.98) at 14q24.1 (RAD51L1), for up to 46 036 invasive breast cancer cases and 46 930 controls from 39 studies, were genotyped. PMID: 21852249
18. findings support the notion that DNA repair genes, in particular RAD51L1, play a role in nasopharyngeal carcinoma etiology and development PMID: 21368091
19. polymorphisms in and haplotypes of the RAD51L1 gene, which is involved in the double-strand break repair pathway, modulate gamma-radiation-induced mutagen sensitivity. PMID: 20610542
20. BCR/ABL fragments were used for identifying the sites of BCR/ABL interaction with RAD51B PMID: 19657362
21. involved in the frequently occurring t(6;14) (p21;q23-->q24) in pulmonary chondroid hamartomas PMID: 11978964
22. Rad51B protein may have a specific function in Holliday junction processing in the homologous recombinational repair pathway in humans PMID: 12441335
23. motif in the N-terminus of Rad51B serves as an NLS that allows Rad51B to localize to the nucleus independent of Rad51C or BRCA2 PMID: 15701685
24. A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). PMID: 19330030

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HGNC: 9822

OMIM: 150699

KEGG: hsa:5890

STRING: 9606.ENSP00000419471

UniGene: Hs.172587