BLK Antibody

1. our results indicated that the BLK rs13277113 polymorphism was involved in the genetic background of RA in Chinese population and the association of BANK1 rs3733197 polymorphism with RA was dependent on the genotype of BLK rs13277113 polymorphism, highlighting B-cell response implicated in the pathogenesis of RA. PMID: 28925718
2. present study suggests a novel association between specific TNFSF4 and BLK gene polymorphisms and allergic rhinitis risk. PMID: 28713926
3. This meta-analysis confirms that polymorphisms in the BLK alleles rs13277113 A/G, rs2736340 T/C, and rs2248932 T/C are associated with susceptibility to SLE in Caucasian and Asian populations. PMID: 27067206
4. Confirm the association of rs548234/ATG5, rs2736340/BLK and rs10516487/BANK1 with systemic lupus erythematosus in Chinese Han and reinforced our hypothesis of their epistasis effect in regulating B-cell signaling in SLE. PMID: 26420661
5. ur study provides evidence that human BLK is a true proto-oncogene capable of inducing tumors, and we demonstrate a novel BLK activity-dependent tumor model suitable for studies of BLK-driven lymphomagenesis and screening of novel BLK inhibitors in vivo. PMID: 28670978
6. rs13277113 GA genotype of BLK is more frequent in Systemic Lupus Erythematosus patients and may have a role in low gene expression and increased flares PMID: 27864698
7. current meta-analysis suggested that FAM167A-BLK rs2736340 polymorphism is associated with several autoimmune diseases PMID: 27105348
8. the SNPs in TNFSF4 and FAM167A-BLK may be involved in asthma and allergic rhinitis gene risk in the Han Chinese cohort. PMID: 27088737
9. The systemic lupus erythematosus variant Ala71Thr of BLK severely decreases protein abundance and binding to BANK1 through impairment of the SH3 domain function. PMID: 26821283
10. Report a novel BLK gene variant in common variable immunodeficiency-patients that causes suppressed B-cell proliferation and reduced ability of B-cells to elicit antigen-specific CD4(+) T-cell responses. PMID: 25926555
11. A major mechanism underlying the BLK association with autoimmune disease involves lowered thresholds for basal B cell receptor signaling, enhanced B cell-T cell interactions, and altered patterns of isotype switching. PMID: 26246128
12. our study reveals a previously unappreciated role of reduced BLK expression on extraperitoneal accumulation of B1a cells in mice, as well as the presence of IgG autoantibodies and B1-like cells in humans. PMID: 25972485
13. Results support previous findings that vaiants in the RHOB and FAM167A-BLK genes may be associated with susceptibility to systemic sclerosis. PMID: 25470816
14. These results place Blk upstream of the p190RhoGAP-RhoA pathway in Galpha13-activated cells, overall representing an opposing signaling module during CXCL12-triggered invasion. PMID: 25025568
15. Report role of BLK genetic variants in confering risk of systemic lupus erythematosus in Chinese population. PMID: 24091983
16. The observations suggested that C8orf13-BLK, in combination with STAT4, plays a pivotal role in creating genetic susceptibility to polymyositis/dermatomyositis in Japanese individuals. PMID: 24632671
17. B-lymphoid tyrosine kinase (Blk) is an oncogene and a potential target for therapy with dasatinib in cutaneous T-cell lymphoma PMID: 24919804
18. results demonstrated that both lupus-associated functional variants contribute to the autoimmune disease association by modulating transcription of BLK in B cells and thus potentially altering immune responses PMID: 24702955
19. Our study confirms evidence for epistasis between BLK and BANK1 in systemic lupus erythematosis from a Chinese population for the first time. PMID: 24085759
20. The BLK region was significantly associated with Kawasaki disease susceptibility in populations of Korean and European descent. PMID: 24023612
21. BANK1 and BLK have roles in B-cell signaling through phospholipase C gamma 2 PMID: 23555801
22. SNPs of the FAM167A-BLK region, but not the BANK1 SNPs, were associated with the development of primary Sjogren's syndrome in Han Chinese. PMID: 23899688
23. This study confirms BANK1 as an RA susceptibility gene and for the first time provides evidence for epistasis between BANK1 and BLK in RA. PMID: 23646104
24. study demonstrated that the loss-of-function BLK-p.A71T mutation is very unlikely to cause MODY; instead, it may modestly influence type 2 diabetes risk through an interaction with obesity PMID: 23224494
25. the functional SNP BLK rs2248932 T/C variant allele was associated with rheumatoid arthritis development PMID: 22740142
26. Blk allele expression differences at the protein level are restricted to early B cells. PMID: 22678060
27. The genetic variants in the promoter region of BLK may cause dysregulation of BLK expression, which might finally contribute to the initiation and progression of systemic lupus erythematosus. PMID: 22313735
28. BCR-ABL downregulates the Blk gene (encoding B-lymphoid kinase) through c-Myc in leukemic stem cells in chronic myeloid leukemia PMID: 22797726
29. Expression of RUNX1 isoforms and its target gene BLK in childhood acute lymphoblastic leukemia. PMID: 22748822
30. Rare and common regulatory variants in BLK are involved in disease susceptibility in systemic lupus erythematosus. PMID: 22696686
31. Single nucleotide polymorphism in BLK gene is associated with Kawasaki disease. PMID: 22446961
32. allelic variation in Blk does not play a major role in determining multifocal motor neuropathy susceptibility. PMID: 22003931
33. This study shows a genetic interaction between BANK1 and BLK, and demonstrates that these molecules interact physically. PMID: 21978998
34. Moderate evidence exists for an association between the BLK rs13277113, rs2248932 variants and systemic lupus erythematosus. PMID: 21152986
35. study evaluated SNP rs2248932 from BLK and further defined its role in systemic lupus erythematosus (SLE) risk; its association with SLE was confirmed in Chinese Han population PMID: 20130895
36. studies found that IRF5, STAT4 and BLK are associated not only with systemic lupus erythematosus, but also rheumatoid arthritis and systemic sclerosis [review] PMID: 20453440
37. our results do not support a major implication of the C8orf13-BLK gene region in susceptibility to Giant cell arteritis PMID: 20156505
38. Results indicate the FAM167A-BLK region may be a shared genetic factor for a number of autoimmune diseases in multiple populations, but the genetic contribution may be grater in Asian populations. PMID: 19740902
39. genetic polymorphism is associated with systemic sclerosis in North-American and European populations PMID: 19796918
40. Our findings indicate that the rs13277113A allele is associated not only with SLE but also with SSc and that the FAM167A-BLK region is a common genetic risk factor for both SLE and SSc. PMID: 20131239
41. transcription of the B cell-specific blk gene is regulated by NERF/ELF-2 and AMl1 PMID: 14970218
42. identified and confirmed through replication two new genetic loci for SLE: a promoter-region allele associated with reduced expression of BLK and increased expression of C8orf13 and variants in the ITGAM-ITGAX region PMID: 18204098
43. The association of the C8orf13-BLK region with systemic lupus erythematosus was replicated in a Japanese population. PMID: 19180478
44. Our data confirmed association of STAT4 (rs7574865, odds ratio (OR) =1.71, P=3.55 x 10(-23)) and BLK (rs13277113, OR=0.77, P=1.34 x 10(-5)) with SLE PMID: 19225526
45. Blk is constitutively tyrosine phosphorylated in malignant cutaneous T-cell lymphoma cell lines and spontaneously active in kinase assays PMID: 19351960
46. STAT4 and BLK displayed a strong genetic association with primary antiphospholipid syndrome. PMID: 19644876
47. Findings point to BLK as a previously unrecognized modulator of beta-cell function, the deficit of which may lead to the development of diabetes. PMID: 19667185
48. Observational study and genome-wide association study of gene-disease association and gene-gene interaction. (HuGE Navigator) PMID: 19503088

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HGNC: 1057

OMIM: 191305

KEGG: hsa:640

STRING: 9606.ENSP00000259089

UniGene: Hs.146591