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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2004 1
2005 4
2006 6
2007 14
2008 5
2009 14
2010 7
2011 14
2012 9
2013 10
2014 7
2015 14
2016 18
2017 7
2018 7
2019 9
2020 1
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129 results
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Page 1
Regulation of Immunity by Butyrophilins.
Rhodes DA, Reith W, Trowsdale J. Rhodes DA, et al. Annu Rev Immunol. 2016 May 20;34:151-72. doi: 10.1146/annurev-immunol-041015-055435. Epub 2016 Jan 11. Annu Rev Immunol. 2016. PMID: 26772212 Review.
Molecules such as BTN3A1 (CD277), myelin oligodendrocyte glycoprotein, and mouse Skint1 and Btnl2, all members of the butyrophilin family, show greater structural and functional diversity than the canonical B7 receptors. ...
Molecules such as BTN3A1 (CD277), myelin oligodendrocyte glycoprotein, and mouse Skint1 and Btnl2, all members of the butyrophilin fa …
Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease.
Zhou F, Cao H, Zuo X, Zhang T, Zhang X, Liu X, Xu R, Chen G, Zhang Y, Zheng X, Jin X, Gao J, Mei J, Sheng Y, Li Q, Liang B, Shen J, Shen C, Jiang H, Zhu C, Fan X, Xu F, Yue M, Yin X, Ye C, Zhang C, Liu X, Yu L, Wu J, Chen M, Zhuang X, Tang L, Shao H, Wu L, Li J, Xu Y, Zhang Y, Zhao S, Wang Y, Li G, Xu H, Zeng L, Wang J, Bai M, Chen Y, Chen W, Kang T, Wu Y, Xu X, Zhu Z, Cui Y, Wang Z, Yang C, Wang P, Xiang L, Chen X, Zhang A, Gao X, Zhang F, Xu J, Zheng M, Zheng J, Zhang J, Yu X, Li Y, Yang S, Yang H, Wang J, Liu J, Hammarström L, Sun L, Wang J, Zhang X. Zhou F, et al. Nat Genet. 2016 Jul;48(7):740-6. doi: 10.1038/ng.3576. Epub 2016 May 23. Nat Genet. 2016. PMID: 27213287
We further identified multiple independent new susceptibility loci in HLA-C, HLA-B, HLA-DPB1 and BTNL2 and an intergenic variant, rs118179173, associated with psoriasis and confirmed the well-established risk allele HLA-C*06:02. ...
We further identified multiple independent new susceptibility loci in HLA-C, HLA-B, HLA-DPB1 and BTNL2 and an intergenic variant, rs1 …
The BTNL2 G16071A gene polymorphism increases granulomatous disease susceptibility: A meta-analysis including FPRP test of 8710 participants.
Tong X, Ma Y, Niu X, Yan Z, Liu S, Peng B, Peng S, Fan H. Tong X, et al. Medicine (Baltimore). 2016 Jul;95(30):e4325. doi: 10.1097/MD.0000000000004325. Medicine (Baltimore). 2016. PMID: 27472712 Free PMC article.
OBJECTIVE: The butyrophilin-like 2 (BTNL2) G16071A gene polymorphism has been implicated in the susceptibility to granulomatous diseases, but the results were inconclusive. ...Interestingly, the results of FPRP test indicated that the BTNL2 G16071A gene polymorphism …
OBJECTIVE: The butyrophilin-like 2 (BTNL2) G16071A gene polymorphism has been implicated in the susceptibility to granulomatous disea …
BTNL2 gene polymorphism and sarcoid uveitis.
Chaperon M, Pacheco Y, Maucort-Boulch D, Iwaz J, Perard L, Broussolle C, Jamilloux Y, Burillon C, Kodjikian L, Calender A, Seve P. Chaperon M, et al. Br J Ophthalmol. 2019 Dec;103(12):1690-1694. doi: 10.1136/bjophthalmol-2018-312949. Epub 2019 Mar 14. Br J Ophthalmol. 2019. PMID: 30872286
As BTNL2 (butyrophilin-like 2) gene polymorphism was found linked with the susceptibility to sarcoidosis, we investigated whether a specific genotype of BTNL2 gene G16071A (or rs2076530) single-nucleotide polymorphism (SNP) would be associated with the risk of sarco …
As BTNL2 (butyrophilin-like 2) gene polymorphism was found linked with the susceptibility to sarcoidosis, we investigated whether a s …
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
Debiec H, Dossier C, Letouzé E, Gillies CE, Vivarelli M, Putler RK, Ars E, Jacqz-Aigrain E, Elie V, Colucci M, Debette S, Amouyel P, Elalaoui SC, Sefiani A, Dubois V, Simon T, Kretzler M, Ballarin J, Emma F, Sampson MG, Deschênes G, Ronco P. Debiec H, et al. J Am Soc Nephrol. 2018 Jul;29(7):2000-2013. doi: 10.1681/ASN.2017111185. Epub 2018 Jun 14. J Am Soc Nephrol. 2018. PMID: 29903748 Free PMC article.
Conditional analysis identified two additional independent risk alleles upstream of HLA-DRB1 (rs28366266, P=3.7×10(-11)) and in the 3' untranslated region of BTNL2 (rs9348883, P=9.4×10(-7)) within introns of HCG23 and LOC101929163 These three risk alleles were independent …
Conditional analysis identified two additional independent risk alleles upstream of HLA-DRB1 (rs28366266, P=3.7×10(-11)) and in the 3' untra …
Butyrophilin-like 2 gene is associated with ulcerative colitis in the Japanese under strong linkage disequilibrium with HLA-DRB1*1502.
Mochida A, Kinouchi Y, Negoro K, Takahashi S, Takagi S, Nomura E, Kakuta Y, Tosa M, Shimosegawa T. Mochida A, et al. Tissue Antigens. 2007 Aug;70(2):128-35. doi: 10.1111/j.1399-0039.2007.00866.x. Tissue Antigens. 2007. PMID: 17610417
In contrast, five polymorphisms were significantly associated with UC, especially three single nucleotide polymorphisms (BTNL2_19, BTNL2_22 and BTNL2_23) were associated as a haplotype. ...The strong LD between BTNL2 and HLA-DRB1 raises another issue a …
In contrast, five polymorphisms were significantly associated with UC, especially three single nucleotide polymorphisms (BTNL2_19, …
Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15.
Traherne JA, Barcellos LF, Sawcer SJ, Compston A, Ramsay PP, Hauser SL, Oksenberg JR, Trowsdale J. Traherne JA, et al. Hum Mol Genet. 2006 Jan 1;15(1):155-61. doi: 10.1093/hmg/ddi436. Epub 2005 Dec 1. Hum Mol Genet. 2006. PMID: 16321988
The implicated gene, BTNL2, is adjacent to DR and is in strong LD with HLA-DRB1. This fact, combined with a sequence relationship between BTNL2 and myelin oligodendrocyte glycoprotein, an autoantigen associated with MS, makes the gene an attractive candidate. ...Fam …
The implicated gene, BTNL2, is adjacent to DR and is in strong LD with HLA-DRB1. This fact, combined with a sequence relationship bet …
Association of BTNL2 single nucleotide polymorphisms with knee osteoarthritis susceptibility.
Sun W, Min H, Zhao L. Sun W, et al. Int J Clin Exp Pathol. 2019 Oct 1;12(10):3921-3927. eCollection 2019. Int J Clin Exp Pathol. 2019. PMID: 31933783 Free PMC article.
OBJECTIVE: To investigate the association between SNP in the BTNL2 gene region and the susceptibility to osteoarthritis of the knee. ...Four SNP in the BTNL2 gene region were selected, whole DNA was extracted using the QIAamp blood DNA purification mini reagent, the …
OBJECTIVE: To investigate the association between SNP in the BTNL2 gene region and the susceptibility to osteoarthritis of the knee. …
The Roles of Genetic Factors in Kawasaki Disease: A Systematic Review and Meta-analysis of Genetic Association Studies.
Xie X, Shi X, Liu M. Xie X, et al. Pediatr Cardiol. 2018 Feb;39(2):207-225. doi: 10.1007/s00246-017-1760-0. Epub 2017 Nov 2. Pediatr Cardiol. 2018. PMID: 29098351 Review.
Besides, genetic variations in BTNL2, CASP3, FCGR2A, FGF23, FGβ, GRIN3A, HLA-E, IL10, ITPKC and TGFBR2 may serve as biomarkers of CALs in KD....
Besides, genetic variations in BTNL2, CASP3, FCGR2A, FGF23, FGβ, GRIN3A, HLA-E, IL10, ITPKC and TGFBR2 may serve as biomarkers of CAL …
Analysis of a functional BTNL2 polymorphism in type 1 diabetes, rheumatoid arthritis, and systemic lupus erythematosus.
Orozco G, Eerligh P, Sánchez E, Zhernakova S, Roep BO, González-Gay MA, López-Nevot MA, Callejas JL, Hidalgo C, Pascual-Salcedo D, Balsa A, González-Escribano MF, Koeleman BP, Martín J. Orozco G, et al. Hum Immunol. 2005 Dec;66(12):1235-41. doi: 10.1016/j.humimm.2006.02.003. Epub 2006 Mar 9. Hum Immunol. 2005. PMID: 16690410
Genotyping of the BTNL2 gene rs2076530 polymorphism was performed by real-time polymerase chain reaction technology, using the TaqMan 5'-allele discrimination assay. ...When the BTNL2 polymorphism was tested conditional on HLA DQB1-DRB1haplotypes, the BTNL2 e …
Genotyping of the BTNL2 gene rs2076530 polymorphism was performed by real-time polymerase chain reaction technology, using the TaqMan …
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