about
Identification of novel single nucleotide substitutions in the NKp30 gene expressed in human natural killer cellsAssociation of HLA-DRB1*0901-DQB1*0303 haplotype with microscopic polyangiitis in JapaneseAssociation of human leukocyte antigen with interstitial lung disease in rheumatoid arthritis: a protective role for shared epitopeThe role of common protective alleles HLA-DRB1*13 among systemic autoimmune diseases.A replication study of the association between the IL12B promoter allele CTCTAA and susceptibility to cerebral malaria in Thai population.Presence of four major haplotypes in human BCMA gene: lack of association with systemic lupus erythematosus and rheumatoid arthritis.Sex-specific association of X-linked Toll-like receptor 7 (TLR7) with male systemic lupus erythematosus.Association of HLA-DRB1*1502-DQB1*0501 haplotype with susceptibility to systemic lupus erythematosus in Thais.Association of a functional polymorphism in the 3'-untranslated region of SPI1 with systemic lupus erythematosus.Variations of human killer cell lectin-like receptors: common occurrence of NKG2-C deletion in the general population.Association of Fcgamma receptor IIb and IIIb polymorphisms with susceptibility to systemic lupus erythematosus in Thais.Association of increased frequencies of HLA-DPB1*05:01 with the presence of anti-Ro/SS-A and anti-La/SS-B antibodies in Japanese rheumatoid arthritis and systemic lupus erythematosus patientsEpistatic interaction between BANK1 and BLK in rheumatoid arthritis: results from a large trans-ethnic meta-analysis.Variations in immune response genes and their associations with multifactorial immune disorders.TLR7 single-nucleotide polymorphisms in the 3' untranslated region and intron 2 independently contribute to systemic lupus erythematosus in Japanese women: a case-control association study.Association of ADAMTS13 polymorphism with cerebral malaria.Association of HLA-G 3' Untranslated Region Polymorphisms with Systemic Lupus Erythematosus in a Japanese Population: A Case-Control Association Study.Role of B cell inhibitory receptor polymorphisms in systemic lupus erythematosus: a negative times a negative makes a positive.Genetics of microscopic polyangiitis in the Japanese population.Diversity of human immune system multigene families and its implication in the genetic background of rheumatic diseases.A compass that points to lupus: genetic studies on type I interferon pathway.Role of STAT4 polymorphisms in systemic lupus erythematosus in a Japanese population: a case-control association study of the STAT1-STAT4 region.Identification of a haplotype block in the 5q31 cytokine gene cluster associated with the susceptibility to severe malaria.Association of IRF5, STAT4 and BLK with systemic lupus erythematosus and other rheumatic diseases.Genetics of ANCA-associated vasculitis in Japan: a role for HLA-DRB1*09:01 haplotype.Identification of genes upregulated in the inflamed colonic lesions of Crohn's disease.The human histocompatibility leukocyte antigen (HLA) haplotype is associated with the onset of postherpetic neuralgia after herpes zoster.Response to: 'HLA-A* 31:01 is not associated with the development of methotrexate pneumonitis in the UK population: results from a genome wide association study' by Bluett et al.Transethnic meta-analysis identifies GSDMA and PRDM1 as susceptibility genes to systemic sclerosis.FcgammaRIIB Ile232Thr transmembrane polymorphism associated with human systemic lupus erythematosus decreases affinity to lipid rafts and attenuates inhibitory effects on B cell receptor signaling.Association of PHRF1-IRF7 region polymorphism with clinical manifestations of systemic lupus erythematosus in a Japanese population.Cumulative association of eight susceptibility genes with systemic lupus erythematosus in a Japanese female population.Exacerbation of Lambert-Eaton myasthenic syndrome caused by an L-type Ca2+ channel antagonist.HLA-A*31:01 and methotrexate-induced interstitial lung disease in Japanese rheumatoid arthritis patients: a multidrug hypersensitivity marker?Replication of the association between the C8orf13-BLK region and systemic lupus erythematosus in a Japanese population.Association of Fcgamma receptor IIA, but not IIB and IIIA, polymorphisms with systemic lupus erythematosus: A family-based association study in Caucasians.Analysis of the association of HLA-DRB1, TNFalpha promoter and TNFR2 (TNFRSF1B) polymorphisms with SLE using transmission disequilibrium test.Association of LILRA2 (ILT1, LIR7) splice site polymorphism with systemic lupus erythematosus and microscopic polyangiitis.The impact of natural selection on an ABCC11 SNP determining earwax type.Association of Fcgamma receptor IIb polymorphism with susceptibility to systemic lupus erythematosus in Chinese: a common susceptibility gene in the Asian populations.
P50
Q28215014-0C6210D5-B773-4AA1-959B-1F9059EBD843Q28275793-8D4FFEFD-5426-4DAC-9886-99EBE4E61EBFQ28730083-E29746D2-C779-4DC9-AA60-BB9A482FA819Q30241539-C4C0F6DC-E52B-49D1-9D22-D968F96A55E4Q33555960-FE3B12B4-87A5-4B5D-A3A5-39726AD1038EQ34088725-FD26BB9D-2CA0-447F-88F3-1BA67379D214Q34115767-31275F32-658D-4F7C-A68B-0A3A6AA9A1E0Q34130000-5BAF4B0E-62E5-4D67-95FD-690A39BCB6B5Q34167593-EA0DE5B1-1CD7-477F-AB5C-13AE6512C01EQ34181555-4124816A-6D27-478E-B2CD-6BBA4D0D275CQ34197831-E81E0019-1B90-4699-82AA-91452AC1BA0AQ34548358-1D13FD76-811F-4D86-91A6-928784DB8D19Q34706667-7CDF23FC-E9D8-43D2-B5A0-2E4031996E68Q35030984-34FAE87D-AEF6-4802-85D6-CA731C630222Q35092905-7B481D64-3116-441E-8F2E-903430315C54Q35680580-519CB87D-19F5-4C15-9AFB-669950016009Q36058691-DEB37ADC-B517-4D93-9BF9-DEA32E50003CQ36583473-42BD3CD2-D4A1-40FA-B144-C0C249D8FCE6Q36679437-4AD3F66F-7484-41CF-ABE6-AF9286E9A0B7Q36737916-9CA78F26-2BDE-4B6B-83BE-4D9AA7876F48Q36854313-74A78577-C34D-44FD-B14F-DD84A4406F9CQ36993267-A687D049-DDDC-4538-AA78-188BFB60585CQ37405835-0187F182-F19B-4F6A-9225-872DB8769C21Q37746659-43D0D296-792B-49C3-A866-690B78166D2DQ38062448-D1217366-F30A-4F49-A263-4677DC6FE906Q39041168-8A5B095E-9A3C-42A8-9A58-48668E4F1728Q39378004-867AE5E1-FDA9-4576-BBF3-B10AFA4C6A2AQ40203190-ED3A38B0-9AA5-446F-A51E-599D79B5688EQ40287055-14EA3E80-E62E-4CEE-BA86-FD95258441C0Q40382431-081B041A-7473-4DE4-BF92-126D1A816359Q43723309-3437DF43-78FC-4AC7-9284-667AE545E0DAQ44303693-41B99431-27CD-4B09-BAC3-DC27ADF99832Q44352408-62B185E8-D8B4-4860-BE56-5CD491F192FCQ45869977-EB07144D-88E5-4743-8E04-8AB378133D05Q46140208-BBB3C82B-78A4-465F-952E-1E996520FD36Q46277866-348E2BF2-3409-4F70-8F9D-9471F36889FBQ46484623-CF456F6A-9478-42E6-8D09-A64C6C88BA00Q46755235-2B840156-96EA-43D9-BBFE-F8FE8C2642B0Q46816983-368AEE1B-BE7E-409E-A49D-DD589D599F3CQ47347629-4E15509F-F9F6-4EA6-B741-DE069E1C4714
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Naoyuki Tsuchiya
@ast
Naoyuki Tsuchiya
@en
Naoyuki Tsuchiya
@es
Naoyuki Tsuchiya
@nl
type
label
Naoyuki Tsuchiya
@ast
Naoyuki Tsuchiya
@en
Naoyuki Tsuchiya
@es
Naoyuki Tsuchiya
@nl
prefLabel
Naoyuki Tsuchiya
@ast
Naoyuki Tsuchiya
@en
Naoyuki Tsuchiya
@es
Naoyuki Tsuchiya
@nl
P106
P1153
7102607073
P31
P496
0000-0002-6776-5580