A multicenter international evaluation of single-tube amplification protocols for sequencing-based typing of HLA-DRB1 and HLA-DRB3,4,5.
about
Molecular genetic studies of natives on Easter Island: evidence of an early European and Amerindian contribution to the Polynesian gene poolOligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.Interaction analysis between HLA-DRB1 shared epitope alleles and MHC class II transactivator CIITA gene with regard to risk of rheumatoid arthritis.The genetic variants at the HLA-DRB1 gene are associated with primary IgA nephropathy in Han Chinese.Importance of human leukocyte antigen (HLA) class I and II alleles on the risk of multiple sclerosis.Late onset myasthenia gravis is associated with HLA DRB1*15:01 in the Norwegian population.Environmental exposures and the risk of multiple sclerosis investigated in a Norwegian case-control study.Refinement of the MHC risk map in a scandinavian primary sclerosing cholangitis population.HLA-B*1301 as a biomarker for genetic susceptibility to hypersensitivity dermatitis induced by trichloroethylene among workers in China.Associations between the PTPN22 1858C->T polymorphism and radiographic joint destruction in patients with rheumatoid arthritis: results from a 10-year longitudinal studyIntrahaplotypic Variants Differentiate Complex Linkage Disequilibrium within Human MHC Haplotypes.Coding variants at hexa-allelic amino acid 13 of HLA-DRB1 explain independent SNP associations with follicular lymphoma risk.Population-specific recombination sites within the human MHC regionActinic Prurigo in Singaporean Chinese: A Positive Association with HLA-DRB1*03:01.Protection against anti-citrullinated protein antibody-positive rheumatoid arthritis is predominantly associated with HLA-DRB1*1301: a meta-analysis of HLA-DRB1 associations with anti-citrullinated protein antibody-positive and anti-citrullinated prIdentification of a novel HLA-DRB1*04:94N allele by polymerase chain reaction sequence-based typing.Identification of the novel allele, HLA-DRB1*09:30, by sequence-based high resolution typing.An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis.CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations
P2860
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P2860
A multicenter international evaluation of single-tube amplification protocols for sequencing-based typing of HLA-DRB1 and HLA-DRB3,4,5.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh
2004年學術文章
@zh-hant
name
A multicenter international ev ...... of HLA-DRB1 and HLA-DRB3,4,5.
@en
A multicenter international ev ...... of HLA-DRB1 and HLA-DRB3,4,5.
@nl
type
label
A multicenter international ev ...... of HLA-DRB1 and HLA-DRB3,4,5.
@en
A multicenter international ev ...... of HLA-DRB1 and HLA-DRB3,4,5.
@nl
prefLabel
A multicenter international ev ...... of HLA-DRB1 and HLA-DRB3,4,5.
@en
A multicenter international ev ...... of HLA-DRB1 and HLA-DRB3,4,5.
@nl
P2093
P2860
P1433
P1476
A multicenter international ev ...... of HLA-DRB1 and HLA-DRB3,4,5.
@en
P2093
Christiansen FT
De Santis D
Rozemuller EH
Tilanus MG
Whidborne R
P2860
P304
P356
10.1111/J.0001-2815.2004.00214.X
P577
2004-05-01T00:00:00Z