Polymorphic structural features of modelled HLA-DQ molecules segregate according to susceptibility or resistance to IDDM (Q70953741)

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15 October 2019

title

Polymorphic structural features of modelled HLA-DQ molecules segregate according to susceptibility or resistance to IDDM (English)

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15 October 2019

author name string

J Routsias

series ordinal

1

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15 October 2019

G K Papadopoulos

series ordinal

2

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15 October 2019

publication date

1 November 1995

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15 October 2019

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15 October 2019

volume

38

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15 October 2019

issue

11

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15 October 2019

page(s)

1251-1261

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A systematic study of HLA class II-beta DNA restriction fragments in insulin-dependent diabetes mellitus

15 October 2019

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Human growth hormone and extracellular domain of its receptor: crystal structure of the complex

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HLA-D region β-chain DNA endonuclease fragments differ between HLA-DR identical healthy and insulin-dependent diabetic individuals

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The amino acid at position 57 of the HLA-DQ beta chain and susceptibility to develop insulin-dependent diabetes mellitus.

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MHC class II interaction with CD4 mediated by a region analogous to the MHC class I binding site for CD8

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Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimer

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Particular HLA-DQ molecules play a dominant role in determining susceptibility or resistance to type 1 (insulin-dependent) diabetes mellitus

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Primarily chronic progressive and relapsing/remitting multiple sclerosis: two immunogenetically distinct disease entities

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Pool sequencing of natural HLA-DR, DQ, and DP ligands reveals detailed peptide motifs, constraints of processing, and general rules

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Dose effect of cis- and trans-encoded HLA-DQ alpha beta heterodimers in IDDM susceptibility

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Molecular cloning of a polymorphic DNA endonuclease fragment associates insulin-dependent diabetes mellitus with HLA-DQ.

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Immunological suppression by human CD8+ T cells is receptor dependent and HLA-DQ restricted

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HLA-DQ beta gene contributes to susceptibility and resistance to insulin-dependent diabetes mellitus

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12 December 2020

Identification of the 64K autoantigen in insulin-dependent diabetes as the GABA-synthesizing enzyme glutamic acid decarboxylase

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HLA-D and -DR antigens in genetic analysis of insulin dependent diabetes mellitus

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Self-peptides from four HLA-DR alleles share hydrophobic anchor residues near the NH2-terminal including proline as a stop signal for trimming

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The human thymic microenvironment: an immunohistologic study

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H-2Dd exploits a four residue peptide binding motif

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New perspectives in cell adhesion: RGD and integrins

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T cell receptor antagonist peptides induce positive selection

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A combination of HLA-DQ beta Asp57-negative and HLA DQ alpha Arg52 confers susceptibility to insulin-dependent diabetes mellitus

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Structure of a Fibronectin Type III Domain from Tenascin Phased by MAD Analysis of the Selenomethionyl Protein

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A genome-wide search for human type 1 diabetes susceptibility genes

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Polymorphic amino acid variations in HLA-DQ are associated with systematic physical property changes and occurrence of IDDM. Members of the Swedish Childhood Diabetes Study

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Crystal structure of the human class II MHC protein HLA-DR1 complexed with an influenza virus peptide

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Traffic signals for lymphocyte recirculation and leukocyte emigration: the multistep paradigm

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Overlapping epitopes encompassing a point mutation (12 Gly-->Arg) in p21 ras can be recognized by HLA-DR, -DP and -DQ restricted T cells

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Immune response to glutamic acid decarboxylase correlates with insulitis in non-obese diabetic mice.

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An evaluation of the performance of an automated procedure for comparative modelling of protein tertiary structure

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What is the basis for HLA-DQ associations with autoimmune disease?

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Structural compartmentalization of MHC class II signaling function.

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HLA-DQ is epistatic to HLA-DR in controlling the immune response to schistosomal antigen in humans

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12 December 2020

Identifiers

DOI

10.1007/BF00401756

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8582533%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

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