Genetic susceptibility factors in type 1 diabetes: linkage, disequilibrium and functional analyses (Q77892057)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914216%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

review article

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title

Genetic susceptibility factors in type 1 diabetes: linkage, disequilibrium and functional analyses (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914216%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

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J X She

1

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9 December 2019

M P Marron

series ordinal

2

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9 December 2019

publication date

1 December 1998

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Current Opinion in Immunology

9 December 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914216%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

volume

10

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9 December 2019

issue

6

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9 December 2019

page(s)

682-689

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The significance of the concordance rate for type 1 (insulin-dependent) diabetes in identical twins.

9 December 2019

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Saturation multipoint linkage mapping of chromosome 6q in type 1 diabetes

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Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility

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Susceptibility to insulin dependent diabetes mellitus maps to a 4.1 kb segment of DNA spanning the insulin gene and associated VNTR.

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Paternally transmitted IDDM2 influences diabetes susceptibility despite biallelic expression of the insulin gene in human pancreas.

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7 January 2021

The paternally inherited insulin gene B allele (1,428 FokI site) confers protection from insulin-dependent diabetes in families

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7 January 2021

Insulin gene region-encoded susceptibility to type 1 diabetes is not restricted to HLA-DR4-positive individuals

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7 January 2021

Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

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7 January 2021

Sometimes it's hot, sometimes it's not

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A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patients.

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The future of genetic studies of complex human diseases

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The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry

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7 January 2021

Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groups

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7 January 2021

Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33.

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Intrafamilial and case-control association analysis of D2S152 in insulin-dependent diabetes

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Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21.

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Evidence for a type 1 diabetes susceptibility locus (IDDM10) on human chromosome 10p11-q11

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7 January 2021

Association of distal chromosome 2q with IDDM in Japanese subjects

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CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus.

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7 January 2021

Association of CTLA-4 gene A-G polymorphism (IDDM12 locus) with acute-onset and insulin-depleted IDDM as well as autoimmune thyroid disease (Graves' disease and Hashimoto's thyroiditis) in the Japanese population

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7 January 2021

The peptide binding motif of the disease associated HLA-DQ (alpha 1* 0501, beta 1* 0201) molecule

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7 January 2021

Use of eluted peptide sequence data to identify the binding characteristics of peptides to the insulin-dependent diabetes susceptibility allele HLA-DQ8 (DQ 3.2).

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7 January 2021

HLA-DQB1 codon 57 is critical for peptide binding and recognition.

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Critical contribution of beta chain residue 57 in peptide binding ability of both HLA-DR and -DQ molecules

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Biochemical characterization of the human diabetes-associated HLA-DQ8 allelic product: similarity to the major histocompatibility complex class II I-A(g)7 protein of non-obese diabetic mice

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T cell epitopes of insulin defined in HLA-DR4 transgenic mice are derived from preproinsulin and proinsulin

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Naturally processed T cell epitopes from human glutamic acid decarboxylase identified using mice transgenic for the type 1 diabetes-associated human MHC class II allele, DRB1*0401.

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Identification of immunodominant T cell epitopes of human glutamic acid decarboxylase 65 by using HLA-DR(alpha1*0101,beta1*0401) transgenic mice.

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Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele

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7 January 2021

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7 January 2021

Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus.

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7 January 2021

The insulin gene is transcribed in the human thymus and transcription levels correlated with allelic variation at the INS VNTR-IDDM2 susceptibility locus for type 1 diabetes.

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7 January 2021

A functional analysis of the role of IGF2 in IDDM2-encoded susceptibility to type 1 diabetes

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7 January 2021

The INS 5' variable number of tandem repeats is associated with IGF2 expression in humans

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7 January 2021

Close genetic linkage between diabetes mellitus and kidd blood group

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7 January 2021

10.1016/S0952-7915(98)80089-7

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914216%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

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