Polymorphisms in the SOD2 and HLA-DRB1 genes are associated with nonfamilial idiopathic dilated cardiomyopathy in Japanese (Q22010438)

MHC class II receptor activity

GOA release 2020-03-11

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GOA release 2020-03-11

dilated cardiomyopathy

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Idiopathic dilated cardiomyopathy

inferred from title

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S Hiroi

1

S

Hiroi

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7 February 2023

H Harada

2

H

Harada

1 reference

7 February 2023

H Nishi

3

H

Nishi

1 reference

7 February 2023

M Satoh

4

M

Satoh

1 reference

7 February 2023

R Nagai

5

R

Nagai

1 reference

7 February 2023

A Kimura

6

A

Biochemical and Biophysical Research Communications

Kimura

1 reference

7 February 2023

language of work or name

English

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publication date

2 August 1999

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published in

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volume

261

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issue

2

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page(s)

332-9

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cites work

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Structural dimorphism in the mitochondrial targeting sequence in the human manganese superoxide dismutase gene. A predictive evidence for conformational change to influence mitochondrial transport and a study of allelic association in Parkinson's di

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Possible involvement of the HLA-DQB1 gene in susceptibility and resistance to human dilated cardiomyopathy.

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HLA A, B and DR typing in idiopathic dilated cardiomyopathy: a search for immune response factors

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Major histocompatibility complex class II gene frequencies by serologic and deoxyribonucleic acid genomic typing in idiopathic dilated cardiomyopathy

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Targeting of pre-ornithine transcarbamylase to mitochondria: definition of critical regions and residues in the leader peptide.

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Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

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Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA

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How mitochondria import proteins

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DNA typing of HLA class II genes in Japanese patients with dilated cardiomyopathy.

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Chronic relapsing pericarditis and dilated cardiomyopathy: serological evidence of persistent enterovirus infection

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Evidence from family studies for autoimmunity in dilated cardiomyopathy

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HLA antigen frequencies in end-stage idiopathic and ischaemic cardiomyopathy

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Human leukocyte antigen class II associations in patients with idiopathic dilated cardiomyopathy. Myocarditis Treatment Trial Investigators

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A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1

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Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase

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Idiopathic Dilated Cardiomyopathy

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Receptor sites involved in posttranslational transport of apocytochrome c into mitochondria: specificity, affinity, and number of sites

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Molecular characterization of inherited carnitine palmitoyltransferase II deficiency

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Neurodegeneration, myocardial injury, and perinatal death in mitochondrial superoxide dismutase-deficient mice

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On signal sequence polymorphisms and diseases of distribution

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Molecular structure and organization of the human manganese superoxide dismutase gene

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Reduced lipid peroxidation in dilated hearts of cardiomyopathic turkeys

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Cardioprotection by nisoldipine: role of timing of administration

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Overexpression of mitochondrial manganese superoxide dismutase promotes the survival of tumor cells exposed to interleukin-1, tumor necrosis factor, selected anticancer drugs, and ionizing radiation.

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Molecular genetics of dilated cardiomyopathy

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HLA and disease associations: detecting the strongest association

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17th Sir Hans Krebs lecture. Signals guiding proteins to their correct locations in mitochondria

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Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

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HLA antigens in idiopathic dilated cardiomyopathy

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Do specific HLA antigens predispose to ischaemic heart disease or idiopathic dilated cardiomyopathy?

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Increased circulating cytokines in patients with myocarditis and cardiomyopathy

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Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

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Dystrophinopathy, the expanding phenotype. Dystrophin abnormalities in X-linked dilated cardiomyopathy

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Familial dilated cardiomyopathy locus maps to chromosome 2q31.

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Mapping a cardiomyopathy locus to chromosome 3p22-p25.

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Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

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7 January 2021

Identifiers

DOI

10.1006/BBRC.1999.1036

1 reference

Consolidated OpenCitations Corpus – April 2017

1001111

1001111

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference