Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy. - Wikidata - awgldk - TriplyDB

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.

http://www.wikidata.org/entity/Q35754519

about

ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene The Role of Mitochondrial Functional Proteins in ROS Production in Ischemic Heart Diseases Mitochondrial dynamics in cardiovascular health and disease Cardiovascular Disease, Mitochondria, and Traditional Chinese Medicine Mitochondria-targeted agents: Future perspectives of mitochondrial pharmaceutics in cardiovascular diseases IL-15Rα deficiency in skeletal muscle alters respiratory function and the proteome of mitochondrial subpopulations independent of changes to the mitochondrial genome Genetic determinants of myocardial dysfunction.Nitric oxide impairs mitochondrial movement in cortical neurons during hypoxia.Mitochondrial mosaics in the liver of 3 infants with mtDNA defects The Genetic Challenges and Opportunities in Advanced Heart Failure Genetic causes of human heart failure.Morphological and functional abnormalities in mitochondria associated with synaptic degeneration in prion disease.Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny Divergent mitochondrial biogenesis responses in human cardiomyopathy Loss of cardiac tetralinoleoyl cardiolipin in human and experimental heart failure.Impairment of myocardial mitochondria in viral myocardial disease and its reflective window in peripheral cells.Molecular mechanisms of inherited cardiomyopathies.Short term exercise induces PGC-1α, ameliorates inflammation and increases mitochondrial membrane proteins but fails to increase respiratory enzymes in aging diabetic hearts.Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals Calreticulin is localized at mitochondria of rat cardiomyocytes and affected by furazolidone.Genetics of inherited cardiomyopathies.Mitochondrial DNA variant for complex I reveals a role in diabetic cardiac remodeling.Mitochondrial ROS Induces Cardiac Inflammation via a Pathway through mtDNA Damage in a Pneumonia-Related Sepsis Model.Genetic basis of Alzheimer's dementia: role of mtDNA mutations.Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup.Megamitochondria in Cardiomyocytes of a Knockout (Klf15-/-) Mouse.Ultrastructural definition of apoptosis in heart failure.Thymidine kinase and mtDNA depletion in human cardiomyopathy: epigenetic and translational evidence for energy starvation.Mitochondria and heart failure: new insights into an energetic problem.Mitochondria in cardiac hypertrophy and heart failure.Mitochondria in the human heart.Dynamic organization of mitochondria in human heart and in myocardial disease The novel mitochondrial 16S rRNA 2336T>C mutation is associated with hypertrophic cardiomyopathy.Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy.Genetic testing for inherited cardiac disease.Mitochondrial cardiomyopathy: pathophysiology, diagnosis, and management.Mitochondrial cytopathies and cardiovascular disease.8-hydroxy-2'-deoxyguanosine and cardiovascular disease: a systematic review.Persistent alterations to the gene expression profile of the heart subsequent to chronic Doxorubicin treatment.Mitochondrial Mutations in Cardiac Disorders.

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Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.

http://www.wikidata.org/entity/Q35754519

description

1998 nî lūn-bûn

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1998年の論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

@zh-mo

1998年論文

@zh-tw

1998年论文

@wuu

1998年论文

@zh

1998年论文

@zh-cn

name

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.

@ast

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.

@en

type

label

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.

@ast

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.

@en

prefLabel

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.

@ast

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.

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The American Journal of Pathology

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Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.

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A Gavazzi

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A Pilotto

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B Dal Bello

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C Campana

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G Magrini

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M Diegoli

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M Viganò

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P2860

Sequence and organization of the human mitochondrial genome

Detection and localization of single base changes by denaturing gradient gel electrophoresis

A new mitochondrial DNA mutation associated with non-insulin-dependent diabetes mellitus

Normal variants of human mitochondrial DNA and translation products: the building of a reference data base

Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects.

Ribosomal RNA and translation.

Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia

Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure.

PCR-SSCP: a method for detection of mutations.

Diseases of the mitochondrial DNA.

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1501-1510

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5

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Eloisa Arbustini

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13475905

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9811342

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mitochondrial DNA

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1853408

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