Literature DB >> 11182713

Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.

A Brega1, J Narula, E Arbustini.   

Abstract

Myocardial tissue is highly dependent on energy supplied by normal mitochondrial function. Therefore defects of energy production or utilization affect the heart in both syndromic and isolated disorders. Knowledge of the peculiar structural, functional, and genetic characteristics of mitochondria provides the basis for identification and classification of mitochondrial defects as well as for establishment of a diagnostic workup useful for related cardiac disorders. This review is therefore dedicated to the characteristics of normal mitochondria and the pathologic alterations of these organelles in various cardiovascular diseases.

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Year:  2001        PMID： 11182713     DOI： 10.1067/mnc.2001.112755

Source DB:  PubMed          Journal:  J Nucl Cardiol        ISSN： 1071-3581            Impact factor:   5.952


  44 in total

Review 1.  Repair of mtDNA in vertebrates.

Authors:  D F Bogenhagen
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

2.  Regulation of mitochondrial gene expression in mammalian cells.

Authors:  G Attardi; A Chomyn; M P King; B Kruse; P L Polosa; N N Murdter
Journal:  Biochem Soc Trans       Date:  1990-08       Impact factor: 5.407

3.  MITOMAP: a human mitochondrial genome database--1998 update.

Authors:  A M Kogelnik; M T Lott; M D Brown; S B Navathe; D C Wallace
Journal:  Nucleic Acids Res       Date:  1998-01-01       Impact factor: 16.971

4.  The mitochondrial A3243G mutation presenting as severe cardiomyopathy.

Authors:  L Vilarinho; F M Santorelli; M J Rosas; C Tavares; M Melo-Pires; S DiMauro
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

5.  Familial cardiomyopathy with cataracts and lactic acidosis: a defect in complex I (NADH-dehydrogenase) of the mitochondria respiratory chain.

Authors:  S Pitkanen; F Merante; D R McLeod; D Applegarth; T Tong; B H Robinson
Journal:  Pediatr Res       Date:  1996-03       Impact factor: 3.756

6.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

7.  Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy.

Authors:  P Richard; R Isnard; L Carrier; O Dubourg; Y Donatien; B Mathieu; G Bonne; F Gary; P Charron; M Hagege; M Komajda; K Schwartz; B Hainque
Journal:  J Med Genet       Date:  1999-07       Impact factor: 6.318

8.  Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

Authors:  M Zeviani; C Gellera; C Antozzi; M Rimoldi; L Morandi; F Villani; V Tiranti; S DiDonato
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Review 9.  Mitochondrial diseases in man and mouse.

Authors:  D C Wallace
Journal:  Science       Date:  1999-03-05       Impact factor: 47.728

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Authors:  E Arbustini; M Diegoli; R Fasani; M Grasso; P Morbini; N Banchieri; O Bellini; B Dal Bello; A Pilotto; G Magrini; C Campana; P Fortina; A Gavazzi; J Narula; M Viganò
Journal:  Am J Pathol       Date:  1998-11       Impact factor: 4.307
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  6 in total

Review 1.  Ultrastructural definition of apoptosis in heart failure.

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2.  Genetic deletion of the mitochondrial phosphate carrier desensitizes the mitochondrial permeability transition pore and causes cardiomyopathy.

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Review 3.  Genetics of dilated cardiomyopathy: practical implications for heart failure management.

Authors:  Andrew N Rosenbaum; Katherine E Agre; Naveen L Pereira
Journal:  Nat Rev Cardiol       Date:  2019-10-11       Impact factor: 32.419

4.  A novel locus for dilated cardiomyopathy maps to canine chromosome 8.

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5.  Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny.

Authors:  Michael V Zaragoza; Martin C Brandon; Marta Diegoli; Eloisa Arbustini; Douglas C Wallace
Journal:  Eur J Hum Genet       Date:  2010-10-27       Impact factor: 4.246

6.  Novel m.15434C>A (p.230L>I) Mitochondrial Cytb Gene Missense Mutation Associated with Dilated Cardiomyopathy.

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  6 in total

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