Literature DB >> 2193491

Oxidative phosphorylation diseases. Disorders of two genomes.

J M Shoffner1, D C Wallace.   

Abstract

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Year:  1990        PMID： 2193491

Source DB:  PubMed          Journal:  Adv Hum Genet        ISSN： 0065-275X


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  28 in total

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2.  Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy.

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3.  Mitochondrial genetics: principles and practice.

Authors:  J M Shoffner; D C Wallace
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Review 4.  Diseases resulting from mitochondrial DNA point mutations.

Authors:  D C Wallace; M T Lott; J M Shoffner; M D Brown
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

5.  Multiple presentation of mitochondrial disorders.

Authors:  A Nissenkorn; A Zeharia; D Lev; A Fatal-Valevski; V Barash; A Gutman; S Harel; T Lerman-Sagie
Journal:  Arch Dis Child       Date:  1999-09       Impact factor: 3.791

6.  Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathies.

Authors:  J M Collombet; H Faure-Vigny; G Mandon; R Dumoulin; S Boissier; A Bernard; B Mousson; G Stepien
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7.  Transfection of mitochondria: strategy towards a gene therapy of mitochondrial DNA diseases.

Authors:  P Seibel; J Trappe; G Villani; T Klopstock; S Papa; H Reichmann
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8.  Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.

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

Authors:  J M van den Ouweland; G J Bruining; D Lindhout; J M Wit; B F Veldhuyzen; J A Maassen
Journal:  Nucleic Acids Res       Date:  1992-02-25       Impact factor: 16.971

10.  Visual dysfunction in patients with mitochondrial myopathies. I. Electrophysiologic impairments.

Authors:  G Ambrosio; R De Marco; L Loffredo; A Magli
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