Literature DB >> 3307933

Maternal genes: mitochondrial diseases.

D C Wallace1.   

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Year:  1987        PMID： 3307933

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  24 in total

1.  Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy.

Authors:  B Melegh; L Seress; T Bedekovics; G Kispál; B Sümegi; K Trombitás; K Méhes
Journal:  J Inherit Metab Dis       Date:  1999-10       Impact factor: 4.982

2.  Effect of 'binary mitochondrial heteroplasmy' on respiration and ATP synthesis: implications for mitochondrial diseases.

Authors:  B Korzeniewski; M Malgat; T Letellier; J P Mazat
Journal:  Biochem J       Date:  2001-08-01       Impact factor: 3.857

Review 3.  Does the mitochondrial DNA play a role in the pathogenesis of diabetes?

Authors:  K D Gerbitz
Journal:  Diabetologia       Date:  1992-12       Impact factor: 10.122

4.  Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.

Authors:  I Nelson; F Degoul; B Obermaier-Kusser; N Romero; C Borrone; C Marsac; J L Vayssiere; K Gerbitz; M Fardeau; G Ponsot; P Lestienne
Journal:  Nucleic Acids Res       Date:  1989-10-25       Impact factor: 16.971

5.  Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorder.

Authors:  V Li; J Hostein; N B Romero; C Marsac; P Mezin; R Bost; F Degoul; M Fardeau; J Fournet
Journal:  Dig Dis Sci       Date:  1992-03       Impact factor: 3.199

6.  Control over the contribution of the mitochondrial membrane potential (DeltaPsi) and proton gradient (DeltapH) to the protonmotive force (Deltap). In silico studies.

Authors:  Jaroslaw Dzbek; Bernard Korzeniewski
Journal:  J Biol Chem       Date:  2008-08-11       Impact factor: 5.157

7.  X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation.

Authors:  X D Bu; J I Rotter
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-15       Impact factor: 11.205

8.  Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.

Authors:  S Mita; B Schmidt; E A Schon; S DiMauro; E Bonilla
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

9.  Partial outlet obstruction of the rabbit bladder results in changes in the mitochondrial genetic system.

Authors:  Y Zhao; R M Levin; S S Levin; C A Nevel; N Haugaard; T H Hsu; A P Hudson
Journal:  Mol Cell Biochem       Date:  1994-12-07       Impact factor: 3.396

Review 10.  Nucleus-driven mutations of human mitochondrial DNA.

Authors:  M Zeviani
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982
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