Mitochondrial disorders

被引：27

作者：

Schapira, AHV ^{[1
]}

机构：

[1] Univ London, Royal Free & Univ Coll Med Sch, Dept Clin Neurosci, London NW3 2PF, England

来源：

BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 1999年 / 1410卷 / 02期

关键词：

D O I：

10.1016/S0005-2728(98)00160-1

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：99 / 102

页数：4

共 13 条

[1] MUTATION OF A NUCLEAR SUCCINATE-DEHYDROGENASE GENE RESULTS IN MITOCHONDRIAL RESPIRATORY-CHAIN DEFICIENCY [J].

BOURGERON, T ;

RUSTIN, P ;

CHRETIEN, D ;

BIRCHMACHIN, M ;

BOURGEOIS, M ;

VIEGASPEQUIGNOT, E ;

MUNNICH, A ;

ROTIG, A .

NATURE GENETICS, 1995, 11 (02) :144-149

[2] Oxidative damage and metabolic dysfunction in Huntington's disease: Selective vulnerability of the basal ganglia [J].

Browne, SE ;

Bowling, AC ;

MacGarvey, U ;

Baik, MJ ;

Berger, SC ;

Muqit, MMK ;

Bird, ED ;

Beal, MF .

ANNALS OF NEUROLOGY, 1997, 41 (05) :646-653

[3] The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy [J].

Cock, HR ;

Tabrizi, SJ ;

Cooper, JM ;

Schapira, AHV .

ANNALS OF NEUROLOGY, 1998, 44 (02) :187-193

[4] RETRACTED: Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer disease (Retracted Article) [J].

Davis, RE ;

Miller, S ;

Herrnstadt, C ;

Ghosh, SS ;

Fahy, E ;

Shinobu, LA ;

Galasko, D ;

Thal, LJ ;

Beal, MF ;

Howell, N ;

Parker, WD .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (09) :4526-4531

[5] DIFFERENT CELLULAR BACKGROUNDS CONFER A MARKED ADVANTAGE TO EITHER MUTANT OR WILD-TYPE MITOCHONDRIAL GENOMES [J].

DUNBAR, DR ;

MOONIE, PA ;

JACOBS, HT ;

HOLT, IJ .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (14) :6562-6566

[6] Mitochondrial defect in Huntington's disease on caudate nucleus [J].

Gu, M ;

Gash, MT ;

Mann, VM ;

JavoyAgid, F ;

Cooper, JM ;

Schapira, AHV .

ANNALS OF NEUROLOGY, 1996, 39 (03) :385-389

[7] Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease [J].

Gu, M ;

Cooper, JM ;

Taanman, JW ;

Schapira, AHV .

ANNALS OF NEUROLOGY, 1998, 44 (02) :177-186

[8] Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes [J].

Hirano, M ;

Shtilbans, A ;

Mayeux, R ;

Davidson, MM ;

DiMauro, S ;

Knowles, JA ;

Schon, EA .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14894-14899

[9] Localization of the Wilson's disease protein product to mitochondria [J].

Lutsenko, S ;

Cooper, MJ .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (11) :6004-6009

[10] MITOCHONDRIAL-FUNCTION AND PARENTAL SEX EFFECT IN HUNTINGTONS-DISEASE [J].

MANN, VM ;

COOPER, JM ;

JAVOYAGID, F ;

AGID, Y ;

JENNER, P ;

SCHAPIRA, AHV .

LANCET, 1990, 336 (8717) :749-749

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