136 related articles for article (PubMed ID: 8515573)
1. Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect.
Angelini C; Melacini P; Valente ML; Reichmann H; Carrozzo R; Fanin M; Vergani L; Boffa GM; Martinuzzi A; Fasoli G
Jpn Heart J; 1993 Jan; 34(1):63-77. PubMed ID: 8515573
[TBL] [Abstract][Full Text] [Related]
2. Single muscle fibre analyses in 2 brothers with succinate dehydrogenase deficiency.
Reichmann H; Angelini C
Eur Neurol; 1994; 34(2):95-8. PubMed ID: 8174601
[TBL] [Abstract][Full Text] [Related]
3. [Complex II (succinate-ubiquinone reductase) deficiency].
Nonaka I
Ryoikibetsu Shokogun Shirizu; 2001; (36):132-4. PubMed ID: 11596343
[No Abstract] [Full Text] [Related]
4. [Parkinson disease--a mitochondrial myopathy?].
Reichmann H; Janetzky B; Klinge M; Riederer P
Nervenarzt; 1993 Apr; 64(4):215-20. PubMed ID: 8506008
[No Abstract] [Full Text] [Related]
5. Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain.
Kennaway NG; Buist NR; Darley-Usmar VM; Papadimitriou A; Dimauro S; Kelley RI; Capaldi RA; Blank NK; D'Agostino A
Pediatr Res; 1984 Oct; 18(10):991-9. PubMed ID: 6093035
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial mutations differentially affect aging, mutability and anesthetic sensitivity in Caenorhabditis elegans.
Hartman PS; Ishii N; Kayser EB; Morgan PG; Sedensky MM
Mech Ageing Dev; 2001 Aug; 122(11):1187-201. PubMed ID: 11389932
[TBL] [Abstract][Full Text] [Related]
7. The contribution of mitochondrial respiratory complexes to the production of reactive oxygen species.
McLennan HR; Degli Esposti M
J Bioenerg Biomembr; 2000 Apr; 32(2):153-62. PubMed ID: 11768748
[TBL] [Abstract][Full Text] [Related]
8. Phenotypic dichotomy in mitochondrial complex II genetic disorders.
Baysal BE; Rubinstein WS; Taschner PE
J Mol Med (Berl); 2001 Sep; 79(9):495-503. PubMed ID: 11692162
[TBL] [Abstract][Full Text] [Related]
9. Cytochrome b560 (QPs1) of mitochondrial succinate-ubiquinone reductase. Immunochemistry, cloning, and nucleotide sequencing.
Yu L; Wei YY; Usui S; Yu CA
J Biol Chem; 1992 Dec; 267(34):24508-15. PubMed ID: 1447196
[TBL] [Abstract][Full Text] [Related]
10. The cDNA sequence of beef heart CII-3, a membrane-intrinsic subunit of succinate-ubiquinone oxidoreductase.
Cochran B; Capaldi RA; Ackrell BA
Biochim Biophys Acta; 1994 Nov; 1188(1-2):162-6. PubMed ID: 7947903
[TBL] [Abstract][Full Text] [Related]
11. Succinate: quinone oxidoreductases. Variations on a conserved theme.
Hägerhäll C
Biochim Biophys Acta; 1997 Jun; 1320(2):107-41. PubMed ID: 9210286
[No Abstract] [Full Text] [Related]
12. Late-onset optic atrophy, ataxia, and myopathy associated with a mutation of a complex II gene.
Birch-Machin MA; Taylor RW; Cochran B; Ackrell BA; Turnbull DM
Ann Neurol; 2000 Sep; 48(3):330-5. PubMed ID: 10976639
[TBL] [Abstract][Full Text] [Related]
13. [Mitochondrial complex II (succinate-ubiquinone oxidoreductase)].
Miki T
Nihon Rinsho; 2002 Apr; 60 Suppl 4():139-43. PubMed ID: 12013837
[No Abstract] [Full Text] [Related]
14. Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules.
Leslie N; Wang X; Peng Y; Valencia CA; Khuchua Z; Hata J; Witte D; Huang T; Bove KE
Hum Pathol; 2016 Mar; 49():27-32. PubMed ID: 26826406
[TBL] [Abstract][Full Text] [Related]
15. A role for mitochondrial enzymes in inherited neoplasia and beyond.
Eng C; Kiuru M; Fernandez MJ; Aaltonen LA
Nat Rev Cancer; 2003 Mar; 3(3):193-202. PubMed ID: 12612654
[TBL] [Abstract][Full Text] [Related]
16. Mitochondrial disorders of the nervous system: clinical, biochemical, and molecular genetic features.
Thyagarajan D; Byrne E
Int Rev Neurobiol; 2002; 53():93-144. PubMed ID: 12512338
[No Abstract] [Full Text] [Related]
17. Comparative study and cDNA cloning of the flavoprotein subunit of mitochondrial complex II (succinate-ubiquinone oxidoreductase: fumarate reductase) from the dog heartworm, Dirofilaria immitis.
Kuramochi T; Kita K; Takamiya S; Kojima S; Hayasaki M
Comp Biochem Physiol B Biochem Mol Biol; 1995 Jul; 111(3):491-502. PubMed ID: 7613771
[TBL] [Abstract][Full Text] [Related]
18. Sequence comparison between the flavoprotein subunit of the fumarate reductase (complex II) of the anaerobic parasitic nematode, Ascaris suum and the succinate dehydrogenase of the aerobic, free-living nematode, Caenorhabditis elegans.
Kuramochi T; Hirawake H; Kojima S; Takamiya S; Furushima R; Aoki T; Komuniecki R; Kita K
Mol Biochem Parasitol; 1994 Dec; 68(2):177-87. PubMed ID: 7739664
[TBL] [Abstract][Full Text] [Related]
19. Hereditary mitochondrial hypertrophic cardiomyopathy with mitochondrial myopathy of skeletal muscle, congenital cataract and lactic acidosis.
van Ekeren GJ; Stadhouders AM; Egberink GJ; Sengers RC; Daniëls O; Kubat K
Virchows Arch A Pathol Anat Histopathol; 1987; 412(1):47-52. PubMed ID: 3120403
[TBL] [Abstract][Full Text] [Related]
20. Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution.
Hirata K; Nakagawa M; Higuchi I; Hashimoto K; Hanada K; Takahashi K; Niiyama T; Izumi K; Sakoda S; Yamada H; Osame M
J Hum Genet; 1999; 44(3):210-4. PubMed ID: 10319590
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
