-
1
-
-
0000041138
-
Enzymatic activities of human skeletal muscle mitochondria: A tool in clinical metabolic research
-
Ernster, L., Ikkos, D. and Luft, R. (1959) Enzymatic activities of human skeletal muscle mitochondria: a tool in clinical metabolic research. Nature, 184, 1851-1854.
-
(1959)
Nature
, vol.184
, pp. 1851-1854
-
-
Ernster, L.1
Ikkos, D.2
Luft, R.3
-
2
-
-
0021345994
-
Mitochondrial myopathies. Clinical, morphological and biochemical aspects
-
Sengers, R.C., Stadhouders, A.M. and Trijbels, J.M. (1984) Mitochondrial myopathies. Clinical, morphological and biochemical aspects. Eur. J. Pediatr., 141, 192-207.
-
(1984)
Eur. J. Pediatr.
, vol.141
, pp. 192-207
-
-
Sengers, R.C.1
Stadhouders, A.M.2
Trijbels, J.M.3
-
3
-
-
0021798888
-
Mitochondrial myopathies
-
DiMauro, S., Bonilla, E., Zeviani, M., Nakagawa, M. and DeVivo, D.C. (1985) Mitochondrial myopathies. Ann. Neurol., 17, 521-538.
-
(1985)
Ann. Neurol.
, vol.17
, pp. 521-538
-
-
DiMauro, S.1
Bonilla, E.2
Zeviani, M.3
Nakagawa, M.4
DeVivo, D.C.5
-
4
-
-
0023717111
-
Disorders of the mitochondrial respiratory chain: Clinical manifestations and diagnostic approach
-
Trijbels, J.M., Sengers, R.C., Ruitenbeek, W., Fischer, J.C., Bakkeren, J.A. and Janssen, A.J. (1988) Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach. Eur. J. Pediatr., 148, 92-97.
-
(1988)
Eur. J. Pediatr.
, vol.148
, pp. 92-97
-
-
Trijbels, J.M.1
Sengers, R.C.2
Ruitenbeek, W.3
Fischer, J.C.4
Bakkeren, J.A.5
Janssen, A.J.6
-
5
-
-
0024363942
-
Mitochondrial encephalomyopathies
-
Lombes, A., Bonilla, E. and DiMauro, S. (1989) Mitochondrial encephalomyopathies. Rev. Neurol. (Paris), 145, 671-689.
-
(1989)
Rev. Neurol. (Paris)
, vol.145
, pp. 671-689
-
-
Lombes, A.1
Bonilla, E.2
DiMauro, S.3
-
6
-
-
0027930832
-
Mitochondrial diseases of muscle
-
Morgan-Hughes, J.A. (1994) Mitochondrial diseases of muscle. Curr. Opin. Neurol., 7, 457-462.
-
(1994)
Curr. Opin. Neurol.
, vol.7
, pp. 457-462
-
-
Morgan-Hughes, J.A.1
-
7
-
-
0026624980
-
Diseases of the mitochondrial DNA
-
Wallace, D.C. (1992) Diseases of the mitochondrial DNA. Annu. Rev. Biochem., 61, 1175-1212.
-
(1992)
Annu. Rev. Biochem.
, vol.61
, pp. 1175-1212
-
-
Wallace, D.C.1
-
8
-
-
0029638664
-
Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease
-
Johns, D.R. (1995) Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease. N. Engl. J. Med., 333, 638-644.
-
(1995)
N. Engl. J. Med.
, vol.333
, pp. 638-644
-
-
Johns, D.R.1
-
9
-
-
0029948860
-
Metabolic myopathies
-
Tein, I. (1996) Metabolic myopathies. Semin. Pediatr. Neurol., 3, 59-98.
-
(1996)
Semin. Pediatr. Neurol.
, vol.3
, pp. 59-98
-
-
Tein, I.1
-
10
-
-
0014170028
-
Circular dimer and catenate forms of mitochondrial DNA in human leukaemic leucocytes
-
Clayton, D.A. and Vinograd, J. (1967) Circular dimer and catenate forms of mitochondrial DNA in human leukaemic leucocytes. J. Pers., 35, 652-657.
-
(1967)
J. Pers.
, vol.35
, pp. 652-657
-
-
Clayton, D.A.1
Vinograd, J.2
-
11
-
-
0014210552
-
Catenated circular DNA molecules in HeLa cell mitochondria
-
Hudson, B. and Vinograd, J. (1967) Catenated circular DNA molecules in HeLa cell mitochondria. Nature, 216, 647-652.
-
(1967)
Nature
, vol.216
, pp. 647-652
-
-
Hudson, B.1
Vinograd, J.2
-
12
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
Anderson, S., Bankier, A.T., Barrell, B.G., de Bruijn, M.H., Coulson, A.R., Drouin, J., Eperon, I.C., Nierlich, D.P., Roe, B.A., Sanger, F., Schreier, P.H., Smith, A.J., Staden, R. and Young, I.G. (1981) Sequence and organization of the human mitochondrial genome. Nature, 290, 457-465.
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
De Bruijn, M.H.4
Coulson, A.R.5
Drouin, J.6
Eperon, I.C.7
Nierlich, D.P.8
Roe, B.A.9
Sanger, F.10
Schreier, P.H.11
Smith, A.J.12
Staden, R.13
Young, I.G.14
-
13
-
-
0021866528
-
Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase
-
Chomyn, A., Mariottini, P., Cleeter, M.W., Ragan, C.I., Matsuno-Yagi, A., Hatefi, Y., Doolittle, R.F. and Attardi, G. (1985) Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase. Nature, 314, 592-597.
-
(1985)
Nature
, vol.314
, pp. 592-597
-
-
Chomyn, A.1
Mariottini, P.2
Cleeter, M.W.3
Ragan, C.I.4
Matsuno-Yagi, A.5
Hatefi, Y.6
Doolittle, R.F.7
Attardi, G.8
-
14
-
-
0023032242
-
URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit
-
Chomyn, A., Cleeter, M.W., Ragan, C.I, Riley, M., Doolittle, R.F. and Attardi, G. (1986) URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit. Science, 234, 614-618.
-
(1986)
Science
, vol.234
, pp. 614-618
-
-
Chomyn, A.1
Cleeter, M.W.2
Ragan, C.I.3
Riley, M.4
Doolittle, R.F.5
Attardi, G.6
-
15
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
Wallace, D.C., Singh, G., Lott, M.T., Hodge, J.A., Schurr, T.G., Lezza, A.M., Elsas, L.J. II and Nikoskelainen, E.K. (1988) Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science, 242, 1427-1430.
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, T.G.5
Lezza, A.M.6
Elsas II, L.J.7
Nikoskelainen, E.K.8
-
16
-
-
0024798264
-
Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA
-
Holt, I.J., Harding, A.E., Cooper, J.M., Schapira, A.H., Toscano, A., Clark, J.B. and Morgan-Hughes, J.A. (1989) Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA. Ann. Neurol., 26, 699-708.
-
(1989)
Ann. Neurol.
, vol.26
, pp. 699-708
-
-
Holt, I.J.1
Harding, A.E.2
Cooper, J.M.3
Schapira, A.H.4
Toscano, A.5
Clark, J.B.6
Morgan-Hughes, J.A.7
-
17
-
-
0024582466
-
Non-invasive diagnosis of mitochondrial myopathy
-
Poulton, J. and Gardiner, R.M. (1989) Non-invasive diagnosis of mitochondrial myopathy. Lancet, 1, 961.
-
(1989)
Lancet
, vol.1
, pp. 961
-
-
Poulton, J.1
Gardiner, R.M.2
-
18
-
-
0025368281
-
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
-
Shoffner, J.M., Lott, M.T., Lezza, A.M., Seibel, P., Ballinger, S.W. and Wallace, D.C. (1990) Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation. Cell, 61, 931-937.
-
(1990)
Cell
, vol.61
, pp. 931-937
-
-
Shoffner, J.M.1
Lott, M.T.2
Lezza, A.M.3
Seibel, P.4
Ballinger, S.W.5
Wallace, D.C.6
-
19
-
-
0025267548
-
A new mitochondrial disease associated with mitochondrial DNA heteroplasmy
-
Holt, I.J., Harding, A.E., Petty, R.K. and Morgan-Hughes, J.A. (1990) A new mitochondrial disease associated with mitochondrial DNA heteroplasmy. Am. J. Hum. Genet., 46, 428-433.
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 428-433
-
-
Holt, I.J.1
Harding, A.E.2
Petty, R.K.3
Morgan-Hughes, J.A.4
-
20
-
-
0025666322
-
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
-
Goto, Y., Nonaka, I. and Horai, S. (1990) A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature, 348, 651-653.
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
21
-
-
0025260002
-
Mitochondrial mutation in fatal infantile cardiomyopathy
-
Tanaka, M., Ino, H., Ohno, K., Hattori, K., Sato, W., Ozawa, T., Tanaka, T. and Itoyama, S. (1990) Mitochondrial mutation in fatal infantile cardiomyopathy. Lancet, 336, 1452.
-
(1990)
Lancet
, vol.336
, pp. 1452
-
-
Tanaka, M.1
Ino, H.2
Ohno, K.3
Hattori, K.4
Sato, W.5
Ozawa, T.6
Tanaka, T.7
Itoyama, S.8
-
22
-
-
0024601360
-
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region
-
Zeviani, M., Servidei, S., Gellera, C., Bertini, E., DiMauro, S. and DiDonato, S. (1989) An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region. Nature, 339, 309-311.
-
(1989)
Nature
, vol.339
, pp. 309-311
-
-
Zeviani, M.1
Servidei, S.2
Gellera, C.3
Bertini, E.4
Dimauro, S.5
DiDonato, S.6
-
23
-
-
0025807222
-
Maternally inherited myopathy and cardiomyopathy: Association with mutation in mitochondrial DNA tRNA(Leu)(UUR)
-
Zeviani, M., Gellera, C., Antozzi, C., Rimoldi, M., Morandi, L., Villani, F., Tiranti, V. and DiDonato, S. (1991) Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR). Lancet, 338, 143-147.
-
(1991)
Lancet
, vol.338
, pp. 143-147
-
-
Zeviani, M.1
Gellera, C.2
Antozzi, C.3
Rimoldi, M.4
Morandi, L.5
Villani, F.6
Tiranti, V.7
DiDonato, S.8
-
24
-
-
0026715879
-
Nucleus-driven mutations of human mitochondrial DNA
-
Zeviani, M. (1992) Nucleus-driven mutations of human mitochondrial DNA. J. Inherited Metab. Dis., 15, 456-471.
-
(1992)
J. Inherited Metab. Dis.
, vol.15
, pp. 456-471
-
-
Zeviani, M.1
-
25
-
-
0026840385
-
Defects of mitochondrial DNA
-
Zeviani, M. and Antozzi, C. (1992) Defects of mitochondrial DNA. Brain Pathol., 2, 121-132.
-
(1992)
Brain Pathol.
, vol.2
, pp. 121-132
-
-
Zeviani, M.1
Antozzi, C.2
-
26
-
-
0021891869
-
The mitochondrial electron transport and oxidative phosphorylation system
-
Hatefi, Y. (1985) The mitochondrial electron transport and oxidative phosphorylation system. Annu. Rev. Biochem., 54, 1015-1069.
-
(1985)
Annu. Rev. Biochem.
, vol.54
, pp. 1015-1069
-
-
Hatefi, Y.1
-
27
-
-
0026487290
-
Sequences of 20 subunits of NADH:ubiquinone oxidoreductase from bovine heart mitochondria. Application of a novel strategy for sequencing proteins using the polymerase chain reaction
-
Walker, J.E., Arizmendi, J.M., Dupuis, A., Fearnley, I.M., Finel, M., Medd, S.M., Pilkington, S.J., Runswick, M.J. and Skehel, J.M. (1992) Sequences of 20 subunits of NADH:ubiquinone oxidoreductase from bovine heart mitochondria. Application of a novel strategy for sequencing proteins using the polymerase chain reaction. J. Mol. Biol., 226, 1051-1072.
-
(1992)
J. Mol. Biol.
, vol.226
, pp. 1051-1072
-
-
Walker, J.E.1
Arizmendi, J.M.2
Dupuis, A.3
Fearnley, I.M.4
Finel, M.5
Medd, S.M.6
Pilkington, S.J.7
Runswick, M.J.8
Skehel, J.M.9
-
28
-
-
0027104114
-
The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains
-
Walker, J.E. (1992) The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains. Quart. Rev. Biophys., 25, 253-324.
-
(1992)
Quart. Rev. Biophys.
, vol.25
, pp. 253-324
-
-
Walker, J.E.1
-
29
-
-
0025760073
-
The respiratorychain NADH dehydrogenase (complex I) of mitochondria
-
Weiss, H., Friedrich, T., Hofhaus, G. and Preis, D. (1991) The respiratorychain NADH dehydrogenase (complex I) of mitochondria. Eur. J. Biochem., 197, 563-576.
-
(1991)
Eur. J. Biochem.
, vol.197
, pp. 563-576
-
-
Weiss, H.1
Friedrich, T.2
Hofhaus, G.3
Preis, D.4
-
30
-
-
0027519561
-
The gene locus of the proton-translocating NADH: Ubiquinone oxidoreductase in Escherichia coli. Organization of the 14 genes and relationship between the derived proteins and subunits of mitochondrial complex I
-
Weidner, U., Geier, S., Ptock, A., Friedrich, T., Leif, H. and Weiss, H. (1993) The gene locus of the proton-translocating NADH: ubiquinone oxidoreductase in Escherichia coli. Organization of the 14 genes and relationship between the derived proteins and subunits of mitochondrial complex I. J. Mol. Biol., 233, 109-122.
-
(1993)
J. Mol. Biol.
, vol.233
, pp. 109-122
-
-
Weidner, U.1
Geier, S.2
Ptock, A.3
Friedrich, T.4
Leif, H.5
Weiss, H.6
-
31
-
-
0031592480
-
Three-dimensional structure of NADH-dehydrogenase from Neurospora crassa by electron microscopy and conical tilt reconstruction
-
Guenebaut, V., Vincentelli, R., Mills, D., Weiss, H. and Leonard, K.R. (1997) Three-dimensional structure of NADH-dehydrogenase from Neurospora crassa by electron microscopy and conical tilt reconstruction. J. Mol. Biol., 265, 409-418.
-
(1997)
J. Mol. Biol.
, vol.265
, pp. 409-418
-
-
Guenebaut, V.1
Vincentelli, R.2
Mills, D.3
Weiss, H.4
Leonard, K.R.5
-
32
-
-
0032540273
-
Three-dimensional structure of bovine NADH:ubiquinone oxidoreductase (complex I) at 22 Å in ice
-
Grigorieff, N. (1998) Three-dimensional structure of bovine NADH:ubiquinone oxidoreductase (complex I) at 22 Å in ice. J. Mol. Biol., 277, 1033-1046.
-
(1998)
J. Mol. Biol.
, vol.277
, pp. 1033-1046
-
-
Grigorieff, N.1
-
33
-
-
0018438631
-
Purification and molecular and enzymic properties of mitochondrial NADH dehydrogenase
-
Galante, Y.M. and Hatefi, Y. (1979) Purification and molecular and enzymic properties of mitochondrial NADH dehydrogenase. Arch. Biochem. Biophys., 192, 559-568.
-
(1979)
Arch. Biochem. Biophys.
, vol.192
, pp. 559-568
-
-
Galante, Y.M.1
Hatefi, Y.2
-
34
-
-
0028269382
-
Catalytic sector of complex I (NADH:ubiquinone oxidoreductase): Subunit stoichiometry and substrateinduced conformation changes
-
Belogrudov, G. and Hatefi, Y. (1994) Catalytic sector of complex I (NADH:ubiquinone oxidoreductase): subunit stoichiometry and substrateinduced conformation changes. Biochemistry, 33, 4571-4576.
-
(1994)
Biochemistry
, vol.33
, pp. 4571-4576
-
-
Belogrudov, G.1
Hatefi, Y.2
-
35
-
-
0021958744
-
EPR studies of iron-sulfur clusters in isolated subunits and subfractions of NADH-ubiquinone oxidoreductase
-
Ohnishi, T., Ragan, C.I. and Hatefi, Y. (1985) EPR studies of iron-sulfur clusters in isolated subunits and subfractions of NADH-ubiquinone oxidoreductase. J. Biol. Chem., 260, 2782-2788.
-
(1985)
J. Biol. Chem.
, vol.260
, pp. 2782-2788
-
-
Ohnishi, T.1
Ragan, C.I.2
Hatefi, Y.3
-
36
-
-
0019888311
-
Studies on the interaction of arylazido-beta-alanyl NAD+ with the mitochondrial NADH dehydrogenase
-
Chen, S. and Guillory, R.J. (1981) Studies on the interaction of arylazido-beta-alanyl NAD+ with the mitochondrial NADH dehydrogenase. J. Biol. Chem., 256, 8318-8323.
-
(1981)
J. Biol. Chem.
, vol.256
, pp. 8318-8323
-
-
Chen, S.1
Guillory, R.J.2
-
37
-
-
0025017864
-
N-arylazido-beta-alanyl-NAD+, a new NAD+ photoaffinity analogue. Synthesis and labeling of mitochondrial NADH dehydrogenase
-
Deng, P.S., Hatefi, Y. and Chen, S. (1990) N-arylazido-beta-alanyl-NAD+, a new NAD+ photoaffinity analogue. Synthesis and labeling of mitochondrial NADH dehydrogenase. Biochemistry, 29, 1094-1098.
-
(1990)
Biochemistry
, vol.29
, pp. 1094-1098
-
-
Deng, P.S.1
Hatefi, Y.2
Chen, S.3
-
38
-
-
0026032458
-
Relationship between mitochondrial NADH-ubiquinone reductase and a bacterial NAD-reducing hydrogenase
-
Pilkington, S.J., Skehel, J.M., Gennis, R.B. and Walker, J.E. (1991) Relationship between mitochondrial NADH-ubiquinone reductase and a bacterial NAD-reducing hydrogenase. Biochemistry, 30, 2166-2175.
-
(1991)
Biochemistry
, vol.30
, pp. 2166-2175
-
-
Pilkington, S.J.1
Skehel, J.M.2
Gennis, R.B.3
Walker, J.E.4
-
39
-
-
0024559488
-
Mitochondrial NADH-ubiquinone reductase: Complementary DNA sequences of import precursors of the bovine and human 24-kDa subunit
-
Pilkington, S.J. and Walker, J.E. (1989) Mitochondrial NADH-ubiquinone reductase: complementary DNA sequences of import precursors of the bovine and human 24-kDa subunit. Biochemistry, 28, 3257-3264.
-
(1989)
Biochemistry
, vol.28
, pp. 3257-3264
-
-
Pilkington, S.J.1
Walker, J.E.2
-
40
-
-
0024350374
-
Mitochondrial NADH:ubiquinone reductase: Complementary DNA sequence of the import precursor of the bovine 75-kDa subunit
-
Runswick, M.J., Gennis, R.B., Feamley, I.M. and Walker, J.E. (1989) Mitochondrial NADH:ubiquinone reductase: complementary DNA sequence of the import precursor of the bovine 75-kDa subunit. Biochemistry, 28, 9452-9459.
-
(1989)
Biochemistry
, vol.28
, pp. 9452-9459
-
-
Runswick, M.J.1
Gennis, R.B.2
Feamley, I.M.3
Walker, J.E.4
-
41
-
-
0025854234
-
A homologue of a nuclear-coded iron-sulfur protein subunit of bovine mitochondrial complex I is encoded in chloroplast genomes
-
Dupuis, A., Skehel, J.M. and Walker, J.E. (1991) A homologue of a nuclear-coded iron-sulfur protein subunit of bovine mitochondrial complex I is encoded in chloroplast genomes. Biochemistry, 30, 2954-2960.
-
(1991)
Biochemistry
, vol.30
, pp. 2954-2960
-
-
Dupuis, A.1
Skehel, J.M.2
Walker, J.E.3
-
42
-
-
0029159804
-
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
-
Bourgeron, T., Rustin, P., Chretien, D., Birch-Machin, M., Bourgeois, M., Viegas-Pequignot, E., Munnich, A. and Rotig, A. (1995) Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. Nature Genet., 11, 144-149.
-
(1995)
Nature Genet.
, vol.11
, pp. 144-149
-
-
Bourgeron, T.1
Rustin, P.2
Chretien, D.3
Birch-Machin, M.4
Bourgeois, M.5
Viegas-Pequignot, E.6
Munnich, A.7
Rotig, A.8
-
43
-
-
0030447468
-
Diagnosis of complex I deficiency in patients with lactic acidemia using skin fibroblast cultures
-
Pitkanen, S., Raha, S. and Robinson, B.H. (1996) Diagnosis of complex I deficiency in patients with lactic acidemia using skin fibroblast cultures. Biochem. Mol. Med., 59, 134-137.
-
(1996)
Biochem. Mol. Med.
, vol.59
, pp. 134-137
-
-
Pitkanen, S.1
Raha, S.2
Robinson, B.H.3
-
44
-
-
0029984559
-
Benign mitochondrial encephalomyopathy in a patient with complex I deficiency
-
Trijbels, J.M., Ruitenbeek, W., Sengers, R.C., Janssen, A.J. and van Oost, B.A. (1996) Benign mitochondrial encephalomyopathy in a patient with complex I deficiency. J. Inherited Metab. Dis., 19, 149-152.
-
(1996)
J. Inherited Metab. Dis.
, vol.19
, pp. 149-152
-
-
Trijbels, J.M.1
Ruitenbeek, W.2
Sengers, R.C.3
Janssen, A.J.4
Van Oost, B.A.5
-
45
-
-
0029745044
-
Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolism
-
Ruitenbeek, W., Wendel, U., Hamel, B.C. and Trijbels, J.M. (1996) Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolism. J. Inherited Metab. Dis., 19, 581-587.
-
(1996)
J. Inherited Metab. Dis.
, vol.19
, pp. 581-587
-
-
Ruitenbeek, W.1
Wendel, U.2
Hamel, B.C.3
Trijbels, J.M.4
-
46
-
-
0026729738
-
The use of chorionic villi in prenatal diagnosis of mitochondriopathies
-
Ruitenbeek, W., Sengers, R.C., Trijbels, J.M., Janssen, A.J. and Bakkeren, J.A. (1992) The use of chorionic villi in prenatal diagnosis of mitochondriopathies. J. Inherited Metab. Dis., 15, 303-306.
-
(1992)
J. Inherited Metab. Dis.
, vol.15
, pp. 303-306
-
-
Ruitenbeek, W.1
Sengers, R.C.2
Trijbels, J.M.3
Janssen, A.J.4
Bakkeren, J.A.5
-
47
-
-
0025944560
-
Leber hereditary optic neuropathy: Identification of the same mitochondrial NDI mutation in six pedigrees
-
Howell, N., Bindoff, L.A., McCullough, D.A., Kubacka, I., Poulton, J., Mackey, D., Taylor, L. and Tumbull, D.M. (1991) Leber hereditary optic neuropathy: identification of the same mitochondrial NDI mutation in six pedigrees. Am. J. Hum. Genet., 49, 939-950.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 939-950
-
-
Howell, N.1
Bindoff, L.A.2
McCullough, D.A.3
Kubacka, I.4
Poulton, J.5
Mackey, D.6
Taylor, L.7
Tumbull, D.M.8
-
48
-
-
0025910614
-
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy
-
Huoponen, K., Vilkki, J., Aula, P., Nikoskelainen, E.K. and Savontaus, M.L. (1991) A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy. Am. J. Hum. Genet., 48, 1147-1153.
-
(1991)
Am. J. Hum. Genet.
, vol.48
, pp. 1147-1153
-
-
Huoponen, K.1
Vilkki, J.2
Aula, P.3
Nikoskelainen, E.K.4
Savontaus, M.L.5
-
49
-
-
0030788482
-
Mitochondrial DNA mutations and pathogenesis
-
Schon, E.A., Bonilla, E. and DiMauro, S. (1997) Mitochondrial DNA mutations and pathogenesis. J. Bioenerg. Biomembr., 29, 131-149.
-
(1997)
J. Bioenerg. Biomembr.
, vol.29
, pp. 131-149
-
-
Schon, E.A.1
Bonilla, E.2
DiMauro, S.3
-
50
-
-
0031900991
-
The myoclonic epilepsy and ragged-Red fiber mutation provides new insights into human mitochondrial function and genetics
-
Chomyn, A. (1998) The myoclonic epilepsy and ragged-Red fiber mutation provides new insights into human mitochondrial function and genetics. Am. J. Hum. Genet., 62, 745-751.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 745-751
-
-
Chomyn, A.1
-
51
-
-
0022965899
-
Seven unidentified reading frames of human mitochondrial DNA encode subunits of the respiratory chain NADH dehydrogenase
-
Attardi, G., Chomyn, A., Doolittle, R.F., Mariottini, P. and Ragan, C.I. (1986) Seven unidentified reading frames of human mitochondrial DNA encode subunits of the respiratory chain NADH dehydrogenase. Cold Spring Harbor Symp. Quant. Biol., 51, 103-114.
-
(1986)
Cold Spring Harbor Symp. Quant. Biol.
, vol.51
, pp. 103-114
-
-
Attardi, G.1
Chomyn, A.2
Doolittle, R.F.3
Mariottini, P.4
Ragan, C.I.5
-
52
-
-
0029059067
-
MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination
-
Enriquez, J.A., Chomyn, A. and Attardi, G. (1995) MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination. Nature Genet., 10, 47-55.
-
(1995)
Nature Genet.
, vol.10
, pp. 47-55
-
-
Enriquez, J.A.1
Chomyn, A.2
Attardi, G.3
-
53
-
-
0030771308
-
Genetic counselling in mitochondrial diseases
-
Warner, T.T. and Schapira, A.H. (1997) Genetic counselling in mitochondrial diseases. Curr. Opin. Neurol., 10, 408-412.
-
(1997)
Curr. Opin. Neurol.
, vol.10
, pp. 408-412
-
-
Warner, T.T.1
Schapira, A.H.2
-
54
-
-
0029816795
-
Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA
-
Jenuth, J.P., Peterson, A.C., Fu, K. and Shoubridge, E.A. (1996) Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA. Nature Genet., 14, 146-151.
-
(1996)
Nature Genet.
, vol.14
, pp. 146-151
-
-
Jenuth, J.P.1
Peterson, A.C.2
Fu, K.3
Shoubridge, E.A.4
-
55
-
-
0028272494
-
Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation
-
de Vries, D., de Wijs, I., Ruitenbeek, W., Begeer, J., Smit, P., Bentlage, H. and van Oost, B. (1994) Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation. J. Neurol. Sci., 124, 77-82.
-
(1994)
J. Neurol. Sci.
, vol.124
, pp. 77-82
-
-
De Vries, D.1
De Wijs, I.2
Ruitenbeek, W.3
Begeer, J.4
Smit, P.5
Bentlage, H.6
Van Oost, B.7
-
56
-
-
17344365132
-
Demonstration of a new pathogenic mutation in human complex I deficiency: A 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit
-
van den Heuvel, L., Ruitenbeek, W., Smeets, R., Gelman-Kohan, Z., Elpeleg, O., Loeffen, J., Trijbels, F., Mariman, E., de Bruijn, D. and Smeitink, J. (1998) Demonstration of a new pathogenic mutation in human complex I deficiency: a 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit. Am. J. Hum. Genet., 62, 262-268.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 262-268
-
-
Van Den Heuvel, L.1
Ruitenbeek, W.2
Smeets, R.3
Gelman-Kohan, Z.4
Elpeleg, O.5
Loeffen, J.6
Trijbels, F.7
Mariman, E.8
De Bruijn, D.9
Smeitink, J.10
-
57
-
-
0023883150
-
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
-
Holt, I.J., Harding, A.E. and Morgan-Hughes, J.A. (1988) Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Nature, 331, 717-719.
-
(1988)
Nature
, vol.331
, pp. 717-719
-
-
Holt, I.J.1
Harding, A.E.2
Morgan-Hughes, J.A.3
-
58
-
-
0025046999
-
Mitochondrial myopathies: Clinical defects
-
Morgan-Hughes, J.A., Cooper, J.M., Holt, I.J., Harding, A.E., Schapira, A.H. and Clark, J.B. (1990) Mitochondrial myopathies: clinical defects. Biochem. Soc. Trans., 18, 523-526.
-
(1990)
Biochem. Soc. Trans.
, vol.18
, pp. 523-526
-
-
Morgan-Hughes, J.A.1
Cooper, J.M.2
Holt, I.J.3
Harding, A.E.4
Schapira, A.H.5
Clark, J.B.6
-
59
-
-
0028286006
-
Molecular basis of mitochondrial DNA disease
-
Brown, M.D. and Wallace, D.C. (1994) Molecular basis of mitochondrial DNA disease. J. Bioenerg. Biomembr., 26, 273-289.
-
(1994)
J. Bioenerg. Biomembr.
, vol.26
, pp. 273-289
-
-
Brown, M.D.1
Wallace, D.C.2
-
60
-
-
0030465635
-
Mitochondrial genetics and human disease
-
Grossman, L.I. and Shoubridge, E.A. (1996) Mitochondrial genetics and human disease. BioEssays, 18, 983-991.
-
(1996)
BioEssays
, vol.18
, pp. 983-991
-
-
Grossman, L.I.1
Shoubridge, E.A.2
-
61
-
-
0023240790
-
Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: Mitochondrial DNA genes sustain seventeen times more mutations
-
Wallace, D.C., Ye, J.H., Neckelmann, S.N., Singh, G., Webster, K.A. and Greenberg, B.D. (1987) Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: mitochondrial DNA genes sustain seventeen times more mutations. Curr. Genet., 12, 81-90.
-
(1987)
Curr. Genet.
, vol.12
, pp. 81-90
-
-
Wallace, D.C.1
Ye, J.H.2
Neckelmann, S.N.3
Singh, G.4
Webster, K.A.5
Greenberg, B.D.6
-
62
-
-
0030298544
-
Isolation, mapping, and genomic structure of an X-linked gene for a subunit of human mitochondrial complex I
-
Zhuchenko, O., Wehnert, M., Bailey, J., Sun, Z.S. and Lee, C.C. (1996) Isolation, mapping, and genomic structure of an X-linked gene for a subunit of human mitochondrial complex I. Genomics, 37, 281-288.
-
(1996)
Genomics
, vol.37
, pp. 281-288
-
-
Zhuchenko, O.1
Wehnert, M.2
Bailey, J.3
Sun, Z.S.4
Lee, C.C.5
-
63
-
-
0027414356
-
Possible X linked congenital mitochondrial cardiomyopathy in three families
-
Orstavik, K.H., Skjorten, F., Hellebostad, M., Haga, P. and Langslet, A. (1993) Possible X linked congenital mitochondrial cardiomyopathy in three families. J. Med. Genet., 30, 269-272.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 269-272
-
-
Orstavik, K.H.1
Skjorten, F.2
Hellebostad, M.3
Haga, P.4
Langslet, A.5
-
64
-
-
0031927247
-
Mutation analysis and tissue distribution of the X-chromosomal mitochondrial NADH:ubiquinone oxidoreductase NDUFA1 gene in fetal and adult human tissues
-
Loeffen, J., Smeets, R., Smeitink, J., Ruitenbeek, W., Janssen, A.J., Mariman, E., Sengers, R.C., Trijbels, F. and van den Heuvel, L. (1998) Mutation analysis and tissue distribution of the X-chromosomal mitochondrial NADH:ubiquinone oxidoreductase NDUFA1 gene in fetal and adult human tissues. J. Inherited Metab. Dis., 21, 210-215.
-
(1998)
J. Inherited Metab. Dis.
, vol.21
, pp. 210-215
-
-
Loeffen, J.1
Smeets, R.2
Smeitink, J.3
Ruitenbeek, W.4
Janssen, A.J.5
Mariman, E.6
Sengers, R.C.7
Trijbels, F.8
Van Den Heuvel, L.9
-
65
-
-
0031582715
-
Modular evolution of the respiratory NADH:ubiquinone oxidoreductase and the origin of its modules
-
Friedrich, T. and Weiss, H. (1997) Modular evolution of the respiratory NADH:ubiquinone oxidoreductase and the origin of its modules. J. Theor. Biol., 187, 529-540.
-
(1997)
J. Theor. Biol.
, vol.187
, pp. 529-540
-
-
Friedrich, T.1
Weiss, H.2
-
66
-
-
0029075136
-
Isolation and characterization of the proton-translocating NADH: Ubiquinone oxidoreductase from Escherichia coli
-
Leif, H., Sled, V.D., Ohnisni, T., Weiss, H. and Friedrich, T. (1995) Isolation and characterization of the proton-translocating NADH: ubiquinone oxidoreductase from Escherichia coli. Eur. J. Biochem., 230, 538-548.
-
(1995)
Eur. J. Biochem.
, vol.230
, pp. 538-548
-
-
Leif, H.1
Sled, V.D.2
Ohnisni, T.3
Weiss, H.4
Friedrich, T.5
-
67
-
-
0027971160
-
NADH dehydrogenase subunit genes in the mitochondrial DNA of yeasts
-
Nosek, J. and Fukuhara, H. (1994) NADH dehydrogenase subunit genes in the mitochondrial DNA of yeasts. J. Bacteriol., 176, 5622-5630.
-
(1994)
J. Bacteriol.
, vol.176
, pp. 5622-5630
-
-
Nosek, J.1
Fukuhara, H.2
-
68
-
-
0027433148
-
A new five-year plan for the U.S. Human Genome Project
-
Collins, F. and Galas, D. (1993) A new five-year plan for the U.S. Human Genome Project. Science, 262, 43-46.
-
(1993)
Science
, vol.262
, pp. 43-46
-
-
Collins, F.1
Galas, D.2
-
69
-
-
0030040319
-
The nuclear-encoded 18 kDa (IP) AQDQ subunit of bovine heart complex I is phosphorylated by the mitochondrial cAMP-dependent protein kinase
-
Papa, S., Sardanelli, A.M., Cocco, T., Speranza, F., Scacco, S.C. and Technikova-Dobrova, Z. (1996) The nuclear-encoded 18 kDa (IP) AQDQ subunit of bovine heart complex I is phosphorylated by the mitochondrial cAMP-dependent protein kinase. FEBS Lett., 379, 299-301.
-
(1996)
FEBS Lett.
, vol.379
, pp. 299-301
-
-
Papa, S.1
Sardanelli, A.M.2
Cocco, T.3
Speranza, F.4
Scacco, S.C.5
Technikova-Dobrova, Z.6
-
70
-
-
0025081416
-
An unusually large multifunctional polypeptide in the erythromycin-producing polyketide synthase of Saccharopolyspora erythraea
-
Cortes, J., Haydock, S.F., Roberts, G.A., Bevitt, D.J. and Leadlay, P.F. (1990) An unusually large multifunctional polypeptide in the erythromycin-producing polyketide synthase of Saccharopolyspora erythraea. Nature, 348, 176-178.
-
(1990)
Nature
, vol.348
, pp. 176-178
-
-
Cortes, J.1
Haydock, S.F.2
Roberts, G.A.3
Bevitt, D.J.4
Leadlay, P.F.5
-
71
-
-
0032571104
-
The 24-kDa subunit of the bovine mitochondrial NADH:ubiquinone oxidoreductase is a G protein
-
Hegde, R. (1998) The 24-kDa subunit of the bovine mitochondrial NADH:ubiquinone oxidoreductase is a G protein. Biochem. Biophys. Res. Commun., 244, 620-629.
-
(1998)
Biochem. Biophys. Res. Commun.
, vol.244
, pp. 620-629
-
-
Hegde, R.1
-
72
-
-
0032540107
-
Cloning of the human mitochondrial 51 kDa subunit (NDUFV1) reveals a 100% antisense homology of its 3′UTR with the 5′UTR of the gamma-interferon inducible protein (IP-30) precursor: Is this a link between mitochondrial myopathy and inflammation?
-
Schuelke, M., Loeffen, J., Mariman, E., Smeitink, J. and van den Heuvel, L. (1998) Cloning of the human mitochondrial 51 kDa subunit (NDUFV1) reveals a 100% antisense homology of its 3′UTR with the 5′UTR of the gamma-interferon inducible protein (IP-30) precursor: is this a link between mitochondrial myopathy and inflammation? Biochem. Biophys. Res. Commun., 245, 599-606.
-
(1998)
Biochem. Biophys. Res. Commun.
, vol.245
, pp. 599-606
-
-
Schuelke, M.1
Loeffen, J.2
Mariman, E.3
Smeitink, J.4
Van Den Heuvel, L.5
-
73
-
-
0031661362
-
Molecular characterization and mutational analysis in the human B17 subunit of the mitochondrial respiratory chain complex I
-
in press
-
Smeitink, J., Loeffen, J., Smeets, R., Triepels, R., Ruitenbeek, W., Trijbels, F. and van den Heuvel, L. (1998) Molecular characterization and mutational analysis in the human B17 subunit of the mitochondrial respiratory chain complex I. Hum. Genet., in press.
-
(1998)
Hum. Genet.
-
-
Smeitink, J.1
Loeffen, J.2
Smeets, R.3
Triepels, R.4
Ruitenbeek, W.5
Trijbels, F.6
Van Den Heuvel, L.7
-
74
-
-
0032054295
-
Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease
-
Hattori, N., Yoshino, H., Tanaka, M., Suzuki, H. and Mizuno, Y. (1998) Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease. Genomics, 49, 52-58.
-
(1998)
Genomics
, vol.49
, pp. 52-58
-
-
Hattori, N.1
Yoshino, H.2
Tanaka, M.3
Suzuki, H.4
Mizuno, Y.5
-
75
-
-
0027097636
-
The human mitochondrial NADH: Ubiquinone oxidoreductase 51-kDa subunit maps adjacent to the glutathione S-transferase PI-I gene on chromosome 11q13
-
Spencer, S.R., Taylor, J.B., Cowell, I.G., Xia, C.L., Pemble, S.E. and Ketterer, B. (1992) The human mitochondrial NADH: ubiquinone oxidoreductase 51-kDa subunit maps adjacent to the glutathione S-transferase PI-I gene on chromosome 11q13. Genomics, 14, 1116-1118.
-
(1992)
Genomics
, vol.14
, pp. 1116-1118
-
-
Spencer, S.R.1
Taylor, J.B.2
Cowell, I.G.3
Xia, C.L.4
Pemble, S.E.5
Ketterer, B.6
-
76
-
-
0029024362
-
Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene
-
de Coo, R., Buddiger, P., Smeets, H., Geurts van Kessel, A., Morgan-Hughes, J., Weghuis, D.O., Overhauser, J. and van Oost, B. (1995) Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene. Genomics, 26, 461-466.
-
(1995)
Genomics
, vol.26
, pp. 461-466
-
-
De Coo, R.1
Buddiger, P.2
Smeets, H.3
Geurts Van Kessel, A.4
Morgan-Hughes, J.5
Weghuis, D.O.6
Overhauser, J.7
Van Oost, B.8
-
77
-
-
0030685792
-
Molecular cloning and characterization of the human mitochondrial NADH:oxidoreductase 10-kDa gene (NDUFV3)
-
de Coo, R.F., Buddiger, P., Smeets, H.J. and van Oost, B.A. (1997) Molecular cloning and characterization of the human mitochondrial NADH:oxidoreductase 10-kDa gene (NDUFV3). Genomics, 45, 434-437.
-
(1997)
Genomics
, vol.45
, pp. 434-437
-
-
De Coo, R.F.1
Buddiger, P.2
Smeets, H.J.3
Van Oost, B.A.4
-
78
-
-
0031577725
-
Identification and primary structure of five human NADH-ubiquinone oxidoreductase subunits
-
Ton, C., Hwang, D.M., Dempsey, A.A. and Liew, C.C. (1997) Identification and primary structure of five human NADH-ubiquinone oxidoreductase subunits. Biochem. Biophys. Res. Commun., 241, 589-594.
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.241
, pp. 589-594
-
-
Ton, C.1
Hwang, D.M.2
Dempsey, A.A.3
Liew, C.C.4
-
79
-
-
0031401865
-
Cloning of the human cDNA sequence encoding the NADH:ubiquinone oxidoreductase MLRQ subunit
-
Kim, J.W., Lee, Y., Kang, H.B., Chose, Y.K., Chung, T.W., Chang, S.Y., Lee, K.S. and Choe, I.S. (1997) Cloning of the human cDNA sequence encoding the NADH:ubiquinone oxidoreductase MLRQ subunit. Biochem. Mol. Biol. Int., 43, 669-675.
-
(1997)
Biochem. Mol. Biol. Int.
, vol.43
, pp. 669-675
-
-
Kim, J.W.1
Lee, Y.2
Kang, H.B.3
Chose, Y.K.4
Chung, T.W.5
Chang, S.Y.6
Lee, K.S.7
Choe, I.S.8
-
80
-
-
0031042378
-
A human cDNA encoding the homologue of NADH: Ubiquinone oxidoreductase subunit B13
-
Pata, I., Tensing, K. and Metspalu, A. (1997) A human cDNA encoding the homologue of NADH: ubiquinone oxidoreductase subunit B13. Biochim. Biophys. Acta, 1350, 115-118.
-
(1997)
Biochim. Biophys. Acta
, vol.1350
, pp. 115-118
-
-
Pata, I.1
Tensing, K.2
Metspalu, A.3
-
81
-
-
0030631582
-
Cloning of the human NADH:ubiquinone oxidoreductase subunit B13: Localization to chromosome 7q32 and identification of a pseudogene on 11p15
-
Russell, M.W., du Manoir, S., Collins, F.S. and Brody, L.C. (1997) Cloning of the human NADH:ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15. Mamm. Genome, 8, 60-61.
-
(1997)
Mamm. Genome
, vol.8
, pp. 60-61
-
-
Russell, M.W.1
Du Manoir, S.2
Collins, F.S.3
Brody, L.C.4
-
82
-
-
0030830977
-
In situ hybridisation mapping of genomic clones for five human respiratory chain complex I genes
-
Dunbar, D.R., Shibasaki, Y., Dobbie, L., Andersson, B. and Brookes, A.J. (1997) In situ hybridisation mapping of genomic clones for five human respiratory chain complex I genes. Cytogenet. Cell. Genet., 78, 21-24.
-
(1997)
Cytogenet. Cell. Genet.
, vol.78
, pp. 21-24
-
-
Dunbar, D.R.1
Shibasaki, Y.2
Dobbie, L.3
Andersson, B.4
Brookes, A.J.5
-
83
-
-
0028292070
-
Assignment of the gene for the human proliferating cell nucleolar protein P120 (NOL1) to chromosome 12p13 by fluorescence in situ hybridization and polymerase chain reaction with somatic cell hybrids
-
Baens, M., Chaffanet, M., Aerssens, J., Cassiman, J.J. and Marynen, P. (1994) Assignment of the gene for the human proliferating cell nucleolar protein P120 (NOL1) to chromosome 12p13 by fluorescence in situ hybridization and polymerase chain reaction with somatic cell hybrids. Genomics, 21, 296-297.
-
(1994)
Genomics
, vol.21
, pp. 296-297
-
-
Baens, M.1
Chaffanet, M.2
Aerssens, J.3
Cassiman, J.J.4
Marynen, P.5
-
84
-
-
0030200921
-
The human B22 subunit of the NADH-ubiquinone oxidoreductase maps to the region of chromosome 8 involved in branchio-otorenal syndrome
-
Gu, J.Z., Lin, X. and Wells, D.E. (1996) The human B22 subunit of the NADH-ubiquinone oxidoreductase maps to the region of chromosome 8 involved in branchio-otorenal syndrome. Genomics, 35, 6-10.
-
(1996)
Genomics
, vol.35
, pp. 6-10
-
-
Gu, J.Z.1
Lin, X.2
Wells, D.E.3
-
85
-
-
0025948124
-
Determination of the cDNA sequence for the human mitochondrial 75-kDa Fe-S protein of NADH-coenzyme Q reductase
-
Chow, W., Ragan, I. and Robinson, B.H. (1991) Determination of the cDNA sequence for the human mitochondrial 75-kDa Fe-S protein of NADH-coenzyme Q reductase. Eur. J. Biochem., 201, 547-550.
-
(1991)
Eur. J. Biochem.
, vol.201
, pp. 547-550
-
-
Chow, W.1
Ragan, I.2
Robinson, B.H.3
-
86
-
-
0030298008
-
Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13
-
Hyslop, S.J., Duncan, A.M., Pitkanen, S. and Robinson, B.H. (1996) Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13. Genomics, 37, 375-380.
-
(1996)
Genomics
, vol.37
, pp. 375-380
-
-
Hyslop, S.J.1
Duncan, A.M.2
Pitkanen, S.3
Robinson, B.H.4
-
87
-
-
0002514555
-
cDNA sequence and chromosomal localization of the NDUFS8 human gene coding for the 23 kDa subunit of the mitochondrial complex I
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Procaccio, V., Depetris, D., Soularue, P., Mattei, M.G., Lunardi, J. and Issartel, J.P. (1997) cDNA sequence and chromosomal localization of the NDUFS8 human gene coding for the 23 kDa subunit of the mitochondrial complex I. Biochim. Biophys. Acta, 1351, 37-41.
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(1997)
Biochim. Biophys. Acta
, vol.1351
, pp. 37-41
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Procaccio, V.1
Depetris, D.2
Soularue, P.3
Mattei, M.G.4
Lunardi, J.5
Issartel, J.P.6
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