-
1
-
-
0037610225
-
Diagnosis and treatment of the hepatic porphyrias
-
M. Lecha, C. Herrero, and D. Ozalla Diagnosis and treatment of the hepatic porphyrias Dermatol. Ther. 16 2003 65 72
-
(2003)
Dermatol. Ther.
, vol.16
, pp. 65-72
-
-
Lecha, M.1
Herrero, C.2
Ozalla, D.3
-
2
-
-
0042283812
-
Guide to porphyrias. A historical and clinical perspective
-
S.E. Foran, and G. Abel Guide to porphyrias. A historical and clinical perspective Am. J. Clin. Pathol. 119 Suppl. 2003 S86 S93
-
(2003)
Am. J. Clin. Pathol.
, vol.119
-
-
Foran, S.E.1
Abel, G.2
-
3
-
-
0029448995
-
The effect of protoporphyrinogen oxidase inhibitors on microsomal and mitochondrial cytochromes
-
J. Krijt, P. Maruna, P. Petrovicky, and V. Janousek The effect of protoporphyrinogen oxidase inhibitors on microsomal and mitochondrial cytochromes Obes. Res. 3 Suppl. 5 1995 785S 788S
-
(1995)
Obes. Res.
, vol.3
, Issue.5
-
-
Krijt, J.1
Maruna, P.2
Petrovicky, P.3
Janousek, V.4
-
5
-
-
0016819667
-
Heme a of cytochrome c oxicase. Structure and properties: Comparisons with hemes B, C, and S and derivatives
-
W.S. Caughey, G.A. Smythe, D.H. O'Keeffe, J.E. Maskasky, and M.I. Smith Heme A of cytochrome c oxicase. Structure and properties: comparisons with hemes B, C, and S and derivatives J. Biol. Chem. 250 1975 7602 7622
-
(1975)
J. Biol. Chem.
, vol.250
, pp. 7602-7622
-
-
Caughey, W.S.1
Smythe, G.A.2
O'Keeffe, D.H.3
Maskasky, J.E.4
Smith, M.I.5
-
6
-
-
0025640889
-
Structural features of cytochrome oxidase
-
M. Saraste Structural features of cytochrome oxidase Q. Rev. Biophys. 23 1990 331 366
-
(1990)
Q. Rev. Biophys.
, vol.23
, pp. 331-366
-
-
Saraste, M.1
-
7
-
-
0037029074
-
Cytochrome oxidase in health and disease
-
A. Barrientos, M.H. Barros, I. Valnot, A. Rotig, P. Rustin, and A. Tzagoloff Cytochrome oxidase in health and disease Gene 286 2002 53 63
-
(2002)
Gene
, vol.286
, pp. 53-63
-
-
Barrientos, A.1
Barros, M.H.2
Valnot, I.3
Rotig, A.4
Rustin, P.5
Tzagoloff, A.6
-
8
-
-
0037660510
-
Yeast models of human mitochondrial diseases
-
A. Barrientos Yeast models of human mitochondrial diseases IUBMB Life 55 2003 83 95
-
(2003)
IUBMB Life
, vol.55
, pp. 83-95
-
-
Barrientos, A.1
-
9
-
-
0023067403
-
Identification and sequence of the gene encoding cytochrome c heme lyase in the yeast Saccharomyces cerevisiae
-
M.E. Dumont, J.F. Ernst, D.M. Hampsey, and F. Sherman Identification and sequence of the gene encoding cytochrome c heme lyase in the yeast Saccharomyces cerevisiae EMBO J. 6 1987 235 241
-
(1987)
EMBO J.
, vol.6
, pp. 235-241
-
-
Dumont, M.E.1
Ernst, J.F.2
Hampsey, D.M.3
Sherman, F.4
-
11
-
-
0024279426
-
Coupling of heme attachment to import of cytochrome c into yeast mitochondria. Studies with heme lyase-deficient mitochondria and altered apocytochromes c
-
M.E. Dumont, J.F. Ernst, and F. Sherman Coupling of heme attachment to import of cytochrome c into yeast mitochondria. Studies with heme lyase-deficient mitochondria and altered apocytochromes c J. Biol. Chem. 263 1988 15928 15937
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 15928-15937
-
-
Dumont, M.E.1
Ernst, J.F.2
Sherman, F.3
-
12
-
-
0025989267
-
Role of cytochrome c heme lyase in mitochondrial import and accumulation of cytochrome c in Saccharomyces cerevisiae
-
M.E. Dumont, T.S. Cardillo, M.K. Hayes, and F. Sherman Role of cytochrome c heme lyase in mitochondrial import and accumulation of cytochrome c in Saccharomyces cerevisiae Mol. Cell. Biol. 11 1991 5487 5496
-
(1991)
Mol. Cell. Biol.
, vol.11
, pp. 5487-5496
-
-
Dumont, M.E.1
Cardillo, T.S.2
Hayes, M.K.3
Sherman, F.4
-
13
-
-
0024408905
-
Import of cytochrome c into mitochondria: Reduction of heme, mediated by NADH and flavin nucleotides, is obligatory for its covalent linkage to apocytochrome c
-
D.W. Nicholson, and W. Neupert Import of cytochrome c into mitochondria: reduction of heme, mediated by NADH and flavin nucleotides, is obligatory for its covalent linkage to apocytochrome c Proc. Natl. Acad. Sci. U. S. A. 86 1989 4340 4344
-
(1989)
Proc. Natl. Acad. Sci. U. S. A.
, vol.86
, pp. 4340-4344
-
-
Nicholson, D.W.1
Neupert, W.2
-
14
-
-
0024474942
-
1 heme lyase and of the two proteolytic processing steps during import into mitochondria
-
1 heme lyase and of the two proteolytic processing steps during import into mitochondria J. Biol. Chem. 264 1989 10156 10168
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 10156-10168
-
-
Nicholson, D.W.1
Stuart, R.A.2
Neupert, W.3
-
15
-
-
0027442655
-
In vitro heme O synthesis by the cyoE gene product from Escherichia coli
-
K. Saiki, T. Mogi, K. Ogura, and Y. Anraku In vitro heme O synthesis by the cyoE gene product from Escherichia coli J. Biol. Chem. 268 1993 26041 26044
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 26041-26044
-
-
Saiki, K.1
Mogi, T.2
Ogura, K.3
Anraku, Y.4
-
17
-
-
0025076235
-
COX10 codes for a protein homologous to the ORF1 product of Paracoccus denitrificans and is required for the synthesis of yeast cytochrome oxidase
-
M.P. Nobrega, F.G. Nobrega, and A. Tzagoloff COX10 codes for a protein homologous to the ORF1 product of Paracoccus denitrificans and is required for the synthesis of yeast cytochrome oxidase J. Biol. Chem. 265 1990 14220 14226
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 14220-14226
-
-
Nobrega, M.P.1
Nobrega, F.G.2
Tzagoloff, A.3
-
18
-
-
0025145542
-
PET genes of Saccharomyces cerevisiae
-
A. Tzagoloff, and C.L. Dieckmann PET genes of Saccharomyces cerevisiae Microbiol. Rev. 54 1990 211 225
-
(1990)
Microbiol. Rev.
, vol.54
, pp. 211-225
-
-
Tzagoloff, A.1
Dieckmann, C.L.2
-
19
-
-
0027086985
-
Heme O biosynthesis in Escherichia coli: The cyoE gene in the cytochrome bo operon encodes a protoheme IX farnesyltransferase
-
K. Saiki, T. Mogi, and Y. Anraku Heme O biosynthesis in Escherichia coli: the cyoE gene in the cytochrome bo operon encodes a protoheme IX farnesyltransferase Biochem. Biophys. Res. Commun. 189 1992 1491 1497
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.189
, pp. 1491-1497
-
-
Saiki, K.1
Mogi, T.2
Anraku, Y.3
-
20
-
-
0028038276
-
Isolation of a human cDNA for heme A:farnesyltransferase by functional complementation of a yeast cox10 mutant
-
D.M. Glerum, and A. Tzagoloff Isolation of a human cDNA for heme A:farnesyltransferase by functional complementation of a yeast cox10 mutant Proc. Natl. Acad. Sci. U. S. A. 91 1994 8452 8456
-
(1994)
Proc. Natl. Acad. Sci. U. S. A.
, vol.91
, pp. 8452-8456
-
-
Glerum, D.M.1
Tzagoloff, A.2
-
21
-
-
0034192365
-
A mutation in the human heme A: Farnesyltransferase gene (COX10) causes cytochrome c oxidase deficiency
-
I. Valnot, J.C. von Kleist-Retzow, A. Barrientos, M. Gorbatyuk, J.W. Taanman, B. Mehaye, P. Rustin, A. Tzagoloff, A. Munnich, and A. Rotig A mutation in the human heme A: farnesyltransferase gene (COX10) causes cytochrome c oxidase deficiency Hum. Mol. Genet. 9 2000 1245 1249
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1245-1249
-
-
Valnot, I.1
Von Kleist-Retzow, J.C.2
Barrientos, A.3
Gorbatyuk, M.4
Taanman, J.W.5
Mehaye, B.6
Rustin, P.7
Tzagoloff, A.8
Munnich, A.9
Rotig, A.10
-
22
-
-
0025917055
-
The heme groups of cytochrome o from Escherichia coli
-
A. Puustinen, and M. Wikstrom The heme groups of cytochrome o from Escherichia coli Proc. Natl. Acad. Sci. U. S. A. 88 1991 6122 6126
-
(1991)
Proc. Natl. Acad. Sci. U. S. A.
, vol.88
, pp. 6122-6126
-
-
Puustinen, A.1
Wikstrom, M.2
-
23
-
-
0035831217
-
Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O
-
M.H. Barros, C.G. Carlson, D.M. Glerum, and A. Tzagoloff Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O FEBS Lett. 492 2001 133 138
-
(2001)
FEBS Lett.
, vol.492
, pp. 133-138
-
-
Barros, M.H.1
Carlson, C.G.2
Glerum, D.M.3
Tzagoloff, A.4
-
24
-
-
0030802910
-
COX15 codes for a mitochondrial protein essential for the assembly of yeast cytochrome oxidase
-
D.M. Glerum, I. Muroff, C. Jin, and A. Tzagoloff COX15 codes for a mitochondrial protein essential for the assembly of yeast cytochrome oxidase J. Biol. Chem. 272 1997 19088 19094
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 19088-19094
-
-
Glerum, D.M.1
Muroff, I.2
Jin, C.3
Tzagoloff, A.4
-
25
-
-
0029930646
-
Low-spin heme a in the heme a biosynthetic protein CtaA from Bacillus subtilis
-
B. Svensson, K.K. Andersson, and L. Hederstedt Low-spin heme A in the heme A biosynthetic protein CtaA from Bacillus subtilis Eur. J. Biochem. 238 1996 287 295
-
(1996)
Eur. J. Biochem.
, vol.238
, pp. 287-295
-
-
Svensson, B.1
Andersson, K.K.2
Hederstedt, L.3
-
26
-
-
0027527547
-
Bacillus subtilis CtaA and CtaB function in haem a biosynthesis
-
B. Svensson, M. Lubben, and L. Hederstedt Bacillus subtilis CtaA and CtaB function in haem A biosynthesis Mol. Microbiol. 10 1993 193 201
-
(1993)
Mol. Microbiol.
, vol.10
, pp. 193-201
-
-
Svensson, B.1
Lubben, M.2
Hederstedt, L.3
-
27
-
-
0028046467
-
Bacillus subtilis CtaA is a heme-containing membrane protein involved in heme a biosynthesis
-
B. Svensson, and L. Hederstedt Bacillus subtilis CtaA is a heme-containing membrane protein involved in heme A biosynthesis J. Bacteriol. 176 1994 6663 6671
-
(1994)
J. Bacteriol.
, vol.176
, pp. 6663-6671
-
-
Svensson, B.1
Hederstedt, L.2
-
28
-
-
0032783754
-
YAH1 of Saccharomyces cerevisiae: A new essential gene that codes for a protein homologous to human adrenodoxin
-
M.H. Barros, and F.G. Nobrega YAH1 of Saccharomyces cerevisiae: a new essential gene that codes for a protein homologous to human adrenodoxin Gene 233 1999 197 203
-
(1999)
Gene
, vol.233
, pp. 197-203
-
-
Barros, M.H.1
Nobrega, F.G.2
-
29
-
-
0033953353
-
A mitochondrial ferredoxin is essential for biogenesis of cellular iron-sulfur proteins
-
H. Lange, A. Kaut, G. Kispal, and R. Lill A mitochondrial ferredoxin is essential for biogenesis of cellular iron-sulfur proteins Proc. Natl. Acad. Sci. U. S. A. 97 2000 1050 1055
-
(2000)
Proc. Natl. Acad. Sci. U. S. A.
, vol.97
, pp. 1050-1055
-
-
Lange, H.1
Kaut, A.2
Kispal, G.3
Lill, R.4
-
30
-
-
0032581215
-
ARH1 of Saccharomyces cerevisiae: A new essential gene that codes for a protein homologous to the human adrenodoxin reductase
-
L. Manzella, M.H. Barros, and F.G. Nobrega ARH1 of Saccharomyces cerevisiae: a new essential gene that codes for a protein homologous to the human adrenodoxin reductase Yeast 14 1998 839 846
-
(1998)
Yeast
, vol.14
, pp. 839-846
-
-
Manzella, L.1
Barros, M.H.2
Nobrega, F.G.3
-
31
-
-
0029882297
-
Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS)
-
L. Schaefer, A. Ballabio, and H.Y. Zoghbi Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS) Genomics 34 1996 166 172
-
(1996)
Genomics
, vol.34
, pp. 166-172
-
-
Schaefer, L.1
Ballabio, A.2
Zoghbi, H.Y.3
-
32
-
-
0035701395
-
Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c
-
Q.P. Schwarz, and T.C. Cox Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c Genomics 79 2002 51 57
-
(2002)
Genomics
, vol.79
, pp. 51-57
-
-
Schwarz, Q.P.1
Cox, T.C.2
-
33
-
-
0036900297
-
Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome
-
S.K. Prakash, T.A. Cormier, A.E. McCall, J.J. Garcia, R. Sierra, B. Haupt, H.Y. Zoghbi, and I.B. Van Den Veyver Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome Hum. Mol. Genet. 11 2002 3237 3248
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 3237-3248
-
-
Prakash, S.K.1
Cormier, T.A.2
McCall, A.E.3
Garcia, J.J.4
Sierra, R.5
Haupt, B.6
Zoghbi, H.Y.7
Van Den Veyver, I.B.8
-
34
-
-
0347987827
-
Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency
-
N. Darin, A.R. Moslemi, S. Lebon, P. Rustin, E. Holme, A. Oldfors, and M. Tulinius Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency Neuropediatrics 34 2003 311 317
-
(2003)
Neuropediatrics
, vol.34
, pp. 311-317
-
-
Darin, N.1
Moslemi, A.R.2
Lebon, S.3
Rustin, P.4
Holme, E.5
Oldfors, A.6
Tulinius, M.7
-
35
-
-
0023889387
-
De Toni-Fanconi-Debre syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency
-
H. Ogier, A. Lombes, H.R. Scholte, B.T. Poll-The, M. Fardeau, J. Alcardi, B. Vignes, P. Niaudet, and J.M. Saudubray de Toni-Fanconi-Debre syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency J. Pediatr. 112 1988 734 739
-
(1988)
J. Pediatr.
, vol.112
, pp. 734-739
-
-
Ogier, H.1
Lombes, A.2
Scholte, H.R.3
Poll-The, B.T.4
Fardeau, M.5
Alcardi, J.6
Vignes, B.7
Niaudet, P.8
Saudubray, J.M.9
-
36
-
-
1542290022
-
Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1
-
S.L. Williams, I. Valnot, P. Rustin, and J.W. Taanman Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1 J. Biol. Chem. 279 2004 7462 7469
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 7462-7469
-
-
Williams, S.L.1
Valnot, I.2
Rustin, P.3
Taanman, J.W.4
-
37
-
-
0142154270
-
Mutations in COX10 result in a defect in mitochondrial heme a biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency
-
H. Antonicka, S.C. Leary, G.H. Guercin, J.N. Agar, R. Horvath, N.G. Kennaway, C.O. Harding, M. Jaksch, and E.A. Shoubridge Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency Hum. Mol. Genet. 12 2003 2693 2702
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 2693-2702
-
-
Antonicka, H.1
Leary, S.C.2
Guercin, G.H.3
Agar, J.N.4
Horvath, R.5
Kennaway, N.G.6
Harding, C.O.7
Jaksch, M.8
Shoubridge, E.A.9
-
38
-
-
0037221950
-
Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy
-
H. Antonicka, A. Mattman, C.G. Carlson, D.M. Glerum, K.C. Hoffbuhr, S.C. Leary, N.G. Kennaway, and E.A. Shoubridge Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy Am. J. Hum. Genet. 72 2003 101 114
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 101-114
-
-
Antonicka, H.1
Mattman, A.2
Carlson, C.G.3
Glerum, D.M.4
Hoffbuhr, K.C.5
Leary, S.C.6
Kennaway, N.G.7
Shoubridge, E.A.8
-
39
-
-
0025104313
-
Isoforms of mammalian cytochrome c oxidase: Correlation with human cytochrome c oxidase deficiency
-
N.G. Kennaway, R.D. Carrero-Valenzuela, G. Ewart, V.K. Balan, R. Lightowlers, Y.Z. Zhang, B.R. Powell, R.A. Capaldi, and N.R. Buist Isoforms of mammalian cytochrome c oxidase: correlation with human cytochrome c oxidase deficiency Pediatr. Res. 28 1990 529 535
-
(1990)
Pediatr. Res.
, vol.28
, pp. 529-535
-
-
Kennaway, N.G.1
Carrero-Valenzuela, R.D.2
Ewart, G.3
Balan, V.K.4
Lightowlers, R.5
Zhang, Y.Z.6
Powell, B.R.7
Capaldi, R.A.8
Buist, N.R.9
-
40
-
-
0036689003
-
Functional genomics in the mouse
-
A.S. Perkins Functional genomics in the mouse Funct. Integr. Genomics 2 2002 81 91
-
(2002)
Funct. Integr. Genomics
, vol.2
, pp. 81-91
-
-
Perkins, A.S.1
|