-
1
-
-
0025055367
-
Biophysical properties of porin pores from mitochondrial outer membrane of eukaryotic cells
-
Benz R. Biophysical properties of porin pores from mitochondrial outer membrane of eukaryotic cells. Experientia. 46:1990;131-137.
-
(1990)
Experientia
, vol.46
, pp. 131-137
-
-
Benz, R.1
-
2
-
-
0030586893
-
A novel mouse mitochondrial voltage-dependent anion channel gene localizes to chromosome 8
-
Sampson M.J., Lovell R.S., Davison D.B., Craigen W.J. A novel mouse mitochondrial voltage-dependent anion channel gene localizes to chromosome 8. Genomics. 36:1996;192-196.
-
(1996)
Genomics
, vol.36
, pp. 192-196
-
-
Sampson, M.J.1
Lovell, R.S.2
Davison, D.B.3
Craigen, W.J.4
-
3
-
-
0030873947
-
Multicopy suppressors of phenotypes resulting from the absence of yeast VDAC encode a VDAC-like protein
-
Blachly-Dyson E., Song J., Wolfgang W.J., Colombini M., Forte M. Multicopy suppressors of phenotypes resulting from the absence of yeast VDAC encode a VDAC-like protein. Mol. Cell. Biol. 17:1997;5727-5738.
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 5727-5738
-
-
Blachly-Dyson, E.1
Song, J.2
Wolfgang, W.J.3
Colombini, M.4
Forte, M.5
-
4
-
-
0023303620
-
A yeast mutant lacking mitochondrial porin is respiratory-deficient, but can recover respiration with simultaneous accumulation of an 86-kd extramitochondrial protein
-
Dihanich M., Suda K., Schatz G. A yeast mutant lacking mitochondrial porin is respiratory-deficient, but can recover respiration with simultaneous accumulation of an 86-kd extramitochondrial protein. EMBO J. 6:1987;723-728.
-
(1987)
EMBO J.
, vol.6
, pp. 723-728
-
-
Dihanich, M.1
Suda, K.2
Schatz, G.3
-
5
-
-
15644371838
-
The role of yeast VDAC genes on the permeability of the mitochondrial outer membrane
-
Lee A.C., Xu X., Blachly-Dyson E., Forte M., Colombini M. The role of yeast VDAC genes on the permeability of the mitochondrial outer membrane. J. Membr. Biol. 161:1998;173-181.
-
(1998)
J. Membr. Biol.
, vol.161
, pp. 173-181
-
-
Lee, A.C.1
Xu, X.2
Blachly-Dyson, E.3
Forte, M.4
Colombini, M.5
-
6
-
-
0029925099
-
Isolation, characterization, and mapping of two mouse mitochondrial voltage-dependent anion channel isoforms
-
Sampson M.J., Lovell R.S., Craigen W.J. Isolation, characterization, and mapping of two mouse mitochondrial voltage-dependent anion channel isoforms. Genomics. 33:1996;283-288.
-
(1996)
Genomics
, vol.33
, pp. 283-288
-
-
Sampson, M.J.1
Lovell, R.S.2
Craigen, W.J.3
-
7
-
-
0030856487
-
The murine VDAC gene family: Conserved structure and function
-
Sampson M.J., Lovell R.S., Craigen W.J. The murine VDAC gene family: conserved structure and function. J. Biol. Chem. 272:1997;18966-18973.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 18966-18973
-
-
Sampson, M.J.1
Lovell, R.S.2
Craigen, W.J.3
-
8
-
-
0032765963
-
Mouse VDAC isoforms expressed in yeast: Channel properties and their roles in mitochondrial outer membrane permeability
-
Xu X., Decker W., Sampson M.J., Craigen W.J., Colombini M. Mouse VDAC isoforms expressed in yeast: Channel properties and their roles in mitochondrial outer membrane permeability. J. Membr. Biol. 170:1999;89-102.
-
(1999)
J. Membr. Biol.
, vol.170
, pp. 89-102
-
-
Xu, X.1
Decker, W.2
Sampson, M.J.3
Craigen, W.J.4
Colombini, M.5
-
9
-
-
0028034636
-
In vitro complex formation between the octamer of mitochondrial creatine kinase and porin
-
Brdiczka D., Kaldis P., Wallimann T. In vitro complex formation between the octamer of mitochondrial creatine kinase and porin. J. Biol. Chem. 269:1994;27640-27644.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 27640-27644
-
-
Brdiczka, D.1
Kaldis, P.2
Wallimann, T.3
-
10
-
-
0027934365
-
The importance of the outer mitochondrial compartment in regulation of energy metabolism
-
Brdiczka D., Wallimann T. The importance of the outer mitochondrial compartment in regulation of energy metabolism. Mol. Cell. Biochem. 133-134:1994;69-83.
-
(1994)
Mol. Cell. Biochem.
, vol.133-134
, pp. 69-83
-
-
Brdiczka, D.1
Wallimann, T.2
-
11
-
-
0025796715
-
Porin interaction with hexokinase and glycerol kinase: Metabolic microcompartmentation of the outer mitochondrial membrane
-
Adams V., Griffin L., Towbin J., Gelb B., Worley K., McCabe E. Porin interaction with hexokinase and glycerol kinase: metabolic microcompartmentation of the outer mitochondrial membrane. Biochem. Med. Metab. Biol. 45:1991;271-291.
-
(1991)
Biochem. Med. Metab. Biol.
, vol.45
, pp. 271-291
-
-
Adams, V.1
Griffin, L.2
Towbin, J.3
Gelb, B.4
Worley, K.5
McCabe, E.6
-
12
-
-
0031852596
-
Further studies on the coupling of mitochondrially bound hexokinase to intramitochondrially compartmented ATP, generated by oxidative phosphorylation
-
de Cerqueira Cesar M., Wilson J.E. Further studies on the coupling of mitochondrially bound hexokinase to intramitochondrially compartmented ATP, generated by oxidative phosphorylation. Arch. Biochem. Biophys. 350:1998;1109-1117.
-
(1998)
Arch. Biochem. Biophys.
, vol.350
, pp. 1109-1117
-
-
De Cerqueira Cesar, M.1
Wilson, J.E.2
-
13
-
-
0029854155
-
ATP flux is controlled by a voltage-gated channel from the mitochondrial outer membrane
-
Rostovtseva T., Colombini M. ATP flux is controlled by a voltage-gated channel from the mitochondrial outer membrane. J. Biol. Chem. 271:1996;28006-28008.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 28006-28008
-
-
Rostovtseva, T.1
Colombini, M.2
-
14
-
-
0028336783
-
Generation of a mouse model for citrullinemia by targeted disruption of the argininosuccinate synthetase gene
-
Patejunas G., Bradley A., Beaudet A.L., O'Brien W.E. Generation of a mouse model for citrullinemia by targeted disruption of the argininosuccinate synthetase gene. Somat. Cell Mol. Genet. 20:1994;55-60.
-
(1994)
Somat. Cell Mol. Genet.
, vol.20
, pp. 55-60
-
-
Patejunas, G.1
Bradley, A.2
Beaudet, A.L.3
O'Brien, W.E.4
-
15
-
-
0024296027
-
Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: A general strategy for targeting mutations to non-selectable genes
-
Mansour S.L., Thomas K.R., Capecchi M.R. Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes. Nature. 336:1988;348-352.
-
(1988)
Nature
, vol.336
, pp. 348-352
-
-
Mansour, S.L.1
Thomas, K.R.2
Capecchi, M.R.3
-
16
-
-
0000742810
-
Production and analysis of chimaeric mice
-
in: E.J. Robertson (Ed.), IRL Press, Oxford
-
A. Bradley, Production and analysis of chimaeric mice, in: E.J. Robertson (Ed.), Teratocarcinomas and Embryonic Stem Cells: A Practical Approach, IRL Press, Oxford, 1987, pp. 113-151.
-
(1987)
Teratocarcinomas and Embryonic Stem Cells: A Practical Approach
, pp. 113-151
-
-
Bradley, A.1
-
17
-
-
0026621796
-
Alpha-inhibin is a tumor-suppressor gene with gonadal specificity in mice
-
Matzuk M.M., Finegold M.J., Su J.G., Hsueh A.J., Bradley A. Alpha-inhibin is a tumor-suppressor gene with gonadal specificity in mice. Nature. 360:1992;313-319.
-
(1992)
Nature
, vol.360
, pp. 313-319
-
-
Matzuk, M.M.1
Finegold, M.J.2
Su, J.G.3
Hsueh, A.J.4
Bradley, A.5
-
18
-
-
0026598614
-
Genomic DNA microextraction: A method to screen numerous samples
-
Ramirez-Solis R., Rivera-Perez J., Wallace J., Wims M., Zheng H., Bradley A. Genomic DNA microextraction: a method to screen numerous samples. Anal. Biochem. 201:1992;331-335.
-
(1992)
Anal. Biochem.
, vol.201
, pp. 331-335
-
-
Ramirez-Solis, R.1
Rivera-Perez, J.2
Wallace, J.3
Wims, M.4
Zheng, H.5
Bradley, A.6
-
19
-
-
0026773795
-
Production of mutant ES cells with a single targeting construct
-
Mortensen R., Conner D., Chao S., Geisterfer-Lowrance A., Seidman J.G. Production of mutant ES cells with a single targeting construct. Mol. Cell. Biol. 12:1992;2391-2395.
-
(1992)
Mol. Cell. Biol.
, vol.12
, pp. 2391-2395
-
-
Mortensen, R.1
Conner, D.2
Chao, S.3
Geisterfer-Lowrance, A.4
Seidman, J.G.5
-
20
-
-
0028059099
-
Deletion of a DNA polymerase beta gene segment in T cells using cell type-specific gene targeting
-
Gu H., Marth J., Orban P., Mossmann H., Rajewsky K. Deletion of a DNA polymerase beta gene segment in T cells using cell type-specific gene targeting. Science. 265:1994;26-28.
-
(1994)
Science
, vol.265
, pp. 26-28
-
-
Gu, H.1
Marth, J.2
Orban, P.3
Mossmann, H.4
Rajewsky, K.5
-
21
-
-
0023277545
-
A single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
-
Chomczynski P., Sacchi N. A single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162:1987;156-159.
-
(1987)
Anal. Biochem.
, vol.162
, pp. 156-159
-
-
Chomczynski, P.1
Sacchi, N.2
-
23
-
-
0032101318
-
Automated analysis of mitochondrial enzymes in cultured skin fibroblasts
-
Williams A.J., Coakley J., Christodoulou J. Automated analysis of mitochondrial enzymes in cultured skin fibroblasts. Anal. Biochem. 259:1998;176-180.
-
(1998)
Anal. Biochem.
, vol.259
, pp. 176-180
-
-
Williams, A.J.1
Coakley, J.2
Christodoulou, J.3
-
24
-
-
0024313144
-
Rapid purification of mitochondrial hexokinase from rat brain by a single affinity chromatography step on Affi-Gel blue
-
Wilson J.E. Rapid purification of mitochondrial hexokinase from rat brain by a single affinity chromatography step on Affi-Gel blue. Prep. Biochem. 19:1989;13-21.
-
(1989)
Prep. Biochem.
, vol.19
, pp. 13-21
-
-
Wilson, J.E.1
-
25
-
-
0030607139
-
Determination of the activities of the enzyme complexes of the electron transport chain in human fibroblasts
-
Krahenbuhl S., Schafer T., Wiesmann U. Determination of the activities of the enzyme complexes of the electron transport chain in human fibroblasts. Clin. Chim. Acta. 253:1996;79-90.
-
(1996)
Clin. Chim. Acta
, vol.253
, pp. 79-90
-
-
Krahenbuhl, S.1
Schafer, T.2
Wiesmann, U.3
-
26
-
-
0032514888
-
A novel isoform of the mitochondrial outer membrane protein VDAC3 via alternative splicing of a three base exon: Functional characteristics and subcellular localization
-
Sampson M.J., Ross L.O., Decker W.K., Craigen W.J. A novel isoform of the mitochondrial outer membrane protein VDAC3 via alternative splicing of a three base exon: Functional characteristics and subcellular localization. J. Biol. Chem. 273:1998;30482-30486.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 30482-30486
-
-
Sampson, M.J.1
Ross, L.O.2
Decker, W.K.3
Craigen, W.J.4
-
27
-
-
0027456823
-
A retrospective study of patients with the hereditary syndrome of congenital cataract, mitochondrial myopathy of heart and skeletal muscle and lactic acidosis
-
van Ekeren G.J., Stadhouders A.M., Smeitink J.A., Sengers R.C. A retrospective study of patients with the hereditary syndrome of congenital cataract, mitochondrial myopathy of heart and skeletal muscle and lactic acidosis. Eur. J. Pediatr. 152:1993;255-259.
-
(1993)
Eur. J. Pediatr.
, vol.152
, pp. 255-259
-
-
Van Ekeren, G.J.1
Stadhouders, A.M.2
Smeitink, J.A.3
Sengers, R.C.4
-
28
-
-
0030665174
-
Aberrant glycolytic metabolism of cancer cells: A remarkable coordination of genetic, transcriptional, post-translational, and mutational events that lead to a critical role for type II hexokinase
-
Mathupala S.P., Rempel A., Pedersen P.L. Aberrant glycolytic metabolism of cancer cells: a remarkable coordination of genetic, transcriptional, post-translational, and mutational events that lead to a critical role for type II hexokinase. J. Bioenerg. Biomembr. 29:1997;339-343.
-
(1997)
J. Bioenerg. Biomembr.
, vol.29
, pp. 339-343
-
-
Mathupala, S.P.1
Rempel, A.2
Pedersen, P.L.3
-
29
-
-
0029866447
-
Oxygen supply and oxygen-dependent gene expression in differentiating embryonic stem cells
-
Gassman M., Fandrey J., Bichet S., Wartenberg M., Marti H.H., Bauer C., Wenger R.H., Acker H. Oxygen supply and oxygen-dependent gene expression in differentiating embryonic stem cells. Proc. Natl. Acad. Sci. USA. 93:1996;2867-2872.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 2867-2872
-
-
Gassman, M.1
Fandrey, J.2
Bichet, S.3
Wartenberg, M.4
Marti, H.H.5
Bauer, C.6
Wenger, R.H.7
Acker, H.8
-
30
-
-
0032401567
-
Cyclophilin-D binds strongly to complexes of the voltage-dependent anion channel and the adenine nucleotide translocase to form the permeability transition pore
-
Crompton M., Virji S., Ward J.M. Cyclophilin-D binds strongly to complexes of the voltage-dependent anion channel and the adenine nucleotide translocase to form the permeability transition pore. Eur. J. Biochem. 258:1998;729-735.
-
(1998)
Eur. J. Biochem.
, vol.258
, pp. 729-735
-
-
Crompton, M.1
Virji, S.2
Ward, J.M.3
-
31
-
-
0344653616
-
Complexes between porin, hexokinase, mitochondrial creatine kinase and adenylate translocator display properties of the permeability transition pore. Implication for regulation of permeability transition by the kinases
-
Beutner G., Ruck A., Riede B., Brdiczka D. Complexes between porin, hexokinase, mitochondrial creatine kinase and adenylate translocator display properties of the permeability transition pore. Implication for regulation of permeability transition by the kinases. Biochim. Biophys. Acta. 1368:1998;7-18.
-
(1998)
Biochim. Biophys. Acta
, vol.1368
, pp. 7-18
-
-
Beutner, G.1
Ruck, A.2
Riede, B.3
Brdiczka, D.4
-
32
-
-
0032387842
-
Direct demonstration of a specific interaction between cyclophilin-D and the adenine nucleotide translocase confirms their role in the mitochondrial permeability transition
-
Woodfield K., Ruck A., Brdiczka D., Halestrap A.P. Direct demonstration of a specific interaction between cyclophilin-D and the adenine nucleotide translocase confirms their role in the mitochondrial permeability transition. Biochem. J. 336:1998;287-290.
-
(1998)
Biochem. J.
, vol.336
, pp. 287-290
-
-
Woodfield, K.1
Ruck, A.2
Brdiczka, D.3
Halestrap, A.P.4
-
33
-
-
0029778849
-
Clinical presentation of mitochondrial disorders in childhood
-
Munnich A., Rotig A., Chretien D., Cormier V., Bourgeron T., Bonnefont J.P., Saudubray J.M., Rustin P. Clinical presentation of mitochondrial disorders in childhood. J. Inherit. Metab. Dis. 19:1996;521-527.
-
(1996)
J. Inherit. Metab. Dis.
, vol.19
, pp. 521-527
-
-
Munnich, A.1
Rotig, A.2
Chretien, D.3
Cormier, V.4
Bourgeron, T.5
Bonnefont, J.P.6
Saudubray, J.M.7
Rustin, P.8
-
34
-
-
0031044985
-
Molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome
-
Adams P.L., Lightowlers R.N., Turnbull D.M. Molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome. Ann. Neurol. 41:1997;268-270.
-
(1997)
Ann. Neurol.
, vol.41
, pp. 268-270
-
-
Adams, P.L.1
Lightowlers, R.N.2
Turnbull, D.M.3
-
35
-
-
0030003760
-
A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria
-
Keightley J.A., Hoffbuhr K.C., Burton M.D., Salas V.M., Johnston W.S., Penn A.M., Buist N.R., Kennaway N.G. A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria. Nature Genet. 12:1996;410-416.
-
(1996)
Nature Genet.
, vol.12
, pp. 410-416
-
-
Keightley, J.A.1
Hoffbuhr, K.C.2
Burton, M.D.3
Salas, V.M.4
Johnston, W.S.5
Penn, A.M.6
Buist, N.R.7
Kennaway, N.G.8
-
36
-
-
0032231458
-
Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA
-
Hanna M.G., Nelson I.P., Rahman S., Lane R.J., Land J., Heales S., Cooper M.J., Schapira A.H., Morgan-Hughes J.A., Wood N.W. Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA. Am. J. Hum. Genet. 63:1998;29-36.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 29-36
-
-
Hanna, M.G.1
Nelson, I.P.2
Rahman, S.3
Lane, R.J.4
Land, J.5
Heales, S.6
Cooper, M.J.7
Schapira, A.H.8
Morgan-Hughes, J.A.9
Wood, N.W.10
-
37
-
-
0031441038
-
No mitochondrial cytochrome oxidase (COX) gene mutations in 18 cases of COX deficiency
-
Parfait B., Percheron A., Chretien D., Rustin P., Munnich A., Rotig A. No mitochondrial cytochrome oxidase (COX) gene mutations in 18 cases of COX deficiency. Hum. Genet. 101:1997;247-250.
-
(1997)
Hum. Genet.
, vol.101
, pp. 247-250
-
-
Parfait, B.1
Percheron, A.2
Chretien, D.3
Rustin, P.4
Munnich, A.5
Rotig, A.6
-
38
-
-
0025145542
-
PET genes of Saccharomyces cerevisiae
-
Tzagoloff A., Dieckmann C.L. 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
-
39
-
-
17344362021
-
SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome
-
Zhu Z., Yao J., Johns T., Fu K., De Bie I., Macmillan C., Cuthbert A.P., Newbold R.F., Wang J., Chevrette M., Brown G.K., Brown R.M., Shoubridge E.A. SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome. Nature Genet. 20:1998;337-343.
-
(1998)
Nature Genet.
, vol.20
, pp. 337-343
-
-
Zhu, Z.1
Yao, J.2
Johns, T.3
Fu, K.4
De Bie, I.5
Macmillan, C.6
Cuthbert, A.P.7
Newbold, R.F.8
Wang, J.9
Chevrette, M.10
Brown, G.K.11
Brown, R.M.12
Shoubridge, E.A.13
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