-
1
-
-
0032541406
-
The formation of respiratory chain complexes in mitochondria is under the proteolytic control of the m-AAA protease
-
H. Arlt G. Steglich R. Perryman The formation of respiratory chain complexes in mitochondria is under the proteolytic control of the m-AAA protease EMBO J. 17 1998 4837 4847
-
(1998)
EMBO J.
, vol.17
, pp. 4837-4847
-
-
Arlt, H.1
Steglich, G.2
Perryman, R.3
-
2
-
-
18044401375
-
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia
-
A. Ashley-Koch E.R. Bonner P.C. Gaskell Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia Neurogenetics 3 2001 91 97
-
(2001)
Neurogenetics
, vol.3
, pp. 91-97
-
-
Ashley-Koch, A.1
Bonner, E.R.2
Gaskell, P.C.3
-
3
-
-
0033166528
-
Identification and characterization of AFG3L2, a novel paraplegin-related gene
-
S. Banfi M.T. Bassi G. Andolfi Identification and characterization of AFG3L2, a novel paraplegin-related gene Genomics 59 1999 51 58
-
(1999)
Genomics
, vol.59
, pp. 51-58
-
-
Banfi, S.1
Bassi, M.T.2
Andolfi, G.3
-
4
-
-
0032745071
-
Mitochondrial enzyme activity in amyotrophic lateral sclerosis: Implications for the role of mitochondria in neuronal cell death
-
G.M. Borthwick M.A. Johnson P.G. Ince Mitochondrial enzyme activity in amyotrophic lateral sclerosis: Implications for the role of mitochondria in neuronal cell death Ann. Neurol. 46 1999 787 790
-
(1999)
Ann. Neurol.
, vol.46
, pp. 787-790
-
-
Borthwick, G.M.1
Johnson, M.A.2
Ince, P.G.3
-
5
-
-
0033957174
-
Clinical, biochemical and molecular genetic correlations in Friedriech's ataxia
-
J.L. Bradley J.C. Blake S. Chamberlain Clinical, biochemical and molecular genetic correlations in Friedriech's ataxia Mol. Genet. 9 2000 275 282
-
(2000)
Mol. Genet.
, vol.9
, pp. 275-282
-
-
Bradley, J.L.1
Blake, J.C.2
Chamberlain, S.3
-
6
-
-
0033781121
-
Hereditary spastic paraplegia caused by mutations in the SPG4 gene
-
J. Burger N. Fonknechten M. Hoeltzenbein Hereditary spastic paraplegia caused by mutations in the SPG4 gene Eur. J. Hum. Genet. 8 2000 771 776
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 771-776
-
-
Burger, J.1
Fonknechten, N.2
Hoeltzenbein, M.3
-
7
-
-
0343238487
-
Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p
-
P.C. Byrne P. Mc Monagle S. Webb Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p Neurology 54 2000 1510 1517
-
(2000)
Neurology
, vol.54
, pp. 1510-1517
-
-
Byrne, P.C.1
Mc Monagle, P.2
Webb, S.3
-
8
-
-
13344270899
-
Freidreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion
-
V. Campuzano Freidreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion Science 271 1996 1423 1427
-
(1996)
Science
, vol.271
, pp. 1423-1427
-
-
Campuzano, V.1
-
9
-
-
0031559896
-
Expression of CuZn superoxide dismutase typical of familial amyotrophic lateral sclerosis induces mitochondrial alteration and increase of cytosolic Ca2+ concentration in transfected neuroblastoma SH-SY5Y cells
-
2+ concentration in transfected neuroblastoma SH-SY5Y cells FEBS Lett. 414 1997 365 368
-
(1997)
FEBS Lett.
, vol.414
, pp. 365-368
-
-
Carri, M.T.1
Ferri, A.2
Battistoni, A.3
-
10
-
-
0032511186
-
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease
-
G. Casari M. De Fusco S. Ciarmatori Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease Cell 93 1998 973 983
-
(1998)
Cell
, vol.93
, pp. 973-983
-
-
Casari, G.1
De Fusco, M.2
Ciarmatori, S.3
-
11
-
-
0034657997
-
Identification and characterization of YME1L1, a novel paraplegin-related gene
-
M. Coppola A. Pizzigoni S. Banfi Identification and characterization of YME1L1, a novel paraplegin-related gene Genomics 66 2000 48 54
-
(2000)
Genomics
, vol.66
, pp. 48-54
-
-
Coppola, M.1
Pizzigoni, A.2
Banfi, S.3
-
12
-
-
0034601407
-
Mitochondrial DNA deletion mutation levels are elevated in ALS brains
-
G.K. Dhaliwal R.P. Grewal Mitochondrial DNA deletion mutation levels are elevated in ALS brains Neuroreport. 11 2000 2507 2509
-
(2000)
Neuroreport.
, vol.11
, pp. 2507-2509
-
-
Dhaliwal, G.K.1
Grewal, R.P.2
-
13
-
-
0028868126
-
Autosomal dominant familial spastic paraplegia: Tight linkage to chromosome 15q
-
J.K. Fink C.-T.B. Wu S.M. Jones Autosomal dominant familial spastic paraplegia: Tight linkage to chromosome 15q Am. J. Hum. Genet. 56 1995 188 192
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 188-192
-
-
Fink, J.K.1
Wu, C.-T.B.2
Jones, S.M.3
-
14
-
-
0034163576
-
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia
-
N. Fonknechten D. Mavel P. Byrne Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia Hum. Mol. Genet. 9 2000 637 644
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 637-644
-
-
Fonknechten, N.1
Mavel, D.2
Byrne, P.3
-
15
-
-
0033912567
-
A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24–2q34
-
B. Fontaine C.-S. Davoine A. Durr A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24–2q34 Am. J. Hum. Genet. 66 2000 702 707
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 702-707
-
-
Fontaine, B.1
Davoine, C.-S.2
Durr, A.3
-
16
-
-
0029744863
-
Decreased cytochrome c oxidase activity but unchanged superoxide dismutase and glutathione peroxidase activities in the spinal cords of patients with amyotrophic lateral sclerosis
-
K. Fujita M. Yamauchi K. Shibayama Decreased cytochrome c oxidase activity but unchanged superoxide dismutase and glutathione peroxidase activities in the spinal cords of patients with amyotrophic lateral sclerosis J. Neurosci. Res. 45 1996 276 281
-
(1996)
J. Neurosci. Res.
, vol.45
, pp. 276-281
-
-
Fujita, K.1
Yamauchi, M.2
Shibayama, K.3
-
17
-
-
0028872909
-
Autosomal dominant familial spastic paraplegia: Reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity
-
S. Gispert N. Santos R. Damen Autosomal dominant familial spastic paraplegia: Reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity Am. J. Hum. Genet. 56 1995 183 187
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 183-187
-
-
Gispert, S.1
Santos, N.2
Damen, R.3
-
18
-
-
0019777963
-
Hereditary “pure” spastic paraplegia: A clinical and genetic study of 22 families
-
A.E. Harding Hereditary “pure” spastic paraplegia: A clinical and genetic study of 22 families J. Neurol. Neurosurg. Psychiat. 44 1981 871 883
-
(1981)
J. Neurol. Neurosurg. Psychiat.
, vol.44
, pp. 871-883
-
-
Harding, A.E.1
-
19
-
-
0032721512
-
Spastin, a novel AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
-
J. Hazan N. Fonknechten D. Mavel Spastin, a novel AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia Nat. Genet. 23 1999 296 303
-
(1999)
Nat. Genet.
, vol.23
, pp. 296-303
-
-
Hazan, J.1
Fonknechten, N.2
Mavel, D.3
-
20
-
-
0027981739
-
Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p
-
J. Hazan B. Fontaine R.P.M. Bruyn Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p Hum. Mol. Genet. 3 1994 1569 1573
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1569-1573
-
-
Hazan, J.1
Fontaine, B.2
Bruyn, R.P.M.3
-
21
-
-
0027363223
-
Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q
-
J. Hazan C. Lamy J. Melki Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q Nat. Genet. 5 1993 163 167
-
(1993)
Nat. Genet.
, vol.5
, pp. 163-167
-
-
Hazan, J.1
Lamy, C.2
Melki, J.3
-
22
-
-
0034727613
-
Mitochondrial analysis in autosomal dominant hereditary spastic paraplegia
-
P. Hedera S. DiMauro E. Bonilla Mitochondrial analysis in autosomal dominant hereditary spastic paraplegia Neurology 55 2000 1591 1592
-
(2000)
Neurology
, vol.55
, pp. 1591-1592
-
-
Hedera, P.1
DiMauro, S.2
Bonilla, E.3
-
23
-
-
0033073735
-
Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q
-
P. Hedera S. Rainer D. Alvarado Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q Am. J. Hum. Genet. 64 1999 563 569
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 563-569
-
-
Hedera, P.1
Rainer, S.2
Alvarado, D.3
-
24
-
-
0034649471
-
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms
-
A. Hentati H.-X. Deng H. Zhai Novel mutations in spastin gene and absence of correlation with age at onset of symptoms Neurology 55 2000 1388 1390
-
(2000)
Neurology
, vol.55
, pp. 1388-1390
-
-
Hentati, A.1
Deng, H.-X.2
Zhai, H.3
-
25
-
-
0028145138
-
Linkage of “pure” autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity
-
A. Hentati M.A. Pericak-Vance W.-Y. Hung Linkage of “pure” autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity Hum. Mol. Genet. 3 1994 1263 1267
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1263-1267
-
-
Hentati, A.1
Pericak-Vance, M.A.2
Hung, W.-Y.3
-
26
-
-
0028067709
-
Linkage of a locus for autosomal dominant spastic paraplegia to chromosome 2p markers
-
A. Hentati M.A. Pericak-Vance F. Lennon Linkage of a locus for autosomal dominant spastic paraplegia to chromosome 2p markers Hum. Mol. Genet. 3 1994 1867 1871
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1867-1871
-
-
Hentati, A.1
Pericak-Vance, M.A.2
Lennon, F.3
-
27
-
-
0031411418
-
Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2–14q24.3
-
S. Huang H. Zhuyu Li Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2–14q24.3 Hum. Genet. 100 1997 620 623
-
(1997)
Hum. Genet.
, vol.100
, pp. 620-623
-
-
Huang, S.1
Zhuyu Li, H.2
-
28
-
-
0028241952
-
X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1CAM gene
-
M. Jouet A. Rosenthal G. Armstrong X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1CAM gene Nat. Genet. 7 1994 402 407
-
(1994)
Nat. Genet.
, vol.7
, pp. 402-407
-
-
Jouet, M.1
Rosenthal, A.2
Armstrong, G.3
-
30
-
-
0032079517
-
Massive mitochondrial degeneration in motor neurones triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1
-
J. Kong Z. Xu Massive mitochondrial degeneration in motor neurones triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1 J. Neurosci. 18 1998 3241 3250
-
(1998)
J. Neurosci.
, vol.18
, pp. 3241-3250
-
-
Kong, J.1
Xu, Z.2
-
31
-
-
0030475162
-
Regulated protein degradation in mitochondria
-
T. Langer W. Neupert Regulated protein degradation in mitochondria Experimentia 52 1996 1069 1076
-
(1996)
Experimentia
, vol.52
, pp. 1069-1076
-
-
Langer, T.1
Neupert, W.2
-
32
-
-
0038913348
-
Linkage and heterogeneity in hereditary spastic paraparesis
-
F. Lennon P.C. Gaskell C. Wolpert Linkage and heterogeneity in hereditary spastic paraparesis Am. J. Hum. Genet. 57 1995 A217
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. A217
-
-
Lennon, F.1
Gaskell, P.C.2
Wolpert, C.3
-
33
-
-
0029775087
-
AAA proteases with catalytic sites on opposite membrane surfaces comprise a proteolytic system for the ATP-dependent degradation of inner membrame proteins in mitochondria
-
K. Leonhard J.M. Hermann R.A. Stuart AAA proteases with catalytic sites on opposite membrane surfaces comprise a proteolytic system for the ATP-dependent degradation of inner membrame proteins in mitochondria EMBO J. 15 1996 4218 4229
-
(1996)
EMBO J.
, vol.15
, pp. 4218-4229
-
-
Leonhard, K.1
Hermann, J.M.2
Stuart, R.A.3
-
34
-
-
0033602381
-
Chaperone-like activity of the AAA domain of the yeast Yme 1 AAA protease
-
K. Leonhard A. Stiegler T. Langer Chaperone-like activity of the AAA domain of the yeast Yme 1 AAA protease Nature 398 1999 348 351
-
(1999)
Nature
, vol.398
, pp. 348-351
-
-
Leonhard, K.1
Stiegler, A.2
Langer, T.3
-
35
-
-
0033782943
-
Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis
-
J.C. Lindsey M.E. Lusher C.J. McDermott Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis J. Med. Genet. 37 2000 759 765
-
(2000)
J. Med. Genet.
, vol.37
, pp. 759-765
-
-
Lindsey, J.C.1
Lusher, M.E.2
McDermott, C.J.3
-
36
-
-
0032568610
-
Localization of the Wilson's disease protein product to mitochondria
-
S. Lutsenko M.J. Cooper Localization of the Wilson's disease protein product to mitochondria Proc. Natl. Acad. Sci. USA 95 1998 6004 6009
-
(1998)
, pp. 6004-6009
-
-
Lutsenko, S.1
Cooper, M.J.2
-
38
-
-
0035957066
-
Paraplegin gene analysis in hereditary spastic paraparesis (HSP) pedigrees in northeast England
-
C.J. McDermott R.K. Dayaratne J. Tomkins Paraplegin gene analysis in hereditary spastic paraparesis (HSP) pedigrees in northeast England Neurology 56 2001 467 471
-
(2001)
Neurology
, vol.56
, pp. 467-471
-
-
McDermott, C.J.1
Dayaratne, R.K.2
Tomkins, J.3
-
39
-
-
0034719042
-
Phenotype of AD-HSP due to mutations in the SPAST gene. Comparison with AD-HSP without mutations
-
P. McMonagle P.C. Byrne B. Fitzgerald Phenotype of AD-HSP due to mutations in the SPAST gene. Comparison with AD-HSP without mutations Neurology 55 2000 1794 1800
-
(2000)
Neurology
, vol.55
, pp. 1794-1800
-
-
McMonagle, P.1
Byrne, P.C.2
Fitzgerald, B.3
-
40
-
-
0345279856
-
Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13–15q15
-
F. Murillo H. Kobayashi E. Pegoraro Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13–15q15 Neurology 53 1999 50 56
-
(1999)
Neurology
, vol.53
, pp. 50-56
-
-
Murillo, F.1
Kobayashi, H.2
Pegoraro, E.3
-
41
-
-
0029042705
-
Multiple genes, including a memeber of the AAA family, are essential for the degradation of unassembled subunit 2 of cytochrome oxidase in yeast mitochondria
-
T. Nakai T. Yasuhara Y. Fujiki Multiple genes, including a memeber of the AAA family, are essential for the degradation of unassembled subunit 2 of cytochrome oxidase in yeast mitochondria Mol. Cell. Biol. 15 1995 4441 4452
-
(1995)
Mol. Cell. Biol.
, vol.15
, pp. 4441-4452
-
-
Nakai, T.1
Yasuhara, T.2
Fujiki, Y.3
-
42
-
-
0029089031
-
Mutations in RCA1 and AFG3 inhibit F1-ATPase assembly in Saccharomyces cerevisiae
-
1-ATPase assembly in Saccharomyces cerevisiae FEBS Lett. 373 1995 66 70
-
(1995)
FEBS Lett.
, vol.373
, pp. 66-70
-
-
Paul, M.-F.1
Tzagoloff, A.2
-
43
-
-
0029163565
-
Degradation of cytochrome oxidase subunits in mutants of yeast lacking cytochrome c and suppression of the degradation by yme1
-
D.A. Pearce F. Shermann Degradation of cytochrome oxidase subunits in mutants of yeast lacking cytochrome c and suppression of the degradation by yme1 J. Biol. Chem. 270 1995 20879 20882
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 20879-20882
-
-
Pearce, D.A.1
Shermann, F.2
-
44
-
-
0033912569
-
A locus for autosomal dominant “pure” hereditary spastic paraplegia maps to chromosome 19ql3
-
E. Reid A.M. Dearlove O. Osborn A locus for autosomal dominant “pure” hereditary spastic paraplegia maps to chromosome 19ql3 Am. J. Hum. Genet. 66 2000 728 732
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 728-732
-
-
Reid, E.1
Dearlove, A.M.2
Osborn, O.3
-
45
-
-
0033362081
-
A new locus for autosomal dominant “pure” hereditary spastic paraplegia mapping to chromosome l2q13, and evidence for further genetic heterogeneity
-
E. Reid M. Dearlove M. Rhodes A new locus for autosomal dominant “pure” hereditary spastic paraplegia mapping to chromosome l2q13, and evidence for further genetic heterogeneity Am. J. Hum. Genet. 65 1999 757 763
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 757-763
-
-
Reid, E.1
Dearlove, M.2
Rhodes, M.3
-
46
-
-
0029803808
-
The role of protein degradation in mitochondrial function and biogenesis
-
M. Rep L.A. Grivell The role of protein degradation in mitochondrial function and biogenesis Curr. Genet. 30 1996 367 380
-
(1996)
Curr. Genet.
, vol.30
, pp. 367-380
-
-
Rep, M.1
Grivell, L.A.2
-
47
-
-
0029837817
-
Three genes for mitochondrial proteins supress null mutations in both Afg3 and Rca1 when overexpressed
-
M. Rep J. Nooy E. Guelin Three genes for mitochondrial proteins supress null mutations in both Afg3 and Rca1 when overexpressed Curr. Genet. 30 1996 206 211
-
(1996)
Curr. Genet.
, vol.30
, pp. 206-211
-
-
Rep, M.1
Nooy, J.2
Guelin, E.3
-
48
-
-
0033821055
-
Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation
-
F.M. Santorelli C. Patrono D. Fortini Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation Neurology 55 2000 702 705
-
(2000)
Neurology
, vol.55
, pp. 702-705
-
-
Santorelli, F.M.1
Patrono, C.2
Fortini, D.3
-
49
-
-
0030019414
-
Ultrastructural study of the synapses in the anterior horn of neurones of patients with amyotrophic lateral sclerosis
-
S. Sasaki M. Iwata Ultrastructural study of the synapses in the anterior horn of neurones of patients with amyotrophic lateral sclerosis Neurosci. Lett. 204 1996 53 56
-
(1996)
Neurosci. Lett.
, vol.204
, pp. 53-56
-
-
Sasaki, S.1
Iwata, M.2
-
50
-
-
0028239867
-
X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus
-
P. Saugier-Veber A. Munnich D. Bonneau X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus Nat. Genet. 6 1994 257 261
-
(1994)
Nat. Genet.
, vol.6
, pp. 257-261
-
-
Saugier-Veber, P.1
Munnich, A.2
Bonneau, D.3
-
51
-
-
0033069503
-
Genetic mapping to 10q23.3–10q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy
-
M. Seri R. Cusano P. Forabosco Genetic mapping to 10q23.3–10q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy Am. J. Hum. Genet. 64 1999 586 593
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 586-593
-
-
Seri, M.1
Cusano, R.2
Forabosco, P.3
-
52
-
-
0026700276
-
Fraternal concordance of types of abnormal hepatocellular mitochondria in Wilson's disease
-
I. Sternlieb Fraternal concordance of types of abnormal hepatocellular mitochondria in Wilson's disease Hepatology 16 1992 728 732
-
(1992)
Hepatology
, vol.16
, pp. 728-732
-
-
Sternlieb, I.1
-
53
-
-
0027988708
-
Yta10p, a member of a novel ATPase family in yeast, is essential for mitochondrial function
-
R. Tauer G. Mannhaupt R. Schnall Yta10p, a member of a novel ATPase family in yeast, is essential for mitochondrial function FEBS Lett. 353 1994 197 200
-
(1994)
FEBS Lett.
, vol.353
, pp. 197-200
-
-
Tauer, R.1
Mannhaupt, G.2
Schnall, R.3
-
54
-
-
0027304446
-
Inactivation of YME1, a putative member of the FtsH-SEC18-PAS1-CDC48 family of putative ATPase-encoding genes, causes increased escape of DNA from mitochondria in Saccharomyces cerevisiae
-
P.E. Thorsness K.H. White T.D. Fox Inactivation of YME1 , a putative member of the FtsH-SEC18-PAS1-CDC48 family of putative ATPase-encoding genes, causes increased escape of DNA from mitochondria in Saccharomyces cerevisiae Mol. Cell. Biol. 13 1993 5418 5426
-
(1993)
Mol. Cell. Biol.
, vol.13
, pp. 5418-5426
-
-
Thorsness, P.E.1
White, K.H.2
Fox, T.D.3
-
55
-
-
67649312686
-
A new member of a family of ATPases is essential for assembly of mitochondrial respiratory chain and ATP synthetase complexes in Saccharomyces cerevisiae
-
A. Tzagoloff J. Yue J. Jang A new member of a family of ATPases is essential for assembly of mitochondrial respiratory chain and ATP synthetase complexes in Saccharomyces cerevisiae Mol. Cell. Biol. 13 1994 5418 5426
-
(1994)
Mol. Cell. Biol.
, vol.13
, pp. 5418-5426
-
-
Tzagoloff, A.1
Yue, J.2
Jang, J.3
-
56
-
-
0033868486
-
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27–3q28
-
G. Vazza M. Zortea E. Boaretto A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27–3q28 Am. J. Hum. Genet. 67 2000 504 509
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 504-509
-
-
Vazza, G.1
Zortea, M.2
Boaretto, E.3
-
57
-
-
0034641262
-
Clinical and pathological findings in hereditary spastic paraparesis with spastin mutation
-
K.D. White P.G. Ince M. Cookson Clinical and pathological findings in hereditary spastic paraparesis with spastin mutation Neurology 55 2000 89 94
-
(2000)
Neurology
, vol.55
, pp. 89-94
-
-
White, K.D.1
Ince, P.G.2
Cookson, M.3
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