-
1
-
-
84858791998
-
Mitochondrial quality control: A matter of life and death for neurons
-
Rugarli EI, Langer T. Mitochondrial quality control: a matter of life and death for neurons. EMBO J. 2012;31(6):1336-1349.
-
(2012)
EMBO J
, vol.31
, Issue.6
, pp. 1336-1349
-
-
Rugarli, E.I.1
Langer, T.2
-
2
-
-
0030008581
-
The YTA10-12 complex, an AAA protease with chaperone-like activity in the inner membrane of mitochondria
-
DOI 10.1016/S0092-8674(00)81271-4
-
Arlt H, Tauer R, Feldmann H, Neupert W, Langer T. The YTA10-12 complex, an AAA protease with chaperone-like activity in the inner membrane of mitochondria. Cell. 1996;85(6):875-885. (Pubitemid 26192138)
-
(1996)
Cell
, vol.85
, Issue.6
, pp. 875-885
-
-
Arlt, H.1
Tauer, R.2
Feldmann, H.3
Neupert, W.4
Langer, T.5
-
3
-
-
79953010046
-
Electron cryomicroscopy structure of a membrane-anchored mitochondrial AAA protease
-
Lee S, Augustin S, Tatsuta T, Gerdes F, Langer T, Tsai FT. Electron cryomicroscopy structure of a membrane-anchored mitochondrial AAA protease. J Biol Chem. 2011;286(6):4404-4411.
-
(2011)
J Biol Chem
, vol.286
, Issue.6
, pp. 4404-4411
-
-
Lee, S.1
Augustin, S.2
Tatsuta, T.3
Gerdes, F.4
Langer, T.5
Tsai, F.T.6
-
4
-
-
0033639076
-
Membrane protein degradation by AAA proteases in mitochondria: Extraction of substrates from either membrane surface
-
Leonhard K, Guiard B, Pellecchia G, Tzagoloff A, Neupert W, Langer T. Membrane protein degradation by AAA proteases in mitochondria: extraction of substrates from either membrane surface. Mol Cell. 2000;5(4):629-638.
-
(2000)
Mol Cell
, vol.5
, Issue.4
, pp. 629-638
-
-
Leonhard, K.1
Guiard, B.2
Pellecchia, G.3
Tzagoloff, A.4
Neupert, W.5
Langer, T.6
-
5
-
-
84858001999
-
Nonsense mutations in the COX1 subunit impair the stability of respiratory chain complexes rather than their assembly
-
Hornig-Do HT, et al. Nonsense mutations in the COX1 subunit impair the stability of respiratory chain complexes rather than their assembly. EMBO J. 2012;31(5):1293-1307.
-
(2012)
EMBO J
, vol.31
, Issue.5
, pp. 1293-1307
-
-
Hornig-Do, H.T.1
-
6
-
-
26844484821
-
The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria
-
DOI 10.1016/j.cell.2005.08.003, PII S0092867405008068
-
Nolden M, Ehses S, Koppen M, Bernacchia A, Rugarli EI, Langer T. The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria. Cell. 2005;123(2):277-289. (Pubitemid 41457217)
-
(2005)
Cell
, vol.123
, Issue.2
, pp. 277-289
-
-
Nolden, M.1
Ehses, S.2
Koppen, M.3
Bernacchia, A.4
Rugarli, E.I.5
Langer, T.6
-
7
-
-
0344736798
-
Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia
-
DOI 10.1083/jcb.200304112
-
Atorino L, et al. Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia. J Cell Biol. 2003;163(4):777-787. (Pubitemid 37517885)
-
(2003)
Journal of Cell Biology
, vol.163
, Issue.4
, pp. 777-787
-
-
Atorino, L.1
Silvestri, L.2
Koppen, M.3
Cassina, L.4
Ballabio, A.5
Marconi, R.6
Langer, T.7
Casari, G.8
-
8
-
-
33846127778
-
Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia
-
DOI 10.1128/MCB.01470-06
-
Koppen M, Metodiev MD, Casari G, Rugarli EI, Langer T. Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia. Mol Cell Biol. 2007;27(2):758-767. (Pubitemid 46080140)
-
(2007)
Molecular and Cellular Biology
, vol.27
, Issue.2
, pp. 758-767
-
-
Koppen, M.1
Metodiev, M.D.2
Casari, G.3
Rugarli, E.I.4
Langer, T.5
-
9
-
-
77950298030
-
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28
-
Di Bella D, et al. Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. Nat Genet. 2010;42(4):313-321.
-
(2010)
Nat Genet
, vol.42
, Issue.4
, pp. 313-321
-
-
Di Bella, D.1
-
10
-
-
80055087830
-
Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases
-
Pierson TM, et al. Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases. PLoS Genet. 2011;7(10):e1002325.
-
(2011)
PLoS Genet
, vol.7
, Issue.10
-
-
Pierson, T.M.1
-
11
-
-
0032511186
-
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease
-
DOI 10.1016/S0092-8674(00)81203-9
-
Casari G, et al. Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease. Cell. 1998;93(6):973-983. (Pubitemid 28280791)
-
(1998)
Cell
, vol.93
, Issue.6
, pp. 973-983
-
-
Casari, G.1
De Fusco, M.2
Ciarmatori, S.3
Zeviani, M.4
Mora, M.5
Fernandez, P.6
De Michele, G.7
Filla, A.8
Cocozza, S.9
Marconi, R.10
Durr, A.11
Fontaine, B.12
Ballabio, A.13
-
12
-
-
65549147202
-
Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration
-
Martinelli P, et al. Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration. Hum Mol Genet. 2009;18(11):2001-2013.
-
(2009)
Hum Mol Genet
, vol.18
, Issue.11
, pp. 2001-2013
-
-
Martinelli, P.1
-
13
-
-
40849142484
-
The mitochondrial protease AFG3L2 is essential for axonal development
-
DOI 10.1523/JNEUROSCI.4677-07.2008
-
Maltecca F, et al. The mitochondrial protease AFG3L2 is essential for axonal development. J Neurosci. 2008;28(11):2827-2836. (Pubitemid 351398887)
-
(2008)
Journal of Neuroscience
, vol.28
, Issue.11
, pp. 2827-2836
-
-
Maltecca, F.1
Aghaie, A.2
Schroeder, D.G.3
Cassina, L.4
Taylor, B.A.5
Phillips, S.J.6
Malaguti, M.7
Previtali, S.8
Guenet, J.-L.9
Quattrini, A.10
Cox, G.A.11
Casari, G.12
-
14
-
-
67651154308
-
Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degeneration
-
Maltecca F, Magnoni R, Cerri F, Cox GA, Quattrini A, Casari G. Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degeneration. J Neurosci. 2009;29(29):9244-9254.
-
(2009)
J Neurosci
, vol.29
, Issue.29
, pp. 9244-9254
-
-
Maltecca, F.1
Magnoni, R.2
Cerri, F.3
Cox, G.A.4
Quattrini, A.5
Casari, G.6
-
15
-
-
76149140917
-
Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1
-
Ehses S, et al. Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1. J Cell Biol. 2009;187(7):1023-1036.
-
(2009)
J Cell Biol
, vol.187
, Issue.7
, pp. 1023-1036
-
-
Ehses, S.1
-
16
-
-
34547601410
-
Mitochondrial Fusion Protects against Neurodegeneration in the Cerebellum
-
DOI 10.1016/j.cell.2007.06.026, PII S0092867407007933
-
Chen H, McCaffery JM, Chan DC. Mitochondrial fusion protects against neurodegeneration in the cerebellum. Cell. 2007;130(3):548-562. (Pubitemid 47198302)
-
(2007)
Cell
, vol.130
, Issue.3
, pp. 548-562
-
-
Chen, H.1
McCaffery, J.M.2
Chan, D.C.3
-
17
-
-
0034489127
-
Cre recombinase expression in cerebellar Purkinje cells
-
Barski JJ, Dethleffsen K, Meyer M. Cre recombinase expression in cerebellar Purkinje cells. Genesis. 2000;28(3-4):93-98.
-
(2000)
Genesis
, vol.28
, Issue.3-4
, pp. 93-98
-
-
Barski, J.J.1
Dethleffsen, K.2
Meyer, M.3
-
18
-
-
79961239061
-
Impaired mitochondrial transport and Parkin-independent degeneration of respiratory chain-deficient dopamine neurons in vivo
-
Sterky FH, Lee S, Wibom R, Olson L, Larsson NG. Impaired mitochondrial transport and Parkin-independent degeneration of respiratory chain-deficient dopamine neurons in vivo. Proc Natl Acad Sci U S A. 2011;108(31):12937-12942.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, Issue.31
, pp. 12937-12942
-
-
Sterky, F.H.1
Lee, S.2
Wibom, R.3
Olson, L.4
Larsson, N.G.5
-
19
-
-
0034011725
-
Atm-deficient mice Purkinje cells show age-dependent defects in calcium spike bursts and calcium currents
-
DOI 10.1016/S0306-4522(99)00581-3, PII S0306452299005813
-
Chiesa N, Barlow C, Wynshaw-Boris A, Strata P, Tempia F. Atm-deficient mice Purkinje cells show age-dependent defects in calcium spike bursts and calcium currents. Neuroscience. 2000;96(3):575-583. (Pubitemid 30136322)
-
(2000)
Neuroscience
, vol.96
, Issue.3
, pp. 575-583
-
-
Chiesa, N.1
Barlow, C.2
Wynshaw-Boris, A.3
Strata, P.4
Tempia, F.5
-
20
-
-
0035070146
-
Calcium dynamics and electrophysiological properties of cerebellar Purkinje cells in SCA1 transgenic mice
-
Inoue T, Lin X, Kohlmeier KA, Orr HT, Zoghbi HY, Ross WN. Calcium dynamics and electrophysiological properties of cerebellar Purkinje cells in SCA1 transgenic mice. J Neurophysiol. 2001;85(4):1750-1760. (Pubitemid 32280613)
-
(2001)
Journal of Neurophysiology
, vol.85
, Issue.4
, pp. 1750-1760
-
-
Inoue, T.1
Lin, X.2
Kohlmeier, K.A.3
Orr, H.T.4
Zoghbi, H.Y.5
Ross, W.N.6
-
21
-
-
34147107973
-
Climbing fiber discharge regulates cerebellar functions by controlling the intrinsic characteristics of Purkinje cell output
-
DOI 10.1152/jn.00627.2006
-
McKay BE, et al. Climbing fiber discharge regulates cerebellar functions by controlling the intrinsic characteristics of purkinje cell output. J Neurophysiol. 2007;97(4):2590-2604. (Pubitemid 46557694)
-
(2007)
Journal of Neurophysiology
, vol.97
, Issue.4
, pp. 2590-2604
-
-
McKay, B.E.1
Engbers, J.D.T.2
Mehaffey, W.H.3
Gordon, G.R.J.4
Molineux, M.L.5
Bains, J.S.6
Turner, R.W.7
-
22
-
-
0033105025
-
Altered physiology of Purkinje neurons in cerebellar slices from transgenic mice with chronic central nervous system expression of interleukin-6
-
DOI 10.1016/S0306-4522(98)00316-9, PII S0306452298003169
-
Nelson TE, Campbell IL, Gruol DL. Altered physiology of Purkinje neurons in cerebellar slices from transgenic mice with chronic central nervous system expression of interleukin-6. Neuroscience. 1999;89(1):127-136. (Pubitemid 29049032)
-
(1999)
Neuroscience
, vol.89
, Issue.1
, pp. 127-136
-
-
Nelson, T.E.1
Campbell, I.L.2
Gruol, D.L.3
-
23
-
-
34547461825
-
Purkinje cell dysfunction and alteration of long-term synaptic plasticity in fetal alcohol syndrome
-
DOI 10.1073/pnas.0607037104
-
Servais L, Hourez R, Bearzatto B, Gall D, Schiffmann SN, Cheron G. Purkinje cell dysfunction and alteration of long-term synaptic plasticity in fetal alcohol syndrome. Proc Natl Acad Sci U S A. 2007;104(23):9858-9863. (Pubitemid 47175356)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.23
, pp. 9858-9863
-
-
Servais, L.1
Hourez, R.2
Bearzatto, B.3
Gall, D.4
Schiffmann, S.N.5
Cheron, G.6
-
24
-
-
0037115030
-
Active contribution of dendrites to the tonic and trimodal patterns of activity in cerebellar Purkinje neurons
-
Womack M, Khodakhah K. Active contribution of dendrites to the tonic and trimodal patterns of activity in cerebellar Purkinje neurons. J Neurosci. 2002;22(24):10603-10612. (Pubitemid 36005133)
-
(2002)
Journal of Neuroscience
, vol.22
, Issue.24
, pp. 10603-10612
-
-
Womack, M.1
Khodakhah, K.2
-
25
-
-
33746299692
-
Regulation of mitochondrial morphology through proteolytic cleavage of OPA1
-
DOI 10.1038/sj.emboj.7601184, PII 7601184
-
Ishihara N, Fujita Y, Oka T, Mihara K. Regulation of mitochondrial morphology through proteolytic cleavage of OPA1. EMBO J. 2006;25(13):2966-2977. (Pubitemid 44106750)
-
(2006)
EMBO Journal
, vol.25
, Issue.13
, pp. 2966-2977
-
-
Ishihara, N.1
Fujita, Y.2
Oka, T.3
Mihara, K.4
-
26
-
-
33845976357
-
Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology
-
DOI 10.1074/jbc.M606059200
-
Duvezin-Caubet S, et al. Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology. J Biol Chem. 2006;281(49):37972-37979. (Pubitemid 46042101)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.49
, pp. 37972-37979
-
-
Duvezin-Caubet, S.1
Jagasia, R.2
Wagener, J.3
Hofmann, S.4
Trifunovic, A.5
Hansson, A.6
Chomyn, A.7
Bauer, M.F.8
Attardi, G.9
Larsson, N.-G.10
Neupert, W.11
Reichert, A.S.12
-
27
-
-
76149093590
-
Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells
-
Head B, Griparic L, Amiri M, Gandre-Babbe S, van der Bliek AM. Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells. J Cell Biol. 2009;187(7):959-966.
-
(2009)
J Cell Biol
, vol.187
, Issue.7
, pp. 959-966
-
-
Head, B.1
Griparic, L.2
Amiri, M.3
Gandre-Babbe, S.4
Van Der Bliek, A.M.5
-
28
-
-
77953933808
-
Mitochondrial dysfunction in NnaD mutant flies and Purkinje cell degeneration mice reveals a role for Nna proteins in neuronal bioenergetics
-
Chakrabarti L, et al. Mitochondrial dysfunction in NnaD mutant flies and Purkinje cell degeneration mice reveals a role for Nna proteins in neuronal bioenergetics. Neuron. 2010;66(6):835-847.
-
(2010)
Neuron
, vol.66
, Issue.6
, pp. 835-847
-
-
Chakrabarti, L.1
-
29
-
-
84857136769
-
Mitochondrial dysfunction and Purkinje cell loss in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)
-
Girard M, et al. Mitochondrial dysfunction and Purkinje cell loss in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS). Proc Natl Acad Sci U S A. 2012;109(5):1661-1666.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, Issue.5
, pp. 1661-1666
-
-
Girard, M.1
-
30
-
-
80052827401
-
Inflammation in the early stages of neurodegenerative pathology
-
Khandelwal PJ, Herman AM, Moussa CE. Inflammation in the early stages of neurodegenerative pathology. J Neuroimmunol. 2011;238(1-2):1-11.
-
(2011)
J Neuroimmunol
, vol.238
, Issue.1-2
, pp. 1-11
-
-
Khandelwal, P.J.1
Herman, A.M.2
Moussa, C.E.3
-
31
-
-
0036616280
-
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells
-
Yamada K, Watanabe M. Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells. Anat Sci Int. 2002;77(2):94-108.
-
(2002)
Anat Sci Int
, vol.77
, Issue.2
, pp. 94-108
-
-
Yamada, K.1
Watanabe, M.2
-
32
-
-
35548986304
-
Microglia: Active sensor and versatile effector cells in the normal and pathologic brain
-
DOI 10.1038/nn1997, PII NN1997
-
Hanisch UK, Kettenmann H. Microglia: active sensor and versatile effector cells in the normal and pathologic brain. Nat Neurosci. 2007;10(11):1387-1394. (Pubitemid 350014685)
-
(2007)
Nature Neuroscience
, vol.10
, Issue.11
, pp. 1387-1394
-
-
Hanisch, U.-K.1
Kettenmann, H.2
-
33
-
-
79959314684
-
In vivo correction of COX deficiency by activation of the AMPK/PGC-1alpha axis
-
Viscomi C, et al. In vivo correction of COX deficiency by activation of the AMPK/PGC-1alpha axis. Cell Metab. 2011;14(1):80-90.
-
(2011)
Cell Metab
, vol.14
, Issue.1
, pp. 80-90
-
-
Viscomi, C.1
-
34
-
-
63449105579
-
Methylation of 12S rRNA is necessary for in vivo stability of the small subunit of the mammalian mitochondrial ribosome
-
Metodiev MD, et al. Methylation of 12S rRNA is necessary for in vivo stability of the small subunit of the mammalian mitochondrial ribosome. Cell Metab. 2009;9(4):386-397.
-
(2009)
Cell Metab
, vol.9
, Issue.4
, pp. 386-397
-
-
Metodiev, M.D.1
-
35
-
-
79955633747
-
MTERF4 regulates translation by targeting the methyltransferase NSUN4 to the mammalian mitochondrial ribosome
-
Camara Y, et al. MTERF4 regulates translation by targeting the methyltransferase NSUN4 to the mammalian mitochondrial ribosome. Cell Metab. 2011;13(5):527-539.
-
(2011)
Cell Metab
, vol.13
, Issue.5
, pp. 527-539
-
-
Camara, Y.1
-
36
-
-
77956658496
-
Human ERAL1 is a mitochondrial RNA chaperone involved in the assembly of the 28S small mitochondrial ribosomal subunit
-
Dennerlein S, Rozanska A, Wydro M, Chrzanowska-Lightowlers ZM, Lightowlers RN. Human ERAL1 is a mitochondrial RNA chaperone involved in the assembly of the 28S small mitochondrial ribosomal subunit. Biochem J. 2010;430(3):551-558.
-
(2010)
Biochem J
, vol.430
, Issue.3
, pp. 551-558
-
-
Dennerlein, S.1
Rozanska, A.2
Wydro, M.3
Chrzanowska-Lightowlers, Z.M.4
Lightowlers, R.N.5
-
37
-
-
84864454280
-
Human C4orf14 interacts with the mitochondrial nucleoid and is involved in the biogenesis of the small mitochondrial ribosomal subunit
-
He J, et al. Human C4orf14 interacts with the mitochondrial nucleoid and is involved in the biogenesis of the small mitochondrial ribosomal subunit. Nucleic Acids Res. 2012;40(13):6097-6108.
-
(2012)
Nucleic Acids Res
, vol.40
, Issue.13
, pp. 6097-6108
-
-
He, J.1
-
38
-
-
78651104165
-
NOA1 is an essential GTPase required for mitochondrial protein synthesis
-
Kolanczyk M, et al. NOA1 is an essential GTPase required for mitochondrial protein synthesis. Mol Biol Cell. 2011;22(1):1-11.
-
(2011)
Mol Biol Cell
, vol.22
, Issue.1
, pp. 1-11
-
-
Kolanczyk, M.1
-
39
-
-
84861392482
-
C7orf30 is necessary for biogenesis of the large subunit of the mitochondrial ribosome
-
Rorbach J, Gammage PA, Minczuk M. C7orf30 is necessary for biogenesis of the large subunit of the mitochondrial ribosome. Nucleic Acids Res. 2012;40(9):4097-4109.
-
(2012)
Nucleic Acids Res
, vol.40
, Issue.9
, pp. 4097-4109
-
-
Rorbach, J.1
Gammage, P.A.2
Minczuk, M.3
-
40
-
-
77956539977
-
ERAL1 is associated with mitochondrial ribosome and elimination of ERAL1 leads to mitochondrial dysfunction and growth retardation
-
Uchiumi T, et al. ERAL1 is associated with mitochondrial ribosome and elimination of ERAL1 leads to mitochondrial dysfunction and growth retardation. Nucleic Acids Res. 2010;38(16):5554-5568.
-
(2010)
Nucleic Acids Res
, vol.38
, Issue.16
, pp. 5554-5568
-
-
Uchiumi, T.1
-
41
-
-
84861414389
-
C7orf30 specifically associates with the large subunit of the mitochondrial ribosome and is involved in translation
-
Wanschers BF, et al. C7orf30 specifically associates with the large subunit of the mitochondrial ribosome and is involved in translation. Nucleic Acids Res. 2012;40(9):4040-4051.
-
(2012)
Nucleic Acids Res
, vol.40
, Issue.9
, pp. 4040-4051
-
-
Wanschers, B.F.1
-
42
-
-
77952472152
-
Mitochondrial translation and beyond: Processes implicated in combined oxidative phosphorylation deficiencies
-
Smits P, Smeitink J, van den Heuvel L. Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficiencies. J Biomed Biotechnol. 2010;2010:737385.
-
(2010)
J Biomed Biotechnol
, vol.2010
, pp. 737385
-
-
Smits, P.1
Smeitink, J.2
Van Den Heuvel, L.3
-
43
-
-
79960555933
-
Human diseases with impaired mitochondrial protein synthesis
-
Rotig A. Human diseases with impaired mitochondrial protein synthesis. Biochim Biophys Acta. 2011;1807(9):1198-1205.
-
(2011)
Biochim Biophys Acta
, vol.1807
, Issue.9
, pp. 1198-1205
-
-
Rotig, A.1
-
44
-
-
84858985882
-
Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans
-
Bayat V, et al. Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans. PLoS Biol. 2012;10(3):e1001288.
-
(2012)
PLoS Biol
, vol.10
, Issue.3
-
-
Bayat, V.1
-
45
-
-
0024353837
-
Expression of the mammalian mitochondrial genome. Stability of mitochondrial translation products as a function of membrane potential
-
Cote C, Poirier J, and Boulet D. Expression of the mammalian mitochondrial genome. Stability of mitochondrial translation products as a function of membrane potential. J Biol Chem. 1989;264(15):8487-8490. (Pubitemid 19151558)
-
(1989)
Journal of Biological Chemistry
, vol.264
, Issue.15
, pp. 8487-8490
-
-
Cote, C.1
Poirier, J.2
Boulet, D.3
|