-
1
-
-
0028935319
-
A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22
-
Tranebjaerg, L., Schwartz, C., Eriksen, H., Andreasson, S., Ponjavic, V., Dahl, A., Stevenson, R., May, M., Arena, F., Barker, D. et al. (1995) A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22. J. Med. Genet., 32, 257-263.
-
(1995)
J. Med. Genet.
, vol.32
, pp. 257-263
-
-
Tranebjaerg, L.1
Schwartz, C.2
Eriksen, H.3
Andreasson, S.4
Ponjavic, V.5
Dahl, A.6
Stevenson, R.7
May, M.8
Arena, F.9
Barker, D.10
-
2
-
-
0002923628
-
Sex-linked deafness of a possibly new type
-
Mohr, J. and Mageroy, K. (1960) Sex-linked deafness of a possibly new type. Acta Genet. Stat. Med., 10, 54-62.
-
(1960)
Acta Genet. Stat. Med.
, vol.10
, pp. 54-62
-
-
Mohr, J.1
Mageroy, K.2
-
3
-
-
16044366597
-
A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness
-
Jin, H., May, M., Tranebjaerg, L., Kendall, E., Fontan, G., Jackson, J., Subramony, S., Arena, F., Lubs, H., Smith, S. et al. (1996) A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness. Nat. Genet., 14, 177-180.
-
(1996)
Nat. Genet.
, vol.14
, pp. 177-180
-
-
Jin, H.1
May, M.2
Tranebjaerg, L.3
Kendall, E.4
Fontan, G.5
Jackson, J.6
Subramony, S.7
Arena, F.8
Lubs, H.9
Smith, S.10
-
4
-
-
0034039615
-
A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndrome
-
Tranebjaerg, L., Hamel, B., Gabreels, F., Renier, W. and Van Ghelue, M. (2000) A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndrome. Eur. J. Hum. Genet., 8, 464-467.
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 464-467
-
-
Tranebjaerg, L.1
Hamel, B.2
Gabreels, F.3
Renier, W.4
Van Ghelue, M.5
-
5
-
-
17944399388
-
Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a gene
-
Tranebjaerg, L., Jensen, P., Van Ghelue, M., Vnencak-Jones, C., Sund, S., Elgjo, K., Jakobsen, J., Lindal, S., Warburg, M., Fuglsang-Frederiksen, A. et al. (2001) Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a gene. Ophthalmic Genet., 22, 207-223.
-
(2001)
Ophthalmic Genet.
, vol.22
, pp. 207-223
-
-
Tranebjaerg, L.1
Jensen, P.2
Van Ghelue, M.3
Vnencak-Jones, C.4
Sund, S.5
Elgjo, K.6
Jakobsen, J.7
Lindal, S.8
Warburg, M.9
Fuglsang-Frederiksen, A.10
-
6
-
-
0034795004
-
A novel deafness/dystonia peptide gene mutation that causes dystonia in female carriers of Mohr-Tranebjaerg syndrome
-
Swerdlow, R. and Wooten, G. (2001) A novel deafness/dystonia peptide gene mutation that causes dystonia in female carriers of Mohr-Tranebjaerg syndrome. Ann. Neurol., 50, 537-540.
-
(2001)
Ann. Neurol.
, vol.50
, pp. 537-540
-
-
Swerdlow, R.1
Wooten, G.2
-
7
-
-
0034971212
-
A family with X-linked dystonia-deafness syndrome with a novel mutation of the DDP gene
-
Ujike, H., Tanabe, Y., Takehisa, Y., Hayabara, T. and Kuroda, S. (2001) A family with X-linked dystonia-deafness syndrome with a novel mutation of the DDP gene. Arch. Neurol., 58, 1004-1007.
-
(2001)
Arch. Neurol.
, vol.58
, pp. 1004-1007
-
-
Ujike, H.1
Tanabe, Y.2
Takehisa, Y.3
Hayabara, T.4
Kuroda, S.5
-
8
-
-
0042767609
-
Clinical and molecular findings in a patient with a novel mutation in the deafness-dystonia peptide (DDP1) gene
-
Binder, J., Hofmann, S., Kreisel, S., Wohrle, J., Bazner, H., Krauss, J., Hennerici, M. and Bauer, M. (2003) Clinical and molecular findings in a patient with a novel mutation in the deafness-dystonia peptide (DDP1) gene. Brain, 126, 1814-1820.
-
(2003)
Brain
, vol.126
, pp. 1814-1820
-
-
Binder, J.1
Hofmann, S.2
Kreisel, S.3
Wohrle, J.4
Bazner, H.5
Krauss, J.6
Hennerici, M.7
Bauer, M.8
-
9
-
-
13444267649
-
A novel intronic mutation in the DDP1 gene in a family with X-linked dystonia-deafness syndrome
-
Ezquerra, M., Campdelacreu, J., Munoz, E., Tolosa, E. and Marti, M. (2005) A novel intronic mutation in the DDP1 gene in a family with X-linked dystonia-deafness syndrome. Arch. Neurol., 62, 306-308.
-
(2005)
Arch. Neurol.
, vol.62
, pp. 306-308
-
-
Ezquerra, M.1
Campdelacreu, J.2
Munoz, E.3
Tolosa, E.4
Marti, M.5
-
10
-
-
32444451348
-
A novel mutation in the gene encoding TIMM8a, a component of the mitochondrial protein translocase complexes, in a Spanish familial case of deafness-dystonia (Mohr-Tranebjaerg) syndrome
-
Aguirre, L., del Castillo, I., Macaya, A., Meda, C., Villamar, M., Moreno-Pelayo, M. and Moreno, F. (2006) A novel mutation in the gene encoding TIMM8a, a component of the mitochondrial protein translocase complexes, in a Spanish familial case of deafness-dystonia (Mohr-Tranebjaerg) syndrome. Am. J. Med. Genet. A, 140, 392-397.
-
(2006)
Am. J. Med. Genet. A
, vol.140
, pp. 392-397
-
-
Aguirre, L.1
del Castillo, I.2
Macaya, A.3
Meda, C.4
Villamar, M.5
Moreno-Pelayo, M.6
Moreno, F.7
-
11
-
-
34548257274
-
Blepharospasm and limb dystonia caused by Mohr-Tranebjaerg syndrome with a novel splice-site mutation in the deafness/dystonia peptide gene
-
Kim, H., Edwards, M., Tyson, J., Quinn, N., Bitner-Glindzicz, M. and Bhatia, K. (2007) Blepharospasm and limb dystonia caused by Mohr-Tranebjaerg syndrome with a novel splice-site mutation in the deafness/dystonia peptide gene. Mov. Disord., 22, 1328-1331.
-
(2007)
Mov. Disord.
, vol.22
, pp. 1328-1331
-
-
Kim, H.1
Edwards, M.2
Tyson, J.3
Quinn, N.4
Bitner-Glindzicz, M.5
Bhatia, K.6
-
12
-
-
56649083543
-
A Spanish sporadic case of deafness-dystonia (Mohr-Tranebjaerg) syndrome with a novel mutation in the gene encoding TIMM8a, a component of the mitochondrial protein translocase complexes
-
Aguirre, L., Perez-Bas, M., Villamar, M., Lopez-Ariztegui, M., Moreno-Pelayo, M., Moreno, F. and del Castillo, I. (2008) A Spanish sporadic case of deafness-dystonia (Mohr-Tranebjaerg) syndrome with a novel mutation in the gene encoding TIMM8a, a component of the mitochondrial protein translocase complexes. Neuromuscul. Disord., 18, 979-981.
-
(2008)
Neuromuscul. Disord.
, vol.18
, pp. 979-981
-
-
Aguirre, L.1
Perez-Bas, M.2
Villamar, M.3
Lopez-Ariztegui, M.4
Moreno-Pelayo, M.5
Moreno, F.6
del Castillo, I.7
-
13
-
-
0033515001
-
Mitochondria and dystonia: the movement disorder connection?
-
Wallace, D. and Murdock, D. (1999) Mitochondria and dystonia: the movement disorder connection? Proc. Natl Acad. Sci. USA, 96, 1817-1819.
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 1817-1819
-
-
Wallace, D.1
Murdock, D.2
-
14
-
-
0033514928
-
Human deafness dystonia syndrome is a mitochondrial disease
-
Koehler, C., Leuenberger, D., Merchant, S., Renold, A., Junne, T. and Schatz, G. (1999) Human deafness dystonia syndrome is a mitochondrial disease. Proc. Natl Acad. Sci. USA, 96, 2141-2146.
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 2141-2146
-
-
Koehler, C.1
Leuenberger, D.2
Merchant, S.3
Renold, A.4
Junne, T.5
Schatz, G.6
-
15
-
-
0034683663
-
Two intermembrane space TIM complexes interact with different domains of Tim23p during its import into mitochondria
-
Davis, A., Sepuri, N., Holder, J., Johnson, A. and Jensen, R. (2000) Two intermembrane space TIM complexes interact with different domains of Tim23p during its import into mitochondria. J. Cell Biol., 150, 1271-1282.
-
(2000)
J. Cell Biol.
, vol.150
, pp. 1271-1282
-
-
Davis, A.1
Sepuri, N.2
Holder, J.3
Johnson, A.4
Jensen, R.5
-
16
-
-
0034387981
-
The role of the TIM8-13 complex in the import of Tim23 into mitochondria
-
Paschen, S., Rothbauer, U., Kaldi, K., Bauer, M., Neupert, W. and Brunner, M. (2000) The role of the TIM8-13 complex in the import of Tim23 into mitochondria. EMBO J., 19, 6392-6400.
-
(2000)
EMBO J.
, vol.19
, pp. 6392-6400
-
-
Paschen, S.1
Rothbauer, U.2
Kaldi, K.3
Bauer, M.4
Neupert, W.5
Brunner, M.6
-
17
-
-
0035813194
-
Role of the deafness dystonia peptide 1 (DDP1) in import of human Tim23 into the inner membrane of mitochondria
-
Rothbauer, U., Hofmann, S., Muhlenbein, N., Paschen, S., Gerbitz, K., Neupert, W., Brunner, M. and Bauer, M. (2001) Role of the deafness dystonia peptide 1 (DDP1) in import of human Tim23 into the inner membrane of mitochondria. J. Biol. Chem., 276, 37327-37334.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 37327-37334
-
-
Rothbauer, U.1
Hofmann, S.2
Muhlenbein, N.3
Paschen, S.4
Gerbitz, K.5
Neupert, W.6
Brunner, M.7
Bauer, M.8
-
18
-
-
0027222059
-
Identification of MIM23, a putative component of the protein import machinery of the mitochondrial inner membrane
-
Dekker, P.J., Keil, P., Rassow, J., Maarse, A.C., Pfanner, N. and Meijer, M. (1993) Identification of MIM23, a putative component of the protein import machinery of the mitochondrial inner membrane. FEBS Lett., 330, 66-70.
-
(1993)
FEBS Lett.
, vol.330
, pp. 66-70
-
-
Dekker, P.J.1
Keil, P.2
Rassow, J.3
Maarse, A.C.4
Pfanner, N.5
Meijer, M.6
-
19
-
-
0027162057
-
MAS6 encodes an essential inner membrane component of the yeast mitochondrial protein import pathway
-
Emtage, J.L. and Jensen, R.E. (1993) MAS6 encodes an essential inner membrane component of the yeast mitochondrial protein import pathway. J. Cell Biol., 122, 1003-1012.
-
(1993)
J. Cell Biol.
, vol.122
, pp. 1003-1012
-
-
Emtage, J.L.1
Jensen, R.E.2
-
20
-
-
0037189583
-
The C66W mutation in the deafness dystonia peptide 1 (DDP1) affects the formation of functional DDP1, TIM13 complexes in the mitochondrial intermembrane space
-
Hofmann, S., Rothbauer, U., Muhlenbein, N., Neupert, W., Gerbitz, K., Brunner, M. and Bauer, M. (2002) The C66W mutation in the deafness dystonia peptide 1 (DDP1) affects the formation of functional DDP1.TIM13 complexes in the mitochondrial intermembrane space. J. Biol. Chem., 277, 23287-23293.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 23287-23293
-
-
Hofmann, S.1
Rothbauer, U.2
Muhlenbein, N.3
Neupert, W.4
Gerbitz, K.5
Brunner, M.6
Bauer, M.7
-
21
-
-
0036501592
-
Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex
-
Roesch, K., Curran, S., Tranebjaerg, L. and Koehler, C. (2002) Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex. Hum. Mol. Genet., 11, 477-486.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 477-486
-
-
Roesch, K.1
Curran, S.2
Tranebjaerg, L.3
Koehler, C.4
-
22
-
-
5744230324
-
The calcium-binding aspartate/glutamate carriers, citrin and aralar1, are new substrates for the DDP1/TIMM8a-TIMM13 complex
-
Roesch, K., Hynds, P., Varga, R., Tranebjaerg, L. and Koehler, C. (2004) The calcium-binding aspartate/glutamate carriers, citrin and aralar1, are new substrates for the DDP1/TIMM8a-TIMM13 complex. Hum. Mol. Genet., 13, 2101-2111.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 2101-2111
-
-
Roesch, K.1
Hynds, P.2
Varga, R.3
Tranebjaerg, L.4
Koehler, C.5
-
23
-
-
2442421175
-
Biogenesis of the protein import channel Tom40 of the mitochondrial outer membrane: intermembrane space components are involved in an early stage of the assembly pathway
-
Wiedemann, N., Truscott, K.N., Pfannschmidt, S., Guiard, B., Meisinger, C. and Pfanner, N. (2004) Biogenesis of the protein import channel Tom40 of the mitochondrial outer membrane: intermembrane space components are involved in an early stage of the assembly pathway. J. Biol. Chem., 279, 18188-18194.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 18188-18194
-
-
Wiedemann, N.1
Truscott, K.N.2
Pfannschmidt, S.3
Guiard, B.4
Meisinger, C.5
Pfanner, N.6
-
24
-
-
1842478040
-
The Tim8-Tim13 complex of Neurospora crassa functions in the assembly of proteins into both mitochondrial membranes
-
Hoppins, S. and Nargang, F. (2004) The Tim8-Tim13 complex of Neurospora crassa functions in the assembly of proteins into both mitochondrial membranes. J. Biol. Chem., 279, 12396-12405.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 12396-12405
-
-
Hoppins, S.1
Nargang, F.2
-
25
-
-
14844307858
-
Assembly of the TOB complex of mitochondria
-
Habib, S., Waizenegger, T., Lech, M., Neupert, W. and Rapaport, D. (2005) Assembly of the TOB complex of mitochondria. J. Biol. Chem., 280, 6434-6440.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 6434-6440
-
-
Habib, S.1
Waizenegger, T.2
Lech, M.3
Neupert, W.4
Rapaport, D.5
-
26
-
-
80055113762
-
Modulated microtubule dynamics enable Hklp2/Kif15 to assemble bipolar spindles
-
in press
-
Florian, S. and Mayer, T. (2011) Modulated microtubule dynamics enable Hklp2/Kif15 to assemble bipolar spindles. Cell Cycle, 10, in press.
-
(2011)
Cell Cycle
, vol.10
-
-
Florian, S.1
Mayer, T.2
-
27
-
-
0033198845
-
Different import pathways through the mitochondrial intermembrane space for inner membrane proteins
-
Leuenberger, D., Bally, N., Schatz, G. and Koehler, C. (1999) Different import pathways through the mitochondrial intermembrane space for inner membrane proteins. EMBO J., 18, 4816-4822.
-
(1999)
EMBO J.
, vol.18
, pp. 4816-4822
-
-
Leuenberger, D.1
Bally, N.2
Schatz, G.3
Koehler, C.4
-
28
-
-
80052579096
-
Multispan mitochondrial outer membrane protein Ugo1 follows a unique Mim1-dependent import pathway
-
Papic, D., Krumpe, K., Dukanovic, J., Dimmer, K.S. and Rapaport, D. (2011) Multispan mitochondrial outer membrane protein Ugo1 follows a unique Mim1-dependent import pathway. J. Cell Biol., 194, 397-405.
-
(2011)
J. Cell Biol.
, vol.194
, pp. 397-405
-
-
Papic, D.1
Krumpe, K.2
Dukanovic, J.3
Dimmer, K.S.4
Rapaport, D.5
-
29
-
-
26244466764
-
Functional and mutational characterization of human MIA40 acting during import into the mitochondrial intermembrane space
-
Hofmann, S., Rothbauer, U., Muhlenbein, N., Baiker, K., Hell, K. and Bauer, M. (2005) Functional and mutational characterization of human MIA40 acting during import into the mitochondrial intermembrane space. J. Mol. Biol., 353, 517-528.
-
(2005)
J. Mol. Biol.
, vol.353
, pp. 517-528
-
-
Hofmann, S.1
Rothbauer, U.2
Muhlenbein, N.3
Baiker, K.4
Hell, K.5
Bauer, M.6
-
30
-
-
0028149597
-
Rupture of the mitochondrial outer membrane impairs porin assembly
-
Smith, M., Hicks, S., Baker, K. and McCauley, R. (1994) Rupture of the mitochondrial outer membrane impairs porin assembly. J. Biol. Chem., 269, 28460-28464.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 28460-28464
-
-
Smith, M.1
Hicks, S.2
Baker, K.3
McCauley, R.4
-
32
-
-
78649413837
-
Mitochondrial fusion and fission in cell life and death
-
Westermann, B. (2010) Mitochondrial fusion and fission in cell life and death. Nat. Rev. Mol. Cell Biol., 11, 872-884.
-
(2010)
Nat. Rev. Mol. Cell Biol.
, vol.11
, pp. 872-884
-
-
Westermann, B.1
-
33
-
-
34250204271
-
The machines that divide and fuse mitochondria
-
Hoppins, S., Lackner, L. and Nunnari, J. (2007) The machines that divide and fuse mitochondria. Annu. Rev. Biochem., 76, 751-780.
-
(2007)
Annu. Rev. Biochem.
, vol.76
, pp. 751-780
-
-
Hoppins, S.1
Lackner, L.2
Nunnari, J.3
-
34
-
-
77955287381
-
Physiological functions of mitochondrial fusion
-
Chen, H. and Chan, D. (2010) Physiological functions of mitochondrial fusion. Ann. N. Y. Acad. Sci., 1201, 21-25.
-
(2010)
Ann. N. Y. Acad. Sci.
, vol.1201
, pp. 21-25
-
-
Chen, H.1
Chan, D.2
-
35
-
-
77956230098
-
Mitochondrial shape changes: orchestrating cell pathophysiology
-
Campello, S. and Scorrano, L. (2010) Mitochondrial shape changes: orchestrating cell pathophysiology. EMBO Rep., 11, 678-684.
-
(2010)
EMBO Rep.
, vol.11
, pp. 678-684
-
-
Campello, S.1
Scorrano, L.2
-
36
-
-
79952291364
-
Molecular mechanisms and physiologic functions of mitochondrial dynamics
-
Otera, H. and Mihara, K. (2011) Molecular mechanisms and physiologic functions of mitochondrial dynamics. J. Biochem., 149, 241-251.
-
(2011)
J. Biochem.
, vol.149
, pp. 241-251
-
-
Otera, H.1
Mihara, K.2
-
37
-
-
0033231549
-
C. elegans dynamin-related protein DRP-1 controls severing of the mitochondrial outer membrane
-
Labrousse, A.M., Zappaterra, M.D., Rube, D.A. and van der Bliek, A.M. (1999) C. elegans dynamin-related protein DRP-1 controls severing of the mitochondrial outer membrane. Mol. Cell, 4, 815-826.
-
(1999)
Mol. Cell
, vol.4
, pp. 815-826
-
-
Labrousse, A.M.1
Zappaterra, M.D.2
Rube, D.A.3
van der Bliek, A.M.4
-
38
-
-
28444487509
-
Bax/Bak-dependent release of DDP/TIMM8a promotes Drp1-mediated mitochondrial fission and mitoptosis during programmed cell death
-
Arnoult, D., Rismanchi, N., Grodet, A., Roberts, R., Seeburg, D., Estaquier, J., Sheng, M. and Blackstone, C. (2005) Bax/Bak-dependent release of DDP/TIMM8a promotes Drp1-mediated mitochondrial fission and mitoptosis during programmed cell death. Curr. Biol., 15, 2112-2118.
-
(2005)
Curr. Biol.
, vol.15
, pp. 2112-2118
-
-
Arnoult, D.1
Rismanchi, N.2
Grodet, A.3
Roberts, R.4
Seeburg, D.5
Estaquier, J.6
Sheng, M.7
Blackstone, C.8
-
39
-
-
0032416346
-
Oxygen and ion concentrations in normoxic and hypoxic brain cells
-
Silver, I. and Erecinska, M. (1998) Oxygen and ion concentrations in normoxic and hypoxic brain cells. Adv. Exp. Med. Biol., 454, 7-16.
-
(1998)
Adv. Exp. Med. Biol.
, vol.454
, pp. 7-16
-
-
Silver, I.1
Erecinska, M.2
-
40
-
-
79955623510
-
During autophagy mitochondria elongate, are spared from degradation and sustain cell viability
-
Gomes, L.C., Di Benedetto, G. and Scorrano, L. (2011) During autophagy mitochondria elongate, are spared from degradation and sustain cell viability. Nat. Cell Biol., 13, 589-598.
-
(2011)
Nat. Cell Biol.
, vol.13
, pp. 589-598
-
-
Gomes, L.C.1
Di Benedetto, G.2
Scorrano, L.3
-
41
-
-
79959987510
-
Tubular network formation protects mitochondria from autophagosomal degradation during nutrient starvation
-
Rambold, A.S., Kostelecky, B., Elia, N. and Lippincott-Schwartz, J. (2011) Tubular network formation protects mitochondria from autophagosomal degradation during nutrient starvation. Proc. Natl Acad. Sci. USA, 108, 10190-10195.
-
(2011)
Proc. Natl Acad. Sci. USA
, vol.108
, pp. 10190-10195
-
-
Rambold, A.S.1
Kostelecky, B.2
Elia, N.3
Lippincott-Schwartz, J.4
-
42
-
-
0023659499
-
Mitochondrial protein import: nucleoside triphosphates are involved in conferring import-competence to precursors
-
Pfanner, N., Tropschug, M. and Neupert, W. (1987) Mitochondrial protein import: nucleoside triphosphates are involved in conferring import-competence to precursors. Cell, 49, 815-823.
-
(1987)
Cell
, vol.49
, pp. 815-823
-
-
Pfanner, N.1
Tropschug, M.2
Neupert, W.3
-
43
-
-
0023644933
-
Distinct steps in the import of ADP/ATP carrier into mitochondria
-
Pfanner, N. and Neupert, W. (1987) Distinct steps in the import of ADP/ATP carrier into mitochondria. J. Biol. Chem., 262, 7528-7536.
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 7528-7536
-
-
Pfanner, N.1
Neupert, W.2
-
44
-
-
0036830531
-
Insertion and assembly of human tom7 into the preprotein translocase complex of the outer mitochondrial membrane
-
Johnston, A., Hoogenraad, J., Dougan, D., Truscott, K., Yano, M., Mori, M., Hoogenraad, N. and Ryan, M. (2002) Insertion and assembly of human tom7 into the preprotein translocase complex of the outer mitochondrial membrane. J. Biol. Chem., 277, 42197-42204.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 42197-42204
-
-
Johnston, A.1
Hoogenraad, J.2
Dougan, D.3
Truscott, K.4
Yano, M.5
Mori, M.6
Hoogenraad, N.7
Ryan, M.8
-
45
-
-
34347236921
-
Organelle isolation: functional mitochondria from mouse liver, muscle and cultured fibroblasts
-
Frezza, C., Cipolat, S. and Scorrano, L. (2007) Organelle isolation: functional mitochondria from mouse liver, muscle and cultured fibroblasts. Nat. Protoc., 2, 287-295.
-
(2007)
Nat. Protoc.
, vol.2
, pp. 287-295
-
-
Frezza, C.1
Cipolat, S.2
Scorrano, L.3
-
46
-
-
34250676869
-
Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunits
-
Bonnet, C., Kaltimbacher, V., Ellouze, S., Augustin, S., Benit, P., Forster, V., Rustin, P., Sahel, J. and Corral-Debrinski, M. (2007) Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunits. Rejuvenation Res., 10, 127-144.
-
(2007)
Rejuvenation Res.
, vol.10
, pp. 127-144
-
-
Bonnet, C.1
Kaltimbacher, V.2
Ellouze, S.3
Augustin, S.4
Benit, P.5
Forster, V.6
Rustin, P.7
Sahel, J.8
Corral-Debrinski, M.9
-
47
-
-
0028214450
-
Analysis of molecular masses and oligomeric states of protein complexes by blue native electrophoresis and isolation of membrane protein complexes by two-dimensional native electrophoresis
-
Schagger, H., Cramer, W.A. and von Jagow, G. (1994) Analysis of molecular masses and oligomeric states of protein complexes by blue native electrophoresis and isolation of membrane protein complexes by two-dimensional native electrophoresis. Anal. Biochem., 217, 220-230.
-
(1994)
Anal. Biochem.
, vol.217
, pp. 220-230
-
-
Schagger, H.1
Cramer, W.A.2
von Jagow, G.3
|