-
1
-
-
0029076820
-
Selective elimination of paternal mitochondrial DNA during mouse embryogenesis
-
Kaneda H., Hayashi J.-I., Takahama S., Taya C., Lindahl K.F., Yonekawa H. Selective elimination of paternal mitochondrial DNA during mouse embryogenesis. Proc. Natl. Acad. Sci. USA. 92:1995;4542-4546.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 4542-4546
-
-
Kaneda, H.1
Hayashi, J.-I.2
Takahama, S.3
Taya, C.4
Lindahl, K.F.5
Yonekawa, H.6
-
2
-
-
0031887129
-
Maternal inheritance of mouse mtDNA in interspecific hybrids: Segregation of the leaked paternal mtDNA followed by the prevention of subsequent paternal leakage
-
Shitara H., Hayashi J.-I., Takahama S., Kaneda H., Yonekawa H. Maternal inheritance of mouse mtDNA in interspecific hybrids: segregation of the leaked paternal mtDNA followed by the prevention of subsequent paternal leakage. Genetics. 148:1998;851-857.
-
(1998)
Genetics
, vol.148
, pp. 851-857
-
-
Shitara, H.1
Hayashi, J.-I.2
Takahama, S.3
Kaneda, H.4
Yonekawa, H.5
-
3
-
-
0028262917
-
Human mitochondria and mitochondrial genome function as a single dynamic cellular unit
-
Hayashi J.-I., Takemitsu M., Goto Y., Nonaka I. Human mitochondria and mitochondrial genome function as a single dynamic cellular unit. J. Cell Biol. 125:1994;43-50.
-
(1994)
J. Cell Biol.
, vol.125
, pp. 43-50
-
-
Hayashi, J.-I.1
Takemitsu, M.2
Goto, Y.3
Nonaka, I.4
-
4
-
-
0025836655
-
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
-
Hayashi J.-I., Ohta S., Kikuchi A., Takemitsu M., Goto Y., Nonaka I. Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction. Proc. Natl. Acad. Sci. USA. 88:1991;10614-10618.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 10614-10618
-
-
Hayashi, J.-I.1
Ohta, S.2
Kikuchi, A.3
Takemitsu, M.4
Goto, Y.5
Nonaka, I.6
-
5
-
-
0033772263
-
Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes
-
Inoue K., Nakada K., Ogura A., Isobe K., Goto Y., Nonaka I., Hayashi J.-I. Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes. Nat. Genet. 26:2000;176-181.
-
(2000)
Nat. Genet.
, vol.26
, pp. 176-181
-
-
Inoue, K.1
Nakada, K.2
Ogura, A.3
Isobe, K.4
Goto, Y.5
Nonaka, I.6
Hayashi, J.-I.7
-
6
-
-
0034881326
-
Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA
-
Nakada K., Inoue K., Ono T., Isobe K., Ogura A., Goto Y., Nonaka I., Hayashi J.-I. Inter-mitochondrial complementation: mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA. Nat. Med. 7:2001;934-940.
-
(2001)
Nat. Med.
, vol.7
, pp. 934-940
-
-
Nakada, K.1
Inoue, K.2
Ono, T.3
Isobe, K.4
Ogura, A.5
Goto, Y.6
Nonaka, I.7
Hayashi, J.-I.8
-
7
-
-
0034938453
-
Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria
-
Ono T., Isobe K., Nakada K., Hayashi J.-I. Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria. Nat. Genet. 28:2001;272-275.
-
(2001)
Nat. Genet.
, vol.28
, pp. 272-275
-
-
Ono, T.1
Isobe, K.2
Nakada, K.3
Hayashi, J.-I.4
-
8
-
-
0026573082
-
(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes
-
(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. Mol. Cell. Biol. 12:1992;480-490.
-
(1992)
Mol. Cell. Biol.
, vol.12
, pp. 480-490
-
-
King, M.P.1
Koga, Y.2
Davidson, M.3
Schon, E.A.4
-
9
-
-
0026608057
-
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts
-
Chomyn A., Martinuzzi A., Yoneda M., Daga A., Hurko O., Johns D., Lai S.T., Nonaka I., Angelini C., Attardi G. MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts. Proc. Natl. Acad. Sci. USA. 89:1992;4221-4225.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 4221-4225
-
-
Chomyn, A.1
Martinuzzi, A.2
Yoneda, M.3
Daga, A.4
Hurko, O.5
Johns, D.6
Lai, S.T.7
Nonaka, I.8
Angelini, C.9
Attardi, G.10
-
10
-
-
0036544879
-
Inter-mitochondrial complementation of mtDNA mutations and nuclear context
-
Attardi G., Enriquez J.A., Cabezas-Herrera J. Inter-mitochondrial complementation of mtDNA mutations and nuclear context. Nat. Genet. 30:2002;360.
-
(2002)
Nat. Genet.
, vol.30
, pp. 360
-
-
Attardi, G.1
Enriquez, J.A.2
Cabezas-Herrera, J.3
-
11
-
-
0034646656
-
Very rare complementation between mitochondria carrying different mitochondrial DNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells
-
Enriquez J.A., Cabezas-Herrera J., Bayona-Bafaluy M.P., Attardi G. Very rare complementation between mitochondria carrying different mitochondrial DNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells. J. Biol. Chem. 275:2000;11207-11215.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 11207-11215
-
-
Enriquez, J.A.1
Cabezas-Herrera, J.2
Bayona-Bafaluy, M.P.3
Attardi, G.4
-
12
-
-
0012887965
-
Inter-mitochondrial complementation of mtDNA mutations and nuclear context
-
authors' reply 361
-
Hayashi J.-I., Nakada K., Ono T. Inter-mitochondrial complementation of mtDNA mutations and nuclear context. Nat. Genet. 30:2002;. authors' reply 361.
-
(2002)
Nat. Genet.
, vol.30
-
-
Hayashi, J.-I.1
Nakada, K.2
Ono, T.3
-
13
-
-
0036906665
-
Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins
-
Legros F., Lombes A., Frachon P., Rojo M. Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins. Mol. Biol. Cell. 13:2002;4343-4354.
-
(2002)
Mol. Biol. Cell
, vol.13
, pp. 4343-4354
-
-
Legros, F.1
Lombes, A.2
Frachon, P.3
Rojo, M.4
-
14
-
-
0037459089
-
Regulation of mitochondrial morphology by membrane potential, and DRP-dependent division and FZO1-dependent fusion reaction in mammalian cells
-
Ishihara N., Jofuku A., Eura Y., Mihara K. Regulation of mitochondrial morphology by membrane potential, and DRP-dependent division and FZO1-dependent fusion reaction in mammalian cells. Biochem. Biophys. Res. Commun. 301:2003;891-898.
-
(2003)
Biochem. Biophys. Res. Commun.
, vol.301
, pp. 891-898
-
-
Ishihara, N.1
Jofuku, A.2
Eura, Y.3
Mihara, K.4
-
15
-
-
0033515075
-
Functional integrity of mitochondrial genomes in human platelets and autopsied brain tissues from aged patients with Alzheimer's disease
-
Ito S., Inoue K., Yanagisawa N., Kaneko M., Hayashi J.-I. Functional integrity of mitochondrial genomes in human platelets and autopsied brain tissues from aged patients with Alzheimer's disease. Proc. Natl. Acad. Sci. USA. 96:1999;2099-2103.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 2099-2103
-
-
Ito, S.1
Inoue, K.2
Yanagisawa, N.3
Kaneko, M.4
Hayashi, J.-I.5
-
16
-
-
0024541837
-
Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases
-
Linnane A.W., Marzuki S., Ozawa T., Tanaka M. Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases. Lancet. 1:1989;642-645.
-
(1989)
Lancet
, vol.1
, pp. 642-645
-
-
Linnane, A.W.1
Marzuki, S.2
Ozawa, T.3
Tanaka, M.4
|