-
2
-
-
0029003553
-
Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness
-
Bacino, C., Prezant, T.R., Bu, X., Fournier, P., Fischel-Ghodsian, N., 1995. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness. Pharmacogenetics 5, 165-172.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 165-172
-
-
Bacino, C.1
Prezant, T.R.2
Bu, X.3
Fournier, P.4
Fischel-Ghodsian, N.5
-
3
-
-
0037406049
-
Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction
-
Carelli, V., Giordano, C., D'amati, G., 2003. Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction. Trends Genet. 19, 257-262.
-
(2003)
Trends Genet.
, vol.19
, pp. 257-262
-
-
Carelli, V.1
Giordano, C.2
D'Amati, G.3
-
4
-
-
0029876984
-
In vivo labeling and analysis of human mitochondrial translation products
-
Chomyn, A., 1996a. In vivo labeling and analysis of human mitochondrial translation products. Methods Enzymol. 264, 197-211.
-
(1996)
Methods Enzymol.
, vol.264
, pp. 197-211
-
-
Chomyn, A.1
-
5
-
-
0029981829
-
Platelet-mediated transformation of human mitochondrial DNA-less cells
-
Chomyn, A., 1996b. Platelet-mediated transformation of human mitochondrial DNA-less cells. Methods Enzymol. 264, 334-339.
-
(1996)
Methods Enzymol.
, vol.264
, pp. 334-339
-
-
Chomyn, A.1
-
6
-
-
0023615466
-
Mechanism of bactericidal action of amino-glycosides
-
Davis, B.D., 1987. Mechanism of bactericidal action of amino-glycosides. Microbiol. Rev. 51, 341-350.
-
(1987)
Microbiol. Rev.
, vol.51
, pp. 341-350
-
-
Davis, B.D.1
-
7
-
-
0018646687
-
Cytoplasmic inheritance of erythromycin resistance in human cells
-
Doersen, C.J., Stanbridge, E.J., 1979. Cytoplasmic inheritance of erythromycin resistance in human cells. Proc. Natl Acad. Sci. USA 76, 4549-4553.
-
(1979)
Proc. Natl. Acad. Sci. USA
, vol.76
, pp. 4549-4553
-
-
Doersen, C.J.1
Stanbridge, E.J.2
-
8
-
-
0032796453
-
Genetic factors in aminoglycoside toxicity
-
Fischel-Ghodsian, N., 1999. Genetic factors in aminoglycoside toxicity. Ann. NY Acad. Sci. 884, 99-109.
-
(1999)
Ann. NY Acad. Sci.
, vol.884
, pp. 99-109
-
-
Fischel-Ghodsian, N.1
-
9
-
-
0041778318
-
Mitochondrial deafness
-
Fischel-Ghodsian, N., 2003. Mitochondrial deafness. Ear. Hear. 24, 303-313.
-
(2003)
Ear. Hear.
, vol.24
, pp. 303-313
-
-
Fischel-Ghodsian, N.1
-
10
-
-
0027515721
-
Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity
-
Fischel-Ghodsian, N., Prezant, T.R., Bu, X., Oztas, S., 1993. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity. Am. J. Otolaryngol. 14, 399-403.
-
(1993)
Am. J. Otolaryngol.
, vol.14
, pp. 399-403
-
-
Fischel-Ghodsian, N.1
Prezant, T.R.2
Bu, X.3
Oztas, S.4
-
11
-
-
0037423202
-
Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium
-
Ghelli, A., Zanna, C., Porcelli, A.M., Schapira, A.H., Martinuzzi, A., Carelli, V., Rugolo, M., 2003. Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium. J. Biol. Chem. 278, 4145-4150.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 4145-4150
-
-
Ghelli, A.1
Zanna, C.2
Porcelli, A.M.3
Schapira, A.H.4
Martinuzzi, A.5
Carelli, V.6
Rugolo, M.7
-
12
-
-
0029011225
-
Mitochondrial DNA diseases: Genotype and phenotype in Leber's hereditary optic neuropathy
-
Harding, A.E., Riordan-Eva, P., Govan, G.G., 1995. Mitochondrial DNA diseases: genotype and phenotype in Leber's hereditary optic neuropathy. Muscle Nerve 3, S82-S84.
-
(1995)
Muscle Nerve
, vol.3
-
-
Harding, A.E.1
Riordan-Eva, P.2
Govan, G.G.3
-
13
-
-
0028944623
-
Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA
-
Hotta, Y., Fujiki, K., Hayakawa, M., Nakajima, A., Kanai, A., Mashima, Y., et al., 1995. Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA. Jpn. J. Ophthalmol. 39, 96-108.
-
(1995)
Jpn. J. Ophthalmol.
, vol.39
, pp. 96-108
-
-
Hotta, Y.1
Fujiki, K.2
Hayakawa, M.3
Nakajima, A.4
Kanai, A.5
Mashima, Y.6
-
14
-
-
0030601096
-
Mutant mtDNA at 1555 a to G in 12S rRNA gene and hypersusceptibility of mitochondrial translation to streptomycin can be co-transferred to rho 0 HeLa cells
-
Inoue, K., Takai, D., Soejima, A., Isobe, K., Yamasoba, T., Oka, Y., et al., 1996. Mutant mtDNA at 1555 A to G in 12S rRNA gene and hypersusceptibility of mitochondrial translation to streptomycin can be co-transferred to rho 0 HeLa cells. Biochem. Biophys. Res. Commun. 223, 496-501.
-
(1996)
Biochem. Biophys. Res. Commun.
, vol.223
, pp. 496-501
-
-
Inoue, K.1
Takai, D.2
Soejima, A.3
Isobe, K.4
Yamasoba, T.5
Oka, Y.6
-
15
-
-
0030869088
-
Clinical spectrum of Leber's hereditary optic neuropathy
-
Kerrison, J.B., Newman, N.J., 1997. Clinical spectrum of Leber's hereditary optic neuropathy. Clin. Neurosci. 4, 295-301.
-
(1997)
Clin. Neurosci.
, vol.4
, pp. 295-301
-
-
Kerrison, J.B.1
Newman, N.J.2
-
16
-
-
0029876987
-
Mitochondria-mediated transformation of human rho(0) cells
-
King, M.P., Attadi, G., 1996. Mitochondria-mediated transformation of human rho(0) cells. Methods Enzymol. 264, 313-334.
-
(1996)
Methods Enzymol.
, vol.264
, pp. 313-334
-
-
King, M.P.1
Attadi, G.2
-
17
-
-
0028990381
-
Mitochondrial toxicity of antiviral drugs
-
Lewis, W., Dalakas, M.C., 1995. Mitochondrial toxicity of antiviral drugs. Nat. Med. 1, 417-422.
-
(1995)
Nat. Med.
, vol.1
, pp. 417-422
-
-
Lewis, W.1
Dalakas, M.C.2
-
18
-
-
0038394378
-
Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virus
-
Mackey, D.A., Fingert, J.H., Luzhansky, J.Z., Mccluskey, P.J., Howell, N., Hall, A.J., et al., 2003. Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virus. Eye 17, 312-317.
-
(2003)
Eye
, vol.17
, pp. 312-317
-
-
Mackey, D.A.1
Fingert, J.H.2
Luzhansky, J.Z.3
Mccluskey, P.J.4
Howell, N.5
Hall, A.J.6
-
19
-
-
0036201070
-
Leber hereditary optic neuropathy
-
Man, P.Y., Turnbull, D.M., Chinnery, P.F., 2002. Leber hereditary optic neuropathy. J. Med. Genet. 39, 162-169.
-
(2002)
J. Med. Genet.
, vol.39
, pp. 162-169
-
-
Man, P.Y.1
Turnbull, D.M.2
Chinnery, P.F.3
-
20
-
-
0028925771
-
Lack of differences among mitochondrial DNA in family members with Leber's hereditary optic neuropathy and differing visual outcomes
-
Mashima, Y., Hiida, Y., Oguchi, Y., 1995. Lack of differences among mitochondrial DNA in family members with Leber's hereditary optic neuropathy and differing visual outcomes. J. Neuroophthalmol. 15, 15-19.
-
(1995)
J. Neuroophthalmol.
, vol.15
, pp. 15-19
-
-
Mashima, Y.1
Hiida, Y.2
Oguchi, Y.3
-
21
-
-
0024328462
-
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
-
Moraes, C.T., Dimauro, S., Zeviani, M., Lombes, A., Shanske, S., Miranda, A.F., et al., 1989. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome. N. Engl. J. Med. 320, 1293-1299.
-
(1989)
N. Engl. J. Med.
, vol.320
, pp. 1293-1299
-
-
Moraes, C.T.1
Dimauro, S.2
Zeviani, M.3
Lombes, A.4
Shanske, S.5
Miranda, A.F.6
-
22
-
-
0242522947
-
Techniques and pitfalls in the detection of pathogenic mitochondrial DNA mutations
-
Moraes, C.T., Atencio, D.P., Oca-Cossio, J., Diaz, F., 2003. Techniques and pitfalls in the detection of pathogenic mitochondrial DNA mutations. J. Mol. Diagn. 5, 197-208.
-
(2003)
J. Mol. Diagn.
, vol.5
, pp. 197-208
-
-
Moraes, C.T.1
Atencio, D.P.2
Oca-Cossio, J.3
Diaz, F.4
-
23
-
-
0029874964
-
Use of fibroblast and lymphoblast cultures for detection of respiratory chain defects
-
Robinson, B.H., 1996. Use of fibroblast and lymphoblast cultures for detection of respiratory chain defects. Methods Enzymol. 264, 454-464.
-
(1996)
Methods Enzymol.
, vol.264
, pp. 454-464
-
-
Robinson, B.H.1
-
24
-
-
0036981804
-
A very large Brazilian pedigree with 1 1778 Leber's hereditary optic neuropathy
-
discussion 178-179
-
Sadun, A.A., Carelli, V., Salomao, S.R., Berezovsky, A., Quiros, P., Sadun, F., et al., 2002. A very large Brazilian pedigree with 1 1778 Leber's hereditary optic neuropathy. Trans Am. Ophthalmol. Soc. 100, 169-178.(discussion 178-179).
-
(2002)
Trans Am. Ophthalmol. Soc.
, vol.100
, pp. 169-178
-
-
Sadun, A.A.1
Carelli, V.2
Salomao, S.R.3
Berezovsky, A.4
Quiros, P.5
Sadun, F.6
-
25
-
-
0042850443
-
Extensive investigation of a large Brazilian pedigree of 11778/haplogroup J Leber hereditary optic neuropathy
-
Sadun, A.A., Carelli, V., Salomao, S.R., Berezovsky, A., Quiros, P.A., Sadun, F., et al., 2003. Extensive investigation of a large Brazilian pedigree of 11778/haplogroup J Leber hereditary optic neuropathy. Am. J. Ophthalmol. 136, 231-238.
-
(2003)
Am. J. Ophthalmol.
, vol.136
, pp. 231-238
-
-
Sadun, A.A.1
Carelli, V.2
Salomao, S.R.3
Berezovsky, A.4
Quiros, P.A.5
Sadun, F.6
-
26
-
-
0028173646
-
H1-receptor antagonists. Comparative tolerability and safety
-
Simons, F.E., 1994. H1-receptor antagonists. Comparative tolerability and safety. Drug Saf. 10, 350-380.
-
(1994)
Drug Saf.
, vol.10
, pp. 350-380
-
-
Simons, F.E.1
-
27
-
-
0038811889
-
Aminoglycoside and its derivatives as ligands to target the ribosome
-
Tok, J.B., Bi, L., 2003. Aminoglycoside and its derivatives as ligands to target the ribosome. Curr. Top. Med. Chem. 3, 1001-1019.
-
(2003)
Curr. Top. Med. Chem.
, vol.3
, pp. 1001-1019
-
-
Tok, J.B.1
Bi, L.2
-
28
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
Wallace, D.C., Singh, G., Lott, M.T., Hodge, J.A., Schurr, T.G., Lezza, A.M., et al., 1988. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science 242, 1427-1430.
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, T.G.5
Lezza, A.M.6
-
29
-
-
0036894733
-
Leber hereditary optic neuropathy associated with use of ephedra alkaloids
-
Warner, R.B., Lee, A.G., 2002. Leber hereditary optic neuropathy associated with use of ephedra alkaloids. Am. J. Ophthalmol. 134, 918-920.
-
(2002)
Am. J. Ophthalmol.
, vol.134
, pp. 918-920
-
-
Warner, R.B.1
Lee, A.G.2
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