M Yoneda|T Miyatake|G Attardi - JoVE Visualize

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Muscle & Nerve. Supplement|January 1, 1995

Heteroplasmic mitochondrial tRNA(Lys) mutation and its complementation in MERRF patient-derived mitochondrial transformantsM Yoneda, T Miyatake, G Attardi

Molecular and Cellular Biology|April 1, 1994

Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organellesM Yoneda, T Miyatake, G Attardi

Biochimica Et Biophysica Acta|May 24, 1995

Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systemsG Attardi, M Yoneda, A Chomyn

Proceedings of the National Academy of Sciences of the United States of America|December 1, 1992

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathyM Yoneda, A Chomyn, A Martinuzzi, et al.

Rinsho Shinkeigaku = Clinical Neurology|September 1, 1989

[Chronic progressive external ophthalmoplegia (CPEO) with deleted mitochondrial DNA]Y Tanno, M Yoneda, Y Ohnishi, et al.

Neurology|November 1, 1991

Simple detection of tRNA(Lys) mutation in myoclonus epilepsy associated with ragged-red fibers (MERRF) by polymerase chain reaction with a mismatched primerM Yoneda, Y Tanno, I Nonaka, et al.

Neurology|March 1, 1987

Dihydrobiopterin synthesis defect: an adult with diurnal fluctuation of symptomsK Tanaka, M Yoneda, T Nakajima, et al.

Biochemistry International|August 1, 1990

A common mitochondrial DNA mutation in the t-RNA(Lys) of patients with myoclonus epilepsy associated with ragged-red fibersM Yoneda, Y Tanno, S Horai, et al.

Biochemical and Biophysical Research Communications|September 16, 1991

Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patientsY Tanno, M Yoneda, I Nonaka, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1988

Two distinct genes for ADP/ATP translocase are expressed at the mRNA level in adult human liverJ Houldsworth, G Attardi

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Showing results (1-10 of 673) with videos related to

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Pageof 68

Muscle & Nerve. Supplement|January 1, 1995

Heteroplasmic mitochondrial tRNA(Lys) mutation and its complementation in MERRF patient-derived mitochondrial transformantsM Yoneda, T Miyatake, G Attardi

Molecular and Cellular Biology|April 1, 1994

Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organellesM Yoneda, T Miyatake, G Attardi

Biochimica Et Biophysica Acta|May 24, 1995

Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systemsG Attardi, M Yoneda, A Chomyn

Proceedings of the National Academy of Sciences of the United States of America|December 1, 1992

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathyM Yoneda, A Chomyn, A Martinuzzi, et al.

Rinsho Shinkeigaku = Clinical Neurology|September 1, 1989

[Chronic progressive external ophthalmoplegia (CPEO) with deleted mitochondrial DNA]Y Tanno, M Yoneda, Y Ohnishi, et al.

Neurology|November 1, 1991

Simple detection of tRNA(Lys) mutation in myoclonus epilepsy associated with ragged-red fibers (MERRF) by polymerase chain reaction with a mismatched primerM Yoneda, Y Tanno, I Nonaka, et al.

Neurology|March 1, 1987

Dihydrobiopterin synthesis defect: an adult with diurnal fluctuation of symptomsK Tanaka, M Yoneda, T Nakajima, et al.

Biochemistry International|August 1, 1990

A common mitochondrial DNA mutation in the t-RNA(Lys) of patients with myoclonus epilepsy associated with ragged-red fibersM Yoneda, Y Tanno, S Horai, et al.

Biochemical and Biophysical Research Communications|September 16, 1991

Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patientsY Tanno, M Yoneda, I Nonaka, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1988

Two distinct genes for ADP/ATP translocase are expressed at the mRNA level in adult human liverJ Houldsworth, G Attardi

Pageof 68