Y I Goto - JoVE Visualize

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Journal of Gravitational Physiology : a Journal of the International Society for Gravitational Physiology|April 17, 2003

Muscle mitochondrial changes by experimental immobility and hindlimb suspensionY I Goto, H Komaki, F Igarashi, et al.

Muscle & Nerve|March 1, 1997

Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two familiesM Ozawa, I Nishino, S Horai, et al.

American Journal of Medical Genetics|August 22, 1997

New autosomal-recessive syndrome of Leber congenital amaurosis, short stature, growth hormone insufficiency, mental retardation, hepatic dysfunction, and metabolic acidosisH Ehara, C Nakano, K Ohno, et al.

Ultrastructural Pathology|July 11, 2006

Mitochondrial disorder, diabetes mellitus, and findings in three muscles, including the heartB Venugopal, K T Wong, Y-I Goto, et al.

The Journal of Biological Chemistry|February 28, 1997

The interorganellar interaction between distinct human mitochondria with deletion mutant mtDNA from a patient with mitochondrial disease and with HeLa mtDNAD Takai, K Inoue, Y i Goto, et al.

Ultrastructural Pathology|December 23, 2006

Mitochondrial disorder, diabetes mellitus, and findings in three muscles, including the heartM Bhattacharjee, B Venugopal, K T Wong, et al.

Nature Medicine|August 2, 2001

Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNAK Nakada, K Inoue, T Ono, et al.

Muscle & Nerve|May 8, 1998

Mitochondrial abnormalities in selenium-deficient myopathyY Osaki, I Nishino, N Murakami, et al.

Biochemical and Biophysical Research Communications|April 16, 1998

Glycogen storage disease type II: identification of four novel missense mutations (D645N, G648S, R672W, R672Q) and two insertions/deletions in the acid alpha-glucosidase locus of patients of differing phenotypeM L Huie, S Tsujino, S Sklower Brooks, et al.

Clinical Genetics|January 19, 2018

NDUFAF3 variants that disrupt mitochondrial complex I assembly may associate with cavitating leukoencephalopathyA Ishiyama, K Muramatsu, S Uchino, et al.

Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:

Pageof 2

Journal of Gravitational Physiology : a Journal of the International Society for Gravitational Physiology|April 17, 2003

Muscle mitochondrial changes by experimental immobility and hindlimb suspensionY I Goto, H Komaki, F Igarashi, et al.

Muscle & Nerve|March 1, 1997

Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two familiesM Ozawa, I Nishino, S Horai, et al.

American Journal of Medical Genetics|August 22, 1997

New autosomal-recessive syndrome of Leber congenital amaurosis, short stature, growth hormone insufficiency, mental retardation, hepatic dysfunction, and metabolic acidosisH Ehara, C Nakano, K Ohno, et al.

Ultrastructural Pathology|July 11, 2006

Mitochondrial disorder, diabetes mellitus, and findings in three muscles, including the heartB Venugopal, K T Wong, Y-I Goto, et al.

The Journal of Biological Chemistry|February 28, 1997

The interorganellar interaction between distinct human mitochondria with deletion mutant mtDNA from a patient with mitochondrial disease and with HeLa mtDNAD Takai, K Inoue, Y i Goto, et al.

Ultrastructural Pathology|December 23, 2006

Mitochondrial disorder, diabetes mellitus, and findings in three muscles, including the heartM Bhattacharjee, B Venugopal, K T Wong, et al.

Nature Medicine|August 2, 2001

Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNAK Nakada, K Inoue, T Ono, et al.

Muscle & Nerve|May 8, 1998

Mitochondrial abnormalities in selenium-deficient myopathyY Osaki, I Nishino, N Murakami, et al.

Biochemical and Biophysical Research Communications|April 16, 1998

Glycogen storage disease type II: identification of four novel missense mutations (D645N, G648S, R672W, R672Q) and two insertions/deletions in the acid alpha-glucosidase locus of patients of differing phenotypeM L Huie, S Tsujino, S Sklower Brooks, et al.

Clinical Genetics|January 19, 2018

NDUFAF3 variants that disrupt mitochondrial complex I assembly may associate with cavitating leukoencephalopathyA Ishiyama, K Muramatsu, S Uchino, et al.

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