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S Horai

Showing results (71-80 of 85) with videos related to

Pageof 9
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Muscle & Nerve|January 14, 1998
A new congenital muscular dystrophy with mitochondrial structural abnormalitiesI Nishino, O Kobayashi, Y Goto, et al.
Human Biology|April 1, 1994
Polymorphisms of complement component I and C1R subcomponent of C1 in nine aboriginal Taiwanese populationsK Umetsu, I Yuasa, T Suzuki, et al.
Journal of Human Genetics|April 27, 2001
Mitochondrial DNA polymorphisms in Yunnan nationalities in ChinaY P Qian, Z T Chu, Q Dai, et al.
Tissue Antigens|March 1, 1981
The HLA antigens of two Negrito populations in the PhilippinesS Horai, K Omoto, T Juji, et al.
Annals of Neurology|March 1, 1994
Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomesY Kawakami, R Sakuta, K Hashimoto, et al.
Journal of the Neurological Sciences|September 1, 1989
Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS)M Yoneda, M Tanaka, M Nishikimi, et al.
Biochemical and Biophysical Research Communications|August 15, 1988
Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathyT Ozawa, M Yoneda, M Tanaka, et al.
The American Journal of Physiology|September 1, 1994
Enzymatic and genetic adaptation of soleus muscle mitochondria to physical training in ratsT Murakami, Y Shimomura, N Fujitsuka, et al.
Nature Medicine|December 2, 1999
The presence of ancient human T-cell lymphotropic virus type I provirus DNA in an Andean mummyH C Li, T Fujiyoshi, H Lou, et al.
American Journal of Human Genetics|September 1, 1996
mtDNA polymorphism in East Asian Populations, with special reference to the peopling of JapanS Horai, K Murayama, K Hayasaka, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Muscle & Nerve|January 14, 1998
A new congenital muscular dystrophy with mitochondrial structural abnormalitiesI Nishino, O Kobayashi, Y Goto, et al.
Human Biology|April 1, 1994
Polymorphisms of complement component I and C1R subcomponent of C1 in nine aboriginal Taiwanese populationsK Umetsu, I Yuasa, T Suzuki, et al.
Journal of Human Genetics|April 27, 2001
Mitochondrial DNA polymorphisms in Yunnan nationalities in ChinaY P Qian, Z T Chu, Q Dai, et al.
Tissue Antigens|March 1, 1981
The HLA antigens of two Negrito populations in the PhilippinesS Horai, K Omoto, T Juji, et al.
Annals of Neurology|March 1, 1994
Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomesY Kawakami, R Sakuta, K Hashimoto, et al.
Journal of the Neurological Sciences|September 1, 1989
Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS)M Yoneda, M Tanaka, M Nishikimi, et al.
Biochemical and Biophysical Research Communications|August 15, 1988
Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathyT Ozawa, M Yoneda, M Tanaka, et al.
The American Journal of Physiology|September 1, 1994
Enzymatic and genetic adaptation of soleus muscle mitochondria to physical training in ratsT Murakami, Y Shimomura, N Fujitsuka, et al.
Nature Medicine|December 2, 1999
The presence of ancient human T-cell lymphotropic virus type I provirus DNA in an Andean mummyH C Li, T Fujiyoshi, H Lou, et al.
American Journal of Human Genetics|September 1, 1996
mtDNA polymorphism in East Asian Populations, with special reference to the peopling of JapanS Horai, K Murayama, K Hayasaka, et al.
Pageof 9