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S Horai

Showing results (41-50 of 85) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1991
A new type of mitochondrial DNA deletion in patients with encephalomyopathyS Miyabayashi, H Hanamizu, H Endo, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 17, 1995
Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAsS Horai, K Hayasaka, R Kondo, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|June 1, 1979
Genetic polymorphism of the fourth component of human complement in JapaneseK Tokunaga, S Horai, K Omoto, 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.
Journal of the Neurological Sciences|January 1, 1992
Is Parkinson's disease a mitochondrial disorder?Y Nakagawa-Hattori, H Yoshino, T Kondo, 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.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|March 1, 1980
Haplotype analysis of the linkage group HLA-A:HLA-B:C4 in Japanese: evidence for the C4 locus being between the HLA-A and HLA-B lociS Horai, K Tokunaga, K Omoto, et al.
Molecular Biology and Evolution|May 1, 1988
Phylogenetic relationships among Japanese, rhesus, Formosan, and crab-eating monkeys, inferred from restriction-enzyme analysis of mitochondrial DNAsK Hayasaka, S Horai, T Gojobori, et al.
International Journal of Epidemiology|October 1, 1993
Seroepidemiological survey of human T-lymphotropic retrovirus among indigenous populations in TaiwanT Ishida, I H Pan, S Horai, et al.
Muscle & Nerve|December 1, 1996
The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)I Nishino, M Komatsu, S Kodama, et al.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
Journal of Inherited Metabolic Disease|January 1, 1991
A new type of mitochondrial DNA deletion in patients with encephalomyopathyS Miyabayashi, H Hanamizu, H Endo, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 17, 1995
Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAsS Horai, K Hayasaka, R Kondo, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|June 1, 1979
Genetic polymorphism of the fourth component of human complement in JapaneseK Tokunaga, S Horai, K Omoto, 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.
Journal of the Neurological Sciences|January 1, 1992
Is Parkinson's disease a mitochondrial disorder?Y Nakagawa-Hattori, H Yoshino, T Kondo, 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.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|March 1, 1980
Haplotype analysis of the linkage group HLA-A:HLA-B:C4 in Japanese: evidence for the C4 locus being between the HLA-A and HLA-B lociS Horai, K Tokunaga, K Omoto, et al.
Molecular Biology and Evolution|May 1, 1988
Phylogenetic relationships among Japanese, rhesus, Formosan, and crab-eating monkeys, inferred from restriction-enzyme analysis of mitochondrial DNAsK Hayasaka, S Horai, T Gojobori, et al.
International Journal of Epidemiology|October 1, 1993
Seroepidemiological survey of human T-lymphotropic retrovirus among indigenous populations in TaiwanT Ishida, I H Pan, S Horai, et al.
Muscle & Nerve|December 1, 1996
The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)I Nishino, M Komatsu, S Kodama, et al.
Pageof 9