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S Horai

Showing results (21-30 of 85) with videos related to

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Nature|December 13, 1990
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesY Goto, I Nonaka, S Horai
Human Genetics|January 1, 1984
Mitochondrial DNA polymorphism in Japanese. I. Analysis with restriction enzymes of six base pair recognitionS Horai, T Gojobori, E Matsunaga
Human Genetics|October 2, 1979
Haplotype analysis of the linkage group HLA-A: HLA-B : Bf in JapaneseS Horai, T Juji, H Nakajima
Journal of Human Genetics|March 18, 2000
Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implicationsM Makino, S Horai, Y Goto, et al.
Journal of Molecular Evolution|September 1, 1995
Molecular phylogeny of gibbons inferred from mitochondrial DNA sequences: preliminary reportS Hayashi, K Hayasaka, O Takenaka, et al.
Neuromuscular Disorders : NMD|June 19, 1998
Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndromeM Makino, S Horai, Y Goto, et al.
Journal of Molecular Evolution|August 1, 1990
Mitochondrial DNA evolution in primates: transition rate has been extremely low in the lemurM Hasegawa, H Kishino, K Hayasaka, et al.
American Journal of Human Genetics|October 1, 1993
An A-to-G transition at nucleotide pair 11084 in the ND4 gene may be an mtDNA polymorphismR Sakuta, Y Goto, I Nonaka, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1976
Further studies on phosphoglucomutase-1 phenotypes in Japanese. i. Comparison of "slow" variantsC Satoh, N Ueda, S Horai, et al.
Human Immunology|July 1, 1982
Cytotoxic T lymphocytes directed against HLA-Bw 35-linked target determinants show differences in sensitivity toward antibiotics during sensitization periodS Horai, E Goulmy, J J van Rood
Pageof 9

Showing results (21-30 of 85) with videos related to

Sort By:
Pageof 9
Nature|December 13, 1990
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesY Goto, I Nonaka, S Horai
Human Genetics|January 1, 1984
Mitochondrial DNA polymorphism in Japanese. I. Analysis with restriction enzymes of six base pair recognitionS Horai, T Gojobori, E Matsunaga
Human Genetics|October 2, 1979
Haplotype analysis of the linkage group HLA-A: HLA-B : Bf in JapaneseS Horai, T Juji, H Nakajima
Journal of Human Genetics|March 18, 2000
Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implicationsM Makino, S Horai, Y Goto, et al.
Journal of Molecular Evolution|September 1, 1995
Molecular phylogeny of gibbons inferred from mitochondrial DNA sequences: preliminary reportS Hayashi, K Hayasaka, O Takenaka, et al.
Neuromuscular Disorders : NMD|June 19, 1998
Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndromeM Makino, S Horai, Y Goto, et al.
Journal of Molecular Evolution|August 1, 1990
Mitochondrial DNA evolution in primates: transition rate has been extremely low in the lemurM Hasegawa, H Kishino, K Hayasaka, et al.
American Journal of Human Genetics|October 1, 1993
An A-to-G transition at nucleotide pair 11084 in the ND4 gene may be an mtDNA polymorphismR Sakuta, Y Goto, I Nonaka, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1976
Further studies on phosphoglucomutase-1 phenotypes in Japanese. i. Comparison of "slow" variantsC Satoh, N Ueda, S Horai, et al.
Human Immunology|July 1, 1982
Cytotoxic T lymphocytes directed against HLA-Bw 35-linked target determinants show differences in sensitivity toward antibiotics during sensitization periodS Horai, E Goulmy, J J van Rood
Pageof 9