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S Horai

Showing results (31-40 of 85) with videos related to

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Journal of the Neurological Sciences|December 1, 1990
Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsiesY Goto, Y Koga, S Horai, et al.
Biochemical and Biophysical Research Communications|May 15, 1996
Detection of DNA fragments encompassing the deletion junction of mitochondrial genomeY Goto, I Nishino, S Horai, et al.
Journal of Molecular Evolution|June 1, 1993
Evolution of hominoid mitochondrial DNA with special reference to the silent substitution rate over the genomeR Kondo, S Horai, Y Satta, et al.
Journal of the Neurological Sciences|April 1, 1993
Mitochondrial DNA mutations at nucleotide positions 3243 and 3271 in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: a comparative studyR Sakuta, Y Goto, S Horai, et al.
Immunology Letters|June 1, 1981
Detection of platelet antibodies by enzyme-linked immunosorbent assay (ELISA) on artificial monolayers of plateletsS Horai, F H Claas, J J van Rood
Immunogenetics|January 1, 1982
Differential recognition of the serologically defined HLA-A2 antigen by allogeneic cytotoxic T cells. I. Population studiesS Horai, J J van der Poel, E Goulmy
Immunology Letters|August 1, 1981
Detection of platelet antibodies by enzyme-linked immunosorbent assay (ELISA). Comparative studies with the indirect immunofluorescence assayS Horai, F H Claas, J J van Rood
Annals of Neurology|June 1, 1992
A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathyY Goto, M Tojo, J Tohyama, et al.
Biken Journal|December 1, 1975
Trypsin-activated complex of human factor B with cobra venom factor (CVF), cleaving C3 and C5 and generating a lytic factor for unsensitized guinea pig erythrocytes. I. Generation of the activated complexA Miyama, T Kato, S Horai, et al.
Biochemical and Biophysical Research Communications|August 15, 1994
A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)Y Goto, K Tsugane, Y Tanabe, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
Journal of the Neurological Sciences|December 1, 1990
Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsiesY Goto, Y Koga, S Horai, et al.
Biochemical and Biophysical Research Communications|May 15, 1996
Detection of DNA fragments encompassing the deletion junction of mitochondrial genomeY Goto, I Nishino, S Horai, et al.
Journal of Molecular Evolution|June 1, 1993
Evolution of hominoid mitochondrial DNA with special reference to the silent substitution rate over the genomeR Kondo, S Horai, Y Satta, et al.
Journal of the Neurological Sciences|April 1, 1993
Mitochondrial DNA mutations at nucleotide positions 3243 and 3271 in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: a comparative studyR Sakuta, Y Goto, S Horai, et al.
Immunology Letters|June 1, 1981
Detection of platelet antibodies by enzyme-linked immunosorbent assay (ELISA) on artificial monolayers of plateletsS Horai, F H Claas, J J van Rood
Immunogenetics|January 1, 1982
Differential recognition of the serologically defined HLA-A2 antigen by allogeneic cytotoxic T cells. I. Population studiesS Horai, J J van der Poel, E Goulmy
Immunology Letters|August 1, 1981
Detection of platelet antibodies by enzyme-linked immunosorbent assay (ELISA). Comparative studies with the indirect immunofluorescence assayS Horai, F H Claas, J J van Rood
Annals of Neurology|June 1, 1992
A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathyY Goto, M Tojo, J Tohyama, et al.
Biken Journal|December 1, 1975
Trypsin-activated complex of human factor B with cobra venom factor (CVF), cleaving C3 and C5 and generating a lytic factor for unsensitized guinea pig erythrocytes. I. Generation of the activated complexA Miyama, T Kato, S Horai, et al.
Biochemical and Biophysical Research Communications|August 15, 1994
A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)Y Goto, K Tsugane, Y Tanabe, et al.
Pageof 9