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Journal of the Neurological Sciences
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December 1, 1990
Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies
Y 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 genome
Y 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 genome
R 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 study
R 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 platelets
S 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 studies
S 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 assay
S 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 myopathy
Y 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 complex
A 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.
Page
of 9
Search research articles
Search
Showing results (31-40 of 85) with videos related to
Sort By:
Page
of 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 biopsies
Y 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 genome
Y 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 genome
R 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 study
R 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 platelets
S 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 studies
S 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 assay
S 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 myopathy
Y 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 complex
A 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.
Page
of 9