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A Tanoue

Showing results (11-20 of 37) with videos related to

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Japanese Journal of Pharmacology|February 11, 2000
Structure and sequence of the mouse V1a and V1b vasopressin receptor genesS Kikuchi, A Tanoue, N Goda, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Deduced amino acid sequence of human prolidase and molecular analyses of prolidase deficiencyF Endo, A Tanoue, A Hata, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1988
Immunoaffinity purification of human erythrocyte prolidaseF Endo, A Tanoue, T Ogata, et al.
Journal of Cardiovascular Pharmacology|January 29, 2002
Functional genomic research of alpha 1-adrenoceptorsG Tsujimoto, S Katsuma, S Shiojima, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Characterization of a point mutation in the pyruvate dehydrogenase E1 alpha gene from two boys with primary lactic acidaemiaH Awata, F Endo, A Tanoue, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Tyrosinaemia type III: immunochemical studies on 4-hydroxyphenylpyruvic acid dioxygenase and molecular cloning of cDNA for the enzymeF Endo, H Awata, A Tanoue, et al.
The Japanese Journal of Human Genetics|December 1, 1992
Sex-determining region Y (SRY) in a patient with 46,XX true hermaphroditismA Tanoue, T Nakamura, F Endo, et al.
Japanese Journal of Pharmacology|January 6, 2000
Characterization of the mouse alpha1D-adrenergic receptor geneK Arai, A Tanoue, N Goda, et al.
EMBO Reports|March 22, 2001
MCM3AP, a novel acetyltransferase that acetylates replication protein MCM3Y Takei, M Swietlik, A Tanoue, et al.
Biochimica Et Biophysica Acta|May 25, 1994
Structural organization and analysis of the human fumarylacetoacetate hydrolase gene in tyrosinemia type IH Awata, F Endo, A Tanoue, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Japanese Journal of Pharmacology|February 11, 2000
Structure and sequence of the mouse V1a and V1b vasopressin receptor genesS Kikuchi, A Tanoue, N Goda, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Deduced amino acid sequence of human prolidase and molecular analyses of prolidase deficiencyF Endo, A Tanoue, A Hata, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1988
Immunoaffinity purification of human erythrocyte prolidaseF Endo, A Tanoue, T Ogata, et al.
Journal of Cardiovascular Pharmacology|January 29, 2002
Functional genomic research of alpha 1-adrenoceptorsG Tsujimoto, S Katsuma, S Shiojima, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Characterization of a point mutation in the pyruvate dehydrogenase E1 alpha gene from two boys with primary lactic acidaemiaH Awata, F Endo, A Tanoue, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Tyrosinaemia type III: immunochemical studies on 4-hydroxyphenylpyruvic acid dioxygenase and molecular cloning of cDNA for the enzymeF Endo, H Awata, A Tanoue, et al.
The Japanese Journal of Human Genetics|December 1, 1992
Sex-determining region Y (SRY) in a patient with 46,XX true hermaphroditismA Tanoue, T Nakamura, F Endo, et al.
Japanese Journal of Pharmacology|January 6, 2000
Characterization of the mouse alpha1D-adrenergic receptor geneK Arai, A Tanoue, N Goda, et al.
EMBO Reports|March 22, 2001
MCM3AP, a novel acetyltransferase that acetylates replication protein MCM3Y Takei, M Swietlik, A Tanoue, et al.
Biochimica Et Biophysica Acta|May 25, 1994
Structural organization and analysis of the human fumarylacetoacetate hydrolase gene in tyrosinemia type IH Awata, F Endo, A Tanoue, et al.
Pageof 4