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Y Hase

Showing results (31-40 of 50) with videos related to

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Human Molecular Genetics|April 1, 1994
Molecular characterization of phenylketonuric mutations in Japanese by analysis of phenylalanine hydroxylase mRNA from lymphoblastsY Okano, Y Hase, H Shintaku, et al.
European Journal of Human Genetics : EJHG|February 13, 2002
Molecular characterisation of glutamate dehydrogenase gene defects in Japanese patients with congenital hyperinsulinism/hyperammonaemiaH Fujioka, Y Okano, H Inada, et al.
Nihon Naibunpi Gakkai Zasshi|October 20, 1989
[Enzyme immunoassay of 17-hydroxyprogesterone in dried blood spot on filter paper using specific antibody for 17-hydroxyprogesterone]Y Kobayashi, Y Nishiguchi, F Watanabe, et al.
Human Genetics|December 22, 1998
Molecular characterization of phenylketonuria in Japanese patientsY Okano, M Asada, Y Kang, et al.
Journal of Medicinal Chemistry|November 22, 1996
Synthesis and biological activity of conformationally restricted analogs of milnacipran: (1S,2R)-1-phenyl-2-[(S)-1-aminopropyl]-N,N-diethylcyclopropanecarboxami de, an efficient noncompetitive N-methyl-D-aspartic acid receptor antagonistS Shuto, S Ono, Y Hase, et al.
Human Mutation|January 1, 1992
Frequency and distribution of phenylketonuric mutations in OrientalsY Okano, Y Hase, D H Lee, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular and population genetics of phenylketonuria in Orientals: correlation between phenotype and genotypeY Okano, Y Hase, D H Lee, et al.
Journal of Medicinal Chemistry|July 21, 1995
(+/-)-(Z)-2-(aminomethyl)-1-phenylcyclopropanecarboxamide derivatives as a new prototype of NMDA receptor antagonistsS Shuto, H Takada, D Mochizuki, et al.
Human Genetics|August 1, 1993
Four novel gene mutations in five Japanese male patients with neonatal or late onset OTC deficiency: application of PCR-single-strand conformation polymorphisms for all exons and adjacent introns [corrected]T Matsuura, R Hoshide, C Setoyama, et al.
The Journal of Biological Chemistry|September 5, 1985
N tau-Ribosylhistidine, a novel histidine derivative in urine of histidinemic patients. Isolation, structure, and tissue levelI Imamura, T Watanabe, Y Sakamoto, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|April 1, 1994
Molecular characterization of phenylketonuric mutations in Japanese by analysis of phenylalanine hydroxylase mRNA from lymphoblastsY Okano, Y Hase, H Shintaku, et al.
European Journal of Human Genetics : EJHG|February 13, 2002
Molecular characterisation of glutamate dehydrogenase gene defects in Japanese patients with congenital hyperinsulinism/hyperammonaemiaH Fujioka, Y Okano, H Inada, et al.
Nihon Naibunpi Gakkai Zasshi|October 20, 1989
[Enzyme immunoassay of 17-hydroxyprogesterone in dried blood spot on filter paper using specific antibody for 17-hydroxyprogesterone]Y Kobayashi, Y Nishiguchi, F Watanabe, et al.
Human Genetics|December 22, 1998
Molecular characterization of phenylketonuria in Japanese patientsY Okano, M Asada, Y Kang, et al.
Journal of Medicinal Chemistry|November 22, 1996
Synthesis and biological activity of conformationally restricted analogs of milnacipran: (1S,2R)-1-phenyl-2-[(S)-1-aminopropyl]-N,N-diethylcyclopropanecarboxami de, an efficient noncompetitive N-methyl-D-aspartic acid receptor antagonistS Shuto, S Ono, Y Hase, et al.
Human Mutation|January 1, 1992
Frequency and distribution of phenylketonuric mutations in OrientalsY Okano, Y Hase, D H Lee, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular and population genetics of phenylketonuria in Orientals: correlation between phenotype and genotypeY Okano, Y Hase, D H Lee, et al.
Journal of Medicinal Chemistry|July 21, 1995
(+/-)-(Z)-2-(aminomethyl)-1-phenylcyclopropanecarboxamide derivatives as a new prototype of NMDA receptor antagonistsS Shuto, H Takada, D Mochizuki, et al.
Human Genetics|August 1, 1993
Four novel gene mutations in five Japanese male patients with neonatal or late onset OTC deficiency: application of PCR-single-strand conformation polymorphisms for all exons and adjacent introns [corrected]T Matsuura, R Hoshide, C Setoyama, et al.
The Journal of Biological Chemistry|September 5, 1985
N tau-Ribosylhistidine, a novel histidine derivative in urine of histidinemic patients. Isolation, structure, and tissue levelI Imamura, T Watanabe, Y Sakamoto, et al.
Pageof 5