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S Kure

Showing results (41-50 of 85) with videos related to

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Biochemical and Biophysical Research Communications|December 31, 1990
One of the two genomic copies of the glycine decarboxylase cDNA has been deleted at a 5' region in a patient with nonketotic hyperglycinemiaT Sakakibara, H Koyata, Y Ishiguro, et al.
The Journal of Pharmacy and Pharmacology|March 14, 2000
Rapid detection of CYP2C18 genotypes by real-time fluorescence polymerase chain reactionM Mizugaki, M Hiratsuka, Y Agatsuma, et al.
Journal of Human Genetics|February 4, 1999
Molecular analysis of methylmalonyl-CoA mutase deficiency: identification of three missense mutations in mut0 patientsH Mikami, M Ogasawara, Y Matsubara, et al.
Brain Research|June 26, 1995
Apoptotic cell death of a temperature-sensitive central neuronal cell lineK Hisanaga, S Kure, D E Bredesen, et al.
Neurology|April 13, 2005
Glycine decarboxylase mutations: a distinctive phenotype of nonketotic hyperglycinemia in adultsA Dinopoulos, S Kure, G Chuck, et al.
Journal of Human Genetics|June 11, 1998
Mutation and polymorphic marker analyses of 65K- and 67K-glutamate decarboxylase genes in two families with pyridoxine-dependent epilepsyS Kure, Y Sakata, S Miyabayashi, et al.
Nihon Juigaku Zasshi. the Japanese Journal of Veterinary Science|June 1, 1979
[Distribution and morphology of brilliant cells in bovine endometritis (author's transl)]W Shirai, S Kure, T Kashima, et al.
Journal of Human Genetics|June 11, 1998
A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemiaS Kure, T Shinka, Y Sakata, et al.
Nihon Juigaku Zasshi. the Japanese Journal of Veterinary Science|February 1, 1979
[Studies on brilliant cells in gastritis of swine (author's transl)]S Kure, W Shirai, T Sato, et al.
Prenatal Diagnosis|August 19, 1999
Prenatal diagnosis of non-ketotic hyperglycinaemia: enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutationsS Kure, M O Rolland, J Leisti, et al.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
Biochemical and Biophysical Research Communications|December 31, 1990
One of the two genomic copies of the glycine decarboxylase cDNA has been deleted at a 5' region in a patient with nonketotic hyperglycinemiaT Sakakibara, H Koyata, Y Ishiguro, et al.
The Journal of Pharmacy and Pharmacology|March 14, 2000
Rapid detection of CYP2C18 genotypes by real-time fluorescence polymerase chain reactionM Mizugaki, M Hiratsuka, Y Agatsuma, et al.
Journal of Human Genetics|February 4, 1999
Molecular analysis of methylmalonyl-CoA mutase deficiency: identification of three missense mutations in mut0 patientsH Mikami, M Ogasawara, Y Matsubara, et al.
Brain Research|June 26, 1995
Apoptotic cell death of a temperature-sensitive central neuronal cell lineK Hisanaga, S Kure, D E Bredesen, et al.
Neurology|April 13, 2005
Glycine decarboxylase mutations: a distinctive phenotype of nonketotic hyperglycinemia in adultsA Dinopoulos, S Kure, G Chuck, et al.
Journal of Human Genetics|June 11, 1998
Mutation and polymorphic marker analyses of 65K- and 67K-glutamate decarboxylase genes in two families with pyridoxine-dependent epilepsyS Kure, Y Sakata, S Miyabayashi, et al.
Nihon Juigaku Zasshi. the Japanese Journal of Veterinary Science|June 1, 1979
[Distribution and morphology of brilliant cells in bovine endometritis (author's transl)]W Shirai, S Kure, T Kashima, et al.
Journal of Human Genetics|June 11, 1998
A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemiaS Kure, T Shinka, Y Sakata, et al.
Nihon Juigaku Zasshi. the Japanese Journal of Veterinary Science|February 1, 1979
[Studies on brilliant cells in gastritis of swine (author's transl)]S Kure, W Shirai, T Sato, et al.
Prenatal Diagnosis|August 19, 1999
Prenatal diagnosis of non-ketotic hyperglycinaemia: enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutationsS Kure, M O Rolland, J Leisti, et al.
Pageof 9