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T Orii

Showing results (11-20 of 397) with videos related to

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Mutation Research|August 1, 1980
High sensitivity but normal DNA-repair activity after UV irradiation in Epstein--Barr virus-transformed lymphoblastoid cell lines from Chediak--Higashi syndromeH Tanaka, T Orii
Clinical Genetics|March 1, 1990
Terminal 7q deletion as a cause of holoprosencephalyM Masuno, T Orii
Japan-Hospitals : the Journal of the Japan Hospital Association|June 8, 1988
Systemization of drug inventory control in the University of Tokyo HospitalT Orii, S Kaihara
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1989
Severity of GM1 gangliosidosis and urinary oligosaccharide excretionY Takahashi, T Orii
Journal of Inherited Metabolic Disease|January 1, 1981
The activity of carbamoyl-phosphate synthetase I and ornithine carbamoyltransferase (OCT) in the intestine and screening for OCT deficiency in the rectal mucosaA Matsushima, T Orii
No to Hattatsu = Brain and Development|March 1, 1992
[Peroxisomal disorders in neurology]T Orii, T Hashimoto
Ryoikibetsu Shokogun Shirizu|September 1, 2001
[Mucopolysaccharidosis (I-VII)]K Sukegawa, T Orii
Journal of Inherited Metabolic Disease|January 1, 1982
Residual activity in fibroblasts from two brothers with the late-onset form of N-acetylgalactosamine-6-sulphate sulphatase deficiencyK Sukegawa, T Orii
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|June 1, 1974
A new type of mucolipidosis with beta-galactosidase dificiency and glycopeptiduriaT Orii, T Nakao
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 22, 1989
Diagnosis of subtypes of GM1 gangliosidosis in vitro and in vivo--using urinary oligosaccharides as substratesY Takahashi, T Orii
Pageof 40

Showing results (11-20 of 397) with videos related to

Sort By:
Pageof 40
Mutation Research|August 1, 1980
High sensitivity but normal DNA-repair activity after UV irradiation in Epstein--Barr virus-transformed lymphoblastoid cell lines from Chediak--Higashi syndromeH Tanaka, T Orii
Clinical Genetics|March 1, 1990
Terminal 7q deletion as a cause of holoprosencephalyM Masuno, T Orii
Japan-Hospitals : the Journal of the Japan Hospital Association|June 8, 1988
Systemization of drug inventory control in the University of Tokyo HospitalT Orii, S Kaihara
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1989
Severity of GM1 gangliosidosis and urinary oligosaccharide excretionY Takahashi, T Orii
Journal of Inherited Metabolic Disease|January 1, 1981
The activity of carbamoyl-phosphate synthetase I and ornithine carbamoyltransferase (OCT) in the intestine and screening for OCT deficiency in the rectal mucosaA Matsushima, T Orii
No to Hattatsu = Brain and Development|March 1, 1992
[Peroxisomal disorders in neurology]T Orii, T Hashimoto
Ryoikibetsu Shokogun Shirizu|September 1, 2001
[Mucopolysaccharidosis (I-VII)]K Sukegawa, T Orii
Journal of Inherited Metabolic Disease|January 1, 1982
Residual activity in fibroblasts from two brothers with the late-onset form of N-acetylgalactosamine-6-sulphate sulphatase deficiencyK Sukegawa, T Orii
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|June 1, 1974
A new type of mucolipidosis with beta-galactosidase dificiency and glycopeptiduriaT Orii, T Nakao
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 22, 1989
Diagnosis of subtypes of GM1 gangliosidosis in vitro and in vivo--using urinary oligosaccharides as substratesY Takahashi, T Orii
Pageof 40