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T Saijo

Showing results (31-40 of 75) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1991
Clinical and biochemical findings in parents of children with vitamin D-dependent rickets Type III Yokota, E Takeda, M Ito, et al.
Biochemical and Biophysical Research Communications|November 12, 1996
Stable restoration of pyruvate dehydrogenase complex in E1-defective human lymphoblastoid cells: evidence that three C-terminal amino acids of E1 alpha are essential for the structural integrity of heterotetrameric E1T Saijo, E Naito, M Ito, et al.
Neuropediatrics|August 1, 1991
Therapeutic effect of sodium dichloroacetate on visual and auditory hallucinations in a patient with MELAST Saijo, E Naito, M Ito, et al.
European Journal of Pediatrics|September 4, 1998
Thiamine-responsive lactic acidaemia: role of pyruvate dehydrogenase complexE Naito, M Ito, I Yokota, et al.
Prostaglandins|December 1, 1983
Pharmacological profile of AA-861, a 5-lipoxygenase inhibitorY Ashida, T Saijo, H Kuriki, et al.
Advances in Prostaglandin, Thromboxane, and Leukotriene Research|January 1, 1985
Antiallergic activity of AA-861, a 5-lipoxygenase inhibitorY Maki, Y Ashida, H Makino, et al.
Acta Paediatrica Japonica : Overseas Edition|February 1, 1990
Effect of long-term treatment with massive doses of 1 alpha-hydroxyvitamin D3 on calcium-phosphate balance in patients with vitamin D-dependent rickets type IIE Takeda, I Yokota, T Saijo, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1990
25-Hydroxyvitamin D-24-hydroxylase in phytohemagglutinin-stimulated lymphocytes: intermediate bioresponse to 1,25-dihydroxyvitamin D3 of cells from parents of patients with vitamin D-dependent rickets type IIE Takeda, I Yokota, M Ito, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Mutation of E1 alpha gene in a female patient with pyruvate dehydrogenase deficiency due to rapid degradation of E1 proteinM Ito, A H Huq, E Naito, et al.
Pediatric Research|July 1, 1991
Demonstration of an unstable variant of pyruvate dehydrogenase protein (E1) in cultured fibroblasts from a patient with congenital lactic acidemiaA H Huq, M Ito, E Naito, et al.
Pageof 8

Showing results (31-40 of 75) with videos related to

Sort By:
Pageof 8
Journal of Inherited Metabolic Disease|January 1, 1991
Clinical and biochemical findings in parents of children with vitamin D-dependent rickets Type III Yokota, E Takeda, M Ito, et al.
Biochemical and Biophysical Research Communications|November 12, 1996
Stable restoration of pyruvate dehydrogenase complex in E1-defective human lymphoblastoid cells: evidence that three C-terminal amino acids of E1 alpha are essential for the structural integrity of heterotetrameric E1T Saijo, E Naito, M Ito, et al.
Neuropediatrics|August 1, 1991
Therapeutic effect of sodium dichloroacetate on visual and auditory hallucinations in a patient with MELAST Saijo, E Naito, M Ito, et al.
European Journal of Pediatrics|September 4, 1998
Thiamine-responsive lactic acidaemia: role of pyruvate dehydrogenase complexE Naito, M Ito, I Yokota, et al.
Prostaglandins|December 1, 1983
Pharmacological profile of AA-861, a 5-lipoxygenase inhibitorY Ashida, T Saijo, H Kuriki, et al.
Advances in Prostaglandin, Thromboxane, and Leukotriene Research|January 1, 1985
Antiallergic activity of AA-861, a 5-lipoxygenase inhibitorY Maki, Y Ashida, H Makino, et al.
Acta Paediatrica Japonica : Overseas Edition|February 1, 1990
Effect of long-term treatment with massive doses of 1 alpha-hydroxyvitamin D3 on calcium-phosphate balance in patients with vitamin D-dependent rickets type IIE Takeda, I Yokota, T Saijo, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1990
25-Hydroxyvitamin D-24-hydroxylase in phytohemagglutinin-stimulated lymphocytes: intermediate bioresponse to 1,25-dihydroxyvitamin D3 of cells from parents of patients with vitamin D-dependent rickets type IIE Takeda, I Yokota, M Ito, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Mutation of E1 alpha gene in a female patient with pyruvate dehydrogenase deficiency due to rapid degradation of E1 proteinM Ito, A H Huq, E Naito, et al.
Pediatric Research|July 1, 1991
Demonstration of an unstable variant of pyruvate dehydrogenase protein (E1) in cultured fibroblasts from a patient with congenital lactic acidemiaA H Huq, M Ito, E Naito, et al.
Pageof 8