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I Matsuda

Showing results (201-210 of 603) with videos related to

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American Journal of Human Genetics|April 1, 1991
A murine model for type III tyrosinemia: lack of immunologically detectable 4-hydroxyphenylpyruvic acid dioxygenase enzyme protein in a novel mouse strain with hypertyrosinemiaF Endo, H Katoh, S Yamamoto, et al.
Journal of Biochemistry|July 7, 1999
Short-chain acyl-CoA-dependent production of oxalate from oxaloacetate by Burkholderia glumae, a plant pathogen which causes grain rot and seedling rot of rice via the oxalate productionH Q Li, I Matsuda, Y Fujise, et al.
Human Genetics|July 29, 2000
Statistical and mutational analysis of chronic granulomatous disease in Japan with special reference to gp91-phox and p22-phox deficiencyF Ishibashi, H Nunoi, F Endo, et al.
Human Genetics|May 19, 1976
Tricho-rhino-phalangeal syndrome. The first case in JapanN Fukushima, M Anakura, S Arashima, et al.
Acta Paediatrica Japonica : Overseas Edition|August 1, 1987
Attempts to investigate the molecular basis of urea cycle disordersI Matsuda, A Hata, Y Jinno, et al.
Pediatrics|September 1, 1990
Self-limited neonatal familial hyperparathyroidism associated with hypercalciuria and renal tubular acidosis in three siblingsS Nishiyama, S Tomoeda, F Inoue, et al.
Journal of Neuroendocrinology|February 20, 2009
Sagittalis nucleus: a novel hypothalamic nucleusH Mori, K-I Matsuda, D W Pfaff, et al.
Horumon to Rinsho. Clinical Endocrinology|February 1, 1983
[Evaluation of ionized calcium--first report]S Nishiyama, H Fujimoto, I Matsuda, et al.
Atherosclerosis|March 1, 1978
The role of hemodynamic factors in arterial wall thickening in the ratI Matsuda, H Niimi, K Moritake, et al.
European Neurology|January 1, 1993
Pontine infarction with pure Millard-Gubler syndrome: precise localization with magnetic resonance imagingY Yasuda, I Matsuda, T Sakagami, et al.
Pageof 61

Showing results (201-210 of 603) with videos related to

Sort By:
Pageof 61
American Journal of Human Genetics|April 1, 1991
A murine model for type III tyrosinemia: lack of immunologically detectable 4-hydroxyphenylpyruvic acid dioxygenase enzyme protein in a novel mouse strain with hypertyrosinemiaF Endo, H Katoh, S Yamamoto, et al.
Journal of Biochemistry|July 7, 1999
Short-chain acyl-CoA-dependent production of oxalate from oxaloacetate by Burkholderia glumae, a plant pathogen which causes grain rot and seedling rot of rice via the oxalate productionH Q Li, I Matsuda, Y Fujise, et al.
Human Genetics|July 29, 2000
Statistical and mutational analysis of chronic granulomatous disease in Japan with special reference to gp91-phox and p22-phox deficiencyF Ishibashi, H Nunoi, F Endo, et al.
Human Genetics|May 19, 1976
Tricho-rhino-phalangeal syndrome. The first case in JapanN Fukushima, M Anakura, S Arashima, et al.
Acta Paediatrica Japonica : Overseas Edition|August 1, 1987
Attempts to investigate the molecular basis of urea cycle disordersI Matsuda, A Hata, Y Jinno, et al.
Pediatrics|September 1, 1990
Self-limited neonatal familial hyperparathyroidism associated with hypercalciuria and renal tubular acidosis in three siblingsS Nishiyama, S Tomoeda, F Inoue, et al.
Journal of Neuroendocrinology|February 20, 2009
Sagittalis nucleus: a novel hypothalamic nucleusH Mori, K-I Matsuda, D W Pfaff, et al.
Horumon to Rinsho. Clinical Endocrinology|February 1, 1983
[Evaluation of ionized calcium--first report]S Nishiyama, H Fujimoto, I Matsuda, et al.
Atherosclerosis|March 1, 1978
The role of hemodynamic factors in arterial wall thickening in the ratI Matsuda, H Niimi, K Moritake, et al.
European Neurology|January 1, 1993
Pontine infarction with pure Millard-Gubler syndrome: precise localization with magnetic resonance imagingY Yasuda, I Matsuda, T Sakagami, et al.
Pageof 61