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I Mineo

Showing results (21-30 of 48) with videos related to

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Medical Journal of Osaka University|March 1, 1983
Kinetic properties of mutant enzymes in erythrocyte phosphofructokinase deficiency and erythrocyte pyruvate kinase deficiencyT Shimizu, M Kuwajima, N Kono, et al.
Gene|April 1, 1997
Cloning and expression of cDNA encoding heart-type isoform of AMP deaminaseX Wang, H Morisaki, K Sermsuvitayawong, et al.
The Journal of Clinical Investigation|August 1, 1985
Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VIII Mineo, N Kono, T Shimizu, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|January 1, 1988
[A family of hereditary xanthinuria: two siblings with peptic ulcer and hypouricemia due to xanthine oxidase deficiency, and a heterozygote (father) with gout]M Kawachi, N Kono, I Mineo, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
Myogenic hyperuricemia in hypoparathyroidismT Nishimura, I Mineo, T Shimizu, et al.
Metabolism: Clinical and Experimental|June 1, 1994
Influence of daily drinking habits on ethanol-induced hyperuricemiaT Nishimura, T Shimizu, I Mineo, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Molecular analysis of mouse Ampd3 gene encoding heart-type isoform of AMP deaminaseT Morisaki, K Sermsuvitayawong, X Wang, et al.
Nephron|January 1, 1992
Decreased renal clearance of xanthine and hypoxanthine in a patient with renal hypouricemia: a new defect in renal handling of purinesM Kawachi, N Kono, H Kiyokawa, et al.
Muscle & Nerve|September 1, 1987
Enhanced release of ammonia and hypoxanthine from exercising muscles in patients with idiopathic hypoparathyroidismN Hara, I Mineo, N Kono, et al.
The New England Journal of Medicine|July 9, 1987
Myogenic hyperuricemia. A common pathophysiologic feature of glycogenosis types III, V, and VIII Mineo, N Kono, N Hara, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Medical Journal of Osaka University|March 1, 1983
Kinetic properties of mutant enzymes in erythrocyte phosphofructokinase deficiency and erythrocyte pyruvate kinase deficiencyT Shimizu, M Kuwajima, N Kono, et al.
Gene|April 1, 1997
Cloning and expression of cDNA encoding heart-type isoform of AMP deaminaseX Wang, H Morisaki, K Sermsuvitayawong, et al.
The Journal of Clinical Investigation|August 1, 1985
Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VIII Mineo, N Kono, T Shimizu, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|January 1, 1988
[A family of hereditary xanthinuria: two siblings with peptic ulcer and hypouricemia due to xanthine oxidase deficiency, and a heterozygote (father) with gout]M Kawachi, N Kono, I Mineo, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
Myogenic hyperuricemia in hypoparathyroidismT Nishimura, I Mineo, T Shimizu, et al.
Metabolism: Clinical and Experimental|June 1, 1994
Influence of daily drinking habits on ethanol-induced hyperuricemiaT Nishimura, T Shimizu, I Mineo, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Molecular analysis of mouse Ampd3 gene encoding heart-type isoform of AMP deaminaseT Morisaki, K Sermsuvitayawong, X Wang, et al.
Nephron|January 1, 1992
Decreased renal clearance of xanthine and hypoxanthine in a patient with renal hypouricemia: a new defect in renal handling of purinesM Kawachi, N Kono, H Kiyokawa, et al.
Muscle & Nerve|September 1, 1987
Enhanced release of ammonia and hypoxanthine from exercising muscles in patients with idiopathic hypoparathyroidismN Hara, I Mineo, N Kono, et al.
The New England Journal of Medicine|July 9, 1987
Myogenic hyperuricemia. A common pathophysiologic feature of glycogenosis types III, V, and VIII Mineo, N Kono, N Hara, et al.
Pageof 5