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M Kouwaki

Showing results (1-10 of 6) with videos related to

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Ryoikibetsu Shokogun Shirizu|May 20, 1998
[Dihydropyrimidine dehydrogenase deficiency]M Kouwaki, Y Wada
Ryoikibetsu Shokogun Shirizu|May 20, 1998
[Malonic, methylmalonic and ethylmalonic acid semialdehyde dehydrogenase deficiency]M Kouwaki, Y Wada
Ryoikibetsu Shokogun Shirizu|May 20, 1998
[Hyperbetaalaninemia]M Kouwaki, Y Wada
International Journal of Molecular Medicine|December 19, 1998
Possible prediction of adverse reactions to fluorouracil by the measurement of urinary dihydrothymine and thymineS Sumi, K Kidouchi, M Kondou, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 29, 1998
Identification of novel mutations in the dihydropyrimidine dehydrogenase gene in a Japanese patient with 5-fluorouracil toxicityM Kouwaki, N Hamajima, S Sumi, et al.
American Journal of Human Genetics|August 27, 1998
Dihydropyrimidinase deficiency: structural organization, chromosomal localization, and mutation analysis of the human dihydropyrimidinase geneN Hamajima, M Kouwaki, P Vreken, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Ryoikibetsu Shokogun Shirizu|May 20, 1998
[Dihydropyrimidine dehydrogenase deficiency]M Kouwaki, Y Wada
Ryoikibetsu Shokogun Shirizu|May 20, 1998
[Malonic, methylmalonic and ethylmalonic acid semialdehyde dehydrogenase deficiency]M Kouwaki, Y Wada
Ryoikibetsu Shokogun Shirizu|May 20, 1998
[Hyperbetaalaninemia]M Kouwaki, Y Wada
International Journal of Molecular Medicine|December 19, 1998
Possible prediction of adverse reactions to fluorouracil by the measurement of urinary dihydrothymine and thymineS Sumi, K Kidouchi, M Kondou, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 29, 1998
Identification of novel mutations in the dihydropyrimidine dehydrogenase gene in a Japanese patient with 5-fluorouracil toxicityM Kouwaki, N Hamajima, S Sumi, et al.
American Journal of Human Genetics|August 27, 1998
Dihydropyrimidinase deficiency: structural organization, chromosomal localization, and mutation analysis of the human dihydropyrimidinase geneN Hamajima, M Kouwaki, P Vreken, et al.
Pageof 1