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M Umeno

Showing results (31-40 of 35) with videos related to

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Applied Optics|February 13, 2008
Determination of Optical Constants of Solgel-Derived Inhomogeneous TiO(2) Thin Films by Spectroscopic Ellipsometry and Transmission SpectroscopyM Mosaddeq-Ur-Rahman, G Yu, K M Krishna, et al.
The American Journal of Tropical Medicine and Hygiene|October 28, 1998
Paralytic ileus due to strongyloidiasis: case report and review of the literatureD Nonaka, K Takaki, M Tanaka, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|February 1, 1984
[A case of Sjögren's syndrome associated with malignant lymphoma]Y Urabe, S Okamura, N Takeichi, et al.
DNA (Mary Ann Liebert, Inc.)|March 1, 1988
Human P450PCN1: sequence, chromosome localization, and direct evidence through cDNA expression that P450PCN1 is nifedipine oxidaseF J Gonzalez, B J Schmid, M Umeno, et al.
Nature|February 4, 1988
Characterization of the common genetic defect in humans deficient in debrisoquine metabolismF J Gonzalez, R C Skoda, S Kimura, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Applied Optics|February 13, 2008
Determination of Optical Constants of Solgel-Derived Inhomogeneous TiO(2) Thin Films by Spectroscopic Ellipsometry and Transmission SpectroscopyM Mosaddeq-Ur-Rahman, G Yu, K M Krishna, et al.
The American Journal of Tropical Medicine and Hygiene|October 28, 1998
Paralytic ileus due to strongyloidiasis: case report and review of the literatureD Nonaka, K Takaki, M Tanaka, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|February 1, 1984
[A case of Sjögren's syndrome associated with malignant lymphoma]Y Urabe, S Okamura, N Takeichi, et al.
DNA (Mary Ann Liebert, Inc.)|March 1, 1988
Human P450PCN1: sequence, chromosome localization, and direct evidence through cDNA expression that P450PCN1 is nifedipine oxidaseF J Gonzalez, B J Schmid, M Umeno, et al.
Nature|February 4, 1988
Characterization of the common genetic defect in humans deficient in debrisoquine metabolismF J Gonzalez, R C Skoda, S Kimura, et al.
Pageof 4