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The Tohoku Journal of Experimental Medicine|April 1, 1997
Management of functional pulmonary atresia with isoproterenol in a neonate with Ebstein's anomalyH Suzuki, M Nakasato, S Sato, et al.American Journal of Medical Genetics|August 5, 2000
Compound heterozygous patient with glycogen storage disease type III: identification of two novel AGL mutations, a donor splice site mutation of Chinese origin and a 1-bp deletion of Japanese originM Okubo, A Horinishi, Y Suzuki, et al.Proceedings of the National Academy of Sciences of the United States of America|January 17, 1995
Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAsS Horai, K Hayasaka, R Kondo, et al.Biochemical and Biophysical Research Communications|August 16, 1993
Mutation of the myelin P0 gene in Charcot-Marie-tooth neuropathy type 1K Hayasaka, A Ohnishi, G Takada, et al.Journal of Molecular Biology|April 5, 1992
Fetal recruitment of anthropoid gamma-globin genes. Findings from phylogenetic analyses involving the 5'-flanking sequences of the psi gamma 1 globin gene of spider monkey Ateles geoffroyiK Hayasaka, D H Fitch, J L Slightom, et al.Biochemistry and Molecular Biology International|November 1, 1996
Isolation and sequence determination of cDNA encoding mouse rab 4 and candidate approach for the beige mutation in miceH Ikeda, T Ikegami, T Mitsui, et al.Applied Optics|October 2, 2010
Tunable 397-nm light source for spectroscopy obtained by frequency doubling of a diode laserK Hayasaka, M Watanabe, H Imajo, et al.The Tohoku Journal of Experimental Medicine|June 1, 1992
The effect of carnitine on the metabolism of valproic acid in epileptic patientsK Sakemi, K Hayasaka, M Tahara, et al.Optics Letters|October 22, 2009
High-power second-harmonic generation with picosecond and hundreds-of-picosecond pulses of a cw mode-locked Ti:sapphire laserM Watanabe, R Ohmukai, K Hayasaka, et al.The Tohoku Journal of Experimental Medicine|September 1, 1977
Methylmalonyl-CoA mutase activity of leukocytes in variants and heterozygotes of methylmalonic acidemiaK Narisawa, T Saito, S Hisa, et al.Pageof 35