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Yasukazu Yamada

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Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Complete and partial deficiencies of hypoxanthine guanine phosphoribosyltransferase (HPRT)]Yasukazu Yamada
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Hypoxanthine guanine phosphoribosyltransferase (HPRT)]Yasukazu Yamada
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[AMP deaminase (AMPD)]Yasukazu Yamada
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Hyperuricemia associated with inborn errors of purine metabolism: screening, enzymatic and genetic diagnosis]Yasukazu Yamada
Nihon Rinsho. Japanese Journal of Clinical Medicine|April 16, 2008
[Deficiencies of hypoxanthine guanine phosphoribosyltransferase (HPRT)]Yasukazu Yamada
Molecular Genetics and Metabolism|October 10, 2006
Molecular analysis of HPRT deficiencies: an update of the spectrum of Asian mutations with novel mutationsYasukazu Yamada, Noriko Nomura, Kenichiro Yamada, et al.
Congenital Anomalies|May 21, 2005
Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutationSeiji Mizuno, Yasukazu Yamada, Kenichiro Yamada, et al.
Gene|November 1, 2011
Identification and characterization of splicing variants of PLEKHA5 (Plekha5) during brain developmentKenichiro Yamada, Noriko Nomura, Arisa Yamano, et al.
Nucleosides, Nucleotides & Nucleic Acids|July 5, 2008
Molecular analysis of hypoxanthine guanine phosphoribosyltransferase (HPRT) deficiencies: novel mutations and the spectrum of Japanese mutationsYasukazu Yamada, Noriko Nomura, Kenichro Yamada, et al.
Journal of Biochemistry|November 7, 2012
Characterization of the mutant β-subunit of β-hexosaminidase for dimer formation responsible for the adult form of Sandhoff disease with the motor neuron disease phenotypeKenichiro Yamada, Yuhei Takado, Yusuke S Kato, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Complete and partial deficiencies of hypoxanthine guanine phosphoribosyltransferase (HPRT)]Yasukazu Yamada
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Hypoxanthine guanine phosphoribosyltransferase (HPRT)]Yasukazu Yamada
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[AMP deaminase (AMPD)]Yasukazu Yamada
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Hyperuricemia associated with inborn errors of purine metabolism: screening, enzymatic and genetic diagnosis]Yasukazu Yamada
Nihon Rinsho. Japanese Journal of Clinical Medicine|April 16, 2008
[Deficiencies of hypoxanthine guanine phosphoribosyltransferase (HPRT)]Yasukazu Yamada
Molecular Genetics and Metabolism|October 10, 2006
Molecular analysis of HPRT deficiencies: an update of the spectrum of Asian mutations with novel mutationsYasukazu Yamada, Noriko Nomura, Kenichiro Yamada, et al.
Congenital Anomalies|May 21, 2005
Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutationSeiji Mizuno, Yasukazu Yamada, Kenichiro Yamada, et al.
Gene|November 1, 2011
Identification and characterization of splicing variants of PLEKHA5 (Plekha5) during brain developmentKenichiro Yamada, Noriko Nomura, Arisa Yamano, et al.
Nucleosides, Nucleotides & Nucleic Acids|July 5, 2008
Molecular analysis of hypoxanthine guanine phosphoribosyltransferase (HPRT) deficiencies: novel mutations and the spectrum of Japanese mutationsYasukazu Yamada, Noriko Nomura, Kenichro Yamada, et al.
Journal of Biochemistry|November 7, 2012
Characterization of the mutant β-subunit of β-hexosaminidase for dimer formation responsible for the adult form of Sandhoff disease with the motor neuron disease phenotypeKenichiro Yamada, Yuhei Takado, Yusuke S Kato, et al.
Pageof 4