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F Endo

Showing results (181-190 of 197) with videos related to

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American Journal of Human Genetics|June 1, 1997
Haplotype and mutation analysis in Japanese patients with Wilson diseaseM S Nanji, V T Nguyen, J H Kawasoe, et al.
The Journal of Clinical Investigation|January 1, 1990
Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypesF Endo, A Tanoue, A Kitano, et al.
Hepatology (Baltimore, Md.)|March 21, 1998
Intracellular distribution of the Wilson's disease gene product (ATPase7B) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's diseaseK Nagano, K Nakamura, K I Urakami, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 24, 1999
Mass screening for Wilson's disease: results and recommendationsY Yamaguchi, T Aoki, S Arashima, et al.
Molecular Genetics and Metabolism|November 14, 2000
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuriaK Tomoeda, H Awata, T Matsuura, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|November 1, 1996
A new blood compatible and permselective hollow fiber membrane for hemodialysisS Yamashita, A Mochizuki, T Nakazaki, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|February 17, 1999
Human ubiquitin-protein ligase Nedd4: expression, subcellular localization and selective interaction with ubiquitin-conjugating enzymesT Anan, Y Nagata, H Koga, et al.
European Journal of Neurology|June 4, 2013
p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese malesK Nakamura, Y Sekijima, K Nakamura, et al.
Journal of Medical Genetics|August 1, 1996
Phenotypic variability in male patients carrying the mutant ornithine transcarbamylase (OTC) allele, Arg40His, ranging from a child with an unfavourable prognosis to an asymptomatic older adultI Matsuda, T Matsuura, A Nishiyori, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|April 5, 2017
Stability of cervical esophagogastrostomy via hand-sewn anastomosis after esophagectomy for esophageal cancerY Akiyama, T Iwaya, F Endo, et al.
Pageof 20

Showing results (181-190 of 197) with videos related to

Sort By:
Pageof 20
American Journal of Human Genetics|June 1, 1997
Haplotype and mutation analysis in Japanese patients with Wilson diseaseM S Nanji, V T Nguyen, J H Kawasoe, et al.
The Journal of Clinical Investigation|January 1, 1990
Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypesF Endo, A Tanoue, A Kitano, et al.
Hepatology (Baltimore, Md.)|March 21, 1998
Intracellular distribution of the Wilson's disease gene product (ATPase7B) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's diseaseK Nagano, K Nakamura, K I Urakami, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 24, 1999
Mass screening for Wilson's disease: results and recommendationsY Yamaguchi, T Aoki, S Arashima, et al.
Molecular Genetics and Metabolism|November 14, 2000
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuriaK Tomoeda, H Awata, T Matsuura, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|November 1, 1996
A new blood compatible and permselective hollow fiber membrane for hemodialysisS Yamashita, A Mochizuki, T Nakazaki, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|February 17, 1999
Human ubiquitin-protein ligase Nedd4: expression, subcellular localization and selective interaction with ubiquitin-conjugating enzymesT Anan, Y Nagata, H Koga, et al.
European Journal of Neurology|June 4, 2013
p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese malesK Nakamura, Y Sekijima, K Nakamura, et al.
Journal of Medical Genetics|August 1, 1996
Phenotypic variability in male patients carrying the mutant ornithine transcarbamylase (OTC) allele, Arg40His, ranging from a child with an unfavourable prognosis to an asymptomatic older adultI Matsuda, T Matsuura, A Nishiyori, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|April 5, 2017
Stability of cervical esophagogastrostomy via hand-sewn anastomosis after esophagectomy for esophageal cancerY Akiyama, T Iwaya, F Endo, et al.
Pageof 20