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Cederbaum

Showing results (711-720 of 783) with videos related to

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Pediatric Research|March 1, 1990
Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapyB Marescau, P P De Deyn, A Lowenthal, et al.
Molecular Genetics and Metabolism|September 30, 2018
Prevalence of comorbid conditions among adult patients diagnosed with phenylketonuriaBarbara K Burton, Kyle Bradford Jones, Stephen Cederbaum, et al.
Molecular Genetics and Metabolism|June 27, 2002
Expression of the liver form of arginase in erythrocytesPhillip S Kim, Ramaswamy K Iyer, Kan V Lu, et al.
Human Genetics|January 1, 1996
Apparent higher frequency of phenylketonuria in the Mexican state of JaliscoA Velázquez, G Bilbao, J L González-Trujillo, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 21, 2010
Arginase I suppresses IL-12/IL-23p40-driven intestinal inflammation during acute schistosomiasisDe'Broski R Herbert, Tatyana Orekov, Amanda Roloson, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 24, 2002
Helicobacter pylori induces macrophage apoptosis by activation of arginase IIAlain P Gobert, Yulan Cheng, Jian-Ying Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 9, 2013
Newborn screening 50 years later: access issues faced by adults with PKUSusan A Berry, Christine Brown, Mitzie Grant, et al.
JCI Insight|September 6, 2019
Hepatic arginase deficiency fosters dysmyelination during postnatal CNS developmentXiao-Bo Liu, Jillian R Haney, Gloria Cantero, et al.
Bioorganic & Medicinal Chemistry|July 9, 2014
Synthesis and fungicidal activity of quinolin-6-yloxyacetamides, a novel class of tubulin polymerization inhibitorsClemens Lamberth, Fiona Murphy Kessabi, Renaud Beaudegnies, et al.
Neurology|December 31, 1997
Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutationsI D Wexler, S G Hemalatha, J McConnell, et al.
Pageof 79

Showing results (711-720 of 783) with videos related to

Sort By:
Pageof 79
Pediatric Research|March 1, 1990
Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapyB Marescau, P P De Deyn, A Lowenthal, et al.
Molecular Genetics and Metabolism|September 30, 2018
Prevalence of comorbid conditions among adult patients diagnosed with phenylketonuriaBarbara K Burton, Kyle Bradford Jones, Stephen Cederbaum, et al.
Molecular Genetics and Metabolism|June 27, 2002
Expression of the liver form of arginase in erythrocytesPhillip S Kim, Ramaswamy K Iyer, Kan V Lu, et al.
Human Genetics|January 1, 1996
Apparent higher frequency of phenylketonuria in the Mexican state of JaliscoA Velázquez, G Bilbao, J L González-Trujillo, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 21, 2010
Arginase I suppresses IL-12/IL-23p40-driven intestinal inflammation during acute schistosomiasisDe'Broski R Herbert, Tatyana Orekov, Amanda Roloson, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 24, 2002
Helicobacter pylori induces macrophage apoptosis by activation of arginase IIAlain P Gobert, Yulan Cheng, Jian-Ying Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 9, 2013
Newborn screening 50 years later: access issues faced by adults with PKUSusan A Berry, Christine Brown, Mitzie Grant, et al.
JCI Insight|September 6, 2019
Hepatic arginase deficiency fosters dysmyelination during postnatal CNS developmentXiao-Bo Liu, Jillian R Haney, Gloria Cantero, et al.
Bioorganic & Medicinal Chemistry|July 9, 2014
Synthesis and fungicidal activity of quinolin-6-yloxyacetamides, a novel class of tubulin polymerization inhibitorsClemens Lamberth, Fiona Murphy Kessabi, Renaud Beaudegnies, et al.
Neurology|December 31, 1997
Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutationsI D Wexler, S G Hemalatha, J McConnell, et al.
Pageof 79