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Stephen D Cederbaum

Showing results (21-30 of 50) with videos related to

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Molecular Genetics and Metabolism|October 10, 2013
Analysis of cases of 3-methylcrotonyl CoA carboxylase deficiency (3-MCCD) in the California newborn screening program reported in the state databaseChristina Lam, Jennifer M Carter, Stephen D Cederbaum, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 5, 2012
Long-term survival of the juvenile lethal arginase-deficient mouse with AAV gene therapyEun K Lee, Chuhong Hu, Ragini Bhargava, et al.
Molecular Genetics and Metabolism|November 13, 2007
Increased plasma and tissue guanidino compounds in a mouse model of hyperargininemiaJoshua L Deignan, Bart Marescau, Justin C Livesay, et al.
Journal of Neuroscience Research|June 15, 2006
Loss of arginase I results in increased proliferation of neural stem cellsSara G Becker-Catania, Teresa L Gregory, Yawei Yang, et al.
Pediatric Research|August 31, 2006
Clinical and functional characterization of a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndromeJosé A Camacho, Rebecca Mardach, Natalia Rioseco-Camacho, et al.
BMC Immunology|June 3, 2009
Bone marrow cell derived arginase I is the major source of allergen-induced lung arginase but is not required for airway hyperresponsiveness, remodeling and lung inflammatory responses in miceKathryn A Niese, Ann R Collier, Amanda R Hajek, et al.
Molecular Genetics and Metabolism|November 1, 2002
Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiencyStephen D Cederbaum, Samantha Koo-McCoy, Ingrid Tein, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|August 19, 2003
Widespread expression of arginase I in mouse tissues. Biochemical and physiological implicationsHong Yu, Paul K Yoo, Claudia C Aguirre, et al.
Molecular and Cellular Biology|June 8, 2002
Mouse model for human arginase deficiencyRamaswamy K Iyer, Paul K Yoo, Rita M Kern, et al.
Molecular Genetics and Metabolism|June 7, 2006
Ornithine deficiency in the arginase double knockout mouseJoshua L Deignan, Justin C Livesay, Paul K Yoo, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Molecular Genetics and Metabolism|October 10, 2013
Analysis of cases of 3-methylcrotonyl CoA carboxylase deficiency (3-MCCD) in the California newborn screening program reported in the state databaseChristina Lam, Jennifer M Carter, Stephen D Cederbaum, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 5, 2012
Long-term survival of the juvenile lethal arginase-deficient mouse with AAV gene therapyEun K Lee, Chuhong Hu, Ragini Bhargava, et al.
Molecular Genetics and Metabolism|November 13, 2007
Increased plasma and tissue guanidino compounds in a mouse model of hyperargininemiaJoshua L Deignan, Bart Marescau, Justin C Livesay, et al.
Journal of Neuroscience Research|June 15, 2006
Loss of arginase I results in increased proliferation of neural stem cellsSara G Becker-Catania, Teresa L Gregory, Yawei Yang, et al.
Pediatric Research|August 31, 2006
Clinical and functional characterization of a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndromeJosé A Camacho, Rebecca Mardach, Natalia Rioseco-Camacho, et al.
BMC Immunology|June 3, 2009
Bone marrow cell derived arginase I is the major source of allergen-induced lung arginase but is not required for airway hyperresponsiveness, remodeling and lung inflammatory responses in miceKathryn A Niese, Ann R Collier, Amanda R Hajek, et al.
Molecular Genetics and Metabolism|November 1, 2002
Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiencyStephen D Cederbaum, Samantha Koo-McCoy, Ingrid Tein, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|August 19, 2003
Widespread expression of arginase I in mouse tissues. Biochemical and physiological implicationsHong Yu, Paul K Yoo, Claudia C Aguirre, et al.
Molecular and Cellular Biology|June 8, 2002
Mouse model for human arginase deficiencyRamaswamy K Iyer, Paul K Yoo, Rita M Kern, et al.
Molecular Genetics and Metabolism|June 7, 2006
Ornithine deficiency in the arginase double knockout mouseJoshua L Deignan, Justin C Livesay, Paul K Yoo, et al.
Pageof 5