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Cederbaum

Showing results (721-730 of 783) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|June 4, 2014
Myocyte-mediated arginase expression controls hyperargininemia but not hyperammonemia in arginase-deficient miceChuhong Hu, Jennifer Kasten, Hana Park, et al.
Metabolism: Clinical and Experimental|September 1, 1992
The pathobiochemistry of uremia and hyperargininemia further demonstrates a metabolic relationship between urea and guanidinosuccinic acidB Marescau, P P De Deyn, I A Qureshi, et al.
Child & Adolescent Social Work Journal : C & A|June 22, 2026
Associations between Local and State Structural Stigma, Minority stress, and Mental Health in a Nationwide Sample of Sexual Minority AdolescentsRory P O'Brien, John R Blosnich, Julie A Cederbaum, et al.
Frontiers in Immunology|August 23, 2013
Arginase 1: an unexpected mediator of pulmonary capillary barrier dysfunction in models of acute lung injuryRudolf Lucas, Istvàn Czikora, Supriya Sridhar, et al.
Journal of Inherited Metabolic Disease|September 12, 2007
The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening studyB K Burton, D K Grange, A Milanowski, et al.
The Journal of Pediatrics|March 18, 2003
Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edemaJonathan D Picker, Ana C Puga, Harvey L Levy, et al.
Early Intervention in Psychiatry|December 1, 2015
McLean OnTrack: a transdiagnostic program for early intervention in first-episode psychosisAnn K Shinn, Kirsten W Bolton, Rakesh Karmacharya, et al.
Molecular Genetics and Metabolism|May 5, 2018
Human hepatocyte transplantation corrects the inherited metabolic liver disorder arginase deficiency in miceStephanie A K Angarita, Brian Truong, Suhail Khoja, et al.
Blood|August 1, 1975
Dominant inheritance of hemophilia A in three generations of womenJ B Graham, E S Barrow, H R Roberts, et al.
Physical Review Letters|August 18, 2025
Neutralization of Multiply Charged Ground-State Ions by Collective Electron Transfer from an EnvironmentLutz Marder, Catmarna Küstner-Wetekam, Nils Kiefer, et al.
Pageof 79

Showing results (721-730 of 783) with videos related to

Sort By:
Pageof 79
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 4, 2014
Myocyte-mediated arginase expression controls hyperargininemia but not hyperammonemia in arginase-deficient miceChuhong Hu, Jennifer Kasten, Hana Park, et al.
Metabolism: Clinical and Experimental|September 1, 1992
The pathobiochemistry of uremia and hyperargininemia further demonstrates a metabolic relationship between urea and guanidinosuccinic acidB Marescau, P P De Deyn, I A Qureshi, et al.
Child & Adolescent Social Work Journal : C & A|June 22, 2026
Associations between Local and State Structural Stigma, Minority stress, and Mental Health in a Nationwide Sample of Sexual Minority AdolescentsRory P O'Brien, John R Blosnich, Julie A Cederbaum, et al.
Frontiers in Immunology|August 23, 2013
Arginase 1: an unexpected mediator of pulmonary capillary barrier dysfunction in models of acute lung injuryRudolf Lucas, Istvàn Czikora, Supriya Sridhar, et al.
Journal of Inherited Metabolic Disease|September 12, 2007
The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening studyB K Burton, D K Grange, A Milanowski, et al.
The Journal of Pediatrics|March 18, 2003
Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edemaJonathan D Picker, Ana C Puga, Harvey L Levy, et al.
Early Intervention in Psychiatry|December 1, 2015
McLean OnTrack: a transdiagnostic program for early intervention in first-episode psychosisAnn K Shinn, Kirsten W Bolton, Rakesh Karmacharya, et al.
Molecular Genetics and Metabolism|May 5, 2018
Human hepatocyte transplantation corrects the inherited metabolic liver disorder arginase deficiency in miceStephanie A K Angarita, Brian Truong, Suhail Khoja, et al.
Blood|August 1, 1975
Dominant inheritance of hemophilia A in three generations of womenJ B Graham, E S Barrow, H R Roberts, et al.
Physical Review Letters|August 18, 2025
Neutralization of Multiply Charged Ground-State Ions by Collective Electron Transfer from an EnvironmentLutz Marder, Catmarna Küstner-Wetekam, Nils Kiefer, et al.
Pageof 79