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Stephen D Cederbaum

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Molecular Therapy : the Journal of the American Society of Gene Therapy|April 16, 2009
Short-term correction of arginase deficiency in a neonatal murine model with a helper-dependent adenoviral vectorChia-Ling Gau, Robin A Rosenblatt, Vincenzo Cerullo, et al.
Molecular Genetics and Metabolism|August 8, 2013
Lethal phenotype in conditional late-onset arginase 1 deficiency in the mouseJennifer Kasten, Chuhong Hu, Ragini Bhargava, et al.
Molecular Genetics and Metabolism|October 3, 2002
Identification of isobutyryl-CoA dehydrogenase and its deficiency in humansTien V Nguyen, Brage S Andresen, Thomas J Corydon, et al.
Molecular Genetics and Metabolism|March 20, 2012
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in CaliforniaNatalie M Gallant, Karen Leydiker, Hao Tang, et al.
Frontiers in Immunology|January 9, 2014
l-Citrulline Protects from Kidney Damage in Type 1 Diabetic MiceMaritza J Romero, Lin Yao, Supriya Sridhar, et al.
Molecular Therapy. Nucleic Acids|June 13, 2022
Intermittent lipid nanoparticle mRNA administration prevents cortical dysmyelination associated with arginase deficiencySuhail Khoja, Xiao-Bo Liu, Brian Truong, et al.
Molecular Genetics and Metabolism|June 20, 2008
Cross-sectional multicenter study of patients with urea cycle disorders in the United StatesMendel Tuchman, Brendan Lee, Uta Lichter-Konecki, et al.
Molecular Therapy. Nucleic Acids|November 30, 2016
Restoring Ureagenesis in Hepatocytes by CRISPR/Cas9-mediated Genomic Addition to Arginase-deficient Induced Pluripotent Stem CellsPatrick C Lee, Brian Truong, Agustin Vega-Crespo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2024
Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participantsAmir Hossein Saeidian, Michael E March, Leila Youssefian, et al.
American Journal of Respiratory Cell and Molecular Biology|May 15, 2012
Protein kinase C-α and arginase I mediate pneumolysin-induced pulmonary endothelial hyperpermeabilityRudolf Lucas, Guang Yang, Boris A Gorshkov, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 16, 2009
Short-term correction of arginase deficiency in a neonatal murine model with a helper-dependent adenoviral vectorChia-Ling Gau, Robin A Rosenblatt, Vincenzo Cerullo, et al.
Molecular Genetics and Metabolism|August 8, 2013
Lethal phenotype in conditional late-onset arginase 1 deficiency in the mouseJennifer Kasten, Chuhong Hu, Ragini Bhargava, et al.
Molecular Genetics and Metabolism|October 3, 2002
Identification of isobutyryl-CoA dehydrogenase and its deficiency in humansTien V Nguyen, Brage S Andresen, Thomas J Corydon, et al.
Molecular Genetics and Metabolism|March 20, 2012
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in CaliforniaNatalie M Gallant, Karen Leydiker, Hao Tang, et al.
Frontiers in Immunology|January 9, 2014
l-Citrulline Protects from Kidney Damage in Type 1 Diabetic MiceMaritza J Romero, Lin Yao, Supriya Sridhar, et al.
Molecular Therapy. Nucleic Acids|June 13, 2022
Intermittent lipid nanoparticle mRNA administration prevents cortical dysmyelination associated with arginase deficiencySuhail Khoja, Xiao-Bo Liu, Brian Truong, et al.
Molecular Genetics and Metabolism|June 20, 2008
Cross-sectional multicenter study of patients with urea cycle disorders in the United StatesMendel Tuchman, Brendan Lee, Uta Lichter-Konecki, et al.
Molecular Therapy. Nucleic Acids|November 30, 2016
Restoring Ureagenesis in Hepatocytes by CRISPR/Cas9-mediated Genomic Addition to Arginase-deficient Induced Pluripotent Stem CellsPatrick C Lee, Brian Truong, Agustin Vega-Crespo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2024
Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participantsAmir Hossein Saeidian, Michael E March, Leila Youssefian, et al.
American Journal of Respiratory Cell and Molecular Biology|May 15, 2012
Protein kinase C-α and arginase I mediate pneumolysin-induced pulmonary endothelial hyperpermeabilityRudolf Lucas, Guang Yang, Boris A Gorshkov, et al.
Pageof 5