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Biochemical and Molecular Medicine
|
October 1, 1996
Loss of function mutations in conserved regions of the human arginase I gene
J G Vockley, B K Goodman, D E Tabor, et al.
Molecular Genetics and Metabolism
|
November 13, 2007
Increased plasma and tissue guanidino compounds in a mouse model of hyperargininemia
Joshua 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 cells
Sara 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) syndrome
José A Camacho, Rebecca Mardach, Natalia Rioseco-Camacho, et al.
The American Journal of Physiology
|
November 1, 1996
Arginase activity in endothelial cells: inhibition by NG-hydroxy-L-arginine during high-output NO production
G M Buga, R Singh, S Pervin, et al.
Gene Therapy
|
December 5, 2014
Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy
C Hu, D S Tai, H Park, et al.
The Journal of Clinical Investigation
|
February 1, 1989
Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysis
W W Grody, C Argyle, R M Kern, et al.
Journal of Interpersonal Violence
|
April 7, 2020
Cumulative Violence Exposure and Alcohol Use Among College Students: Adverse Childhood Experiences and Dating Violence
Carolina Villamil Grest, Julie A Cederbaum, Daniel S Lee, et al.
The Journal of Clinical Investigation
|
June 19, 2002
Biotin dependency due to a defect in biotin transport
Rebecca Mardach, Janos Zempleni, Barry Wolf, et al.
Physical Review Letters
|
January 15, 2011
Interatomic electronic decay driven by nuclear motion
Nicolas Sisourat, Hendrik Sann, Nikolai V Kryzhevoi, et al.
Page
of 79
Search research articles
Search
Showing results (681-690 of 783) with videos related to
Sort By:
Page
of 79
Biochemical and Molecular Medicine
|
October 1, 1996
Loss of function mutations in conserved regions of the human arginase I gene
J G Vockley, B K Goodman, D E Tabor, et al.
Molecular Genetics and Metabolism
|
November 13, 2007
Increased plasma and tissue guanidino compounds in a mouse model of hyperargininemia
Joshua 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 cells
Sara 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) syndrome
José A Camacho, Rebecca Mardach, Natalia Rioseco-Camacho, et al.
The American Journal of Physiology
|
November 1, 1996
Arginase activity in endothelial cells: inhibition by NG-hydroxy-L-arginine during high-output NO production
G M Buga, R Singh, S Pervin, et al.
Gene Therapy
|
December 5, 2014
Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy
C Hu, D S Tai, H Park, et al.
The Journal of Clinical Investigation
|
February 1, 1989
Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysis
W W Grody, C Argyle, R M Kern, et al.
Journal of Interpersonal Violence
|
April 7, 2020
Cumulative Violence Exposure and Alcohol Use Among College Students: Adverse Childhood Experiences and Dating Violence
Carolina Villamil Grest, Julie A Cederbaum, Daniel S Lee, et al.
The Journal of Clinical Investigation
|
June 19, 2002
Biotin dependency due to a defect in biotin transport
Rebecca Mardach, Janos Zempleni, Barry Wolf, et al.
Physical Review Letters
|
January 15, 2011
Interatomic electronic decay driven by nuclear motion
Nicolas Sisourat, Hendrik Sann, Nikolai V Kryzhevoi, et al.
Page
of 79