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The Journal of Biological Chemistry|September 18, 2009
Catabolism of 4-hydroxyacids and 4-hydroxynonenal via 4-hydroxy-4-phosphoacyl-CoAsGuo-Fang Zhang, Rajan S Kombu, Takhar Kasumov, et al.
Neurology|April 16, 2017
Phenotype of GABA-transaminase deficiencyMary Kay Koenig, Ryan Hodgeman, James J Riviello, et al.
Annals of Neurology|August 2, 2003
Murine succinate semialdehyde dehydrogenase deficiencyManeesh Gupta, Boris M Hogema, Markus Grompe, et al.
Journal of Medicinal Chemistry|May 2, 2022
Discovery and Optimization of 5-Hydroxy-Diclofenac toward a New Class of Ligands with Nanomolar Affinity for the CaMKIIα Hub DomainYongsong Tian, Mohamed A Shehata, Stine Juul Gauger, et al.
Journal of Inherited Metabolic Disease|April 30, 2019
Maternal glutamine supplementation in murine succinic semialdehyde dehydrogenase deficiency, a disorder of γ-aminobutyric acid metabolismMadalyn N Brown, Dana C Walters, Michelle A Schmidt, et al.
Neurology|August 14, 2015
Natural history of succinic semialdehyde dehydrogenase deficiency through adulthoodSamuel Lapalme-Remis, Evan Cole Lewis, Christine De Meulemeester, et al.
Molecular Genetics and Metabolism Reports|December 18, 2020
Zellweger spectrum disorder: A cross-sectional study of symptom prevalence using input from family caregiversMousumi Bose, David D Cuthbertson, Marsha A Fraser, et al.
Biochimica Et Biophysica Acta|August 25, 2009
Hepatocyte transplantation (HTx) corrects selected neurometabolic abnormalities in murine intermediate maple syrup urine disease (iMSUD)Kristen J Skvorak, Elizabeth J Hager, Erland Arning, et al.
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