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Organic Letters|December 20, 2011
New rhodamine nitroxide based fluorescent probes for intracellular hydroxyl radical identification in living cellsNazmiye B Yapici, Steffen Jockusch, Alberto Moscatelli, et al.
Human Mutation|March 26, 2003
Mutations in the AUH gene cause 3-methylglutaconic aciduria type IT B Nga Ly, Verena Peters, K Michael Gibson, et al.
Bioorganic & Medicinal Chemistry Letters|March 11, 2016
Anti-inflammatory, analgesic and antioxidant activities of novel kyotorphin-nitroxide hybrid moleculesWei Bi, Yue Bi, Xiang Gao, et al.
Brain Research|May 2, 2006
Succinic semialdehyde dehydrogenase deficiency: GABAB receptor-mediated functionAndrea Buzzi, Ying Wu, Marina V Frantseva, et al.
European Journal of Medicinal Chemistry|April 9, 2011
Novel β-carboline-tripeptide conjugates attenuate mesenteric ischemia/reperfusion injury in the ratWei Bi, Yue Bi, Ping Xue, et al.
Experimental Neurology|January 18, 2008
A ketogenic diet rescues the murine succinic semialdehyde dehydrogenase deficient phenotypeKirk Nylen, Jose Luis Perez Velazquez, Sergei S Likhodii, et al.
Molecular Genetics & Genomic Medicine|March 5, 2019
Rett syndrome (MECP2) and succinic semialdehyde dehydrogenase (ALDH5A1) deficiency in a developmentally delayed femaleMadalyn Brown, Paula Ashcraft, Erland Arning, et al.
Sleep|January 1, 2010
Polysomnographic abnormalities in succinic semialdehyde dehydrogenase (SSADH) deficiencyPhillip L Pearl, Sadat Shamim, William H Theodore, et al.
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