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Clinical and Translational Science|October 17, 2013
Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndromePuya G Yazdi, Hailing Su, Svetlana Ghimbovschi, et al.Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|November 28, 2024
Longevity, enhanced memory, and altered density of dendritic spines in hippocampal CA3 and dentate gyrus after hemizygous deletion of Pde 2a in miceKarsten Baumgärtel, Nicola J Broadbent, Hailing Su, et al.Plos One|October 20, 2010
VCP associated inclusion body myopathy and paget disease of bone knock-in mouse model exhibits tissue pathology typical of human diseaseMallikarjun Badadani, Angèle Nalbandian, Giles D Watts, et al.Neuroscience Letters|July 1, 2009
Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndromeHailing Su, Weiwei Fan, Pinar E Coskun, et al.Pageof 3