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American Journal of Medical Genetics. Part A|May 14, 2011
A novel mutation in PYCR1 causes an autosomal recessive cutis laxa with premature aging features in a familyDar-Shong Lin, Chun-Yan Yeung, Hsuan-Liang Liu, et al.Gene|October 17, 2013
De novo MECP2 duplication derived from paternal germ line result in dysmorphism and developmental delayDar-Shong Lin, Tzu-Po Chuang, Ming-Fu Chiang, et al.Cells|January 20, 2019
Oxidative Insults and Mitochondrial DNA Mutation Promote Enhanced Autophagy and Mitophagy Compromising Cell Viability in Pluripotent Cell Model of Mitochondrial DiseaseDar-Shong Lin, Yu-Wen Huang, Che-Sheng Ho, et al.Oncotarget|November 2, 2017
Inflexibility of AMPK-mediated metabolic reprogramming in mitochondrial diseaseDar-Shong Lin, Shu-Huei Kao, Che-Sheng Ho, et al.American Journal of Medical Genetics. Part A|November 5, 2011
Compound heterozygous mutations in PYCR1 further expand the phenotypic spectrum of De Barsy syndromeDar-Shong Lin, Jui-Hsing Chang, Hsuan-Liang Liu, et al.Pageof 2