Showing results (211-220 of 11,950) with videos related to
Sort By:
Pageof 1,195
Human Molecular Genetics|June 12, 2016
A reduction in Drp1-mediated fission compromises mitochondrial health in autosomal recessive spastic ataxia of Charlevoix SaguenayTeisha Y Bradshaw, Lisa E L Romano, Emma J Duncan, et al.Human Molecular Genetics|June 12, 2016
Genome-wide interrogation reveals hundreds of long intergenic noncoding RNAs that associate with cardiometabolic traitsRachel L Ballantyne, Xuan Zhang, Sara Nuñez, et al.Human Molecular Genetics|June 12, 2016
Tead1 regulates the expression of Peripheral Myelin Protein 22 during Schwann cell developmentCamila Lopez-Anido, Yannick Poitelon, Chetna Gopinath, et al.Human Molecular Genetics|June 12, 2016
Disruption of the astrocytic TNFR1-GDNF axis accelerates motor neuron degeneration and disease progression in amyotrophic lateral sclerosisLiliana Brambilla, Giulia Guidotti, Francesca Martorana, et al.Human Molecular Genetics|July 15, 2016
A genome-wide association meta-analysis on apolipoprotein A-IV concentrationsClaudia Lamina, Salome Friedel, Stefan Coassin, et al.Human Molecular Genetics|September 22, 2017
Overexpression of microRNAs from the Gtl2-Rian locus contributes to postnatal death in miceSoichiro Kumamoto, Nozomi Takahashi, Kayo Nomura, et al.Human Molecular Genetics|September 22, 2017
SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase Cɛ) impairing TORC2-dependent AKT activationDiana Alcantara, Frances Elmslie, Martine Tetreault, et al.Human Molecular Genetics|September 22, 2017
Expression of the neuropathy-associated MTMR2 gene rescues MTM1-associated myopathyMatthieu A Raess, Belinda S Cowling, Dimitri L Bertazzi, et al.Human Molecular Genetics|September 22, 2017
Homozygous KIDINS220 loss-of-function variants in fetuses with cerebral ventriculomegaly and limb contracturesI-L Mero, H H Mørk, Y Sheng, et al.Human Molecular Genetics|September 16, 2017
Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early deathSiqi Cao, Laura L Smith, Sergio R Padilla-Lopez, et al.Pageof 1,195