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JCI Insight|October 5, 2016
Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophyRachael A Powis, Evangelia Karyka, Penelope Boyd, et al.
Molecular Biology of the Cell|December 24, 2005
The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleusHeike Laser, Laura Conforti, Giacomo Morreale, et al.
Human Molecular Genetics|January 13, 2006
The neuroprotective WldS gene regulates expression of PTTG1 and erythroid differentiation regulator 1-like gene in mice and human cellsThomas H Gillingwater, Thomas M Wishart, Philip E Chen, et al.
Elife|July 22, 2017
Pro-death NMDA receptor signaling is promoted by the GluN2B C-terminus independently of Dapk1Jamie McQueen, Tomás J Ryan, Sean McKay, et al.
Cellular and Molecular Gastroenterology and Hepatology|February 5, 2021
SMN Depleted Mice Offer a Robust and Rapid Onset Model of Nonalcoholic Fatty Liver DiseaseMarc-Olivier Deguise, Chantal Pileggi, Yves De Repentigny, et al.
The Journal of Endocrinology|June 3, 2024
ATP-binding cassette family C member 1 constrains metabolic responses to high-fat diet in male miceElisa Villalobos, Allende Miguelez-Crespo, Ruth A Morgan, et al.
Acta Neuropathologica Communications|December 22, 2019
Comparative profiling of the synaptic proteome from Alzheimer's disease patients with focus on the APOE genotypeRaphael Hesse, Maica Llavero Hurtado, Rosemary J Jackson, et al.
The FEBS Journal|January 29, 2022
The mitochondrial protein Sideroflexin 3 (SFXN3) influences neurodegeneration pathways in vivoLeire M Ledahawsky, Maria Eirini Terzenidou, Ruairidh Edwards, et al.
Cells|September 9, 2022
Modelling Neurological Diseases in Large Animals: Criteria for Model Selection and Clinical AssessmentSamantha L Eaton, Fraser Murdoch, Nina M Rzechorzek, et al.
JCI Insight|September 9, 2025
Prenatal SMN-dependent defects in translation uncover reversible primary cilia phenotypes in spinal muscular atrophyFederica Genovese, Yu-Ting Huang, Anna Al Motyl, et al.
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