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Gene|February 21, 2006
Efficient recombination-based methods for bacterial artificial chromosome fusion and mutagenesisBryce L Sopher, Albert R La SpadaHeliyon|June 25, 2020
Tight expression regulation of senataxin, linked to motor neuron disease and ataxia, is required to avert cell-cycle block and nucleolus disassemblyCraig L Bennett, Bryce L Sopher, Albert R La SpadaMammalian Genome : Official Journal of the International Mammalian Genome Society|February 9, 2006
The Purkinje cell degeneration 5J mutation is a single amino acid insertion that destabilizes Nna1 proteinLisa Chakrabarti, James T Neal, Michael Miles, et al.Human Molecular Genetics|November 14, 2003
Interference of Crx-dependent transcription by ataxin-7 involves interaction between the glutamine regions and requires the ataxin-7 carboxy-terminal region for nuclear localizationShiming Chen, Guang-Hua Peng, Xuejiao Wang, et al.Vision Research|July 8, 2008
The zinc-binding domain of Nna1 is required to prevent retinal photoreceptor loss and cerebellar ataxia in Purkinje cell degeneration (pcd) miceLisa Chakrabarti, Jeremiah Eng, Refugio A Martinez, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 13, 2020
4E-BP1 Protects Neurons from Misfolded Protein Stress and Parkinson's Disease Toxicity by Inducing the Mitochondrial Unfolded Protein ResponseSomasish Ghosh Dastidar, Michael T Pham, Matthew B Mitchell, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 11, 2011
Spinocerebellar ataxia type 7 cerebellar disease requires the coordinated action of mutant ataxin-7 in neurons and glia, and displays non-cell-autonomous bergmann glia degenerationStephanie A Furrer, Mathini S Mohanachandran, Sarah M Waldherr, et al.Human Molecular Genetics|April 11, 2015
Proteolytic cleavage of ataxin-7 promotes SCA7 retinal degeneration and neurological dysfunctionStephan J Guyenet, Shona S Mookerjee, Amy Lin, et al.Cerebrum : the Dana Forum on Brain Science|February 13, 2019
A Novel Therapy for Huntington's DiseaseAlbert R La SpadaAutophagy|August 31, 2012
PPARGC1A/PGC-1α, TFEB and enhanced proteostasis in Huntington disease: defining regulatory linkages between energy production and protein-organelle quality controlAlbert R La SpadaPageof 16