Showing results (51-60 of 87) with videos related to

Sort By:
Pageof 9
Science Translational Medicine|June 12, 2010
Systemic delivery of scAAV9 expressing SMN prolongs survival in a model of spinal muscular atrophyChiara F Valori, Ke Ning, Matthew Wyles, et al.
European Journal of Biochemistry|July 11, 1998
The gene for the human Src-like adaptor protein (hSLAP) is located within the 64-kb intron of the thyroglobulin geneP H Meijerink, P Yanakiev, I Zorn, et al.
Biochemical Pharmacology|January 15, 1988
Kinetics of in vitro decarboxylation and the in vivo metabolism of 2-18F- and 6-18F-fluorodopa in the hooded ratP Cumming, M Häusser, W R Martin, et al.
Australian and New Zealand Journal of Medicine|February 1, 1990
Chronic non-A, non-B hepatitis: lack of correlation between biochemical and morphological activity, and effects of immunosuppressive therapy on disease progressionM N Schoeman, C Liddle, M Bilous, et al.
BMJ Open Science|January 20, 2022
Methodological standards, quality of reporting and regulatory compliance in animal research on amyotrophic lateral sclerosis: a systematic reviewJoana G Fernandes, Nuno H Franco, Andrew J Grierson, et al.
Development (Cambridge, England)|September 27, 2021
Lamb1a regulates atrial growth by limiting second heart field addition during zebrafish heart developmentChristopher J Derrick, Eric J G Pollitt, Ashley Sanchez Sevilla Uruchurtu, et al.
Journal of Neurochemistry|January 9, 2001
Phosphorylation of thr(668) in the cytoplasmic domain of the Alzheimer's disease amyloid precursor protein by stress-activated protein kinase 1b (Jun N-terminal kinase-3)C L Standen, J Brownlees, A J Grierson, et al.
Plos One|January 29, 2013
No evidence for cardiac dysfunction in Kif6 mutant miceAbdul Hameed, Ellen Bennett, Barbara Ciani, et al.
Journal of Neuropathology and Experimental Neurology|December 6, 2003
The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin geneStephen B Wharton, Christopher J McDermott, Andrew J Grierson, et al.
Annals of Neurology|December 19, 2003
Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutationChristopher J McDermott, Andrew J Grierson, Jonathan D Wood, et al.
Pageof 9