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Frontiers in Cell and Developmental Biology|July 16, 2021
Loss of Deacetylation Enzymes Hdac6 and Sirt2 Promotes Acetylation of Cytoplasmic Tubulin, but Suppresses Axonemal Acetylation in Zebrafish CiliaPaweł K Łysyganicz, Niedharsan Pooranachandran, Xinming Liu, et al.Journal of Epidemiology and Community Health|January 31, 2009
No increase in HIV or sexually transmissible infection testing following a social marketing campaign among men who have sex with menR Guy, J Goller, D Leslie, et al.The International Journal on Drug Policy|February 13, 2018
Prevalence and correlates of recent injecting drug use among gay and bisexual men in Australia: Results from the FLUX studyH Bui, I Zablotska-Manos, M Hammoud, et al.Human Molecular Genetics|October 24, 2002
Charcot-Marie-Tooth disease neurofilament mutations disrupt neurofilament assembly and axonal transportJanet Brownlees, Steven Ackerley, Andrew J Grierson, et al.Brain Research. Molecular Brain Research|June 14, 2005
Quantitative analysis of tau isoform transcripts in sporadic tauopathiesJ W Connell, T Rodriguez-Martin, G M Gibb, et al.Journal of Cell Science|March 5, 2004
Parkinson's disease alpha-synuclein mutations exhibit defective axonal transport in cultured neuronsAnirban R Saha, Josephine Hill, Michelle A Utton, et al.Free Radical Biology & Medicine|April 24, 2013
S[+] Apomorphine is a CNS penetrating activator of the Nrf2-ARE pathway with activity in mouse and patient fibroblast models of amyotrophic lateral sclerosisRichard J Mead, Adrian Higginbottom, Scott P Allen, et al.Autophagy|June 20, 2020
Neutrophils use selective autophagy receptor Sqstm1/p62 to target Staphylococcus aureus for degradation in vivo in zebrafishJosie F Gibson, Tomasz K Prajsnar, Christopher J Hill, et al.Journal of Neurochemistry|May 21, 2009
Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patientsPaul R Kasher, Kurt J De Vos, Stephen B Wharton, et al.Human Molecular Genetics|August 30, 2007
Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria contentKurt J De Vos, Anna L Chapman, Maria E Tennant, et al.Pageof 9