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Autophagy|May 10, 2016
Defective recognition of LC3B by mutant SQSTM1/p62 implicates impairment of autophagy as a pathogenic mechanism in ALS-FTLDAlice Goode, Kevin Butler, Jed Long, et al.Bone|November 3, 2012
The S349T mutation of SQSTM1 links Keap1/Nrf2 signalling to Paget's disease of boneTao Wright, Sarah L Rea, Alice Goode, et al.Biochimica Et Biophysica Acta|March 20, 2014
Paget disease of bone-associated UBA domain mutations of SQSTM1 exert distinct effects on protein structure and functionAlice Goode, Jed E Long, Barry Shaw, et al.Frontiers in Chemistry|May 22, 2023
Conformational analysis and interaction of the Staphylococcus aureus transmembrane peptidase AgrB with its AgrD propeptide substratePhilip Bardelang, Ewan J Murray, Isobel Blower, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 12, 2011
A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's diseaseFernando Gianfrancesco, Domenico Rendina, Marco Di Stefano, et al.Pageof 2