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Journal of Visualized Experiments : Jove|February 1, 2021
Building a Simple and Versatile Illumination System for Optogenetic ExperimentsPhillip Kyriakakis, Lourdes Fernandez de Cossio, Patrick Wade Howard, et al.European Journal of Cancer (Oxford, England : 1990)|August 31, 2001
Cancer survival increases in Europe, but international differences remain wideM Sant, R Capocaccia, M P Coleman, et al.Brain : a Journal of Neurology|January 13, 2005
The slow Wallerian degeneration gene, WldS, inhibits axonal spheroid pathology in gracile axonal dystrophy miceWeiqian Mi, Bogdan Beirowski, Thomas H Gillingwater, et al.ALTEX|May 25, 2017
From in vivo to in vitro: The medical device testing paradigm shiftDayna Kerecman Myers, Alan M Goldberg, Albrecht Poth, et al.Journal of Clinical Epidemiology|July 27, 2001
Coffee consumption and serum aminotransferases in middle-aged Japanese menS Honjo, S Kono, M P Coleman, et al.ACS Synthetic Biology|January 5, 2018
Biosynthesis of Orthogonal Molecules Using Ferredoxin and Ferredoxin-NADP+ Reductase Systems Enables Genetically Encoded PhyB OptogeneticsPhillip Kyriakakis, Marianne Catanho, Nicole Hoffner, et al.The European Journal of Neuroscience|January 19, 2005
A rat model of slow Wallerian degeneration (WldS) with improved preservation of neuromuscular synapsesRobert Adalbert, Thomas H Gillingwater, Jane E Haley, et al.Neurobiology of Disease|November 20, 2019
Mitochondrial impairment activates the Wallerian pathway through depletion of NMNAT2 leading to SARM1-dependent axon degenerationAndrea Loreto, Ciaran S Hill, Victoria L Hewitt, et al.Current Biology : CB|March 7, 2017
NMN Deamidase Delays Wallerian Degeneration and Rescues Axonal Defects Caused by NMNAT2 Deficiency In VivoMichele Di Stefano, Andrea Loreto, Giuseppe Orsomando, et al.Cell Death and Differentiation|April 29, 2006
NAD(+) and axon degeneration revisited: Nmnat1 cannot substitute for Wld(S) to delay Wallerian degenerationL Conforti, G Fang, B Beirowski, et al.Pageof 101