Distinct expression patterns of mitochondrially localized YFP in neuronal subsets in the retina of three transgenic mouse lines

por Burgess, Robert W, Fuerst, Peter G
Publicado 2010

Self-awareness in the retina

por Garrett, Andrew M, Burgess, Robert W
Publicado 2015

Accumulating Evidence for Axonal Translation in Neuronal Homeostasis

por Spaulding, Emily L., Burgess, Robert W.
Publicado 2017

Editorial: Axonopathy in Neurodegenerative Disease

por Burgess, Robert W., Crish, Samuel D.
Publicado 2018

Model validity for preclinical studies in precision medicine: precisely how precise do we need to be?

por Tadenev, Abigail L. D., Burgess, Robert W.
Publicado 2019

Cell adhesion to agrin presented as a nanopatterned substrate is consistent with an interaction with the extracellular matrix and not transmembrane adhesion molecules

por Wolfram, Tobias, Spatz, Joachim P, Burgess, Robert W
Publicado 2008

The Synaptic Protein Syntaxin1 Is Required for Cellularization of Drosophila Embryos

por Burgess, Robert W., Deitcher, David L., Schwarz, Thomas L.
Publicado 1997

Agrin Isoforms with Distinct Amino Termini: Differential Expression, Localization, and Function

por Burgess, Robert W., Skarnes, William C., Sanes, Joshua R.
Publicado 2000

Introduction to mechanisms of neural circuit formation

por Weiner, Joshua A., Jontes, James D., Burgess, Robert W.
Publicado 2013

DSCAMs: restoring balance to developmental forces

por Garrett, Andrew M., Tadenev, Abigail L. D., Burgess, Robert W.
Publicado 2012

An Integrated Approach to Studying Rare Neuromuscular Diseases Using Animal and Human Cell-Based Models

por Hines, Timothy J., Lutz, Cathleen, Murray, Stephen A., Burgess, Robert W.
Publicado 2022

Replacing the PDZ-interacting C-termini of DSCAM and DSCAML1 with epitope tags causes different phenotypic severity in different cell populations

por Garrett, Andrew M, Tadenev, Abigail LD, Hammond, Yuna T, Fuerst, Peter G, Burgess, Robert W
Publicado 2016

A MusD Retrotransposon Insertion in the Mouse Slc6a5 Gene Causes Alterations in Neuromuscular Junction Maturation and Behavioral Phenotypes

por Bogdanik, Laurent P., Chapman, Harold D., Miers, Kathy E., Serreze, David V., Burgess, Robert W.
Publicado 2012

A Mouse Model of Heritable Cerebrovascular Disease

por Sproule, Thomas J., Sled, John G., Wentzell, Jill, Wang, Bing, Henkelman, R. Mark, Roopenian, Derry C., Burgess, Robert W.
Publicado 2010

A Spontaneous Mutation in Contactin 1 in the Mouse

por Davisson, Muriel T., Bronson, Roderick T., Tadenev, Abigail L. D., Motley, William W., Krishnaswamy, Arjun, Seburn, Kevin L., Burgess, Robert W.
Publicado 2011

A Novel Mouse Dscam Mutation Inhibits Localization and Shedding of DSCAM

por Schramm, R. Dee, Li, Shuai, Harris, Belinda S., Rounds, Ryan P., Burgess, Robert W., Ytreberg, F. Marty, Fuerst, Peter G.
Publicado 2012

Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease

por Bogdanik, Laurent P., Sleigh, James N., Tian, Cong, Samuels, Mark E., Bedard, Karen, Seburn, Kevin L., Burgess, Robert W.
Publicado 2013

Dominant, toxic gain-of-function mutations in gars lead to non-cell autonomous neuropathology

por Grice, Stuart J., Sleigh, James N., Motley, William W., Liu, Ji-Long, Burgess, Robert W., Talbot, Kevin, Cader, M. Zameel
Publicado 2015

Two-photon NADH imaging exposes boundaries of oxygen diffusion in cortical vascular supply regions

por Kasischke, Karl A, Lambert, Elton M, Panepento, Ben, Sun, Anita, Gelbard, Harris A, Burgess, Robert W, Foster, Thomas H, Nedergaard, Maiken
Publicado 2011

Analysis of Expression Pattern and Genetic Deletion of Netrin5 in the Developing Mouse

por Garrett, Andrew M., Jucius, Thomas J., Sigaud, Liam P. R., Tang, Fu-Lei, Xiong, Wen-Cheng, Ackerman, Susan L., Burgess, Robert W.
Publicado 2016