Altered terminal Schwann cell morphology precedes denervation in SOD1 mice von Carrasco, Dario I., Seburn, Kevin L., Pinter, Martin J.

Volltext

Lack of Neuropathy-Related Phenotypes in Hint1 Knockout Mice von Seburn, Kevin L, Morelli, Kathryn H, Jordanova, Albena, Burgess, Robert W

Volltext

Abnormal response of distal Schwann cells to denervation in a mouse model of motor neuron disease von Carrasco, Dario I., Bahr, Ben A., Seburn, Kevin L., Pinter, Martin J.

Volltext

Neuromuscular Disease Models and Analysis von Burgess, Robert W., Cox, Gregory A., Seburn, Kevin L.

Volltext

Age, experience and genetic background influence treadmill walking in mice von Wooley, Christine M, Xing, Shuqin, Burgess, Robert W, Cox, Gregory A, Seburn, Kevin L

Volltext

single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination von Patton, Bruce L, Wang, Bing, Tarumi, Yukie S, Seburn, Kevin L, Burgess, Robert W

Volltext

Nerve terminal degeneration is independent of muscle fiber genotype in SOD1 mice von Carrasco, Dario I, Bichler, Edyta K, Seburn, Kevin L, Pinter, Martin J

Volltext

Motor terminal degeneration unaffected by activity changes in SOD1(G93A) mice; a possible role for glycolysis von Carrasco, Dario I, Bichler, Edyta K, Rich, Mark M, Wang, Xueyong, Seburn, Kevin L, Pinter, Martin J

Volltext

Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot-Marie-Tooth Type 2d von Spaulding, Emily L, Sleigh, James N, Morelli, Kathryn H, Pinter, Martin J, Burgess, Robert W, Seburn, Kevin L

Volltext

Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels von Motley, William W, Seburn, Kevin L, Nawaz, Mir Hussain, Miers, Kathy E, Cheng, Jun, Antonellis, Anthony, Green, Eric D, Talbot, Kevin, Yang, Xiang-Lei, Fischbeck, Kenneth H, Burgess, Robert W

Volltext

Strain-specific hyperkyphosis and megaesophagus in Add1 null mice von Robledo, Raymond F., Seburn, Kevin L., Nicholson, Anthony, Peters, Luanne L.

Volltext

Mutations in a P-type ATPase gene cause axonal degeneration von Zhu, Xianjun, Libby, Richard T, de Vries, Wilhelmine N, Smith, Richard S, Wright, Dana L, Bronson, Roderick T, Seburn, Kevin L, John, Simon W M

Volltext

Nerve Terminal Degeneration Is Independent of Muscle Fiber Genotype in SOD1G93A Mice von Carrasco, Dario I., Bichler, Edyta K., Seburn, Kevin L., Pinter, Martin J.

Volltext

An Active Dominant Mutation of Glycyl-tRNA Synthetase Causes Neuropathy in a Charcot-Marie-Tooth 2D Mouse Model von Seburn, Kevin L., Nangle, Leslie A., Cox, Gregory A., Schimmel, Paul, Burgess, Robert W.

Volltext

Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes von Morelli, Kathryn H., Seburn, Kevin L., Schroeder, David G., Spaulding, Emily L., Dionne, Loiuse A., Cox, Gregory A., Burgess, Robert W.

Volltext

The harlequin mouse mutation downregulates apoptosis-inducing factor von Klein, Jeffrey A., Longo-Guess, Chantal M., Rossmann, Marlies P., Seburn, Kevin L., Hurd, Ronald E., Frankel, Wayne N., Bronson, Roderick T., Ackerman, Susan L.

Volltext

Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunit von Traka, Maria, Seburn, Kevin L, Popko, Brian

Volltext

An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations von Stum, Morgane, McLaughlin, Heather M., Kleinbrink, Erica L., Miers, Kathy E., Ackerman, Susan L., Seburn, Kevin L., Antonellis, Anthony, Burgess, Robert W.

Volltext

A Novel ENU-Induced Mfn2 Mutation Causes Motor Deficits in Mice without Causing Peripheral Neuropathy von Hines, Timothy J, Bailey, Janice, Liu, Hedi, Guntur, Anyonya R, Seburn, Kevin L, Pratt, Samia L, Funke, Jonathan R, Tarantino, Lisa M, Burgess, Robert W

Volltext

Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease von Bogdanik, Laurent P, Sleigh, James N, Tian, Cong, Samuels, Mark E, Bedard, Karen, Seburn, Kevin L, Burgess, Robert W

Volltext