日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

A Novel ENU-Induced Mfn2 Mutation Causes Motor Deficits in Mice without Causing Peripheral Neuropathy

ENU 诱发的新型 Mfn2 突变导致小鼠运动障碍,但不会引起周围神经病变

Timothy J Hines, Janice Bailey, Hedi Liu, Anyonya R Guntur, Kevin L Seburn, Samia L Pratt, Jonathan R Funke, Lisa M Tarantino, Robert W Burgess

Genetic analysis of Pycr1 and Pycr2 in mice

小鼠 Pycr1 和 Pycr2 的基因分析

Morgane G Stum, Abigail L D Tadenev, Kevin L Seburn, Kathy E Miers, Pak P Poon, Christopher R McMaster, Carolyn Robinson, Coleen Kane, Kathleen A Silva, Paul F Cliften, John P Sundberg, Laura G Reinholdt, Simon W M John, Robert W Burgess

Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot-Marie-Tooth Type 2d

两种 2 型 Charcot-Marie-Tooth 病小鼠模型的神经肌肉接头突触缺陷

Emily L Spaulding, James N Sleigh, Kathryn H Morelli, Martin J Pinter, Robert W Burgess, Kevin L Seburn

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

E3 泛素连接酶 LRSAM1 的缺失使 Charcot-Marie-Tooth 病小鼠模型中的外周轴突对退化敏感

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

Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6

患有 Pla2g6 突变的人类婴儿神经轴索营养不良症的小鼠模型中的星形胶质细胞中的 Ca2+ 信号传导严重紊乱

Mikhail Strokin, Kevin L Seburn, Gregory A Cox, Kimberly A Martens, Georg Reiser

A spontaneous mutation in contactin 1 in the mouse

小鼠接触蛋白 1 的自发突变

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

An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations

氨酰-tRNA 合成酶突变导致外周轴突变性机制的评估

Morgane Stum, Heather M McLaughlin, Erica L Kleinbrink, Kathy E Miers, Susan L Ackerman, Kevin L Seburn, Anthony Antonellis, Robert W Burgess