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

Altered terminal Schwann cell morphology precedes denervation in SOD1 mice

SOD1小鼠中,终末雪旺细胞形态的改变先于神经支配丧失。

Carrasco, Dario I; Seburn, Kevin L; Pinter, Martin J

Abnormal response of distal Schwann cells to denervation in a mouse model of motor neuron disease

在运动神经元疾病小鼠模型中,远端雪旺细胞对去神经支配的反应异常

Carrasco, Dario I; Bahr, Ben A; Seburn, Kevin L; Pinter, Martin J

Metabolite profile of a mouse model of Charcot-Marie-Tooth type 2D neuropathy: implications for disease mechanisms and interventions

Charcot-Marie-Tooth 2D 型神经病小鼠模型的代谢物谱:对疾病机制和干预措施的启示

Bais, Preeti; Beebe, Kirk; Morelli, Kathryn H; Currie, Meagan E; Norberg, Sara N; Evsikov, Alexei V; Miers, Kathy E; Seburn, Kevin L; Guergueltcheva, Velina; Kremensky, Ivo; Jordanova, Albena; Bult, Carol J; Burgess, Robert W

Lack of neuropathy-related phenotypes in hint1 knockout mice

hint1基因敲除小鼠缺乏神经病变相关表型

Seburn, Kevin L; Morelli, Kathryn H; Jordanova, Albena; Burgess, Robert W

Motor terminal degeneration unaffected by activity changes in SOD1(G93A) mice; a possible role for glycolysis

SOD1(G93A)小鼠的运动末梢退化不受活动变化的影响;糖酵解可能发挥作用

Carrasco, Dario I; Bichler, Edyta K; Rich, Mark M; Wang, Xueyong; Seburn, Kevin L; Pinter, Martin J

Mutations in a P-type ATPase gene cause axonal degeneration.

P型ATPase基因突变会导致轴突变性

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

A novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations

一种携带D1005G-Npc1突变的尼曼-匹克C型疾病小鼠模型,该突变与常见的人类突变相似。

Maue, Robert A; Burgess, Robert W; Wang, Bing; Wooley, Christine M; Seburn, Kevin L; Vanier, Marie T; Rogers, Maximillian A; Chang, Catherine C; Chang, Ta-Yuan; Harris, Brent T; Graber, David J; Penatti, Carlos A A; Porter, Donna M; Szwergold, Benjamin S; Henderson, Leslie P; Totenhagen, John W; Trouard, Theodore P; Borbon, Ivan A; Erickson, Robert P

Strain-specific hyperkyphosis and megaesophagus in Add1 null mice

Add1基因敲除小鼠的品系特异性脊柱后凸和巨食管症

Robledo, Raymond F; Seburn, Kevin L; Nicholson, Anthony; Peters, Luanne L

Nerve terminal degeneration is independent of muscle fiber genotype in SOD1 mice

在SOD1小鼠中,神经末梢退化与肌肉纤维基因型无关。

Carrasco, Dario I; Bichler, Edyta K; Seburn, Kevin L; Pinter, Martin J

An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy.

小鼠甘氨酰-tRNA合成酶(GARS)中由ENU诱导的突变导致周围感觉和运动表型,从而建立了夏科-马里-图斯2D型周围神经病变模型

Achilli Francesca, Bros-Facer Virginie, Williams Hazel P, Banks Gareth T, AlQatari Mona, Chia Ruth, Tucci Valter, Groves Michael, Nickols Carole D, Seburn Kevin L, Kendall Rachel, Cader Muhammed Z, Talbot Kevin, van Minnen Jan, Burgess Robert W, Brandner Sebastian, Martin Joanne E, Koltzenburg Martin, Greensmith Linda, Nolan Patrick M, Fisher Elizabeth M C