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

Repeat-associated non-AUG translation as a common mechanism for the polyGln ataxias

重复序列相关的非AUG翻译是多聚谷氨酰胺共济失调的常见机制

Banez-Coronel, Monica; Zu, Tao; Aldridge, Madeline; Guo, Shu; Ajredini, Ramadan; Morrison, Deborah; Tays, Alexis B; Duvick, Lisa A; Pletnikova, Olga; Yachnis, Anthony T; Troncoso, Juan C; Paulson, Henry L; McLoughlin, Hayley S; Ashizawa, Tetsuo; Subramony, S H; Orr, Harry T; Ranum, Laura P W

Neural basis for mutant ATAXIN-1 induced respiratory dysfunction in mouse models of spinocerebellar ataxia type 1

突变型共济失调1型小鼠模型中ATAXIN-1诱导呼吸功能障碍的神经基础

Soles, Alyssa; Grittner, Jessica; Douglas, Kaia; Yang, Praseuth; Duvick, Lisa; O'Callaghan, Brennon; Barnett, Ryan; Chau, Christine; Cosiquien, Roj; Rainwater, Orion; Serres, Shannah; Dougherty, Brendan; Orr, Harry T; Cvetanovic, Marija

An expanded polyglutamine in ATAXIN1 results in a loss-of-function that exacerbates severity of Multiple Sclerosis in an EAE mouse model

ATAXIN1 中多聚谷氨酰胺的扩增导致其功能丧失,从而加剧 EAE 小鼠模型中多发性硬化症的严重程度。

Talukdar, Gourango; Duvick, Lisa; Yang, Praseuth; O'Callaghan, Brennon; Fuchs, Gavin J; Cvetanovic, Marija; Orr, Harry T

Striatal pathology in Spinocerebellar Ataxia Type 1 mice: A comparative study with Huntington's disease

脊髓小脑性共济失调1型小鼠纹状体病理:与亨廷顿病的比较研究

Goel, Pragya; Yang, Praseuth; Duvick, Lisa; Rainwater, Orion; Serres, Shannah; O'Callaghan, Brennon; Gomez-Pastor, Rocio; Mehkary, Mustafa; Gall-Duncan, Terence; Langfelder, Peter; Yang, X William; Pearson, Christopher E; Rothwell, Patrick E; Orr, Harry T

Dysregulation of zebrin-II cell subtypes in the cerebellum is a shared feature across polyglutamine ataxia mouse models and patients

小脑中 zebrin-II 细胞亚型的失调是多聚谷氨酰胺共济失调小鼠模型和患者的共同特征

Luke C Bartelt, Pawel M Switonski, Grażyna Adamek, Fabiana Longo, Juliana Carvalho, Lisa A Duvick, Sabrina I Jarrah, Hayley S McLoughlin, Daniel R Scoles, Stefan M Pulst, Harry T Orr, Court Hull, Craig B Lowe, Albert R La Spada0

Mapping SCA1 regional vulnerabilities reveals neural and skeletal muscle contributions to disease

绘制 SCA1 区域脆弱性图可揭示神经和骨骼肌对疾病的贡献

Lisa Duvick, W Michael Southern, Kellie A Benzow, Zoe N Burch, Hillary P Handler, Jason S Mitchell, Hannah Kuivinen, Udaya Gadiparthi, Praseuth Yang, Alyssa Soles, Carrie A Sheeler, Orion Rainwater, Shannah Serres, Erin B Lind, Tessa Nichols-Meade, Yun You, Brennon O'Callaghan, Huda Y Zoghbi, Marija

Expanded ATXN1 alters transcription and calcium signaling in SCA1 human motor neurons differentiated from induced pluripotent stem cells.

扩增的 ATXN1 会改变由诱导多能干细胞分化而来的 SCA1 人类运动神经元的转录和钙信号传导

Sheeler Carrie, Labrada Emmanuel, Duvick Lisa, Thompson Leslie M, Zhang Ying, Orr Harry T, Cvetanovic Marija

A Neural Basis for Mutant ATAXIN-1 Induced Respiratory Dysfunction in Mouse Models of Spinocerebellar Ataxia Type 1

突变型共济失调1型小鼠模型中ATAXIN-1诱导呼吸功能障碍的神经基础

Soles, Alyssa; Grittner, Jessica; Douglas, Kaia; Yang, Praseuth; Barnett, Ryan; Chau, Christine; Cosiquien, Roj; Duvick, Lisa; Rainwater, Orion; Serres, Shannah; Orr, Harry; Dougherty, Brendan; Cvetanovic, Marija

Decreasing mutant ATXN1 nuclear localization improves a spectrum of SCA1-like phenotypes and brain region transcriptomic profiles

降低突变型 ATXN1 的核定位可改善一系列 SCA1 样表型和脑区转录组谱

Hillary P Handler, Lisa Duvick, Jason S Mitchell, Marija Cvetanovic, Molly Reighard, Alyssa Soles, Kathleen B Mather, Orion Rainwater, Shannah Serres, Tessa Nichols-Meade, Stephanie L Coffin, Yun You, Brian L Ruis, Brennon O'Callaghan, Christine Henzler, Huda Y Zoghbi, Harry T Orr

Delineating regional vulnerability in the neurodegenerative disease SCA1 using a conditional mutant ATXN1 mouse

使用条件突变 ATXN1 小鼠描绘神经退行性疾病 SCA1 的区域脆弱性

Lisa Duvick, W Michael Southern, Kellie Benzow, Zoe N Burch, Hillary P Handler, Jason S Mitchell, Hannah Kuivinen, Udaya Keerthy Gadiparthi, Praseuth Yang, Alyssa Soles, Carrie Scheeler, Orion Rainwater, Shannah Serres, Erin Lind, Tessa Nichols-Meade, Brennon O'Callaghan, Huda Y Zoghbi, Marija Cveta