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

Neuronal Cell-Cycle Re-entry Defines Divergent Outcomes Through Replication-Dependent DNA Damage in ALS

神经元细胞周期再进入通过ALS中复制依赖性DNA损伤决定不同的结局

Plessis-Belair, Jonathan; Sher, Roger B

Nuclear Import Defects Drive Cell Cycle Dysregulation in Neurodegeneration

核输入缺陷驱动神经退行性疾病中的细胞周期失调

Plessis-Belair, Jonathan; Russo, Taylor; Riessland, Markus; Sher, Roger B

LINE-1 retrotransposition in a mouse TDP-43 model of neurodegeneration marks motor cortex neurons for cell-intrinsic and cell non-autonomous programmed cell death.

在小鼠 TDP-43 神经退行性疾病模型中,LINE-1 逆转座标记运动皮层神经元发生细胞内在和非细胞自主的程序性细胞死亡。

Korada Shreevidya, Tam Oliver H, Greco Hunter C, Hammell Molly Gale, Dubnau Josh, Sher Roger B

Validity of the 2021 Traumatic Encephalopathy Syndrome Criteria for CTE pathology

2021年创伤性脑病综合征诊断标准对慢性创伤性脑病病理的有效性

Plessis-Belair, Jonathan; Russo, Taylor; Riessland, Markus; Sher, Roger B; Groot, Colin; Calandri, Ismael Luis; Bader, Ilse; Bocancea, Diana I; de Bruin, Hannah; Carrigan, Maria; Kamps, Suzie; de Koning, Lotte A; Mastenbroek, Sophie E; Rikken, Roos M; van Tol, Bastiaan G J; Vermeiren, Marie R; Wesseling, Alex J; Xia, Ye; Teunissen, Charlotte E; van de Giessen, Elsmarieke; Barkhof, Frederik; Jonkman, Laura E; van der Lee, Sven J; de Boer, Casper; Rozemuller, Annemieke JM; Duits, Floor; Tijms, Betty M; van der Flier, Wiesje M; Pijnenburg, Yolande AL; Coomans, Emma M; Ossenkoppele, Rik; Jenkins, Dorea P; Davis, Laura; Belk, Jennifer; Ackerman, Michelle; Carter, Shelby; Hamlett, Eric D; Carroll, Steven L; Mez, Jesse; Dwyer, Brigid; Alosco, Michael L; Yew, Belinda; Pritchett, Alexandra; Fernández, Natalia Bernal; Hicks, Amelia J; Abdolmohammadi, Bobak; Durape, Shruti; Uretsky, Madeline; Ryder, Megan H; Faheem, Farwa; Novak, Sophia; Martin, Brett; Palmisano, Joseph N; Nowinski, Christopher J; Tripodis, Yorghos; Dams‐O'Connor, Kristen; Goldstein, Lee E; Katz, Douglas I; Cantu, Robert C; Kowall, Neil W; Stern, Robert A; Alvarez, Victor E; Huber, Bertrand Russell; Crary, John F; Stein, Thor D; Daneshvar, Daniel H; McKee, Ann C

NEMF mutations in mice illustrate how Importin-β specific nuclear transport defects recapitulate neurodegenerative disease hallmarks

小鼠的NEMF突变表明,Importin-β特异性核转运缺陷如何重现神经退行性疾病的特征。

Plessis-Belair, Jonathan; Ravano, Kathryn; Han, Ellen; Janniello, Aubrey; Molina, Catalina; Sher, Roger B

Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease

在运动神经元疾病的突变型动力蛋白p150Glued小鼠模型中鉴定生存相关的数量性状基因座

Alexander, Guillermo M; Heiman-Patterson, Terry D; Bearoff, Frank; Sher, Roger B; Hennessy, Laura; Terek, Shannon; Caccavo, Nicole; Cox, Gregory A; Philip, Vivek M; Blankenhorn, Elizabeth A

Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

作者更正:NEMF基因突变会损害核糖体相关的质量控制,而这些突变与神经肌肉疾病有关。

Martin, Paige B; Kigoshi-Tansho, Yu; Sher, Roger B; Ravenscroft, Gianina; Stauffer, Jennifer E; Kumar, Rajesh; Yonashiro, Ryo; Müller, Tina; Griffith, Christopher; Allen, William; Pehlivan, Davut; Harel, Tamar; Zenker, Martin; Howting, Denise; Schanze, Denny; Faqeih, Eissa A; Almontashiri, Naif A M; Maroofian, Reza; Houlden, Henry; Mazaheri, Neda; Galehdari, Hamid; Douglas, Ganka; Posey, Jennifer E; Ryan, Monique; Lupski, James R; Laing, Nigel G; Joazeiro, Claudio A P; Cox, Gregory A

Functional rescue in a mouse model of congenital muscular dystrophy with megaconial myopathy

在先天性肌营养不良伴巨锥肌病的鼠模型中实现功能性挽救

Sayed-Zahid, Ambreen A; Sher, Roger B; Sukoff Rizzo, Stacey J; Anderson, Laura C; Patenaude, Kathryn E; Cox, Gregory A

Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease

遗传背景对突变型动力蛋白p150Glued小鼠运动神经元疾病模型的发病和寿命的影响

Heiman-Patterson, Terry D; Blankenhorn, Elizabeth P; Sher, Roger B; Jiang, Juliann; Welsh, Priscilla; Dixon, Meredith C; Jeffrey, Jeremy I; Wong, Philip; Cox, Gregory A; Alexander, Guillermo M

A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesis

一种先天性肌营养不良症,伴有线粒体结构异常,由磷脂酰胆碱从头合成缺陷引起。

Mitsuhashi, Satomi; Ohkuma, Aya; Talim, Beril; Karahashi, Minako; Koumura, Tomoko; Aoyama, Chieko; Kurihara, Mana; Quinlivan, Ros; Sewry, Caroline; Mitsuhashi, Hiroaki; Goto, Kanako; Koksal, Burcu; Kale, Gulsev; Ikeda, Kazutaka; Taguchi, Ryo; Noguchi, Satoru; Hayashi, Yukiko K; Nonaka, Ikuya; Sher, Roger B; Sugimoto, Hiroyuki; Nakagawa, Yasuhito; Cox, Gregory A; Topaloglu, Haluk; Nishino, Ichizo