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

Epigenetic priming of neural progenitors by Notch enhances Sonic hedgehog signaling and establishes gliogenic competence

Notch通过表观遗传调控神经祖细胞,增强Sonic hedgehog信号通路,并建立胶质细胞生成能力。

Tran, Luuli N; Shinde, Ashwini; Schuster, Kristen H; Sabaawy, Aiman; Dale, Emily; Welch, Madalynn J; Isner, Trevor J; Nunez, Sylvia A; García-Moreno, Fernando; Sagerström, Charles G; Appel, Bruce H; Franco, Santos J

ASOs are an effective treatment for disease-associated oligodendrocyte signatures in premanifest and symptomatic SCA3 mice.

ASO 可有效治疗 SCA3 前驱期和症状期小鼠的疾病相关少突胶质细胞特征

Schuster Kristen H, Zalon Annie J, DiFranco Danielle M, Putka Alexandra F, Stec Nicholas R, Jarrah Sabrina I, Naeem Arsal, Haque Zaid, Zhang Hanrui, Guan Yuanfang, McLoughlin Hayley S

Antisense Oligonucleotide Silencing Reverses Abnormal Neurochemistry in Spinocerebellar Ataxia 3 Mice

反义寡核苷酸沉默逆转脊髓小脑性共济失调3型小鼠的异常神经化学

McLoughlin, Hayley S; Gundry, Katherine; Rainwater, Orion; Schuster, Kristen H; Wellik, Isabel G; Zalon, Annie J; Benneyworth, Michael A; Eberly, Lynn E; Öz, Gülin

Blood levels of neurofilament light are associated with disease progression in a mouse model of spinocerebellar ataxia type 3

在脊髓小脑性共济失调3型小鼠模型中,神经丝轻链的血液水平与疾病进展相关

Mengel, David; Wellik, Isabel G; Schuster, Kristen H; Jarrah, Sabrina I; Wacker, Madeleine; Ashraf, Naila S; Öz, Gülin; Synofzik, Matthis; Costa, Maria do Carmo; McLoughlin, Hayley S

Blood neurofilament light chain levels are associated with disease progression in a transgenic SCA3 mouse model

在转基因SCA3小鼠模型中,血液神经丝轻链水平与疾病进展相关。

Mengel, David; Wellik, Isabel G; Schuster, Kristen H; Jarrah, Sabrina I; Wacker, Madeleine; Ashraf, Naila S; Öz, Gülin; Synofzik, Matthis; do Carmo Costa, Maria; McLoughlin, Hayley S

Pathogenetic Mechanisms Underlying Spinocerebellar Ataxia Type 3 Are Altered in Primary Oligodendrocyte Culture.

原代少突胶质细胞培养改变了脊髓小脑性共济失调3型的发病机制

Schuster Kristen H, Putka Alexandra F, McLoughlin Hayley S