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

Histone H2A variant H2A.B is enriched in transcriptionally active and replicating HSV-1 lytic chromatin

组蛋白 H2A 变体 H2A.B 在转录活性和复制的 HSV-1 裂解染色质中富集

Esteban Flores Cortes, Sarah M Saddoris, Arryn K Owens, Rebecca Gibeault, Daniel P Depledge, Luis M Schang

Histone H2A variant H2A.B is enriched in transcriptionally active HSV-1 lytic chromatin

组蛋白H2A变体H2A.B在转录活跃的HSV-1裂解染色质中富集。

Flores, Esteban; Saddoris, Sarah M; Owens, Arryn K; Gibeault, Rebecca; Depledge, Daniel P; Schang, Luis M

Field dataset of punctual observations of soil properties and vegetation types distributed along soil moisture gradients in France

法国土壤湿度梯度分布的土壤性质和植被类型点观测实地数据集

Gayet, Guillaume; Botcazou, François; Gibeault-Rousseau, Jean-Manuel; Hubert-Moy, Laurence; Rapinel, Sébastien; Lemercier, Blandine

An Essential Viral Transcription Activator Modulates Chromatin Dynamics

一种重要的病毒转录激活因子调节染色质动力学

Gibeault, Rebecca L; Conn, Kristen L; Bildersheim, Michael D; Schang, Luis M

Effect of genetic background on the phenotype of the Smn2B/- mouse model of spinal muscular atrophy

遗传背景对脊髓性肌萎缩症Smn2B/-小鼠模型表型的影响

Eshraghi, Mehdi; McFall, Emily; Gibeault, Sabrina; Kothary, Rashmi

Cytoskeletal Linker Protein Dystonin Is Not Critical to Terminal Oligodendrocyte Differentiation or CNS Myelination

细胞骨架连接蛋白肌张力蛋白对终末少突胶质细胞分化或中枢神经系统髓鞘形成并非至关重要。

Kornfeld, Samantha F; Lynch-Godrei, Anisha; Bonin, Sawyer R; Gibeault, Sabrina; De Repentigny, Yves; Kothary, Rashmi

Disruption in the autophagic process underlies the sensory neuropathy in dystonia musculorum mice

自噬过程中断是肌张力障碍小鼠感觉神经病变的根本原因

Andrew Ferrier, Yves De Repentigny, Anisha Lynch-Godrei, Sabrina Gibeault, Walaa Eid, Daniel Kuo, Xiaohui Zha, Rashmi Kothary

Viral reprogramming of the Daxx histone H3.3 chaperone during early Epstein-Barr virus infection

早期 Epstein-Barr 病毒感染期间 Daxx 组蛋白 H3.3 分子伴侣的病毒重编程

Kevin Tsai, Lilian Chan, Rebecca Gibeault, Kristen Conn, Jayaraju Dheekollu, John Domsic, Ronen Marmorstein, Luis M Schang, Paul M Lieberman

Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI

神经元肌张力障碍蛋白亚型 2 的转基因表达可部分挽救遗传性感觉自主神经病 VI 型肌张力障碍小鼠模型的疾病表型

Ferrier, Andrew; Sato, Tadasu; De Repentigny, Yves; Gibeault, Sabrina; Bhanot, Kunal; O'Meara, Ryan W; Lynch-Godrei, Anisha; Kornfeld, Samantha F; Young, Kevin G; Kothary, Rashmi