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

The ups and downs of Pax6 in neural stem cells

Pax6在神经干细胞中的起伏

Shohayeb, Belal; Cooper, Helen M

Hydrocephalus in Nfix(-/-) Mice Is Underpinned by Changes in Ependymal Cell Physiology.

Nfix(-/-) 小鼠的脑积水是由室管膜细胞生理变化引起的

Harkins Danyon, Harvey Tracey J, Atterton Cooper, Miller Ingrid, Currey Laura, Oishi Sabrina, Kasherman Maria, Davila Raul Ayala, Harris Lucy, Green Kathryn, Piper Hannah, Parton Robert G, Thor Stefan, Cooper Helen M, Piper Michael

Adherens Junctions: Guardians of Cortical Development

黏着连接:皮层发育的守护者

Veeraval, Lenin; O'Leary, Conor J; Cooper, Helen M

DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome

DCC基因突变最新进展:先天性镜像运动、孤立性胼胝体发育不全和发育性裂脑综合征

Marsh, Ashley P L; Edwards, Timothy J; Galea, Charles; Cooper, Helen M; Engle, Elizabeth C; Jamuar, Saumya S; Méneret, Aurélie; Moutard, Marie-Laure; Nava, Caroline; Rastetter, Agnès; Robinson, Gail; Rouleau, Guy; Roze, Emmanuel; Spencer-Smith, Megan; Trouillard, Oriane; Billette de Villemeur, Thierry; Walsh, Christopher A; Yu, Timothy W; Heron, Delphine; Sherr, Elliott H; Richards, Linda J; Depienne, Christel; Leventer, Richard J; Lockhart, Paul J

DCC Confers Susceptibility to Depression-like Behaviors in Humans and Mice and Is Regulated by miR-218

DCC 使人类和小鼠易患抑郁样行为,并受 miR-218 调控

Torres-Berrío, Angélica; Lopez, Juan Pablo; Bagot, Rosemary C; Nouel, Dominique; Dal Bo, Gregory; Cuesta, Santiago; Zhu, Lei; Manitt, Colleen; Eng, Conrad; Cooper, Helen M; Storch, Kai-Florian; Turecki, Gustavo; Nestler, Eric J; Flores, Cecilia

Sonic hedgehog and notch signaling can cooperate to regulate neurogenic divisions of neocortical progenitors.

Sonic hedgehog 和 notch 信号通路可以协同调节新皮层祖细胞的神经发生分裂

Dave Richa K, Ellis Tammy, Toumpas Melissa C, Robson Jonathan P, Julian Elaine, Adolphe Christelle, Bartlett Perry F, Cooper Helen M, Reynolds Brent A, Wainwright Brandon J

Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling

与常染色体显性遗传性进行性眼外肌麻痹相关的Twinkle基因突变会导致解旋酶功能受损和体内mtDNA复制停滞。

Goffart, Steffi; Cooper, Helen M; Tyynismaa, Henna; Wanrooij, Sjoerd; Suomalainen, Anu; Spelbrink, Johannes N