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

Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humans

CELSR1基因的双等位基因变异会导致人类脑畸形、神经发育障碍和癫痫。

Bonardi, Claudia M; Møller, Rikke S; Ruiz-Reig, Nuria; Chai, Guoliang; Madsen, Camilla G; Bayat, Allan; Hammer, Trine B; Fenger, Christina D; Gardella, Elena; Gawlinski, Pawel; Dawidziuk, Mateusz; Wiszniewski, Wojciech; Bekiesinska-Figatowska, Monika; Cabet, Sara; Rossi, Massimiliano; Lesca, Gaetan; Gouy, Evan; Jepsen, Birgit; Mieszczanek, Tomasz S; Sanchez Russo, Rossana; Barr, Eileen E; Õunap, Katrin; Ilves, Pilvi; Wojcik, Monica H; Aittaleb, Mohamed; Brusgaard, Klaus; Tissir, Fadel; Rubboli, Guido

Loss of DIAPH3 accelerates glioma genesis in mice

DIAPH3 缺失会加速小鼠神经胶质瘤的发生。

Chehade, Georges; Durá, Irene; Ruiz-Reig, Nuria; Damiani, Devid; Lau, Eva On-Chai; Lelotte, Julie; Joudiou, Nicolas; Aittaleb, Mohamed; Tissir, Fadel

Auts2 enhances neurogenesis and promotes expansion of the cerebral cortex.

Auts2 增强神经发生并促进大脑皮层的扩张

Boucherie Cédric, Alkailani Maisa, Jossin Yves, Ruiz-Reig Nuria, Mahdi Asma, Aldaalis Arwa, Aittaleb Mohamed, Tissir Fadel

Competing Programs Shape Cortical Sensorimotor-Association Axis Development.

相互竞争的程序塑造皮层感觉运动联合轴的发育

Tsyporin Jeremiah, Zhang Menglei, Qi Cai, Segal Ashlea, Finn Thomas, Kim Hyojin, Choi Sang-Hun, Li Xinyun, Bandiera Sara, Pavlovic Ivan, Kim Suel-Kee, Shibata Akemi, Onishi Kohei, Zhang Ziqin, Hammarlund Elijah, Su Graham, Salla Nikkita, Kachko Joy, Hawley Christi, Li Shuiyu, Doyle Daniel Z, Peng Xueyan, Nottoli Timothy, Ruiz-Reig Nuria, Tissir Fadel, Nakagawa Yasushi, Herzog Erica, Ma Shaojie, Gobeske Kevin, Pattabiraman Kartik, Shimogori Tomomi, Duque Alvaro, Fornito Alex, Huang Hao, Shibata Mikihito, Chen Bin, Sestan Nenad

DIAPH3 predicts survival of patients with MGMT-methylated glioblastoma

DIAPH3 可预测 MGMT 甲基化胶质母细胞瘤患者的生存率

Georges Chehade, Nady El Hajj, Mohamed Aittaleb, Maisa I Alkailani, Yosra Bejaoui, Asma Mahdi, Arwa A H Aldaalis, Michael Verbiest, Julie Lelotte, Nuria Ruiz-Reig, Irene Durá, Christian Raftopoulos, Nicolas Tajeddine, Fadel Tissir

Aberrant generation of dentate gyrus granule cells is associated with epileptic susceptibility in p53 conditional knockout mice

齿状回颗粒细胞异常生成与 p53 条件性敲除小鼠的癫痫易感性有关

Nuria Ruiz-Reig #, Georges Chehade #, Xavier Yerna, Irene Durá, Philippe Gailly, Fadel Tissir

Inhibitory synapse dysfunction and epileptic susceptibility associated with KIF2A deletion in cortical interneurons

皮质中间神经元 KIF2A 缺失与抑制性突触功能障碍和癫痫易感性相关

Nuria Ruiz-Reig, Dario García-Sánchez, Olivier Schakman, Philippe Gailly, Fadel Tissir

KIF2A deficiency causes early-onset neurodegeneration

KIF2A 缺乏导致早发性神经退行性疾病

Nuria Ruiz-Reig, Georges Chehade, Janne Hakanen, Mohamed Aittaleb, Keimpe Wierda, Joris De Wit, Laurent Nguyen, Philippe Gailly, Fadel Tissir

DIAPH3 deficiency links microtubules to mitotic errors, defective neurogenesis, and brain dysfunction

DIAPH3 缺陷与微管与有丝分裂错误、神经发生缺陷和脑功能障碍有关

Eva On-Chai Lau, Devid Damiani #, Georges Chehade #, Nuria Ruiz-Reig, Rana Saade, Yves Jossin, Mohamed Aittaleb, Olivier Schakman, Nicolas Tajeddine, Philippe Gailly, Fadel Tissir

DIAPH3 deficiency links microtubules to mitotic errors, defective neurogenesis, and brain dysfunction

DIAPH3 缺陷将微管与有丝分裂错误、神经发生缺陷和脑功能障碍联系起来

Eva On-Chai Lau,Devid Damiani #,Georges Chehade #,Nuria Ruiz-Reig,Rana Saade,Yves Jossin,Mohamed Aittaleb,Olivier Schakman,Nicolas Tajeddine,Philippe Gailly,Fadel Tissir