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

Targeting Glioma Stem Cells: Therapeutic Opportunities and Challenges

靶向胶质瘤干细胞:治疗机遇与挑战

Mahdi, Asma; Aittaleb, Mohamed; Tissir, Fadel

A Celsr3 Mutation Linked to Tourette Disorder Disrupts Cortical Dendritic Patterning and Striatal Cholinergic Interneuron Excitability.

与图雷特综合征相关的 Celsr3 突变会破坏皮质树突模式和纹状体胆碱能中间神经元的兴奋性。

Nasello Cara, Yilmaz G Duygu, Poppi Lauren A, Kowalski Tess F, Ho-Nguyen K T, Wu Junbing, Matrongolo Matthew, Thackray Joshua K, Shi Anna, Carayannopoulos Nicolas L, Cheedalla Nithisha, McGinnis Julianne, Chen Jasmine, Khondker Adyan, Tissir Fadel, Heiman Gary A, Tischfield Jay A, Tischfield Max A

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

Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice

人类高置信度图雷特综合征基因的突变会影响小鼠的感觉运动行为、奖赏学习和纹状体多巴胺。

Nasello, Cara; Poppi, Lauren A; Wu, Junbing; Kowalski, Tess F; Thackray, Joshua K; Wang, Riley; Persaud, Angelina; Mahboob, Mariam; Lin, Sherry; Spaseska, Rodna; Johnson, C K; Gordon, Derek; Tissir, Fadel; Heiman, Gary A; Tischfield, Jay A; Bocarsly, Miriam; Tischfield, Max A

Editorial: Advances in understanding synaptic function and its dysfunction in neurological disorders

社论:对突触功能及其在神经系统疾病中功能障碍的理解进展

Mohammad, Farhan; Shaikh, Mohd Farooq; Syed, Yasir Ahmed; Tissir, Fadel

Linking Cell Polarity to Cortical Development and Malformations

细胞极性与皮层发育和畸形之间的联系

Hakanen, Janne; Ruiz-Reig, Nuria; Tissir, Fadel

p73 regulates ependymal planar cell polarity by modulating actin and microtubule cytoskeleton

p73通过调节肌动蛋白和微管细胞骨架来调控室管膜平面细胞极性

Fuertes-Alvarez, Sandra; Maeso-Alonso, Laura; Villoch-Fernandez, Javier; Wildung, Merit; Martin-Lopez, Marta; Marshall, Clayton; Villena-Cortes, Alberto J; Diez-Prieto, Inmaculada; Pietenpol, Jennifer A; Tissir, Fadel; Lizé, Muriel; Marques, Margarita M; Marin, Maria C