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

First evaluation of genetic diversity and population structure of Phelsuma inexpectata (Gekkonidae), a critically endangered gecko endemic to Reunion Island

对留尼汪岛特有的极度濒危壁虎——异斑日行守宫(壁虎科)的遗传多样性和种群结构进行了首次评估

Gomard, Yann; Sanchez, Mickaël; Caubit, Margot; Roesch, Markus A; Bonanno, Alicia; Clémencet, Johanna

Single-Nucleus Analysis of Human White Adipose Tissue Reveals Adipocyte Subsets with Distinct Metabolic Profiles

人类白色脂肪组织单核分析揭示具有不同代谢特征的脂肪细胞亚群

Efthymiou, Vissarion; Ghosh, Adhideb; Kodani, Sean D; Caubit, Xavier; Fasano, Laurent; Ali, Waqar; Poulos, Lindsay S; Camara, Henrique; Gupta, Anushka; Belaidouni, Yasmine; Booeshaghi, A Sina; Yang, Shiyi; Rastogi, Ruchir; Shamsi, Farnaz; Vernon, Ashley; Streets, Aaron; Tseng, Yu-Hua; Patti, Mary Elizabeth

Correction: Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviors

更正:皮质纹状体回路成分中靶向删除Tshz3可分离核心自闭症行为

Caubit, Xavier; Gubellini, Paolo; Roubertoux, Pierre L; Carlier, Michèle; Molitor, Jordan; Chabbert, Dorian; Metwaly, Mehdi; Salin, Pascal; Fatmi, Ahmed; Belaidouni, Yasmine; Brosse, Lucie; Kerkerian-Le Goff, Lydia; Fasano, Laurent

Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviors

皮质纹状体回路成分中的 Tshz3 靶向缺失会导致核心自闭症行为

Xavier Caubit #, Paolo Gubellini #, Pierre L Roubertoux #, Michèle Carlier #, Jordan Molitor, Dorian Chabbert, Mehdi Metwaly, Pascal Salin, Ahmed Fatmi, Yasmine Belaidouni, Lucie Brosse, Lydia Kerkerian-Le Goff, Laurent Fasano

Haploinsufficiency of the mouse Tshz3 gene leads to kidney defects

小鼠 Tshz3 基因单倍体不足导致肾脏缺陷

Irene Sanchez-Martin, Pedro Magalhães, Parisa Ranjzad, Ahmed Fatmi, Fabrice Richard, Thien Phong Vu Manh, Andrew J Saurin, Guylène Feuillet, Colette Denis, Adrian S Woolf, Joost P Schanstra, Petra Zürbig, Xavier Caubit, Laurent Fasano

Camk2a-Cre and Tshz3 Expression in Mouse Striatal Cholinergic Interneurons: Implications for Autism Spectrum Disorder

Camk2a-Cre 和 Tshz3 在小鼠纹状体胆碱能中间神经元中的表达:对自闭症谱系障碍的启示

Caubit, Xavier; Arbeille, Elise; Chabbert, Dorian; Desprez, Florence; Messak, Imane; Fatmi, Ahmed; Habermann, Bianca; Gubellini, Paolo; Fasano, Laurent

TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons

TSHZ3基因缺失会导致自闭症综合征和皮质投射神经元缺陷。

Caubit, Xavier; Gubellini, Paolo; Andrieux, Joris; Roubertoux, Pierre L; Metwaly, Mehdi; Jacq, Bernard; Fatmi, Ahmed; Had-Aissouni, Laurence; Kwan, Kenneth Y; Salin, Pascal; Carlier, Michèle; Liedén, Agne; Rudd, Eva; Shinawi, Marwan; Vincent-Delorme, Catherine; Cuisset, Jean-Marie; Lemaitre, Marie-Pierre; Abderrehamane, Fatimetou; Duban, Bénédicte; Lemaitre, Jean-François; Woolf, Adrian S; Bockenhauer, Detlef; Severac, Dany; Dubois, Emeric; Zhu, Ying; Sestan, Nenad; Garratt, Alistair N; Lydia Kerkerian-Le, Goff; Fasano, Laurent

TSHZ3 and SOX9 regulate the timing of smooth muscle cell differentiation in the ureter by reducing myocardin activity

TSHZ3 和 SOX9 通过降低心肌素活性来调节输尿管平滑肌细胞分化的时间

Elise Martin, Xavier Caubit, Rannar Airik, Christine Vola, Ahmed Fatmi, Andreas Kispert, Laurent Fasano

Teashirt-3, a novel regulator of muscle differentiation, associates with BRG1-associated factor 57 (BAF57) to inhibit myogenin gene expression.

Teashirt-3 是一种新型的肌肉分化调节因子,它与 BRG1 相关因子 57 (BAF57) 结合,抑制肌生成素基因的表达

Faralli Hervé, Martin Elise, Coré Nathalie, Liu Qi-Cai, Filippi Pierre, Dilworth F Jeffrey, Caubit Xavier, Fasano Laurent

Teashirt 3 regulates development of neurons involved in both respiratory rhythm and airflow control

Teashirt 3 调节参与呼吸节律和气流控制的神经元的发育

Xavier Caubit, Muriel Thoby-Brisson, Nicolas Voituron, Pierre Filippi, Michelle Bévengut, Hervé Faralli, Sébastien Zanella, Gilles Fortin, Gérard Hilaire, Laurent Fasano