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

Imaging Human Pancreatic Endocrinogenesis During Early Prenatal Life

早期产前生命阶段人类胰腺内分泌发生过程的成像

Villalba, Adrian; Gitton, Yorick; Aiello, Virginie; Toupin, Maryne; Mazaud-Guittot, Séverine; Chédotal, Alain; Scharfmann, Raphaël

Probing the origin of matching functional jaws: roles of Dlx5/6 in cranial neural crest cells

探究功能性颌骨的起源:Dlx5/6在颅神经嵴细胞中的作用

Shimizu, Miki; Narboux-Nême, Nicolas; Gitton, Yorick; de Lombares, Camille; Fontaine, Anastasia; Alfama, Gladys; Kitazawa, Taro; Kawamura, Yumiko; Heude, Eglantine; Marshall, Lindsey; Higashiyama, Hiroki; Wada, Youichiro; Kurihara, Yukiko; Kurihara, Hiroki; Levi, Giovanni

The untold stories of the speech gene, the FOXP2 cancer gene

鲜为人知的语言基因故事,FOXP2 癌症基因

Herrero, Maria Jesus; Gitton, Yorick

The Dlx5 and Foxg1 transcription factors, linked via miRNA-9 and -200, are required for the development of the olfactory and GnRH system.

Dlx5 和 Foxg1 转录因子通过 miRNA-9 和 -200 连接,是嗅觉和 GnRH 系统发育所必需的

Garaffo Giulia, Conte Daniele, Provero Paolo, Tomaiuolo Daniela, Luo Zheng, Pinciroli Patrizia, Peano Clelia, D'Atri Ilaria, Gitton Yorick, Etzion Talya, Gothilf Yoav, Gays Dafne, Santoro Massimo M, Merlo Giorgio R

Transitory expression of Dlx5 and Dlx6 in maxillary arch epithelial precursors is essential for upper jaw morphogenesis

上颌弓上皮前体细胞中Dlx5和Dlx6的短暂表达对上颌形态发生至关重要

Gitton, Yorick; Narboux-Nême, Nicolas; Levi, Giovanni

Efficient CPP-mediated Cre protein delivery to developing and adult CNS tissues

高效地利用CPP介导的Cre蛋白递送至发育中和成年的中枢神经系统组织

Gitton, Yorick; Tibaldi, Lorenzo; Dupont, Edmond; Levi, Giovanni; Joliot, Alain

Role of heat-shock factor 2 in cerebral cortex formation and as a regulator of p35 expression

热休克因子2在大脑皮层形成中的作用及其作为p35表达调节因子的作用

Chang, Yunhua; Ostling, Päivi; Akerfelt, Malin; Trouillet, Diane; Rallu, Murielle; Gitton, Yorick; El Fatimy, Rachid; Fardeau, Vivienne; Le Crom, Stéphane; Morange, Michel; Sistonen, Lea; Mezger, Valérie

Brain abnormalities, defective meiotic chromosome synapsis and female subfertility in HSF2 null mice

HSF2基因敲除小鼠出现脑部异常、减数分裂染色体联会缺陷和雌性生育力低下。

Kallio, Marko; Chang, Yunhua; Manuel, Martine; Alastalo, Tero-Pekka; Rallu, Murielle; Gitton, Yorick; Pirkkala, Lila; Loones, Marie-Thérèse; Paslaru, Liliana; Larney, Severine; Hiard, Sophie; Morange, Michel; Sistonen, Lea; Mezger, Valérie