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

PHEX(L222P) Mutation Increases Phex Expression in a New ENU Mouse Model for XLH Disease

PHEX(L222P)突变增加新型ENU小鼠XLH疾病模型中Phex的表达

El Hakam, Carole; Parenté, Alexis; Baraige, Fabienne; Magnol, Laetitia; Forestier, Lionel; Di Meo, Florent; Blanquet, Véronique

Reduced Notch signalling leads to postnatal skeletal muscle hypertrophy in Pofut1cax/cax mice.

Notch 信号传导减弱导致 Pofut1cax/cax 小鼠出生后骨骼肌肥大

Al Jaam Bilal, Heu Katy, Pennarubia Florian, Segelle Alexandre, Magnol Laetitia, Germot Agnès, Legardinier Sébastien, Blanquet Véronique, Maftah Abderrahman

A new Otogelin ENU mouse model for autosomal-recessive nonsyndromic moderate hearing impairment

一种用于研究常染色体隐性遗传非综合征型中度听力障碍的新型 Otogelin ENU 小鼠模型

El Hakam Kamareddin, Carole; Magnol, Laetitia; Blanquet, Veronique

A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome

一种新的Abcg1-U2af1区域三体小鼠模型揭示了唐氏综合征组合遗传密码的复杂性

Pereira, Patricia Lopes; Magnol, Laetitia; Sahún, Ignasi; Brault, Véronique; Duchon, Arnaud; Prandini, Paola; Gruart, Agnès; Bizot, Jean-Charles; Chadefaux-Vekemans, Bernadette; Deutsch, Samuel; Trovero, Fabrice; Delgado-García, José María; Antonarakis, Stylianos E; Dierssen, Mara; Herault, Yann

KIT is required for hepatic function during mouse post-natal development

KIT是小鼠出生后发育过程中肝脏功能所必需的

Magnol, Laetitia; Chevallier, Marie-Clémence; Nalesso, Valérie; Retif, Stéphanie; Fuchs, Helmut; Klempt, Martina; Pereira, Patricia; Riottot, Michel; Andrzejewski, Sandra; Doan, Bich-Thuy; Panthier, Jean-Jacques; Puech, Anne; Beloeil, Jean-Claude; de Angelis, Martin Hrabe; Hérault, Yann