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

Two distinct fetal-type signatures characterize juvenile myelomonocytic leukemia

幼年型骨髓单核细胞白血病具有两种不同的胎儿型特征。

Strullu, Marion; Arfeuille, Chloé; Caye-Eude, Aurélie; Maillard, Loïc; Lainey, Elodie; Piques, Florian; Cassinat, Bruno; Guimiot, Fabien; Dalle, Jean-Hugues; Baruchel, André; Chomienne, Christine; Bonnet, Dominique; Souyri, Michèle; Cavé, Hélène

Mapping the developmental profile of ventricular zone-derived neurons in the human cerebellum

绘制人类小脑室区衍生神经元的发育图谱

Erickson, Anders W; Tan, Henry; Hendrikse, Liam D; Millman, Jake; Thomson, Zachary; Golser, Joseph; Khan, Omar; He, Guanyi; Bach, Kathleen; Mishra, Arpit Suresh; Kopic, Janja; Krsnik, Zeljka; Encha-Razavi, Ferechte; Petrilli, Giulia; Guimiot, Fabien; Silvestri, Evelina; Aldinger, Kimberly A; Taylor, Michael D; Millen, Kathleen J; Haldipur, Parthiv

Biallelic null RAB3GAP1 variants impair cortical development and autophagy in Warburg Micro syndrome: evidence from fetal brain tissue and patient fibroblasts

双等位基因缺失的 RAB3GAP1 变异体损害 Warburg Micro 综合征的皮质发育和自噬:来自胎儿脑组织和患者成纤维细胞的证据

Emma Noël,Fabien Guimiot,Yline Capri,Marianne Alison,Asha Baskaran,Clémence Delcour,David Germanaud,Sophie Lebon,Caroline Storey,Nicolas de Roux,Adeline Orts-Del'Immagine

Radial Microbrain (Micrencephaly) Is Caused by a Recurrent Variant in the RTTN Gene

放射状小脑畸形(小脑畸形)是由RTTN基因的复发性变异引起的。

Gins, Clarisse; Guimiot, Fabien; Drunat, Séverine; Prévost, Clemence; Rosenblatt, Jonathan; Capri, Yline; Letard, Pascaline; Khung-Savatovsky, Suonavy; Mahi Henni, Mohamed Amine; Elalaoui, Siham Chafai; Alison, Marianne; Guilmin Crepon, Sophie; Gressens, Pierre; Verloes, Alain; Basto, Renata; El Ghouzzi, Vincent; Passemard, Sandrine

MPDZ Pathogenic Variants Cause Obstructive Ventriculomegaly Related to Diencephalosynapsis and Third Ventricle Atresia

MPDZ致病变异导致梗阻性脑室扩大,与间脑融合和第三脑室闭锁相关

Cabet, Sara; Ghersi-Egea, Jean-François; Khung-Savatovsky, Suonavy; Guimiot, Fabien; Putoux, Audrey; Sabatier, Isabelle; Fernandez, Carla; Raymond, Laure; Mortreux, Jérémie; Laurichesse Delmas, Hélène; Cuillier, Fabrice Eric; Ho, Fabien; Lesca, Gaetan; Alessandri, Jean-Luc; Guibaud, Laurent

Long-term Efficacy and Safety of a Hyaluronic Acid-Based Dermal Filler With Tri-Hyal Technology to Enhance Lip Volume

采用Tri-Hyal技术的透明质酸基皮肤填充剂在增强唇部容量方面的长期疗效和安全性

Kestemont, Philippe; Fanian, Ferial; Garcia, Philippe; Grand-Vincent, Anne; Benadiba, Laurent; Delmar, Henry; Bodokh, Isaac; Brun, Patrick; Braccini, Frédéric; Desouches, Christophe; Paris, Jérôme; Guimiot, Ismahane; Salomon, Catherine; Trévidic, Patrick

A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex

细胞命运决策图揭示了人类发育新皮层中大量绕过中间祖细胞的直接神经发生

Laure Coquand #, Clarisse Brunet Avalos #, Anne-Sophie Macé, Sarah Farcy, Amandine Di Cicco, Marusa Lampic, Ryszard Wimmer, Betina Bessières, Tania Attie-Bitach, Vincent Fraisier, Pierre Sens, Fabien Guimiot, Jean-Baptiste Brault, Alexandre D Baffet

New ZNHIT3 Variants Disrupting snoRNP Assembly Cause Prenatal PEHO Syndrome with Isolated Hydrops

破坏 snoRNP 组装的新 ZNHIT3 变体导致产前 PEHO 综合征和孤立性积水

Md Lutfur Rahman, Adeline A Bonnard, Feng Wang, Lyse Ruaud, Fabien Guimiot, Yangping Li, Ines Defer, Yilin Wang, Virginie Marchand, Yuri Motorin, Bing Yao, Séverine Drunat, Homa Ghalei

Immunologic aspects of preeclampsia

先兆子痫的免疫学方面

Boulanger, Henri; Bounan, Stéphane; Mahdhi, Amel; Drouin, Dominique; Ahriz-Saksi, Salima; Guimiot, Fabien; Rouas-Freiss, Nathalie

Reply to Pubpeer anonymous contributors: incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1

回复 Pubpeer 匿名贡献者:6q16 缺失(包括 SIM1)的不完全外显率和表型变异性

El Khattabi, Laila; Guimiot, Fabien; Delahaye-Duriez, Andrée