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

Fetal-restricted hematopoietic progenitors arise from hemogenic endothelium in vitelline and umbilical arteries

胎儿特有的造血祖细胞来源于卵黄动脉和脐动脉中的造血内皮细胞。

Barone, Cristiana; Quattrini, Giulia; Muratore, Alessandro; Anselmi, Giorgio; Park, Yurim; Mehmood, Naeema T; Morganti, Elena; Orsenigo, Roberto; Timóteo-Ferreira, Filipa; Cazzola, Anna; Patelli, Arianna; Milanesi, Thea; Nesti, Bianca; Soares-da-Silva, Francisca; Nicholls, Matthew; Zambelli, Gloria; Mauri, Mario; Bombelli, Silvia; De Marco, Sofia; D'Aliberti, Deborah; Spinelli, Silvia; Bonalume, Veronica; Domingues, Alison; Naghavi Alhosseini, Mahdieh; Sala, Gianluca; Colonna, Arianna; D'Errico, Elisabetta; D'Orlando, Cristina; Bianchi, Cristina; Perego, Roberto A; Meneveri, Raffaella; Cumano, Ana; Brunelli, Silvia; De Bruijn, Marella F T R; Ditadi, Andrea; Fantin, Alessandro; Piazza, Rocco; Azzoni, Emanuele

Bloodhounds chasing the origin of blood cells

寻血猎犬追寻血细胞的起源

Randolph, Lauren N; Castiglioni, Claudia; Tavian, Manuela; Sturgeon, Christopher M; Ditadi, Andrea

Refined and benchmarked homemade media for cost-effective, weekend-free human pluripotent stem cell culture.

经过改进和基准测试的自制培养基,可实现经济高效、无需周末的人类多能干细胞培养。

Truszkowski Lukasz, Bottini Sveva, Bianchi Sara, Scrivano Mirko G, Ramondo Giulia Ferrari, Belluci Linda, Bell Helen, Becca Silvia, Snijders Kirsten E, Savorè Giulia, Sozza Federica, Ricca Irene, Rubinetto Cristina, Ferrara Luana, Neri Francesco, Ditadi Andrea, Oliviero Savatore, Balmas Elisa, Elton Catherine, Bertero Alessandro

Let Me Speak! A Reviewers' Guide to Writing a Successful Meeting Abstract

让我发言!审稿人撰写成功会议摘要指南

Sturgeon, Christopher M; Ditadi, Andrea

Wnt signaling controls the specification of definitive and primitive hematopoiesis from human pluripotent stem cells

Wnt信号通路控制着人类多能干细胞分化为终末造血和原始造血细胞。

Sturgeon, Christopher M; Ditadi, Andrea; Awong, Geneve; Kennedy, Marion; Keller, Gordon

Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness.

人类腺苷酸激酶 2 缺乏症会导致严重的造血缺陷,并伴有感觉神经性耳聋

Lagresle-Peyrou Chantal, Six Emmanuelle M, Picard Capucine, Rieux-Laucat Frédéric, Michel Vincent, Ditadi Andrea, Demerens-de Chappedelaine Corinne, Morillon Estelle, Valensi Françoise, Simon-Stoos Karen L, Mullikin James C, Noroski Lenora M, Besse Céline, Wulffraat Nicolas M, Ferster Alina, Abecasis Manuel M, Calvo Fabien, Petit Christine, Candotti Fabio, Abel Laurent, Fischer Alain, Cavazzana-Calvo Marina