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

Erratum to: "Optimizing CRISPR methodology for precise gene editing in the erythroid cell line BEL-A with high efficiency generation of a sickle cell anemia model"

更正:“优化 CRISPR 方法,以在红系细胞系 BEL-A 中进行精确基因编辑,并高效构建镰状细胞贫血模型”

Daniels, Deborah E; Hawksworth, Joseph; El Hoss, Sara; Oyawoye, Fatima O; Ferrer-Vicens, Ivan; Wilson, Marieangela C; Frayne, Jan

MMS22L is a novel key actor of normal and pathological erythropoiesis

MMS22L是正常和病理性红细胞生成过程中的一个新型关键因子

Colin, Elia; Ferrer-Vicens, Ivan; Brook, Dror; Salma, Mohammad; Andrieu-Soler, Charlotte; Bayard, Elisa; Fernandes, Alicia; Brouzes, Chantal; Lefèvre, Carine; Duval, Romain; Dussiot, Michaël; Trovati, Thiago; Courtois, Geneviève; Azouzi, Slim; Zarhrate, Mohammed; Lambilliotte, Anne; Park, Sophie; Carpentier, Benjamin; Colard, Martin; Manceau, Sandra; Moshous, Despina; Mayeux, Patrick; Gautier, Emilie-Fleur; Miccio, Annarita; Soulier, Jean; Vainchenker, William; Shlush, Liran; Da Costa, Lydie; Frayne, Jan; Soler, Eric; Hermine, Olivier; Couronné, Lucile

Optimizing CRISPR methodology for precise gene editing in the erythroid cell line BEL-A with high efficiency generation of a sickle cell anemia model

优化 CRISPR 技术,以高效构建镰状细胞贫血模型,从而在红系细胞系 BEL-A 中实现精准基因编辑。

Daniels, Deborah E; Hawksworth, Joseph; El Hoss, Sara; Oyawoye, Fatima O; Ferrer-Vicens, Ivan; Wilson, Marieangela C; Frayne, Jan

Enhancement of red blood cell transfusion compatibility using CRISPR-mediated erythroblast gene editing

利用CRISPR介导的成红细胞基因编辑增强红细胞输注相容性

Hawksworth, Joseph; Satchwell, Timothy J; Meinders, Marjolein; Daniels, Deborah E; Regan, Fiona; Thornton, Nicole M; Wilson, Marieangela C; Dobbe, Johannes Gg; Streekstra, Geert J; Trakarnsanga, Kongtana; Heesom, Kate J; Anstee, David J; Frayne, Jan; Toye, Ashley M

Secretory factors from OP9 stromal cells delay differentiation and increase the expansion potential of adult erythroid cells in vitro.

OP9 基质细胞分泌的因子可延缓分化,并增加体外成红细胞的扩增潜力

Trakarnsanga Kongtana, Wilson Marieangela C, Heesom Kate J, Andrienko Tatyana N, Srisawat Chatchawan, Frayne Jan

Structure of insoluble rat sperm glyceraldehyde-3-phosphate dehydrogenase (GAPDH) via heterotetramer formation with Escherichia coli GAPDH reveals target for contraceptive design

通过与大肠杆菌GAPDH形成异源四聚体解析不溶性大鼠精子甘油醛-3-磷酸脱氢酶(GAPDH)的结构,揭示了其作为避孕药设计靶点的价值。

Frayne, Jan; Taylor, Abby; Cameron, Gus; Hadfield, Andrea T