Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes
SRP19 和 SRPRA 基因的人类遗传缺陷会导致严重的先天性中性粒细胞减少症,并伴有独特的蛋白质组变化。
期刊:Blood
影响因子:23.1
doi:10.1182/blood.2022016783
Linder, Monika I; Mizoguchi, Yoko; Hesse, Sebastian; Csaba, Gergely; Tatematsu, Megumi; Łyszkiewicz, Marcin; Ziȩtara, Natalia; Jeske, Tim; Hastreiter, Maximilian; Rohlfs, Meino; Liu, Yanshan; Grabowski, Piotr; Ahomaa, Kaarin; Maier-Begandt, Daniela; Schwestka, Marko; Pazhakh, Vahid; Isiaku, Abdulsalam I; Briones Miranda, Brenda; Blombery, Piers; Saito, Megumu K; Rusha, Ejona; Alizadeh, Zahra; Pourpak, Zahra; Kobayashi, Masao; Rezaei, Nima; Unal, Ekrem; Hauck, Fabian; Drukker, Micha; Walzog, Barbara; Rappsilber, Juri; Zimmer, Ralf; Lieschke, Graham J; Klein, Christoph