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

Fancl-mutant mice reveal central role of monoubiquitination in Fanconi anemia and a model for therapeutic gene editing

Fancl突变小鼠揭示了单泛素化在范可尼贫血症中的核心作用,并为治疗性基因编辑提供了一种模型。

Liu, Lu; Glaser, Astrid; Isiaku, Abdulsalam I; Fairfax, Kirsten; Casolari, Debora A; Ristovski, Angelina; Murphy, Vincent; van Twest, Sylvie; Henrikus, Sarah S; Heraud-Farlow, Jacki; Granger, Elissah; Novakovic, Stevan; Monks O'Byrne, Sophie F; Tsui, Vanessa; Conyers, Rachel; Gonda, Thomas J; Crismani, Wayne; D'Andrea, Richard J; Heierhorst, Jörg; Deans, Andrew J

Beyond blood pressure and glucose: exploring potential biochemical predictors of cardiovascular disease risk in patients with type 2 diabetes mellitus and co-morbid hypertension

超越血压和血糖:探索2型糖尿病合并高血压患者心血管疾病风险的潜在生化预测因子

Basil, Bruno; Mohammed, Jamila Aminu; Mba, Izuchukwu Nnachi; Nkemakolam, Isiaku Mary; Myke-Mbata, Blessing Kenechi

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。

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