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

Tropomyosin isoforms encoded by TPM2 control the actin-bundling activity of fascin-1.

由 TPM2 编码的原肌球蛋白同工型控制着 fascin-1 的肌动蛋白束集活性

Siatkowska Małgorzata, Robaszkiewicz Katarzyna, Rousová Andrea, Navrátil Jiří, Knopfová Lucia, Talián Gábor, Beneš Petr, Moraczewska Joanna

A Novel Variant in TPM3 Causing Muscle Weakness and Concomitant Hypercontractile Phenotype

TPM3基因新变异导致肌肉无力及伴随的过度收缩表型

Robaszkiewicz, Katarzyna; Siatkowska, Małgorzata; Wadman, Renske I; Kamsteeg, Erik-Jan; Chen, Zhiyong; Merve, Ashirwad; Parton, Matthew; Bugiardini, Enrico; de Bie, Charlotte; Moraczewska, Joanna

Troponin and a Myopathy-Linked Mutation in TPM3 Inhibit Cofilin-2-Induced Thin Filament Depolymerization

肌钙蛋白和TPM3中与肌病相关的突变抑制cofilin-2诱导的细丝解聚

Robaszkiewicz, Katarzyna; Wróbel, Julia; Moraczewska, Joanna

Mutations Q93H and E97K in TPM2 Disrupt Ca-Dependent Regulation of Actin Filaments

TPM2 中的 Q93H 和 E97K 突变破坏了肌动蛋白丝的钙依赖性调节

Śliwinska, Małgorzata; Robaszkiewicz, Katarzyna; Wasąg, Piotr; Moraczewska, Joanna

Congenital myopathy-related mutations in tropomyosin disrupt regulatory function through altered actin affinity and tropomodulin binding

先天性肌病相关的原肌球蛋白突变会通过改变肌动蛋白亲和力和原肌球蛋白调节蛋白结合能力来破坏其调节功能。

Moraczewska, Joanna; Robaszkiewicz, Katarzyna; Śliwinska, Małgorzata; Czajkowska, Marta; Ly, Thu; Kostyukova, Alla; Wen, Han; Zheng, Wenjun