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Biochimica Et Biophysica Acta|July 4, 2012
Functional effects of congenital myopathy-related mutations in gamma-tropomyosin geneKatarzyna Robaszkiewicz, Elżbieta Dudek, Andrzej A Kasprzak, et al.
The FEBS Journal|July 14, 2025
Myopathy-linked mutations in TPM2 and their impact on troponin-mediated regulation of actomyosin contractilityRecep Küçükdogru, Katarzyna Robaszkiewicz, Małgorzata Siatkowska, et al.
Analytical Biochemistry|July 9, 2009
Differential binding of tropomyosin isoforms to actin modified with m-maleimidobenzoyl-N-hydroxysuccinimide ester and fluorescein-5-isothiocyanateRadosław Skórzewski, Katarzyna Robaszkiewicz, Justyna Jarzebińska, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 29, 2023
Mechanochemical consequences of myopathy-linked mutations in Tpm2.2 on striated muscle contractilityRecep Küçükdogru, Peter Franz, Remigiusz Worch, et al.
The FEBS Journal|February 16, 2019
Congenital myopathy-related mutations in tropomyosin disrupt regulatory function through altered actin affinity and tropomodulin bindingJoanna Moraczewska, Katarzyna Robaszkiewicz, Małgorzata Śliwinska, et al.
Biological Research|August 31, 2025
Tropomyosin isoforms encoded by TPM2 control the actin-bundling activity of fascin-1Małgorzata Siatkowska, Katarzyna Robaszkiewicz, Andrea Rousová, et al.
International Journal of Molecular Sciences|November 25, 2023
A Novel Variant in TPM3 Causing Muscle Weakness and Concomitant Hypercontractile PhenotypeKatarzyna Robaszkiewicz, Małgorzata Siatkowska, Renske I Wadman, et al.
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