Dmitrii I. Levitsky
Moscow, MOW 119071, Russian Federation
Last Updated: 09/26/2026
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Found 47 publications
Novel Mutation Lys30Glu in the TPM1 Gene Leads to Pediatric Left Ventricular Non-Compaction and Dilated Cardiomyopathy via Impairment of Structural and Functional Properties of Cardiac Tropomyosin.
Journal: International journal of molecular sciences
Published: October 31, 2024
Functional and Structural Properties of Cytoplasmic Tropomyosin Isoforms Tpm1.8 and Tpm1.9.
Journal: International journal of molecular sciences
Published: May 14, 2024
Myopathy-causing mutation R91P in the TPM3 gene drastically impairs structural and functional properties of slow skeletal muscle tropomyosin γβ-heterodimer.
Journal: Archives of biochemistry and biophysics
Published: November 07, 2023
Neurofilament Light Protein Rod Domain Exhibits Structural Heterogeneity.
Journal: Biomolecules
Published: November 06, 2023
Structural and Functional Properties of Tropomyosin Isoforms Tpm4.1 and Tpm2.1.
Journal: Biochemistry. Biokhimiia
Published: September 25, 2023
Novel Mutation Glu98Lys in Cardiac Tropomyosin Alters Its Structure and Impairs Myocardial Relaxation.
Journal: International journal of molecular sciences
Published: July 01, 2023
Structural and Functional Properties of Kappa Tropomyosin.
Journal: International journal of molecular sciences
Published: March 27, 2023
Properties of Cardiac Myosin with Cardiomyopathic Mutations in Essential Light Chains.
Journal: Biochemistry. Biokhimiia
Published: December 12, 2022
De Novo Asp219Val Mutation in Cardiac Tropomyosin Associated with Hypertrophic Cardiomyopathy.
Journal: International journal of molecular sciences
Published: November 19, 2022
Impact of Troponin in Cardiomyopathy Development Caused by Mutations in Tropomyosin.
Journal: International journal of molecular sciences
Published: November 17, 2022
Last Updated: 09/26/2026