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7. Myopathy-causing mutation R91P in the TPM3 gene drastically impairs structural and functional properties of slow skeletal muscle tropomyosin γβ-heterodimer

12. Novel Mutation Glu98Lys in Cardiac Tropomyosin Alters Its Structure and Impairs Myocardial Relaxation

13. Structural and Functional Properties of Kappa Tropomyosin

14. Novel Antitubercular Agent-Loaded Liposomal Vesicles: Optimization, Characterization, and Cytotoxicity Studies

15. De Novo Asp219Val Mutation in Cardiac Tropomyosin Associated with Hypertrophic Cardiomyopathy

16. Impact of Troponin in Cardiomyopathy Development Caused by Mutations in Tropomyosin

21. De Novo Asp219Val Mutation in Cardiac Tropomyosin Associated with Hypertrophic Cardiomyopathy.

22. Type 1 Diabetes Impairs Cardiomyocyte Contractility in the Left and Right Ventricular Free Walls but Preserves It in the Interventricular Septum

26. Effects of myopathy-causing mutations R91P and R245G in the TPM3 gene on structural and functional properties of slow skeletal muscle tropomyosin

28. Mechanisms of disturbance of the contractile function of slow skeletal muscles induced by myopathic mutations in the tropomyosinTPM3gene

33. The effects of cardiomyopathy-associated mutations in the head-to-tail overlap junction of α-tropomyosin on its properties and interaction with actin

41. Structural and functional effects of two stabilizing substitutions, D137L and G126R, in the middle part of a-tropomyosin molecule

43. The isoforms of α-actin and myosin affect the Ca2+ regulation of the actin-myosin interaction in the heart.

44. Functional and Structural Properties of Cytoplasmic Tropomyosin Isoforms Tpm1.8 and Tpm1.9.

45. The isoforms of α-actin and myosin affect the Ca 2+ regulation of the actin-myosin interaction in the heart.

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