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Showing results (61-70 of 85) with videos related to

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Pflugers Archiv : European Journal of Physiology|October 6, 2006
Functional effects of the DCM mutant Gly159Asp troponin C in skinned muscle fibresLaura C Preston, Simon Lipscomb, Paul Robinson, et al.
European Heart Journal|May 3, 2018
Transcatheter aortic valve implantation: current status and future perspectivesT J Cahill, M Chen, K Hayashida, et al.
Scientific Reports|December 3, 2017
Molecular mechanisms of dysfunction of muscle fibres associated with Glu139 deletion in TPM2 geneYurii S Borovikov, Nikita A Rysev, Olga E Karpicheva, et al.
Physics in Medicine and Biology|February 13, 2010
Vortex formation and recirculation zones in left anterior descending artery stenoses: computational fluid dynamics analysisD G Katritsis, A Theodorakakos, I Pantos, et al.
International Journal of Molecular Sciences|July 2, 2021
Molecular Mechanisms of the Deregulation of Muscle Contraction Induced by the R90P Mutation in Tpm3.12 and the Weakening of This Effect by BDM and W7Yurii S Borovikov, Daria D Andreeva, Stanislava V Avrova, et al.
Archives of Biochemistry and Biophysics|December 31, 2013
Gly126Arg substitution causes anomalous behaviour of α-skeletal and β-smooth tropomyosins during the ATPase cycleNikita A Rysev, Ilya A Nevzorov, Stanislava V Avrova, et al.
International Journal of Molecular Sciences|December 15, 2018
The Primary Causes of Muscle Dysfunction Associated with the Point Mutations in Tpm3.12; Conformational Analysis of Mutant Proteins as a Tool for Classification of MyopathiesYurii S Borovikov, Olga E Karpicheva, Armen O Simonyan, et al.
Biochemical and Biophysical Research Communications|May 25, 2018
The reason for the low Ca<sup>2+</sup>-sensitivity of thin filaments associated with the Glu41Lys mutation in the TPM2 gene is "freezing" of tropomyosin near the outer domain of actin and inhibition of actin monomer switching off during the ATPase cycleStanislava V Avrova, Olga E Karpicheva, Nikita A Rysev, et al.
Biochemical and Biophysical Research Communications|November 4, 2017
The reason for a high Ca<sup>2+</sup>-sensitivity associated with Arg91Gly substitution in TPM2 gene is the abnormal behavior and high flexibility of tropomyosin during the ATPase cycleYurii S Borovikov, Armen O Simonyan, Olga E Karpicheva, et al.
Archives of Biochemistry and Biophysics|April 3, 2016
Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca(2+)-sensitivity and suppress the modulation of Ca(2+)-sensitivity by troponin I phosphorylationAndrew E Messer, Christopher R Bayliss, Mohammed El-Mezgueldi, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
Pflugers Archiv : European Journal of Physiology|October 6, 2006
Functional effects of the DCM mutant Gly159Asp troponin C in skinned muscle fibresLaura C Preston, Simon Lipscomb, Paul Robinson, et al.
European Heart Journal|May 3, 2018
Transcatheter aortic valve implantation: current status and future perspectivesT J Cahill, M Chen, K Hayashida, et al.
Scientific Reports|December 3, 2017
Molecular mechanisms of dysfunction of muscle fibres associated with Glu139 deletion in TPM2 geneYurii S Borovikov, Nikita A Rysev, Olga E Karpicheva, et al.
Physics in Medicine and Biology|February 13, 2010
Vortex formation and recirculation zones in left anterior descending artery stenoses: computational fluid dynamics analysisD G Katritsis, A Theodorakakos, I Pantos, et al.
International Journal of Molecular Sciences|July 2, 2021
Molecular Mechanisms of the Deregulation of Muscle Contraction Induced by the R90P Mutation in Tpm3.12 and the Weakening of This Effect by BDM and W7Yurii S Borovikov, Daria D Andreeva, Stanislava V Avrova, et al.
Archives of Biochemistry and Biophysics|December 31, 2013
Gly126Arg substitution causes anomalous behaviour of α-skeletal and β-smooth tropomyosins during the ATPase cycleNikita A Rysev, Ilya A Nevzorov, Stanislava V Avrova, et al.
International Journal of Molecular Sciences|December 15, 2018
The Primary Causes of Muscle Dysfunction Associated with the Point Mutations in Tpm3.12; Conformational Analysis of Mutant Proteins as a Tool for Classification of MyopathiesYurii S Borovikov, Olga E Karpicheva, Armen O Simonyan, et al.
Biochemical and Biophysical Research Communications|May 25, 2018
The reason for the low Ca<sup>2+</sup>-sensitivity of thin filaments associated with the Glu41Lys mutation in the TPM2 gene is "freezing" of tropomyosin near the outer domain of actin and inhibition of actin monomer switching off during the ATPase cycleStanislava V Avrova, Olga E Karpicheva, Nikita A Rysev, et al.
Biochemical and Biophysical Research Communications|November 4, 2017
The reason for a high Ca<sup>2+</sup>-sensitivity associated with Arg91Gly substitution in TPM2 gene is the abnormal behavior and high flexibility of tropomyosin during the ATPase cycleYurii S Borovikov, Armen O Simonyan, Olga E Karpicheva, et al.
Archives of Biochemistry and Biophysics|April 3, 2016
Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca(2+)-sensitivity and suppress the modulation of Ca(2+)-sensitivity by troponin I phosphorylationAndrew E Messer, Christopher R Bayliss, Mohammed El-Mezgueldi, et al.
Pageof 9