검색결과 : 4건
| No. | Article |
|---|---|
| 1 |
The molecular mechanism of muscle dysfunction associated with the R133W mutation in Tpm2.2 Borovikov YS, Karpicheva OE, Avrova SV, Simonyan AO, Sirenko VV, Redwood CS Biochemical and Biophysical Research Communications, 523(1), 258, 2020 |
| 2 |
The molecular mechanisms of a high Ca2+-sensitivity and muscle weakness associated with the Ala155Thr substitution in Tpm3.12 Avrova SV, Karpicheva OE, Simonyan AO, Sirenko VV, Redwood CS, Borovikov YS Biochemical and Biophysical Research Communications, 515(2), 372, 2019 |
| 3 |
The reason for the low Ca2+-sensitivity of thin filaments associated with the Glu41 Lys 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 cycle Avrova SV, Karpicheva OE, Rysev NA, Simonyan AO, Sirenko VV, Redwood CS, Borovikov YS Biochemical and Biophysical Research Communications, 502(2), 209, 2018 |
| 4 |
The reason for a high Ca2+-sensitivity associated with Arg91Gly substitution in TPM2 gene is the abnormal behavior and high. flexibility of tropomyosin during the ATPase cycle Borovikov YS, Simonyan AO, Karpicheva OE, Avrova SV, Rysev NA, Sirenko VV, Piers A, Redwood CS Biochemical and Biophysical Research Communications, 494(3-4), 681, 2017 |