Showing 1 - 7 results of 7 for search 'Piers, A', query time: 0.02s
Refine Results
-
1
-
2
Functional investigation of beta-tropomyosin mutations that cause congenital skeletal myopathies by Piers, A, Robinson, P, Redwood, C
Published 2011Conference item -
3
Assaying protein palmitoylation in plants by Taylor Laura, Hemsley Piers A, Grierson Claire S
Published 2008-01-01
Article -
4
The nemaline myopathy-causing E117K mutation in β-tropomyosin reduces thin filament activation. by Karpicheva, O, Robinson, P, Piers, A, Borovikov, Y, Redwood, C
Published 2013Journal article -
5
Molecular mechanisms of dysfunction of muscle fibres associated with Glu139 deletion in TPM2 gene by Borovikov, Y, Rysev, N, Karpicheva, O, Sirenko, V, Avrova, S, Piers, A, Redwood, C
Published 2017Journal article -
6
-
7
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 by Borovikov, Y, Simonyan, A, Karpicheva, O, Avrova, S, Rysev, N, Sirenko, V, Piers, A, Redwood, C
Published 2017Journal article