|Mechanistic heterogeneity in contractile properties of α-tropomyosin (TPM1) mutants associated with inherited cardiomyopathies|
TM Gupte, F Haque, B Gangadharan, MS Sunitha, S Mukherjee, ...
Journal of Biological Chemistry 290 (11), 7003-7015, 2015
|Molecular mechanisms and structural features of cardiomyopathy-causing troponin T mutants in the tropomyosin overlap region|
B Gangadharan, MS Sunitha, S Mukherjee, RR Chowdhury, F Haque, ...
Proceedings of the National Academy of Sciences 114 (42), 11115-11120, 2017
|A New Humanized Mouse Model for Studying Inherited Cardiomyopathic Mutations in the MYH7 Gene|
F Haque, M Sarikhani, S Mukherjee, NR Sundaresan, JA Mercer
Biophysical Journal 112 (3), 264a, 2017
|A new humanized mouse model for studying inherited cardiomyopathies caused by mutations in the MYH7 gene|
F Haque, S Mukherjee, JA Mercer
MOLECULAR BIOLOGY OF THE CELL 26, 2015
|Molecular Mechanism of Cardiomyopathy-Causing Mutations in Alpha-Tropomyosin|
TM Gupte, F Haque, B Gangadharan, M Sunitha, S Nag, R Sowdhamini, ...
Biophysical Journal 106 (2), 350a, 2014
|350a Monday, February 17, 2014|
TM Gupte, F Haque, B Gangadharan, M Sunitha, JA Mercer
|Validation of in silico prediction on the function of α-tropomyosin through designed point mutation and in vitro biochemical assays|
MS Sunitha, F Haque, TM Gupte, JA Mercer, JA Spudich, R Sowdhamini