Mohammed El‐Mezgueldi

Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients

Steven B. Marston, Massimiliano Memo, Andrew E. Messer et al. · Human Molecular Genetics · 2013 · 82 citations · Full text

The Effect of Mutations in α-Tropomyosin (E40K and E54K) That Cause Familial Dilated Cardiomyopathy on the Regulatory Mechanism of Cardiac Muscle Thin Filaments

M Mirza, Paul Robinson, Elena Kremneva et al. · Journal of Biological Chemistry · 2007 · 72 citations · Full text

3-D image reconstruction of reconstituted smooth muscle thin filaments containing calponin: Visualization of interactions between F-actin and Calponin

Julie L. Hodgkinson, Mohammed El‐Mezgueldi, Roger Craig et al. · Journal of Molecular Biology · 1997 · 70 citations · Full text

Engineering, Protein Assembly, Microscopy +24

Structural and functional characterization of a cell cycle associated HDAC1/2 complex reveals the structural basis for complex assembly and nucleosome targeting

Toshimasa Itoh, Louise Fairall, Frederick W. Muskett et al. · Nucleic Acids Research · 2015 · 62 citations · Full text

Dimeric Chromatin, Molecular Biology, Genomic Mechanism +19

Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca2+-sensitivity and suppress the modulation of Ca2+-sensitivity by troponin I phosphorylation

Andrew E. Messer, Christopher R. Bayliss, Mohammed El‐Mezgueldi et al. · Archives of Biochemistry and Biophysics · 2016 · 61 citations · Full text