-
161
-
162
Functional investigation of troponin with the homozygous HCM mutation, TNNT2 K280N, obtained from an explanted heart
Published 2012Conference item -
163
-
164
Effects of DCM mutations in thin filament regulatory proteins on contractile function
Published 2005Conference item -
165
Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency.
Published 2009Journal article -
166
Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
Published 2004Journal article -
167
Two DCM mutations in cardiac tropomyosin alter thin filament function by different mechanisms
Published 2007Conference item -
168
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
Published 2005Journal article -
169
Structure-function relationships of eight mutations in troponin and tropomyosin that cause dilated cardiomyopathy
Published 2004Conference item -
170
-
171
Stochastic specification of primordial germ cells from mesoderm precursors in axolotl embryos.
Published 2014Journal article -
172
-
173
Crystal structure of the C1 domain of cardiac myosin binding protein-C: implications for hypertrophic cardiomyopathy.
Published 2008Journal article -
174
-
175
-
176
-
177
-
178
Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.
Published 2002Journal article -
179
-
180