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Plos Genetics
|
October 31, 2017
Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian development
Liam A Ridge, Karen Mitchell, Ali Al-Anbaki, et al.
The American Journal of Pathology
|
September 23, 2017
Myofilament Remodeling and Function Is More Impaired in Peripartum Cardiomyopathy Compared with Dilated Cardiomyopathy and Ischemic Heart Disease
Ilse A E Bollen, Elisabeth Ehler, Karin Fleischanderl, et al.
Cells
|
March 11, 2023
Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in <i>ACTN2</i>
Sophie Broadway-Stringer, He Jiang, Kirsty Wadmore, et al.
Basic Research in Cardiology
|
February 27, 2021
Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant
He Jiang, Charlotte Hooper, Matthew Kelly, et al.
Cell Reports Methods
|
May 9, 2023
Generation of left ventricle-like cardiomyocytes with improved structural, functional, and metabolic maturity from human pluripotent stem cells
Nicola Dark, Marie-Victoire Cosson, Lorenza I Tsansizi, et al.
Human Molecular Genetics
|
May 29, 2008
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy
Christian Geier, Katja Gehmlich, Elisabeth Ehler, et al.
Circulation. Cardiovascular Genetics
|
September 15, 2016
Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction
Robert Hastings, Carin P de Villiers, Charlotte Hooper, et al.
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Showing results (111-120 of 117) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 117 results.
Plos Genetics
|
October 31, 2017
Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian development
Liam A Ridge, Karen Mitchell, Ali Al-Anbaki, et al.
The American Journal of Pathology
|
September 23, 2017
Myofilament Remodeling and Function Is More Impaired in Peripartum Cardiomyopathy Compared with Dilated Cardiomyopathy and Ischemic Heart Disease
Ilse A E Bollen, Elisabeth Ehler, Karin Fleischanderl, et al.
Cells
|
March 11, 2023
Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in <i>ACTN2</i>
Sophie Broadway-Stringer, He Jiang, Kirsty Wadmore, et al.
Basic Research in Cardiology
|
February 27, 2021
Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant
He Jiang, Charlotte Hooper, Matthew Kelly, et al.
Cell Reports Methods
|
May 9, 2023
Generation of left ventricle-like cardiomyocytes with improved structural, functional, and metabolic maturity from human pluripotent stem cells
Nicola Dark, Marie-Victoire Cosson, Lorenza I Tsansizi, et al.
Human Molecular Genetics
|
May 29, 2008
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy
Christian Geier, Katja Gehmlich, Elisabeth Ehler, et al.
Circulation. Cardiovascular Genetics
|
September 15, 2016
Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction
Robert Hastings, Carin P de Villiers, Charlotte Hooper, et al.
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of 12