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Geroscience
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October 2, 2023
Phenoage and longitudinal changes on transthoracic echocardiography in Alström syndrome: a disease of accelerated ageing?
Leena Patel, Ashwin Roy, Amor Mia B Alvior, et al.
Molecular Genetics and Metabolism
|
September 7, 2024
Characterisation of infantile cardiomyopathy in Alström syndrome using ALMS1 knockout induced pluripotent stem cell derived cardiomyocyte model
Leena Patel, Ashwin Roy, Jonathan Barlow, et al.
Cardiovascular Research
|
November 11, 2010
Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations
Katja Gehmlich, Petros Syrris, Emma Peskett, et al.
Molecular Biosystems
|
December 2, 2014
Changes in the cardiac metabolome caused by perhexiline treatment in a mouse model of hypertrophic cardiomyopathy
Katja Gehmlich, Michael S Dodd, J William Allwood, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
September 10, 2017
Age- and strain-related aberrant Ca<sup>2+</sup> release is associated with sudden cardiac death in the ACTC E99K mouse model of hypertrophic cardiomyopathy
Christina T Rowlands, Thomas Owen, Saheed Lawal, et al.
Circulation. Cardiovascular Genetics
|
April 8, 2014
Truncating plakophilin-2 mutations in arrhythmogenic cardiomyopathy are associated with protein haploinsufficiency in both myocardium and epidermis
Torsten B Rasmussen, Peter H Nissen, Johan Palmfeldt, et al.
Journal of Molecular and Cellular Cardiology
|
December 5, 2016
Aberrant developmental titin splicing and dysregulated sarcomere length in Thymosin β4 knockout mice
Nicola Smart, Johannes Riegler, Cameron W Turtle, et al.
Journal of Molecular and Cellular Cardiology
|
June 19, 2026
Structural, biophysical and cellular assessment of filamin C M82K: A test case for VUS interpretation in cardiomyopathy
Maya Noureddine, Bethany A I Jones, Oseloka C M Oliobi, et al.
Scientific Reports
|
July 26, 2023
Chronic activation of human cardiac fibroblasts in vitro attenuates the reversibility of the myofibroblast phenotype
Caitlin Hall, Jonathan P Law, Jasmeet S Reyat, et al.
Nature Communications
|
June 30, 2016
MLP and CARP are linked to chronic PKCα signalling in dilated cardiomyopathy
Stephan Lange, Katja Gehmlich, Alexander S Lun, et al.
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of 7
Search research articles
Search
Showing results (41-50 of 65) with videos related to
Sort By:
Page
of 7
Geroscience
|
October 2, 2023
Phenoage and longitudinal changes on transthoracic echocardiography in Alström syndrome: a disease of accelerated ageing?
Leena Patel, Ashwin Roy, Amor Mia B Alvior, et al.
Molecular Genetics and Metabolism
|
September 7, 2024
Characterisation of infantile cardiomyopathy in Alström syndrome using ALMS1 knockout induced pluripotent stem cell derived cardiomyocyte model
Leena Patel, Ashwin Roy, Jonathan Barlow, et al.
Cardiovascular Research
|
November 11, 2010
Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations
Katja Gehmlich, Petros Syrris, Emma Peskett, et al.
Molecular Biosystems
|
December 2, 2014
Changes in the cardiac metabolome caused by perhexiline treatment in a mouse model of hypertrophic cardiomyopathy
Katja Gehmlich, Michael S Dodd, J William Allwood, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
September 10, 2017
Age- and strain-related aberrant Ca<sup>2+</sup> release is associated with sudden cardiac death in the ACTC E99K mouse model of hypertrophic cardiomyopathy
Christina T Rowlands, Thomas Owen, Saheed Lawal, et al.
Circulation. Cardiovascular Genetics
|
April 8, 2014
Truncating plakophilin-2 mutations in arrhythmogenic cardiomyopathy are associated with protein haploinsufficiency in both myocardium and epidermis
Torsten B Rasmussen, Peter H Nissen, Johan Palmfeldt, et al.
Journal of Molecular and Cellular Cardiology
|
December 5, 2016
Aberrant developmental titin splicing and dysregulated sarcomere length in Thymosin β4 knockout mice
Nicola Smart, Johannes Riegler, Cameron W Turtle, et al.
Journal of Molecular and Cellular Cardiology
|
June 19, 2026
Structural, biophysical and cellular assessment of filamin C M82K: A test case for VUS interpretation in cardiomyopathy
Maya Noureddine, Bethany A I Jones, Oseloka C M Oliobi, et al.
Scientific Reports
|
July 26, 2023
Chronic activation of human cardiac fibroblasts in vitro attenuates the reversibility of the myofibroblast phenotype
Caitlin Hall, Jonathan P Law, Jasmeet S Reyat, et al.
Nature Communications
|
June 30, 2016
MLP and CARP are linked to chronic PKCα signalling in dilated cardiomyopathy
Stephan Lange, Katja Gehmlich, Alexander S Lun, et al.
Page
of 7