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J Peter van Tintelen

Showing results (51-60 of 232) with videos related to

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Human Mutation|February 14, 2015
The ARVD/C genetic variants database: 2014 updateElisabetta Lazzarini, Jan D H Jongbloed, Kalliopi Pilichou, et al.
Circulation. Genomic and Precision Medicine|October 20, 2020
Long-Term Follow-Up Study on the Uptake of Genetic Counseling and Predictive DNA Testing in Inherited Cardiac ConditionsLieke M van den Heuvel, Maxiem O van Teijlingen, Wilma van der Roest, et al.
ESC Heart Failure|July 17, 2022
Blood-based biomarkers for the prediction of hypertrophic cardiomyopathy prognosis: a systematic review and meta-analysisMark Jansen, Sila Algül, Laurens P Bosman, et al.
Histopathology|March 13, 2016
Phospholamban p.Arg14del cardiomyopathy is characterized by phospholamban aggregates, aggresomes, and autophagic degradationWouter P Te Rijdt, J Peter van Tintelen, Aryan Vink, et al.
Cardiovascular Research|March 26, 2003
A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kineticsW Antoinette Groenewegen, Connie R Bezzina, J Peter van Tintelen, et al.
European Journal of Human Genetics : EJHG|May 5, 2019
Informing relatives at risk of inherited cardiac conditions: experiences and attitudes of healthcare professionals and counseleesLieke M van den Heuvel, Mette J Huisinga, Yvonne M Hoedemaekers, et al.
American Journal of Physiology. Heart and Circulatory Physiology|July 18, 2020
Desmin is essential for the structure and function of the sinoatrial node: implications for increased arrhythmogenesisManolis Mavroidis, Nikolaos C Athanasiadis, Pavlos Rigas, et al.
Genetics in Medicine Open|November 10, 2025
Evaluation of DNA-poli: Study protocol of a randomized controlled trial to assess a digital platform for family cascade genetic testing and predictive genetic counselingMarlies N van Lingen, Janine V Meulenkamp, Marten A Siemelink, et al.
International Journal of Molecular Sciences|September 23, 2022
Towards a Better Understanding of Genotype-Phenotype Correlations and Therapeutic Targets for Cardiocutaneous Genes: The Importance of Functional Studies above PredictionMathilde C S C Vermeer, Daniela Andrei, Luisa Marsili, et al.
European Journal of Heart Failure|March 3, 2015
A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle-specific genesMagdalena Harakalova, Gijs Kummeling, Arjan Sammani, et al.
Pageof 24

Showing results (51-60 of 232) with videos related to

Sort By:
Pageof 24
Human Mutation|February 14, 2015
The ARVD/C genetic variants database: 2014 updateElisabetta Lazzarini, Jan D H Jongbloed, Kalliopi Pilichou, et al.
Circulation. Genomic and Precision Medicine|October 20, 2020
Long-Term Follow-Up Study on the Uptake of Genetic Counseling and Predictive DNA Testing in Inherited Cardiac ConditionsLieke M van den Heuvel, Maxiem O van Teijlingen, Wilma van der Roest, et al.
ESC Heart Failure|July 17, 2022
Blood-based biomarkers for the prediction of hypertrophic cardiomyopathy prognosis: a systematic review and meta-analysisMark Jansen, Sila Algül, Laurens P Bosman, et al.
Histopathology|March 13, 2016
Phospholamban p.Arg14del cardiomyopathy is characterized by phospholamban aggregates, aggresomes, and autophagic degradationWouter P Te Rijdt, J Peter van Tintelen, Aryan Vink, et al.
Cardiovascular Research|March 26, 2003
A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kineticsW Antoinette Groenewegen, Connie R Bezzina, J Peter van Tintelen, et al.
European Journal of Human Genetics : EJHG|May 5, 2019
Informing relatives at risk of inherited cardiac conditions: experiences and attitudes of healthcare professionals and counseleesLieke M van den Heuvel, Mette J Huisinga, Yvonne M Hoedemaekers, et al.
American Journal of Physiology. Heart and Circulatory Physiology|July 18, 2020
Desmin is essential for the structure and function of the sinoatrial node: implications for increased arrhythmogenesisManolis Mavroidis, Nikolaos C Athanasiadis, Pavlos Rigas, et al.
Genetics in Medicine Open|November 10, 2025
Evaluation of DNA-poli: Study protocol of a randomized controlled trial to assess a digital platform for family cascade genetic testing and predictive genetic counselingMarlies N van Lingen, Janine V Meulenkamp, Marten A Siemelink, et al.
International Journal of Molecular Sciences|September 23, 2022
Towards a Better Understanding of Genotype-Phenotype Correlations and Therapeutic Targets for Cardiocutaneous Genes: The Importance of Functional Studies above PredictionMathilde C S C Vermeer, Daniela Andrei, Luisa Marsili, et al.
European Journal of Heart Failure|March 3, 2015
A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle-specific genesMagdalena Harakalova, Gijs Kummeling, Arjan Sammani, et al.
Pageof 24