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Frontiers in Physiology
|
June 29, 2023
Corrigendum: Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: the impact of full-length dystrophin deficiency
Josè Manuel Pioner, Lorenzo Santini, Chiara Palandri, et al.
Circulation Research
|
February 6, 2023
Slower Calcium Handling Balances Faster Cross-Bridge Cycling in Human <i>MYBPC3</i> HCM
Josè Manuel Pioner, Giulia Vitale, Sonette Steczina, et al.
Circulation. Genomic and Precision Medicine
|
August 26, 2020
Spatial and Functional Distribution of <i>MYBPC3</i> Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy
Adam S Helms, Andrea D Thompson, Amelia A Glazier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy
Claire Horvat, Renee Johnson, Lien Lam, et al.
Psychiatry Research
|
August 3, 2024
Genetic determinants of coping, resilience and self-esteem in schizophrenia suggest a primary role for social factors and hippocampal neurogenesis
Francesco Mazzarotto, Palmiero Monteleone, Alessandra Minelli, et al.
Genome Medicine
|
January 31, 2019
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy
Roddy Walsh, Francesco Mazzarotto, Nicola Whiffin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 27, 2021
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
Francesco Mazzarotto, Megan H Hawley, Matteo Beltrami, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Quantifying evidence toward pathogenicity for rare phenotypes: The case of succinate dehydrogenase genes, SDHB and SDHD
Alice Garrett, Chey Loveday, Laura King, et al.
Circulation
|
January 28, 2020
Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy
Francesco Mazzarotto, Upasana Tayal, Rachel J Buchan, et al.
Circulation
|
May 5, 2021
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy
Elizabeth Jordan, Laiken Peterson, Tomohiko Ai, et al.
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of 5
Search research articles
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Showing results (21-30 of 41) with videos related to
Sort By:
Page
of 5
Frontiers in Physiology
|
June 29, 2023
Corrigendum: Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: the impact of full-length dystrophin deficiency
Josè Manuel Pioner, Lorenzo Santini, Chiara Palandri, et al.
Circulation Research
|
February 6, 2023
Slower Calcium Handling Balances Faster Cross-Bridge Cycling in Human <i>MYBPC3</i> HCM
Josè Manuel Pioner, Giulia Vitale, Sonette Steczina, et al.
Circulation. Genomic and Precision Medicine
|
August 26, 2020
Spatial and Functional Distribution of <i>MYBPC3</i> Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy
Adam S Helms, Andrea D Thompson, Amelia A Glazier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy
Claire Horvat, Renee Johnson, Lien Lam, et al.
Psychiatry Research
|
August 3, 2024
Genetic determinants of coping, resilience and self-esteem in schizophrenia suggest a primary role for social factors and hippocampal neurogenesis
Francesco Mazzarotto, Palmiero Monteleone, Alessandra Minelli, et al.
Genome Medicine
|
January 31, 2019
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy
Roddy Walsh, Francesco Mazzarotto, Nicola Whiffin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 27, 2021
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
Francesco Mazzarotto, Megan H Hawley, Matteo Beltrami, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Quantifying evidence toward pathogenicity for rare phenotypes: The case of succinate dehydrogenase genes, SDHB and SDHD
Alice Garrett, Chey Loveday, Laura King, et al.
Circulation
|
January 28, 2020
Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy
Francesco Mazzarotto, Upasana Tayal, Rachel J Buchan, et al.
Circulation
|
May 5, 2021
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy
Elizabeth Jordan, Laiken Peterson, Tomohiko Ai, et al.
Page
of 5