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David Winlaw

Showing results (41-50 of 54) with videos related to

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BMJ Open|August 18, 2019
Study protocol: NITric oxide during cardiopulmonary bypass to improve Recovery in Infants with Congenital heart defects (NITRIC trial): a randomised controlled trialLuregn J Schlapbach, Stephen Brian Horton, Debbie Amanda Long, et al.
The American Journal of Cardiology|June 7, 2017
Hospital Inpatient Costs for Single Ventricle Patients Surviving the Fontan ProcedureLi Huang, Chris Schilling, Kim M Dalziel, et al.
Heart, Lung & Circulation|May 24, 2016
Congenital Heart Disease Requires a Lifetime Continuum of Care: A Call for a Regional RegistryDavid Celermajer, Geoff Strange, Rachael Cordina, et al.
Critical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine|December 4, 2023
Statistical analysis plan for the NITric oxide during cardiopulmonary bypass to improve Recovery in Infants with Congenital heart defects (NITRIC) trialKristen S Gibbons, Luregn J Schlapbach, Stephen B Horton, et al.
Biorxiv : the Preprint Server for Biology|December 25, 2025
LncRNA H19 Upregulation Links Hypoplastic Left Heart Syndrome to Impaired PINK1/Parkin-Mediated Mitophagy and Ischemic VulnerabilityXuebin Fu, Conrad L Epting, Anshuman Sinha, et al.
Nature Communications|January 22, 2026
Neural crest cell-derived DKK1 and NEDD4 modulate Wnt signalling in the second heart field to orchestrate outflow tract developmentSophie Wiszniak, Dimuthu Alankarage, Iman Lohraseb, et al.
Cancer Research|August 16, 2013
A novel class of anticancer compounds targets the actin cytoskeleton in tumor cellsJustine R Stehn, Nikolas K Haass, Teresa Bonello, et al.
The Journal of Cell Biology|June 22, 2011
Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across speciesLi Qian, Joshua D Wythe, Jiandong Liu, et al.
Genome Medicine|January 8, 2026
DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defectsGregor Dombrowsky, Liselot van der Laan, Ananília Silva, et al.
Human Molecular Genetics|January 9, 2013
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of FallotHeather J Cordell, Ana Töpf, Chrysovalanto Mamasoula, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
BMJ Open|August 18, 2019
Study protocol: NITric oxide during cardiopulmonary bypass to improve Recovery in Infants with Congenital heart defects (NITRIC trial): a randomised controlled trialLuregn J Schlapbach, Stephen Brian Horton, Debbie Amanda Long, et al.
The American Journal of Cardiology|June 7, 2017
Hospital Inpatient Costs for Single Ventricle Patients Surviving the Fontan ProcedureLi Huang, Chris Schilling, Kim M Dalziel, et al.
Heart, Lung & Circulation|May 24, 2016
Congenital Heart Disease Requires a Lifetime Continuum of Care: A Call for a Regional RegistryDavid Celermajer, Geoff Strange, Rachael Cordina, et al.
Critical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine|December 4, 2023
Statistical analysis plan for the NITric oxide during cardiopulmonary bypass to improve Recovery in Infants with Congenital heart defects (NITRIC) trialKristen S Gibbons, Luregn J Schlapbach, Stephen B Horton, et al.
Biorxiv : the Preprint Server for Biology|December 25, 2025
LncRNA H19 Upregulation Links Hypoplastic Left Heart Syndrome to Impaired PINK1/Parkin-Mediated Mitophagy and Ischemic VulnerabilityXuebin Fu, Conrad L Epting, Anshuman Sinha, et al.
Nature Communications|January 22, 2026
Neural crest cell-derived DKK1 and NEDD4 modulate Wnt signalling in the second heart field to orchestrate outflow tract developmentSophie Wiszniak, Dimuthu Alankarage, Iman Lohraseb, et al.
Cancer Research|August 16, 2013
A novel class of anticancer compounds targets the actin cytoskeleton in tumor cellsJustine R Stehn, Nikolas K Haass, Teresa Bonello, et al.
The Journal of Cell Biology|June 22, 2011
Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across speciesLi Qian, Joshua D Wythe, Jiandong Liu, et al.
Genome Medicine|January 8, 2026
DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defectsGregor Dombrowsky, Liselot van der Laan, Ananília Silva, et al.
Human Molecular Genetics|January 9, 2013
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of FallotHeather J Cordell, Ana Töpf, Chrysovalanto Mamasoula, et al.
Pageof 6