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Nicholas Watkins

Showing results (31-40 of 45) with videos related to

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Computational Biology and Chemistry|May 15, 2007
Improving the power to detect differentially expressed genes in comparative microarray experiments by including information from self-self hybridizationsArief Gusnanto, Brian Tom, Philippa Burns, et al.
Analytical Chemistry|February 19, 2008
On-chip single-copy real-time reverse-transcription PCR in isolated picoliter dropletsN Reginald Beer, Elizabeth K Wheeler, Lorenna Lee-Houghton, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|July 24, 2020
Convalescent plasma treatment for SARS-CoV-2 infection: analysis of the first 436 donors in England, 22 April to 12 May 2020Heli Harvala, Jennifer Mehew, Matthew L Robb, et al.
Prenatal Diagnosis|January 28, 2022
Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomaliesYiming Wang, Elena Greenfeld, Nicholas Watkins, et al.
Protein Science : a Publication of the Protein Society|October 2, 2007
Functional analysis of the GTPases EngA and YhbZ encoded by Salmonella typhimuriumHeather K Lamb, Paul Thompson, Catherine Elliott, et al.
Canadian Journal of Kidney Health and Disease|June 8, 2026
Canadian Society of Nephrology Commentary on the 2025 Kidney Disease Improving Global Outcomes Clinical Practice Guidelines for Autosomal Dominant Polycystic Kidney DiseaseMatthew B Lanktree, Nick Ashawasega, Micheli Bevilacqua, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 3, 2021
The role of digital tools in the delivery of genomic medicine: enhancing patient-centered careSalma Shickh, Sara A Rafferty, Marc Clausen, et al.
Genetics in Medicine Open|September 22, 2025
Framework for standardized genetic testing recommendations for chronic kidney disease in OntarioAngela Du, Kaitlyn Lemay, Amit Bagga, et al.
Clinical Genetics|September 5, 2020
Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiencyMaian Roifman, Kirsten M Niles, Lauren MacNeil, et al.
Cancers|July 12, 2025
Advancing the Landscape of Clinical Actionability in Von Hippel-Lindau Syndrome: An Evidence-Based Framework from the INT<sup>2</sup>GRATE Oncology ConsortiumDiane R Koeller, McKenzie Walker, Busra Unal, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Computational Biology and Chemistry|May 15, 2007
Improving the power to detect differentially expressed genes in comparative microarray experiments by including information from self-self hybridizationsArief Gusnanto, Brian Tom, Philippa Burns, et al.
Analytical Chemistry|February 19, 2008
On-chip single-copy real-time reverse-transcription PCR in isolated picoliter dropletsN Reginald Beer, Elizabeth K Wheeler, Lorenna Lee-Houghton, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|July 24, 2020
Convalescent plasma treatment for SARS-CoV-2 infection: analysis of the first 436 donors in England, 22 April to 12 May 2020Heli Harvala, Jennifer Mehew, Matthew L Robb, et al.
Prenatal Diagnosis|January 28, 2022
Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomaliesYiming Wang, Elena Greenfeld, Nicholas Watkins, et al.
Protein Science : a Publication of the Protein Society|October 2, 2007
Functional analysis of the GTPases EngA and YhbZ encoded by Salmonella typhimuriumHeather K Lamb, Paul Thompson, Catherine Elliott, et al.
Canadian Journal of Kidney Health and Disease|June 8, 2026
Canadian Society of Nephrology Commentary on the 2025 Kidney Disease Improving Global Outcomes Clinical Practice Guidelines for Autosomal Dominant Polycystic Kidney DiseaseMatthew B Lanktree, Nick Ashawasega, Micheli Bevilacqua, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 3, 2021
The role of digital tools in the delivery of genomic medicine: enhancing patient-centered careSalma Shickh, Sara A Rafferty, Marc Clausen, et al.
Genetics in Medicine Open|September 22, 2025
Framework for standardized genetic testing recommendations for chronic kidney disease in OntarioAngela Du, Kaitlyn Lemay, Amit Bagga, et al.
Clinical Genetics|September 5, 2020
Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiencyMaian Roifman, Kirsten M Niles, Lauren MacNeil, et al.
Cancers|July 12, 2025
Advancing the Landscape of Clinical Actionability in Von Hippel-Lindau Syndrome: An Evidence-Based Framework from the INT<sup>2</sup>GRATE Oncology ConsortiumDiane R Koeller, McKenzie Walker, Busra Unal, et al.
Pageof 5