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F Pearson

Showing results (221-230 of 247) with videos related to

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Frontiers in Genetics|October 31, 2022
Allelic diversity of the pharmacogene CYP2D6 in New Zealand Māori and Pacific peoplesLeonie M Hitchman, Allamanda Faatoese, Tony R Merriman, et al.
Human Genetics|November 10, 2014
Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predispositionGemma L Moir-Meyer, John F Pearson, Felicity Lose, et al.
AIDS Research and Human Retroviruses|March 14, 2017
Quantification of Residual Germinal Center Activity and HIV-1 DNA and RNA Levels Using Fine Needle Biopsies of Lymph Nodes During Antiretroviral TherapyWilliam J Hey-Nguyen, Yin Xu, Chester F Pearson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 19, 2014
Serum phosphorylated neurofilament-heavy chain levels in multiple sclerosis patientsM M Gresle, Y Liu, L F Dagley, et al.
Medrxiv : the Preprint Server for Health Sciences|August 30, 2024
Preoperative Exposure to Fine Particulate Matter and Risk of Postoperative Complications: A Single Center Observational Cohort Bayesian AnalysisJohn F Pearson, Cameron K Jacobson, Calvin S Riss, et al.
Nature Immunology|April 12, 2024
Blimp-1 and c-Maf regulate immune gene networks to protect against distinct pathways of pathobiont-induced colitisMarisol Alvarez-Martinez, Luke S Cox, Claire F Pearson, et al.
Acta Anaesthesiologica Scandinavica|April 26, 2026
Bayesian Analysis of Postoperative Complication Risk Associated With Preoperative Exposure to Fine Particulate Matter: A Single-Center Cohort StudyJohn F Pearson, Cameron K Jacobson, Calvin S Riss, et al.
Scientific Reports|May 17, 2018
Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathyCameron J Lacey, Kit Doudney, Paul G Bridgman, et al.
Plos One|July 7, 2012
The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissuesAnna P Pilbrow, Lasse Folkersen, John F Pearson, et al.
Neurobiology of Aging|May 2, 2025
Presenilin 1 hemizygosity has no overt deleterious phenotypic outcomes in sheep: Potential implications for therapeutic targets in Alzheimer's diseaseNatasha E Mckean, Jun Liu, Skye R Rudiger, et al.
Pageof 25

Showing results (221-230 of 247) with videos related to

Sort By:
Pageof 25
Frontiers in Genetics|October 31, 2022
Allelic diversity of the pharmacogene CYP2D6 in New Zealand Māori and Pacific peoplesLeonie M Hitchman, Allamanda Faatoese, Tony R Merriman, et al.
Human Genetics|November 10, 2014
Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predispositionGemma L Moir-Meyer, John F Pearson, Felicity Lose, et al.
AIDS Research and Human Retroviruses|March 14, 2017
Quantification of Residual Germinal Center Activity and HIV-1 DNA and RNA Levels Using Fine Needle Biopsies of Lymph Nodes During Antiretroviral TherapyWilliam J Hey-Nguyen, Yin Xu, Chester F Pearson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 19, 2014
Serum phosphorylated neurofilament-heavy chain levels in multiple sclerosis patientsM M Gresle, Y Liu, L F Dagley, et al.
Medrxiv : the Preprint Server for Health Sciences|August 30, 2024
Preoperative Exposure to Fine Particulate Matter and Risk of Postoperative Complications: A Single Center Observational Cohort Bayesian AnalysisJohn F Pearson, Cameron K Jacobson, Calvin S Riss, et al.
Nature Immunology|April 12, 2024
Blimp-1 and c-Maf regulate immune gene networks to protect against distinct pathways of pathobiont-induced colitisMarisol Alvarez-Martinez, Luke S Cox, Claire F Pearson, et al.
Acta Anaesthesiologica Scandinavica|April 26, 2026
Bayesian Analysis of Postoperative Complication Risk Associated With Preoperative Exposure to Fine Particulate Matter: A Single-Center Cohort StudyJohn F Pearson, Cameron K Jacobson, Calvin S Riss, et al.
Scientific Reports|May 17, 2018
Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathyCameron J Lacey, Kit Doudney, Paul G Bridgman, et al.
Plos One|July 7, 2012
The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissuesAnna P Pilbrow, Lasse Folkersen, John F Pearson, et al.
Neurobiology of Aging|May 2, 2025
Presenilin 1 hemizygosity has no overt deleterious phenotypic outcomes in sheep: Potential implications for therapeutic targets in Alzheimer's diseaseNatasha E Mckean, Jun Liu, Skye R Rudiger, et al.
Pageof 25