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Kathryn Scott

Showing results (1-10 of 21) with videos related to

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Immunology and Allergy Clinics of North America|April 26, 2022
Pharmacogenomics of Drug Hypersensitivity: Technology and TranslationRebecca Kuruvilla, Kathryn Scott, Sir Munir Pirmohamed
Urology|December 13, 2021
Robotic Assisted Caval Replacement for Recurrent Renal Cell Carcinoma Invading the Wall of the Inferior Vena CavaKathryn Scott, Jared Manwaring, Kwame Amankwah, et al.
Clinical and Translational Science|May 7, 2010
Association of a polymorphic variant of the adiponectin gene with insulin resistance in african americansClaudia Specchia, Kathryn Scott, Paolo Fortina, et al.
Law and Human Behavior|September 15, 2022
Evaluator empathy in risk assessment interviewsKathryn Scott, Marcus T Boccaccini, Gabriele Trupp, et al.
Haematologica|July 22, 2008
Genetic variation in genes expressed in the germinal center and risk of B cell lymphoma among CaucasiansKathryn Scott, Peter J Adamson, Eleanor V Willett, et al.
Thorax|April 23, 2022
COVID-19 associated phrenic nerve mononeuritis: a case seriesSheonagh MacPhail Law, Kathryn Scott, Ahmed Alkarn, et al.
Blood|June 8, 2007
RAG1 and BRCA2 polymorphisms in non-Hodgkin lymphomaKathryn Scott, Peter J Adamson, Sharon L Barrans, et al.
Clinical and Translational Science|December 21, 2010
Variants in genes involved in functional pathways associated with hypertension in African AmericansMaria P Martinez Cantarin, Adam Ertel, Stephanie Deloach, et al.
BMJ Open|January 15, 2018
A study protocol for a non-randomised comparison trial evaluating the feasibility and effectiveness of a mobile cognitive-behavioural programme with integrated coaching for anxious adults in primary careEva Szigethy, Francis Solano, Meredith Wallace, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 30, 2013
Developmental dysplasia of the hip: linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration familyGeorge J Feldman, Javad Parvizi, Mark Levenstien, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Immunology and Allergy Clinics of North America|April 26, 2022
Pharmacogenomics of Drug Hypersensitivity: Technology and TranslationRebecca Kuruvilla, Kathryn Scott, Sir Munir Pirmohamed
Urology|December 13, 2021
Robotic Assisted Caval Replacement for Recurrent Renal Cell Carcinoma Invading the Wall of the Inferior Vena CavaKathryn Scott, Jared Manwaring, Kwame Amankwah, et al.
Clinical and Translational Science|May 7, 2010
Association of a polymorphic variant of the adiponectin gene with insulin resistance in african americansClaudia Specchia, Kathryn Scott, Paolo Fortina, et al.
Law and Human Behavior|September 15, 2022
Evaluator empathy in risk assessment interviewsKathryn Scott, Marcus T Boccaccini, Gabriele Trupp, et al.
Haematologica|July 22, 2008
Genetic variation in genes expressed in the germinal center and risk of B cell lymphoma among CaucasiansKathryn Scott, Peter J Adamson, Eleanor V Willett, et al.
Thorax|April 23, 2022
COVID-19 associated phrenic nerve mononeuritis: a case seriesSheonagh MacPhail Law, Kathryn Scott, Ahmed Alkarn, et al.
Blood|June 8, 2007
RAG1 and BRCA2 polymorphisms in non-Hodgkin lymphomaKathryn Scott, Peter J Adamson, Sharon L Barrans, et al.
Clinical and Translational Science|December 21, 2010
Variants in genes involved in functional pathways associated with hypertension in African AmericansMaria P Martinez Cantarin, Adam Ertel, Stephanie Deloach, et al.
BMJ Open|January 15, 2018
A study protocol for a non-randomised comparison trial evaluating the feasibility and effectiveness of a mobile cognitive-behavioural programme with integrated coaching for anxious adults in primary careEva Szigethy, Francis Solano, Meredith Wallace, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 30, 2013
Developmental dysplasia of the hip: linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration familyGeorge J Feldman, Javad Parvizi, Mark Levenstien, et al.
Pageof 3