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G Bailey

Showing results (381-390 of 566) with videos related to

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Experimental Physiology|November 22, 2021
The within- and between-day reliability of cerebrovascular reactivity using traditional and novel analytical approachesJodie L Koep, Max E Weston, Alan R Barker, et al.
Anesthesia and Analgesia|April 9, 1999
Tracheal extubation of deeply anesthetized pediatric patients: a comparison of isoflurane and sevofluraneR D Valley, J T Ramza, P Calhoun, et al.
Preventive Medicine|March 25, 2023
Economic evaluation of exercise interventions for individuals with cancer: A systematic reviewYufan Wang, Alexandra L McCarthy, Sandra C Hayes, et al.
Angewandte Chemie (International Ed. in English)|March 13, 2023
Polydopamine as a Visible-Light Photosensitiser for Photoinitiated PolymerisationChristopher G Bailey, Mitchell D Nothling, Lucy L Fillbrook, et al.
Journal of Microbiology & Biology Education|October 1, 2021
Online Tools for Teaching Cancer BioinformaticsMason D Taylor, Bryn Mendenhall, Calvin S Woods, et al.
Haematologica|October 26, 2010
OCT-1 function varies with cell lineage but is not influenced by BCR-ABLJane R Engler, Andrew C W Zannettino, Charles G Bailey, et al.
American Journal of Physiology. Heart and Circulatory Physiology|June 26, 2012
Remote ischemic preconditioning prevents reduction in brachial artery flow-mediated dilation after strenuous exerciseTom G Bailey, Gurpreet K Birk, N Timothy Cable, et al.
Biosecurity and Bioterrorism : Biodefense Strategy, Practice, and Science|February 23, 2012
Decontamination after a release of B. anthracis sporesChris G Campbell, Robert D Kirvel, Adam H Love, et al.
American Journal of Clinical Pathology|October 22, 2020
Clinicopathologic Characterization of Hypocellular Acute Myeloid Leukemia (AML) Showed Fewer Genetic Abnormalities Involving Cell Proliferation and NPM1 When Compared With Nonhypocellular AMLEric Carlsen, Nathanael G Bailey, Nidhi Aggarwal, et al.
Nature Genetics|August 3, 2004
Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19Heng F Seow, Stefan Bröer, Angelika Bröer, et al.
Pageof 57

Showing results (381-390 of 566) with videos related to

Sort By:
Pageof 57
Experimental Physiology|November 22, 2021
The within- and between-day reliability of cerebrovascular reactivity using traditional and novel analytical approachesJodie L Koep, Max E Weston, Alan R Barker, et al.
Anesthesia and Analgesia|April 9, 1999
Tracheal extubation of deeply anesthetized pediatric patients: a comparison of isoflurane and sevofluraneR D Valley, J T Ramza, P Calhoun, et al.
Preventive Medicine|March 25, 2023
Economic evaluation of exercise interventions for individuals with cancer: A systematic reviewYufan Wang, Alexandra L McCarthy, Sandra C Hayes, et al.
Angewandte Chemie (International Ed. in English)|March 13, 2023
Polydopamine as a Visible-Light Photosensitiser for Photoinitiated PolymerisationChristopher G Bailey, Mitchell D Nothling, Lucy L Fillbrook, et al.
Journal of Microbiology & Biology Education|October 1, 2021
Online Tools for Teaching Cancer BioinformaticsMason D Taylor, Bryn Mendenhall, Calvin S Woods, et al.
Haematologica|October 26, 2010
OCT-1 function varies with cell lineage but is not influenced by BCR-ABLJane R Engler, Andrew C W Zannettino, Charles G Bailey, et al.
American Journal of Physiology. Heart and Circulatory Physiology|June 26, 2012
Remote ischemic preconditioning prevents reduction in brachial artery flow-mediated dilation after strenuous exerciseTom G Bailey, Gurpreet K Birk, N Timothy Cable, et al.
Biosecurity and Bioterrorism : Biodefense Strategy, Practice, and Science|February 23, 2012
Decontamination after a release of B. anthracis sporesChris G Campbell, Robert D Kirvel, Adam H Love, et al.
American Journal of Clinical Pathology|October 22, 2020
Clinicopathologic Characterization of Hypocellular Acute Myeloid Leukemia (AML) Showed Fewer Genetic Abnormalities Involving Cell Proliferation and NPM1 When Compared With Nonhypocellular AMLEric Carlsen, Nathanael G Bailey, Nidhi Aggarwal, et al.
Nature Genetics|August 3, 2004
Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19Heng F Seow, Stefan Bröer, Angelika Bröer, et al.
Pageof 57