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V Morgan

Showing results (221-230 of 278) with videos related to

Pageof 28
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The Journal of Clinical Investigation|August 18, 2015
SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defectsSarah J Fletcher, Ben Johnson, Gillian C Lowe, et al.
Evidence-Based Complementary and Alternative Medicine : Ecam|July 7, 2023
Anti-Inflammatory and Antimicrobial Effects of <i>Eucalyptus</i> spp. Essential Oils: A Potential Valuable Use for an Industry ByproductEmilly S Salvatori, Letícia V Morgan, Samara Ferrarini, et al.
The Journal of Clinical Investigation|May 30, 2009
Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystoniaManju A Kurian, Juan Zhen, Shu-Yuan Cheng, et al.
Evidence-Based Complementary and Alternative Medicine : Ecam|March 17, 2021
Anti-Inflammatory Effects of <i>Campomanesia xanthocarpa</i> Seed Extract Obtained from Supercritical CO<sub>2</sub>Fernanda Petry, Bruna B Dall'Orsoleta, Mikaela Scatolin, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 21, 2025
The Role of Race/Ethnicity on the Association between Neighborhood Deprivation and Breast Cancer Outcomes among Kentucky Patients with Breast Cancer (2010-2022)Breyanna Walker, Elinita Pollard, Sydney P Howard, et al.
The Review of Scientific Instruments|June 1, 2022
A compact x-ray diffraction system for dynamic compression experiments on pulsed-power generatorsT Ao, D V Morgan, B S Stoltzfus, et al.
Journal of Thrombosis and Haemostasis : JTH|August 6, 2021
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and HemostasisKaryn Megy, Kate Downes, Marie-Christine Morel-Kopp, et al.
American Journal of Human Genetics|November 27, 2010
Whole-exome-sequencing-based discovery of human FADD deficiencyAlexandre Bolze, Minji Byun, David McDonald, et al.
Acta Neuropathologica Communications|December 6, 2014
Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndromeArthur B McKie, Atif Alsaedi, Julie Vogt, et al.
Brain : a Journal of Neurology|September 14, 2010
Phospholipase C beta 1 deficiency is associated with early-onset epileptic encephalopathyManju A Kurian, Esther Meyer, Grace Vassallo, et al.
Pageof 28

Showing results (221-230 of 278) with videos related to

Sort By:
Pageof 28
The Journal of Clinical Investigation|August 18, 2015
SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defectsSarah J Fletcher, Ben Johnson, Gillian C Lowe, et al.
Evidence-Based Complementary and Alternative Medicine : Ecam|July 7, 2023
Anti-Inflammatory and Antimicrobial Effects of <i>Eucalyptus</i> spp. Essential Oils: A Potential Valuable Use for an Industry ByproductEmilly S Salvatori, Letícia V Morgan, Samara Ferrarini, et al.
The Journal of Clinical Investigation|May 30, 2009
Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystoniaManju A Kurian, Juan Zhen, Shu-Yuan Cheng, et al.
Evidence-Based Complementary and Alternative Medicine : Ecam|March 17, 2021
Anti-Inflammatory Effects of <i>Campomanesia xanthocarpa</i> Seed Extract Obtained from Supercritical CO<sub>2</sub>Fernanda Petry, Bruna B Dall'Orsoleta, Mikaela Scatolin, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 21, 2025
The Role of Race/Ethnicity on the Association between Neighborhood Deprivation and Breast Cancer Outcomes among Kentucky Patients with Breast Cancer (2010-2022)Breyanna Walker, Elinita Pollard, Sydney P Howard, et al.
The Review of Scientific Instruments|June 1, 2022
A compact x-ray diffraction system for dynamic compression experiments on pulsed-power generatorsT Ao, D V Morgan, B S Stoltzfus, et al.
Journal of Thrombosis and Haemostasis : JTH|August 6, 2021
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and HemostasisKaryn Megy, Kate Downes, Marie-Christine Morel-Kopp, et al.
American Journal of Human Genetics|November 27, 2010
Whole-exome-sequencing-based discovery of human FADD deficiencyAlexandre Bolze, Minji Byun, David McDonald, et al.
Acta Neuropathologica Communications|December 6, 2014
Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndromeArthur B McKie, Atif Alsaedi, Julie Vogt, et al.
Brain : a Journal of Neurology|September 14, 2010
Phospholipase C beta 1 deficiency is associated with early-onset epileptic encephalopathyManju A Kurian, Esther Meyer, Grace Vassallo, et al.
Pageof 28