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E Morrison

Showing results (831-840 of 971) with videos related to

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The Journal of Infectious Diseases|May 2, 2007
Accelerated detection of Mycobacterium tuberculosis genes essential for bacterial survival in guinea pigs, compared with miceSanjay K Jain, S Moises Hernandez-Abanto, Qi-Jian Cheng, et al.
Journal of the American Society of Nephrology : JASN|March 30, 2016
Vasopressin Regulates Extracellular Vesicle Uptake by Kidney Collecting Duct CellsWilna Oosthuyzen, Kathleen M Scullion, Jessica R Ivy, et al.
Hypertension (Dallas, Tex. : 1979)|May 17, 2017
First-in-Man Demonstration of Direct Endothelin-Mediated Natriuresis and DiuresisRobert W Hunter, Rebecca Moorhouse, Tariq E Farrah, et al.
Brain : a Journal of Neurology|April 22, 2017
A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UKSarah Morgan, Aleksey Shatunov, William Sproviero, et al.
Kidney International|August 31, 2024
Myeloperoxidase-ANCA IgG induces different forms of small vessel vasculitis based on type of synergistic immune stimuliPeiqi Hu, Hong Xiao, Marco A Alba, et al.
Neurology|May 7, 2013
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson diseaseGavin Hudson, Mike Nalls, Jonathan R Evans, et al.
The American Journal of Surgical Pathology|June 30, 2009
Fluorescence in situ hybridization (FISH) as an ancillary diagnostic tool in the diagnosis of melanomaPedram Gerami, Susan S Jewell, Larry E Morrison, et al.
Nature|January 18, 2008
NLRX1 is a regulator of mitochondrial antiviral immunityChris B Moore, Daniel T Bergstralh, Joseph A Duncan, et al.
Nature Communications|September 25, 2025
A specific gene expression program underlies antigen archiving by lymphatic endothelial cells in mammalian lymph nodesRyan M Sheridan, Thu A Doan, Cormac J Lucas, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 18, 2003
No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disordersAzlina Ahmad-Annuar, Paresh Shah, Majid Hafezparast, et al.
Pageof 98

Showing results (831-840 of 971) with videos related to

Sort By:
Pageof 98
The Journal of Infectious Diseases|May 2, 2007
Accelerated detection of Mycobacterium tuberculosis genes essential for bacterial survival in guinea pigs, compared with miceSanjay K Jain, S Moises Hernandez-Abanto, Qi-Jian Cheng, et al.
Journal of the American Society of Nephrology : JASN|March 30, 2016
Vasopressin Regulates Extracellular Vesicle Uptake by Kidney Collecting Duct CellsWilna Oosthuyzen, Kathleen M Scullion, Jessica R Ivy, et al.
Hypertension (Dallas, Tex. : 1979)|May 17, 2017
First-in-Man Demonstration of Direct Endothelin-Mediated Natriuresis and DiuresisRobert W Hunter, Rebecca Moorhouse, Tariq E Farrah, et al.
Brain : a Journal of Neurology|April 22, 2017
A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UKSarah Morgan, Aleksey Shatunov, William Sproviero, et al.
Kidney International|August 31, 2024
Myeloperoxidase-ANCA IgG induces different forms of small vessel vasculitis based on type of synergistic immune stimuliPeiqi Hu, Hong Xiao, Marco A Alba, et al.
Neurology|May 7, 2013
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson diseaseGavin Hudson, Mike Nalls, Jonathan R Evans, et al.
The American Journal of Surgical Pathology|June 30, 2009
Fluorescence in situ hybridization (FISH) as an ancillary diagnostic tool in the diagnosis of melanomaPedram Gerami, Susan S Jewell, Larry E Morrison, et al.
Nature|January 18, 2008
NLRX1 is a regulator of mitochondrial antiviral immunityChris B Moore, Daniel T Bergstralh, Joseph A Duncan, et al.
Nature Communications|September 25, 2025
A specific gene expression program underlies antigen archiving by lymphatic endothelial cells in mammalian lymph nodesRyan M Sheridan, Thu A Doan, Cormac J Lucas, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 18, 2003
No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disordersAzlina Ahmad-Annuar, Paresh Shah, Majid Hafezparast, et al.
Pageof 98