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P Atkinson

Showing results (711-720 of 730) with videos related to

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Immunity|December 10, 2013
Intracellular complement activation sustains T cell homeostasis and mediates effector differentiationM Kathryn Liszewski, Martin Kolev, Gaelle Le Friec, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
Impaired complement regulation drives chronic lung allograft dysfunction after lung transplantationHrishikesh S Kulkarni, Laneshia K Tague, Daniel R Calabrese, et al.
American Journal of Human Genetics|August 12, 1999
Genetic linkage of hyper-IgE syndrome to chromosome 4B Grimbacher, A A Schäffer, S M Holland, et al.
American Journal of Human Genetics|July 5, 2001
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3R A Ophoff, J DeYoung, S K Service, et al.
Neurology|September 5, 2020
Lesion evolution and neurodegeneration in RVCL-S: A monogenic microvasculopathyAndria L Ford, Victoria W Chin, Slim Fellah, et al.
CJEM|December 28, 2022
Does point-of-care ultrasonography improve diagnostic accuracy in emergency department patients with undifferentiated hypotension? An international randomized controlled trial from the SHOC-ED investigatorsM Peach, J Milne, L Diegelmann, et al.
JCI Insight|August 5, 2020
Local complement activation is associated with primary graft dysfunction after lung transplantationHrishikesh S Kulkarni, Kristy Ramphal, Lina Ma, et al.
Cureus|September 24, 2020
Does Point of Care Ultrasound Improve Resuscitation Markers in Undifferentiated Hypotension? An International Randomized Controlled Trial From The Sonography in Hypotension and Cardiac Arrest in the Emergency Department (SHoC-ED) SeriesPaul Atkinson, Luke Taylor, James Milne, et al.
Nature|March 15, 2017
3D structures of individual mammalian genomes studied by single-cell Hi-CTim J Stevens, David Lando, Srinjan Basu, et al.
Human Molecular Genetics|March 30, 2021
The rare C9 P167S risk variant for age-related macular degeneration increases polymerization of the terminal component of the complement cascadeO McMahon, T M Hallam, S Patel, et al.
Pageof 73

Showing results (711-720 of 730) with videos related to

Sort By:
Pageof 73
Immunity|December 10, 2013
Intracellular complement activation sustains T cell homeostasis and mediates effector differentiationM Kathryn Liszewski, Martin Kolev, Gaelle Le Friec, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
Impaired complement regulation drives chronic lung allograft dysfunction after lung transplantationHrishikesh S Kulkarni, Laneshia K Tague, Daniel R Calabrese, et al.
American Journal of Human Genetics|August 12, 1999
Genetic linkage of hyper-IgE syndrome to chromosome 4B Grimbacher, A A Schäffer, S M Holland, et al.
American Journal of Human Genetics|July 5, 2001
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3R A Ophoff, J DeYoung, S K Service, et al.
Neurology|September 5, 2020
Lesion evolution and neurodegeneration in RVCL-S: A monogenic microvasculopathyAndria L Ford, Victoria W Chin, Slim Fellah, et al.
CJEM|December 28, 2022
Does point-of-care ultrasonography improve diagnostic accuracy in emergency department patients with undifferentiated hypotension? An international randomized controlled trial from the SHOC-ED investigatorsM Peach, J Milne, L Diegelmann, et al.
JCI Insight|August 5, 2020
Local complement activation is associated with primary graft dysfunction after lung transplantationHrishikesh S Kulkarni, Kristy Ramphal, Lina Ma, et al.
Cureus|September 24, 2020
Does Point of Care Ultrasound Improve Resuscitation Markers in Undifferentiated Hypotension? An International Randomized Controlled Trial From The Sonography in Hypotension and Cardiac Arrest in the Emergency Department (SHoC-ED) SeriesPaul Atkinson, Luke Taylor, James Milne, et al.
Nature|March 15, 2017
3D structures of individual mammalian genomes studied by single-cell Hi-CTim J Stevens, David Lando, Srinjan Basu, et al.
Human Molecular Genetics|March 30, 2021
The rare C9 P167S risk variant for age-related macular degeneration increases polymerization of the terminal component of the complement cascadeO McMahon, T M Hallam, S Patel, et al.
Pageof 73