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Showing results (801-810 of 910) with videos related to

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Neurosurgery|April 3, 2023
Global Neurosurgery: Progress and Resolutions at the 75th World Health AssemblyRoxanna M Garcia, Kemel A Ghotme, Anastasia Arynchyna-Smith, et al.
Journal of Internal Medicine|July 16, 2024
High viral loads combined with inflammatory markers predict disease severity in hospitalized COVID-19 patients: Results from the NOR-Solidarity trialHans-Kittil Viermyr, Bente Halvorsen, Ellen Lund Sagen, et al.
The Journal of Allergy and Clinical Immunology|October 11, 2022
Duodenal inflammation in common variable immunodeficiency has altered transcriptional response to virusesMari Kaarbø, Mingyi Yang, Johannes R Hov, et al.
Frontiers in Immunology|September 28, 2018
IL-6 Receptor Inhibition by Tocilizumab Attenuated Expression of C5a Receptor 1 and 2 in Non-ST-Elevation Myocardial InfarctionHilde L Orrem, Per H Nilsson, Søren E Pischke, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 21, 2006
Enhanced T-cell expression of RANK ligand in acute coronary syndrome: possible role in plaque destabilizationWiggo J Sandberg, Arne Yndestad, Erik Øie, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2023
A Systematic Review of the use of Precision Diagnostics in Monogenic DiabetesRinki Murphy, Kevin Colclough, Toni I Pollin, et al.
European Journal of Human Genetics : EJHG|November 30, 2018
De novo truncating variants in PHF21A cause intellectual disability and craniofacial anomaliesKohei Hamanaka, Yuji Sugawara, Takeyoshi Shimoji, et al.
Journal of Neuroimmunology|November 5, 2015
Body mass index influence interferon-beta treatment response in multiple sclerosisSilje Stokke Kvistad, Kjell-Morten Myhr, Trygve Holmøy, et al.
Scientific Reports|October 6, 2021
NEIL3-deficiency increases gut permeability and contributes to a pro-atherogenic metabolic phenotypeTom Rune Karlsen, Xiang Yi Kong, Sverre Holm, et al.
Orphanet Journal of Rare Diseases|September 27, 2014
STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneityKetil Heimdal, Monica Sanchez-Guixé, Ingvild Aukrust, et al.
Pageof 91

Showing results (801-810 of 910) with videos related to

Sort By:
Pageof 91
Neurosurgery|April 3, 2023
Global Neurosurgery: Progress and Resolutions at the 75th World Health AssemblyRoxanna M Garcia, Kemel A Ghotme, Anastasia Arynchyna-Smith, et al.
Journal of Internal Medicine|July 16, 2024
High viral loads combined with inflammatory markers predict disease severity in hospitalized COVID-19 patients: Results from the NOR-Solidarity trialHans-Kittil Viermyr, Bente Halvorsen, Ellen Lund Sagen, et al.
The Journal of Allergy and Clinical Immunology|October 11, 2022
Duodenal inflammation in common variable immunodeficiency has altered transcriptional response to virusesMari Kaarbø, Mingyi Yang, Johannes R Hov, et al.
Frontiers in Immunology|September 28, 2018
IL-6 Receptor Inhibition by Tocilizumab Attenuated Expression of C5a Receptor 1 and 2 in Non-ST-Elevation Myocardial InfarctionHilde L Orrem, Per H Nilsson, Søren E Pischke, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 21, 2006
Enhanced T-cell expression of RANK ligand in acute coronary syndrome: possible role in plaque destabilizationWiggo J Sandberg, Arne Yndestad, Erik Øie, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2023
A Systematic Review of the use of Precision Diagnostics in Monogenic DiabetesRinki Murphy, Kevin Colclough, Toni I Pollin, et al.
European Journal of Human Genetics : EJHG|November 30, 2018
De novo truncating variants in PHF21A cause intellectual disability and craniofacial anomaliesKohei Hamanaka, Yuji Sugawara, Takeyoshi Shimoji, et al.
Journal of Neuroimmunology|November 5, 2015
Body mass index influence interferon-beta treatment response in multiple sclerosisSilje Stokke Kvistad, Kjell-Morten Myhr, Trygve Holmøy, et al.
Scientific Reports|October 6, 2021
NEIL3-deficiency increases gut permeability and contributes to a pro-atherogenic metabolic phenotypeTom Rune Karlsen, Xiang Yi Kong, Sverre Holm, et al.
Orphanet Journal of Rare Diseases|September 27, 2014
STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneityKetil Heimdal, Monica Sanchez-Guixé, Ingvild Aukrust, et al.
Pageof 91