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Showing results (181-190 of 206) with videos related to

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Frontiers in Immunology|August 21, 2023
Identification of eight novel proteasome variants in five unrelated cases of proteasome-associated autoinflammatory syndromes (PRAAS)Jonas Johannes Papendorf, Frédéric Ebstein, Sara Alehashemi, et al.
Lancet (London, England)|October 18, 2015
Outcomes after thrombus aspiration for ST elevation myocardial infarction: 1-year follow-up of the prospective randomised TOTAL trialSanjit S Jolly, John A Cairns, Salim Yusuf, et al.
Neurology. Genetics|December 7, 2022
Somatic Variants in SVIL in Cerebral AneurysmsPui Man Rosalind Lai, Jee-Yeon Ryu, Sang-Cheol Park, et al.
The New England Journal of Medicine|March 17, 2016
Loss of B Cells in Patients with Heterozygous Mutations in IKAROSH S Kuehn, B Boisson, C Cunningham-Rundles, et al.
Digestion|December 1, 2006
Use of sedation for routine diagnostic upper gastrointestinal endoscopy: a European Society of Gastrointestinal Endoscopy Survey of National Endoscopy Society MembersS D Ladas, L Aabakken, J-F Rey, et al.
Translational Stroke Research|August 23, 2023
A Transcriptomic Comparative Study of Cranial VasculatureJianing Zhang, Jee-Yeon Ryu, Selena-Rae Tirado, et al.
Blood|April 20, 2021
SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulationOttavia M Delmonte, Jenna R E Bergerson, Tomoki Kawai, et al.
Science (New York, N.Y.)|September 13, 2014
Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4Hye Sun Kuehn, Weiming Ouyang, Bernice Lo, et al.
Nature Genetics|October 28, 2017
Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic diseaseChi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
Nature Genetics|June 20, 2017
Germline hypomorphic CARD11 mutations in severe atopic diseaseChi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
Pageof 21

Showing results (181-190 of 206) with videos related to

Sort By:
Pageof 21
Frontiers in Immunology|August 21, 2023
Identification of eight novel proteasome variants in five unrelated cases of proteasome-associated autoinflammatory syndromes (PRAAS)Jonas Johannes Papendorf, Frédéric Ebstein, Sara Alehashemi, et al.
Lancet (London, England)|October 18, 2015
Outcomes after thrombus aspiration for ST elevation myocardial infarction: 1-year follow-up of the prospective randomised TOTAL trialSanjit S Jolly, John A Cairns, Salim Yusuf, et al.
Neurology. Genetics|December 7, 2022
Somatic Variants in SVIL in Cerebral AneurysmsPui Man Rosalind Lai, Jee-Yeon Ryu, Sang-Cheol Park, et al.
The New England Journal of Medicine|March 17, 2016
Loss of B Cells in Patients with Heterozygous Mutations in IKAROSH S Kuehn, B Boisson, C Cunningham-Rundles, et al.
Digestion|December 1, 2006
Use of sedation for routine diagnostic upper gastrointestinal endoscopy: a European Society of Gastrointestinal Endoscopy Survey of National Endoscopy Society MembersS D Ladas, L Aabakken, J-F Rey, et al.
Translational Stroke Research|August 23, 2023
A Transcriptomic Comparative Study of Cranial VasculatureJianing Zhang, Jee-Yeon Ryu, Selena-Rae Tirado, et al.
Blood|April 20, 2021
SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulationOttavia M Delmonte, Jenna R E Bergerson, Tomoki Kawai, et al.
Science (New York, N.Y.)|September 13, 2014
Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4Hye Sun Kuehn, Weiming Ouyang, Bernice Lo, et al.
Nature Genetics|October 28, 2017
Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic diseaseChi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
Nature Genetics|June 20, 2017
Germline hypomorphic CARD11 mutations in severe atopic diseaseChi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
Pageof 21