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Niemela

Showing results (171-180 of 206) with videos related to

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Lancet (London, England)|September 7, 2010
Double-dose versus standard-dose clopidogrel and high-dose versus low-dose aspirin in individuals undergoing percutaneous coronary intervention for acute coronary syndromes (CURRENT-OASIS 7): a randomised factorial trialShamir R Mehta, Jean-Francois Tanguay, John W Eikelboom, et al.
The Journal of Clinical Investigation|November 28, 2023
Disease-associated AIOLOS variants lead to immune deficiency/dysregulation by haploinsufficiency and redefine AIOLOS functional domainsHye Sun Kuehn, Inga S Sakovich, Julie E Niemela, et al.
The Journal of Allergy and Clinical Immunology|June 5, 2023
TCF3 haploinsufficiency defined by immune, clinical, gene-dosage, and murine studiesBrigette Boast, Shubham Goel, Luis I González-Granado, et al.
Journal of the American College of Cardiology|November 30, 2019
Timing of Staged Nonculprit Artery Revascularization in Patients With ST-Segment Elevation Myocardial Infarction: COMPLETE TrialDavid A Wood, John A Cairns, Jia Wang, et al.
JACC. Cardiovascular Interventions|April 15, 2026
Percutaneous Coronary Intervention in Frail Patients Undergoing Transcatheter Aortic Valve Replacement: A NOTION-3 SubstudyHanna Ratcovich, Lene Holmvang, Golnaz Sadjadieh, et al.
Nature Communications|June 22, 2023
Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signalingCristiane J Nunes-Santos, HyeSun Kuehn, Brigette Boast, et al.
Journal of Clinical Immunology|May 6, 2021
Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel MutationsSaul Oswaldo Lugo-Reyes, Nina Pastor, Edith González-Serrano, et al.
Nature Immunology|October 30, 2013
Dominant-activating germline mutations in the gene encoding the PI(3)K catalytic subunit p110δ result in T cell senescence and human immunodeficiencyCarrie L Lucas, Hye Sun Kuehn, Fang Zhao, et al.
Blood|September 22, 2023
Natural history study of patients with familial platelet disorder with associated myeloid malignancyLea Cunningham, Matthew Merguerian, Katherine R Calvo, et al.
The Journal of Clinical Investigation|June 12, 2018
Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiencyDavid Boutboul, Hye Sun Kuehn, Zoé Van de Wyngaert, et al.
Pageof 21

Showing results (171-180 of 206) with videos related to

Sort By:
Pageof 21
Lancet (London, England)|September 7, 2010
Double-dose versus standard-dose clopidogrel and high-dose versus low-dose aspirin in individuals undergoing percutaneous coronary intervention for acute coronary syndromes (CURRENT-OASIS 7): a randomised factorial trialShamir R Mehta, Jean-Francois Tanguay, John W Eikelboom, et al.
The Journal of Clinical Investigation|November 28, 2023
Disease-associated AIOLOS variants lead to immune deficiency/dysregulation by haploinsufficiency and redefine AIOLOS functional domainsHye Sun Kuehn, Inga S Sakovich, Julie E Niemela, et al.
The Journal of Allergy and Clinical Immunology|June 5, 2023
TCF3 haploinsufficiency defined by immune, clinical, gene-dosage, and murine studiesBrigette Boast, Shubham Goel, Luis I González-Granado, et al.
Journal of the American College of Cardiology|November 30, 2019
Timing of Staged Nonculprit Artery Revascularization in Patients With ST-Segment Elevation Myocardial Infarction: COMPLETE TrialDavid A Wood, John A Cairns, Jia Wang, et al.
JACC. Cardiovascular Interventions|April 15, 2026
Percutaneous Coronary Intervention in Frail Patients Undergoing Transcatheter Aortic Valve Replacement: A NOTION-3 SubstudyHanna Ratcovich, Lene Holmvang, Golnaz Sadjadieh, et al.
Nature Communications|June 22, 2023
Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signalingCristiane J Nunes-Santos, HyeSun Kuehn, Brigette Boast, et al.
Journal of Clinical Immunology|May 6, 2021
Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel MutationsSaul Oswaldo Lugo-Reyes, Nina Pastor, Edith González-Serrano, et al.
Nature Immunology|October 30, 2013
Dominant-activating germline mutations in the gene encoding the PI(3)K catalytic subunit p110δ result in T cell senescence and human immunodeficiencyCarrie L Lucas, Hye Sun Kuehn, Fang Zhao, et al.
Blood|September 22, 2023
Natural history study of patients with familial platelet disorder with associated myeloid malignancyLea Cunningham, Matthew Merguerian, Katherine R Calvo, et al.
The Journal of Clinical Investigation|June 12, 2018
Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiencyDavid Boutboul, Hye Sun Kuehn, Zoé Van de Wyngaert, et al.
Pageof 21