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Fabio Candotti

Showing results (121-130 of 143) with videos related to

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The Journal of Clinical Investigation|September 20, 2016
FOXP3+ Tregs require WASP to restrain Th2-mediated food allergyWillem S Lexmond, Jeremy A Goettel, Jonathan J Lyons, et al.
Clinical Genetics|February 15, 2021
Immune deficiency, autoimmune disease and intellectual disability: A pleiotropic disorder caused by biallelic variants in the TPP2 geneIsis Atallah, Mathieu Quinodoz, Belinda Campos-Xavier, et al.
Frontiers in Immunology|June 17, 2021
Transcriptomic Signature Differences Between SARS-CoV-2 and Influenza Virus Infected PatientsStéphanie Bibert, Nicolas Guex, Joao Lourenco, et al.
The New England Journal of Medicine|June 5, 2014
Actionable diagnosis of neuroleptospirosis by next-generation sequencingMichael R Wilson, Samia N Naccache, Erik Samayoa, et al.
American Journal of Human Genetics|June 6, 2015
Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutationsJennifer J Johnston, Katie L Lewis, David Ng, et al.
Journal of Clinical Immunology|June 21, 2023
Correction to: New Dominant‑Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130‑Dependent Hyper‑IgE SyndromeTiphaine Arlabosse, Marie Materna, Orbicia Riccio, et al.
Journal of Clinical Immunology|May 31, 2019
Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI SyndromeStefano Volpi, Antonella Insalaco, Roberta Caorsi, et al.
Journal of Clinical Immunology|June 5, 2023
New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE SyndromeTiphaine Arlabosse, Marie Materna, Orbicia Riccio, et al.
Nature Genetics|December 2, 2008
Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafnessChantal Lagresle-Peyrou, Emmanuelle M Six, Capucine Picard, et al.
The Journal of Allergy and Clinical Immunology|August 15, 2024
Variants in IGLL1 cause a broad phenotype from agammaglobulinemia to transient hypogammaglobulinemiaMaarja Soomann, Viktor Bily, Magdeldin Elgizouli, et al.
Pageof 15

Showing results (121-130 of 143) with videos related to

Sort By:
Pageof 15
The Journal of Clinical Investigation|September 20, 2016
FOXP3+ Tregs require WASP to restrain Th2-mediated food allergyWillem S Lexmond, Jeremy A Goettel, Jonathan J Lyons, et al.
Clinical Genetics|February 15, 2021
Immune deficiency, autoimmune disease and intellectual disability: A pleiotropic disorder caused by biallelic variants in the TPP2 geneIsis Atallah, Mathieu Quinodoz, Belinda Campos-Xavier, et al.
Frontiers in Immunology|June 17, 2021
Transcriptomic Signature Differences Between SARS-CoV-2 and Influenza Virus Infected PatientsStéphanie Bibert, Nicolas Guex, Joao Lourenco, et al.
The New England Journal of Medicine|June 5, 2014
Actionable diagnosis of neuroleptospirosis by next-generation sequencingMichael R Wilson, Samia N Naccache, Erik Samayoa, et al.
American Journal of Human Genetics|June 6, 2015
Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutationsJennifer J Johnston, Katie L Lewis, David Ng, et al.
Journal of Clinical Immunology|June 21, 2023
Correction to: New Dominant‑Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130‑Dependent Hyper‑IgE SyndromeTiphaine Arlabosse, Marie Materna, Orbicia Riccio, et al.
Journal of Clinical Immunology|May 31, 2019
Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI SyndromeStefano Volpi, Antonella Insalaco, Roberta Caorsi, et al.
Journal of Clinical Immunology|June 5, 2023
New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE SyndromeTiphaine Arlabosse, Marie Materna, Orbicia Riccio, et al.
Nature Genetics|December 2, 2008
Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafnessChantal Lagresle-Peyrou, Emmanuelle M Six, Capucine Picard, et al.
The Journal of Allergy and Clinical Immunology|August 15, 2024
Variants in IGLL1 cause a broad phenotype from agammaglobulinemia to transient hypogammaglobulinemiaMaarja Soomann, Viktor Bily, Magdeldin Elgizouli, et al.
Pageof 15