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Anne Puel

Showing results (111-120 of 296) with videos related to

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Acta Microbiologica Et Immunologica Hungarica|June 10, 2017
A gain-of-function mutation of STAT1: A novel genetic factor contributing to chronic mucocutaneous candidiasisNarges Eslami, Marzieh Tavakol, Mehrnaz Mesdaghi, et al.
Journal of Clinical Immunology|November 2, 2022
IRAK1 Duplication in MECP2 Duplication Syndrome Does Not Increase Canonical NF-κB-Induced InflammationIlona Gottschalk, Uwe Kölsch, Dimitrios L Wagner, et al.
The Journal of Pediatrics|May 2, 2006
Autosomal recessive interleukin-1 receptor-associated kinase 4 deficiency in fourth-degree relativesMaría Cardenes, Horst von Bernuth, Ayoze García-Saavedra, et al.
Cell Genomics|February 23, 2023
Genetic adaptation to pathogens and increased risk of inflammatory disorders in post-Neolithic EuropeGaspard Kerner, Anna-Lena Neehus, Quentin Philippot, et al.
American Journal of Human Genetics|November 11, 2021
Identification of discriminative gene-level and protein-level features associated with pathogenic gain-of-function and loss-of-function variantsCigdem Sevim Bayrak, David Stein, Aayushee Jain, et al.
Frontiers in Immunology|February 13, 2020
<i>Aspergillus fumigatus</i> Infection in Humans With STAT3-Deficiency Is Associated With Defective Interferon-Gamma and Th17 ResponsesFrançois Danion, Vishukumar Aimanianda, Jagadeesh Bayry, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|October 25, 2008
Rhinoscleroma: a French national retrospective study of epidemiological and clinical featuresLoïc de Pontual, Philippe Ovetchkine, Diana Rodriguez, et al.
Journal of Medical Genetics|September 5, 2006
IRAK4 and NEMO mutations in otherwise healthy children with recurrent invasive pneumococcal diseaseCheng-Lung Ku, Capucine Picard, Melinda Erdös, et al.
Plos One|January 13, 2012
A mild form of SLC29A3 disorder: a frameshift deletion leads to the paradoxical translation of an otherwise noncoding mRNA splice variantAlexandre Bolze, Avinash Abhyankar, Audrey V Grant, et al.
BMC Surgery|September 23, 2023
Interventional pulmonary procedures and their outcomes in patients with STAT3 hyper IgE syndromeSeyed Alireza Mahdaviani, Soodeh Ghadimi, Mazdak Fallahi, et al.
Pageof 30

Showing results (111-120 of 296) with videos related to

Sort By:
Pageof 30
Acta Microbiologica Et Immunologica Hungarica|June 10, 2017
A gain-of-function mutation of STAT1: A novel genetic factor contributing to chronic mucocutaneous candidiasisNarges Eslami, Marzieh Tavakol, Mehrnaz Mesdaghi, et al.
Journal of Clinical Immunology|November 2, 2022
IRAK1 Duplication in MECP2 Duplication Syndrome Does Not Increase Canonical NF-κB-Induced InflammationIlona Gottschalk, Uwe Kölsch, Dimitrios L Wagner, et al.
The Journal of Pediatrics|May 2, 2006
Autosomal recessive interleukin-1 receptor-associated kinase 4 deficiency in fourth-degree relativesMaría Cardenes, Horst von Bernuth, Ayoze García-Saavedra, et al.
Cell Genomics|February 23, 2023
Genetic adaptation to pathogens and increased risk of inflammatory disorders in post-Neolithic EuropeGaspard Kerner, Anna-Lena Neehus, Quentin Philippot, et al.
American Journal of Human Genetics|November 11, 2021
Identification of discriminative gene-level and protein-level features associated with pathogenic gain-of-function and loss-of-function variantsCigdem Sevim Bayrak, David Stein, Aayushee Jain, et al.
Frontiers in Immunology|February 13, 2020
<i>Aspergillus fumigatus</i> Infection in Humans With STAT3-Deficiency Is Associated With Defective Interferon-Gamma and Th17 ResponsesFrançois Danion, Vishukumar Aimanianda, Jagadeesh Bayry, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|October 25, 2008
Rhinoscleroma: a French national retrospective study of epidemiological and clinical featuresLoïc de Pontual, Philippe Ovetchkine, Diana Rodriguez, et al.
Journal of Medical Genetics|September 5, 2006
IRAK4 and NEMO mutations in otherwise healthy children with recurrent invasive pneumococcal diseaseCheng-Lung Ku, Capucine Picard, Melinda Erdös, et al.
Plos One|January 13, 2012
A mild form of SLC29A3 disorder: a frameshift deletion leads to the paradoxical translation of an otherwise noncoding mRNA splice variantAlexandre Bolze, Avinash Abhyankar, Audrey V Grant, et al.
BMC Surgery|September 23, 2023
Interventional pulmonary procedures and their outcomes in patients with STAT3 hyper IgE syndromeSeyed Alireza Mahdaviani, Soodeh Ghadimi, Mazdak Fallahi, et al.
Pageof 30