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Matthieu Bouaziz

Showing results (11-20 of 19) with videos related to

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Arthritis and Rheumatism|August 29, 2013
A regulatory variant in CCR6 is associated with susceptibility to antitopoisomerase-positive systemic sclerosisEugénie Koumakis, Matthieu Bouaziz, Philippe Dieudé, et al.
Elife|March 15, 2018
IRF4 haploinsufficiency in a family with Whipple's diseaseAntoine Guérin, Gaspard Kerner, Nico Marr, et al.
Annals of the Rheumatic Diseases|August 17, 2012
TGFβ receptor gene variants in systemic sclerosis-related pulmonary arterial hypertension: results from a multicentre EUSTAR study of European Caucasian patientsEugénie Koumakis, Julien Wipff, Philippe Dieudé, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 2018
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated <i>RPSA</i> exonsAlexandre Bolze, Bertrand Boisson, Barbara Bosch, et al.
The Journal of Experimental Medicine|August 3, 2018
The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomavirusesSarah Jill de Jong, Amandine Créquer, Irina Matos, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 29, 2021
Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 DeficiencyTom Le Voyer, Sonoko Sakata, Miyuki Tsumura, et al.
Science Immunology|June 17, 2018
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activityVivien Béziat, Juan Li, Jian-Xin Lin, et al.
Science Immunology|December 23, 2018
Tuberculosis and impaired IL-23-dependent IFN-γ immunity in humans homozygous for a common <i>TYK2</i> missense variantStéphanie Boisson-Dupuis, Noe Ramirez-Alejo, Zhi Li, et al.
The Journal of Clinical Investigation|July 4, 2018
Inherited p40phox deficiency differs from classic chronic granulomatous diseaseAnnemarie van de Geer, Alejandro Nieto-Patlán, Douglas B Kuhns, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Arthritis and Rheumatism|August 29, 2013
A regulatory variant in CCR6 is associated with susceptibility to antitopoisomerase-positive systemic sclerosisEugénie Koumakis, Matthieu Bouaziz, Philippe Dieudé, et al.
Elife|March 15, 2018
IRF4 haploinsufficiency in a family with Whipple's diseaseAntoine Guérin, Gaspard Kerner, Nico Marr, et al.
Annals of the Rheumatic Diseases|August 17, 2012
TGFβ receptor gene variants in systemic sclerosis-related pulmonary arterial hypertension: results from a multicentre EUSTAR study of European Caucasian patientsEugénie Koumakis, Julien Wipff, Philippe Dieudé, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 2018
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated <i>RPSA</i> exonsAlexandre Bolze, Bertrand Boisson, Barbara Bosch, et al.
The Journal of Experimental Medicine|August 3, 2018
The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomavirusesSarah Jill de Jong, Amandine Créquer, Irina Matos, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 29, 2021
Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 DeficiencyTom Le Voyer, Sonoko Sakata, Miyuki Tsumura, et al.
Science Immunology|June 17, 2018
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activityVivien Béziat, Juan Li, Jian-Xin Lin, et al.
Science Immunology|December 23, 2018
Tuberculosis and impaired IL-23-dependent IFN-γ immunity in humans homozygous for a common <i>TYK2</i> missense variantStéphanie Boisson-Dupuis, Noe Ramirez-Alejo, Zhi Li, et al.
The Journal of Clinical Investigation|July 4, 2018
Inherited p40phox deficiency differs from classic chronic granulomatous diseaseAnnemarie van de Geer, Alejandro Nieto-Patlán, Douglas B Kuhns, et al.
Pageof 2