N. Jeremiah

发表

RAS-associated lymphoproliferative disease evolves into severe juvenile myelo-monocytic leukemia.

F. Rieux-Laucat, A. Fischer, H. Cavé, 2014, Blood.

Heterozygous RELA mutations cause early-onset systemic lupus erythematosus by hijacking the NF-κB pathway towards transcriptional activation of type-I Interferon genes

F. Rieux-Laucat, C. Bodemer, C. Picard, 2020, bioRxiv.

Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations.

T. Molina, F. Rieux-Laucat, A. Fischer, 2014, The Journal of clinical investigation.

Severe Pulmonary Fibrosis as the First Manifestation of Interferonopathy (TMEM173 Mutation).

F. Rieux-Laucat, P. Reix, J. Dubus, 2016, Chest.

Stimulator of Interferon Genes-Associated Vasculopathy With Onset in Infancy: A Mimic of Childhood Granulomatosis With Polyangiitis.

F. Rieux-Laucat, Y. Crow, G. Rice, 2015, JAMA dermatology.

Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part one

J. Stinson, J. Jaremko, A. Goris, 2017, Pediatric Rheumatology.

Severe combined immunodeficiency in stimulator of interferon genes (STING) V154M/wild‐type mice

F. Rieux-Laucat, Y. Crow, Sophie Jung, 2019, The Journal of allergy and clinical immunology.

Efficacy of the Janus kinase 1/2 inhibitor ruxolitinib in the treatment of vasculopathy associated with TMEM173-activating mutations in 3 children.

F. Rieux-Laucat, A. Fischer, C. Bodemer, 2016, The Journal of allergy and clinical immunology.

Overview of STING-associated vasculopathy with onset in infancy (SAVI) among 21 patients.

T. Molina, F. Rieux-Laucat, A. Fischer, 2020, The journal of allergy and clinical immunology. In practice.

VPS33B regulates protein sorting into and maturation of α-granule progenitor organelles in mouse megakaryocytes.

F. Rieux-Laucat, S. Watson, G. Ariceta, 2015, Blood.

Intrinsic antiproliferative activity of the innate sensor STING in T lymphocytes

F. Rieux-Laucat, A. Fischer, C. Picard, 2017, The Journal of experimental medicine.

Are RASopathies new monogenic predisposing conditions to the development of systemic lupus erythematosus? Case report and systematic review of the literature.

F. Rieux-Laucat, H. Cavé, B. Bader-Meunier, 2013, Seminars in arthritis and rheumatism.

Genetic tools for analysis of FoxP3+ regulatory T cells in vivo.

A. Liston, N. Jeremiah, 2011, Methods in molecular biology.

Disease‐associated mutations identify a novel region in human STING necessary for the control of type I interferon signaling

F. Rieux-Laucat, C. Bodemer, C. Wouters, 2017, The Journal of allergy and clinical immunology.

RELA tunes innate-like interferon I/III responses in human T cells

P. Benaroch, N. Manel, J. Nikolic, 2023, The Journal of experimental medicine.

Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations.

T. Molina, F. Rieux-Laucat, A. Fischer, 2014, The Journal of clinical investigation.

Severe Pulmonary Fibrosis as the First Manifestation of Interferonopathy (TMEM173 Mutation).

F. Rieux-Laucat, P. Reix, J. Dubus, 2016, Chest.

Stimulator of Interferon Genes-Associated Vasculopathy With Onset in Infancy: A Mimic of Childhood Granulomatosis With Polyangiitis.

F. Rieux-Laucat, Y. Crow, G. Rice, 2015, JAMA dermatology.