Type I interferon in patients with systemic autoimmune rheumatic disease is associated with haematological abnormalities and specific autoantibody profiles
John A. Reynolds
,
Tracy Briggs
,
Gillian Rice
,
Sathya Darmalinggam
,
Vincent Bondet
,
et al.
Journal articles
pasteur-02173399v1
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Microglial Priming as Trained Immunity in the Brain
Michael Haley
,
David Brough
,
Jessica Quintin
,
Stuart Allan
Journal articles
pasteur-02873942v1
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Efficacy of the Janus kinase 1/2 inhibitor ruxolitinib in the treatment of vasculopathy associated with TMEM173-activating mutations in 3 children
Marie-Louise Frémond
,
Mathieu Paul Rodero
,
Nadia Jeremiah
,
Alexandre Belot
,
Eric Jeziorski
,
et al.
Journal articles
hal-01911048v1
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Use of ruxolitinib in COPA syndrome manifesting as life-threatening alveolar haemorrhage
Marie-Louise Frémond
,
Marie Legendre
,
Michael Fayon
,
Annick Clement
,
Emilie Filhol-Blin
,
et al.
Journal articles
pasteur-02376257v1
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OP0107 HETEROZYGOUS MUTATIONS IN COPA ARE ASSOCIATED WITH ENHANCED TYPE I INTERFERON SIGNALLING
Marie-Louise Frémond
,
Alice Lepelley
,
Carolina Uggenti
,
Maria José Martin-Niclos
,
Marine Depp
,
et al.
Conference papers
pasteur-03251879v1
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Comment on: ‘Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors’ by Giannelou et al : mutations in TRNT1 result in a constitutive activation of type I interferon signalling
Marie-Louise Frémond
,
Isabelle Melki
,
Sven Kracker
,
Vincent Bondet
,
Darragh Duffy
,
et al.
Journal articles
pasteur-01819255v1
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Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling
Alice Lepelley
,
Maria José Martin-Niclos
,
Melvin Le Bihan
,
Joseph A. Marsh
,
Carolina Uggenti
,
et al.
Journal articles
pasteur-02933253v1
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PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunity
Anne-Laure Mathieu
,
Estelle Verronese
,
Gillian I. Rice
,
Fanny Fouyssac
,
Yves Bertrand
,
et al.
Journal articles
hal-01917848v1
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Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
Marije E.C. Meuwissen
,
Rachel Schot
,
Sofija Buta
,
Grétel Oudesluijs
,
Sigrid Tinschert
,
et al.
Journal articles
pasteur-02070980v1
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Characterization of samhd1 Morphant Zebrafish Recapitulates Features of the Human Type I Interferonopathy Aicardi-Goutières Syndrome
Paul Kasher
,
Emma Jenkinson
,
Valérie Briolat
,
David Gent
,
Catherine Morrissey
,
et al.
Journal articles
pasteur-02558343v1
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Detection of interferon alpha protein reveals differential levels and cellular sources in disease.
Mathieu P. Rodero
,
Jérémie Decalf
,
Vincent Bondet
,
David Hunt
,
Gillian I. Rice
,
et al.
Journal articles
pasteur-01534181v1
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Anti-MDA5 juvenile idiopathic inflammatory myopathy: a specific subgroup defined by differentially enhanced interferon-α signalling
Isabelle Melki
,
Hervé Devilliers
,
Cyril Gitiaux
,
Vincent Bondet
,
Darragh Duffy
,
et al.
Journal articles
pasteur-02383120v1
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Overview of STING-Associated Vasculopathy with Onset in Infancy (SAVI) Among 21 Patients
Marie-Louise Frémond
,
Alice Hadchouel
,
Laureline Berteloot
,
Isabelle Melki
,
Violaine Bresson
,
et al.
Journal articles
hal-03228789v1
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