Kolexia
Crow Yanick
Génétique médicale
Hôpital Necker Enfants Malades
Paris, France
180 Activités
0 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Maladies auto-immunes du système nerveux Malformations du système nerveux Lupus érythémateux disséminé Calcinose Inflammation Morsures et piqûres Kystes Leucoencéphalopathies Maladies auto-immunes

Industries

{{person.topindus1.name}}
{{person.topindus1.tot}} collaboration(s)
Dernière en {{person.topindus1.last}}
{{person.topindus2.name}}
{{person.topindus2.tot}} collaboration(s)
Dernière en {{person.topindus2.last}}
{{person.topindus3.name}}
{{person.topindus3.tot}} collaboration(s)
Dernière en {{person.topindus3.last}}
{{person.topindus4.name}}
{{person.topindus4.tot}} collaboration(s)
Dernière en {{person.topindus4.last}}

Dernières activités

Interface Gain-of-Function Mutations in TLR7 Cause Systemic and Neuro-inflammatory Disease.
Journal of clinical immunology   07 février 2024
IFN: Genotype-phenotype Characterization Study on Genetic Diseases With Immune and Neurological Dysfunctions
Essai Clinique (Imagine Institute)   23 janvier 2024
Mutations in the non-catalytic polyproline motif destabilize TREX1 and amplify cGAS-STING signaling.
bioRxiv : the preprint server for biology   04 janvier 2024
ARF1 prevents aberrant type I interferon induction by regulating STING activation and recycling.
Nature communications   01 novembre 2023
Elevated serum interferon-alpha associates with flare risk in juvenile-onset systemic lupus erythematosus
Proceedings of the 29th European Paediatric Rheumatology Congress   17 octobre 2023
Case report: Clinical and neuroradiological longitudinal follow-up in Leukoencephalopathy with Calcifications and Cysts during treatment with bevacizumab.
Frontiers in neurology   20 septembre 2023
LB1726 Pathogenic contribution of ADAR1 mutations to severe plaque psoriasis
The Journal of investigative dermatology   01 septembre 2023
JAK Inhibition in Aicardi-Goutières Syndrome: a Monocentric Multidisciplinary Real-World Approach Study.
Journal of clinical immunology   12 mai 2023
Molecular characterization of an intronic RNASEH2B variant in a patient with Aicardi-Goutières syndrome.
European journal of medical genetics   11 février 2023
Type I Interferonopathy due to a Homozygous Loss-of-Inhibitory Function Mutation in STAT2.
Journal of clinical immunology   08 février 2023