Allelic repertoire of the humanMHC class IMICA gene

Nassima Fodil, Laurent Laloux, Valérie Wanner, +7

Immunogenetics

HistocompatibilityImmunogeneticsAllelic RepertoireGeneticsAutoimmunity +1

Regulated in development and DNA damage responses 1 (REDD1) links stress with IL-1β–mediated familial Mediterranean fever attack through autophagy-driven neutrophil extracellular traps

Panagiotis Skendros, Akrivi Chrysanthopoulou, François Rousset, +17

Journal of Allergy and Clinical Immunology

InflammationHost ResponseDisease MechanismImmune Cell DevelopmentAutoinflammatory Disorders +12

MICA haplotypic diversity

Nassima Fodil, Philippe Pellet, Laurent Laloux, +3

Immunogenetics

BiologyGenetic DiversityBiodiversityMolecular EcologyNatural Sciences +6

Effects of Sleep Deprivation and Reversal of Diurnal Activity on Protein Metabolism of Young Men

N. S. Scrimshaw, Jean‐Pierre Habicht, Philippe Pellet, +2

American Journal of Clinical Nutrition

NutritionSleepEnergy HomeostasisSleep DisorderDiurnal Activity +8

Cloning and functional characterization of the human fractalkine receptor promoter regions

Alexandre Garin, Philippe Pellet, Philippe Déterre, +2

Biochemical Journal

Deleterious Genetic Influence of CX3CR1 Genotypes on HIV-1 Disease Progression

Sophie Faure, Laurence Meyer, Emmanuelle Génin, +4

JAIDS Journal of Acquired Immune Deficiency Syndromes

The productive gene for <i>alpha</i>-H chain disease protein MAL is highly modified by insertion-deletion processes.

Andréas Tsapis, M Bentaboulet, Philippe Pellet, +4

The Journal of Immunology

Molecular analysis of a t(9;14)(p11;q32) translocation occurring in a case of human alpha heavy chain disease.

Philippe Pellet, R Berger, Alain Bernheim, +2

PubMed

Germline ATG2B/GSKIP-containing 14q32 duplication predisposes to early clonal hematopoiesis leading to myeloid neoplasms

Jean Pegliasco, Pierre Hirsch, Christophe Marzac, +28

Leukemia

Hematological MalignancyDuplication PredisposesEarly Clonal HematopoiesisGeneticsHematology +7

Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity

Viviana Marin‐Esteban, Jenny Youn, Blandine Beaupain, +11

Haematologica