Publications and ressources

NKp46 is a diagnostic biomarker and may be a therapeutic target in gastrointestinal T-cell lymphoproliferative diseases: a CELAC study.

Olivier Hermine

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A deep intronic splice mutation of STAT3 underlies hyper IgE syndrome by negative dominance.

Jean-Laurent CASANOVA

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PAXX and Xlf interplay revealed by impaired CNS development and immunodeficiency of double KO mice.

Jean-Pierre De Villartay

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Prevalence and risk factors for latent tuberculosis infection among healthcare workers in Morocco.

Laurent Abel , Aurélie Cobat, Jocelyn Quistrebert

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New Publication

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Modulation of the gut microbiota to improve innate resistance.

Nadine CERF-BENSUSSAN

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Pleiotropic effects for Parkin and LRRK2 in leprosy type-1 reactions and Parkinson's disease.

Laurent Abel , Aurélie Cobat, Alexandre Alcaïs

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Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations.

Lydie Burglen, Nadia Bahi-Buisson

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Ex vivo generated human T-lymphoid progenitors as a tool to accelerate immune reconstitution after partially HLA compatible hematopoietic stem cell transplantation or after gene therapy.

Isabelle André, Laura SIMONS, Kuiying MA, Marina Cavazzana

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Generation of adult human T-cell progenitors for immunotherapeutic applications.

Corinne de Chappedelaine, Ranjita MOIRANGTHEM, Chantal LAGRESLE-PEYROU, Antonio Rausell, Marina Cavazzana, Isabelle André

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TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology.

Aurore Carre

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Impaired telomere integrity and rRNA biogenesis in PARN-deficient patients and knock-out models.

Patrick Revy

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De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene.

Vincent Cantagrel

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Casein kinase 1ε and 1α as novel players in polycystic kidney disease and mechanistic targets for (R)-roscovitine and (S)-CR8.

Sophie Saunier

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Recent advances in celiac disease and refractory celiac disease.

Nadine CERF-BENSUSSAN

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