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Publications by Marita Bosticardo

Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis

American Journal of Human Genetics
Genetics
2019English

447. Lentiviral Gene Therapy in a Preclinical Model of Omenn Syndrome

Molecular Therapy
Molecular MedicineMolecular BiologyPharmacologyMedicineGeneticsDrug Discovery
2015English

A Hypomorphic R229Q Rag2 Mouse Mutant Recapitulates Human Omenn Syndrome

Journal of Clinical Investigation
Medicine
2007English

CCL16/LEC Powerfully Triggers Effector and Antigen-Presenting Functions of Macrophages and Enhances T Cell Cytotoxicity

Journal of Leukocyte Biology
AllergyImmunologyCell Biology
2003English

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