Mutations in <i>STAT3</i> and <i>IL12RB1</i> impair the development of human IL-17–producing T cells

Ludovic de Beaucoudrey, Anne Puel, Orchidée Filipe‐Santos, +42

The Journal of Experimental Medicine

Cdk2 suppresses cellular senescence induced by the c-myc oncogene

Stefano Campaner, Mirko Doni, Per Hydbring, +11

Nature Cell Biology

Signal TransductionCell RegulationC-myc OncogeneCellular SenescenceCell Cycle +3

Development of myelofibrosis in mice genetically impaired for GATA-1 expression (GATA-1low mice)

Alessandro M. Vannucchi, Lucia Bianchi, Cristina Cellai, +5

Blood

Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: Inconsistent correlation between forkhead box protein 3 expression and disease severity

Eleonora Gambineri, L Perroni, Laura Passerini, +22

Journal of Allergy and Clinical Immunology

Primary ImmunodeficiencyAutoimmune DiseaseDisease MechanismDisease SeverityImmunodeficiencies +13

GATA-1 as a Regulator of Mast Cell Differentiation Revealed by the Phenotype of the GATA-1low Mouse Mutant

Anna Ritá Migliaccio, Rosa Alba Rana, Massimo Sanchez, +6

The Journal of Experimental Medicine

A pathobiologic pathway linking thrombopoietin, GATA-1, and TGF-β1 in the development of myelofibrosis

Alessandro M. Vannucchi, Lucia Bianchi, Francesco Paoletti, +10

Blood

Abnormalities of GATA-1 in Megakaryocytes from Patients with Idiopathic Myelofibrosis

Alessandro M. Vannucchi, Alessandro Pancrazzi, Paola Guglielmelli, +7

American Journal Of Pathology

InflammationHematological MalignancyAutoimmune DiseaseGranulocyteHematology +6

Accentuated response to phenylhydrazine and erythropoietin in mice genetically impaired for their GATA-1 expression (GATA-1low mice)

Alessandro M. Vannucchi, Lucia Bianchi, Cristina Cellai, +10

Blood

CACP syndrome: identification of five novel mutations and of the first case of UPD in the largest European cohort

Sara Ciullini Mannurita, Marina Vignoli, Lucia Bianchi, +8

European Journal of Human Genetics

Largest European CohortMendelian DisorderGenetic DisorderPathologyMolecular Medicine +4

Myc, Cdk2 and cellular senescence: Old players, new game

Stefano Campaner, Mirko Doni, Alessandro Verrecchia, +3

Cell Cycle