Associated Papers
Epidermodysplasia Verruciformis and Vδ2 γδ T-cell Expansion in STK4 Deficiency.
Ying W et al.
Journal of Clinical Immunology, 2024
39110273 (PubMed )
Supplement: 10875_2024_1780_MOESM2_ESM.xlsx › S3_Immunophenotype_review
Hematopoietic stem cell transplantation in serine/threonine kinase 4 (STK4) deficiency: Report of two cases and literature review.
Uygun V et al.
Pediatric Transplantation, 2023
A Novel STK4 Mutation Impairs T Cell Immunity Through Dysregulation of Cytokine-Induced Adhesion and Chemotaxis Genes.
Guennoun A et al.
Journal of Clinical Immunology, 2021
A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis.
Sharafian S et al.
Journal of Clinical Immunology, 2019
Noncanonical Hippo Signalling in the Regulation of Leukocyte Function.
Kurz ARM et al.
Trends in Immunology, 2018
EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency.
Schipp C et al.
Frontiers in Immunology, 2018
F-actin remodeling defects as revealed in primary immunodeficiency disorders.
Janssen WJ et al.
Clinical Immunology (orlando, Fla.), 2016
MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival.
Nehme NT et al.
Blood, 2012
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