Junfeng Wu
Chongqing, China
Last Updated: 09/26/2026
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Found 15 publications
A novel linker region truncating variant in BCL10 underlies a leaky immunodeficiency phenotype.
Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Published: April 29, 2026
Janus kinase inhibitor therapy for the treatment of spondyloenchondrodysplasia with immune dysregulation due to novel ACP5 variants: a multicenter study.
Journal: Frontiers in immunology
Published: January 15, 2026
Novel Compound Heterozygous Mutations in HOIP Result in Autoinflammation and Immunodeficiency.
Journal: Journal of clinical immunology
Published: December 24, 2024
Editorial: Case Reports in Pediatric Rheumatology 2022.
Journal: Frontiers in pediatrics
Published: January 04, 2023
A Multicenter Cohort Study of Immune Dysregulation Disorders Caused by ELF4 Variants in China.
Journal: Journal of clinical immunology
Published: December 30, 2022
Loss of Function Mutation in ELF4 Causes Autoinflammatory and Immunodeficiency Disease in Human.
Journal: Journal of clinical immunology
Published: October 30, 2021
WASp Deficiency Selectively Affects the TCR Diversity of Different Memory T Cell Subsets in WAS Chimeric Mice.
Journal: Frontiers in immunology
Published: October 14, 2021
Multicentric Carpo-Tarsal Osteolysis Syndrome Mimicking Juvenile Idiopathic Arthritis: Two Case Reports and Review of the Literature.
Journal: Frontiers in pediatrics
Published: July 22, 2021
Molecular and Phenotypic Characterization of Nine Patients with STAT1 GOF Mutations in China.
Journal: Journal of clinical immunology
Published: June 12, 2019
Last Updated: 09/26/2026