Hailun Li
Paris, France
Last Updated: 09/26/2026
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Found 9 publications
Inherited human TFIIIA deficiency disrupts T cell development.
Journal: medRxiv : the preprint server for health sciences
Published: July 10, 2026
Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis.
Journal: The Journal of experimental medicine
Published: October 27, 2025
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function.
Journal: Nature immunology
Published: December 16, 2024
2q33 Deletions Underlying Syndromic and Non-syndromic CTLA4 Deficiency.
Journal: Journal of clinical immunology
Published: June 25, 2024
Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation.
Journal: The Journal of clinical investigation
Published: April 02, 2024
Tuberculosis in otherwise healthy adults with inherited TNF deficiency.
Journal: Nature
Published: January 07, 2024
Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency.
Journal: Journal of clinical immunology
Published: November 13, 2023
Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases.
Journal: The Journal of experimental medicine
Published: July 06, 2023
Showing 1-9 of 9
Last Updated: 09/26/2026