Erika Mina-Della
Darlinghurst, NSW, Australia
Last Updated: 09/26/2026
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Found 17 publications
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
Correction to: A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries.
Journal: Journal of clinical immunology
Published: September 19, 2024
A Novel Heterozygous Variant in AICDA Impairs Ig Class Switching and Somatic Hypermutation in Human B Cells and is Associated with Autosomal Dominant HIGM2 Syndrome.
Journal: Journal of clinical immunology
Published: September 24, 2023
FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice.
Journal: Cell
Published: July 26, 2023
Atypical Autosomal Recessive AID Deficiency-Yet Another Piece of the Hyper-IgM Puzzle.
Journal: Journal of clinical immunology
Published: March 15, 2022
Molecular requirements for human lymphopoiesis as defined by inborn errors of immunity.
Journal: Stem cells (Dayton, Ohio)
Published: October 16, 2020
Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A.
Journal: The Journal of experimental medicine
Published: July 23, 2020
cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing.
Journal: Nature genetics
Published: July 03, 2020
A Novel Targeted Amplicon Next-Generation Sequencing Gene Panel for the Diagnosis of Common Variable Immunodeficiency Has a High Diagnostic Yield: Results from the Perth CVID Cohort Study.
Journal: The Journal of molecular diagnostics : JMD
Published: April 27, 2020
IRF4 haploinsufficiency in a family with Whipple's disease.
Journal: eLife
Published: September 28, 2017
Last Updated: 09/26/2026