Associated Papers
Molecular Classification of Primary Immunodeficiencies of T Lymphocytes.
Comrie WA et al.
Advances in Immunology, 2018
The disease-linked Glu-26-Lys mutant version of Coronin 1A exhibits pleiotropic and pathway-specific signaling defects.
Ojeda V et al.
Molecular Biology of the Cell, 2015
The expanding spectrum of human coronin 1A deficiency.
Moshous D et al.
Current Allergy and Asthma Reports, 2014
Compound heterozygous CORO1A mutations in siblings with a mucocutaneous-immunodeficiency syndrome of epidermodysplasia verruciformis-HPV, molluscum contagiosum and granulomatous tuberculoid leprosy.
Stray-Pedersen A et al.
Journal of Clinical Immunology, 2014
On guard: coronin proteins in innate and adaptive immunity.
Pieters J et al.
Nature Reviews. Immunology, 2013
The Wilms' tumor suppressor Wt1 regulates Coronin 1B expression in the epicardium.
Hsu WH et al.
Experimental Cell Research, 2013
Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation.
Moshous D et al.
The Journal of Allergy and Clinical Immunology, 2013
Mast cell function is not altered by Coronin-1A deficiency.
Arandjelovic S et al.
Journal of Leukocyte Biology, 2010
The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency.
Shiow LR et al.
Nature Immunology, 2008
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