Linda Shawver-Monaco
Philadelphia, Panama
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Genome-wide analyses and functional profiling of human NK cell lines.
Journal: Molecular immunology
Published: March 08, 2018
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder.
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder.
Journal: The Journal of allergy and clinical immunology
Published: August 17, 2015
A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism.
Journal: The Journal of allergy and clinical immunology
Published: June 01, 2015
Practical NK cell phenotyping and variability in healthy adults.
Journal: Immunologic research
Published: May 28, 2015
Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56(bright) subset.
Journal: Blood
Published: February 01, 2013
Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency.
Journal: The Journal of allergy and clinical immunology
Published: November 02, 2012
Human immunodeficiency-causing mutation defines CD16 in spontaneous NK cell cytotoxicity.
Journal: The Journal of clinical investigation
Published: May 17, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026