Associated Papers
Mutations of MRGPRX2, drug sensitivity, and genetic markers related to disease.
Ratnayake SH et al.
The Journal of Allergy and Clinical Immunology. Global, 2025
MRGPRX2 gain-of-function mutation drives enhanced mast cell reactivity in chronic spontaneous urticaria.
Ye D et al.
The Journal of Allergy and Clinical Immunology, 2025
The structure, function, and pharmacology of MRGPRs.
Cao C et al.
Trends in Pharmacological Sciences, 2023
Naturally Occurring Missense MRGPRX2 Variants Display Loss of Function Phenotype for Mast Cell Degranulation in Response to Substance P, Hemokinin-1, Human β-Defensin-3, and Icatibant.
Alkanfari I et al.
Journal of Immunology (baltimore, Md. : 1950), 2018
XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.
Talukder AK et al.
Plos One, 2015
25905921 (PubMed )
Supplement: pone.0123569.s008.xls › BC9_ERR166333
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 884.336
A probabilistic model to predict clinical phenotypic traits from genome sequencing.
Chen YC et al.
Plos Computational Biology, 2014
25188385 (PubMed )
Supplement: pcbi.1003825.s014.xlsx › TableS12
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