Associated Papers
Caution in interpreting MRGPRX2 N62S as a disease-driving variant in chronic spontaneous urticaria.
Martín M et al.
The Journal of Allergy and Clinical Immunology, 2025
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 prevalence of genetic variants of the Mas-related G-protein-coupled receptor X2 in patients does not explain perioperative hypersensitivity reactions to neuromuscular blocking agents.
Dziadowiec A et al.
Frontiers in Pharmacology, 2025
The structure, function, and pharmacology of MRGPRs.
Cao C et al.
Trends in Pharmacological Sciences, 2023
Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank.
Park J et al.
Cell Reports. Medicine, 2022
Inflamed Ulcerative Colitis Regions Associated With MRGPRX2-Mediated Mast Cell Degranulation and Cell Activation Modules, Defining a New Therapeutic Target.
Chen E et al.
Gastroenterology, 2021
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.
Calender A et al.
Bmc Medical Genomics, 2018
29510755 (PubMed )
Supplement: 12920_2018_338_MOESM6_ESM.xlsx › T2
Somatic signature of brain-specific single nucleotide variations in sporadic Alzheimer's disease.
Parcerisas A et al.
Journal of Alzheimer's Disease : Jad, 2014
25024348 (PubMed )
Supplement: sj-xls-6-alz-10.3233_jad-140891.xls › P1C
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