Associated Papers
Molecular Pathogenesis of Inherited Platelet Dysfunction.
Rodríguez-Alén A et al.
Biomolecules, 2025
Middle Eastern Genetic Variation Improves Clinical Annotation of the Human Genome.
Ramaswamy S et al.
Journal of Personalized Medicine, 2022
35330423 (PubMed )
Supplement: jpm-12-00423-s001.zip › Supplementary_Table.xlsx › Supp_Table2
A Global Map of G Protein Signaling Regulation by RGS Proteins.
Masuho I et al.
Cell, 2020
33007266 (PubMed )
Supplement: mmc5.xlsx › RGS2
The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals.
Cao Y et al.
Cell Research, 2020
32355288 (PubMed )
Supplement: 41422_2020_322_MOESM14_ESM.xlsx › S7
Human Missense Mutations in Regulator of G Protein Signaling 2 Affect the Protein Function Through Multiple Mechanisms.
Phan HTN et al.
Molecular Pharmacology, 2017
Regulators of G protein signaling: role in hematopoiesis, megakaryopoiesis and platelet function.
Louwette S et al.
Journal of Thrombosis and Haemostasis : Jth, 2012
Platelet Gs hypofunction and abnormal morphology resulting from a heterozygous RGS2 mutation.
Noé L et al.
Journal of Thrombosis and Haemostasis : Jth, 2010
Select a paper to view details