Varaico: Literature-Extracted Genetic Variants

Gene:SELPLG
Variant:p.M62I
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SELPLG

NM_003006.4:p.M62I

Associated Papers

The effects of SCARB2 and SELPLG gene polymorphisms on EV71 infection in hand, foot and mouth disease.

Duan FY et al.

Biomolecules & Biomedicine, 2023

Targeting SELPLG/P-selectin glycoprotein ligand 1 in preclinical ARDS: Genetic and epigenetic regulation of the SELPLG promoter.

Sun X et al.

Pulmonary Circulation, 2023

Genome-Wide Association Study in African Americans with Acute Respiratory Distress Syndrome Identifies the Selectin P Ligand Gene as a Risk Factor.

Bime C et al.

American Journal of Respiratory and Critical Care Medicine, 2018

Correlations of platelet-leukocyte aggregates with P-selectin S290N and P-selectin glycoprotein ligand-1 M62I genetic polymorphisms in patients with acute ischemic stroke.

Tao L et al.

Journal of the Neurological Sciences, 2016

DiMeX: A Text Mining System for Mutation-Disease Association Extraction.

Mahmood AS et al.

Plos One, 2016

Somatic Variations in Cervical Cancers in Indian Patients.

Das P et al.

Plos One, 2016

27829003 (PubMed )
Supplement: pone.0165878.s001.xlsx › somatic_cosmic_hit.list

The sex-specific association of Met62Ile gene polymorphism in P-selectin glycoprotein ligand (PSGL-1) with carotid plaque presence: preliminary study.

Zivković M et al.

Molecular Biology Reports, 2012

Innate immunity and non-Hodgkin's lymphoma (NHL) related genes in a nested case-control study for gastric cancer risk.

Park SK et al.

Plos One, 2012

23028900 (PubMed )
Supplement: pone.0045274.s001.xlsx › Innate

Contribution of SELP and PSGL-1 genotypes and haplotypes to the presence of coronary heart disease in Tunisians.

Ghazouani L et al.

Molecular Biology Reports, 2011

Triangulation of the human, chimpanzee, and Neanderthal genome sequences identifies potentially compensated mutations.

Zhang G et al.

Human Mutation, 2010

21064102 (PubMed )
Supplement: supplement_1.pdf

The P-selectin gene polymorphism Val168Met: a novel risk marker for the occurrence of primary ventricular fibrillation during acute myocardial infarction.

Elmas E et al.

Journal of Cardiovascular Electrophysiology, 2010

Combined effects of genetic polymorphisms of P-selectin and P-selectin glycoprotein ligand-1 on the binding of platelets to monocytes.

Panzer S et al.

Thrombosis Research, 2010

The adhesion mediated by the P-selectin P-selectin glycoprotein ligand-1 (PSGL-1) couple is stronger for shorter PSGL-1 variants.

Barbaux S et al.

Journal of Leukocyte Biology, 2010

SELP and SELPLG genetic variation is associated with cell surface measures of SELP and SELPLG: the Atherosclerosis Risk in Communities Carotid MRI Study.

Volcik KA et al.

Clinical Chemistry, 2009

Evaluation of resequencing on number of tag SNPs of 13 atherosclerosis-related genes in Thai population.

Tocharoentanaphol C et al.

Journal of Human Genetics, 2008

Specific P-selectin and P-selectin glycoprotein ligand-1 genotypes/haplotypes are associated with risk of incident CHD and ischemic stroke: the Atherosclerosis Risk in Communities (ARIC) study.

Volcik KA et al.

Atherosclerosis, 2007

SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis.

Fenoglio C et al.

Neuroscience Letters, 2006

P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis.

Scalabrini D et al.

Neuroscience Letters, 2005

SELPLG gene polymorphisms in relation to plasma SELPLG levels and coronary artery disease.

Tregouet DA et al.

Annals of Human Genetics, 2003

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