Cargando…

Blood Pressure Levels in Male Carriers of Arg82Cys in CD300LG

The genetics of hypertension has been scrutinized in large-scale genome-wide association studies (GWAS) with a large number of common genetic variants identified, each exerting subtle effects on disease susceptibility. An amino acid polymorphism, p.Arg82Cys, in CD300LG was recently found to be assoc...

Descripción completa

Detalles Bibliográficos
Autores principales:	Støy, Julie, Grarup, Niels, Hørlyck, Arne, Ibsen, Liselotte, Rungby, Jørgen, Poulsen, Per Løgstrup, Brandslund, Ivan, Christensen, Cramer, Hansen, Torben, Pedersen, Oluf, Møller, Niels, Kampmann, Ulla
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2014
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196928/ https://www.ncbi.nlm.nih.gov/pubmed/25314291 http://dx.doi.org/10.1371/journal.pone.0109646

Ejemplares similares

Reduced CD300LG mRNA tissue expression, increased intramyocellular lipid content and impaired glucose metabolism in healthy male carriers of Arg82Cys in CD300LG: a novel genometabolic cross-link between CD300LG and common metabolic phenotypes
por: Støy, Julie, et al.
Publicado: (2015)

The Arg82Cys Polymorphism of the Protein Nepmucin Implies a Role in HDL Metabolism
por: Metz, Sophia, et al.
Publicado: (2022)

Sequencing reveals protective and pathogenic effects on development of diabetes of rare GLIS3 variants
por: Sun, Jihua, et al.
Publicado: (2019)

CD300LG improves the cytotoxic activity of CIK
por: Wang, Qiuyue, et al.
Publicado: (2017)

Studies of the Association of Arg72Pro of Tumor Suppressor Protein p53 with Type 2 Diabetes in a Combined Analysis of 55,521 Europeans
por: Burgdorf, Kristoffer Sølvsten, et al.
Publicado: (2011)

Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein
por: Dominguez-Valentin, Mev, et al.
Publicado: (2014)

The Type 2 Diabetes Risk Allele of TMEM154-rs6813195 Associates with Decreased Beta Cell Function in a Study of 6,486 Danes
por: Harder, Marie Neergaard, et al.
Publicado: (2015)

Three months of melatonin treatment reduces insulin sensitivity in patients with type 2 diabetes—A randomized placebo‐controlled crossover trial
por: Lauritzen, Esben S., et al.
Publicado: (2022)

GLP-1 Receptor Agonist Treatment in Morbid Obesity and Type 2 Diabetes Due to Pathogenic Homozygous Melanocortin-4 Receptor Mutation: A Case Report
por: Iepsen, Eva W., et al.
Publicado: (2020)

CD82 palmitoylation site mutations at Cys5+Cys74 affect EGFR internalization and metabolism through recycling pathway: CD82 palmitoylation mutation can regulate the localization of EGFR
por: Bu, Jingya, et al.
Publicado: (2022)

Increased frequency of rare missense PPP1R3B variants among Danish patients with type 2 diabetes
por: Niazi, Robina Khan, et al.
Publicado: (2019)

Combined Analyses of 20 Common Obesity Susceptibility Variants
por: Sandholt, Camilla Helene, et al.
Publicado: (2010)

Studies of association of AGPAT6 variants with type 2 diabetes and related metabolic phenotypes in 12,068 Danes
por: Snogdal, Lena Sønder, et al.
Publicado: (2013)

The effect of diabetes and the diabetogenic TBC1D4 p.Arg684ter variant on kidney function in Inuit in Greenland
por: Overvad, Maria, et al.
Publicado: (2023)

The effect of diabetes and the common diabetogenic TBC1D4 p.Arg684Ter variant on cardiovascular risk in Inuit in Greenland
por: Overvad, Maria, et al.
Publicado: (2020)

High Prevalence of Diabetes-Predisposing Variants in MODY Genes Among Danish Women With Gestational Diabetes Mellitus
por: Gjesing, Anette P., et al.
Publicado: (2017)

Correction: Genetic Variant SCL2A2 Is Associated with Risk of Cardiovascular Disease – Assessing the Individual and Cumulative Effect of 46 Type 2 Diabetes Related Genetic Variants
por: Borglykke, Anders, et al.
Publicado: (2013)

Genetic Variant SCL2A2 Is Associated with Risk of Cardiovascular Disease – Assessing the Individual and Cumulative Effect of 46 Type 2 Diabetes Related Genetic Variants
por: Borglykke, Anders, et al.
Publicado: (2012)

Parity and type 2 diabetes mellitus: a study of insulin resistance and β-cell function in women with multiple pregnancies
por: Iversen, Ditte Smed, et al.
Publicado: (2016)

The Cys-Arg/N-End Rule Pathway Is a General Sensor of Abiotic Stress in Flowering Plants
por: Vicente, Jorge, et al.
Publicado: (2017)

Association Testing of Novel Type 2 Diabetes Risk Alleles in the JAZF1, CDC123/CAMK1D, TSPAN8, THADA, ADAMTS9, and NOTCH2 Loci With Insulin Release, Insulin Sensitivity, and Obesity in a Population-Based Sample of 4,516 Glucose-Tolerant Middle-Aged Danes
por: Grarup, Niels, et al.
Publicado: (2008)

Impact of rs361072 in the Phosphoinositide 3-Kinase p110β Gene on Whole-Body Glucose Metabolism and Subunit Protein Expression in Skeletal Muscle
por: Ribel-Madsen, Rasmus, et al.
Publicado: (2010)

Dynamic Changes in Endothelial Cell Adhesion Molecule Nepmucin/CD300LG Expression under Physiological and Pathological Conditions
por: Umemoto, Eiji, et al.
Publicado: (2013)

LG24 and sex chromosomes
por: Huang, Rong, et al.
Publicado: (2015)

Association of general health and lifestyle factors with the salivary microbiota – Lessons learned from the ADDITION-PRO cohort
por: Poulsen, Casper Sahl, et al.
Publicado: (2022)

A novel apolipoprotein E mutation (p.Arg150Cys) in a Chinese patient with lipoprotein glomerulopathy
por: Ku, Ming, et al.
Publicado: (2019)

Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma
por: Marques, Ana Maria, et al.
Publicado: (2018)

CACNA1S Arg528Cys mutation in a young Chinese man with thyrotoxic hypokalemic periodic paralysis
por: Rezkalla, Nader, et al.
Publicado: (2020)

D’ domain region Arg782-Cys799 of von Willebrand factor contributes to factor VIII binding
por: Przeradzka, Małgorzata A., et al.
Publicado: (2020)

Physiologic Characterization of Type 2 Diabetes–Related Loci
por: Grarup, Niels, et al.
Publicado: (2010)

The PNPLA3 rs738409 G-Allele Associates with Reduced Fasting Serum Triglyceride and Serum Cholesterol in Danes with Impaired Glucose Regulation
por: Krarup, Nikolaj Thure, et al.
Publicado: (2012)

Do Gene Variants Influencing Adult Adiposity Affect Birth Weight? A Population-Based Study of 24 Loci in 4,744 Danish Individuals
por: Andersson, Ehm A., et al.
Publicado: (2010)

Vejle Diabetes Biobank – a resource for studies of the etiologies of diabetes and its comorbidities
por: Petersen, Eva Rabing Brix, et al.
Publicado: (2016)

PYODERMA VEGETANS WITH lg A DEFICIENCY
por: Kumar, Sandeep, et al.
Publicado: (2010)

The mirror map for invertible LG models
por: Kreuzer, M
Publicado: (1994)

Congenital erythropoietic porphyria with two mutations of the uroporphyrinogen III synthase gene (Cys73Arg, Thr228Met)
por: Gucev, Zoran, et al.
Publicado: (2011)

A rare cause of primary adrenal insufficiency due to a homozygous Arg188Cys mutation in the STAR gene
por: Burget, Lukas, et al.
Publicado: (2018)

A novel fibrinogen mutation: FGA g. 3057 C > T (p. Arg104 > Cys) impairs fibrinogen secretion
por: Marchi, R., et al.
Publicado: (2017)

SCN11A Arg225Cys mutation causes nociceptive pain without detectable peripheral nerve pathology
por: Castoro, Ryan, et al.
Publicado: (2018)

Identification of p.Arg205Cys in CASR in an autosomal dominant hypocalcaemia type 1 pedigree: A case report
por: Ji, Yubing, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_mhbt2ijtuooiicpls23lh8fga7