Common genetic variants associate with serum phosphorus concentration. - Wikidata - awgldk - TriplyDB

Common genetic variants associate with serum phosphorus concentration.

Common genetic variants associate with serum phosphorus concentration.

http://www.wikidata.org/entity/Q35153194

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GWAS of 126,559 individuals identifies genetic variants associated with educational attainment Regulation of serum phosphate Serum Biochemical Phenotypes in the Domestic Dog A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1 The population genetics of chronic kidney disease: insights from the MYH9-APOL1 locus.Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis.Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations Fibroblast growth factor 23 is elevated before parathyroid hormone and phosphate in chronic kidney disease.Association studies of calcium-sensing receptor (CaSR) polymorphisms with serum concentrations of glucose and phosphate, and vascular calcification in renal transplant recipients.Heritability of serum sodium concentration: evidence for sex- and ethnic-specific effects.The Envy of Scholars: Applying the Lessons of the Framingham Heart Study to the Prevention of Chronic Kidney Disease Common and rare variants associated with kidney stones and biochemical traits.Con: Phosphate binders in chronic kidney disease Gene-by-Diet Interactions Affect Serum 1,25-Dihydroxyvitamin D Levels in Male BXD Recombinant Inbred Mice.Pharmacogenetic analysis of cinacalcet response in secondary hyperparathyroidism patients.Decreased transcriptional activity of calcium-sensing receptor gene promoter 1 is associated with calcium nephrolithiasis.Can features of phosphate toxicity appear in normophosphatemia?Rare coding variants in ALPL are associated with low serum alkaline phosphatase and low bone mineral density.Evidence for extensive pleiotropy among pharmacogenes.Association Study of Reported Significant Loci at 5q35.3, 7p14.3, 13q14.1 and 16p12.3 with Urolithiasis in Chinese Han Ethnicity Disorders of phosphorus homeostasis.Inositol pyrophosphates: between signalling and metabolism.Genetic diseases of renal phosphate handling.The Significance of the Bifunctional Kinase/Phosphatase Activities of Diphosphoinositol Pentakisphosphate Kinases (PPIP5Ks) for Coupling Inositol Pyrophosphate Cell Signaling to Cellular Phosphate Homeostasis.Genetic Variants Associated with Circulating Parathyroid Hormone.Chemical tools for interrogating inositol pyrophosphate structure and function.The intestinal phosphate transporter NaPi-IIb (Slc34a2) is required to protect bone during dietary phosphate restriction.A replication study for three nephrolithiasis loci at 5q35.3, 7p14.3 and 13q14.1 in the Japanese population.Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics.Associations between polymorphisms related to calcium metabolism and human height: the Tromsø Study.Habitual Intakes, Food Sources and Excretions of Phosphorus and Calcium in Three German Study Collectives.Renal phosphate handling and inherited disorders of phosphate reabsorption: an update.Genetic Analysis of Rare Human Variants of Regulators of G Protein Signaling Proteins and Their Role in Human Physiology and Disease

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P2860

Common genetic variants associate with serum phosphorus concentration.

http://www.wikidata.org/entity/Q35153194

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Common genetic variants associate with serum phosphorus concentration.

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Common genetic variants associate with serum phosphorus concentration.

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type

label

Common genetic variants associate with serum phosphorus concentration.

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Common genetic variants associate with serum phosphorus concentration.

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Common genetic variants associate with serum phosphorus concentration.

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Common genetic variants associate with serum phosphorus concentration.

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Journal of the American Society of Nephrology

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Common genetic variants associate with serum phosphorus concentration.

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Ann-Kristin Petersen

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Caroline S Fox

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Dan E Arking

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Daniel Levy

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Dorothy B Hausman

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Frank J A van Rooij

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Harry Campbell

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Ian H de Boer

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Jacqueline C M Witteman

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Janina S Ried

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P2860

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

Identification and characterization of a novel inositol hexakisphosphate kinase

Mutation of the mouse klotho gene leads to a syndrome resembling ageing

The Rotterdam Study: 2010 objectives and design update

Phosphate regulation of vascular smooth muscle cell calcification

The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting

How fibroblast growth factor 23 works

Homozygous ablation of fibroblast growth factor-23 results in hyperphosphatemia and impaired skeletogenesis, and reverses hypophosphatemia in Phex-deficient mice

Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities

Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts

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1223-1232

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10.1681/ASN.2009111104

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7

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21

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Heinz Erich Wichmann

Thomas Meitinger

Christian Gieger

Fernando Rivadeneira

Eric Boerwinkle

Cornelia M. van Duijn

Caroline Hayward

André Uitterlinden

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2010-06-17T00:00:00Z

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