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Clinical Observation on Bone Metabolism Induced by Chronic Renal Insufficiency
Pathways
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PI3K-Akt signaling pathway
Homo sapiens (human)
one gene
Endocrine and other factor-regulated calcium reabsorption
Homo sapiens (human)
one gene
Cancer Gene Census
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SLC34A3
Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3
CLCN5
Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22
DMP1
Elucidation of the sequence and the genomic organization of the human dentin matrix acidic phosphoprotein 1 (DMP1) gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II
PHEX
Expression and cloning of the human X-linked hypophosphatemia gene cDNA
FGF23
Physiological regulation and disorders of phosphate metabolism--pivotal role of fibroblast growth factor 23
Phosphate and FGF-23
Fibroblast growth factor 23 impairs phosphorus and vitamin D metabolism in vivo and suppresses 25-hydroxyvitamin D-1alpha-hydroxylase expression in vitro
ENPP1
Plasma cell membrane glycoprotein PC-1. cDNA cloning of the human molecule, amino acid sequence, and chromosomal location
Autophosphorylation of PC-1 (alkaline phosphodiesterase I/nucleotide pyrophosphatase) and analysis of the active site
Membrane glycoprotein PC-1 and insulin resistance in non-insulin-dependent diabetes mellitus
CYP2R1
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes
VDR
Membrane Localization, Caveolin-3 Association and Rapid Actions of Vitamin D Receptor in Cardiac Myocytes
Identity between TRAP and SMCC complexes indicates novel pathways for the function of nuclear receptors and diverse mammalian activators
The interaction of the vitamin D receptor with nuclear receptor corepressors and coactivators
The chromatin-remodeling complex WINAC targets a nuclear receptor to promoters and is impaired in Williams syndrome
Antagonistic action of a 25-carboxylic ester analogue of 1alpha, 25-dihydroxyvitamin D3 is mediated by a lack of ligand-induced vitamin D receptor interaction with coactivators
CYP27B1
Association of the CYP27B1 C(-1260)A polymorphism with autoimmune Addison's disease
Vitamin D pathway gene variants and prostate cancer prognosis
Comprehensive association analysis of nine candidate genes with serum 25-hydroxy vitamin D levels among healthy Caucasian subjects