Pages that link to "Q50335713"
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The following pages link to Inactivating mutations in the 25-hydroxyvitamin D3 1alpha-hydroxylase gene in patients with pseudovitamin D-deficiency rickets (Q50335713):
Displaying 50 items.
- rickets (Q183392) (← links)
- Requirement of PDZ domains for the stimulation of the epithelial Ca2+ channel TRPV5 by the NHE regulating factor NHERF2 and the serum and glucocorticoid inducible kinase SGK1 (Q24338748) (← links)
- Resurrection of vitamin D deficiency and rickets (Q24685737) (← links)
- Nuclear receptors in bone physiology and diseases (Q26853017) (← links)
- The pleiomorphic actions of vitamin D and its importance for children (Q27023112) (← links)
- Vitamin D, calcium homeostasis and aging (Q28073460) (← links)
- Genetic Disorders of Vitamin D Metabolism (Q28315373) (← links)
- Drug Off-Target Effects Predicted Using Structural Analysis in the Context of a Metabolic Network Model (Q28475693) (← links)
- ECaC: the gatekeeper of transepithelial Ca2+ transport (Q30748005) (← links)
- Cloning of the mouse 25-hydroxyvitamin D(3)-1alpha-hydroxylase (CYP1alpha) gene (Q30874046) (← links)
- The epithelial calcium channels TRPV5 and TRPV6: regulation and implications for disease (Q30984121) (← links)
- Expression cloning of ligand biosynthetic enzymes (Q31027868) (← links)
- Overview of regulatory cytochrome P450 enzymes of the vitamin D pathway (Q31943559) (← links)
- Identification of a novel rat microsomal vitamin D3 25-hydroxylase (Q33199700) (← links)
- Vitamin D resistance (Q33586593) (← links)
- The biology and pathology of vitamin D control in bone (Q33608847) (← links)
- Hormone regulation of chondrocyte differentiation and endochondral bone formation (Q33690388) (← links)
- In vivo function of VDR in gene expression-VDR knock-out mice (Q33694984) (← links)
- Genetic disorders of vitamin D biosynthesis (Q33802784) (← links)
- Genetic mutation in the human 25-hydroxyvitamin D3 1alpha-hydroxylase gene causes vitamin D-dependent rickets type I. (Q33804590) (← links)
- Vitamin D, parathyroid hormone, and calcium: a complex regulatory network (Q33810886) (← links)
- Vitamin D: metabolism (Q33888727) (← links)
- Genetic disorders of calcium and phosphorus metabolism (Q33967990) (← links)
- Calcium and vitamin D. Diagnostics and therapeutics. (Q34032541) (← links)
- Vitamin D 1 alpha-hydroxylase (Q34038595) (← links)
- Vitamin D deficiency and disorders of vitamin D metabolism (Q34061547) (← links)
- Drug-metabolizing enzymes, polymorphisms and interindividual response to environmental toxicants (Q34093080) (← links)
- CYP27B1 null mice with LacZreporter gene display no 25-hydroxyvitamin D3-1alpha-hydroxylase promoter activity in the skin (Q34248328) (← links)
- Genetic variation in CYP27B1 is associated with congestive heart failure in patients with hypertension (Q34283862) (← links)
- Genetics of vitamin D 1alpha-hydroxylase deficiency in 17 families (Q34388188) (← links)
- Enzymatic studies on the key enzymes of vitamin D metabolism; 1 alpha-hydroxylase (CYP27B1) and 24-hydroxylase (CYP24). (Q34423337) (← links)
- Vitamin D deficiency and rickets (Q34436381) (← links)
- Molecular-pathogenetic classification of genetic disorders of the skeleton (Q34561450) (← links)
- Vitamin D: Metabolism, Molecular Mechanism of Action, and Pleiotropic Effects. (Q34621641) (← links)
- Vitamin D dependent rickets type I (Q34799180) (← links)
- Structure-function relationships of vitamin D including ligand recognition by the vitamin D receptor (Q34993158) (← links)
- Minireview: nuclear receptor regulation of osteoclast and bone remodeling (Q35054970) (← links)
- The investigation of hypocalcaemia and rickets (Q35115497) (← links)
- Acute phosphate restriction leads to impaired fracture healing and resistance to BMP-2. (Q35156052) (← links)
- Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets (Q35673317) (← links)
- Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A. (Q35680001) (← links)
- Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array (Q35685774) (← links)
- Rapid modulation of osteoblast ion channel responses by 1alpha,25(OH)2-vitamin D3 requires the presence of a functional vitamin D nuclear receptor (Q36160245) (← links)
- Targeted ablation of the 25-hydroxyvitamin D 1alpha -hydroxylase enzyme: evidence for skeletal, reproductive, and immune dysfunction (Q36312727) (← links)
- Molecular cloning, characterization, and promoter analysis of the human 25-hydroxyvitamin D3-1alpha-hydroxylase gene (Q36387859) (← links)
- Coordinated control of renal Ca2+ handling (Q36414495) (← links)
- Human cytochromes P450 in health and disease (Q36512912) (← links)
- Regulation of phosphate homeostasis by PTH, vitamin D, and FGF23. (Q36649088) (← links)
- CYP24A1 and CYP27B1 polymorphisms modulate vitamin D metabolism in colon cancer cells. (Q36778121) (← links)
- Association of the vitamin D metabolism gene CYP27B1 with type 1 diabetes (Q36803789) (← links)