Impact of Vitamin D on Expression of SIRT7 and CYP24A1 in Human Breast Cancer Cells - Research in Veterinary Science and Medicine
Presymptomatic diagnosis of CYP24A1-related infantile idiopathic hypercalcemia: A case report - ScienceDirect
A Case of “Late-Onset” Idiopathic Infantile Hypercalcemia Secondary to Mutations in the CYP24A1 Gene - Endocrine Practice
Calcium problems associated with CYP24A1 (a Vitamin D gene) – Oct 2017 | VitaminDWiki
Schéma de la régulation transcriptionelle de l'expression de CYP24A1... | Download Scientific Diagram
CYP24A1-induced vitamin D insufficiency promotes breast cancer growth
Associations of CYP24A1 copy number variation with vitamin D deficiency and insulin secretion
Mutations in CYP24A1 and Idiopathic Infantile Hypercalcemia | NEJM
A CYP24A1 Gene Mutation: A Rare Cause of Adult Onset Recurrent Nephrolithiasis | Journal of Case Reports in Medicine
CYP24A1 - an overview | ScienceDirect Topics
CYP24A1 Gene - GeneCards | CP24A Protein | CP24A Antibody
Combined role of vitamin D status and CYP24A1 in the transition to systemic lupus erythematosus | Annals of the Rheumatic Diseases
CYP24A1 - an overview | ScienceDirect Topics
Regulation of expression of CYP27B1 and CYP24A1 by 1α,25(OH) 2 D, PTH,... | Download Scientific Diagram
CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype
Expression of CYP24A1 and other multiple sclerosis risk genes in peripheral blood indicates response to vitamin D in homeostatic and inflammatory conditions | Genes & Immunity
Astemizole Synergizes Calcitriol Antiproliferative Activity by Inhibiting CYP24A1 and Upregulating VDR: A Novel Approach for Breast Cancer Therapy | PLOS ONE
Contribution of CYP27B1 and CYP24A1 genetic variations to the incidence of acute coronary syndrome and to vitamin D serum level
CYP24A1 Regulation in Health and Disease - ScienceDirect
Vitamin D 3 cascade and involved enzymes. Modulation of CYP24A1 by... | Download Scientific Diagram
Ratio of 25(OH)D-to-24,25(OH)2D: A new test to confirm 24-hydroxylase ( CYP24A1) deficiency as the cause of hypercalcemia - Mayo Clinic
Loss-of-Function Mutations of CYP24A1, the Vitamin D 24-Hydroxylase Gene, Cause Long-standing Hypercalciuric Nephrolithiasis and Nephrocalcinosis - ScienceDirect
