![A Case of “Late-Onset” Idiopathic Infantile Hypercalcemia Secondary to Mutations in the CYP24A1 Gene - Endocrine Practice A Case of “Late-Onset” Idiopathic Infantile Hypercalcemia Secondary to Mutations in the CYP24A1 Gene - Endocrine Practice](https://www.endocrinepractice.org/cms/asset/934ac3ef-c2f7-4da4-9eae-548ce865ea76/gr1.jpg)
A Case of “Late-Onset” Idiopathic Infantile Hypercalcemia Secondary to Mutations in the CYP24A1 Gene - Endocrine Practice
![Loss-of-Function Mutations of CYP24A1, the Vitamin D 24-Hydroxylase Gene, Cause Long-standing Hypercalciuric Nephrolithiasis and Nephrocalcinosis - ScienceDirect Loss-of-Function Mutations of CYP24A1, the Vitamin D 24-Hydroxylase Gene, Cause Long-standing Hypercalciuric Nephrolithiasis and Nephrocalcinosis - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022534713034642-gr2.jpg)
Loss-of-Function Mutations of CYP24A1, the Vitamin D 24-Hydroxylase Gene, Cause Long-standing Hypercalciuric Nephrolithiasis and Nephrocalcinosis - ScienceDirect
![Impact of Vitamin D on Expression of SIRT7 and CYP24A1 in Human Breast Cancer Cells - Research in Veterinary Science and Medicine Impact of Vitamin D on Expression of SIRT7 and CYP24A1 in Human Breast Cancer Cells - Research in Veterinary Science and Medicine](https://veterinaryscimed.com/content/122/2022/2/1/img/RVSM-2-1-g001.png)
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 Presymptomatic diagnosis of CYP24A1-related infantile idiopathic hypercalcemia: A case report - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1769721220308107-gr1.jpg)
Presymptomatic diagnosis of CYP24A1-related infantile idiopathic hypercalcemia: A case report - ScienceDirect
![CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype](https://www.degruyter.com/document/doi/10.1515/cclm-2018-1208/asset/graphic/j_cclm-2018-1208_fig_001.jpg)
CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype
![Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1 in: Endocrinology, Diabetes & Metabolism Case Reports Volume 2019 Issue 1 (2019) Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1 in: Endocrinology, Diabetes & Metabolism Case Reports Volume 2019 Issue 1 (2019)](https://edm.bioscientifica.com/view/journals/edm/2019/1/EDM19-0114fig1.jpeg)
Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1 in: Endocrinology, Diabetes & Metabolism Case Reports Volume 2019 Issue 1 (2019)
![Expression of CYP24A1 and other multiple sclerosis risk genes in peripheral blood indicates response to vitamin D in homeostatic and inflammatory conditions | Genes & Immunity Expression of CYP24A1 and other multiple sclerosis risk genes in peripheral blood indicates response to vitamin D in homeostatic and inflammatory conditions | Genes & Immunity](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41435-021-00144-6/MediaObjects/41435_2021_144_Fig1_HTML.png)
Expression of CYP24A1 and other multiple sclerosis risk genes in peripheral blood indicates response to vitamin D in homeostatic and inflammatory conditions | Genes & Immunity
![Nutrients | Free Full-Text | Hypercalcemia in Pregnancy Due to CYP24A1 Mutations: Case Report and Review of the Literature Nutrients | Free Full-Text | Hypercalcemia in Pregnancy Due to CYP24A1 Mutations: Case Report and Review of the Literature](https://pub.mdpi-res.com/nutrients/nutrients-14-02518/article_deploy/html/images/nutrients-14-02518-ag-550.jpg?1655457127)
Nutrients | Free Full-Text | Hypercalcemia in Pregnancy Due to CYP24A1 Mutations: Case Report and Review of the Literature
![CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype](https://www.degruyter.com/document/doi/10.1515/cclm-2018-1208/asset/graphic/j_cclm-2018-1208_fig_003.jpg)
CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype
![Figure 1 from CYP3A4 Induction by Rifampin: An Alternative Pathway for Vitamin D Inactivation in Patients With CYP24A1 Mutations | Semantic Scholar Figure 1 from CYP3A4 Induction by Rifampin: An Alternative Pathway for Vitamin D Inactivation in Patients With CYP24A1 Mutations | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/3551a5c558c3349b416f2ce0fbfb5d9386123430/2-Figure1-1.png)
Figure 1 from CYP3A4 Induction by Rifampin: An Alternative Pathway for Vitamin D Inactivation in Patients With CYP24A1 Mutations | Semantic Scholar
![Characterization of a Cleavable Fusion of Human CYP24A1 with Adrenodoxin Reveals the Variable Role of Hydrophobics in Redox Partner Binding | Biochemistry Characterization of a Cleavable Fusion of Human CYP24A1 with Adrenodoxin Reveals the Variable Role of Hydrophobics in Redox Partner Binding | Biochemistry](https://pubs.acs.org/cms/10.1021/acs.biochem.1c00770/asset/images/medium/bi1c00770_0008.gif)
Characterization of a Cleavable Fusion of Human CYP24A1 with Adrenodoxin Reveals the Variable Role of Hydrophobics in Redox Partner Binding | Biochemistry
Characterization of a Cleavable Fusion of Human CYP24A1 with Adrenodoxin Reveals the Variable Role of Hydrophobics in Redox Partner Binding | Biochemistry
![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 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](https://www.mayoclinic.org/-/media/kcms/gbs/medical-professionals/images/2018/07/23/16/43/vitamind_fig1_767px.jpg)
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
![A CYP24A1 Gene Mutation: A Rare Cause of Adult Onset Recurrent Nephrolithiasis | Journal of Case Reports in Medicine A CYP24A1 Gene Mutation: A Rare Cause of Adult Onset Recurrent Nephrolithiasis | Journal of Case Reports in Medicine](http://jocrm.org/sites/default/files/styles/large/public/2019_8_3_27.jpg?itok=1Ix7Y6c5)
A CYP24A1 Gene Mutation: A Rare Cause of Adult Onset Recurrent Nephrolithiasis | Journal of Case Reports in Medicine
![Schéma de la régulation transcriptionelle de l'expression de CYP24A1... | Download Scientific Diagram Schéma de la régulation transcriptionelle de l'expression de CYP24A1... | Download Scientific Diagram](https://www.researchgate.net/profile/Jean-Marc-Lobaccaro/publication/6642309/figure/fig2/AS:601724519718921@1520473713484/Schema-de-la-regulation-transcriptionelle-de-lexpression-de-CYP24A1-par-le-recepteur-de_Q320.jpg)
Schéma de la régulation transcriptionelle de l'expression de CYP24A1... | Download Scientific Diagram
![Cancers | Free Full-Text | Relative Expression of Vitamin D Hydroxylases, CYP27B1 and CYP24A1, and of Cyclooxygenase-2 and Heterogeneity of Human Colorectal Cancer in Relation to Age, Gender, Tumor Location, and Malignancy: Cancers | Free Full-Text | Relative Expression of Vitamin D Hydroxylases, CYP27B1 and CYP24A1, and of Cyclooxygenase-2 and Heterogeneity of Human Colorectal Cancer in Relation to Age, Gender, Tumor Location, and Malignancy:](https://www.mdpi.com/cancers/cancers-04-00763/article_deploy/html/images/cancers-04-00763-g001.png)
Cancers | Free Full-Text | Relative Expression of Vitamin D Hydroxylases, CYP27B1 and CYP24A1, and of Cyclooxygenase-2 and Heterogeneity of Human Colorectal Cancer in Relation to Age, Gender, Tumor Location, and Malignancy:
![Figure 1 from 1,25-(OH)2D-24 Hydroxylase (CYP24A1) Deficiency as a Cause of Nephrolithiasis. | Semantic Scholar Figure 1 from 1,25-(OH)2D-24 Hydroxylase (CYP24A1) Deficiency as a Cause of Nephrolithiasis. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/def152feaafe2d55d396a0cb6ef3ef0108c4d434/2-Figure1-1.png)
Figure 1 from 1,25-(OH)2D-24 Hydroxylase (CYP24A1) Deficiency as a Cause of Nephrolithiasis. | Semantic Scholar
![Kinetic analysis of human CYP24A1 metabolism of vitamin D via the C24‐oxidation pathway - Tieu - 2014 - The FEBS Journal - Wiley Online Library Kinetic analysis of human CYP24A1 metabolism of vitamin D via the C24‐oxidation pathway - Tieu - 2014 - The FEBS Journal - Wiley Online Library](https://febs.onlinelibrary.wiley.com/cms/asset/ff1902a3-0946-41c3-a919-d1ce6c710702/febs12862-toc-0001-m.jpg?trick=1673235427481)
Kinetic analysis of human CYP24A1 metabolism of vitamin D via the C24‐oxidation pathway - Tieu - 2014 - The FEBS Journal - Wiley Online Library
Regulation of expression of CYP27B1 and CYP24A1 by 1α,25(OH) 2 D, PTH,... | Download Scientific Diagram
![Combined role of vitamin D status and CYP24A1 in the transition to systemic lupus erythematosus | Annals of the Rheumatic Diseases Combined role of vitamin D status and CYP24A1 in the transition to systemic lupus erythematosus | Annals of the Rheumatic Diseases](https://ard.bmj.com/content/annrheumdis/76/1/153/F1.large.jpg)
Combined role of vitamin D status and CYP24A1 in the transition to systemic lupus erythematosus | Annals of the Rheumatic Diseases
![Major causes of high CYP24A1 expression. Besides VD metabolites, other... | Download Scientific Diagram Major causes of high CYP24A1 expression. Besides VD metabolites, other... | Download Scientific Diagram](https://www.researchgate.net/publication/6899494/figure/fig3/AS:601696455626816@1520467022991/Major-causes-of-high-CYP24A1-expression-Besides-VD-metabolites-other-ligands-of-the-VDR.png)