Search
for
Sort by
Research 31–60 of 1000+
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Rickets and Alopecia with Resistance to 1,25-Dihydroxyvitamin D: Two Different Clinical Courses with Two Different Cellular Defects*
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Non-nutritional rickets: Approach, precision medicine, and outcomes
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Genetic Disorders and Defects in Vitamin D Action
- A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses
- Characterization of Rickets Type II Model Rats to Reveal Functions of Vitamin D and Vitamin D Receptor
- Editorial: Vitamin D 1α-Hydroxylase Knockout Mice as a Hereditary Rickets Animal Model
- In vivo function of VDR in gene expression-VDR knock-out mice
- Atrichia with papular lesions
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Congenital Atrichia: A Case Report
- Mechanism of Vitamin D Receptor Action
- Vitamin Deficiency, Dependency, and Toxicity
- Vitamins
- Satoyoshi Syndrome: A Cause of Alopecia Universalis in Association with Neurologic and Bony Abnormalities
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Receptors in trichology: Hot spots for hair regeneration
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>