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Research 61–90 of 423
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Editorial: Vitamin D 1α-Hydroxylase Knockout Mice as a Hereditary Rickets Animal Model
- The combined use of intravenous and oral calcium for the treatment of vitamin D dependent rickets type II (VDDRII)
- Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation
- Normalization of Mineral Ion Homeostasis by Dietary Means Prevents Hyperparathyroidism, Rickets, and Osteomalacia, But Not Alopecia in Vitamin D Receptor-Ablated Mice<sup>1</sup>
- Normalization of Mineral Ion Homeostasis by Dietary Means Prevents Hyperparathyroidism, Rickets, and Osteomalacia, But Not Alopecia in Vitamin D Receptor-Ablated Mice
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- The effect of 1,25-dihydroxyvitamin D3 on the growth and differentiation of cultured human outer root sheath cells from normal subjects and patients with vitamin D-dependent rickets type II with alopecia
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Vitamin D: More Than a “Bone-a-Fide” Hormone
- Genetic Disorders and Defects in Vitamin D Action
- In vivo function of VDR in gene expression-VDR knock-out mice
- Vitamin D and the Parenteral Nutrition Patient
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- 4 Vitamin D resistance
- Generation of Genetically Modified Rats Using CRISPR/Cas9 Genome-Editing System to Reveal Novel Vitamin D Actions
- Treatme nt of vitamin-D and calcium to children with hair defluvium
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The role of vitamin D receptor mutations in the development of alopecia
- A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Atrichia with papular lesions
- Hair Loss in Paediatric and Adolescent Age Group: A Clinico-Pathological Analysis in a Tertiary Health Care Centre
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Nonfebrile Seizures in Pediatrics: Key Points to Remember
- Congenital Atrichia: A Case Report
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed