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Research 31–60 of 1000+
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Tryptophan Missense Mutation in the Ligand‐Binding Domain of the Vitamin D Receptor Causes Severe Resistance to 1,25‐Dihydroxyvitamin D
- A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
- Nonfebrile Seizures in Pediatrics: Key Points to Remember
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3
- 4 Vitamin D resistance
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Vitamin D‐dependent rickets Type II with alopecia: two case reports and review of the literature
- 1,25-dihydroxyvitamin D resistance, rickets, and alopecia
- An unusual presentation of vitamin D dependent rickets type 2 with low 25 (OH) D3 levels and alopecia: a case report of two siblings
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Vitamin D-dependent Rickets Type II
- Type II Vitamin D Dependent Rickets: A Case Report
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Rickets with alopecia: An inborn error of vitaminD metabolism
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Generation of Genetically Modified Rats Using CRISPR/Cas9 Genome-Editing System to Reveal Novel Vitamin D Actions
- Vitamin D-dependent rickets type II. Defective induction of 25-hydroxyvitamin D3-24-hydroxylase by 1,25-dihydroxyvitamin D3 in cultured skin fibroblasts.
- Vitamin D-Dependent Rickets Type II with Alopecia: A Rare Case Report.
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Two siblings with vitamin-D-dependent rickets type II: No recurrence of rickets for 14 years after cessation of therapy
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Vitamin D resistance
- Characterization of Rickets Type II Model Rats to Reveal Functions of Vitamin D and Vitamin D Receptor
- Persistent hyperparathyroidism in vitamin D-dependent rickets type 2A does not prevent normalization of hypophosphatemia or healing of the rickets
- Vitamin D and the Parenteral Nutrition Patient
- Hair Loss in Systemic Disease
- Vitamin D: More Than a “Bone-a-Fide” Hormone