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Research 61–90 of 1000+
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- 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
- Rickets with alopecia: An inborn error of vitaminD metabolism
- 1,25-dihydroxyvitamin D resistance, rickets, and alopecia
- The role of vitamin D receptor mutations in the development of alopecia
- Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function <i>VDR</i> mutation
- Generation of Genetically Modified Rats Using CRISPR/Cas9 Genome-Editing System to Reveal Novel Vitamin D Actions
- Rickets and Alopecia with Resistance to 1,25-Dihydroxyvitamin D: Two Different Clinical Courses with Two Different Cellular Defects*
- Treatme nt of vitamin-D and calcium to children with hair defluvium
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Non-nutritional rickets: Approach, precision medicine, and outcomes
- Calcitriol-Resistant Rickets With Alopecia
- Calcitriol-resistant rickets with alopecia
- 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
- The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3
- Tryptophan Missense Mutation in the Ligand‐Binding Domain of the Vitamin D Receptor Causes Severe Resistance to 1,25‐Dihydroxyvitamin D
- Atrichia with papular lesions
- Congenital Atrichia: A Case Report
- In vivo function of VDR in gene expression-VDR knock-out mice
- Hair Loss in Paediatric and Adolescent Age Group: A Clinico-Pathological Analysis in a Tertiary Health Care Centre
- Atrichia congenita with papular lesions: A rare cause of pediatric 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
- Nonfebrile Seizures in Pediatrics: Key Points to Remember