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Research 361–390 of 1000+
- A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
- Targeting Expression of the Human Vitamin D Receptor to the Keratinocytes of Vitamin D Receptor Null Mice Prevents Alopecia
- Chapter 28. Vitamin D: Production, Metabolism, Mechanism of Action, and Clinical Requirements
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- 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
- Modulation of Vitamin D Receptor Activity by the Corepressor Hairless: Differential Effects of Hairless Isoforms
- The Expression of Vitamin D-Upregulated Protein 1 in Skin and its Interaction with Sciellin in Cultured Keratinocytes
- Role of vitamin D and calcium signaling in epidermal wound healing
- Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers
- The nutritional biochemistry of wool and hair follicles
- Vitamin D and calcium signaling in epidermal stem cells and their regeneration
- Vitamin D and the Skin: A Review for Dermatologists
- 4 Vitamin D resistance
- Absence of vitamin D receptor (VDR)‐mediated PPARγ suppression causes alopecia in VDR‐null mice
- The future of vitamin D in dermatology.
- Vitamin D-Dependent Rickets Type II with Alopecia: A Rare Case Report.
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- The Tumor Suppressor Actions of the Vitamin D Receptor in Skin
- Immunofluorescence Tomography: High-resolution 3-D reconstruction by serial-sectioning of methacrylate embedded tissues and alignment of 2-D immunofluorescence images
- Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
- Vitamin D Resistance and Alopecia
- The atypical ‘hippocampal’ glutamate receptor coupled to phospholipase D that controls stretch‐sensitivity in primary mechanosensory nerve endings is homomeric purely metabotropic GluK2
- 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
- Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia
- Hereditary vitamin D rickets: a case series in a family
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- Type II Vitamin D Dependent Rickets: A Case Report
- Functional analysis of vitamin D receptor (VDR) using adenovirus vector
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes