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Research 121–150 of 235
- Generation of Genetically Modified Rats Using CRISPR/Cas9 Genome-Editing System to Reveal Novel Vitamin D Actions
- Benign Cutaneous Eruptions After Transplantation
- Calcineurin-based immunosuppression in renal transplantation : focus on efficacy, the role of steroids, and the cardiovascular risk
- National scientific medical meeting 1996 abstracts
- Central nervous system involvement in autoimmune polyglandular syndrome
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Endogenous Hypercortisolism in a Patient With Addison’s Disease: An Unusual Case of Adrenal Cortical Adenoma
- APECED: JAK Inhibition in an Adult Case with Long-Term Follow-up
- Polyglandular autoimmune syndrome type 4 with GAD antibody and dystonia
- The impact of VDR expression and regulation in vivo
- 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
- Rickets with alopecia: An inborn error of vitaminD metabolism
- The Role of Interferon-γ in Autoimmune Polyendocrine Syndrome Type 1
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Queen Anne sign
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- BH02 Overcoming genetic drivers in alopecia areata: hair regrowth in a patient with the <i>AIRE</i> gene mutation treated with ruxolitinib
- Sindrom Fahr: Kalsifikasi Intraserebral Patologis
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Skin abnormalities generated by temporally controlled RXRα mutations in mouse epidermis
- Evolution and Function of Vitamin D
- The role of vitamin D receptor mutations in the development of alopecia
- 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
- The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses
- Serum brain‐derived neurotrophic factor and vitamin D: Two concordant players controlling depression among alopecia areata and vitiligo patients: A case–control study