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Research 91–120 of 1000+
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- The clinical spectrum of parathyroid disease
- Functional characterization and unraveling the structural determinants of novel steroid hydroxylase CYP154C7 from Streptomyces sp. PAMC26508
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Insights into male androgenetic alopecia using comparative transcriptome profiling: hypoxia-inducible factor-1 and Wnt/β-catenin signalling pathways
- A case of 21-hydroxylase deficiency in Turner′s syndrome and literature review
- Mister XX
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Serotoninergic and melatoninergic systems are fully expressed in human skin
- Vitamin D metabolism and function in the skin
- 1,25-dihydroxyvitamin D resistance, rickets, and alopecia
- Nonclassic adrenal hyperplasia
- 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
- Hair Follicle Biology and Topical Minoxidil: Possible Mechanisms of Action
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Inhibition of 17α-hydroxylase/C17,20 lyase reduces gating deficits consequent to dopaminergic activation
- Urinary steroids in women with androgenic alopecia
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Inflammatory perifollicular fibrosis and alopecia
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Type II Vitamin D Dependent Rickets: A Case Report
- Ovarian intratumoral 21-hydroxylase deficiency in a postmenopausal hirsute woman
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Hypoxia Treatment of Adipose Mesenchymal Stem Cells Promotes the Growth of Dermal Papilla Cells via HIF-1α and ERK1/2 Signaling Pathways
- Role of neurosteroids in ischemic postconditioning-induced attenuation of cerebral ischemia-evoked neuronal injury and behavioral deficits in mice
- Acne Scar Management: Minoxidil as a Promising Approach or a Mirage?
- Vitamin D-dependent Rickets Type II