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Research 181–210 of 1000+
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- CYP21A2 Mutations in Women with Polycystic Ovary Syndrome (PCOS)
- Stem Cells and their Niches
- Pharmacotherapy of plexiform neurofibromas in patients with neurofibromatosis type 1. Possible adverse events and their management
- Vitamin D metabolism and function in the skin
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- 1α,25(OH)2-Dihydroxyvitamin D3/VDR protects the skin from UVB-induced tumor formation by interacting with the β-catenin pathway
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Hair follicle development and related gene and protein expression of skins in Rex rabbits during the first 8 weeks of life
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- The potential role of hsa_circ_0001079 in androgenetic alopecia via sponging hsa‐miR‐136‐5p
- Virilizing insulinoma
- Androgen excess: a hallmark of polycystic ovary syndrome
- Does Vitamin D play a role on Msx1 homeoprotein expression involving an endogenous antisense mRNA?*1
- Drug Repositioning: New Approaches and Future Prospects for Life-Debilitating Diseases and the COVID-19 Pandemic Outbreak
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- Activation of Polyamine Catabolism Profoundly Alters Tissue Polyamine Pools and Affects Hair Growth and Female Fertility in Transgenic Mice Overexpressing Spermidine/SpermineN 1-Acetyltransferase
- Androgen sensitivity gateway to COVID‐19 disease severity
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Role of Stearoyl-CoA Desaturase-1 in Skin Integrity and Whole Body Energy Balance
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings