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Research 841–870 of 1000+
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Intratumoral <i>De Novo</i> Steroid Synthesis Activates Androgen Receptor in Castration-Resistant Prostate Cancer and Is Upregulated by Treatment with CYP17A1 Inhibitors
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- New aspects of vitamin D metabolism and action — addressing the skin as source and target
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Molecular basis of androgen insensitivity
- Spermidine/spermine-<i>N</i><sup>1</sup>-acetyltransferase: a key metabolic regulator
- Defective trophoblast function in mice with a targeted mutation of Ets2
- Targeted Inactivation of Gh/Tissue Transglutaminase II
- Corticotropin-releasing hormone: An autocrine hormone that promotes lipogenesis in human sebocytes
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Inflammatory Cytokine TNFα Promotes the Long-Term Expansion of Primary Hepatocytes in 3D Culture
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Human Hair Keratin‐Associated Proteins (KAPs)
- A Novel Marker of Tissue Junctions, Collagen XXII
- On the Role of Melatonin in Skin Physiology and Pathology
- Lipoatrophy and severe metabolic disturbance in mice with fat-specific deletion of PPARγ
- Epigenetics of Colorectal Cancer
- Regulation of adult stem cell quiescence and its functions in the maintenance of tissue integrity
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Biotin and biotinidase deficiency
- Wnt signaling induces epithelial differentiation during cutaneous wound healing
- Expression of Hypothalamic–Pituitary–Thyroid Axis RelatedGenes in the Human Skin
- Genetic Disorders and Defects in Vitamin D Action
- Estrogen and androgen signaling in the pathogenesis of BPH
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Regulation of Involucrin Gene Expression