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Research 511–540 of 683
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- The Pharmacology of Regenerative Medicine
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Coactivator MED1 Ablation in Keratinocytes Results in Hair-Cycling Defects and Epidermal Alterations
- Expression of truncated latent TGF-β-binding protein modulates TGF-β signaling
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Necl2 regulates epidermal adhesion and wound repair
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- The influence of interferon on healthy and diseased skin
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling
- Distinct Developmental Functions of Prostasin (CAP1/PRSS8) Zymogen and Activated Prostasin
- Keratinocyte-derived follistatin regulates epidermal homeostasis and wound repair
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- MEX3A regulates <i>Lgr5</i> <sup>+</sup> stem cell maintenance in the developing intestinal epithelium
- Normal Pubertal Development in Daughters of Women With PCOS: A Controlled Study
- Epidemiological study of prostate cancer (EPICAP): a population-based case–control study in France
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Genetic Hair Disorders: A Review
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Live imaging reveals chromatin compaction transitions and dynamic transcriptional bursting during stem cell differentiation in vivo
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- The Genetic Architecture of Alopecia Areata
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function