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Research 751–780 of 1000+
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Toll-like receptor-targeted anti-tumor therapies: Advances and challenges
- Progress in studies of epidermal stem cells and their application in skin tissue engineering
- Functional Skin Grafts: Where Biomaterials Meet Stem Cells
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Long and short non-coding RNA and radiation response: a review
- Myotonic Dystrophy—A Progeroid Disease?
- The nude gene and the skin
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Expression of truncated latent TGF-β-binding protein modulates TGF-β signaling
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Role of Phenylalanine and Its Metabolites in Health and Neurological Disorders
- Krtap11-1, a hair keratin-associated protein, as a possible crucial element for the physical properties of hair shafts
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3
- Membrane androgen receptors may mediate androgen reinforcement
- Ku80 as a Novel Receptor for Thymosin β4 That Mediates Its Intracellular Activity Different from G-actin Sequestering
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Aging in the sebaceous gland
- Hypoxia in Cell Reprogramming and the Epigenetic Regulations
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Intracrine and Myotrophic Roles of 5α-Reductase and Androgens
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Using the zebrafish lateral line to uncover novel mechanisms of action and prevention in drug-induced hair cell death
- Physiological Insights from the Vitamin D Receptor Knockout Mouse
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Rab5c-mediated endocytic trafficking regulates hematopoietic stem and progenitor cell development via Notch and AKT signaling