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Research 301–330 of 1000+
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Developmental and functional roles of androgen and interactive signals for external genitalia and erectile tissues
- Cyclin D3 deficiency inhibits skin tumor development, but does not affect normal keratinocyte proliferation
- Mutant Cx43 in Skin Differentiation and Disease
- Divergent roles of HDAC1 and HDAC2 in the regulation of epidermal development and tumorigenesis
- Sostdc1 defines the size and number of skin appendage placodes
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- Role of the Notch Ligand Delta1 in Embryonic and Adult Mouse Epidermis
- The Study of Growth Factors in Patients with Androgenic Alopecia
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Co-expression of PADI isoforms during progenitor differentiation enables functional diversity
- Comparative Skin Transcriptomics Reveals Key Regulators of Cashmere Fiber Production in Inner Mongolian Goats
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Pathological sequelae of long-haul COVID
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Phospholipase C 1 is required for skin stem cell lineage commitment
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Relation of Skin Polyamines to the Hairless Phenotype in Transgenic Mice Overexpressing Spermidine/Spermine N1-Acetyltransferase
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Keratinocyte-derived follistatin regulates epidermal homeostasis and wound repair
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- Cell death in skin function, inflammation, and disease
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2