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Research 841–870 of 1000+
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Ethanol intake patterns in female mice: Influence of allopregnanolone and the inhibition of its synthesis
- Review of hair follicle dermal cells
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Preclinical Pharmacology, Antitumor Activity, and Development of Pharmacodynamic Markers for the Novel, Potent AKT Inhibitor CCT128930
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Long and short non-coding RNA and radiation response: a review
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Deletion of the <i>Sox21</i> gene drastically affects hair lipids
- Androgens/Androgen Receptor in the Management of Skin Diseases
- Hair & Cutaneous Development
- The role of WNT10B in physiology and disease: A 10-year update
- Pitfalls of PCR-Based Strategy for Genotyping <i>Cre-Loxp</i> Mice
- The Impact of Sulforaphane on Sex-Specific Conditions and Hormone Balance: A Comprehensive Review
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Dynamic expression of ornithine decarboxylase in hair growth
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Skin Stearoyl-CoA Desaturase Genes
- Hair follicle morphogenesis and epidermal homeostasis in we/we wal/wal mice with postnatal alopecia
- A Novel Marker of Tissue Junctions, Collagen XXII
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Liver and Kidney Dysfunction in Wistar Rats Exposed to Municipal Landfill Leachate
- Keratin intermediate filaments in the colon: guardians of epithelial homeostasis
- Hair follicle stem cell replication stress drives IFI16/STING-dependent inflammation in hidradenitis suppurativa