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Research 391–420 of 1000+
- A practical guide for the study of human and murine sebaceous glands <i>in situ</i>
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Repairing the lungs one breath at a time: How dedicated or facultative are you?
- Defining a Region of the Human Keratin 6a Gene That Confers Inducible Expression in Stratified Epithelia of Transgenic Mice
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Endocrine controls of primary adult human stem cell biology: Thyroid hormones stimulate keratin 15 expression, apoptosis, and differentiation in human hair follicle epithelial stem cells in situ and in vitro
- Dermoscopic Approach to a Small Round to Oval Hairless Patch on the Scalp
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Against the Rules: Human Keratin K80
- The cDNA-deduced amino acid sequence for trichohyalin, a differentiation marker in the hair follicle, contains a 23 amino acid repeat.
- Deciphering the functions of the hair follicle infundibulum in skin physiology and disease
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Biochemical and immunohistochemical analyses of keratin expression in basal cell carcinoma
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Hair Keratins and Hair Follicle–Specific Epithelial Keratins
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Thyroxine (T4) may promote re-epithelialisation and angiogenesis in wounded human skin ex vivo
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Genetically separable determinants of hair keratin gene expression
- Self‐organizing hair peg‐like structures from dissociated skin progenitor cells: New insights for human hair follicle organoid engineering and Turing patterning in an asymmetric morphogenetic field
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep
- Keratin expression by corneal and limbal stem cells during development
- Induction of Hard Keratin Expression in Non-Nail-Matrical Keratinocytes by Nail-Matrical Fibroblasts through Epithelial-Mesenchymal Interactions
- Involucrin: A Constituent of Cross-Linked Envelopes and Marker of Squamous Maturation
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis