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Research 751–780 of 1000+
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Hair follicle immune privilege and its collapse in alopecia areata
- A Nonredundant Human Protein Chip for Antibody Screening and Serum Profiling
- Gene Array Profiling and Immunomodulation Studies Define a Cell-Mediated Immune Response Underlying the Pathogenesis of Alopecia Areata in a Mouse Model and Humans
- Generation of folliculogenic human epithelial stem cells from induced pluripotent stem cells
- Order from disorder: Self-organization in mammalian hair patterning
- Visualising Androgen Receptor Activity in Male and Female Mice
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Regulated Proenkephalin Expression in Human Skin and Cultured Skin Cells
- Genomic Organization, Transcriptomic Analysis, and Functional Characterization of Avian α- and β-Keratins in Diverse Feather Forms
- Exosomal Micro RNAs Derived from Dermal Papilla Cells Mediate Hair Follicle Stem Cell Proliferation and Differentiation
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- The Pharmacology of Regenerative Medicine
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Transcriptomic analyses of regenerating adult feathers in chicken
- The developmental basis of fingerprint pattern formation and variation
- The nude gene and the skin
- Exploiting Unique Features of Microneedles to Modulate Immunity
- Ichthyosis with confetti: clinics, molecular genetics and management
- Runx3 is involved in hair shape determination
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Development of pluripotent stem cell-derived epidermal organoids that generate effective extracellular vesicles in skin regeneration
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- The Genetics of Human Skin Disease
- Hard Keratin IF and Associated Proteins
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis