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Research 391–420 of 1000+
- Psoriasiform skin reaction due to Brazilian keratin treatment
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Hair keratin KRT81 is expressed in normal and breast cancer cells and contributes to their invasiveness
- Stem cell apoptosis in HIV‐1 alopecia
- The Effects of an Oral Supplementation of a Natural Keratin Hydrolysate on Skin Aging: A Randomized, Double‐Blind, Placebo‐Controlled Clinical Study in Healthy Women
- Cyclosporin A-induced hair growth in mice is associated with inhibition of calcineurin-dependent activation of NFAT in follicular keratinocytes
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Effective high-throughput isolation of enriched platelets and circulating pro-angiogenic cells to accelerate skin-wound healing
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- Expression of epidermal keratins and filaggrin during human fetal skin development.
- Keratins: the hair shaft's backbone revealed
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Beyond Expectations
- Characterization of sciellin, a precursor to the cornified envelope of human keratinocytes
- Structural changes in the trichocyte intermediate filaments accompanying the transition from the reduced to the oxidized form
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Pathogenesis of pili annulati
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Analysis of cosmetic residues on a single human hair by ATR FT-IR microspectroscopy
- Follicular Hybrid Cyst With Isthmic-Catagen, Pilomatrical, and Syringocystadenoma Papilliferum Components
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis
- Generalized trichoepitheliomas with alopecia and myasthenia gravis: Clinicopathologic and immunohistochemical study and comparison with classic and desmoplastic trichoepithelioma
- New keratin isolates: actives for natural hair protection.