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Research 931–960 of 1000+
- Characters of KRT80 and its roles in neoplasms diseases
- Spatial transcriptomics of a giant pilomatricoma
- Crosstalk between vimentin and keratins in viral infection: Implications across the viral life cycle
- Green‐Prepared Magnesium Silicate Sprays Enhance the Repair of Burn‐Skin Wound and Appendages Regeneration in Rats and Minipigs
- scMC learns biological variation through the alignment of multiple single-cell genomics datasets
- Skin shedding and tissue regeneration in African spiny mice (Acomys)
- A stretchable wireless wearable bioelectronic system for multiplexed monitoring and combination treatment of infected chronic wounds
- Types I and II Keratin Intermediate Filaments
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Human Female Hair Follicles Are a Direct, Nonclassical Target for Thyroid-Stimulating Hormone
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- 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
- Genomic Organization, Transcriptomic Analysis, and Functional Characterization of Avian α- and β-Keratins in Diverse Feather Forms
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Biomarkers of alopecia areata disease activity and response to corticosteroid treatment
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- An integrated model of alopecia areata biomarkers highlights both TH1 and TH2 upregulation
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Multifaceted role of keratins in epithelial cell differentiation and transformation
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Against the Rules: Human Keratin K80
- Recently Identified Forms of Epidermolysis Bullosa
- Skin inflammation activates intestinal stromal fibroblasts and promotes colitis