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Research 331–360 of 1000+
- Novel Strategy for Hair Regeneration: Exosomes and Collagenous Sequences of Human a1(XVII) Chain Enhance Hair Follicle Stem Cell Activity by Regulating the hsa-novel-238a-CASP9 Axis
- Overexpression of mIGF-1 in Keratinocytes Improves Wound Healing and Accelerates Hair Follicle Formation and Cycling in Mice
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Spatial Distribution and Functional Impact of Human Scalp Hair Follicle Microbiota
- The New Keratin Nomenclature
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Investigation on Microecology of Hair Root Fungi in Androgenetic Alopecia Patients
- Insights into male androgenetic alopecia using comparative transcriptome profiling: hypoxia-inducible factor-1 and Wnt/β-catenin signalling pathways
- The citrullinating enzyme PADI4 governs progenitor cell proliferation and translation in developing hair follicles
- Cross‐linked features of mouse pelage hair resistant to detergent extraction
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Emerging Trends and Focus in Human Skin Microbiome Over the Last Decade: A Bibliometric Analysis and Literature Review
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Expression of Hypothalamic–Pituitary–Thyroid Axis RelatedGenes in the Human Skin
- Biochemical Evidence That Small Proline-rich Proteins and Trichohyalin Function in Epithelia by Modulation of the Biomechanical Properties of Their Cornified Cell Envelopes
- Identification of drug-specific public TCR driving severe cutaneous adverse reactions
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Two Mechanisms Regulate Keratin K15 Expression In Keratinocytes: Role of PKC/AP-1 and FOXM1 Mediated Signalling
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Developmental genetics of color pattern establishment in cats
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Special Biochemical Features of the Hair Follicle
- Multiomics global landscape of stemness-related gene clusters in adipose-derived mesenchymal stem cells
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- An outline of SARS-CoV-2 pathogenesis and the complement cascade of immune system