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Research 391–420 of 1000+
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Myotonic Dystrophy—A Progeroid Disease?
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Sebaceous adenitis in Swedish dogs, a retrospective study of 104 cases
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Transglutaminase Activity Is Conserved in Stratified Epithelia and Skin Appendages of Mammals and Birds
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Transcriptome Sequencing and Mass Spectrometry Reveal Genes Involved in the Non-mendelian Inheritance-Mediated Feather Growth Rate in Chicken
- Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman
- Aberrant Activation of the Hedgehog Signaling Pathway in Malignant Hematological Neoplasms
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- A Comprehensive Review of Acne Vulgaris
- Exosome-based Therapies for Androgenetic Alopecia: Mechanisms, MicroRNAs, and Clinical Prospects
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- Molecular Mechanisms Regulating Hair Follicle Development
- The JAK/STAT signaling pathway: from bench to clinic
- Cell death by cornification
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- Androgen sensitivity gateway to COVID‐19 disease severity
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- Frizzled Receptors in Development and Disease
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Pathology of Mouse Models of Accelerated Aging