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Research 331–360 of 1000+
- Fibroblast growth factors: key players in regeneration and tissue repair
- The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside
- Zeb2 recruits HDAC–NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination
- The Pathobiology of Skin Aging
- Resting no more: re‐defining telogen, the maintenance stage of the hair growth cycle
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Dermal papilla-induced hair differentiation of adult epithelial stem cells from human skin
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Structure and expression of genes for a class of cysteine-rich proteins of the cuticle layers of differentiating wool and hair follicles.
- Role of FGFR2-signaling in the pathogenesis of acne
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- SARS-CoV-2 Non-Structural Proteins and Their Roles in Host Immune Evasion
- Oxidative DNA Damage Accelerates Skin Inflammation in Pristane-Induced Lupus Model
- Progenitor Cell Dysfunctions Underlie Some Diabetic Complications
- Alleviation of Multidrug Resistance by Flavonoid and Non-Flavonoid Compounds in Breast, Lung, Colorectal and Prostate Cancer
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Xenobiotica-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models
- PPAR-<i>γ</i> Agonists and Their Role in Primary Cicatricial Alopecia
- A kindred with mutant IKAROS and autoimmunity