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Research 421–450 of 1000+
- Effects of Periplaneta americana extracts on the growth and proliferation of cutaneous interstitial cells in cutaneous-wound healing
- Familial Dyskeratotic Comedones: A Case Report and Literature Review
- Environmental Air Pollutants Affecting Skin Functions with Systemic Implications
- Transgenic mice provide new insights into the role of TGF-alpha during epidermal development and differentiation.
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Identification of Stem Cell Populations in Sweat Glands and Ducts Reveals Roles in Homeostasis and Wound Repair
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- WNT Signaling in Disease
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- FGF Family: From Drug Development to Clinical Application
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Keratins and disease at a glance
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- The molecular basis of human keratin disorders
- Roles of the Hedgehog Signaling Pathway in Epidermal and Hair Follicle Development, Homeostasis, and Cancer
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- New clinico‐genetic classification of trichothiodystrophy
- Receptor activator of NF-κB (RANK) stimulates the proliferation of epithelial cells of the epidermo-pilosebaceous unit
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases
- The developmental basis of fingerprint pattern formation and variation
- Protective Effects of Melatonin on the Skin: Future Perspectives
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Madarosis: A marker of many Maladies
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis