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Research 691–720 of 1000+
- Cronkhite-Canada Syndrome Associated With Superficial Esophageal Carcinoma: A Case Report and Literature Review
- Potential Treatment of Steroid‐Resistant Alopecia Areata Using Allogeneic Exosomes Derived From Adipose Tissue Mesenchymal Stromal Cells: A Case Report
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- The anatomical distribution of lentiginous melanoma (lentigo maligna and lentigo maligna melanoma): Differences according to sex
- Side effects of vitamins, amino acids, nutrition, and complementary and alternative medicine
- Clinical case of a patient with progressive supranuclear palsy – from symptom to diagnosis
- Three Cases of Canine Dermatomyositis-Like Disease
- Patient Satisfaction and Quality of Life Among Adult Women with Androgenetic Alopecia Using 5% Topical Minoxidil.
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Vitamin A regulates dermal papilla cell proliferation and apoptosis under heat stress via IGF1 and Wnt10b signaling
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- Madarosis: A marker of many Maladies
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- 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
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Tissue engineering of skin and regenerative medicine for wound care
- Matriptase: Potent Proteolysis on the Cell Surface
- The malignant capacity of skin tumours induced by expression of a mutant H-ras transgene depends on the cell type targeted
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- 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
- Cell death in the skin
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Development and homeostasis of the sebaceous gland
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis