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Research 361–390 of 1000+
- Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- Vitamin A regulates dermal papilla cell proliferation and apoptosis under heat stress via IGF1 and Wnt10b signaling
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Optimization and Characterization of TSG-Enriched Polygonum multiflorum Extract and Its Dual Mechanism Against Androgenetic Alopecia via 5α-Reductase Inhibition and Wnt/β-Catenin Activation
- Trichological disorders in Organ Transplant Recipients - case report and literature review.
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- The Dickkopf Protein Family in Non-Neoplastic Disorders: Emerging Roles and Therapeutic Targeting
- Bioinspired engineering ADSC nanovesicles thermosensitive hydrogel enhance autophagy of dermal papilla cells for androgenetic alopecia treatment
- Bioengineered skin organoids: from development to applications
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- The Genetics of Human Skin Disease
- Distinct tooth regeneration systems deploy a conserved battery of genes
- The malignant capacity of skin tumours induced by expression of a mutant H-ras transgene depends on the cell type targeted
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- The role of WNT10B in physiology and disease: A 10-year update
- Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models
- Extracellular vesicles in age-related diseases: disease pathogenesis, intervention, and biomarker
- Essential Oils and Melatonin as Functional Ingredients in Dogs
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Analogs of human genetic skin disease in domesticated animals