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Research 931–960 of 1000+
- Scar Inhibition in Wound Healing: Mechanisms, Design, and Recent Advances
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Selective Pituitary Resistance to Thyroid Hormone: Clinical Hyperthyroidism with High TSH on Levothyroxine Administration in I-131 Ablated “Graves Disease”
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Evolution of Trichocyte Keratins
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Faculty Opinions recommendation of Local positive feedback regulation determines cell shape in root hair cells.
- A missense mutation in Lama3 causes androgen alopecia
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Beneficial Effects of Deoxyshikonin on Delayed Wound Healing in Diabetic Mice
- Hair follicles modulate skin barrier function
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- The Opportunities and Challenges regarding Induced Platelets from Human Pluripotent Stem Cells
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- Skin Regeneration
- Ichthyosis
- Planar Cell Polarity Cadherin Celsr1 Regulates Skin Hair Patterning in the Mouse
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Molecular Evolution and Protein Structure Variation of Dkk Family
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Receptor tyrosine kinase Kit action in skin melanocytes: is it exclusively cell autonomous?
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Male sex hormone and reduced plakoglobin jointly impair atrial conduction and cardiac sodium currents
- The Roles of Smad2 and Smad3 in Mouse Skin Development
- Viewpoint 2