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Research 61–90 of 240
- The ITGB6 gene: its role in experimental and clinical biology
- Safety of Common Medications for Treating Dermatology Disorders in Pregnant Women
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Research on Keratins Reveals Unexpected Link Between Hair Disorders and Dental Decay
- Complications of Self‐Injected Facial Fillers: A Treatment Conundrum in the UK
- Ectodermal Organ Stem Cells: Morphogenesis, Population Regenerative Behavior, and Evo-Devo
- Cutaneous thrombosis and ANCA-positive vasculitis associated with propylthiouracil therapy
- Post-steroid panniculitis: a lost and forgotten entity?
- Use of chemotherapy during human pregnancy
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Cosmetics and Cosmeceutical Applications of Chitin, Chitosan and Their Derivatives
- Stem cell niches in mammals
- Long-term complications of Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN): the spectrum of chronic problems in patients who survive an episode of SJS/TEN necessitates multidisciplinary follow-up
- Platelet‐rich plasma and regenerative dentistry
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Cutaneous and Mucosal Manifestations Associated with Celiac Disease
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Psychocutaneous disease
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Hairless is a nuclear receptor corepressor essential for skin function
- Development and Prospects of Organ Replacement Regenerative Therapy
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- Laser Resurfacing
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature