Search
for
Sort by
Research 661–690 of 1000+
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- WNT Signaling in Disease
- 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
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- Epidermal Development in Mammals: Key Regulators, Signals from Beneath, and Stem Cells
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus
- Telogen Effluvium: A Review
- Receptor activator of NF-κB (RANK) stimulates the proliferation of epithelial cells of the epidermo-pilosebaceous unit
- Morphea: progress to date and the road ahead
- The developmental basis of fingerprint pattern formation and variation
- Protective Effects of Melatonin on the Skin: Future Perspectives
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- RANKL Induces Organized Lymph Node Growth by Stromal Cell Proliferation
- Necl2 regulates epidermal adhesion and wound repair
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Keratinocyte biology and pathology
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- Plastic surgery : indications, operations, and outcomes
- The role of WNT10B in physiology and disease: A 10-year update
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Topically Applied Minoxidil in Baldness
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene