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Research 481–510 of 1000+
- Usefulness of Dermoscopy to Provide Accurate Assessment of Skin Cancers
- Efficacy and patient-reported outcomes in advanced non-small cell lung cancer patients receiving aumolertinib as first-line therapy: a real-world study
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Animals in Dermatology
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Poster presentationsDP11 Bright, eosinophilic intracytoplasmic inclusion bodies: a rare presentation of acquired epidermodysplasia verruciformis with widespread human papillomavirus infection in a transplant recipient
- 026 Altered Skin Wound Healing in Homeobox Gene Msx-2 Knockout Mice
- Expression of Cyclooxygenase Isozymes During Morphogenesis and Cycling of Pelage Hair Follicles in Mouse Skin: Precocious Onset of the First Catagen Phase and Alopecia upon Cyclooxygenase-2 Overexpression
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Cell death in the skin
- A slow-cycling LGR5 tumour population mediates basal cell carcinoma relapse after therapy
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- The molecular basis of human keratin disorders
- Protein kinase Cepsilon is linked to 12-O-tetradecanoylphorbol-13-acetate-induced tumor necrosis factor-alpha ectodomain shedding and the development of metastatic squamous cell carcinoma in protein kinase Cepsilon transgenic mice.
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Interleukin 6 and STAT3 regulate p63 isoform expression in keratinocytes during regeneration
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Sox9 expression in canine epithelial skin tumors
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- miR-129-5p Participates in Hair Follicle Growth by Targeting HOXC13 in Rabbit
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Amphiregulin in Fibrotic Diseases and Cancer