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Research 841–870 of 1000+
- ChatGPT in medicine: Evaluating psoriasis patient concerns
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Hair Follicle Development in Mouse Pluripotent Stem Cell-Derived Skin Organoids
- Role of Cytotoxic T Cells in Chronic Alopecia Areata
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus
- Control by a hair’s breadth: the role of microRNAs in the skin
- The nude gene and the skin
- Dermoscopic findings in scalp psoriasis and seborrheic dermatitis; Two new signs; Signet ring vessel and hidden hair
- Natural Sources of Therapeutic Agents Used in Skin Conditions
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Alopecia and Associated Toxic Agents: A Systematic Review
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- HAIR LOSS AND REGENERATION PERFORMED ON ANIMAL MODELS
- Epigallocatechin-3 Gallate Inhibits STAT-1/JAK2/IRF-1/HLA-DR/HLA-B and Reduces CD8 MKG2D Lymphocytes of Alopecia Areata Patients
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Iron Metabolism of the Skin: Recycling versus Release
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Eccrine angiomatous hamartoma
- Transcription Regulation and Protein Subcellular Localization of the Truncated Basic Hair Keratin hHb1-ΔN in Human Breast Cancer Cells
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation