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Research 181–210 of 1000+
- A single-cell transcriptomic atlas elucidates the hair cycle and apoptosis mechanisms in goat hair follicles
- Role of Extracellular Vesicles as Mediators of Cell Communication and Novel Biomarkers in Sepsis
- Disorders of Keratinization
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Effect of Sun exposure-induced ferroptosis mechanisms on pathology and potential biological processes of primary melanoma by microarray data analysis
- 1616 Cross-comparison of inflammatory skin disease transcriptomics identifies PTEN as a pathogenic disease classifier in cutaneous lupus erythematosus
- Avanços terapêuticos no tratamento da alopecia androgenética: Uma revisão das evidências científicas atuais
- Identification of Biomarkers in Affected Hair Follicles from Chronic Discoid LupusErythematosus by Weighted Gene Co-Expression Network Analysis
- JAK-STAT pathway-associated skin diseases: a refined functional framework for inflammatory skin diseases
- Immunostaining study of cytokeratins in human hair follicle development
- Evaluation of oxidative stress markers in Androgenetic Alopecia Patients
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- A nonsense variant in <i>KRT31</i> is associated with autosomal-dominant monilethrix
- Idiopathic Hirsutism*
- Genetic hair and nail disorders
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Malignant Melanoma and Its Stromal Nonimmune Microecosystem
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Lentiginous melanoma. A clinically malignant entity that histopathologically seems benign. Case study harbouring BRAF V 600R mutation
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Editorial: Androgen-dependent diseases and their treatment
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- Case Report: A case of Rothmund–Thomson syndrome-like phenotype with an ANAPC1 variant of uncertain significance and observed hair improvement
- Temporal triangular alopecia and a review of 52 past cases
- A Case of Kerion Celsi Caused by Microsporum gypseum (Arthroderma gypseum ) in a Child
- A Chinese–Japanese boy with black dot ringworm due to <i>Trichophyton violaceum</i>