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Research 181–210 of 1000+
- The genetics of hair shaft disorders
- Clinical Applications of Extracellular Vesicles: Promises and Pitfalls
- Proteome Analysis of Human Hair Shaft
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Prolonged Incubation Period for<i>Cryptococcus gattii</i>Infection in Cat, Alaska, USA
- Combination Antiretroviral Therapy and the Risk of Myocardial Infarction
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Evaluation of Androgen Receptor Expression and Its Association with Clinicopathological Features in Iraqi Women with Breast Cancer
- Exosomes: Biology, Sources and Isolation Techniques
- Extracellular Vesicles in Skin: Biological Function and Therapeutic Potential
- Primary cutaneous diffuse large B‑cell lymphoma of the scalp: A case report and brief review of the literature
- Exosomes in precision dermatology: From biomarkers to targeted therapeutics in personalized care
- A single-cell transcriptomic atlas elucidates the hair cycle and apoptosis mechanisms in goat hair follicles
- Disorders of Keratinization
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Exosomes as a novel pathway for regulating development and diseases of the skin (Review)
- Role of Extracellular Vesicles as Mediators of Cell Communication and Novel Biomarkers in Sepsis
- Avanços terapêuticos no tratamento da alopecia androgenética: Uma revisão das evidências científicas atuais
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Thrombophilia and Polycythemia in a Woman With Budd-Chiari Syndrome
- 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
- 1616 Cross-comparison of inflammatory skin disease transcriptomics identifies PTEN as a pathogenic disease classifier in cutaneous lupus erythematosus
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- 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
- Idiopathic Hirsutism*
- Genetic hair and nail disorders