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Research 721–750 of 1000+
- A keratin 15 containing stem cell population from the hair follicle contributes to squamous papilloma development in the mouse
- Genetic Analysis of Androgen Receptors in Development and Disease
- Membrane androgen receptors may mediate androgen reinforcement
- Office Diagnosis of Hair Shaft Defects
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- The dermatological consequences of obesity
- The G60S Connexin43 Mutant Regulates Hair Growth and Hair Fiber Morphology in a Mouse Model of Human Oculodentodigital Dysplasia
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
- Stem cell identification-<i>in vivo</i> lineage analysis versus <i>in vitro</i> isolation and clonal expansion
- High incidence of severe hand–foot syndrome during capecitabine–docetaxel combination chemotherapy
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Bendamustine: an Old Drug in the New Era for Patients with Non-Hodgkin Lymphomas and Chronic Lymphocytic Leukemia
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- Disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus A infection
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Topical polyhydroxy acid treatment for autosomal recessive congenital ichthyosis in the golden retriever: a prospective pilot study
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Telogen elongation in the hair cycle of <i>ob/ob</i> mice
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- Becker's Nevus Syndrome
- Therapeutic inhibition of keratinocyte TRPV3 sensory channel by local anesthetic dyclonine
- At the Root: Cutaneous Langerhans Cell Histiocytosis
- Value of dermoscopy for the diagnosis of monilethrix
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- 199 Impairment of notch 1 signaling is a common defect in lesions from patients with hidradenitis suppurativa
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma
- 572 Defining chronic wound types in recessive dystrophic epidermolysis bullosa patients for clinical outcome assessment
- Real-world safety of Tepotinib: Insights from the Food and Drug Administration Adverse Event Reporting System