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Research 721–750 of 1000+
- 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
- Stem cell identification-<i>in vivo</i> lineage analysis versus <i>in vitro</i> isolation and clonal expansion
- 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
- 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
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Becker's Nevus Syndrome
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- Therapeutic inhibition of keratinocyte TRPV3 sensory channel by local anesthetic dyclonine
- Value of dermoscopy for the diagnosis of monilethrix
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- 572 Defining chronic wound types in recessive dystrophic epidermolysis bullosa patients for clinical outcome assessment
- 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
- Real-world safety of Tepotinib: Insights from the Food and Drug Administration Adverse Event Reporting System
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Current Progress Regarding Cordyceps militaris, Its Metabolite Function, and Its Production
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi
- Seasonal Variability in Transcript Expression of Type I and Type II Keratins in Wool Follicles of Lustrous Fleece-Producing Magra Sheep
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- Successful Management of Netherton Syndrome Using IVIG and Dupilumab: A Case Report
- PCSK9: From Nature’s Loss to Patient’s Gain