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Research 421–450 of 1000+
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Eyelash Transplantation Using Leg Hair by Follicular Unit Extraction
- Sox9 expression in canine epithelial skin tumors
- Werner′s syndrome
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- A 4kb Fragment of the Desmocollin 3 Promoter Directs Reporter Gene Expression to Parakeratotic Epidermis and Primary Hair Follicles
- Signal integrator function of CXXC5 in Cancer
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Animals in Dermatology
- A case of chronic kidney disease patient with rapid deterioration of renal function, hair loss, and spontaneous resolution of facial warts after COVID‐19 infection
- Loss of TET2 Tips the Scales Toward Tumorigenesis
- Hypotrichosis in a child with olmsted syndrome
- Toxic and Metabolic Disorders of the Nervous System
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- The Three-Dimensional Human Skin Reconstruct Model: a Tool to Study Normal Skin and Melanoma Progression
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Biotin Supplementation Ameliorates Murine Colitis by Preventing NF-κB Activation
- Multifaceted role of keratins in epithelial cell differentiation and transformation
- The Female Pattern Hair Loss: Review of Etiopathogenesis and Diagnosis
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Utility of GLI1 RNA Chromogenic in Situ Hybridization in Distinguishing Basal Cell Carcinoma From Histopathologic Mimics
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Melanotrichoblastoma: A Histopathological Case Report of a Rare Pigmented Variant of Trichoblastoma
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma