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Research 571–600 of 695
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Congenital atrichia associated with situs inversus and mesocardia
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- TRPV3 Ion Channel: From Gene to Pharmacology
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Folliculotropic CD8+ mycosis fungoides associated with diffuse mucosal involvement
- Phytochemicals for Hair Health Targeting Growth Signaling Molecules in Hair Follicular Stem Cells: A New Strategy for Hair Growth
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Mucocutaneous findings in hematolymphoid neoplasms: An observational study
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- DP15 Syphilis: the chameleon disease. A case series of unexpected mimicry
- Linear and Unilateral Basaloid Follicular Hamartoma Along Blaschko’s Lines in an Elderly Patient: A Rare Presentation
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Cutaneous manifestations of hypothyroidism: An observational study in a tertiary care center of Eastern India
- “Degeneration” in Dermatopathology
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Painful thickened skin on the soles of the feet
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Pioneers in Dermatology and Venereology: An Interview with Professor Danilo V. Stevanovic
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- Fibroblasts: Origins, definitions, and functions in health and disease
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Expression of Hypothalamic–Pituitary–Thyroid Axis RelatedGenes in the Human Skin
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome