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Research 421–450 of 1000+
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis
- Monilethrix – Case report of a rare disease
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Utility of trichoscopy
- Approach to Alopecia in Dogs in Clinical Practice
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Continuous MEK inhibition by AZD6244 (ARRY-142886) results in exhaustion of the cutaneous keratinocytic stem cell pool and resembles senescence driven skin aging
- The sebaceous gland revisited: Friend and adversary
- LB1034 Meta-analysis of scalp transcriptome defines alopecia areata subtypes and molecular response to four (4) treatments with jak inhibiting properties
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Skin-inspired phototherapeutic cryogel ameliorates infected wound healing by orchestrating mechanotransduction and immunomodulation
- Trichotillomania
- Beyond Wavy Hairs
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- The Link Between Obesity and the Skin
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- Neurological post‐acute sequelae of SARS‐CoV‐2 infection
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Type 2 Cytokine–Dependent Skin Barrier Regulation in Personalized 2-Dimensional and 3-Dimensional Skin Models of Atopic Dermatitis: A Pilot Study