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Research 271–300 of 1000+
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- DKK4 as a novel candidate marker for Zhexi Angora rabbit wool quality
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium
- Current Genetics in Hair Diseases
- Multiomics Analysis of the Response to Ritlecitinib in Alopecia Areata Subtypes and Correlation With Efficacy
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- The Effects of Spermidine on Functional and Transcriptomic Markers in Human Primary Keratinocytes
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Keratin 79 is a PPARA target that is highly expressed by liver damage
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Development and Maintenance of Epidermal Stem Cells in Skin Adnexa
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Canonical prolactin signaling and global mRNA expression in the skin of Holstein heifers carrying the SLICK1 allele of the prolactin receptor gene
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Nestin is a marker of unipotent embryonic and adult progenitors differentiating into an epithelial cell lineage of the hair follicles
- Congenital atrichia with papular lesions
- A Mouse Model of Androgenetic Alopecia
- The genetic basis of dermatophytosis skin infection susceptibility
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Spatial transcriptomics of a giant pilomatricoma
- Interleukin-1 Induces Transcription of Keratin K6 in Human Epidermal Keratinocytes
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia