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Research 30 of 671
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Generation of the Krt24-CreERT2 Mouse Line Targeting Outer Bulge Hair Follicle Cells
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Annotation of sheep keratin intermediate filament genes and their patterns of expression
- Association analysis of polymorphisms in six keratin genes with wool traits in sheep
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil
- GCN5-mediated H3K27cr regulates hair follicle stem cell migration and hair follicle development through KRT80 activation
- Dermatopathology and molecular genetics
- Genome-wide identification, characterization, and expression analysis of keratin genes (KRTs) family in yak (Bos grunniens)
- 731 Generation of a laser capture microdissection and RNAseq-based human anagen hair follicle transcriptome atlas
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Generating mouse models of degenerative diseases using Cre/lox-mediated in vivo mosaic cell ablation
- Single-Cell Sequencing Reveals Differential Cell Types in Skin Tissues of Liaoning Cashmere Goats and Key Genes Related Potentially to the Fineness of Cashmere Fiber
- UNRAVELING MINK HAIR KERATIN GENES