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Research 30 of 731
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Characters of KRT80 and its roles in neoplasms diseases
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Hair keratin KRT81 is expressed in normal and breast cancer cells and contributes to their invasiveness
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- 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
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- GCN5-mediated H3K27cr regulates hair follicle stem cell migration and hair follicle development through KRT80 activation
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Generation of the Krt24-CreERT2 Mouse Line Targeting Outer Bulge Hair Follicle Cells
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Ovine KRT81 Variants and Their Influence on Selected Wool Traits of Commercial Value
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family
- Annotation of sheep keratin intermediate filament genes and their patterns of expression
- Analysis of differential expression of hair follicle tissue transcriptome in Hetian sheep undergoing different periodic changes
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Keratins and disease at a glance