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Research 30 of 508
- Characters of KRT80 and its roles in neoplasms diseases
- GCN5-mediated H3K27cr regulates hair follicle stem cell migration and hair follicle development through KRT80 activation
- 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
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- 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
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- Ovine KRT81 Variants and Their Influence on Selected Wool Traits of Commercial Value
- 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
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Annotation of sheep keratin intermediate filament genes and their patterns of expression
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Ichthyosis with confetti: clinics, molecular genetics and management
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- Association analysis of polymorphisms in six keratin genes with wool traits in sheep
- Keratins: the hair shaft's backbone revealed
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- Genome-wide identification, characterization, and expression analysis of keratin genes (KRTs) family in yak (Bos grunniens)