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Research 30 of 508
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Characters of KRT80 and its roles in neoplasms diseases
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- 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
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- 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
- GCN5-mediated H3K27cr regulates hair follicle stem cell migration and hair follicle development through KRT80 activation
- Generation of the Krt24-CreERT2 Mouse Line Targeting Outer Bulge Hair Follicle Cells
- KRT72 wt Allele
- Ovine KRT81 Variants and Their Influence on Selected Wool Traits of Commercial Value
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- 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
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Heterozygous <i>KRT32</i> variant is responsible for autosomal dominant loose anagen hair syndrome
- A comparative proteomic-based study identifies essential factors involved in hair follicle growth in inner Mongolia cashmere goats
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep