Search
for
Sort by
Research 30 of 444
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- KRT72 wt Allele
- 702 dsRNA induces ectopic KRT9 expression via WNT/β-catenin-mediated signaling
- 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.
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Mice Expressing a Mutant Krt75 (K6hf) Allele Develop Hair and Nail Defects Resembling Pachyonychia Congenita
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Keratin 79 is a PPARA target that is highly expressed by liver damage
- Differential transcriptomics and metabolomics analyses of the skin of coarse and fine Liaoning cashmere goats
- Multi-omics analysis of functional substances and expression verification in cashmere fineness
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Hedgehog signaling maintains hair follicle stem cell phenotype in young and aged human skin
- Dynamic changes of genomic methylation profiles at different growth stages in Chinese Tan sheep
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Ovine Hair Follicle Stem Cells Derived from Single Vibrissae Reconstitute Haired Skin