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- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- Caractérisation d’une modification «bigarré» de la couleur du pelage chez le chat domestique
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Identification and profiling of microRNA between back and belly Skin in Rex rabbits (Oryctolagus cuniculus)
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- A Comprehensive Review on Skin Pigmentation-Types, Causes, and Treatment
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Skin Pigmentation Types, Causes and Treatment—A Review
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Dynamic changes of genomic methylation profiles at different growth stages in Chinese Tan sheep
- The role of WNT10B in physiology and disease: A 10-year update
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Sex Identification of Feather Color in Geese and the Expression of Melanin in Embryonic Dorsal Skin Feather Follicles