A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats

Selkirk Rex: Morphological and Genetic Characterization of a New Cat Breed

(2012) Serina Filler et al.   JOURNAL OF HEREDITY

A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis

(2012) Atsushi Fujimoto et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

First WNK4-Hypokalemia Animal Model Identified by Genome-Wide Association in Burmese Cats

(2012) Barbara Gandolfi et al.   PLoS One

A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hair

(2012) Muhammad Tariq et al.   Scientific Reports

The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis

(2012) Chen Siang Ng et al.   PLoS Genetics

Enhancements to the ADMIXTURE algorithm for individual ancestry estimation

(2011) David H Alexander et al.   BMC BIOINFORMATICS

Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture

(2010) Yutaka Shimomura et al.   AMERICAN JOURNAL OF HUMAN GENETICS

pegas: an R package for population genetics with an integrated-modular approach

(2010) E. Paradis   BIOINFORMATICS

Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families

(2010) Naveed Wasif et al.   HUMAN GENETICS

Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene

(2010) Takashi KURAMOTO et al.   JOURNAL OF VETERINARY MEDICAL SCIENCE

The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71

(2010) Barbara Gandolfi et al.   MAMMALIAN GENOME

APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex

(2010) Yutaka Shimomura et al.   NATURE

Identification of aU2HRgene mutation in Turkish families with Marie Unna hereditary hypotrichosis

(2009) S. Düzenli et al.   CLINICAL AND EXPERIMENTAL DERMATOLOGY

Fast model-based estimation of ancestry in unrelated individuals

(2009) D. H. Alexander et al.   GENOME RESEARCH

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

(2009) Yaran Wen et al.   NATURE GENETICS

Coat Variation in the Domestic Dog Is Governed by Variants in Three Genes

(2009) E. Cadieu et al.   SCIENCE

The human keratins: biology and pathology

(2008) Roland Moll et al.   HISTOCHEMISTRY AND CELL BIOLOGY

Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)

(2008) Zahid Azeem et al.   HUMAN GENETICS