Associated Papers
PCR-based detection of hereditary mutations in SLC2A9, BTBD17, and NECAP1 among native Korean dog breeds.
Kang M et al.
Journal of Veterinary Science, 2025
40765230 (PubMed )
Supplement: jvs-26-e48-s001.xls › Supplementary_Table_1
Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture.
Meadows JRS et al.
Genome Biology, 2023
37582787 (PubMed )
Supplement: 13059_2023_3023_MOESM1_ESM.xlsx › Table_S16
Inheritance of Monogenic Hereditary Skin Disease and Related Canine Breeds.
Marín-García PJ et al.
Veterinary Sciences, 2022
Genetics of inherited skin disorders in dogs.
Leeb T et al.
Veterinary Journal (london, England : 1997), 2022
SUV39H2 epigenetic silencing controls fate conversion of epidermal stem and progenitor cells.
Balmer P et al.
The Journal of Cell Biology, 2021
A splice site variant in the SUV39H2 gene in Greyhounds with nasal parakeratosis.
Bauer A et al.
Animal Genetics, 2018
Genetic testing in veterinary dermatology.
Leeb T et al.
Veterinary Dermatology, 2017
Activity and specificity of the human SUV39H2 protein lysine methyltransferase.
Schuhmacher MK et al.
Biochimica Et Biophysica Acta, 2015
A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation.
Jagannathan V et al.
Plos Genetics, 2013
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