Reprint
Molecular Basis of Inherited Diseases in Companion Animals
Edited by
April 2021
232 pages
- ISBN978-3-0365-0472-8 (Hardback)
- ISBN978-3-0365-0473-5 (PDF)
This book is a reprint of the Special Issue Molecular Basis of Inherited Diseases in Companion Animals that was published in
Biology & Life Sciences
Summary
This book includes a collection of publications describing the molecular etiology of inherited diseases and conditions in companion animals (dogs and cats). In addition to contributing to the health of companion animals, this research also benefits humans that have similar types of diseases.
Format
- Hardback
License
© 2022 by the authors; CC BY-NC-ND license
Keywords
Canis familiaris; dermatology; immunology; animal model; skin; TLR7; toll-like receptor; syndecan binding protein; syntenin-1; systemic lupus erythematosus; SLE; CLE; whole-genome sequencing; craniomandibular osteopathy; calvarial hyperostotic syndrome; Caffey disease; infantile cortical hyperostosis; rare disease; SLC37A2; COL1A1; SLC35D1; Canis lupus familiaris; whole-genome sequence; animal model; genodermatosis; skin; dermatology; keratinocyte; SAM syndrome; precision medicine; Canis lupus familiaris; dog; dermatology; skin; desmosome; acantholysis; calcium; animal model; veterinary medicine; precision medicine; feline; Felis catus; brain malformation; BMP12; neurodevelopment; genetics; genomics; mendelian traits; genome-wide association study; whole genome sequencing; Canis lupus familiaris; whole genome sequencing; dog; mitochondrion; phosphoenolpyruvate-carboxykinase; inborn error of metabolism; precision medicine; inborn error of metabolism; encephalopathy; SSADHD; ALDH5A1; GABA; 4-hydroxybutyric acid; succinic semialdehyde; encephalopathy; whole-genome sequencing; precision medicine; GWAS; inherited; dog; Canis lupus familiaris; whole genome sequence; wgs; dermatology; genodermatosis; skin; laminin; precision medicine; Bardet–Biedl syndrome (BBS); primary cilia; ciliopathy; BBS8; progressive retinal atrophy (PRA); retinitis pigmentosa; canine; dystrophinopathy; Duchenne; immunohistochemistry; precision medicine; Canis familiaris; whole-genome sequencing; rare disease; precision medicine; neurometabolic disorder; Canis lupus familiaris; animal model; genodermatosis; dermatology; skin; CHILD syndrome; ILVEN; epidermal nevus; precision medicine; diabetes mellitus; Burmese cats; susceptibility; single-nucleotide polymorphism; genetic markers; LIPH; obesity; genetics; companion animals; metabolic disease; comparative genomics; dogs; cats; horses; Canis familiaris; whole-genome sequencing; rare disease; contactin; neurological disorder; Leonberger; Saint Bernard; Labrador retriever; n/a