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Palabras clave – provistas por la editorial

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; genodermatosis; keratinocyte; SAM syndrome; precision medicine; dog; desmosome; acantholysis; calcium; veterinary medicine; feline; Felis catus; brain malformation; BMP12; neurodevelopment; genetics; genomics; mendelian traits; genome-wide association study; whole genome sequencing; mitochondrion; phosphoenolpyruvate-carboxykinase; inborn error of metabolism; encephalopathy; SSADHD; ALDH5A1; GABA; 4-hydroxybutyric acid; succinic semialdehyde; GWAS; inherited; whole genome sequence; wgs; laminin; Bardet–Biedl syndrome (BBS); primary cilia; ciliopathy; BBS8; progressive retinal atrophy (PRA); retinitis pigmentosa; canine; dystrophinopathy; Duchenne; immunohistochemistry; neurometabolic disorder; CHILD syndrome; ILVEN; epidermal nevus; diabetes mellitus; Burmese cats; susceptibility; single-nucleotide polymorphism; genetic markers; LIPH; obesity; companion animals; metabolic disease; comparative genomics; dogs; cats; horses; contactin; neurological disorder; Leonberger; Saint Bernard; Labrador retriever; n/a