Molecular Basis of Inherited Diseases in Companion Animals

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.

Bibliographic Details
Format: eBook
Language:English
Published: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2021
Subjects:
CLE
dog
n/a
SLE
wgs
Online Access:Open Access: DOAB: description of the publication
Open Access: DOAB, download the publication
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653 |a 4-hydroxybutyric acid 
653 |a acantholysis 
653 |a ALDH5A1 
653 |a animal model 
653 |a Bardet-Biedl syndrome (BBS) 
653 |a BBS8 
653 |a BMP12 
653 |a brain malformation 
653 |a Burmese cats 
653 |a Caffey disease 
653 |a calcium 
653 |a calvarial hyperostotic syndrome 
653 |a canine 
653 |a Canis familiaris 
653 |a Canis lupus familiaris 
653 |a cats 
653 |a CHILD syndrome 
653 |a ciliopathy 
653 |a CLE 
653 |a COL1A1 
653 |a companion animals 
653 |a comparative genomics 
653 |a contactin 
653 |a craniomandibular osteopathy 
653 |a dermatology 
653 |a desmosome 
653 |a diabetes mellitus 
653 |a dog 
653 |a dogs 
653 |a Duchenne 
653 |a dystrophinopathy 
653 |a encephalopathy 
653 |a epidermal nevus 
653 |a feline 
653 |a Felis catus 
653 |a GABA 
653 |a genetic markers 
653 |a genetics 
653 |a genodermatosis 
653 |a genome-wide association study 
653 |a genomics 
653 |a GWAS 
653 |a horses 
653 |a ILVEN 
653 |a immunohistochemistry 
653 |a immunology 
653 |a inborn error of metabolism 
653 |a infantile cortical hyperostosis 
653 |a inherited 
653 |a keratinocyte 
653 |a Labrador retriever 
653 |a laminin 
653 |a Leonberger 
653 |a LIPH 
653 |a mendelian traits 
653 |a metabolic disease 
653 |a mitochondrion 
653 |a n/a 
653 |a neurodevelopment 
653 |a neurological disorder 
653 |a neurometabolic disorder 
653 |a obesity 
653 |a phosphoenolpyruvate-carboxykinase 
653 |a precision medicine 
653 |a primary cilia 
653 |a progressive retinal atrophy (PRA) 
653 |a rare disease 
653 |a retinitis pigmentosa 
653 |a Saint Bernard 
653 |a SAM syndrome 
653 |a single-nucleotide polymorphism 
653 |a skin 
653 |a SLC35D1 
653 |a SLC37A2 
653 |a SLE 
653 |a SSADHD 
653 |a succinic semialdehyde 
653 |a susceptibility 
653 |a syndecan binding protein 
653 |a syntenin-1 
653 |a systemic lupus erythematosus 
653 |a TLR7 
653 |a toll-like receptor 
653 |a veterinary medicine 
653 |a wgs 
653 |a whole genome sequence 
653 |a whole genome sequencing 
653 |a whole-genome sequence 
653 |a whole-genome sequencing 
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