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.
Format: | eBook |
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Language: | English |
Published: |
Basel, Switzerland
MDPI - Multidisciplinary Digital Publishing Institute
2021
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Subjects: | |
Online Access: | Open Access: DOAB: description of the publication Open Access: DOAB, download the publication |
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720 | 1 | |a Bannasch, Danika |4 oth | |
720 | 1 | |a Friedenberg, Steven |4 edt | |
720 | 1 | |a Friedenberg, Steven |4 oth | |
245 | 0 | 0 | |a Molecular Basis of Inherited Diseases in Companion Animals |
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520 | |a 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. | ||
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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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