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.
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Year of Publication: | 2021 |
Language: | English |
Physical Description: | 1 electronic resource (232 p.) |
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100 | 1 | |a Bannasch, Danika |4 edt | |
245 | 1 | 0 | |a Molecular Basis of Inherited Diseases in Companion Animals |
260 | |a Basel, Switzerland |b MDPI - Multidisciplinary Digital Publishing Institute |c 2021 | ||
300 | |a 1 electronic resource (232 p.) | ||
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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. | ||
546 | |a English | ||
650 | 7 | |a Research & information: general |2 bicssc | |
650 | 7 | |a Biology, life sciences |2 bicssc | |
653 | |a Canis familiaris | ||
653 | |a dermatology | ||
653 | |a immunology | ||
653 | |a animal model | ||
653 | |a skin | ||
653 | |a TLR7 | ||
653 | |a toll-like receptor | ||
653 | |a syndecan binding protein | ||
653 | |a syntenin-1 | ||
653 | |a systemic lupus erythematosus | ||
653 | |a SLE | ||
653 | |a CLE | ||
653 | |a whole-genome sequencing | ||
653 | |a craniomandibular osteopathy | ||
653 | |a calvarial hyperostotic syndrome | ||
653 | |a Caffey disease | ||
653 | |a infantile cortical hyperostosis | ||
653 | |a rare disease | ||
653 | |a SLC37A2 | ||
653 | |a COL1A1 | ||
653 | |a SLC35D1 | ||
653 | |a Canis lupus familiaris | ||
653 | |a whole-genome sequence | ||
653 | |a genodermatosis | ||
653 | |a keratinocyte | ||
653 | |a SAM syndrome | ||
653 | |a precision medicine | ||
653 | |a dog | ||
653 | |a desmosome | ||
653 | |a acantholysis | ||
653 | |a calcium | ||
653 | |a veterinary medicine | ||
653 | |a feline | ||
653 | |a Felis catus | ||
653 | |a brain malformation | ||
653 | |a BMP12 | ||
653 | |a neurodevelopment | ||
653 | |a genetics | ||
653 | |a genomics | ||
653 | |a mendelian traits | ||
653 | |a genome-wide association study | ||
653 | |a whole genome sequencing | ||
653 | |a mitochondrion | ||
653 | |a phosphoenolpyruvate-carboxykinase | ||
653 | |a inborn error of metabolism | ||
653 | |a encephalopathy | ||
653 | |a SSADHD | ||
653 | |a ALDH5A1 | ||
653 | |a GABA | ||
653 | |a 4-hydroxybutyric acid | ||
653 | |a succinic semialdehyde | ||
653 | |a GWAS | ||
653 | |a inherited | ||
653 | |a whole genome sequence | ||
653 | |a wgs | ||
653 | |a laminin | ||
653 | |a Bardet-Biedl syndrome (BBS) | ||
653 | |a primary cilia | ||
653 | |a ciliopathy | ||
653 | |a BBS8 | ||
653 | |a progressive retinal atrophy (PRA) | ||
653 | |a retinitis pigmentosa | ||
653 | |a canine | ||
653 | |a dystrophinopathy | ||
653 | |a Duchenne | ||
653 | |a immunohistochemistry | ||
653 | |a neurometabolic disorder | ||
653 | |a CHILD syndrome | ||
653 | |a ILVEN | ||
653 | |a epidermal nevus | ||
653 | |a diabetes mellitus | ||
653 | |a Burmese cats | ||
653 | |a susceptibility | ||
653 | |a single-nucleotide polymorphism | ||
653 | |a genetic markers | ||
653 | |a LIPH | ||
653 | |a obesity | ||
653 | |a companion animals | ||
653 | |a metabolic disease | ||
653 | |a comparative genomics | ||
653 | |a dogs | ||
653 | |a cats | ||
653 | |a horses | ||
653 | |a contactin | ||
653 | |a neurological disorder | ||
653 | |a Leonberger | ||
653 | |a Saint Bernard | ||
653 | |a Labrador retriever | ||
776 | |z 3-0365-0472-9 | ||
776 | |z 3-0365-0473-7 | ||
700 | 1 | |a Friedenberg, Steven |4 edt | |
700 | 1 | |a Bannasch, Danika |4 oth | |
700 | 1 | |a Friedenberg, Steven |4 oth | |
906 | |a BOOK | ||
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