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.
שמור ב:
| פורמט: | Online |
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| שפה: | אנגלית |
| יצא לאור: |
MDPI - Multidisciplinary Digital Publishing Institute
2021
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| נושאים: | |
| גישה מקוונת: | ONIX_20210501_9783036504728_303 |
| תגים: |
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
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| _version_ | 1869524539339177984 |
|---|---|
| collection | Directory of Open Access Books |
| description | 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 | Online |
| id | doab-20.500.12854ir-68557 |
| institution | Directory of Open Access Books |
| language | eng |
| publishDate | 2021 |
| publishDateRange | 2021 |
| publishDateSort | 2021 |
| publisher | MDPI - Multidisciplinary Digital Publishing Institute |
| publisherStr | MDPI - Multidisciplinary Digital Publishing Institute |
| record_format | ojs |
| spelling | doab-20.500.12854ir-685572024-03-28T03:33:42Z Molecular Basis of Inherited Diseases in Companion Animals Bannasch, Danika Friedenberg, Steven 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 thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PS Biology, life sciences 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. 2021-05-01T15:14:40Z 2021-05-01T15:14:40Z 2021 book ONIX_20210501_9783036504728_303 9783036504728 9783036504735 https://directory.doabooks.org/handle/20.500.12854/68557 eng application/octet-stream Attribution 4.0 International https://mdpi.com/books/pdfview/book/3578 https://mdpi.com/books/pdfview/book/3578 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-0365-0473-5 10.3390/books978-3-0365-0473-5 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783036504728 9783036504735 232 Basel, Switzerland open access |
| spellingShingle | 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 thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PS Biology, life sciences Molecular Basis of Inherited Diseases in Companion Animals |
| title | Molecular Basis of Inherited Diseases in Companion Animals |
| title_full | Molecular Basis of Inherited Diseases in Companion Animals |
| title_fullStr | Molecular Basis of Inherited Diseases in Companion Animals |
| title_full_unstemmed | Molecular Basis of Inherited Diseases in Companion Animals |
| title_short | Molecular Basis of Inherited Diseases in Companion Animals |
| title_sort | molecular basis of inherited diseases in companion animals |
| topic | 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 thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PS Biology, life sciences |
| topic_facet | 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 thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PS Biology, life sciences |
| url | ONIX_20210501_9783036504728_303 |