Feedback

X
Molecular Basis of Inherited Diseases in Companion Animals

Molecular Basis of Inherited Diseases in Companion Animals

0 Ungluers have Faved this Work
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.

This book is included in DOAB.

Why read this book? Have your say.

You must be logged in to comment.

Rights Information

Are you the author or publisher of this work? If so, you can claim it as yours by registering as an Unglue.it rights holder.

Downloads

This work has been downloaded 374 times via unglue.it ebook links.
  1. 51 - pdf (CC BY) at Unglue.it.
  2. 319 - pdf (CC BY) at res.mdpi.com.

Keywords

  • 4-hydroxybutyric acid
  • acantholysis
  • ALDH5A1
  • animal model
  • Bardet–Biedl syndrome (BBS)
  • BBS8
  • Biology, Life Sciences
  • BMP12
  • brain malformation
  • Burmese cats
  • Caffey disease
  • Calcium
  • calvarial hyperostotic syndrome
  • canine
  • Canis familiaris
  • Canis lupus familiaris
  • Cats
  • CHILD syndrome
  • ciliopathy
  • CLE
  • COL1A1
  • Companion Animals
  • Comparative genomics
  • contactin
  • craniomandibular osteopathy
  • Dermatology
  • desmosome
  • Diabetes Mellitus
  • dog
  • Dogs
  • Duchenne
  • dystrophinopathy
  • encephalopathy
  • epidermal nevus
  • feline
  • Felis catus
  • GABA
  • Genetic Markers
  • Genetics
  • genodermatosis
  • Genome-Wide Association Study
  • Genomics
  • GWAS
  • Horses
  • ILVEN
  • immunohistochemistry
  • immunology
  • inborn error of metabolism
  • infantile cortical hyperostosis
  • inherited
  • keratinocyte
  • Labrador retriever
  • laminin
  • Leonberger
  • LIPH
  • Mathematics & science
  • mendelian traits
  • metabolic disease
  • mitochondrion
  • n/a
  • neurodevelopment
  • neurological disorder
  • neurometabolic disorder
  • Obesity
  • phosphoenolpyruvate-carboxykinase
  • precision medicine
  • primary cilia
  • progressive retinal atrophy (PRA)
  • rare disease
  • Reference, information & interdisciplinary subjects
  • Research & information: general
  • retinitis pigmentosa
  • Saint Bernard
  • SAM syndrome
  • single-nucleotide polymorphism
  • Skin
  • SLC35D1
  • SLC37A2
  • SLE
  • SSADHD
  • succinic semialdehyde
  • susceptibility
  • syndecan binding protein
  • syntenin-1
  • systemic lupus erythematosus
  • TLR7
  • toll-like receptor
  • Veterinary medicine
  • wgs
  • whole genome sequence
  • whole genome sequencing
  • whole-genome sequence
  • whole-genome sequencing

Links

DOI: 10.3390/books978-3-0365-0473-5

Editions

edition cover

Share

Copy/paste this into your site: