Choose an application

• Reference Manager
• EndNote
• RefWorks (Direct export to RefWorks)

This eBook presents illustrative examples of genetic chaperonopathies affecting primarily nerves and muscles and discusses molecular mechanisms and treatment targeting chaperones, i.e., chaperonotherapy.

small-Hsp --- Hsp60/CCT/BBS --- Indirect/Secondary Chaperonopathies --- Genetic Chaperonopathies --- Hsp40/DnaJ --- chaperonotherapy

Choose an application

• Reference Manager
• EndNote
• RefWorks (Direct export to RefWorks)

This eBook presents illustrative examples of genetic chaperonopathies affecting primarily nerves and muscles and discusses molecular mechanisms and treatment targeting chaperones, i.e., chaperonotherapy.

small-Hsp --- Hsp60/CCT/BBS --- Indirect/Secondary Chaperonopathies --- Genetic Chaperonopathies --- Hsp40/DnaJ --- chaperonotherapy

Choose an application

• Reference Manager
• EndNote
• RefWorks (Direct export to RefWorks)

Ingénieur-architecte diplômé de l’université de Louvain, formé au paysagisme à l’université de Genève, Bas Smets dirige une agence spécialisée dans la conception de stratégies paysagères et l’aménagement d’espaces publics. Fondé à Bruxelles en 2007, le Bureau Bas Smets emploie aujourd’hui quinze architectes et paysagistes, et réalise des projets à toutes les échelles, du développement territorial aux infrastructures, et de l’aménagement de centres urbains aux jardins.Bas Smets enseigne le paysagisme à l’école d’architecture de La Cambre à Bruxelles, et à l’École spéciale d’architecture à Paris, et il fut lauréat en 2008 des ‘Nouveaux Albums des Jeunes Architectes et Paysagistes’. Ses projets ont fait l’objet d’une première exposition personnelle en 2013-2014, qui fut montrée au International Arts Campus de Singel à Anvers, au Palais des beaux-arts de Charleroi, et au centre d’architecture Arc-en-rêve à Bordeaux. En tant que paysagiste, Bas Smets utilise la photo à la fois comme outil du projet, et dans ses expositions. Les deux entretiens menés avec lui nous ont permis d’en savoir plus sur sa pratique de la photographie, qui met en œuvre des moyens simples (iPhone) mais développe une dimension plus complexe sous la forme de montages qu’il appelle des « atlas ». À l’opposé de la photographie d’architecture professionnelle, Bas Smets expérimente des dispositifs qui rendent compte de la dimension du temps et des limites floues du projet de paysage. "This book revolves around five landscape projects. Each one is presented as a story about transforming a land - given terrain - into a 'landscape' and altering its perception".

712 --- Smets, Bas --- Bureau Bas Smets --- 712.07 --- 712.039 --- Landschapsarchitectuur ; 5 projecten ; 2007-2017 ; Bas Smets --- Bureau Bas Smets ; BBS --- Belgische landschapschapsarchitecten --- Luchtfotografie ; als tool voor de landschapsontwerper --- Landschapsarchitectuur --- Landschaps- en tuinarchitectuur ; tuin- en landschapsarchitecten (A - Z) --- Landschaps- en tuinarchitectuur ; 2000 - 2050 --- Paysage --- Paysage rural --- Paysage urbain --- Projet de paysage --- Landscape architects --- Architectes paysagistes --- Typologie urbaine --- Analyse du paysage

Choose an application

• Reference Manager
• EndNote
• RefWorks (Direct export to RefWorks)

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.

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 --- Bardet-Biedl syndrome (BBS)

Choose an application

• Reference Manager
• EndNote
• RefWorks (Direct export to RefWorks)

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.

Research & information: general --- Biology, life sciences --- 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