Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene.
about
Dystonia and Paroxysmal Dyskinesias: Under-Recognized Movement Disorders in Domestic Animals? A Comparison with Human Dystonia/Paroxysmal Dyskinesias.DNA testing in neurologic diseasesA MusD retrotransposon insertion in the mouse Slc6a5 gene causes alterations in neuromuscular junction maturation and behavioral phenotypesMutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease.A novel syndrome of lethal familial hyperekplexia associated with brain malformation.Classification of Involuntary Movements in Dogs: Myoclonus and MyotoniaGlycine transporters as novel therapeutic targets in schizophrenia, alcohol dependence and pain.Constitutive endocytosis and turnover of the neuronal glycine transporter GlyT2 is dependent on ubiquitination of a C-terminal lysine clusterMicroarray gene expression profiling of neural tissues in bovine spastic paresisInternational Veterinary Epilepsy Task Force's current understanding of idiopathic epilepsy of genetic or suspected genetic origin in purebred dogsGenome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins.A canine BCAN microdeletion associated with episodic falling syndromeDistinct phenotypes in zebrafish models of human startle disease.How selective sweeps in domestic animals provide new insight into biological mechanisms.Molecular mechanisms of glycine transporter GlyT2 mutations in startle disease.Copy number variation in the genomes of domestic animals.Identification of congenital muscular dystonia 2 associated with an inherited GlyT2 defect in Belgian Blue cattle from the United Kingdom.Detection of Regional Variation in Selection Intensity within Protein-Coding Genes Using DNA Sequence Polymorphism and Divergence.A novel movement disorder in related male Labrador Retrievers characterized by extreme generalized muscular stiffness.
P2860
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P2860
Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene.
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Startle disease in Irish wolfh ...... lycine transporter GlyT2 gene.
@ast
Startle disease in Irish wolfh ...... lycine transporter GlyT2 gene.
@en
type
label
Startle disease in Irish wolfh ...... lycine transporter GlyT2 gene.
@ast
Startle disease in Irish wolfh ...... lycine transporter GlyT2 gene.
@en
prefLabel
Startle disease in Irish wolfh ...... lycine transporter GlyT2 gene.
@ast
Startle disease in Irish wolfh ...... lycine transporter GlyT2 gene.
@en
P2093
P2860
P50
P1476
Startle disease in Irish wolfh ...... lycine transporter GlyT2 gene.
@en
P2093
Deborah Capper
G Diane Shelton
Jean-François Vanbellinghen
Jennifer L Gill
Robert J Higgins
P2860
P304
P356
10.1016/J.NBD.2011.03.010
P577
2011-03-17T00:00:00Z