Slitrks as emerging candidate genes involved in neuropsychiatric disorders - Wikidata - awgldk - TriplyDB

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

http://www.wikidata.org/entity/Q34634305

about

SLITRK6 mutations cause myopia and deafness in humans and mice Pediatric Autoimmune Disorders Associated with Streptococcal Infections and Tourette's Syndrome in Preclinical Studies.From Genetics to Epigenetics: New Perspectives in Tourette Syndrome Research Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.Structural basis for LAR-RPTP/Slitrk complex-mediated synaptic adhesion Structure of Slitrk2-PTPδ complex reveals mechanisms for splicing-dependent trans-synaptic adhesion Using mice to model Obsessive Compulsive Disorder: From genes to circuits.Porcine SLITRK1: Molecular cloning and characterization Neurobiology of obsessive-compulsive disorder: insights into neural circuitry dysfunction through mouse genetics Rare Synaptogenesis-Impairing Mutations in SLITRK5 Are Associated with Obsessive Compulsive Disorder.Learning From Animal Models of Obsessive-Compulsive Disorder Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism.Slitrk5 Mediates BDNF-Dependent TrkB Receptor Trafficking and Signaling.Slitrks control excitatory and inhibitory synapse formation with LAR receptor protein tyrosine phosphatases.Lmx1a and Lmx1b regulate mitochondrial functions and survival of adult midbrain dopaminergic neurons Protein tyrosine phosphatases PTPδ, PTPσ, and LAR: presynaptic hubs for synapse organization Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology Slitrk Missense Mutations Associated with Neuropsychiatric Disorders Distinctively Impair Slitrk Trafficking and Synapse Formation The leucine-rich repeat superfamily of synaptic adhesion molecules: LRRTMs and Slitrks.Putting the Pieces Together in Gilles de la Tourette Syndrome: Exploring the Link Between Clinical Observations and the Biological Basis of Dysfunction.Role of microRNAs in central nervous system development and pathology.New insights into the control of neurotrophic growth factor receptor signaling: implications for nervous system development and repair.Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early development.Rodent models of obsessive compulsive disorder: Evaluating validity to interpret emerging neurobiology.Slitrk gene duplication and expression in the developing zebrafish nervous system.Lrig1 is a cell-intrinsic modulator of hippocampal dendrite complexity and BDNF signaling.Genome-Wide Association Study of Male Sexual Orientation.Progress in Genetic Studies of Tourette's Syndrome.Disruption of Ninjurin1 Leads to Repetitive and Anxiety-Like Behaviors in Mice.Leucine-rich repeat-containing synaptic adhesion molecules as organizers of synaptic specificity and diversity.Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.Genome-wide association study results for educational attainment aid in identifying genetic heterogeneity of schizophrenia

P2860

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P2860

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

http://www.wikidata.org/entity/Q34634305

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

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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

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

@ast

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

@en

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

@nl

type

label

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

@ast

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

@en

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

@nl

prefLabel

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

@ast

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

@en

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

@nl

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P356

J.TINS.2011.01.001

P1433

Trends in Neurosciences

P1476

Slitrks as emerging candidate genes involved in neuropsychiatric disorders

@en

P2093

Catia C Proenca

http://www.w3.org/2001/XMLSchema#string

Francis S Lee

http://www.w3.org/2001/XMLSchema#string

Kate P Gao

http://www.w3.org/2001/XMLSchema#string

Sergey V Shmelkov

http://www.w3.org/2001/XMLSchema#string

Shahin Rafii

http://www.w3.org/2001/XMLSchema#string

P2860

The netrin protein family

Slit proteins bind Robo receptors and have an evolutionarily conserved role in repulsive axon guidance

AMIGO, a transmembrane protein implicated in axon tract development, defines a novel protein family with leucine-rich repeats

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

The netrin-G1 ligand NGL-1 promotes the outgrowth of thalamocortical axons

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

LRIG1 restricts growth factor signaling by enhancing receptor ubiquitylation and degradation

Hematopoietic origin of pathological grooming in Hoxb8 mutant mice

Cortico-striatal synaptic defects and OCD-like behaviours in Sapap3-mutant mice.

P304

143-153

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scholarly article

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10.1016/J.TINS.2011.01.001

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3

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34

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2011-03-01T00:00:00Z

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49830610

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21315458

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3051006

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