Progress towards a cellular neurobiology of reading disability. - Wikidata - awgldk - TriplyDB

Progress towards a cellular neurobiology of reading disability.

Progress towards a cellular neurobiology of reading disability.

http://www.wikidata.org/entity/Q30475697

about

Genetic advances in the study of speech and language disorders Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice Developmental Learning Disorders: From Generic Interventions to Individualized Remediation Transcriptional program of ciliated epithelial cells reveals new cilium and centrosome components and links to human disease Defects in ultrasonic vocalization of cadherin-6 knockout mice.Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.A theoretical molecular network for dyslexia: integrating available genetic findings.The dyslexia candidate gene DYX1C1 is a potential marker of poor survival in breast cancer.A dyslexia-associated variant in DCDC2 changes gene expression.Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes.Layer I neocortical ectopia: cellular organization and local cortical circuitry.Genetic influences of resting state fMRI activity in language-related brain regions in healthy controls and schizophrenia patients: a pilot study.Pleiotropic functions of EAPII/TTRAP/TDP2: cancer development, chemoresistance and beyond KIAA0319 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.Translating dyslexia across species.Approach to epigenetic analysis in language disorders The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.The Roles of Genes in the Neuronal Migration and Neurite Outgrowth Network in Developmental Dyslexia: Single- and Multiple-Risk Genetic Variants.Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis.Knockout Mice for Dyslexia Susceptibility Gene Homologs KIAA0319 and KIAA0319L have Unaffected Neuronal Migration but Display Abnormal Auditory Processing.The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems.Understanding Heritability: What it is and What it is Not

P2860

Q24609855-FE7A153B-2CA8-4DF9-89E5-39411D12910D Q24630169-05FF5C37-AF59-4608-9361-FA5367CC8565 Q26770407-9360B592-A804-4CA3-A203-EDABABC34765 Q28118826-837710AE-A13E-474E-8110-4E14F4B6E790 Q28711712-7B720851-4681-414D-8ADE-FB6CDDBB57B2 Q30358905-B4E1E29E-E066-4647-BA50-33B49DE11F92 Q34144455-3F0AD456-B18E-49D3-9BB5-1A189F1799CC Q34178564-ABEC9FD1-85A7-4139-A23B-1866AA904785 Q34648864-68AE1ADD-7D16-45F5-B699-A78267D4187F Q34750026-77BBDF27-AE87-4877-8DCD-42CC7397E184 Q34865771-77CCBF6E-6C50-4FB9-B098-655D9AC0F2CF Q35596967-6E515193-D88A-4CFC-A64D-99A1AAAF1E23 Q35600743-A444FB03-2F3F-4F62-BBC8-1E5E9DFDC0DC Q37208967-D80BD8DE-C87E-450E-8901-F5C135028967 Q38890401-503AF55C-DF95-451C-88E8-95A36B892996 Q40505104-011575CD-BBE1-4B6F-90F5-73A63A295093 Q41130845-2173F00B-A272-4609-ADAD-107CEC255447 Q41577410-4EA602A8-2D67-46A1-8BCB-2ED61C690792 Q45942481-6B65D98C-90DD-4C6F-87AD-4E3E5C8AEAD5 Q47633155-01768714-C726-40E4-A507-EC30ECD704B6 Q47848734-3C65665C-5ABC-48B0-8CF9-0F1093847A85 Q55894384-4585848B-02AB-453A-B618-3658210CBAD5

P2860

Progress towards a cellular neurobiology of reading disability.

http://www.wikidata.org/entity/Q30475697

description

2009 nî lūn-bûn

@nan

2009 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Progress towards a cellular neurobiology of reading disability.

@ast

Progress towards a cellular neurobiology of reading disability.

@en

type

label

Progress towards a cellular neurobiology of reading disability.

@ast

Progress towards a cellular neurobiology of reading disability.

@en

prefLabel

Progress towards a cellular neurobiology of reading disability.

@ast

Progress towards a cellular neurobiology of reading disability.

@en

P1433

Q30475697-37D15872-0263-4981-A309-7558FA577C29

P1476

Q30475697-8B74779D-9957-4614-B65F-44435D6E7B20

P2093

Q30475697-1128B776-B968-4CAD-B5D1-9AE438BA08B8

Q30475697-66CA17B2-846A-41E4-B48A-340964F64F64

Q30475697-6D5539FA-DBD6-46DB-8B04-ACFF8ADE18C2

Q30475697-77ACFA9A-2944-4E51-B341-DA58289EBEA5

P2860

Q30475697-01D4E67F-0576-4BA2-8F43-4BE2459EC8B5

Q30475697-0473394F-2EE5-4703-9F7E-42ADD2BC0C20

Q30475697-078D7CD5-E8D7-4AA6-B6C6-954F6F8F2FB0

Q30475697-09B12615-6B6B-4779-8B51-CC48BE61C437

Q30475697-0A89D5BB-7957-4ABA-BF30-C048D48CAE7E

Q30475697-0C564923-B735-4B65-8F5E-AEEA828A1001

Q30475697-0E319838-7EEE-43A3-9E72-B6C92D61F79C

Q30475697-100C69DF-2B5C-43D0-99AD-D35A7DD14521

Q30475697-1054B112-655F-49E9-96C8-F03D2CF0A718

Q30475697-1FCEE97E-0424-446A-8D3E-7978A760C645

P304

Q30475697-E1A393F0-85D8-4DDC-96A9-D4BE23989599

P31

Q30475697-9D02BD77-066A-48DF-A7D4-630D66221CFF

P356

Q30475697-CB2FB22F-9E14-4DF8-92CB-0B978E489CB1

P433

Q30475697-75CB6D46-7DA2-41A8-8821-3ECCB17E4E58

P478

Q30475697-AB231B49-1955-4CD4-B67E-21E0C50C658D

P577

Q30475697-5E3D2D1D-2C7E-4286-8763-136B62A44A75

P5875

Q30475697-543ECEB7-C361-4FFA-94CA-095813838867

P698

Q30475697-D0692C67-A4A3-444A-894B-A4801B62B682

P921

Q30475697-33FEDAE5-53B1-42A6-A1EA-5586E15465DB

P932

Q30475697-7A72A885-C2C6-4739-ACD1-9ECECBEDF1B0

P356

J.NBD.2009.06.019

P1433

Neurobiology of Disease

P1476

Progress towards a cellular neurobiology of reading disability.

@en

P2093

Christopher J Gibson

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

Jeffrey R Gruen

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

Joseph J LoTurco

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

Lisa A Gabel

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

P2860

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia

DCDC2 is associated with reading disability and modulates neuronal development in the brain.

DYX1C1 functions in neuronal migration in developing neocortex

The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway

Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

Evidence for linkage of spelling disability to chromosome 15

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Strong association of de novo copy number mutations with autism

P304

173-180

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

P31

scholarly article

P356

10.1016/J.NBD.2009.06.019

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

P433

2

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

P478

38

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

P577

2009-07-17T00:00:00Z

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

P5875

26680477

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

P698

19616627

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

P921

P932

2854314

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