The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia - Wikidata - thesis-toulmin - TriplyDB

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

http://www.wikidata.org/entity/Q30482949

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The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P Zika virus disrupts molecular fingerprinting of human neurospheres GTF2IRD2 from the Williams-Beuren critical region encodes a mobile-element-derived fusion protein that antagonizes the action of its related family members Globularity and language-readiness: generating new predictions by expanding the set of genes of interest The adapter protein Nck: role of individual SH3 and SH2 binding modules for protein interactions in T lymphocytes The genetics of reading disabilities: from phenotypes to candidate genes Progress towards a cellular neurobiology of reading disability.Essential role of the N-terminal region of TFII-I in viability and behavior.The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation.The RNA-binding protein SFPQ orchestrates an RNA regulon to promote axon viability 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.Tau-mediated nuclear depletion and cytoplasmic accumulation of SFPQ in Alzheimer's and Pick's disease.The effects of embryonic knockdown of the candidate dyslexia susceptibility gene homologue Dyx1c1 on the distribution of GABAergic neurons in the cerebral cortex.The DBHS proteins SFPQ, NONO and PSPC1: a multipurpose molecular scaffold Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children.Biochemistry and biology of the inducible multifunctional transcription factor TFII-I: 10 years later Cytoplasmic mislocalization of RNA splicing factors and aberrant neuronal gene splicing in TDP-43 transgenic pig brain.Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs.Genes, Gender, Environment, and Novel Functions of Estrogen Receptor Beta in the Susceptibility to Neurodevelopmental Disorders.A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.Molecular genetics of dyslexia: an overview.Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.Role of Splice Variants of Gtf2i, a Transcription Factor Localizing at Postsynaptic Sites, and Its Relation to Neuropsychiatric Diseases.Approach to epigenetic analysis in language disorders Novel splice variants in the 5'UTR of Gtf2i expressed in the rat brain: alternative 5'UTRs and differential expression in the neuronal dendrites.Non-nuclear Pool of Splicing Factor SFPQ Regulates Axonal Transcripts Required for Normal Motor Development.Long intervening non-coding RNA 00320 is human brain-specific and highly expressed in the cortical white matter.Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis.Ancestral Variations of the PCDHG Gene Cluster Predispose to Dyslexia in a Multiplex Family.Molecular genetics and molecular biology of dyslexia.Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1.Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome.

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P2860

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

http://www.wikidata.org/entity/Q30482949

description

2008 nî lūn-bûn

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2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2008 թվականի ապրիլին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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The complex of TFII-I, PARP1, ...... euronal migration and dyslexia

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The complex of TFII-I, PARP1, ...... euronal migration and dyslexia

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The complex of TFII-I, PARP1, ...... euronal migration and dyslexia

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The complex of TFII-I, PARP1, ...... euronal migration and dyslexia

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The complex of TFII-I, PARP1, ...... euronal migration and dyslexia

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The complex of TFII-I, PARP1, ...... euronal migration and dyslexia

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Ananda L Roy

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Isabel Tapia-Páez

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Satu Massinen

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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

TFII-I enhances activation of the c-fos promoter through interactions with upstream elements

TFII-I regulates Vbeta promoter activity through an initiator element

Evidence for linkage of spelling disability to chromosome 15

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

Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

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