Related references
Note: Only part of the references are listed.Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia
Alistair T. Pagnamenta et al.
BIOLOGICAL PSYCHIATRY (2010)
The Effect of Variation in Expression of the Candidate Dyslexia Susceptibility Gene Homolog Kiaa0319 on Neuronal Migration and Dendritic Morphology in the Rat
Veronica J. Peschansky et al.
CEREBRAL CORTEX (2010)
Genetics of developmental dyslexia
Thomas S. Scerri et al.
EUROPEAN CHILD & ADOLESCENT PSYCHIATRY (2010)
Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample
Penelope A. Lind et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
DIP2A Functions as a FSTL1 Receptor
Noriyuki Ouchi et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Partial 7q11.23 deletions further implicate GTF2I and GTF2IRD1 as the main genes responsible for the Williams-Beuren syndrome neurocognitive profile
A. Antonell et al.
JOURNAL OF MEDICAL GENETICS (2010)
S100B/RAGE-dependent activation of microglia via NF-κB and AP-1 Co-regulation of COX-2 expression by S100B, IL-1β and TNF-α
Roberta Bianchi et al.
NEUROBIOLOGY OF AGING (2010)
Progress towards a cellular neurobiology of reading disability
Lisa A. Gabel et al.
NEUROBIOLOGY OF DISEASE (2010)
The Universal Protein Resource (UniProt) in 2010
Rolf Apweiler et al.
NUCLEIC ACIDS RESEARCH (2010)
Tiam1 as a Signaling Mediator of Nerve Growth Factor-Dependent Neurite Outgrowth
Shahrzad Shirazi Fard et al.
PLOS ONE (2010)
Fragile X mental retardation 1 and Filamin A interact genetically in Drosophila long-term memory
Francois V. Bolduc et al.
FRONTIERS IN NEURAL CIRCUITS (2010)
Identification of Novel Dyslexia Candidate Genes Through the Analysis of a Chromosomal Deletion
G. Poelmans et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2009)
Lifespan changes in working memory in fragile X premutation males
Kim M. Cornish et al.
BRAIN AND COGNITION (2009)
Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
Nathalie Van der Aa et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2009)
Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia
Satu Massinen et al.
HUMAN MOLECULAR GENETICS (2009)
Promotion of Neurite Extension by Protrudin Requires Its Interaction with Vesicle-associated Membrane Protein-associated Protein
Shotaro Saita et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Molecular characterization of the DYX1C1 gene and its application as a cancer biomarker
Yun-Ji Kim et al.
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY (2009)
A novel role for DYX1C1, a chaperone protein for both Hsp70 and Hsp90, in breast cancer
Yuxin Chen et al.
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY (2009)
Fragile X mental retardation protein is required for chemically-induced long-term potentiation of the hippocampus in adult mice
Yuze Shang et al.
JOURNAL OF NEUROCHEMISTRY (2009)
Regulation of Glucose Transporter 3 Surface Expression by the AMP-Activated Protein Kinase Mediates Tolerance to Glutamate Excitation in Neurons
Petronela Weisova et al.
JOURNAL OF NEUROSCIENCE (2009)
Dyslexia: The evolution of a scientific concept
Jack M. Fletcher
JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY (2009)
HDAC2 negatively regulates memory formation and synaptic plasticity
Ji-Song Guan et al.
NATURE (2009)
Further evidence for DYX1C1 as a susceptibility factor for dyslexia
Faten Dahdouh et al.
PSYCHIATRIC GENETICS (2009)
The Genetics of Reading Disability
Tracey L. Petryshen et al.
CURRENT PSYCHIATRY REPORTS (2009)
A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene
Megan Y. Dennis et al.
PLOS GENETICS (2009)
Functional Skills of Individuals With Fragile X Syndrome: A Lifespan Cross-Sectional Analysis
Donald B. Bailey et al.
AJIDD-AMERICAN JOURNAL ON INTELLECTUAL AND DEVELOPMENTAL DISABILITIES (2009)
A Virtual Reality Test Identifies the Visuospatial Strengths of Adolescents with Dyslexia
Elizabeth A. Attree et al.
CYBERPSYCHOLOGY & BEHAVIOR (2009)
Association of Reading Disability on Chromosome 6p22 in the Afrikaner Population
Jill V. Platko et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2008)
Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a dutch sib-pair collection
Carolien G. F. de Kovel et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2008)
Association of the KIAA0319 Dyslexia Susceptibility Gene With Reading Skills in the General Population
Silvia Paracchini et al.
AMERICAN JOURNAL OF PSYCHIATRY (2008)
Coordination of actin filament and microtubule dynamics during neurite outgrowth
Andrew W. Schaefer et al.
DEVELOPMENTAL CELL (2008)
Neurobiological and Experiential Origins of Dyslexia: An Introduction
Maureen Hoskyn
DEVELOPMENTAL NEUROPSYCHOLOGY (2008)
Chronic estradiol treatment improves brain homeostasis during aging in female rats
Ana Alonso et al.
ENDOCRINOLOGY (2008)
The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia
Isabel Tapia-Paez et al.
FASEB JOURNAL (2008)
NF-κB regulates netrin-1 expression and affects the conditional tumor suppressive activity of the netrin-1 receptors
Andrea Paradisi et al.
GASTROENTEROLOGY (2008)
A novel HSP90 chaperone complex regulates intracellular vesicle transport
Gregor P. Lotz et al.
JOURNAL OF CELL SCIENCE (2008)
Like father, like son: Periventricular nodular heterotopia and nonverbal learning disorder
Marcia V. McCann et al.
JOURNAL OF CHILD NEUROLOGY (2008)
Association between polymorphisms in the vesicle-associated membrane protein-associated protein A (VAPA) gene on chromosome 18p and bipolar disorder
Falk W. Lohoff et al.
JOURNAL OF NEURAL TRANSMISSION (2008)
Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample
Kerstin U. Ludwig et al.
JOURNAL OF NEURAL TRANSMISSION (2008)
The KIAA0319-Like (KIAA0319L) Gene on Chromosome 1p34 as a Candidate for Reading Disabilities
Jillian M. Couto et al.
JOURNAL OF NEUROGENETICS (2008)
Molecular mechanisms controlling midline crossing by precerebellar neurons
Thomas Di Meglio et al.
JOURNAL OF NEUROSCIENCE (2008)
Receptor for advanced glycation end products (RAGE) mediates neuronal differentiation and neurite outgrowth
Lingyan Wang et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2008)
Dock4 Regulates Dendritic Development in Hippocampal Neurons
Shuhei Ueda et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2008)
P53 regulates glucose metabolism through an IKK-NF-κB pathway and inhibits cell transformation
Keiko Kawauchi et al.
NATURE CELL BIOLOGY (2008)
Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat
T. J. Burbridge et al.
NEUROSCIENCE (2008)
Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21
Johannes Schumacher et al.
PSYCHIATRIC GENETICS (2008)
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample
Kerstin U. Ludwig et al.
PSYCHIATRIC GENETICS (2008)
The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms
Antonio Velayos-Baeza et al.
HUMAN MOLECULAR GENETICS (2008)
HMGB1 as an autocrine stimulus in human T98G glioblastoma cells: role in cell growth and migration
Rosaria Bassi et al.
JOURNAL OF NEURO-ONCOLOGY (2008)
The activity of hsp90α promoter is regulated by NF-κB transcription factors
M. Ammirante et al.
ONCOGENE (2008)
Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children
E. L. Meaburn et al.
MOLECULAR PSYCHIATRY (2008)
Polymorphism of DCDC2 Reveals Differences in Cortical Morphology of Healthy Individuals-A Preliminary Voxel Based Morphometry Study
Shashwath A. Meda et al.
BRAIN IMAGING AND BEHAVIOR (2008)
Paying attention to reading: The neurobiology of reading and dyslexia
Sally E. Shaywitz et al.
DEVELOPMENT AND PSYCHOPATHOLOGY (2008)
Disruption of neuronal migration by RNAi of dyx1c1 results in neocortical and hippocampal malformations
Glenn D. Rosen et al.
CEREBRAL CORTEX (2007)
Association of short-term memory with a variant within DYX1C1 in developmental dyslexia
C. Marino et al.
GENES BRAIN AND BEHAVIOR (2007)
A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability
Michelle Luciano et al.
BIOLOGICAL PSYCHIATRY (2007)
Alternative splicing in the dyslexia-associated gene KIAA0319
Antonio Velayos-Baeza et al.
MAMMALIAN GENOME (2007)
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia
Zoran Brkanac et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2007)
Genetics of dyslexia:: the evolving landscape
Johannes Schumacher et al.
JOURNAL OF MEDICAL GENETICS (2007)
The novel cargo Alcadein induces vesicle association of kinesin-1 motor components and activates axonal transport
Yoichi Araki et al.
EMBO JOURNAL (2007)
Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1
Steven W. Threlkeld et al.
BRAIN RESEARCH BULLETIN (2007)
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia
Heidi Anthoni et al.
HUMAN MOLECULAR GENETICS (2007)
Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17
Timothy C. Bates et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2007)
17 beta-estradiol induces IL-1 alpha gene expression in rheumatoid fibroblast-like synovial cells through estrogen receptor alpha (ER alpha) and augmentation of transcriptional activity of Sp1 by dissociating histone deacetylase 2 from ER alpha
Yuka Itoh et al.
JOURNAL OF IMMUNOLOGY (2007)
Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham study
Sudha Seshadri et al.
BMC MEDICAL GENETICS (2007)
Dock4 is regulated by RhoG and promotes Rac-dependent cell migration
Kiyo Hiramoto et al.
EXPERIMENTAL CELL RESEARCH (2006)
DYX1C1 functions in neuronal migration in developing neocortex
Y. Wang et al.
NEUROSCIENCE (2006)
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia
D. Harold et al.
MOLECULAR PSYCHIATRY (2006)
Common KIBRA alleles are associated with human memory performance
Andreas Papassotiropoulos et al.
SCIENCE (2006)
From genes to behavior in developmental dyslexia
Albert M. Galaburda et al.
NATURE NEUROSCIENCE (2006)
CCL2 regulates angiogenesis via activation of Ets-1 transcription factor
Svetlana M. Stamatovic et al.
JOURNAL OF IMMUNOLOGY (2006)
The evolving doublecortin (DCX) superfamily
Orly Reiner et al.
BMC GENOMICS (2006)
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
S Paracchini et al.
HUMAN MOLECULAR GENETICS (2006)
被撤回的出版物: Identification of T-cadherin as a novel target of DNA methyltransferase 3B and its role in the suppression of nerve growth factor-mediated neurite outgrowth in PC12 cells (Retracted article. See vol. 293, pg. 3592, 2018)
SM Bai et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour
A Meyer-Lindenberg et al.
NATURE REVIEWS NEUROSCIENCE (2006)
Common and divergent roles for members of the mouse DCX superfamily
Frederic M. Coquelle et al.
CELL CYCLE (2006)
Genomewide scan for real-word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity
RP Igo et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2006)
mRNPs, polysomes or granules: FMRP in neuronal protein synthesis
Francesca Zalfa et al.
CURRENT OPINION IN NEUROBIOLOGY (2006)
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
J Schumacher et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
DCDC2 is associated with reading disability and modulates neuronal development in the brain
HY Meng et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort
HY Meng et al.
HUMAN GENETICS (2005)
The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia
K Hannula-Jouppi et al.
PLOS GENETICS (2005)
A genome scan in multigenerational families with dyslexia: identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency
WH Raskind et al.
MOLECULAR PSYCHIATRY (2005)
A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia
C Marino et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2005)
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia
N Cope et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Deleted in colorectal cancer binding netrin-1 mediates cell substrate adhesion and recruits Cdc42, Rac1, Pak1, and N-WASP into an intracellular signaling complex that promotes growth cone expansion
M Shekarabi et al.
JOURNAL OF NEUROSCIENCE (2005)
No support for association between Dyslexia Susceptibility 1 Candidate 1 and developmental dyslexia
NA Cope et al.
MOLECULAR PSYCHIATRY (2005)
No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy
G Bellini et al.
JOURNAL OF MOLECULAR NEUROSCIENCE (2005)
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene
M Peyrard-Janvid et al.
HUMAN GENETICS (2004)
A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5
GYR Hsiung et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2004)
NF-KB and AP-1 connection:: Mechanism of NF-κB-Dependent regulation of AP-1 activity
S Fujioka et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family
CGF de Kovel et al.
JOURNAL OF MEDICAL GENETICS (2004)
Developmental expression of receptor for advanced glycation end products (RAGE), amphoterin and sulfoglucuronyl (HNK-1) carbohydrate in mouse cerebellum and their role in neurite outgrowth and cell migration
DKH Chou et al.
JOURNAL OF NEUROCHEMISTRY (2004)
Support for EKN1 as the susceptibility locus for dyslexia on 15q21
KG Wigg et al.
MOLECULAR PSYCHIATRY (2004)
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States
C Francks et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses
KE Deffenbacher et al.
HUMAN GENETICS (2004)
FMRP and its target RNAs: fishing for the specificity
M Veneri et al.
NEUROREPORT (2004)
Linkage analyses of four regions previously implicated in dyslexia: Confirmation of a locus on chromosome 15q
NH Chapman et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2004)
GOstat: find statistically overrepresented Gene Ontologies within a group of genes
T Beissbarth et al.
BIOINFORMATICS (2004)
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK
TS Scerri et al.
JOURNAL OF MEDICAL GENETICS (2004)
High mobility group B proteins facilitate strong estrogen receptor binding to classical and half-site estrogen response elements and relax binding selectivity
D Das et al.
MOLECULAR ENDOCRINOLOGY (2004)
Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100 Canadian families
J Tzenova et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2004)
Human SLITRK family genes: genomic organization and expression profiling in normal brain and brain tumor tissue
J Aruga et al.
GENE (2003)
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
M Taipale et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
A transcription map of the 6p22.3 reading disability locus identifying candidate genes
ER Londin et al.
BMC GENOMICS (2003)
Word reading and reading-related skills in adolescents with Williams syndrome
Y Levy et al.
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY (2003)
A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32
N Kaminen et al.
JOURNAL OF MEDICAL GENETICS (2003)
S100B in brain damage and neurodegeneration
M Rothermundt et al.
MICROSCOPY RESEARCH AND TECHNIQUE (2003)
Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans
SP Robertson et al.
NATURE GENETICS (2003)
Control of dendritic development by the Drosophila fragile X-related gene involves the small GTPase Rac1
A Lee et al.
DEVELOPMENT (2003)
Presynaptic proteins in the prefrontal cortex of patients with schizophrenia and rats with abnormal prefrontal development
ND Halim et al.
MOLECULAR PSYCHIATRY (2003)
The calsyntenins - A family of postsynaptic membrane proteins with distinct neuronal expression patterns
G Hintsch et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2002)
Targeted mutation of Cyln2 in the Williams syndrome critical region links CLIP-115 haploinsufficiency to neurodevelopmental abnormalities in mice
CC Hoogenraad et al.
NATURE GENETICS (2002)
Evidence for linkage and association with reading disability, on 6p21.3-22
DE Kaplan et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
GAPs in slit-robo signaling
A Ghose et al.
BIOESSAYS (2002)
Glial protein S100B modulates long-term neuronal synaptic plasticity
H Nishiyama et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
A novel NF-κB-inducing kinase-MAPK signaling pathway up-regulates NF-κB activity in melanoma cells
P Dhawan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families
TL Petryshen et al.
JOURNAL OF MEDICAL GENETICS (2002)
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
SE Fisher et al.
NATURE GENETICS (2002)
Evidence that GRIP, a PDZ-domain protein which is expressed in the embryonic forebrain, co-activates transcription with DLX homeodomain proteins
GY Yu et al.
DEVELOPMENTAL BRAIN RESEARCH (2001)
Signal transduction in neuronal migration: Roles of GTPase activating proteins and the small GTPase Cdc42 in the Slit-Robo pathway
K Wong et al.
CELL (2001)
A dominant gene for developmental dyslexia on chromosome 3
J Nopola-Hemmi et al.
JOURNAL OF MEDICAL GENETICS (2001)
Learning to read in Williams syndrome: Looking beneath the surface of atypical reading development
E Laing et al.
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY (2001)
Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia
TL Petryshen et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2001)
JAK2 activates TFII-I and regulates its interaction with extracellular signal-regulated kinase
DW Kim et al.
MOLECULAR AND CELLULAR BIOLOGY (2001)
Hierarchical organization of guidance receptors: Silencing of netrin attraction by slit through a Robo/DCC receptor complex
E Stein et al.
SCIENCE (2001)
Coregulation of neurite outgrowth and cell survival by amphoterin and S100 proteins through receptor for advanced glycation end products (RAGE) activation
HJ Huttunen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Two translocations of chromosome 15q associated with dyslexia
J Nopola-Hemmi et al.
JOURNAL OF MEDICAL GENETICS (2000)
DNMT1 binds HDAC2 and a new co-repressor, DMAP1, to form a complex at replication foci
MR Rountree et al.
NATURE GENETICS (2000)
Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q
DW Morris et al.
HUMAN MOLECULAR GENETICS (2000)
Male prevalence for reading disability is found in a large sample of Black and White children free from ascertainment bias
KA Flannery et al.
JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY (2000)