Genetic and protein interaction studies between the ciliary dyslexia candidate genes DYX1C1 and DCDC2
暂无分享,去创建一个
J. Kere | I. Tapia-Páez | J. Gopalakrishnan | Steffen Erkelenz | A. Bieder | G. Chandrasekar | Arpit Wason
[1] H. Omran,et al. Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility , 2021, PLoS genetics.
[2] T. Werge,et al. PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia , 2020, Nature Communications.
[3] J. Kere,et al. Dyslexia Candidate Gene and Ciliary Gene Expression Dynamics During Human Neuronal Differentiation , 2020, Molecular Neurobiology.
[4] T. Tang,et al. Loss of CPAP in developing mouse brain and its functional implication for human primary microcephaly , 2020, Journal of Cell Science.
[5] Zhiheng Xu,et al. The association of microcephaly protein WDR62 with CPAP/IFT88 is required for cilia formation and neocortical development. , 2019, Human molecular genetics.
[6] Xiaoqun Wang,et al. Cenpj Regulates Cilia Disassembly and Neurogenesis in the Developing Mouse Cortex , 2019, The Journal of Neuroscience.
[7] A. Ustione,et al. Establishment of the early cilia preassembly protein complex during motile ciliogenesis , 2018, Proceedings of the National Academy of Sciences.
[8] G. Benítez-King,et al. Primary cilia formation is diminished in schizophrenia and bipolar disorder: A possible marker for these psychiatric diseases , 2017, Schizophrenia Research.
[9] W. Sale,et al. Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms , 2017, PLoS genetics.
[10] F. Oswald,et al. The FOXP2-Driven Network in Developmental Disorders and Neurodegeneration , 2017, Front. Cell. Neurosci..
[11] Shane A. McCarthy,et al. X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3 , 2017, Nature Communications.
[12] A. Trulioff,et al. Primary Cilia as a Possible Link between Left-Right Asymmetry and Neurodevelopmental Diseases , 2017, Genes.
[13] Richard J. Thompson,et al. Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis. , 2016, Journal of hepatology.
[14] S. Saunier,et al. DCDC2 Mutations Cause Neonatal Sclerosing Cholangitis , 2016, Human mutation.
[15] J. Kere,et al. Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs , 2016, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[16] A. Hyman,et al. Molecular basis for CPAP-tubulin interaction in controlling centriolar and ciliary length , 2016, Nature Communications.
[17] R. Henkelman,et al. Zebrafish models of idiopathic scoliosis link cerebrospinal fluid flow defects to spine curvature , 2016, Science.
[18] Tianhua Zhou,et al. Emerging roles of NudC family: from molecular regulation to clinical implications , 2016, Science China Life Sciences.
[19] A. Hyman,et al. CPAP promotes timely cilium disassembly to maintain neural progenitor pool , 2016, The EMBO journal.
[20] L. Leatherbury,et al. DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia , 2016, PLoS genetics.
[21] M. Daly,et al. A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology. , 2015, American journal of human genetics.
[22] X. Liu,et al. A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation. , 2015, Human molecular genetics.
[23] Xiumin Yan,et al. Characterization of Tetratricopeptide Repeat-Containing Proteins Critical for Cilia Formation and Function , 2015, PloS one.
[24] Donald M. Bell,et al. Cenpj/CPAP regulates progenitor divisions and neuronal migration in the cerebral cortex downstream of Ascl1 , 2015, Nature Communications.
[25] J. Kere,et al. DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling. , 2015, American journal of human genetics.
[26] D. Castro,et al. Transcriptional control of vertebrate neurogenesis by the proneural factor Ascl1 , 2014, Front. Cell. Neurosci..
[27] J. Kere. The molecular genetics and neurobiology of developmental dyslexia as model of a complex phenotype. , 2014, Biochemical and biophysical research communications.
[28] J. Loturco,et al. The Dyslexia-Associated Gene Dcdc2 Is Required for Spike-Timing Precision in Mouse Neocortex , 2014, Biological Psychiatry.
[29] Alison L. Reynolds,et al. Unexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller population , 2014, European Journal of Human Genetics.
[30] H. Omran,et al. DYX1C1 is required for axonemal dynein assembly and ciliary motility , 2013, Nature Genetics.
[31] J. Kere,et al. The Zebrafish Orthologue of the Dyslexia Candidate Gene DYX1C1 Is Essential for Cilia Growth and Function , 2013, PloS one.
[32] Carsten O. Daub,et al. Molecular Networks of DYX1C1 Gene Show Connection to Neuronal Migration Genes and Cytoskeletal Proteins , 2013, Biological Psychiatry.
[33] T. Stearns,et al. Transcriptional Program of Ciliated Epithelial Cells Reveals New Cilium and Centrosome Components and Links to Human Disease , 2012, PloS one.
[34] M. von Zastrow,et al. A Simple Cell-Based Assay Reveals That Diverse Neuropsychiatric Risk Genes Converge on Primary Cilia , 2012, PloS one.
[35] P. ’. ‘t Hoen,et al. Exploring the Transcriptome of Ciliated Cells Using In Silico Dissection of Human Tissues , 2012, PloS one.
[36] T. Tang,et al. CPAP is required for cilia formation in neuronal cells , 2012, Biology Open.
[37] J. Amatruda,et al. Studying synthetic lethal interactions in the zebrafish system: insight into disease genes and mechanisms , 2011, Disease Models & Mechanisms.
[38] Juha Kere,et al. Increased Expression of the Dyslexia Candidate Gene DCDC2 Affects Length and Signaling of Primary Cilia in Neurons , 2011, PloS one.
[39] A. Munnich,et al. KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes , 2011, Nature Genetics.
[40] Colin A. Johnson,et al. TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum , 2011, Nature Genetics.
[41] F. Alkuraya,et al. Novel CENPJ mutation causes Seckel syndrome , 2010, Journal of Medical Genetics.
[42] Jeffrey R. Gruen,et al. Progress towards a cellular neurobiology of reading disability , 2010, Neurobiology of Disease.
[43] V. Sheffield,et al. BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly , 2010, Proceedings of the National Academy of Sciences.
[44] J. Kere,et al. Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia. , 2009, Human molecular genetics.
[45] T. Tang,et al. CPAP is a cell-cycle regulated protein that controls centriole length , 2009, Nature Cell Biology.
[46] P. Gönczy,et al. Overly Long Centrioles and Defective Cell Division upon Excess of the SAS-4-Related Protein CPAP , 2009, Current Biology.
[47] E. Nigg,et al. Control of Centriole Length by CPAP and CP110 , 2009, Current Biology.
[48] Qinhong Cao,et al. A novel role for DYX1C1, a chaperone protein for both Hsp70 and Hsp90, in breast cancer , 2009, Journal of Cancer Research and Clinical Oncology.
[49] J. Kere,et al. The complex of TFII‐I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia , 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[50] V. Sheffield,et al. Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning. , 2008, Human molecular genetics.
[51] R. Devlin,et al. Transcriptional profiling of mucociliary differentiation in human airway epithelial cells. , 2007, American journal of respiratory cell and molecular biology.
[52] G. D. Rosen,et al. DYX1C1 functions in neuronal migration in developing neocortex , 2006, Neuroscience.
[53] G. Eichele,et al. The DCX Superfamily 1: Common and Divergent Roles for Members of the Mouse DCX Superfamily , 2006, Cell cycle.
[54] S. Fisher,et al. Dissection of epistasis in oligogenic Bardet–Biedl syndrome , 2006, Nature.
[55] P. Skudlarski,et al. DCDC2 is associated with reading disability and modulates neuronal development in the brain. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[56] Hussain Jafri,et al. A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size , 2005, Nature Genetics.
[57] K. Nakayama,et al. Interaction of U‐box‐type ubiquitin‐protein ligases (E3s) with molecular chaperones , 2004, Genes to cells : devoted to molecular & cellular mechanisms.
[58] Tanya M. Teslovich,et al. Comparative Genomics Identifies a Flagellar and Basal Body Proteome that Includes the BBS5 Human Disease Gene , 2004, Cell.
[59] Heikki Lyytinen,et al. A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[60] A. Valencia,et al. p23 and HSP20/α‐crystallin proteins define a conserved sequence domain present in other eukaryotic protein families , 2002, FEBS letters.
[61] Thomas D. Schmittgen,et al. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.
[62] D. Toft,et al. Crystal Structure and Activity of Human p23, a Heat Shock Protein 90 Co-chaperone* , 2000, The Journal of Biological Chemistry.
[63] G. Blatch,et al. The tetratricopeptide repeat: a structural motif mediating protein-protein interactions. , 1999, BioEssays : news and reviews in molecular, cellular and developmental biology.
[64] N. Geschwind,et al. Developmental dyslexia: Four consecutive patients with cortical anomalies , 1985, Annals of neurology.
[65] E. Valente,et al. Primary cilia in neurodevelopmental disorders , 2014, Nature Reviews Neurology.
[66] Andreas Ziegler,et al. Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. , 2006, American journal of human genetics.
[67] Hilde van der Togt,et al. Publisher's Note , 2003, J. Netw. Comput. Appl..
[68] M. Westerfield. The zebrafish book : a guide for the laboratory use of zebrafish (Danio rerio) , 1995 .