PMC Links for Gene (Select 291130) - PMC

Select item 24241111.

POSTNATAL ANALYSIS OF THE EFFECT OF EMBRYONIC KNOCKDOWN AND OVEREXPRESSION OF CANDIDATE DYSLEXIA SUSCEPTIBILITY GENE DCDC2

Timothy J. Burbridge, Yu Wang, Amy J. Volz, Veronica J. Peschansky, Lauren Lisann, Albert M. Galaburda, Joseph J. Lo Turco, Glenn D. Rosen

Neuroscience. Author manuscript; available in PMC 2009 Mar 27.

Published in final edited form as: Neuroscience. 2008 Mar 27; 152(3): 723–733. Published online 2008 Jan 19. doi: 10.1016/j.neuroscience.2008.01.020

PMCID:: PMC2424111

Abstract Article PDF–3.7M

Select item 50047502.

Mutation of the Dyslexia-Associated Gene Dcdc2 Enhances Glutamatergic Synaptic Transmission Between Layer 4 Neurons in Mouse Neocortex

Alicia Che, Dongnhu T. Truong, R. Holly Fitch, Joseph J. LoTurco

Cereb Cortex. 2016 Sep; 26(9): 3705–3718. Published online 2016 Aug 30. doi: 10.1093/cercor/bhv168

PMCID:: PMC5004750

Abstract Article PDF–2.7M

Select item 48397513.

Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population

Yuping Zhang, Jun Li, Shuang Song, Twila Tardif, Margit Burmeister, Sandra M. Villafuerte, Mengmeng Su, Catherine McBride, Hua Shu

PLoS One. 2016; 11(4): e0153603. Published online 2016 Apr 21. doi: 10.1371/journal.pone.0153603

PMCID:: PMC4839751

Abstract Article PDF–410K

Select item 42411684.

Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability

Dongnhu T. Truong, Alicia Che, Amanda R. Rendall, Caitlin E. Szalkowski, Joseph J. LoTurco, Albert M. Galaburda, R. Holly Fitch

Genes Brain Behav. Author manuscript; available in PMC 2015 Nov 1.

Published in final edited form as: Genes Brain Behav. 2014 Nov; 13(8): 802–811. Published online 2014 Sep 3. doi: 10.1111/gbb.12170

PMCID:: PMC4241168

Abstract Article PDF–711K

Select item 40259765.

The dyslexia-associated gene Dcdc2 is required for spike-timing precision in mouse neocortex

Alicia Che, Matthew J. Girgenti, Joseph LoTurco

Biol Psychiatry. Author manuscript; available in PMC 2015 Sep 1.

Published in final edited form as: Biol Psychiatry. 2014 Sep 1; 76(5): 387–396. Published online 2013 Oct 4. doi: 10.1016/j.biopsych.2013.08.018

PMCID:: PMC4025976

Abstract Article PDF–1.8M

Select item 35184516.

Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability

Natalie Cope, John D. Eicher, Haiying Meng, Christopher J. Gibson, Karl Hager, Cheryl Lacadie, Robert K. Fulbright, R. Todd Constable, Grier P. Page, Jeffrey R. Gruen

Neuroimage. Author manuscript; available in PMC 2013 Oct 15.

Published in final edited form as: Neuroimage. 2012 Oct 15; 63(1): 148–156. Published online 2012 Jun 27. doi: 10.1016/j.neuroimage.2012.06.037

PMCID:: PMC3518451

Abstract Article PDF–521K

Select item 12789347.

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

Haiying Meng, Shelley D. Smith, Karl Hager, Matthew Held, Jonathan Liu, Richard K. Olson, Bruce F. Pennington, John C. DeFries, Joel Gelernter, Thomas O'Reilly-Pol, Stefan Somlo, Pawel Skudlarski, Sally E. Shaywitz, Bennett A. Shaywitz, Karen Marchione, Yu Wang, Murugan Paramasivam, Joseph J. LoTurco, Grier P. Page, Jeffrey R. Gruen

Proc Natl Acad Sci U S A. 2005 Nov 22; 102(47): 17053–17058. Published online 2005 Nov 8. doi: 10.1073/pnas.0508591102

Correction in:: Proc Natl Acad Sci U S A. 2005 Dec 20; 102(51): 18763.

PMCID:: PMC1278934

Abstract Article PDF–806K

Select item 31168258.

Increased Expression of the Dyslexia Candidate Gene DCDC2 Affects Length and Signaling of Primary Cilia in Neurons

Satu Massinen, Marie-Estelle Hokkanen, Hans Matsson, Kristiina Tammimies, Isabel Tapia-Páez, Vanina Dahlström-Heuser, Juha Kuja-Panula, Jan Burghoorn, Kristian E. Jeppsson, Peter Swoboda, Myriam Peyrard-Janvid, Rune Toftgård, Eero Castrén, Juha Kere

PLoS One. 2011; 6(6): e20580. Published online 2011 Jun 16. doi: 10.1371/journal.pone.0020580

PMCID:: PMC3116825

Abstract Article PDF–1.3M

Select item 29873409.

Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample

Penelope A Lind, Michelle Luciano, Margaret J Wright, Grant W Montgomery, Nicholas G Martin, Timothy C Bates

Eur J Hum Genet. 2010 Jun; 18(6): 668–673. Published online 2010 Jan 13. doi: 10.1038/ejhg.2009.237

PMCID:: PMC2987340

Abstract Article PDF–351K

Select item 438386210.

A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation

M'hamed Grati, Imen Chakchouk, Qi Ma, Mariem Bensaid, Alexandra Desmidt, Nouha Turki, Denise Yan, Aissette Baanannou, Rahul Mittal, Nabil Driss, Susan Blanton, Amjad Farooq, Zhongmin Lu, Xue Zhong Liu, Saber Masmoudi

Hum Mol Genet. 2015 May 1; 24(9): 2482–2491. Published online 2015 Jan 18. doi: 10.1093/hmg/ddv009

PMCID:: PMC4383862

Abstract Article PDF–1.1M

Select item 321262211.

Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice

Lisa A. Gabel, Ioana Marin, Joseph J. LoTurco, Alicia Che, Cara Murphy, Monica Manglani, Stephanie Kass

Genes Brain Behav. Author manuscript; available in PMC 2012 Nov 1.

Published in final edited form as: Genes Brain Behav. 2011 Nov; 10(8): 868–875. Published online 2011 Oct 19. doi: 10.1111/j.1601-183X.2011.00727.x

PMCID:: PMC3212622

Abstract Article PDF–736K

Select item 317072412.

Dcdc2 knockout mice display exacerbated developmental disruptions following knockdown of Dcx

Yu Wang, Xiuyin Yin, Glenn Rosen, Lisa Gabel, Sarah M. Guadiana, Matthew R Sarkisian, Albert M. Galaburda, Joseph J. LoTurco

Neuroscience. Author manuscript; available in PMC 2012 Sep 8.

Published in final edited form as: Neuroscience. 2011 Sep 8; 190: 398–408. Published online 2011 Jun 13. doi: 10.1016/j.neuroscience.2011.06.010

PMCID:: PMC3170724

Abstract Article PDF–3.3M

Select item 428967713.

DCDC2 Mutations Cause a Renal-Hepatic Ciliopathy by Disrupting Wnt Signaling

Markus Schueler, Daniela A. Braun, Gayathri Chandrasekar, Heon Yung Gee, Timothy D. Klasson, Jan Halbritter, Andrea Bieder, Jonathan D. Porath, Rannar Airik, Weibin Zhou, Joseph J. LoTurco, Alicia Che, Edgar A. Otto, Detlef Böckenhauer, Neil J. Sebire, Tomas Honzik, Peter C. Harris, Sarah J. Koon, Meral Gunay-Aygun, Sophie Saunier, Klaus Zerres, Nadina Ortiz Bruechle, Joost P.H. Drenth, Laurence Pelletier, Isabel Tapia-Páez, Richard P. Lifton, Rachel H. Giles, Juha Kere, Friedhelm Hildebrandt

Am J Hum Genet. 2015 Jan 8; 96(1): 81–92. doi: 10.1016/j.ajhg.2014.12.002

PMCID:: PMC4289677

Abstract Article PDF–2.3M

Select item 155040214.

The evolving doublecortin (DCX) superfamily

Orly Reiner, Frédéric M Coquelle, Bastian Peter, Talia Levy, Anna Kaplan, Tamar Sapir, Irit Orr, Naama Barkai, Gregor Eichele, Sven Bergmann

BMC Genomics. 2006; 7: 188. Published online 2006 Jul 26. doi: 10.1186/1471-2164-7-188

PMCID:: PMC1550402

Abstract Article PDF–2.9M

Select item 317805915.

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas

Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042

PMCID:: PMC3178059

Abstract Article PDF–1.0M

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