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Results: 1 to 20 of 94

Similar articles for PubMed (Select 23036959)

1.

Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteins.

Tammimies K, Vitezic M, Matsson H, Le Guyader S, Bürglin TR, Ohman T, Strömblad S, Daub CO, Nyman TA, Kere J, Tapia-Páez I.

Biol Psychiatry. 2013 Mar 15;73(6):583-90. doi: 10.1016/j.biopsych.2012.08.012. Epub 2012 Oct 1.

PMID:
23036959
2.

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

Massinen S, Tammimies K, Tapia-Páez I, Matsson H, Hokkanen ME, Söderberg O, Landegren U, Castrén E, Gustafsson JA, Treuter E, Kere J.

Hum Mol Genet. 2009 Aug 1;18(15):2802-12. doi: 10.1093/hmg/ddp215. Epub 2009 May 7.

3.

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

Tapia-Páez I, Tammimies K, Massinen S, Roy AL, Kere J.

FASEB J. 2008 Aug;22(8):3001-9. doi: 10.1096/fj.07-104455. Epub 2008 Apr 29.

4.

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

Taipale M, Kaminen N, Nopola-Hemmi J, Haltia T, Myllyluoma B, Lyytinen H, Muller K, Kaaranen M, Lindsberg PJ, Hannula-Jouppi K, Kere J.

Proc Natl Acad Sci U S A. 2003 Sep 30;100(20):11553-8. Epub 2003 Sep 3.

5.

The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation.

Tammimies K, Tapia-Páez I, Rüegg J, Rosin G, Kere J, Gustafsson JÅ, Nalvarte I.

Mol Endocrinol. 2012 Apr;26(4):619-29. doi: 10.1210/me.2011-1376. Epub 2012 Mar 1.

PMID:
22383464
6.

DYX1C1 placed in a molecular context.

LoTurco JJ, Tarkar A.

Biol Psychiatry. 2013 Mar 15;73(6):497-8. doi: 10.1016/j.biopsych.2013.01.025. No abstract available.

PMID:
23438632
7.

The dyslexia candidate gene DYX1C1 is a potential marker of poor survival in breast cancer.

Rosin G, Hannelius U, Lindström L, Hall P, Bergh J, Hartman J, Kere J.

BMC Cancer. 2012 Feb 29;12:79. doi: 10.1186/1471-2407-12-79.

8.

A novel role for DYX1C1, a chaperone protein for both Hsp70 and Hsp90, in breast cancer.

Chen Y, Zhao M, Wang S, Chen J, Wang Y, Cao Q, Zhou W, Liu J, Xu Z, Tong G, Li J.

J Cancer Res Clin Oncol. 2009 Sep;135(9):1265-76. doi: 10.1007/s00432-009-0568-6. Epub 2009 Mar 11.

PMID:
19277710
9.

Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations.

Rosen GD, Bai J, Wang Y, Fiondella CG, Threlkeld SW, LoTurco JJ, Galaburda AM.

Cereb Cortex. 2007 Nov;17(11):2562-72. Epub 2007 Jan 11.

10.

DYX1C1 functions in neuronal migration in developing neocortex.

Wang Y, Paramasivam M, Thomas A, Bai J, Kaminen-Ahola N, Kere J, Voskuil J, Rosen GD, Galaburda AM, Loturco JJ.

Neuroscience. 2006 Dec 1;143(2):515-22. Epub 2006 Sep 20.

PMID:
16989952
11.

No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy.

Bellini G, Bravaccio C, Calamoneri F, Donatella Cocuzza M, Fiorillo P, Gagliano A, Mazzone D, del Giudice EM, Scuccimarra G, Militerni R, Pascotto A.

J Mol Neurosci. 2005;27(3):311-4.

PMID:
16280601
12.

The effects of embryonic knockdown of the candidate dyslexia susceptibility gene homologue Dyx1c1 on the distribution of GABAergic neurons in the cerebral cortex.

Currier TA, Etchegaray MA, Haight JL, Galaburda AM, Rosen GD.

Neuroscience. 2011 Jan 13;172:535-46. doi: 10.1016/j.neuroscience.2010.11.002. Epub 2010 Nov 9.

13.

Breakthroughs in the search for dyslexia candidate genes.

McGrath LM, Smith SD, Pennington BF.

Trends Mol Med. 2006 Jul;12(7):333-41. Epub 2006 Jun 16. Review.

PMID:
16781891
14.

Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population.

Venkatesh SK, Siddaiah A, Padakannaya P, Ramachandra NB.

Psychiatr Genet. 2014 Feb;24(1):10-20. doi: 10.1097/YPG.0000000000000009.

PMID:
24362368
15.

Evolutionary diversification of DYX1C1 transcripts via an HERV-H LTR integration event.

Kim YJ, Huh JW, Kim DS, Han K, Kim HM, Kim HS.

Genes Genet Syst. 2011;86(4):277-84.

16.

The genetic lexicon of dyslexia.

Paracchini S, Scerri T, Monaco AP.

Annu Rev Genomics Hum Genet. 2007;8:57-79. Review.

PMID:
17444811
17.

Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.

Wigg KG, Feng Y, Crosbie J, Tannock R, Kennedy JL, Ickowicz A, Malone M, Schachar R, Barr CL.

Genes Brain Behav. 2008 Nov;7(8):877-86. doi: 10.1111/j.1601-183X.2008.00425.x.

PMID:
19076634
18.

Progress towards a cellular neurobiology of reading disability.

Gabel LA, Gibson CJ, Gruen JR, LoTurco JJ.

Neurobiol Dis. 2010 May;38(2):173-80. doi: 10.1016/j.nbd.2009.06.019. Epub 2009 Jul 17. Review.

19.

Exploring the transcriptome of ciliated cells using in silico dissection of human tissues.

Ivliev AE, 't Hoen PA, van Roon-Mom WM, Peters DJ, Sergeeva MG.

PLoS One. 2012;7(4):e35618. doi: 10.1371/journal.pone.0035618. Epub 2012 Apr 25.

20.

The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function.

Chandrasekar G, Vesterlund L, Hultenby K, Tapia-Páez I, Kere J.

PLoS One. 2013 May 1;8(5):e63123. doi: 10.1371/journal.pone.0063123. Print 2013.

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