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Items: 1 to 20 of 67

1.

An SNP in an ultraconserved regulatory element affects Dlx5/Dlx6 regulation in the forebrain.

Poitras L, Yu M, Lesage-Pelletier C, Macdonald RB, Gagné JP, Hatch G, Kelly I, Hamilton SP, Rubenstein JL, Poirier GG, Ekker M.

Development. 2010 Sep;137(18):3089-97. doi: 10.1242/dev.051052. Epub 2010 Aug 11.

2.

Ultrasonic vocalizations in mouse models for speech and socio-cognitive disorders: insights into the evolution of vocal communication.

Fischer J, Hammerschmidt K.

Genes Brain Behav. 2011 Feb;10(1):17-27. doi: 10.1111/j.1601-183X.2010.00610.x. Review.

3.

Estrogen-dependent transcription of the NEL-like 2 (NELL2) gene and its role in protection from cell death.

Choi EJ, Kim DH, Kim JG, Kim DY, Kim JD, Seol OJ, Jeong CS, Park JW, Choi MY, Kang SG, Costa ME, Ojeda SR, Lee BJ.

J Biol Chem. 2010 Aug 6;285(32):25074-84. doi: 10.1074/jbc.M110.100545. Epub 2010 Jun 10.

4.

Rac1 regulates neuronal polarization through the WAVE complex.

Tahirovic S, Hellal F, Neukirchen D, Hindges R, Garvalov BK, Flynn KC, Stradal TE, Chrostek-Grashoff A, Brakebusch C, Bradke F.

J Neurosci. 2010 May 19;30(20):6930-43. doi: 10.1523/JNEUROSCI.5395-09.2010.

5.

Guidance molecules in synapse formation and plasticity.

Shen K, Cowan CW.

Cold Spring Harb Perspect Biol. 2010 Apr;2(4):a001842. doi: 10.1101/cshperspect.a001842. Epub 2010 Mar 10. Review.

6.

MicroRNAs in neuronal development, function and dysfunction.

Saba R, Schratt GM.

Brain Res. 2010 Jun 18;1338:3-13. doi: 10.1016/j.brainres.2010.03.107. Epub 2010 Apr 7. Review.

PMID:
20380818
7.

MicroRNAs potentiate neural development.

Fineberg SK, Kosik KS, Davidson BL.

Neuron. 2009 Nov 12;64(3):303-9. doi: 10.1016/j.neuron.2009.10.020. Review.

8.

Human-specific transcriptional regulation of CNS development genes by FOXP2.

Konopka G, Bomar JM, Winden K, Coppola G, Jonsson ZO, Gao F, Peng S, Preuss TM, Wohlschlegel JA, Geschwind DH.

Nature. 2009 Nov 12;462(7270):213-7. doi: 10.1038/nature08549.

9.

Looking BAC at striatal signaling: cell-specific analysis in new transgenic mice.

Valjent E, Bertran-Gonzalez J, Hervé D, Fisone G, Girault JA.

Trends Neurosci. 2009 Oct;32(10):538-47. doi: 10.1016/j.tins.2009.06.005. Epub 2009 Sep 16. Review.

PMID:
19765834
10.

A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.

Enard W, Gehre S, Hammerschmidt K, Hölter SM, Blass T, Somel M, Brückner MK, Schreiweis C, Winter C, Sohr R, Becker L, Wiebe V, Nickel B, Giger T, Müller U, Groszer M, Adler T, Aguilar A, Bolle I, Calzada-Wack J, Dalke C, Ehrhardt N, Favor J, Fuchs H, Gailus-Durner V, Hans W, Hölzlwimmer G, Javaheri A, Kalaydjiev S, Kallnik M, Kling E, Kunder S, Mossbrugger I, Naton B, Racz I, Rathkolb B, Rozman J, Schrewe A, Busch DH, Graw J, Ivandic B, Klingenspor M, Klopstock T, Ollert M, Quintanilla-Martinez L, Schulz H, Wolf E, Wurst W, Zimmer A, Fisher SE, Morgenstern R, Arendt T, de Angelis MH, Fischer J, Schwarz J, Pääbo S.

Cell. 2009 May 29;137(5):961-71. doi: 10.1016/j.cell.2009.03.041.

11.

FOXP2 as a molecular window into speech and language.

Fisher SE, Scharff C.

Trends Genet. 2009 Apr;25(4):166-77. doi: 10.1016/j.tig.2009.03.002. Epub 2009 Mar 21. Review.

PMID:
19304338
12.

The evolution of Fox genes and their role in development and disease.

Hannenhalli S, Kaestner KH.

Nat Rev Genet. 2009 Apr;10(4):233-40. doi: 10.1038/nrg2523. Review.

13.

Expression analysis and mutation detection of DLX5 and DLX6 in autism.

Nakashima N, Yamagata T, Mori M, Kuwajima M, Suwa K, Momoi MY.

Brain Dev. 2010 Feb;32(2):98-104. doi: 10.1016/j.braindev.2008.12.021. Epub 2009 Feb 4.

PMID:
19195802
14.

A functional genetic link between distinct developmental language disorders.

Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE.

N Engl J Med. 2008 Nov 27;359(22):2337-45. doi: 10.1056/NEJMoa0802828. Epub 2008 Nov 5.

15.

Dichotomous anatomical properties of adult striatal medium spiny neurons.

Gertler TS, Chan CS, Surmeier DJ.

J Neurosci. 2008 Oct 22;28(43):10814-24. doi: 10.1523/JNEUROSCI.2660-08.2008.

16.

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders.

Liu X, Novosedlik N, Wang A, Hudson ML, Cohen IL, Chudley AE, Forster-Gibson CJ, Lewis SM, Holden JJ.

Eur J Hum Genet. 2009 Feb;17(2):228-35. doi: 10.1038/ejhg.2008.148. Epub 2008 Aug 27.

17.

Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.

Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SD, Nolan PM, Pääbo S, Channon KM, Costa RM, Eilers J, Ehret G, Rawlins JN, Fisher SE.

Curr Biol. 2008 Mar 11;18(5):354-62. doi: 10.1016/j.cub.2008.01.060.

18.

WAVE1 controls neuronal activity-induced mitochondrial distribution in dendritic spines.

Sung JY, Engmann O, Teylan MA, Nairn AC, Greengard P, Kim Y.

Proc Natl Acad Sci U S A. 2008 Feb 26;105(8):3112-6. doi: 10.1073/pnas.0712180105. Epub 2008 Feb 14.

19.

Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.

Haesler S, Rochefort C, Georgi B, Licznerski P, Osten P, Scharff C.

PLoS Biol. 2007 Dec;5(12):e321.

20.

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders.

Vernes SC, Spiteri E, Nicod J, Groszer M, Taylor JM, Davies KE, Geschwind DH, Fisher SE.

Am J Hum Genet. 2007 Dec;81(6):1232-50. Epub 2007 Oct 31.

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