Les publications de l'équipe Groszer.

Altered social behavior in mice carrying a cortical Foxp2 deletion.

Medvedeva VP, Rieger MA, Vieth B, Mombereau C, Ziegenhain C, Ghosh T, Cressant A, Enard W, Granon S, Dougherty JD, Groszer M.
2018 Hum Mol Genet. doi: 10.1093/hmg/ddy372. [Epub ahead of print]

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Thalamic WNT3 Secretion Spatiotemporally Regulates the Neocortical Ribosome Signature and mRNA Translation to Specify Neocortical Cell Subtypes

Kraushar ML, Viljetic B, Wijeratne HR, Thompson K, Jiao X, Pike JW, Medvedeva V, Groszer M, Kiledjian M, Hart RP, Rasin MR.
2015 J Neurosci.5;35(31):10911-26

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Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance

Schreiweis C, Bornschein U, Burguière E, Kerimoglu C, Schreiter S, Dannemann M, Goyal S, Rea E, French CA, Puliyadi R, Groszer M, Fisher SE, Mundry R, Winter C, Hevers W, Pääbo S, Enard W, Graybiel AM.
2014 Proc Natl Acad Sci U S A. 30;111(39):14253-8

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An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning

French CA, Jin X, Campbell TG, Gerfen E, Groszer M, Fisher SE, Costa RM (2012). Mol Psychiatry.17(11):1077-85. doi: 10.1038/mp.2011.105. 2011 Aug 30.


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Transcriptome sequencing during mouse brain development identifies long non-coding RNAs functionally involved in neurogenic commitment

Aprea J, Prenninger S, Dori M, Ghosh T, Monasor LS, Wessendorf E, Zocher S, Massalini S, Alexopoulou D, Lesche M, Dahl A, Groszer M, Hiller M, Calegari F (2013). EMBO J 32:3145-3160.

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