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Items: 32


Spared cognitive and behavioral functions prior to epilepsy onset in a rat model of subcortical band heteropia.

Martineau FS, Fournier L, Buhler E, Watrin F, Sargolini F, Manent JB, Poucet B, Represa A.

Brain Res. 2019 Jan 25. pii: S0006-8993(19)30052-6. doi: 10.1016/j.brainres.2019.01.030. [Epub ahead of print]


Spontaneous epileptiform activity in a rat model of bilateral subcortical band heterotopia.

Sahu S, Buhler E, Vermoyal JC, Watrin F, Represa A, Manent JB.

Epilepsia. 2019 Feb;60(2):337-348. doi: 10.1111/epi.14633. Epub 2018 Dec 30.


Direct and Collateral Alterations of Functional Cortical Circuits in a Rat Model of Subcortical Band Heterotopia.

Plantier V, Watrin F, Buhler E, Martineau FS, Sahu S, Manent JB, Bureau I, Represa A.

Cereb Cortex. 2018 Dec 7. doi: 10.1093/cercor/bhy307. [Epub ahead of print]


Correct Laminar Positioning in the Neocortex Influences Proper Dendritic and Synaptic Development.

Martineau FS, Sahu S, Plantier V, Buhler E, Schaller F, Fournier L, Chazal G, Kawasaki H, Represa A, Watrin F, Manent JB.

Cereb Cortex. 2018 Aug 1;28(8):2976-2990. doi: 10.1093/cercor/bhy113.


A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations.

Conti V, Carabalona A, Pallesi-Pocachard E, Leventer RJ, Schaller F, Parrini E, Deparis AA, Watrin F, Buhler E, Novara F, Lise S, Pagnamenta AT, Kini U, Taylor JC, Zuffardi O, Represa A, Keays DA, Guerrini R, Falace A, Cardoso C.

J Vis Exp. 2017 Dec 1;(130). doi: 10.3791/53570.


Cytomegalovirus Infection of the Rat Developing Brain In Utero Prominently Targets Immune Cells and Promotes Early Microglial Activation.

Cloarec R, Bauer S, Luche H, Buhler E, Pallesi-Pocachard E, Salmi M, Courtens S, Massacrier A, Grenot P, Teissier N, Watrin F, Schaller F, Adle-Biassette H, Gressens P, Malissen M, Stamminger T, Streblow DN, Bruneau N, Szepetowski P.

PLoS One. 2016 Jul 29;11(7):e0160176. doi: 10.1371/journal.pone.0160176. eCollection 2016.


Epilepsy in young Tsc1(+/-) mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex.

Gataullina S, Lemaire E, Wendling F, Kaminska A, Watrin F, Riquet A, Ville D, Moutard ML, de Saint Martin A, Napuri S, Pedespan JM, Eisermann M, Bahi-Buisson N, Nabbout R, Chiron C, Dulac O, Huberfeld G.

Epilepsia. 2016 Apr;57(4):648-59. doi: 10.1111/epi.13325. Epub 2016 Feb 13.


Causes and consequences of gray matter heterotopia.

Watrin F, Manent JB, Cardoso C, Represa A.

CNS Neurosci Ther. 2015 Feb;21(2):112-22. doi: 10.1111/cns.12322. Epub 2014 Sep 2. Review.


Selective suppression of excessive GluN2C expression rescues early epilepsy in a tuberous sclerosis murine model.

Lozovaya N, Gataullina S, Tsintsadze T, Tsintsadze V, Pallesi-Pocachard E, Minlebaev M, Goriounova NA, Buhler E, Watrin F, Shityakov S, Becker AJ, Bordey A, Milh M, Scavarda D, Bulteau C, Dorfmuller G, Delalande O, Represa A, Cardoso C, Dulac O, Ben-Ari Y, Burnashev N.

Nat Commun. 2014 Aug 1;5:4563. doi: 10.1038/ncomms5563.


Normotopic cortex is the major contributor to epilepsy in experimental double cortex.

Petit LF, Jalabert M, Buhler E, Malvache A, Peret A, Chauvin Y, Watrin F, Represa A, Manent JB.

Ann Neurol. 2014 Sep;76(3):428-42. doi: 10.1002/ana.24237. Epub 2014 Aug 11.


TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway.

Falace A, Buhler E, Fadda M, Watrin F, Lippiello P, Pallesi-Pocachard E, Baldelli P, Benfenati F, Zara F, Represa A, Fassio A, Cardoso C.

Proc Natl Acad Sci U S A. 2014 Feb 11;111(6):2337-42. doi: 10.1073/pnas.1316294111. Epub 2014 Jan 27.


Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.

Conti V, Carabalona A, Pallesi-Pocachard E, Parrini E, Leventer RJ, Buhler E, McGillivray G, Michel FJ, Striano P, Mei D, Watrin F, Lise S, Pagnamenta AT, Taylor JC, Kini U, Clayton-Smith J, Novara F, Zuffardi O, Dobyns WB, Scheffer IE, Robertson SP, Berkovic SF, Represa A, Keays DA, Cardoso C, Guerrini R.

Brain. 2013 Nov;136(Pt 11):3378-94. doi: 10.1093/brain/awt249. Epub 2013 Sep 20.


Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.

Rieusset A, Schaller F, Unmehopa U, Matarazzo V, Watrin F, Linke M, Georges B, Bischof J, Dijkstra F, Bloemsma M, Corby S, Michel FJ, Wevrick R, Zechner U, Swaab D, Dudley K, Bezin L, Muscatelli F.

PLoS Genet. 2013;9(9):e1003752. doi: 10.1371/journal.pgen.1003752. Epub 2013 Sep 5.


Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero.

Salmi M, Bruneau N, Cillario J, Lozovaya N, Massacrier A, Buhler E, Cloarec R, Tsintsadze T, Watrin F, Tsintsadze V, Zimmer C, Villard C, Lafitte D, Cardoso C, Bao L, Lesca G, Rudolf G, Muscatelli F, Pauly V, Khalilov I, Durbec P, Ben-Ari Y, Burnashev N, Represa A, Szepetowski P.

Brain. 2013 Aug;136(Pt 8):2457-73. doi: 10.1093/brain/awt161. Epub 2013 Jul 5.


A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene.

Schaller F, Watrin F, Sturny R, Massacrier A, Szepetowski P, Muscatelli F.

Hum Mol Genet. 2010 Dec 15;19(24):4895-905. doi: 10.1093/hmg/ddq424. Epub 2010 Sep 28.


H19 acts as a trans regulator of the imprinted gene network controlling growth in mice.

Gabory A, Ripoche MA, Le Digarcher A, Watrin F, Ziyyat A, Forné T, Jammes H, Ainscough JF, Surani MA, Journot L, Dandolo L.

Development. 2009 Oct;136(20):3413-21. doi: 10.1242/dev.036061. Epub 2009 Sep 17.


Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome.

Zanella S, Watrin F, Mebarek S, Marly F, Roussel M, Gire C, Diene G, Tauber M, Muscatelli F, Hilaire G.

J Neurosci. 2008 Feb 13;28(7):1745-55. doi: 10.1523/JNEUROSCI.4334-07.2008.


Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region.

Le Meur E, Watrin F, Landers M, Sturny R, Lalande M, Muscatelli F.

Dev Biol. 2005 Oct 15;286(2):587-600. Epub 2005 Aug 29.


Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression.

Andrieu D, Watrin F, Niinobe M, Yoshikawa K, Muscatelli F, Fernandez PA.

Gene Expr Patterns. 2003 Dec;3(6):761-5.


T cell development in TCR beta enhancer-deleted mice: implications for alpha beta T cell lineage commitment and differentiation.

Leduc I, Hempel WM, Mathieu N, Verthuy C, Bouvier G, Watrin F, Ferrier P.

J Immunol. 2000 Aug 1;165(3):1364-73.


The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region.

Boccaccio I, Glatt-Deeley H, Watrin F, Roëckel N, Lalande M, Muscatelli F.

Hum Mol Genet. 1999 Dec;8(13):2497-505.


Deletion of the mouse T-cell receptor beta gene enhancer blocks alphabeta T-cell development.

Bouvier G, Watrin F, Naspetti M, Verthuy C, Naquet P, Ferrier P.

Proc Natl Acad Sci U S A. 1996 Jul 23;93(15):7877-81.


TCR beta and TCR alpha gene enhancers confer tissue- and stage-specificity on V(D)J recombination events.

Capone M, Watrin F, Fernex C, Horvat B, Krippl B, Wu L, Scollay R, Ferrier P.

EMBO J. 1993 Nov;12(11):4335-46.


Differential expression of the proto-oncogenes c-abl and c-mos in developing mouse germ cells.

Iwaoki Y, Matsuda H, Mutter GL, Watrin F, Wolgemuth DJ.

Exp Cell Res. 1993 Jun;206(2):212-9.


List of cloned mouse genes with unique expression patterns during spermatogenesis.

Wolgemuth DJ, Watrin F.

Mamm Genome. 1991;1(4):283-8. No abstract available.


Expression of homeobox genes during spermatogenesis.

Wolgemuth DJ, Viviano CM, Watrin F.

Ann N Y Acad Sci. 1991;637:300-12. Review. No abstract available.


Anti-müllerian hormone and freemartinism: inhibition of germ cell development and induction of seminiferous cord-like structures in rat fetal ovaries exposed in vitro to purified bovine AMH.

Vigier B, Watrin F, Magre S, Tran D, Garrigou O, Forest MG, Josso N.

Reprod Nutr Dev. 1988;28(4B):1113-28. Erratum in: Reprod Nutr Dev 1988;28 Suppl 1:199.


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