4 départements de recherche
750 employés
45 nationalités
55 équipes de recherche
16 lauréats ERC
260 publications par an
24000 m² de laboratoires

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Fondation universite de Strasbourg

Publications de Yann HERAULT

  • Modeling human disease in rodents by CRISPR/Cas9 genome editing.

    Birling MC(1), Herault Y(2)(3)(4)(5)(6), Pavlovic G(2).

    Mamm Genome 4 juillet 2017

  • Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition.

    Arbogast T(1)(2)(3)(4), Iacono G(5), Chevalier C(1)(2)(3)(4), Afinowi NO(6), Houbaert X(7), van Eede MC(8), Laliberte C(8), Birling MC(9), Linda K(10), Meziane H(9), Selloum M(9), Sorg T(9), Nadif Kasri N(10), Koolen DA(10), Stunnenberg HG(5), Henkelman RM(8), Kopanitsa M(6), Humeau Y(7), De Vries BBA(10), Herault Y(1)(2)(3)(4)(9).

    PLoS Genet 13 juillet 2017

  • Nox4 genetic inhibition in experimental hypertension and metabolic syndrome.

    Bouabout G(1), Ayme-Dietrich E(2), Jacob H(1), Champy MF(1), Birling MC(1), Pavlovic G(1), Madeira L(2), Fertak LE(1), Petit-Demouliere B(1), Sorg T(1), Herault Y(1), Mudgett J(3), Monassier L(4).

    Arch Cardiovasc Dis 4 novembre 2017

  • Prevalence of sexual dimorphism in mammalian phenotypic traits.

    Karp NA(1)(2), Mason J(3), Beaudet AL(4), Benjamini Y(5), Bower L(6), Braun RE(7), Brown SDM(8), Chesler EJ(7), Dickinson ME(9), Flenniken AM(10), Fuchs H(11), Angelis MH(11)(12)(13), Gao X(14), Guo S(14), Greenaway S(8), Heller R(5), Herault Y(15)(16)(17)(18)(19), Justice MJ(20), Kurbatova N(5), Lelliott CJ(21), Lloyd KCK(6), Mallon AM(8), Mank JE(22), Masuya H(23), McKerlie C(10)(24), Meehan TF(3), Mott RF(25), Murray SA(7), Parkinson H(3), Ramirez-Solis R(21), Santos L(8), Seavitt JR(4), Smedley D(26), Sorg T(15)(16)(17)(18)(19), Speak AO(21), Steel KP(21)(27), Svenson KL(7); International Mouse Phenotyping Consortium, Wakana S(23), West D(28), Wells S(8), Westerberg H(8), Yaacoby S(5), White JK(7)(21).

    Nat Commun 26 juin 2017

  • Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse.

    Ung DC(1,)(2), Iacono G(3), Meziane H(4), Blanchard E(1,)(5,)(6), Papon MA(1,)(2), Selten M(7), van Rhijn JR(7), Montjean R(8,)(9,)(10,)(11), Rucci J(8,)(9,)(10,)(11), Martin S(12), Fleet A(13), Birling MC(4), Marouillat S(1,)(2), Roepman R(14,)(15), Selloum M(4), Lux A(4), Thepault RA(1,)(2), Hamel P(13), Mittal K(16), Vincent JB(16), Dorseuil O(8,)(9,)(10,)(11), Stunnenberg HG(3), Billuart P(8,)(9,)(10,)(11), Nadif Kasri N(7,)(14), Herault Y(4,)(17,)(18,)(19,)(20), Laumonnier F(1,)(2,)(6).

    Mol Psychiatry 18 avril 2017

  • Rodent models in Down syndrome research: impact and future opportunities.

    Herault Y(1)(2)(3)(4)(5), Delabar JM(5)(6)(7)(8), Fisher EMC(5)(9)(10), Tybulewicz VLJ(5)(10)(11)(12), Yu E(5)(13)(14), Brault V(15)(2)(3)(4).

    Dis Model Mech 1 octobre 2017

  • Synaptic dysfunction in amygdala in intellectual disorder models.

    Aincy M(1), Meziane H(2), Herault Y(3), Humeau Y(4).

    Prog Neuropsychopharmacol Biol Psychiatry 31 juillet 2017

  • WD40-repeat 47, a microtubule-associated protein, is essential for brain development and autophagy.

    Kannan M(1)(2)(3)(4)(5), Bayam E(1)(2)(3)(4), Wagner C(1)(2)(3)(4), Rinaldi B(6), Kretz PF(1)(2)(3)(4), Tilly P(1)(2)(3)(4), Roos M(7), McGillewie L(8), Bar S(6), Minocha S(5), Chevalier C(1)(2)(3)(4), Po C(9); Sanger Mouse Genetics Project, Chelly J(1)(2)(3)(4), Mandel JL(1)(2)(3)(4), Borgatti R(10), Piton A(1)(2)(3)(4), Kinnear C(8), Loos B(7), Adams DJ(11), Herault Y(1)(2)(3)(4), Collins SC(1)(2)(3)(4)(12), Friant S(6), Godin JD(1)(2)(3)(4), Yalcin B(13)(2)(3)(4).

    Proc Natl Acad Sci U S A 12 octobre 2017

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