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750 employés
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Publications de Yann HERAULT

  • How Does Circadian Rhythm Impact Salt Sensitivity of Blood Pressure in Mice? A Study in Two Close C57Bl/6 Substrains.

    Combe R(1), Mudgett J(2), El Fertak L(1), Champy MF(1), Ayme-Dietrich E(3), Petit-Demoulière B(1), Sorg T(1), Herault Y(1), Madwed JB(2), Monassier L(1,)(3).

    PLoS One 18 avril 2016

  • Physiological Expression of AMPKgamma2RG Mutation Causes Wolff-Parkinson-White Syndrome and Induces Kidney Injury in Mice.

    Yang X(1), Mudgett J(2), Bou-About G(3), Champy MF(3), Jacobs H(3), Monassier L(4), Pavlovic G(3), Sorg T(3), Herault Y(3), Petit-Demouliere B(3), Lu K(1), Feng W(1), Wang H(5), Ma LJ(1), Askew R(2), Erion MD(1), Kelley DE(1), Myers RW(1), Li C(1), Guan HP(6).

    J Biol Chem 4 novembre 2016

  • Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes.

    Arbogast T(1,)(2,)(3,)(4), Ouagazzal AM(1,)(2,)(3,)(4), Chevalier C(1,)(2,)(3,)(4), Kopanitsa M(5), Afinowi N(5), Migliavacca E(6,)(7), Cowling BS(1,)(2,)(3,)(4), Birling MC(8), Champy MF(8), Reymond A(6), Herault Y(1,)(2,)(3,)(4,)(8).

    PLoS Genet 12 février 2016

  • The DNA methyltransferase DNMT3C protects male germ cells from transposon activity.

    Barau J(1), Teissandier A(1,)(2), Zamudio N(1), Roy S(3), Nalesso V(4,)(5,)(6), Herault Y(4,)(5,)(6), Guillou F(3), Bourc'his D(7).

    Science 18 novembre 2016

  • Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.

    Hrabe de Angelis M, Nicholson G, Selloum M, White JK, Morgan H, Ramirez-Solis R, Sorg T, Wells S, Fuchs H, Fray M, Adams DJ, Adams NC, Adler T, Aguilar-Pimentel A, Ali-Hadji D, Amann G, AndrE P, Atkins S, Auburtin A, Ayadi A, Becker J, Becker L, Bedu E, Bekeredjian R, Birling MC, Blake A, Bottomley J, Bowl MR, Brault V, Busch DH, Bussell JN, Calzada-Wack J, Cater H, Champy MF, Charles P, Chevalier C, Chiani F, Codner GF, Combe R, Cox R, Dalloneau E, Dierich A, Di Fenza A, Doe B, Duchon A, Eickelberg O, Esapa CT, Fertak LE, Feigel T, Emelyanova I, Estabel J, Favor J, Flenniken A, Gambadoro A, Garrett L, Gates H, Gerdin AK, Gkoutos G, Greenaway S, Glasl L, Goetz P, Da Cruz IG, Gotz A, Graw J, Guimond A, Hans W, Hicks G, Holter SM, Hofler H, Hancock JM, Hoehndorf R, Hough T, Houghton R, Hurt A, Ivandic B, Jacobs H, Jacquot S, Jones N, Karp NA, Katus HA, Kitchen S, Klein-Rodewald T, Klingenspor M, Klopstock T, Lalanne V, Leblanc S, Lengger C, le Marchand E, Ludwig T, Lux A, McKerlie C, Maier H, Mandel JL, Marschall S, Mark M, Melvin DG, Meziane H, Micklich K, Mittelhauser C, Monassier L, Moulaert D, Muller S, Naton B, Neff F, Nolan PM, Nutter LM, Ollert M, Pavlovic G, Pellegata NS, Peter E, Petit-Demouliere B, Pickard A, Podrini C, Potter P, Pouilly L, Puk O, Richardson D, Rousseau S, Quintanilla-Fend L, Quwailid MM, Racz I, Rathkolb B, Riet F, Rossant J, Roux M, Rozman J, Ryder E, Salisbury J, Santos L, Schable KH, Schiller E, Schrewe A, Schulz H, Steinkamp R, Simon M, Stewart M, Stoger C, Stoger T, Sun M, Sunter D, Teboul L, Tilly I, Tocchini-Valentini GP, Tost M, Treise I, Vasseur L, Velot E, Vogt-Weisenhorn D, Wagner C, Walling A, Wattenhofer-Donze M, Weber B, Wendling O, Westerberg H, Willershauser M, Wolf E, Wolter A, Wood J, Wurst W, Yildirim AO, Zeh R, Zimmer A, Zimprich A; EUMODIC Consortium, Holmes C, Steel KP, Herault Y, Gailus-Durner V, Mallon AM, Brown SD.

    Nat Genet Sep 2015

  • Applying the ARRIVE Guidelines to an In Vivo Database.

    Karp NA(1), Meehan TF(2), Morgan H(3), Mason JC(2), Blake A(3), Kurbatova N(2), Smedley D(1), Jacobsen J(1), Mott RF(4), Iyer V(5), Matthews P(5), Melvin DG(1), Wells S(3), Flenniken AM(6), Masuya H(7), Wakana S(7), White JK(8), Lloyd KC(9), Reynolds CL(10), Paylor R(11), West DB(12), Svenson KL(13), Chesler EJ(13), de Angelis MH(14), Tocchini-Valentini GP(15), Sorg T(16), Herault Y(16), Parkinson H(2), Mallon AM(3), Brown SD(3).

    PLoS Biol 20 mai 2015

  • Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration.

    Dubos A(1), Castells-Nobau A(2), Meziane H(3), Oortveld MA(2), Houbaert X(4), Iacono G(5), Martin C(4), Mittelhaeuser C(3), Lalanne V(3), Kramer JM(2), Bhukel A(6), Quentin C(7), Slabbert J(8), Verstreken P(8), Sigrist SJ(7), Messaddeq N(9), Birling MC(3), Selloum M(3), Stunnenberg HG(5), Humeau Y(4), Schenck A(10), Herault Y(11).

    Hum Mol Genet 1 décembre 2015

  • Deletion of the App-Runx1 region in mice models human partial monosomy 21.

    Arbogast T(1), Raveau M(1), Chevalier C(1), Nalesso V(1), Dembele D(1), Jacobs H(2), Wendling O(2), Roux M(3), Duchon A(1), Herault Y(4).

    Dis Model Mech Jun 2015

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