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A mu-delta opioid receptor brain atlas reveals neuronal co-occurrence in subcortical networks.

Erbs E(1), Faget L, Scherrer G, Matifas A, Filliol D, Vonesch JL, Koch M, Kessler P, Hentsch D, Birling MC, Koutsourakis M, Vasseur L, Veinante P, Kieffer BL, Massotte D.
Brain Struct Funct 2015 Mar;220(2):677-702

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An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism.

Meziane H(1), Schaller F(2), Bauer S(2), Villard C(3), Matarazzo V(2), Riet F(1), Guillon G(4), Lafitte D(3), Desarmenien MG(4), Tauber M(5), Muscatelli F(6).
Biol Psychiatry 2015 Jul 15;78(2):85-94

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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 2015 Sep;47(9):969-78

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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 2015 May 20;13(5):e1002151

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Blastocyst genotyping for quality control of mouse mutant archives: an ethical and economical approach.

Scavizzi F(1), Ryder E(2), Newman S(2), Raspa M(1), Gleeson D(2), Wardle-Jones H(2), Montoliu L(3,)(4), Fernandez A(3,)(4), Dessain ML(5), Larrigaldie V(5), Khorshidi Z(6), Vuolteenaho R(7), Soininen R(7), André P(8), Jacquot S(8), Hong Y(9), de Angelis MH(9), Ramirez-Solis R(2), Doe B(10).
Transgenic Res 2015 Oct;24(5):921-7

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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 2015 Dec 1;24(23):6736-55

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Contribution of serotonin to cardiac remodeling associated with hypertensive diastolic ventricular dysfunction in rats.

Ayme-Dietrich E(1), Marzak H, Lawson R, Mokni W, Wendling O, Combe R, Becker J, El Fertak L, Champy MF, Matz R, Andriantsitohaina R, Doly S, Boutourlinsky K, Maroteaux L, Monassier L.
J Hypertens 2015 Nov;33(11):2310-21

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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 2015 Jun;8(6):623-34

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INFRAFRONTIER--providing mutant mouse resources as research tools for the international scientific community.

INFRAFRONTIER Consortium.
Nucleic Acids Res 2015 Jan;43(database issue):D1171–D1175

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LXR-Mediated ABCA1 Expression and Function Are Modulated by High Glucose and PRMT2.

Hussein MA(1), Shrestha E(1), Ouimet M(2), Barrett TJ(2), Leone S(1), Moore KJ(2), Herault Y(3), Fisher EA(2), Garabedian MJ(1).
Plos One 2015 Aug 19;10(8):e0135218

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Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App region.

Brault V(1), Duchon A(1), Romestaing C(2), Sahun I(3), Pothion S(4), Karout M(1), Borel C(5), Dembele D(1), Bizot JC(6), Messaddeq N(1), Sharp AJ(7), Roussel D(2), Antonarakis SE(8), Dierssen M(3), Herault Y(9).
Plos Genet 2015 Mar 24;11(3):e1005062

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Principles and application of LIMS in mouse clinics.

Maier H(1), Schutt C(2), Steinkamp R(2), Hurt A(2), Schneltzer E(2), Gormanns P(2), Lengger C(2), Griffiths M(3), Melvin D(3), Agrawal N(3), Alcantara R(3), Evans A(3), Gannon D(3), Holroyd S(3), Kipp C(3), Raj NP(3), Richardson D(3), LeBlanc S(4), Vasseur L(4), Masuya H(5), Kobayashi K(5), Suzuki T(5), Tanaka N(5), Wakana S(5), Walling A(6), Clary D(7), Gallegos J(8), Fuchs H(2), de Angelis MH(9,)(10,)(11), Gailus-Durner V(2).
Mamm Genome 2015 Oct;26(9-10):467-81

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Shifting eating to the circadian rest phase misaligns the peripheral clocks with the master SCN clock and leads to a metabolic syndrome.

Mukherji A(1), Kobiita A(1), Damara M(1), Misra N(1), Meziane H(2), Champy MF(2), Chambon P(3).
Proc Natl Acad Sci U S A 2015 Dec 1;112(48):E6691-8

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