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Journal Abstract Search

389 related items for PubMed ID: 18419324

  • 1. The possible interplay of synaptic and clock genes in autism spectrum disorders.
    Bourgeron T.
    Cold Spring Harb Symp Quant Biol; 2007; 72():645-54. PubMed ID: 18419324
    [Abstract] [Full Text] [Related]

  • 2. A synaptic trek to autism.
    Bourgeron T.
    Curr Opin Neurobiol; 2009 Apr; 19(2):231-4. PubMed ID: 19545994
    [Abstract] [Full Text] [Related]

  • 3. [Autism: more evidence of a genetic cause].
    Bourgeron T, Leboyer M, Delorme R.
    Bull Acad Natl Med; 2009 Feb; 193(2):299-304; discussion 304-5. PubMed ID: 19718887
    [Abstract] [Full Text] [Related]

  • 4. Analysis of four neuroligin genes as candidates for autism.
    Ylisaukko-oja T, Rehnström K, Auranen M, Vanhala R, Alen R, Kempas E, Ellonen P, Turunen JA, Makkonen I, Riikonen R, Nieminen-von Wendt T, von Wendt L, Peltonen L, Järvelä I.
    Eur J Hum Genet; 2005 Dec; 13(12):1285-92. PubMed ID: 16077734
    [Abstract] [Full Text] [Related]

  • 5. Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit.
    Radyushkin K, Hammerschmidt K, Boretius S, Varoqueaux F, El-Kordi A, Ronnenberg A, Winter D, Frahm J, Fischer J, Brose N, Ehrenreich H.
    Genes Brain Behav; 2009 Jun; 8(4):416-25. PubMed ID: 19243448
    [Abstract] [Full Text] [Related]

  • 6. Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.
    Liu Y, Du Y, Liu W, Yang C, Liu Y, Wang H, Gong X.
    PLoS One; 2013 Jun; 8(2):e56639. PubMed ID: 23468870
    [Abstract] [Full Text] [Related]

  • 7. Key role for gene dosage and synaptic homeostasis in autism spectrum disorders.
    Toro R, Konyukh M, Delorme R, Leblond C, Chaste P, Fauchereau F, Coleman M, Leboyer M, Gillberg C, Bourgeron T.
    Trends Genet; 2010 Aug; 26(8):363-72. PubMed ID: 20609491
    [Abstract] [Full Text] [Related]

  • 8. [Autism, genetics and synaptic function alterations].
    Perche O, Laumonnier F, Baala L, Ardourel MY, Menuet A, Robin V, Mortaud S, Montécot-Dubourg C, Richard O, Pichon J, Briault S.
    Pathol Biol (Paris); 2010 Oct; 58(5):381-6. PubMed ID: 20181440
    [Abstract] [Full Text] [Related]

  • 9. [Autism spectrum disorder and genes for synaptic proteins].
    Shishido E.
    Brain Nerve; 2012 Jan; 64(1):65-70. PubMed ID: 22223503
    [Abstract] [Full Text] [Related]

  • 10. Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism.
    El-Kordi A, Winkler D, Hammerschmidt K, Kästner A, Krueger D, Ronnenberg A, Ritter C, Jatho J, Radyushkin K, Bourgeron T, Fischer J, Brose N, Ehrenreich H.
    Behav Brain Res; 2013 Aug 15; 251():41-9. PubMed ID: 23183221
    [Abstract] [Full Text] [Related]

  • 11. Familial deletion within NLGN4 associated with autism and Tourette syndrome.
    Lawson-Yuen A, Saldivar JS, Sommer S, Picker J.
    Eur J Hum Genet; 2008 May 15; 16(5):614-8. PubMed ID: 18231125
    [Abstract] [Full Text] [Related]

  • 12. Advances in behavioral genetics: mouse models of autism.
    Moy SS, Nadler JJ.
    Mol Psychiatry; 2008 Jan 15; 13(1):4-26. PubMed ID: 17848915
    [Abstract] [Full Text] [Related]

  • 13. [The structure and patterns of sleep in autism spectrum disorders].
    Lázár AS, Bódizs R.
    Psychiatr Hung; 2008 Jan 15; 23(2):109-28. PubMed ID: 18956612
    [Abstract] [Full Text] [Related]

  • 14. Sleep in children with autistic spectrum disorder.
    Cortesi F, Giannotti F, Ivanenko A, Johnson K.
    Sleep Med; 2010 Aug 15; 11(7):659-64. PubMed ID: 20605110
    [Abstract] [Full Text] [Related]

  • 15. Genetic factors and epigenetic factors for autism: endoplasmic reticulum stress and impaired synaptic function.
    Momoi T, Fujita E, Senoo H, Momoi M.
    Cell Biol Int; 2009 Dec 16; 34(1):13-9. PubMed ID: 20001973
    [Abstract] [Full Text] [Related]

  • 16. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
    Jamain S, Quach H, Betancur C, Råstam M, Colineaux C, Gillberg IC, Soderstrom H, Giros B, Leboyer M, Gillberg C, Bourgeron T, Paris Autism Research International Sibpair Study.
    Nat Genet; 2003 May 16; 34(1):27-9. PubMed ID: 12669065
    [Abstract] [Full Text] [Related]

  • 17. SHANK3 variant as a cause of nonsyndromal autism in an 11-year-old boy and a review of published literature.
    Kanani F, Study D, Balasubramanian M.
    Clin Dysmorphol; 2018 Oct 16; 27(4):113-115. PubMed ID: 29939863
    [Abstract] [Full Text] [Related]

  • 18. Disorder-associated mutations lead to functional inactivation of neuroligins.
    Chih B, Afridi SK, Clark L, Scheiffele P.
    Hum Mol Genet; 2004 Jul 15; 13(14):1471-7. PubMed ID: 15150161
    [Abstract] [Full Text] [Related]

  • 19. SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles.
    Castermans D, Volders K, Crepel A, Backx L, De Vos R, Freson K, Meulemans S, Vermeesch JR, Schrander-Stumpel CT, De Rijk P, Del-Favero J, Van Geet C, Van De Ven WJ, Steyaert JG, Devriendt K, Creemers JW.
    Hum Mol Genet; 2010 Apr 01; 19(7):1368-78. PubMed ID: 20071347
    [Abstract] [Full Text] [Related]

  • 20. Genes associated with autism spectrum disorder.
    Li X, Zou H, Brown WT.
    Brain Res Bull; 2012 Sep 01; 88(6):543-52. PubMed ID: 22688012
    [Abstract] [Full Text] [Related]

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