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Journal Abstract Search

233 related items for PubMed ID: 16844227

  • 1. Neuroanatomical, molecular genetic, and behavioral correlates of fragile X syndrome.
    Koukoui SD, Chaudhuri A.
    Brain Res Rev; 2007 Jan; 53(1):27-38. PubMed ID: 16844227
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  • 4. Differential translation and fragile X syndrome.
    Vanderklish PW, Edelman GM.
    Genes Brain Behav; 2005 Aug; 4(6):360-84. PubMed ID: 16098135
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  • 6. Fragile X syndrome: from molecular genetics to therapy.
    D'Hulst C, Kooy RF.
    J Med Genet; 2009 Sep; 46(9):577-84. PubMed ID: 19724010
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  • 7. microRNAs and Fragile X Syndrome.
    Lin SL.
    Adv Exp Med Biol; 2015 Sep; 888():107-21. PubMed ID: 26663181
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  • 9. Anatomical phenotyping in a mouse model of fragile X syndrome with magnetic resonance imaging.
    Ellegood J, Pacey LK, Hampson DR, Lerch JP, Henkelman RM.
    Neuroimage; 2010 Nov 15; 53(3):1023-9. PubMed ID: 20304074
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  • 10. The behavioral phenotype of FMR1 mutations.
    Boyle L, Kaufmann WE.
    Am J Med Genet C Semin Med Genet; 2010 Nov 15; 154C(4):469-76. PubMed ID: 20981777
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  • 11. Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.
    Jacquemont S, Curie A, des Portes V, Torrioli MG, Berry-Kravis E, Hagerman RJ, Ramos FJ, Cornish K, He Y, Paulding C, Neri G, Chen F, Hadjikhani N, Martinet D, Meyer J, Beckmann JS, Delange K, Brun A, Bussy G, Gasparini F, Hilse T, Floesser A, Branson J, Bilbe G, Johns D, Gomez-Mancilla B.
    Sci Transl Med; 2011 Jan 05; 3(64):64ra1. PubMed ID: 21209411
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  • 12. Exceptional good cognitive and phenotypic profile in a male carrying a mosaic mutation in the FMR1 gene.
    Govaerts LC, Smit AE, Saris JJ, VanderWerf F, Willemsen R, Bakker CE, De Zeeuw CI, Oostra BA.
    Clin Genet; 2007 Aug 05; 72(2):138-44. PubMed ID: 17661818
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  • 13. Mechanism-based approaches to treating fragile X.
    Dölen G, Carpenter RL, Ocain TD, Bear MF.
    Pharmacol Ther; 2010 Jul 05; 127(1):78-93. PubMed ID: 20303363
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  • 14. Molecular and cellular aspects of mental retardation in the Fragile X syndrome: from gene mutation/s to spine dysmorphogenesis.
    De Rubeis S, Fernández E, Buzzi A, Di Marino D, Bagni C.
    Adv Exp Med Biol; 2012 Jul 05; 970():517-51. PubMed ID: 22351071
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  • 15. Whole-brain expression analysis of FMRP in adult monkey and its relationship to cognitive deficits in fragile X syndrome.
    Zangenehpour S, Cornish KM, Chaudhuri A.
    Brain Res; 2009 Apr 06; 1264():76-84. PubMed ID: 19368811
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  • 16. Clinical aspects of the fragile X syndrome.
    Brown WT.
    Results Probl Cell Differ; 2012 Apr 06; 54():273-9. PubMed ID: 22009358
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  • 17. Early postnatal plasticity in neocortex of Fmr1 knockout mice.
    Desai NS, Casimiro TM, Gruber SM, Vanderklish PW.
    J Neurophysiol; 2006 Oct 06; 96(4):1734-45. PubMed ID: 16823030
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  • 18. Fragile X mental retardation protein is required for chemically-induced long-term potentiation of the hippocampus in adult mice.
    Shang Y, Wang H, Mercaldo V, Li X, Chen T, Zhuo M.
    J Neurochem; 2009 Nov 06; 111(3):635-46. PubMed ID: 19659572
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  • 20. The Prader-Willi phenotype of fragile X syndrome.
    Nowicki ST, Tassone F, Ono MY, Ferranti J, Croquette MF, Goodlin-Jones B, Hagerman RJ.
    J Dev Behav Pediatr; 2007 Apr 06; 28(2):133-8. PubMed ID: 17435464
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