BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

238 related articles for article (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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The fragile X syndrome: exploring its molecular basis and seeking a treatment.
    Bardoni B; Davidovic L; Bensaid M; Khandjian EW
    Expert Rev Mol Med; 2006 Apr; 8(8):1-16. PubMed ID: 16626504
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Developmental expression of FMRP in the astrocyte lineage: implications for fragile X syndrome.
    Pacey LK; Doering LC
    Glia; 2007 Nov; 55(15):1601-9. PubMed ID: 17823967
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Differential translation and fragile X syndrome.
    Vanderklish PW; Edelman GM
    Genes Brain Behav; 2005 Aug; 4(6):360-84. PubMed ID: 16098135
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The developmental roles of FMRP.
    Till SM
    Biochem Soc Trans; 2010 Apr; 38(2):507-10. PubMed ID: 20298211
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. microRNAs and Fragile X Syndrome.
    Lin SL
    Adv Exp Med Biol; 2015; 888():107-21. PubMed ID: 26663181
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cognitive and behavioral profile of fragile X boys: correlations to molecular data.
    Backes M; Genç B; Schreck J; Doerfler W; Lehmkuhl G; von Gontard A
    Am J Med Genet; 2000 Nov; 95(2):150-6. PubMed ID: 11078566
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 53(3):1023-9. PubMed ID: 20304074
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The behavioral phenotype of FMR1 mutations.
    Boyle L; Kaufmann WE
    Am J Med Genet C Semin Med Genet; 2010 Nov; 154C(4):469-76. PubMed ID: 20981777
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 3(64):64ra1. PubMed ID: 21209411
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 72(2):138-44. PubMed ID: 17661818
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mechanism-based approaches to treating fragile X.
    Dölen G; Carpenter RL; Ocain TD; Bear MF
    Pharmacol Ther; 2010 Jul; 127(1):78-93. PubMed ID: 20303363
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 970():517-51. PubMed ID: 22351071
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 1264():76-84. PubMed ID: 19368811
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical aspects of the fragile X syndrome.
    Brown WT
    Results Probl Cell Differ; 2012; 54():273-9. PubMed ID: 22009358
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Early postnatal plasticity in neocortex of Fmr1 knockout mice.
    Desai NS; Casimiro TM; Gruber SM; Vanderklish PW
    J Neurophysiol; 2006 Oct; 96(4):1734-45. PubMed ID: 16823030
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 111(3):635-46. PubMed ID: 19659572
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India.
    Guruju MR; Lavanya K; Thelma BK; Sujatha M; OmSai VR; Nagarathna V; Amarjyothi P; Jyothi A; Anandaraj MP
    J Clin Neurosci; 2009 Oct; 16(10):1305-10. PubMed ID: 19560928
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 28(2):133-8. PubMed ID: 17435464
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.