These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

63 related articles for article (PubMed ID: 9246495)

  • 21. A new regulatory pathway for fragile X syndrome?
    Hansen RS; Laird CD
    Nat Med; 2002 Nov; 8(11):1204-5. PubMed ID: 12411943
    [No Abstract]   [Full Text] [Related]  

  • 22. Fragile X mental retardation: misregulation of protein synthesis in the developing brain?
    Feng Y
    Microsc Res Tech; 2002 May; 57(3):145-7. PubMed ID: 12112449
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Single-strand conformation polymorphism analysis in the FMR1 gene.
    Castellví-Bel S; Sánchez A; Badenas C; Mallolas J; Barceló A; Jiménez D; Villa M; Estivill X; Milà M
    Am J Med Genet; 1999 May; 84(3):262-5. PubMed ID: 10331603
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Preface: fragile X syndrome: frontiers of understanding gene-brain-behavior relationships.
    Crnic LS; Hagerman R
    Ment Retard Dev Disabil Res Rev; 2004; 10(1):1-2. PubMed ID: 14994281
    [No Abstract]   [Full Text] [Related]  

  • 25. [Fragile X syndrome, a disease caused by defects in an RNA-binding protein].
    Siomi MC; Siomi H
    Tanpakushitsu Kakusan Koso; 2003 Mar; 48(4 Suppl):480-6. PubMed ID: 12696157
    [No Abstract]   [Full Text] [Related]  

  • 26. [Experimental therapeutic models for fragile X syndrome].
    de Diego-Otero Y
    Rev Neurol; 2001 Oct; 33 Suppl 1():S70-6. PubMed ID: 12447824
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular phenotype of Fragile X syndrome: FMRP, FXRPs, and protein targets.
    Kaufmann WE; Cohen S; Sun HT; Ho G
    Microsc Res Tech; 2002 May; 57(3):135-44. PubMed ID: 12112448
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Translational complexity of the fragile x mental retardation protein: insights from the fly.
    Broadie K; Pan L
    Mol Cell; 2005 Mar; 17(6):757-9. PubMed ID: 15780932
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome.
    Koekkoek SK; Yamaguchi K; Milojkovic BA; Dortland BR; Ruigrok TJ; Maex R; De Graaf W; Smit AE; VanderWerf F; Bakker CE; Willemsen R; Ikeda T; Kakizawa S; Onodera K; Nelson DL; Mientjes E; Joosten M; De Schutter E; Oostra BA; Ito M; De Zeeuw CI
    Neuron; 2005 Aug; 47(3):339-52. PubMed ID: 16055059
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouse.
    Bakker CE; de Diego Otero Y; Bontekoe C; Raghoe P; Luteijn T; Hoogeveen AT; Oostra BA; Willemsen R
    Exp Cell Res; 2000 Jul; 258(1):162-70. PubMed ID: 10912798
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Methylation and expression of the FMR1 gene].
    Pintado E; Morón FJ
    Rev Neurol; 2001 Oct; 33 Suppl 1():S57-62. PubMed ID: 12447821
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular screening for fragile X syndrome among Indonesian children with developmental disability.
    Faradz SM; Buckley M; Lam-Po-Tang ; Leigh D; Holden JJ
    Am J Med Genet; 1999 Apr; 83(4):350-1. PubMed ID: 10208179
    [No Abstract]   [Full Text] [Related]  

  • 33. A methylation PCR approach for detection of fragile X syndrome.
    Panagopoulos I; Lassen C; Kristoffersson U; Aman P
    Hum Mutat; 1999; 14(1):71-9. PubMed ID: 10447261
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A phenotypic and molecular characterization of the fmr1-tm1Cgr fragile X mouse.
    Yan QJ; Asafo-Adjei PK; Arnold HM; Brown RE; Bauchwitz RP
    Genes Brain Behav; 2004 Dec; 3(6):337-59. PubMed ID: 15544577
    [TBL] [Abstract][Full Text] [Related]  

  • 35. RNAs that interact with the fragile X syndrome RNA binding protein FMRP.
    Sung YJ; Conti J; Currie JR; Brown WT; Denman RB
    Biochem Biophys Res Commun; 2000 Sep; 275(3):973-80. PubMed ID: 10973830
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fragile X gene.
    Hecht F
    Science; 1991 Sep; 253(5027):1467. PubMed ID: 1896850
    [No Abstract]   [Full Text] [Related]  

  • 37. Fragile X Syndrome Due to a Frameshift Deletion: A Rare Mechanism.
    Arora V; Takkar A; Mehta A; Malleda N; Kumar P
    Indian J Pediatr; 2022 Sep; 89(9):945. PubMed ID: 35857264
    [No Abstract]   [Full Text] [Related]  

  • 38. Neural progenitor cells from an adult patient with fragile X syndrome.
    Schwartz PH; Tassone F; Greco CM; Nethercott HE; Ziaeian B; Hagerman RJ; Hagerman PJ
    BMC Med Genet; 2005 Jan; 6():2. PubMed ID: 15649335
    [TBL] [Abstract][Full Text] [Related]  

  • 39. snRNAs contain specific SMN-binding domains that are essential for snRNP assembly.
    Yong J; Golembe TJ; Battle DJ; Pellizzoni L; Dreyfuss G
    Mol Cell Biol; 2004 Apr; 24(7):2747-56. PubMed ID: 15024064
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sequence-specific interaction of U1 snRNA with the SMN complex.
    Yong J; Pellizzoni L; Dreyfuss G
    EMBO J; 2002 Mar; 21(5):1188-96. PubMed ID: 11867547
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.