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 *

133 related articles for article (PubMed ID: 11562939)

  • 1. Annexin-1 is abnormally expressed in fragile X syndrome: two-dimensional electrophoresis study in lymphocytes.
    Sun HT; Cohen S; Kaufmann WE
    Am J Med Genet; 2001 Sep; 103(1):81-90. PubMed ID: 11562939
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype, molecular phenotype, and cognitive phenotype: correlations in fragile X syndrome.
    Kaufmann WE; Abrams MT; Chen W; Reiss AL
    Am J Med Genet; 1999 Apr; 83(4):286-95. PubMed ID: 10208163
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: a new perspective.
    Loesch DZ; Huggins RM; Bui QM; Taylor AK; Hagerman RJ
    Am J Med Genet A; 2003 Apr; 118A(2):127-34. PubMed ID: 12655493
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Selective Deletion of Astroglial FMRP Dysregulates Glutamate Transporter GLT1 and Contributes to Fragile X Syndrome Phenotypes In Vivo.
    Higashimori H; Schin CS; Chiang MS; Morel L; Shoneye TA; Nelson DL; Yang Y
    J Neurosci; 2016 Jul; 36(27):7079-94. PubMed ID: 27383586
    [TBL] [Abstract][Full Text] [Related]  

  • 6. FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome.
    Abrams MT; Kaufmann WE; Rousseau F; Oostra BA; Wolozin B; Taylor CV; Lishaa N; Morel ML; Hoogeveen A; Reiss AL
    Am J Med Genet; 1999 Jan; 82(1):25-30. PubMed ID: 9916838
    [TBL] [Abstract][Full Text] [Related]  

  • 7. FMRP expression as a potential prognostic indicator in fragile X syndrome.
    Tassone F; Hagerman RJ; Iklé DN; Dyer PN; Lampe M; Willemsen R; Oostra BA; Taylor AK
    Am J Med Genet; 1999 May; 84(3):250-61. PubMed ID: 10331602
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The fragile X syndrome.
    Hoogeveen AT; Oostra BA
    J Inherit Metab Dis; 1997 Jun; 20(2):139-51. PubMed ID: 9211186
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cells.
    Schrier M; Severijnen LA; Reis S; Rife M; van't Padje S; van Cappellen G; Oostra BA; Willemsen R
    Exp Neurol; 2004 Oct; 189(2):343-53. PubMed ID: 15380484
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics.
    de Vries BB; Severijnen LA; Jacobs A; Olmer R; Halley DJ; Oostra BA; Willemsen R
    J Med Genet; 2003 Jul; 40(7):535-9. PubMed ID: 12843328
    [No Abstract]   [Full Text] [Related]  

  • 11. Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?
    Salat U; Bardoni B; Wöhrle D; Steinbach P
    J Med Genet; 2000 Nov; 37(11):842-50. PubMed ID: 11073538
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evidence that fragile X mental retardation protein is a negative regulator of translation.
    Laggerbauer B; Ostareck D; Keidel EM; Ostareck-Lederer A; Fischer U
    Hum Mol Genet; 2001 Feb; 10(4):329-38. PubMed ID: 11157796
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Expression of the FMR1 gene.
    Tassone F; Hagerman PJ
    Cytogenet Genome Res; 2003; 100(1-4):124-8. PubMed ID: 14526172
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Expression of fragile X mental retardation-1 gene with nuclear export signal mutation changes the expression profiling of mouse cerebella immortal neuronal cell.
    Hu L; Chen Y; Evers S; Shen Y
    Proteomics; 2005 Oct; 5(15):3979-90. PubMed ID: 16130171
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.
    Taylor AK; Safanda JF; Fall MZ; Quince C; Lang KA; Hull CE; Carpenter I; Staley LW; Hagerman RJ
    JAMA; 1994 Feb; 271(7):507-14. PubMed ID: 8301764
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fragile X-like behaviors and abnormal cortical dendritic spines in cytoplasmic FMR1-interacting protein 2-mutant mice.
    Han K; Chen H; Gennarino VA; Richman R; Lu HC; Zoghbi HY
    Hum Mol Genet; 2015 Apr; 24(7):1813-23. PubMed ID: 25432536
    [TBL] [Abstract][Full Text] [Related]  

  • 18. FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association.
    Feng Y; Absher D; Eberhart DE; Brown V; Malter HE; Warren ST
    Mol Cell; 1997 Dec; 1(1):109-18. PubMed ID: 9659908
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Transcription of the FMR1 gene in individuals with fragile X syndrome.
    Tassone F; Hagerman RJ; Chamberlain WD; Hagerman PJ
    Am J Med Genet; 2000; 97(3):195-203. PubMed ID: 11449488
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures.
    Myrick LK; Deng PY; Hashimoto H; Oh YM; Cho Y; Poidevin MJ; Suhl JA; Visootsak J; Cavalli V; Jin P; Cheng X; Warren ST; Klyachko VA
    Proc Natl Acad Sci U S A; 2015 Jan; 112(4):949-56. PubMed ID: 25561520
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.