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 *

131 related articles for article (PubMed ID: 18403614)

  • 1. A single nucleotide variant in the FMR1 CGG repeat results in a "Pseudodeletion" and is not associated with the fragile X syndrome phenotype.
    Cecconi M; Forzano F; Rinaldi R; Cappellacci S; Grammatico P; Faravelli F; Dagna Bricarelli F; Di Maria E; Grasso M
    J Mol Diagn; 2008 May; 10(3):272-5. PubMed ID: 18403614
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel polymorphism in the FMR1 gene: implications for clinical testing of fragile X syndrome.
    Thyagarajan B; Bower M; Berger M; Jones S; Dolan M; Wang X
    Arch Pathol Lab Med; 2008 Jan; 132(1):95-8. PubMed ID: 18181681
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1.
    Datta S; Alam MP; Majumdar SS; Mehta AK; Maiti S; Wadhwa N; Brahmachari V
    Chromosome Res; 2011 May; 19(4):445-55. PubMed ID: 21499798
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in
    Tekendo-Ngongang C; Grochowsky A; Solomon BD; Yano ST
    Genes (Basel); 2021 Oct; 12(11):. PubMed ID: 34828275
    [No Abstract]   [Full Text] [Related]  

  • 5. Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene.
    Milà M; Castellví-Bel S; Sánchez A; Lázaro C; Villa M; Estivill X
    J Med Genet; 1996 Apr; 33(4):338-40. PubMed ID: 8730293
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene.
    Wang H; Zhu X; Gui B; Cheung WC; Shi M; Yang Z; Kwok KY; Lim R; Pietilä S; Zhu Y; Choy KW
    J Vis Exp; 2019 Sep; (151):. PubMed ID: 31566610
    [TBL] [Abstract][Full Text] [Related]  

  • 7. FMR1 CGG repeat lengths mediate different regulation of reporter gene expression in comparative transient and locus specific integration assays.
    Sølvsten C; Nielsen AL
    Gene; 2011 Oct; 486(1-2):15-22. PubMed ID: 21767618
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome.
    Meijer H; de Graaff E; Merckx DM; Jongbloed RJ; de Die-Smulders CE; Engelen JJ; Fryns JP; Curfs PM; Oostra BA
    Hum Mol Genet; 1994 Apr; 3(4):615-20. PubMed ID: 8069307
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Promoter-bound trinucleotide repeat mRNA drives epigenetic silencing in fragile X syndrome.
    Colak D; Zaninovic N; Cohen MS; Rosenwaks Z; Yang WY; Gerhardt J; Disney MD; Jaffrey SR
    Science; 2014 Feb; 343(6174):1002-5. PubMed ID: 24578575
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype.
    Collins SC; Coffee B; Benke PJ; Berry-Kravis E; Gilbert F; Oostra B; Halley D; Zwick ME; Cutler DJ; Warren ST
    PLoS One; 2010 Mar; 5(3):e9476. PubMed ID: 20221430
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients.
    Grasso M; Faravelli F; Lo Nigro C; Chiurazzi P; Sperandeo MP; Argusti A; Pomponi MG; Lecora M; Sebastio GF; Perroni L; Andria G; Neri G; Bricarelli FD
    Am J Med Genet; 1999 Jul; 85(3):311-6. PubMed ID: 10398249
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spontaneous rescue of a FMR1 repeat expansion and review of deletions in the FMR1 non-coding region.
    Erbs E; Fenger-Grøn J; Jacobsen CM; Lildballe DL; Rasmussen M
    Eur J Med Genet; 2021 Aug; 64(8):104244. PubMed ID: 34022415
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diminished ovarian reserve is not observed in infertility patients with high normal CGG repeats on the fragile X mental retardation 1 (FMR1) gene.
    Schufreider A; McQueen DB; Lee SM; Allon R; Uhler ML; Davie J; Feinberg EC
    Hum Reprod; 2015 Nov; 30(11):2686-92. PubMed ID: 26345686
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expression.
    Grønskov K; Hjalgrim H; Bjerager MO; Brøndum-Nielsen K
    Am J Hum Genet; 1997 Oct; 61(4):961-7. PubMed ID: 9382110
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome.
    Todd PK; Oh SY; Krans A; Pandey UB; Di Prospero NA; Min KT; Taylor JP; Paulson HL
    PLoS Genet; 2010 Dec; 6(12):e1001240. PubMed ID: 21170301
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome.
    Xie N; Gong H; Suhl JA; Chopra P; Wang T; Warren ST
    PLoS One; 2016; 11(10):e0165499. PubMed ID: 27768763
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Chromatin changes caused by CGG repeat expansion in fmr1 gene].
    Yudkin DV; Lemskaya NA; Grischenko IV; Dolskiy AA
    Mol Biol (Mosk); 2015; 49(2):205-11. PubMed ID: 26065250
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Contraction of fully expanded FMR1 alleles to the normal range: predisposing haplotype or rare events?
    Maia N; Loureiro JR; Oliveira B; Marques I; Santos R; Jorge P; Martins S
    J Hum Genet; 2017 Feb; 62(2):269-275. PubMed ID: 27784894
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing.
    Ardui S; Race V; Zablotskaya A; Hestand MS; Van Esch H; Devriendt K; Matthijs G; Vermeesch JR
    Hum Mutat; 2017 Mar; 38(3):324-331. PubMed ID: 27883256
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population.
    Garcia Arocena D; Breece KE; Hagerman PJ
    Hum Genet; 2003 Oct; 113(5):371-6. PubMed ID: 12905066
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.