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 *

497 related articles for article (PubMed ID: 12905066)

  • 1. 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]  

  • 2. Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population.
    Patsalis PC; Sismani C; Stylianou S; Ioannou P; Joseph G; Manoli P; Holden JJ; Hettinger JA
    Am J Med Genet; 1999 May; 84(3):217-20. PubMed ID: 10331595
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.
    Eichler EE; Macpherson JN; Murray A; Jacobs PA; Chakravarti A; Nelson DL
    Hum Mol Genet; 1996 Mar; 5(3):319-30. PubMed ID: 8852655
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fragile X founder effects and new mutations in Finland.
    Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; Wang D; Ju W; Nolin S; Dobkin C; Ryynänen M; Brown WT
    Am J Med Genet; 1996 Jul; 64(1):226-33. PubMed ID: 8826481
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Methylation mosaicism of 5'-(CGG)(n)-3' repeats in fragile X, premutation and normal individuals.
    Genç B; Müller-Hartmann H; Zeschnigk M; Deissler H; Schmitz B; Majewski F; von Gontard A; Doerfler W
    Nucleic Acids Res; 2000 May; 28(10):2141-52. PubMed ID: 10773084
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular diagnosis of fragile X syndrome and distribution of CGG repeats in the FMR-1 gene in Taiwanese.
    Wang YC; Li C; Lin ML; Lin WH; Li SY
    J Formos Med Assoc; 2000 May; 99(5):402-7. PubMed ID: 10870330
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.
    Eichler EE; Hammond HA; Macpherson JN; Ward PA; Nelson DL
    Hum Mol Genet; 1995 Dec; 4(12):2199-208. PubMed ID: 8634688
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.
    Gunter C; Paradee W; Crawford DC; Meadows KA; Newman J; Kunst CB; Nelson DL; Schwartz C; Murray A; Macpherson JN; Sherman SL; Warren ST
    Hum Mol Genet; 1998 Nov; 7(12):1935-46. PubMed ID: 9811938
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CGG repeat interruptions in the FMR1 gene in patients with infantile autism.
    Poon PM; Chen QL; Lai KY; Wong CK; Pang CP
    Clin Chem Lab Med; 1998 Aug; 36(8):649-53. PubMed ID: 9806479
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X alleles.
    Larsen LA; Armstrong JS; Grønskov K; Hjalgrim H; Macpherson JN; Brøndum-Nielsen K; Hasholt L; Nørgaard-Pedersen B; Vuust J
    Am J Med Genet; 2000 Jul; 93(2):99-106. PubMed ID: 10869110
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia.
    Larsen LA; Vuust J; Nystad M; Evseeva I; Van Ghelue M; Tranebjaerg L
    Eur J Hum Genet; 2001 Sep; 9(9):724-7. PubMed ID: 11571563
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Instability of a premutation-sized CGG repeat in FMR1 YAC transgenic mice.
    Peier AM; Nelson DL
    Genomics; 2002 Oct; 80(4):423-32. PubMed ID: 12376097
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Instability of a (CGG)98 repeat in the Fmr1 promoter.
    Bontekoe CJ; Bakker CE; Nieuwenhuizen IM; van der Linde H; Lans H; de Lange D; Hirst MC; Oostra BA
    Hum Mol Genet; 2001 Aug; 10(16):1693-9. PubMed ID: 11487573
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles.
    Dombrowski C; Lévesque S; Morel ML; Rouillard P; Morgan K; Rousseau F
    Hum Mol Genet; 2002 Feb; 11(4):371-8. PubMed ID: 11854169
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Instability of the CGG repeat at the FRAXA locus and variable phenotypic expression in a large fragile X pedigree.
    Pintado E; de Diego Y; Hmadcha A; Carrasco M; Sierra J; Lucas M
    J Med Genet; 1995 Nov; 32(11):907-8. PubMed ID: 8592340
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. FMR1 premutation allele (CGG)81 is stable in mice.
    Bontekoe CJ; de Graaff E; Nieuwenhuizen IM; Willemsen R; Oostra BA
    Eur J Hum Genet; 1997; 5(5):293-8. PubMed ID: 9412786
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.