BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 8242066)

  • 1. Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins.
    Richards RI; Holman K; Yu S; Sutherland GR
    Hum Mol Genet; 1993 Sep; 2(9):1429-35. PubMed ID: 8242066
    [TBL] [Abstract][Full Text] [Related]  

  • 2. High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome.
    Hornstra IK; Nelson DL; Warren ST; Yang TP
    Hum Mol Genet; 1993 Oct; 2(10):1659-65. PubMed ID: 8268919
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Purification of nuclear proteins from human HeLa cells that bind specifically to the unstable tandem repeat (CGG)n in the human FMR1 gene.
    Deissler H; Behn-Krappa A; Doerfler W
    J Biol Chem; 1996 Feb; 271(8):4327-34. PubMed ID: 8626781
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human Ku antigen tightly binds and stabilizes a tetrahelical form of the Fragile X syndrome d(CGG)n expanded sequence.
    Uliel L; Weisman-Shomer P; Oren-Jazan H; Newcomb T; Loeb LA; Fry M
    J Biol Chem; 2000 Oct; 275(42):33134-41. PubMed ID: 10924524
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fragile X syndrome without CCG amplification has an FMR1 deletion.
    Gedeon AK; Baker E; Robinson H; Partington MW; Gross B; Manca A; Korn B; Poustka A; Yu S; Sutherland GR
    Nat Genet; 1992 Aug; 1(5):341-4. PubMed ID: 1302032
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Methylation analysis of CGG sites in the CpG island of the human FMR1 gene.
    Hansen RS; Gartler SM; Scott CR; Chen SH; Laird CD
    Hum Mol Genet; 1992 Nov; 1(8):571-8. PubMed ID: 1301165
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island.
    Gu Y; Shen Y; Gibbs RA; Nelson DL
    Nat Genet; 1996 May; 13(1):109-13. PubMed ID: 8673086
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.
    Kremer EJ; Pritchard M; Lynch M; Yu S; Holman K; Baker E; Warren ST; Schlessinger D; Sutherland GR; Richards RI
    Science; 1991 Jun; 252(5013):1711-4. PubMed ID: 1675488
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Methylation of expanded CCG triplet repeat DNA from fragile X syndrome patients enhances nucleosome exclusion.
    Wang YH; Griffith J
    J Biol Chem; 1996 Sep; 271(38):22937-40. PubMed ID: 8798475
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients.
    de Graaff E; Rouillard P; Willems PJ; Smits AP; Rousseau F; Oostra BA
    Hum Mol Genet; 1995 Jan; 4(1):45-9. PubMed ID: 7711733
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fragile-X syndrome: unique genetics of the heritable unstable element.
    Yu S; Mulley J; Loesch D; Turner G; Donnelly A; Gedeon A; Hillen D; Kremer E; Lynch M; Pritchard M
    Am J Hum Genet; 1992 May; 50(5):968-80. PubMed ID: 1570846
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.
    Ritchie RJ; Knight SJ; Hirst MC; Grewal PK; Bobrow M; Cross GS; Davies KE
    Hum Mol Genet; 1994 Dec; 3(12):2115-21. PubMed ID: 7881407
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Transmitting males and carrier females in fragile X--revisited.
    Loesch DZ; Hay DA; Mulley J
    Am J Med Genet; 1994 Jul; 51(4):392-9. PubMed ID: 7943005
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.
    Chaudhary AG; Hussein IR; Abuzenadah A; Gari M; Bassiouni R; Sogaty S; Lary S; Al-Quaiti M; Al Balwi M; Al Qahtani M
    Pediatr Neurol; 2014 Apr; 50(4):368-76. PubMed ID: 24630283
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation.
    Snow K; Tester DJ; Kruckeberg KE; Schaid DJ; Thibodeau SN
    Hum Mol Genet; 1994 Sep; 3(9):1543-51. PubMed ID: 7833909
    [TBL] [Abstract][Full Text] [Related]  

  • 19. CGG-repeat dynamics and
    Zhou Y; Kumari D; Sciascia N; Usdin K
    Mol Autism; 2016; 7():42. PubMed ID: 27713816
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of the gene FMR2, associated with FRAXE mental retardation.
    Gecz J; Gedeon AK; Sutherland GR; Mulley JC
    Nat Genet; 1996 May; 13(1):105-8. PubMed ID: 8673085
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.