BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 8957513)

  • 1. Inability to induce fragile sites at CTG repeats in congenital myotonic dystrophy.
    Wenger SL; Giangreco CA; Tarleton J; Wessel HB
    Am J Med Genet; 1996 Dec; 66(1):60-3. PubMed ID: 8957513
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophy.
    Jalal SM; Lindor NM; Michels VV; Buckley DD; Hoppe DA; Sarkar G; Dewald GW
    Am J Med Genet; 1993 Jun; 46(4):441-3. PubMed ID: 8357018
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosomal fragile site expression in dogs: I. Breed specific differences.
    Stone DM; Jacky PB; Hancock DD; Prieur DJ
    Am J Med Genet; 1991 Aug; 40(2):214-22. PubMed ID: 1910263
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Myotonic dystrophy gene analysis in affected Israeli families.
    Achiron A; Magal N; Shem-Tov N; Noy S; Shohat M; Gadoth N
    Isr J Med Sci; 1994 Aug; 30(8):622-5. PubMed ID: 8045745
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expression of folate sensitive and aphidicolin induced chromosomal fragile sites in familial neuroblastoma.
    Ankathil R; Kusumakumary P; Priyakumary T; Krishnan Nair M
    J Exp Clin Cancer Res; 2002 Sep; 21(3):383-8. PubMed ID: 12385582
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein.
    Sarafidou T; Kahl C; Martinez-Garay I; Mangelsdorf M; Gesk S; Baker E; Kokkinaki M; Talley P; Maltby EL; French L; Harder L; Hinzmann B; Nobile C; Richkind K; Finnis M; Deloukas P; Sutherland GR; Kutsche K; Moschonas NK; Siebert R; Gécz J;
    Genomics; 2004 Jul; 84(1):69-81. PubMed ID: 15203205
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations.
    Rubinsztein DC; Leggo J; Amos W; Barton DE; Ferguson-Smith MA
    Hum Mol Genet; 1994 Nov; 3(11):2031-5. PubMed ID: 7874122
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy.
    Tsilfidis C; MacKenzie AE; Mettler G; Barceló J; Korneluk RG
    Nat Genet; 1992 Jun; 1(3):192-5. PubMed ID: 1303233
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [DNA analysis of a pedigree with myotonic dystrophy in Songjiang county, Shanghai].
    Xie H; Zheng H; Zheng S; Deng B; Xu J; Cui Y; Wang Y; Xu Z; Ren D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Oct; 17(5):319-22. PubMed ID: 11024209
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Myotonic dystrophy: another case of too many repeats?
    Shelbourne P; Johnson K
    Hum Mutat; 1992; 1(3):183-9. PubMed ID: 1301924
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DNA analysis in a suspected individual with myotonic dystrophy family history and her abortus.
    Bi X; Xie H; Zheng H; Ding S; Zhang S; Wang Y; Xu Z; Ren D
    Chin Med J (Engl); 2002 Nov; 115(11):1628-31. PubMed ID: 12609075
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Human chromosome fragility.
    Lukusa T; Fryns JP
    Biochim Biophys Acta; 2008 Jan; 1779(1):3-16. PubMed ID: 18078840
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Direct detection of novel expanded trinucleotide repeats in the human genome.
    Schalling M; Hudson TJ; Buetow KH; Housman DE
    Nat Genet; 1993 Jun; 4(2):135-9. PubMed ID: 8348150
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Excess thymidine induces folate sensitive fragile sites.
    Sutherland GR; Baker E; Fratini A
    Am J Med Genet; 1985 Oct; 22(2):433-43. PubMed ID: 4050872
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations.
    Krummel KA; Roberts LR; Kawakami M; Glover TW; Smith DI
    Genomics; 2000 Oct; 69(1):37-46. PubMed ID: 11013073
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The lower incidence of myotonic dystrophy in Ashkenazic Jews compared to North African Jews is associated with a significantly lower number of CTG trinucleotide repeats.
    Mor-Cohen R; Magal N; Gadoth N; Achiron A; Shohat T; Shohat M
    Isr J Med Sci; 1997 Mar; 33(3):190-3. PubMed ID: 9313789
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus.
    Filippova GN; Thienes CP; Penn BH; Cho DH; Hu YJ; Moore JM; Klesert TR; Lobanenkov VV; Tapscott SJ
    Nat Genet; 2001 Aug; 28(4):335-43. PubMed ID: 11479593
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Bromodeoxyuridine induces chromosomal fragile sites in the canine genome.
    Stone DM; Stephens KE
    Am J Med Genet; 1993 Apr; 46(2):198-202. PubMed ID: 8484410
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.
    Hunter AG; Jacob P; O'Hoy K; MacDonald I; Mettler G; Tsilfidis C; Korneluk RG
    Am J Med Genet; 1993 Feb; 45(3):401-7. PubMed ID: 8434633
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Expression of new fragile sites detected in lymphoproliferative processes].
    Fundia AF; Slavutsky IR; Larripa IB
    Sangre (Barc); 1990 Feb; 35(1):4-9. PubMed ID: 2139745
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.