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 *

145 related articles for article (PubMed ID: 8418955)

  • 1. Epigenetic inheritance based on DNA methylation.
    Holliday R
    EXS; 1993; 64():452-68. PubMed ID: 8418955
    [No Abstract]   [Full Text] [Related]  

  • 2. Hereditary unstable DNA: a new explanation for some old genetic questions?
    Sutherland GR; Haan EA; Kremer E; Lynch M; Pritchard M; Yu S; Richards RI
    Lancet; 1991 Aug; 338(8762):289-92. PubMed ID: 1677119
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The unstable and methylatable mutations causing the fragile X syndrome.
    Rousseau F; Heitz D; Mandel JL
    Hum Mutat; 1992; 1(2):91-6. PubMed ID: 1301206
    [No Abstract]   [Full Text] [Related]  

  • 4. Fragile X syndrome and other dynamic mutation diseases.
    Sutherland GR; Richards RI
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():77-85. PubMed ID: 8629146
    [No Abstract]   [Full Text] [Related]  

  • 5. DNA methylation and genomic imprinting in mammals.
    Sasaki H; Allen ND; Surani MA
    EXS; 1993; 64():469-86. PubMed ID: 8418956
    [No Abstract]   [Full Text] [Related]  

  • 6. Fragile X expression is decreased by 5-azacytidine and S-adenosylhomocysteine.
    Mixon JC; Dev VG
    Am J Hum Genet; 1983 Nov; 35(6):1270-5. PubMed ID: 6196967
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The fragile-X syndrome, IV. Progress towards the identification of linked restriction fragment length variants (RFLVs).
    Holden JJ; Wang HS; White BN
    Am J Med Genet; 1984 Jan; 17(1):259-73. PubMed ID: 6324593
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic mapping of the human X chromosome: linkage analysis of the q26-q28 region that includes the fragile X locus and isolation of expressed sequences.
    Mandel JL; Arveiler B; Camerino G; Hanauer A; Heilig R; Koenig M; Oberlé I
    Cold Spring Harb Symp Quant Biol; 1986; 51 Pt 1():195-203. PubMed ID: 3472716
    [No Abstract]   [Full Text] [Related]  

  • 9. Molecular genetics of the human X chromosome.
    Davies KE
    J Med Genet; 1985 Aug; 22(4):243-9. PubMed ID: 2995673
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage.
    Warren ST; Knight SJ; Peters JF; Stayton CL; Consalez GG; Zhang FP
    Proc Natl Acad Sci U S A; 1990 May; 87(10):3856-60. PubMed ID: 2339126
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microsatellites and disease: a new paradigm.
    Wrogemann K; Biancalana V; Devys D; Imbert G; Trottier Y; Mandel JL
    EXS; 1993; 67():141-52. PubMed ID: 8400686
    [No Abstract]   [Full Text] [Related]  

  • 12. Concerning the role of X-inactivation and DNA methylation in fragile X syndrome.
    Migeon BR
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):291-8. PubMed ID: 1605203
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular basis of genetic instability of triplet repeats.
    Wells RD
    J Biol Chem; 1996 Feb; 271(6):2875-8. PubMed ID: 8621672
    [No Abstract]   [Full Text] [Related]  

  • 14. Dynamic mutations: a new class of mutations causing human disease.
    Richards RI; Sutherland GR
    Cell; 1992 Sep; 70(5):709-12. PubMed ID: 1516128
    [No Abstract]   [Full Text] [Related]  

  • 15. Unstable triplet repeat diseases.
    Monckton DG; Caskey CT
    Circulation; 1995 Jan; 91(2):513-20. PubMed ID: 7805257
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CpG islands.
    Antequera F; Bird A
    EXS; 1993; 64():169-85. PubMed ID: 8418949
    [No Abstract]   [Full Text] [Related]  

  • 17. [Unstable DNA sequence and methylation in fragile X syndrome].
    Fu SD; Shen Y; Fan Y
    Zhonghua Yi Xue Za Zhi; 1994 Oct; 74(10):611-4, 646-7. PubMed ID: 7842338
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.
    Patterson M; Bell M; Schwartz C; Davies K
    Am J Med Genet; 1988; 30(1-2):581-91. PubMed ID: 3177471
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Strategy for molecular cloning of the fragile X site DNA.
    Warren ST; Zhang FP; Sutcliffe JS; Peters JF
    Am J Med Genet; 1988; 30(1-2):613-23. PubMed ID: 3177473
    [TBL] [Abstract][Full Text] [Related]  

  • 20. DNA methylation represses FMR-1 transcription in fragile X syndrome.
    Sutcliffe JS; Nelson DL; Zhang F; Pieretti M; Caskey CT; Saxe D; Warren ST
    Hum Mol Genet; 1992 Sep; 1(6):397-400. PubMed ID: 1301913
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.