BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

343 related articles for article (PubMed ID: 10894953)

  • 1. DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.
    Tuck-Muller CM; Narayan A; Tsien F; Smeets DF; Sawyer J; Fiala ES; Sohn OS; Ehrlich M
    Cytogenet Cell Genet; 2000; 89(1-2):121-8. PubMed ID: 10894953
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNA hypomethylation, cancer, the immunodeficiency, centromeric region instability, facial anomalies syndrome and chromosomal rearrangements.
    Ehrlich M
    J Nutr; 2002 Aug; 132(8 Suppl):2424S-2429S. PubMed ID: 12163705
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Subcellular distribution of HP1 proteins is altered in ICF syndrome.
    Luciani JJ; Depetris D; Missirian C; Mignon-Ravix C; Metzler-Guillemain C; Megarbane A; Moncla A; Mattei MG
    Eur J Hum Genet; 2005 Jan; 13(1):41-51. PubMed ID: 15470359
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.
    Miniou P; Jeanpierre M; Blanquet V; Sibella V; Bonneau D; Herbelin C; Fischer A; Niveleau A; Viegas-Péquignot E
    Hum Mol Genet; 1994 Dec; 3(12):2093-102. PubMed ID: 7881405
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF).
    Ehrlich M; Jackson K; Weemaes C
    Orphanet J Rare Dis; 2006 Mar; 1():2. PubMed ID: 16722602
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells.
    Gisselsson D; Shao C; Tuck-Muller CM; Sogorovic S; Pålsson E; Smeets D; Ehrlich M
    Chromosoma; 2005 Jul; 114(2):118-26. PubMed ID: 15856360
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DNA demethylation and pericentromeric rearrangements of chromosome 1.
    Ji W; Hernandez R; Zhang XY; Qu GZ; Frady A; Varela M; Ehrlich M
    Mutat Res; 1997 Sep; 379(1):33-41. PubMed ID: 9330620
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prolonged culture of normal chorionic villus cells yields ICF syndrome-like chromatin decondensation and rearrangements.
    Tsien F; Fiala ES; Youn B; Long TI; Laird PW; Weissbecker K; Ehrlich M
    Cytogenet Genome Res; 2002; 98(1):13-21. PubMed ID: 12584436
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Satellite DNA hypomethylation vs. overall genomic hypomethylation in ovarian epithelial tumors of different malignant potential.
    Qu G; Dubeau L; Narayan A; Yu MC; Ehrlich M
    Mutat Res; 1999 Jan; 423(1-2):91-101. PubMed ID: 10029684
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replication.
    Hassan KM; Norwood T; Gimelli G; Gartler SM; Hansen RS
    Hum Genet; 2001 Oct; 109(4):452-62. PubMed ID: 11702227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies.
    Turleau C; Cabanis MO; Girault D; Ledeist F; Mettey R; Puissant H; Prieur M; de Grouchy J
    Am J Med Genet; 1989 Mar; 32(3):420-4. PubMed ID: 2729362
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes.
    Ehrlich M; Buchanan KL; Tsien F; Jiang G; Sun B; Uicker W; Weemaes CM; Smeets D; Sperling K; Belohradsky BH; Tommerup N; Misek DE; Rouillard JM; Kuick R; Hanash SM
    Hum Mol Genet; 2001 Dec; 10(25):2917-31. PubMed ID: 11741835
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2.
    Kondo T; Bobek MP; Kuick R; Lamb B; Zhu X; Narayan A; Bourc'his D; Viegas-Péquignot E; Ehrlich M; Hanash SM
    Hum Mol Genet; 2000 Mar; 9(4):597-604. PubMed ID: 10699183
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A FISH study of chromosome fusion in the ICF syndrome: involvement of paracentric heterochromatin but not of the centromeres themselves.
    Sumner AT; Mitchell AR; Ellis PM
    J Med Genet; 1998 Oct; 35(10):833-5. PubMed ID: 9783707
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.
    Jeanpierre M; Turleau C; Aurias A; Prieur M; Ledeist F; Fischer A; Viegas-Pequignot E
    Hum Mol Genet; 1993 Jun; 2(6):731-5. PubMed ID: 8102570
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Defective de novo methylation of viral and cellular DNA sequences in ICF syndrome cells.
    Tao Q; Huang H; Geiman TM; Lim CY; Fu L; Qiu GH; Robertson KD
    Hum Mol Genet; 2002 Sep; 11(18):2091-102. PubMed ID: 12189161
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome.
    Dupont C; Guimiot F; Perrin L; Marey I; Smiljkovski D; Le Tessier D; Lebugle C; Baumann C; Bourdoncle P; Tabet AC; Aboura A; Benzacken B; Dupont JM
    Clin Genet; 2012 Aug; 82(2):187-92. PubMed ID: 21554265
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [ICF syndrome. Immunodeficiency, chromosomal centromere instability, facial anomalies. Case report and literature review].
    Kieback P; Wendisch H; Lorenz P; Hinkel K
    Monatsschr Kinderheilkd; 1992 Feb; 140(2):91-4. PubMed ID: 1557060
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosome instability in ICF syndrome: formation of micronuclei from multibranched chromosomes 1 demonstrated by fluorescence in situ hybridization.
    Sawyer JR; Swanson CM; Wheeler G; Cunniff C
    Am J Med Genet; 1995 Mar; 56(2):203-9. PubMed ID: 7625446
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Non-random length distribution of individual telomeres in immunodeficiency, centromeric instability and facial anomalies syndrome, type I.
    Sagie S; Edni O; Weinberg J; Toubiana S; Kozlovski T; Frostig T; Katzin N; Bar-Am I; Selig S
    Hum Mol Genet; 2017 Nov; 26(21):4244-4256. PubMed ID: 28973513
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.