BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

223 related articles for article (PubMed ID: 21559330)

  • 21. Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient.
    Heyn H; Vidal E; Sayols S; Sanchez-Mut JV; Moran S; Medina I; Sandoval J; Simó-Riudalbas L; Szczesna K; Huertas D; Gatto S; Matarazzo MR; Dopazo J; Esteller M
    Epigenetics; 2012 Jun; 7(6):542-50. PubMed ID: 22595875
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Altered intra-nuclear organisation of heterochromatin and genes in ICF syndrome.
    Jefferson A; Colella S; Moralli D; Wilson N; Yusuf M; Gimelli G; Ragoussis J; Volpi EV
    PLoS One; 2010 Jun; 5(6):e11364. PubMed ID: 20613881
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions.
    Yehezkel S; Segev Y; Viegas-Péquignot E; Skorecki K; Selig S
    Hum Mol Genet; 2008 Sep; 17(18):2776-89. PubMed ID: 18558631
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease.
    Ehrlich M
    Clin Immunol; 2003 Oct; 109(1):17-28. PubMed ID: 14585272
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Immunodeficiency, Centromeric Region Instability, and Facial Anomalies Syndrome (ICF) in a Boy with Variable Clinical and Immunological Presentations.
    Bemanian MH; Arshi S; Nabavi M; Vafaee-Shahi M; Fallahpour M; Shokri S; Rezaeifar A; Shahzadi H; Atashrazm F
    Iran J Allergy Asthma Immunol; 2021 Apr; 20(2):249-254. PubMed ID: 33904683
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and Immunological Characterization of ICF Syndrome in Japan.
    Kamae C; Imai K; Kato T; Okano T; Honma K; Nakagawa N; Yeh TW; Noguchi E; Ohara A; Shigemura T; Takahashi H; Takakura S; Hayashi M; Honma A; Watanabe S; Shigemori T; Ohara O; Sasaki H; Kubota T; Morio T; Kanegane H; Nonoyama S
    J Clin Immunol; 2018 Nov; 38(8):927-937. PubMed ID: 30353301
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Molecular landscape of modified histones in Drosophila heterochromatic genes and euchromatin-heterochromatin transition zones.
    Yasuhara JC; Wakimoto BT
    PLoS Genet; 2008 Jan; 4(1):e16. PubMed ID: 18208336
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genome-Wide DNA Methylation Analysis Identifies Novel Hypomethylated Non-Pericentromeric Genes with Potential Clinical Implications in ICF Syndrome.
    Simo-Riudalbas L; Diaz-Lagares A; Gatto S; Gagliardi M; Crujeiras AB; Matarazzo MR; Esteller M; Sandoval J
    PLoS One; 2015; 10(7):e0132517. PubMed ID: 26161907
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Cell cycle-dependent accumulation of histone H3.3 and euchromatic histone modifications in pericentromeric heterochromatin in response to a decrease in DNA methylation levels.
    Sugimura K; Fukushima Y; Ishida M; Ito S; Nakamura M; Mori Y; Okumura K
    Exp Cell Res; 2010 Oct; 316(17):2731-46. PubMed ID: 20599948
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The gene mutations and subtelomeric DNA methylation in immunodeficiency, centromeric instability and facial anomalies syndrome.
    Hu H; Chen C; Shi S; Li B; Duan S
    Autoimmunity; 2019; 52(5-6):192-198. PubMed ID: 31476899
    [TBL] [Abstract][Full Text] [Related]  

  • 34. DNMT3B PWWP mutations cause hypermethylation of heterochromatin.
    Taglini F; Kafetzopoulos I; Rolls W; Musialik KI; Lee HY; Zhang Y; Marenda M; Kerr L; Finan H; Rubio-Ramon C; Gautier P; Wapenaar H; Kumar D; Davidson-Smith H; Wills J; Murphy LC; Wheeler A; Wilson MD; Sproul D
    EMBO Rep; 2024 Mar; 25(3):1130-1155. PubMed ID: 38291337
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Germline genes hypomethylation and expression define a molecular signature in peripheral blood of ICF patients: implications for diagnosis and etiology.
    Velasco G; Walton EL; Sterlin D; Hédouin S; Nitta H; Ito Y; Fouyssac F; Mégarbané A; Sasaki H; Picard C; Francastel C
    Orphanet J Rare Dis; 2014 Apr; 9():56. PubMed ID: 24742017
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Three novel DNMT3B mutations in Japanese patients with ICF syndrome.
    Shirohzu H; Kubota T; Kumazawa A; Sado T; Chijiwa T; Inagaki K; Suetake I; Tajima S; Wakui K; Miki Y; Hayashi M; Fukushima Y; Sasaki H
    Am J Med Genet; 2002 Sep; 112(1):31-7. PubMed ID: 12239717
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9.
    Kloeckener-Gruissem B; Betts DR; Zankl A; Berger W; Güngör T
    Am J Med Genet A; 2005 Jul; 136(1):31-7. PubMed ID: 15952214
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability and facial anomalies syndrome with distinctive genome-wide DNA hypomethylation.
    Unoki M; Velasco G; Kori S; Arita K; Daigaku Y; Yeung WKA; Fujimoto A; Ohashi H; Kubota T; Miyake K; Sasaki H
    Hum Mol Genet; 2023 Apr; 32(9):1439-1456. PubMed ID: 36458887
    [TBL] [Abstract][Full Text] [Related]  

  • 40. DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.
    Jiang YL; Rigolet M; Bourc'his D; Nigon F; Bokesoy I; Fryns JP; Hultén M; Jonveaux P; Maraschio P; Mégarbané A; Moncla A; Viegas-Péquignot E
    Hum Mutat; 2005 Jan; 25(1):56-63. PubMed ID: 15580563
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.