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 *

150 related articles for article (PubMed ID: 18854353)

  • 1. The Cohesin loading factor NIPBL recruits histone deacetylases to mediate local chromatin modifications.
    Jahnke P; Xu W; Wülling M; Albrecht M; Gabriel H; Gillessen-Kaesbach G; Kaiser FJ
    Nucleic Acids Res; 2008 Nov; 36(20):6450-8. PubMed ID: 18854353
    [TBL] [Abstract][Full Text] [Related]  

  • 2. HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle.
    Deardorff MA; Bando M; Nakato R; Watrin E; Itoh T; Minamino M; Saitoh K; Komata M; Katou Y; Clark D; Cole KE; De Baere E; Decroos C; Di Donato N; Ernst S; Francey LJ; Gyftodimou Y; Hirashima K; Hullings M; Ishikawa Y; Jaulin C; Kaur M; Kiyono T; Lombardi PM; Magnaghi-Jaulin L; Mortier GR; Nozaki N; Petersen MB; Seimiya H; Siu VM; Suzuki Y; Takagaki K; Wilde JJ; Willems PJ; Prigent C; Gillessen-Kaesbach G; Christianson DW; Kaiser FJ; Jackson LG; Hirota T; Krantz ID; Shirahige K
    Nature; 2012 Sep; 489(7415):313-7. PubMed ID: 22885700
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The effect of Nipped-B-like (Nipbl) haploinsufficiency on genome-wide cohesin binding and target gene expression: modeling Cornelia de Lange syndrome.
    Newkirk DA; Chen YY; Chien R; Zeng W; Biesinger J; Flowers E; Kawauchi S; Santos R; Calof AL; Lander AD; Xie X; Yokomori K
    Clin Epigenetics; 2017; 9():89. PubMed ID: 28855971
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Regional chromatin decompaction in Cornelia de Lange syndrome associated with NIPBL disruption can be uncoupled from cohesin and CTCF.
    Nolen LD; Boyle S; Ansari M; Pritchard E; Bickmore WA
    Hum Mol Genet; 2013 Oct; 22(20):4180-93. PubMed ID: 23760082
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A cohesin-independent role for NIPBL at promoters provides insights in CdLS.
    Zuin J; Franke V; van Ijcken WF; van der Sloot A; Krantz ID; van der Reijden MI; Nakato R; Lenhard B; Wendt KS
    PLoS Genet; 2014 Feb; 10(2):e1004153. PubMed ID: 24550742
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Regulation of the cohesin-loading factor NIPBL: Role of the lncRNA NIPBL-AS1 and identification of a distal enhancer element.
    Zuin J; Casa V; Pozojevic J; Kolovos P; van den Hout MCGN; van Ijcken WFJ; Parenti I; Braunholz D; Baron Y; Watrin E; Kaiser FJ; Wendt KS
    PLoS Genet; 2017 Dec; 13(12):e1007137. PubMed ID: 29261648
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The zinc finger repressor, ZBP-89, recruits histone deacetylase 1 to repress vimentin gene expression.
    Wu Y; Zhang X; Salmon M; Zehner ZE
    Genes Cells; 2007 Aug; 12(8):905-18. PubMed ID: 17663720
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular characterization of a mosaic NIPBL deletion in a Cornelia de Lange patient with severe phenotype.
    Gervasini C; Parenti I; Picinelli C; Azzollini J; Masciadri M; Cereda A; Selicorni A; Russo S; Finelli P; Larizza L
    Eur J Med Genet; 2013 Mar; 56(3):138-43. PubMed ID: 23313159
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients.
    Schoumans J; Wincent J; Barbaro M; Djureinovic T; Maguire P; Forsberg L; Staaf J; Thuresson AC; Borg A; Nordgren A; Malm G; Anderlid BM
    Eur J Hum Genet; 2007 Feb; 15(2):143-9. PubMed ID: 17106445
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cornelia de Lange syndrome case due to genomic rearrangements including NIPBL.
    Ratajska M; Wierzba J; Pehlivan D; Xia Z; Brundage EK; Cheung SW; Stankiewicz P; Lupski JR; Limon J
    Eur J Med Genet; 2010; 53(6):378-82. PubMed ID: 20727427
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Father-to-daughter transmission of Cornelia de Lange syndrome caused by a mutation in the 5' untranslated region of the NIPBL Gene.
    Borck G; Zarhrate M; Cluzeau C; Bal E; Bonnefont JP; Munnich A; Cormier-Daire V; Colleaux L
    Hum Mutat; 2006 Aug; 27(8):731-5. PubMed ID: 16799922
    [TBL] [Abstract][Full Text] [Related]  

  • 12. NIPBL Controls RNA Biogenesis to Prevent Activation of the Stress Kinase PKR.
    Yuen KC; Xu B; Krantz ID; Gerton JL
    Cell Rep; 2016 Jan; 14(1):93-102. PubMed ID: 26725122
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interaction with members of the heterochromatin protein 1 (HP1) family and histone deacetylation are differentially involved in transcriptional silencing by members of the TIF1 family.
    Nielsen AL; Ortiz JA; You J; Oulad-Abdelghani M; Khechumian R; Gansmuller A; Chambon P; Losson R
    EMBO J; 1999 Nov; 18(22):6385-95. PubMed ID: 10562550
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Recruitment of chromatin-modifying enzymes by CTIP2 promotes HIV-1 transcriptional silencing.
    Marban C; Suzanne S; Dequiedt F; de Walque S; Redel L; Van Lint C; Aunis D; Rohr O
    EMBO J; 2007 Jan; 26(2):412-23. PubMed ID: 17245431
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DNMT3B interacts with hSNF2H chromatin remodeling enzyme, HDACs 1 and 2, and components of the histone methylation system.
    Geiman TM; Sankpal UT; Robertson AK; Zhao Y; Zhao Y; Robertson KD
    Biochem Biophys Res Commun; 2004 May; 318(2):544-55. PubMed ID: 15120635
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MBP-1 physically associates with histone deacetylase for transcriptional repression.
    Ghosh AK; Steele R; Ray RB
    Biochem Biophys Res Commun; 1999 Jul; 260(2):405-9. PubMed ID: 10403782
    [TBL] [Abstract][Full Text] [Related]  

  • 17. MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange Syndrome.
    Parenti I; Diab F; Gil SR; Mulugeta E; Casa V; Berutti R; Brouwer RWW; Dupé V; Eckhold J; Graf E; Puisac B; Ramos F; Schwarzmayr T; Gines MM; van Staveren T; van IJcken WFJ; Strom TM; Pié J; Watrin E; Kaiser FJ; Wendt KS
    Cell Rep; 2020 May; 31(7):107647. PubMed ID: 32433956
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromatin-associated regulation of HIV-1 transcription: implications for the development of therapeutic strategies.
    Quivy V; De Walque S; Van Lint C
    Subcell Biochem; 2007; 41():371-96. PubMed ID: 17484137
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Biochemical and structural characterization of HDAC8 mutants associated with Cornelia de Lange syndrome spectrum disorders.
    Decroos C; Christianson NH; Gullett LE; Bowman CM; Christianson KE; Deardorff MA; Christianson DW
    Biochemistry; 2015 Oct; 54(42):6501-13. PubMed ID: 26463496
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutation.
    Selicorni A; Russo S; Gervasini C; Castronovo P; Milani D; Cavalleri F; Bentivegna A; Masciadri M; Domi A; Divizia MT; Sforzini C; Tarantino E; Memo L; Scarano G; Larizza L
    Clin Genet; 2007 Aug; 72(2):98-108. PubMed ID: 17661813
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.