BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 21777673)

  • 1. Esco2 promotes neuronal differentiation by repressing Notch signaling.
    Leem YE; Choi HK; Jung SY; Kim BJ; Lee KY; Yoon K; Qin J; Kang JS; Kim ST
    Cell Signal; 2011 Nov; 23(11):1876-84. PubMed ID: 21777673
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.
    Gordillo M; Vega H; Trainer AH; Hou F; Sakai N; Luque R; Kayserili H; Basaran S; Skovby F; Hennekam RC; Uzielli ML; Schnur RE; Manouvrier S; Chang S; Blair E; Hurst JA; Forzano F; Meins M; Simola KO; Raas-Rothschild A; Schultz RA; McDaniel LD; Ozono K; Inui K; Zou H; Jabs EW
    Hum Mol Genet; 2008 Jul; 17(14):2172-80. PubMed ID: 18411254
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Establishment and characterization of Roberts syndrome and SC phocomelia model medaka (Oryzias latipes).
    Morita A; Nakahira K; Hasegawa T; Uchida K; Taniguchi Y; Takeda S; Toyoda A; Sakaki Y; Shimada A; Takeda H; Yanagihara I
    Dev Growth Differ; 2012 Jun; 54(5):588-604. PubMed ID: 22694322
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Variations in dysfunction of sister chromatid cohesion in esco2 mutant zebrafish reflect the phenotypic diversity of Roberts syndrome.
    Percival SM; Thomas HR; Amsterdam A; Carroll AJ; Lees JA; Yost HJ; Parant JM
    Dis Model Mech; 2015 Aug; 8(8):941-55. PubMed ID: 26044958
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The non-redundant function of cohesin acetyltransferase Esco2: some answers and new questions.
    Whelan G; Kreidl E; Peters JM; Eichele G
    Nucleus; 2012 Jul; 3(4):330-4. PubMed ID: 22614755
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Roberts syndrome in an Indian patient with humeroradial synostosis, congenital elbow contractures and a novel homozygous splice variant in ESCO2.
    Schneeberger PE; Nayak SS; Fuchs S; Kutsche K; Girisha KM
    Am J Med Genet A; 2020 Nov; 182(11):2793-2796. PubMed ID: 32783269
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An ever-changing landscape in Roberts syndrome biology: Implications for macromolecular damage.
    Mfarej MG; Skibbens RV
    PLoS Genet; 2020 Dec; 16(12):e1009219. PubMed ID: 33382686
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2.
    Faramarz A; Balk JA; van Schie JJM; Oostra AB; Ghandour CA; Rooimans MA; Wolthuis RMF; de Lange J
    PLoS One; 2020; 15(1):e0220348. PubMed ID: 31935221
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A zebrafish model of Roberts syndrome reveals that Esco2 depletion interferes with development by disrupting the cell cycle.
    Mönnich M; Kuriger Z; Print CG; Horsfield JA
    PLoS One; 2011; 6(5):e20051. PubMed ID: 21637801
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Stimulation of mTORC1 with L-leucine rescues defects associated with Roberts syndrome.
    Xu B; Lee KK; Zhang L; Gerton JL
    PLoS Genet; 2013; 9(10):e1003857. PubMed ID: 24098154
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ikaros represses the transcriptional response to Notch signaling in T-cell development.
    Kleinmann E; Geimer Le Lay AS; Sellars M; Kastner P; Chan S
    Mol Cell Biol; 2008 Dec; 28(24):7465-75. PubMed ID: 18852286
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Improved transcription and translation with L-leucine stimulation of mTORC1 in Roberts syndrome.
    Xu B; Gogol M; Gaudenz K; Gerton JL
    BMC Genomics; 2016 Jan; 17():25. PubMed ID: 26729373
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The effects of conformational heterogeneity on the binding of the Notch intracellular domain to effector proteins: a case of biologically tuned disorder.
    Bertagna A; Toptygin D; Brand L; Barrick D
    Biochem Soc Trans; 2008 Apr; 36(Pt 2):157-66. PubMed ID: 18363556
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of Nepro, a gene required for the maintenance of neocortex neural progenitor cells downstream of Notch.
    Muroyama Y; Saito T
    Development; 2009 Dec; 136(23):3889-93. PubMed ID: 19906856
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Roberts Syndrome Individual With Differential Genotoxin Sensitivity and a DNA Damage Response Defect.
    McKay MJ; Craig J; Kalitsis P; Kozlov S; Verschoor S; Chen P; Lobachevsky P; Vasireddy R; Yan Y; Ryan J; McGillivray G; Savarirayan R; Lavin MF; Ramsay RG; Xu H
    Int J Radiat Oncol Biol Phys; 2019 Apr; 103(5):1194-1202. PubMed ID: 30508616
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetically induced redox stress occurs in a yeast model for Roberts syndrome.
    Mfarej MG; Skibbens RV
    G3 (Bethesda); 2022 Feb; 12(2):. PubMed ID: 34897432
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.
    Mengen E; Kotan LD; Ucakturk SA; Topaloglu AK; Yuksel B
    J Coll Physicians Surg Pak; 2018 May; 28(5):403-405. PubMed ID: 29690975
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromatin determinants of the inner-centromere rely on replication factors with functions that impart cohesion.
    Abe T; Kawasumi R; Arakawa H; Hori T; Shirahige K; Losada A; Fukagawa T; Branzei D
    Oncotarget; 2016 Oct; 7(42):67934-67947. PubMed ID: 27636994
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hypopigmented patches in Roberts/SC phocomelia syndrome occur via aneuploidy susceptibility.
    Sezer A; Kayhan G; Zenker M; Percin EF
    Eur J Med Genet; 2019 Dec; 62(12):103608. PubMed ID: 30590172
    [TBL] [Abstract][Full Text] [Related]  

  • 20. RBP-J promotes the maturation of neuronal progenitors.
    Komine O; Nagaoka M; Hiraoka Y; Hoshino M; Kawaguchi Y; Pear WS; Tanaka K
    Dev Biol; 2011 Jun; 354(1):44-54. PubMed ID: 21443869
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.