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 *

323 related articles for article (PubMed ID: 22988450)

  • 1. Diverse developmental disorders from the one ring: distinct molecular pathways underlie the cohesinopathies.
    Horsfield JA; Print CG; Mönnich M
    Front Genet; 2012; 3():171. PubMed ID: 22988450
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The expanding phenotypes of cohesinopathies: one ring to rule them all!
    Piché J; Van Vliet PP; Pucéat M; Andelfinger G
    Cell Cycle; 2019 Nov; 18(21):2828-2848. PubMed ID: 31516082
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Cornelia de Lange Syndrome mutations in SMC1A cause cohesion defects in yeast.
    Chen J; Floyd EN; Dawson DS; Rankin S
    Genetics; 2023 Oct; 225(2):. PubMed ID: 37650609
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies.
    Ball AR; Chen YY; Yokomori K
    Biochim Biophys Acta; 2014 Mar; 1839(3):191-202. PubMed ID: 24269489
    [TBL] [Abstract][Full Text] [Related]  

  • 6. How many roads lead to cohesinopathies?
    Banerji R; Skibbens RV; Iovine MK
    Dev Dyn; 2017 Nov; 246(11):881-888. PubMed ID: 28422453
    [TBL] [Abstract][Full Text] [Related]  

  • 7. BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome.
    García-Gutiérrez P; García-Domínguez M
    Front Mol Biosci; 2021; 8():709232. PubMed ID: 34386522
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multifactorial origins of heart and gut defects in nipbl-deficient zebrafish, a model of Cornelia de Lange Syndrome.
    Muto A; Calof AL; Lander AD; Schilling TF
    PLoS Biol; 2011 Oct; 9(10):e1001181. PubMed ID: 22039349
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cohesinopathies of a feather flock together.
    Skibbens RV; Colquhoun JM; Green MJ; Molnar CA; Sin DN; Sullivan BJ; Tanzosh EE
    PLoS Genet; 2013; 9(12):e1004036. PubMed ID: 24367282
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Roles of the sister chromatid cohesion apparatus in gene expression, development, and human syndromes.
    Dorsett D
    Chromosoma; 2007 Feb; 116(1):1-13. PubMed ID: 16819604
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cohesin: functions beyond sister chromatid cohesion.
    Mehta GD; Kumar R; Srivastava S; Ghosh SK
    FEBS Lett; 2013 Aug; 587(15):2299-312. PubMed ID: 23831059
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cohesin mediates Esco2-dependent transcriptional regulation in a zebrafish regenerating fin model of Roberts Syndrome.
    Banerji R; Skibbens RV; Iovine MK
    Biol Open; 2017 Dec; 6(12):1802-1813. PubMed ID: 29084713
    [TBL] [Abstract][Full Text] [Related]  

  • 13. L-leucine partially rescues translational and developmental defects associated with zebrafish models of Cornelia de Lange syndrome.
    Xu B; Sowa N; Cardenas ME; Gerton JL
    Hum Mol Genet; 2015 Mar; 24(6):1540-55. PubMed ID: 25378554
    [TBL] [Abstract][Full Text] [Related]  

  • 14. RAD21 mutations cause a human cohesinopathy.
    Deardorff MA; Wilde JJ; Albrecht M; Dickinson E; Tennstedt S; Braunholz D; Mönnich M; Yan Y; Xu W; Gil-Rodríguez MC; Clark D; Hakonarson H; Halbach S; Michelis LD; Rampuria A; Rossier E; Spranger S; Van Maldergem L; Lynch SA; Gillessen-Kaesbach G; Lüdecke HJ; Ramsay RG; McKay MJ; Krantz ID; Xu H; Horsfield JA; Kaiser FJ
    Am J Hum Genet; 2012 Jun; 90(6):1014-27. PubMed ID: 22633399
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cornelia de Lange Syndrome as Paradigm of Chromatinopathies.
    Parenti I; Kaiser FJ
    Front Neurosci; 2021; 15():774950. PubMed ID: 34803598
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cornelia de Lange syndrome, cohesin, and beyond.
    Liu J; Krantz ID
    Clin Genet; 2009 Oct; 76(4):303-14. PubMed ID: 19793304
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Zebrafish as a Model to Study Cohesin and Cohesinopathies.
    Muto A; Schilling TF
    Methods Mol Biol; 2017; 1515():177-196. PubMed ID: 27797080
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Functional links between Drosophila Nipped-B and cohesin in somatic and meiotic cells.
    Gause M; Webber HA; Misulovin Z; Haller G; Rollins RA; Eissenberg JC; Bickel SE; Dorsett D
    Chromosoma; 2008 Feb; 117(1):51-66. PubMed ID: 17909832
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cohesin biology and the cohesinopathies: Abstracts from the Second Biennial Conference, Pontignano, Italy, 2009.
    Musio A; Krantz ID
    Am J Med Genet A; 2010 Jul; 152A(7):1630-40. PubMed ID: 20583191
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Esco2 regulates cx43 expression during skeletal regeneration in the zebrafish fin.
    Banerji R; Eble DM; Iovine MK; Skibbens RV
    Dev Dyn; 2016 Jan; 245(1):7-21. PubMed ID: 26434741
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.