420 related articles for article (PubMed ID: 22039349)
1. 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]
2. 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]
3. Using mouse and zebrafish models to understand the etiology of developmental defects in Cornelia de Lange Syndrome.
Kawauchi S; Santos R; Muto A; Lopez-Burks ME; Schilling TF; Lander AD; Calof AL
Am J Med Genet C Semin Med Genet; 2016 Jun; 172(2):138-45. PubMed ID: 27120001
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome.
Kawauchi S; Calof AL; Santos R; Lopez-Burks ME; Young CM; Hoang MP; Chua A; Lao T; Lechner MS; Daniel JA; Nussenzweig A; Kitzes L; Yokomori K; Hallgrimsson B; Lander AD
PLoS Genet; 2009 Sep; 5(9):e1000650. PubMed ID: 19763162
[TBL] [Abstract][Full Text] [Related]
6. Nipbl and mediator cooperatively regulate gene expression to control limb development.
Muto A; Ikeda S; Lopez-Burks ME; Kikuchi Y; Calof AL; Lander AD; Schilling TF
PLoS Genet; 2014 Sep; 10(9):e1004671. PubMed ID: 25255084
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. CyclinD1 Down-Regulation and Increased Apoptosis Are Common Features of Cohesinopathies.
Fazio G; Gaston-Massuet C; Bettini LR; Graziola F; Scagliotti V; Cereda A; Ferrari L; Mazzola M; Cazzaniga G; Giordano A; Cotelli F; Bellipanni G; Biondi A; Selicorni A; Pistocchi A; Massa V
J Cell Physiol; 2016 Mar; 231(3):613-22. PubMed ID: 26206533
[TBL] [Abstract][Full Text] [Related]
12. Disruption of NIPBL/Scc2 in Cornelia de Lange Syndrome provokes cohesin genome-wide redistribution with an impact in the transcriptome.
Garcia P; Fernandez-Hernandez R; Cuadrado A; Coca I; Gomez A; Maqueda M; Latorre-Pellicer A; Puisac B; Ramos FJ; Sandoval J; Esteller M; Mosquera JL; Rodriguez J; Pié J; Losada A; Queralt E
Nat Commun; 2021 Jul; 12(1):4551. PubMed ID: 34315879
[TBL] [Abstract][Full Text] [Related]
13. Reduction of Nipbl impairs cohesin loading locally and affects transcription but not cohesion-dependent functions in a mouse model of Cornelia de Lange Syndrome.
Remeseiro S; Cuadrado A; Kawauchi S; Calof AL; Lander AD; Losada A
Biochim Biophys Acta; 2013 Dec; 1832(12):2097-102. PubMed ID: 23920377
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Drosophila Nipped-B Mutants Model Cornelia de Lange Syndrome in Growth and Behavior.
Wu Y; Gause M; Xu D; Misulovin Z; Schaaf CA; Mosarla RC; Mannino E; Shannon M; Jones E; Shi M; Chen WF; Katz OL; Sehgal A; Jongens TA; Krantz ID; Dorsett D
PLoS Genet; 2015 Nov; 11(11):e1005655. PubMed ID: 26544867
[TBL] [Abstract][Full Text] [Related]
16. Cornelia de Lange Syndrome: NIPBL haploinsufficiency downregulates canonical Wnt pathway in zebrafish embryos and patients fibroblasts.
Pistocchi A; Fazio G; Cereda A; Ferrari L; Bettini LR; Messina G; Cotelli F; Biondi A; Selicorni A; Massa V
Cell Death Dis; 2013 Oct; 4(10):e866. PubMed ID: 24136230
[TBL] [Abstract][Full Text] [Related]
17. Cornelia de Lange syndrome mutations in NIPBL can impair cohesin-mediated DNA loop extrusion.
Panarotto M; Davidson IF; Litos G; Schleiffer A; Peters JM
Proc Natl Acad Sci U S A; 2022 May; 119(18):e2201029119. PubMed ID: 35476527
[TBL] [Abstract][Full Text] [Related]
18. NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome.
Tonkin ET; Wang TJ; Lisgo S; Bamshad MJ; Strachan T
Nat Genet; 2004 Jun; 36(6):636-41. PubMed ID: 15146185
[TBL] [Abstract][Full Text] [Related]
19. Genetic enhancement of limb defects in a mouse model of Cornelia de Lange syndrome.
Lopez-Burks ME; Santos R; Kawauchi S; Calof AL; Lander AD
Am J Med Genet C Semin Med Genet; 2016 Jun; 172(2):146-54. PubMed ID: 27120109
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
