212 related articles for article (PubMed ID: 26206533)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA.
Revenkova E; Focarelli ML; Susani L; Paulis M; Bassi MT; Mannini L; Frattini A; Delia D; Krantz I; Vezzoni P; Jessberger R; Musio A
Hum Mol Genet; 2009 Feb; 18(3):418-27. PubMed ID: 18996922
[TBL] [Abstract][Full Text] [Related]
10. Impairment of Retinoic Acid Signaling in Cornelia de Lange Syndrome Fibroblasts.
Fazio G; Bettini LR; Rigamonti S; Meta D; Biondi A; Cazzaniga G; Selicorni A; Massa V
Birth Defects Res; 2017 Oct; 109(16):1268-1276. PubMed ID: 28752682
[TBL] [Abstract][Full Text] [Related]
11. Structural aspects of HDAC8 mechanism and dysfunction in Cornelia de Lange syndrome spectrum disorders.
Deardorff MA; Porter NJ; Christianson DW
Protein Sci; 2016 Nov; 25(11):1965-1976. PubMed ID: 27576763
[TBL] [Abstract][Full Text] [Related]
12. Overall and allele-specific expression of the SMC1A gene in female Cornelia de Lange syndrome patients and healthy controls.
Parenti I; Rovina D; Masciadri M; Cereda A; Azzollini J; Picinelli C; Limongelli G; Finelli P; Selicorni A; Russo S; Gervasini C; Larizza L
Epigenetics; 2014 Jul; 9(7):973-9. PubMed ID: 24756084
[TBL] [Abstract][Full Text] [Related]
13. Could a patient with SMC1A duplication be classified as a human cohesinopathy?
Baquero-Montoya C; Gil-Rodríguez MC; Teresa-Rodrigo ME; Hernández-Marcos M; Bueno-Lozano G; Bueno-Martínez I; Remeseiro S; Fernández-Hernández R; Bassecourt-Serra M; Rodríguez de Alba M; Queralt E; Losada A; Puisac B; Ramos FJ; Pié J
Clin Genet; 2014 May; 85(5):446-51. PubMed ID: 23683030
[TBL] [Abstract][Full Text] [Related]
14. Mutations and variants in the cohesion factor genes NIPBL, SMC1A, and SMC3 in a cohort of 30 unrelated patients with Cornelia de Lange syndrome.
Pié J; Gil-Rodríguez MC; Ciero M; López-Viñas E; Ribate MP; Arnedo M; Deardorff MA; Puisac B; Legarreta J; de Karam JC; Rubio E; Bueno I; Baldellou A; Calvo MT; Casals N; Olivares JL; Losada A; Hegardt FG; Krantz ID; Gómez-Puertas P; Ramos FJ
Am J Med Genet A; 2010 Apr; 152A(4):924-9. PubMed ID: 20358602
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Mutation spectrum and genotype-phenotype correlation in Cornelia de Lange syndrome.
Mannini L; Cucco F; Quarantotti V; Krantz ID; Musio A
Hum Mutat; 2013 Dec; 34(12):1589-96. PubMed ID: 24038889
[TBL] [Abstract][Full Text] [Related]
17. Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes.
Yuan B; Pehlivan D; Karaca E; Patel N; Charng WL; Gambin T; Gonzaga-Jauregui C; Sutton VR; Yesil G; Bozdogan ST; Tos T; Koparir A; Koparir E; Beck CR; Gu S; Aslan H; Yuregir OO; Al Rubeaan K; Alnaqeb D; Alshammari MJ; Bayram Y; Atik MM; Aydin H; Geckinli BB; Seven M; Ulucan H; Fenercioglu E; Ozen M; Jhangiani S; Muzny DM; Boerwinkle E; Tuysuz B; Alkuraya FS; Gibbs RA; Lupski JR
J Clin Invest; 2015 Feb; 125(2):636-51. PubMed ID: 25574841
[TBL] [Abstract][Full Text] [Related]
18. Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation.
Deardorff MA; Kaur M; Yaeger D; Rampuria A; Korolev S; Pie J; Gil-Rodríguez C; Arnedo M; Loeys B; Kline AD; Wilson M; Lillquist K; Siu V; Ramos FJ; Musio A; Jackson LS; Dorsett D; Krantz ID
Am J Hum Genet; 2007 Mar; 80(3):485-94. PubMed ID: 17273969
[TBL] [Abstract][Full Text] [Related]
19. Mutant cohesin affects RNA polymerase II regulation in Cornelia de Lange syndrome.
Mannini L; C Lamaze F; Cucco F; Amato C; Quarantotti V; Rizzo IM; Krantz ID; Bilodeau S; Musio A
Sci Rep; 2015 Nov; 5():16803. PubMed ID: 26581180
[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]
