209 related articles for article (PubMed ID: 19738907)
1. The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2.
van der Lelij P; Godthelp BC; van Zon W; van Gosliga D; Oostra AB; Steltenpool J; de Groot J; Scheper RJ; Wolthuis RM; Waisfisz Q; Darroudi F; Joenje H; de Winter JP
PLoS One; 2009 Sep; 4(9):e6936. PubMed ID: 19738907
[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. 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]
4. Esco1 and Esco2 regulate distinct cohesin functions during cell cycle progression.
Alomer RM; da Silva EML; Chen J; Piekarz KM; McDonald K; Sansam CG; Sansam CL; Rankin S
Proc Natl Acad Sci U S A; 2017 Sep; 114(37):9906-9911. PubMed ID: 28847955
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. G1-Cyclin2 (Cln2) promotes chromosome hypercondensation in eco1/ctf7 rad61 null cells during hyperthermic stress in Saccharomyces cerevisiae.
Buskirk S; Skibbens RV
G3 (Bethesda); 2022 Jul; 12(8):. PubMed ID: 35736360
[TBL] [Abstract][Full Text] [Related]
10. The replicative helicase MCM recruits cohesin acetyltransferase ESCO2 to mediate centromeric sister chromatid cohesion.
Ivanov MP; Ladurner R; Poser I; Beveridge R; Rampler E; Hudecz O; Novatchkova M; Hériché JK; Wutz G; van der Lelij P; Kreidl E; Hutchins JR; Axelsson-Ekker H; Ellenberg J; Hyman AA; Mechtler K; Peters JM
EMBO J; 2018 Aug; 37(15):. PubMed ID: 29930102
[TBL] [Abstract][Full Text] [Related]
11. Temporal Regulation of ESCO2 Degradation by the MCM Complex, the CUL4-DDB1-VPRBP Complex, and the Anaphase-Promoting Complex.
Minamino M; Tei S; Negishi L; Kanemaki MT; Yoshimura A; Sutani T; Bando M; Shirahige K
Curr Biol; 2018 Aug; 28(16):2665-2672.e5. PubMed ID: 30100344
[TBL] [Abstract][Full Text] [Related]
12. Multivalent interaction of ESCO2 with the replication machinery is required for sister chromatid cohesion in vertebrates.
Bender D; Da Silva EML; Chen J; Poss A; Gawey L; Rulon Z; Rankin S
Proc Natl Acad Sci U S A; 2020 Jan; 117(2):1081-1089. PubMed ID: 31879348
[TBL] [Abstract][Full Text] [Related]
13. Cohesin acetyltransferase Esco2 is a cell viability factor and is required for cohesion in pericentric heterochromatin.
Whelan G; Kreidl E; Wutz G; Egner A; Peters JM; Eichele G
EMBO J; 2012 Jan; 31(1):71-82. PubMed ID: 22101327
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. The cohesin modifier ESCO2 is stable during DNA replication.
Jevitt AM; Rankin BD; Chen J; Rankin S
Chromosome Res; 2023 Jan; 31(1):6. PubMed ID: 36708487
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Two human orthologues of Eco1/Ctf7 acetyltransferases are both required for proper sister-chromatid cohesion.
Hou F; Zou H
Mol Biol Cell; 2005 Aug; 16(8):3908-18. PubMed ID: 15958495
[TBL] [Abstract][Full Text] [Related]
18. DNA double-strand breaks trigger genome-wide sister-chromatid cohesion through Eco1 (Ctf7).
Unal E; Heidinger-Pauli JM; Koshland D
Science; 2007 Jul; 317(5835):245-8. PubMed ID: 17626885
[TBL] [Abstract][Full Text] [Related]
19. Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion.
Vega H; Waisfisz Q; Gordillo M; Sakai N; Yanagihara I; Yamada M; van Gosliga D; Kayserili H; Xu C; Ozono K; Jabs EW; Inui K; Joenje H
Nat Genet; 2005 May; 37(5):468-70. PubMed ID: 15821733
[TBL] [Abstract][Full Text] [Related]
20. Cul4-Ddb1 ubiquitin ligases facilitate DNA replication-coupled sister chromatid cohesion through regulation of cohesin acetyltransferase Esco2.
Sun H; Zhang J; Xin S; Jiang M; Zhang J; Li Z; Cao Q; Lou H
PLoS Genet; 2019 Feb; 15(2):e1007685. PubMed ID: 30779731
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
