The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2
about
Ribosomopathies: Global process, tissue specific defectsMechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathiesCohesinopathies of a feather flock togetherThe ancient and evolving roles of cohesin in gene expression and DNA repairCohesin: functions beyond sister chromatid cohesionCohesin acetyltransferase Esco2 is a cell viability factor and is required for cohesion in pericentric heterochromatinThe non-redundant function of cohesin acetyltransferase Esco2: some answers and new questions.Essential genes for astroglial development and axon pathfinding during zebrafish embryogenesis.Defective sister chromatid cohesion is synthetically lethal with impaired APC/C function.Cohesin proteins promote ribosomal RNA production and protein translation in yeast and human cells.Sister acts: coordinating DNA replication and cohesion establishment.Stimulation of mTORC1 with L-leucine rescues defects associated with Roberts syndrome.Complex elaboration: making sense of meiotic cohesin dynamicsImproved transcription and translation with L-leucine stimulation of mTORC1 in Roberts syndromeSororin actively maintains sister chromatid cohesion.Arabidopsis CHROMOSOME TRANSMISSION FIDELITY 7 (AtCTF7/ECO1) is required for DNA repair, mitosis and meiosis.Cohesinopathies, gene expression, and chromatin organization.Cohesin: a critical chromatin organizer in mammalian gene regulationDiverse developmental disorders from the one ring: distinct molecular pathways underlie the cohesinopathies.Roberts syndrome: A deficit in acetylated cohesin leads to nucleolar dysfunction.BAF180 promotes cohesion and prevents genome instability and aneuploidy.Genome stability: What we have learned from cohesinopathies.How many roads lead to cohesinopathies?Eco1 is important for DNA damage repair in S. cerevisiae.Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage SyndromeTranslational mechanisms at work in the cohesinopathies.A sliding scale: the many faces of Ctf7/Eco1 cohesion establishment factor in DNA repair.Cohesin acetyltransferase Esco2 regulates SAC and kinetochore functions via maintaining H4K16 acetylation during mouse oocyte meiosis.The Opposing Actions of Arabidopsis CHROMOSOME TRANSMISSION FIDELITY7 and WINGS APART-LIKE1 and 2 Differ in Mitotic and Meiotic Cells.The replicative helicase MCM recruits cohesin acetyltransferase ESCO2 to mediate centromeric sister chromatid cohesion
P2860
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P2860
The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2
description
2009 nî lūn-bûn
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2009 թուականին հրատարակուած գիտական յօդուած
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2009 թվականին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
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name
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@ast
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@en
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@en-gb
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@nl
type
label
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@ast
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@en
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@en-gb
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@nl
altLabel
The Cellular Phenotype of Robe ...... by Ectopic Expression of ESCO2
@en
prefLabel
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@ast
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@en
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@en-gb
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@nl
P2093
P2860
P1433
P1476
The cellular phenotype of Robe ...... by ectopic expression of ESCO2
@en
P2093
Anneke B Oostra
Barbara C Godthelp
Djoke van Gosliga
Firouz Darroudi
Jan de Groot
Johan P de Winter
Jûrgen Steltenpool
Petra van der Lelij
Rik J Scheper
Rob M Wolthuis
P2860
P356
10.1371/JOURNAL.PONE.0006936
P407
P577
2009-01-01T00:00:00Z