Pages that link to "Q21142763"

The following pages link to The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2 (Q21142763):

Displaying 39 items.

• Ribosomopathies: Global process, tissue specific defects (Q26781112) (← links)
• Cohesin and human disease: lessons from mouse models (Q26783549) (← links)
• Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies (Q26861558) (← links)
• Cohesinopathies of a feather flock together (Q26999444) (← links)
• The ancient and evolving roles of cohesin in gene expression and DNA repair (Q27014855) (← links)
• Cohesin: functions beyond sister chromatid cohesion (Q28294084) (← links)
• Cohesin acetyltransferase Esco2 is a cell viability factor and is required for cohesion in pericentric heterochromatin (Q28512361) (← links)
• The non-redundant function of cohesin acetyltransferase Esco2: some answers and new questions (Q29347246) (← links)
• Essential genes for astroglial development and axon pathfinding during zebrafish embryogenesis (Q30497206) (← links)
• Defective sister chromatid cohesion is synthetically lethal with impaired APC/C function. (Q30667509) (← links)
• Cohesin Proteins Promote Ribosomal RNA Production and Protein Translation in Yeast and Human Cells (Q34311599) (← links)
• Sister acts: coordinating DNA replication and cohesion establishment (Q34411870) (← links)
• Stimulation of mTORC1 with L-leucine rescues defects associated with Roberts syndrome. (Q35008883) (← links)
• Complex elaboration: making sense of meiotic cohesin dynamics (Q35812288) (← links)
• Improved transcription and translation with L-leucine stimulation of mTORC1 in Roberts syndrome (Q35884792) (← links)
• Sororin actively maintains sister chromatid cohesion (Q36712636) (← links)
• Arabidopsis CHROMOSOME TRANSMISSION FIDELITY 7 (AtCTF7/ECO1) is required for DNA repair, mitosis and meiosis (Q37298383) (← links)
• Cohesinopathies, gene expression, and chromatin organization (Q37733997) (← links)
• Cohesin: a critical chromatin organizer in mammalian gene regulation (Q37919509) (← links)
• The Ubiquitin/SUMO Pathway and Radial Ray Deficiency Syndromes (Q37991103) (← links)
• Diverse developmental disorders from the one ring: distinct molecular pathways underlie the cohesinopathies (Q38044384) (← links)
• Roberts syndrome: A deficit in acetylated cohesin leads to nucleolar dysfunction (Q38233048) (← links)
• BAF180 promotes cohesion and prevents genome instability and aneuploidy (Q38786462) (← links)
• Genome stability: What we have learned from cohesinopathies. (Q38811354) (← links)
• How many roads lead to cohesinopathies? (Q39250491) (← links)
• Eco1 is important for DNA damage repair in S. cerevisiae. (Q39595930) (← links)
• Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome (Q42078992) (← links)
• Translational mechanisms at work in the cohesinopathies (Q42391399) (← links)
• A sliding scale: the many faces of Ctf7/Eco1 cohesion establishment factor in DNA repair (Q42708986) (← links)
• Cohesin acetyltransferase Esco2 regulates SAC and kinetochore functions via maintaining H4K16 acetylation during mouse oocyte meiosis (Q47767068) (← links)
• The Opposing Actions of Arabidopsis CHROMOSOME TRANSMISSION FIDELITY7 and WINGS APART-LIKE1 and 2 Differ in Mitotic and Meiotic Cells. (Q48253582) (← links)
• The replicative helicase MCM recruits cohesin acetyltransferase ESCO2 to mediate centromeric sister chromatid cohesion (Q57753489) (← links)
• Can corruption of chromosome cohesion create a conduit to cancer? (Q83423039) (← links)
• Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2 (Q92626488) (← links)
• VU1199-F (Q98134603) (← links)
• VU1199-F SV40 (Q98134605) (← links)
• VU1199-F SV40+GFP-ESCO2 (Q98134607) (← links)
• VU1199-F SV40+V5-ESCO2 (Q98134609) (← links)
• Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion (Q98778525) (← links)