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UnknownPot1 and cell cycle progression cooperate in telomere length regulation.
Not available
S-EPMC2516480 | biostudies-literature
UnknownRad59-facilitated acquisition of Y' elements by short telomeres delays the onset of senescence.
Not available
S-EPMC4222662 | biostudies-literature
UnknownHeterozygous <i>RPA2</i> variant as a novel genetic cause of telomere biology disorders.
Not available
S-EPMC11444173 | biostudies-literature
UnknownStructural Insights into Yeast Telomerase Recruitment to Telomeres.
Not available
S-EPMC5839504 | biostudies-literature
UnknownTERT expression attenuates metabolic disorders in obese mice by promoting adipose stem and progenitor cell expansion and differentiation.
Not available
S-EPMC12550303 | biostudies-literature
UnknownUFMylation of MRE11 is essential for telomere length maintenance and hematopoietic stem cell survival.
Not available
S-EPMC8462904 | biostudies-literature
UnknownTOP3A amplification and ATRX inactivation are mutually exclusive events in pediatric osteosarcomas using ALT.
Not available
S-EPMC9549729 | biostudies-literature
ProteomicsSearching for new members of the SLX4 complex and for SLX4-complex members that are SUMOylated in vitro
The project was initially aimed at identifying new members of the SLX4 complex as well as members of the complex that are SUMOylated in vitro. The project was also aimed at assessing whether SUMOylation may change the compositon of the complex by reducing complex association of SUMOylated partners. ...
ORGANISM(S): Homo sapiens (Human) 
2020-03-05 | PXD012425 | Pride
Slx4 scaffold Protein sumoylation Interactome 
ProteomicsSearching for binding partners of the SLX4 577-795 region and assessing the impact of the SLX4 D614G and L618P cancer patient-derived mutations on their association with SLX4
The project was aimed at identifying new binding partners of SLX4 that associate with a region spanning the conserved amphipathic helix of SLX4 and the downstream BTB domain. It was also aimed at assessing which of those partners might have their association with SLX4 abrogated by the cancer patient...
ORGANISM(S): Homo sapiens (Human) 
2020-03-05 | PXD012426 | Pride
Slx4 scaffold Protein-protein binding domain Cancer associated mutations Interactome 
UnknownInherited human Apollo deficiency causes severe bone marrow failure and developmental defects.
Not available
S-EPMC11022855 | biostudies-literature
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