Structure, dynamics and functions of promyelocytic leukaemia nuclear bodies
By R. Bernardi, P. Pandolfi. Nature reviews. Molecular cell biology, 2007
923 citations recorded by the source corpus.
Subfields: Hematology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/496508a97eb44dd2b9a3a63789ea38e250033d18
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Citations in the corpus
- A PML-PPARδ pathway for fatty acid oxidation regulates haematopoietic stem cell maintenance (2012, background): “The PML (promyelocytic leukemia) tumor-suppressor gene, originally cloned at the break point of the t(15;17) chromosomal translocation of acute promyelocytic leukemia, has a key role in the maintenance of HSCs16.”
- The SUMO pathway: emerging mechanisms that shape specificity, conjugation and recognition (2010, background): “This process is exemplified by the base excision repair enzyme thymine DNA glycosylase (TDG), promyelocytic leukaemia protein (PML) and the transcription factor DAXX, and has been reviewed previousl”
- Biogenesis and Function of Nuclear Bodies (2011, background): “nuclear domain 10, ND10), is essential for PML-NB formation since human leukemia and solid tumors cells in which the PML gene is inactivated and pml-/- mouse cells fail to assemble PML-NBs [24].”
- Genome-wide identification of Polycomb-associated RNAs by RIP-seq (2010, background): “Because misregulation of Polycomb proteins is often associated with cancer, we intersected PRC2-interacting RNAs with oncogene and tumor suppressor loci (Sparmann and van Lohuizen, 2006; Bernardi and Pandolfi, 2007; Miremadi et al., 2007; Rajasekhar and Begemann, 2007; Simon and Lange, 2008).”
- Phase Transitions in the Assembly of Multi-Valent Signaling Proteins (2012, background): “These include promyelocytic leukaemia nuclear bodies, Cajal bodies, P bodies and P granule”
- Liquid phase condensation in cell physiology and disease (2017, background): “Given the ability of a small subset of proteins to drive phase separation, how might these proteins recruit other molecules into the droplet? Important insights have come from recent work using repetitive domains of the binding partners small ubiquitin-like modifier (SUMO) and the SUMO interacting m”