Pages that link to "Q24540662"
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The following pages link to Proteolytic cleavage of MLL generates a complex of N- and C-terminal fragments that confers protein stability and subnuclear localization (Q24540662):
Displaying 50 items.
- Leukemia proto-oncoprotein MLL forms a SET1-like histone methyltransferase complex with menin to regulate Hox gene expression (Q24297027) (← links)
- Taspase1: a threonine aspartase required for cleavage of MLL and proper HOX gene expression (Q24300473) (← links)
- Histone methyltransferase MLL1 regulates MDR1 transcription and chemoresistance (Q24300652) (← links)
- PRMT6-mediated methylation of R2 in histone H3 antagonizes H3 K4 trimethylation (Q24303480) (← links)
- Physical association and coordinate function of the H3 K4 methyltransferase MLL1 and the H4 K16 acetyltransferase MOF (Q24305335) (← links)
- Menin associates with a trithorax family histone methyltransferase complex and with the hoxc8 locus (Q24313196) (← links)
- A novel nuclear interactor of ARF and MDM2 (NIAM) that maintains chromosomal stability (Q24316305) (← links)
- Pro isomerization in MLL1 PHD3-bromo cassette connects H3K4me readout to CyP33 and HDAC-mediated repression (Q24319024) (← links)
- New insight into the molecular mechanisms of MLL-associated leukemia (Q24336625) (← links)
- Crosstalk between O-GlcNAcylation and proteolytic cleavage regulates the host cell factor-1 maturation pathway (Q24338891) (← links)
- (Q24544453) (redirect page) (← links)
- Uncleaved TFIIA is a substrate for taspase 1 and active in transcription (Q24548040) (← links)
- Taspase1 functions as a non-oncogene addiction protease that coordinates cancer cell proliferation and apoptosis (Q24603213) (← links)
- Hoxa9 and Meis1 are key targets for MLL-ENL-mediated cellular immortalization (Q24603527) (← links)
- Limited proteolysis differentially modulates the stability and subcellular localization of domains of RPGRIP1 that are distinctly affected by mutations in Leber's congenital amaurosis (Q24673292) (← links)
- MLL repression domain interacts with histone deacetylases, the polycomb group proteins HPC2 and BMI-1, and the corepressor C-terminal-binding protein (Q24679773) (← links)
- The structure of the FYR domain of transforming growth factor beta regulator 1 (Q27661982) (← links)
- The super elongation complex (SEC) and MLL in development and disease (Q27692038) (← links)
- NDUFAF7 methylates arginine 85 in the NDUFS2 subunit of human complex I (Q28115826) (← links)
- Modulation of cell cycle by graded expression of MLL-AF4 fusion oncoprotein (Q28247462) (← links)
- Interaction of AF4 wild-type and AF4.MLL fusion protein with SIAH proteins: indication for t(4;11) pathobiology? (Q28268824) (← links)
- Bioassays to monitor Taspase1 function for the identification of pharmacogenetic inhibitors (Q28478269) (← links)
- Overexpression of the catalytically impaired Taspase1 T234V or Taspase1 D233A variants does not have a dominant negative effect in T(4;11) leukemia cells (Q28483263) (← links)
- Neuronal Kmt2a/Mll1 histone methyltransferase is essential for prefrontal synaptic plasticity and working memory (Q28512874) (← links)
- Histone and DNA methylation defects at Hox genes in mice expressing a SET domain-truncated form of Mll. (Q28589560) (← links)
- Regulation of MLL1 H3K4 methyltransferase activity by its core components (Q29614518) (← links)
- Cleavage of TFIIA by Taspase1 activates TRF2-specified mammalian male germ cell programs (Q30409932) (← links)
- Disordered epigenetic regulation in MLL-related leukemia (Q30422159) (← links)
- De novo mutations in MLL cause Wiedemann-Steiner syndrome (Q30458307) (← links)
- Functional anatomy of polycomb and trithorax chromatin landscapes in Drosophila embryos (Q33399874) (← links)
- Alternative epigenetic chromatin states of polycomb target genes (Q33523037) (← links)
- c-Myb binds MLL through menin in human leukemia cells and is an important driver of MLL-associated leukemogenesis (Q33604849) (← links)
- On the use of resampling tests for evaluating statistical significance of binding-site co-occurrence (Q33621990) (← links)
- MLL-AF9-induced leukemogenesis requires coexpression of the wild-type Mll allele. (Q33694927) (← links)
- Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes. (Q33807995) (← links)
- Mixed lineage leukemia: a structure-function perspective of the MLL1 protein (Q33943731) (← links)
- Zebrafish mll gene is essential for hematopoiesis (Q33969764) (← links)
- MLL associates specifically with a subset of transcriptionally active target genes (Q34078397) (← links)
- A pharmacologic inhibitor of the protease Taspase1 effectively inhibits breast and brain tumor growth (Q34100090) (← links)
- The role of the MLL gene in infant leukemia (Q34287512) (← links)
- Taspase1 cleaves MLL1 to activate cyclin E for HER2/neu breast tumorigenesis (Q34452426) (← links)
- The molecular mechanics of mixed lineage leukemia (Q34516051) (← links)
- Proteolysis of MLL family proteins is essential for taspase1-orchestrated cell cycle progression. (Q34563234) (← links)
- MLL becomes functional through intra-molecular interaction not by proteolytic processing (Q34989041) (← links)
- Proteolytically cleaved MLL subunits are susceptible to distinct degradation pathways (Q35041289) (← links)
- DOT1L, the H3K79 methyltransferase, is required for MLL-AF9-mediated leukemogenesis (Q35083276) (← links)
- HOXC6 Is transcriptionally regulated via coordination of MLL histone methylase and estrogen receptor in an estrogen environment (Q35127065) (← links)
- MLL 5 protein forms intranuclear foci, and overexpression inhibits cell cycle progression (Q35554133) (← links)
- Minireview: NAD+, a circadian metabolite with an epigenetic twist (Q35646078) (← links)
- ECSASB2 mediates MLL degradation during hematopoietic differentiation (Q35750333) (← links)