Pages that link to "Q24559974"
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The following pages link to Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias (Q24559974):
Displaying 50 items.
- MSF (MLL septin-like fusion), a fusion partner gene of MLL, in a therapy-related acute myeloid leukemia with a t(11;17)(q23;q25) (Q22009898) (← links)
- MLL2: A new mammalian member of the trx/MLL family of genes (Q22010267) (← links)
- The cloning, mapping and expression of a novel gene, BRL, related to the AF10 leukaemia gene (Q22010950) (← links)
- The interaction between EEN and Abi-1, two MLL fusion partners, and synaptojanin and dynamin: implications for leukaemogenesis (Q22253881) (← links)
- The human homolog of Escherichia coli Orn degrades small single-stranded RNA and DNA oligomers (Q22254252) (← links)
- Protein interactions of the MLL PHD fingers modulate MLL target gene regulation in human cells (Q24291156) (← links)
- The human formin-binding protein 17 (FBP17) interacts with sorting nexin, SNX2, and is an MLL-fusion partner in acute myelogeneous leukemia (Q24291407) (← links)
- Monoubiquitination of human histone H2B: the factors involved and their roles in HOX gene regulation (Q24297025) (← links)
- Genes on chromosomes 4, 9, and 19 involved in 11q23 abnormalities in acute leukemia share sequence homology and/or common motifs (Q24309063) (← links)
- Acute mixed-lineage leukemia t(4;11)(q21;q23) generates an MLL-AF4 fusion product (Q24310468) (← links)
- Cloning of ELL, a gene that fuses to MLL in a t(11;19)(q23;p13.1) in acute myeloid leukemia (Q24310726) (← links)
- The t(10;11)(p13;q14) in the U937 cell line results in the fusion of the AF10 gene and CALM, encoding a new member of the AP-3 clathrin assembly protein family (Q24314354) (← links)
- ELL binding regulates U19/Eaf2 intracellular localization, stability, and transactivation (Q24316696) (← links)
- Leucine-zipper dimerization motif encoded by the AF17 gene fused to ALL-1 (MLL) in acute leukemia (Q24317124) (← links)
- New insight into the molecular mechanisms of MLL-associated leukemia (Q24336625) (← links)
- Inhibition of nuclear import by protein kinase B (Akt) regulates the subcellular distribution and activity of the forkhead transcription factor AFX. (Q24514761) (← links)
- Panhandle and reverse-panhandle PCR enable cloning of der(11) and der(other) genomic breakpoint junctions of MLL translocations and identify complex translocation of MLL, AF-4, and CDK6. (Q24536146) (← links)
- The elongation domain of ELL is dispensable but its ELL-associated factor 1 interaction domain is essential for MLL-ELL-induced leukemogenesis (Q24550876) (← links)
- Leukemic HRX fusion proteins inhibit GADD34-induced apoptosis and associate with the GADD34 and hSNF5/INI1 proteins (Q24554418) (← links)
- EEN encodes for a member of a new family of proteins containing an Src homology 3 domain and is the third gene located on chromosome 19p13 that fuses to MLL in human leukemia (Q24564948) (← links)
- Rearrangements of the retinoic acid receptor alpha and promyelocytic leukemia zinc finger genes resulting from t(11;17)(q23;q21) in a patient with acute promyelocytic leukemia (Q24597732) (← links)
- Hoxa9 and Meis1 are key targets for MLL-ENL-mediated cellular immortalization (Q24603527) (← links)
- Aberrant overexpression and function of the miR-17-92 cluster in MLL-rearranged acute leukemia (Q24624389) (← links)
- The hybrid PAX3-FKHR fusion protein of alveolar rhabdomyosarcoma transforms fibroblasts in culture (Q24632107) (← links)
- Regulation of mir-196b by MLL and its overexpression by MLL fusions contributes to immortalization (Q24646499) (← links)
- Retrovirus-mediated gene transfer of MLL-ELL transforms primary myeloid progenitors and causes acute myeloid leukemias in mice (Q24647139) (← links)
- Alterations of the PPP2R1B gene located at 11q23 in human colorectal cancers (Q24669975) (← links)
- Identification of a gene at 11q23 encoding a guanine nucleotide exchange factor: evidence for its fusion with MLL in acute myeloid leukemia (Q24670279) (← 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)
- Systematic Classification of Mixed-Lineage Leukemia Fusion Partners Predicts Additional Cancer Pathways (Q26771880) (← links)
- Leukemogenic rearrangements at the mixed lineage leukemia gene (MLL)-multiple rather than a single mechanism (Q26830271) (← links)
- Chromatin signatures of cancer (Q27024162) (← links)
- Catalytic and functional roles of conserved amino acids in the SET domain of the S. cerevisiae lysine methyltransferase Set1 (Q27935081) (← links)
- MLL2, the second human homolog of the Drosophila trithorax gene, maps to 19q13.1 and is amplified in solid tumor cell lines (Q28142772) (← links)
- Rapid isolation of chromosomal breakpoints from patients with t(4;11) acute lymphoblastic leukemia: implications for basic and clinical research (Q28203245) (← links)
- Identification and characterization of EBP, a novel EEN binding protein that inhibits Ras signaling and is recruited into the nucleus by the MLL-EEN fusion protein (Q28208684) (← links)
- The ENL moiety of the childhood leukemia-associated MLL-ENL oncoprotein recruits human Polycomb 3 (Q28213852) (← links)
- Structure and function of RNA polymerase II elongation factor ELL. Identification of two overlapping ELL functional domains that govern its interaction with polymerase and the ternary elongation complex (Q28247009) (← links)
- Modulation of cell cycle by graded expression of MLL-AF4 fusion oncoprotein (Q28247462) (← links)
- HRX leukemic fusion proteins form a heterocomplex with the leukemia-associated protein SET and protein phosphatase 2A (Q28253208) (← links)
- Therapy-related myeloid leukemia (Q28284888) (← links)
- Cloning and characterization of the t(X;11) breakpoint from a leukemic cell line identify a new member of the forkhead gene family (Q28287300) (← links)
- Misguided transcriptional elongation causes mixed lineage leukemia (Q28471927) (← links)
- Identification of chromatin remodeling genes Arid4a and Arid4b as leukemia suppressor genes (Q28592846) (← links)
- Mouse Af9 is a controller of embryo patterning, like Mll, whose human homologue fuses with Af9 after chromosomal translocation in leukemia (Q28594037) (← links)
- The history of cancer epigenetics (Q29617273) (← links)
- The MYO1F, unconventional myosin type 1F, gene is fused to MLL in infant acute monocytic leukemia with a complex translocation involving chromosomes 7, 11, 19 and 22. (Q30160238) (← links)
- Structure of AF3p21, a new member of mixed lineage leukemia (MLL) fusion partner proteins-implication for MLL-induced leukemogenesis (Q30167808) (← links)
- ENL, the MLL fusion partner in t(11;19), binds to the c-Abl interactor protein 1 (ABI1) that is fused to MLL in t(10;11)+. (Q30175153) (← links)
- A novel gene, FGA7, is fused to RUNX1/AML1 in a t(4;21)(q28;q22) in a patient with T-cell acute lymphoblastic leukemia (Q30747544) (← links)