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1 tients harbor a translocation involving MLL (mixed lineage leukemia).
2 sociated with infant acute lymphoblastic and mixed lineage leukemia.
3 s cytogenetics in acute myeloid leukemia and mixed lineage leukemia.
4 an inv(8)(p11q13) from a patient with acute mixed lineage leukemia.
5 ole and is a potential therapeutic target in mixed lineage leukemia.
6 ing response to therapy, of 35 patients with mixed-lineage leukemia.
7 methyltranferases (H3K4MTs) MLL3 and MLL4 in mixed-lineage leukemia.
8 -CSF pathway, that resemble a B cell/myeloid mixed-lineage leukemia.
9 F23, and NUP98-TOP1 physically interact with mixed lineage leukemia 1 (MLL1) and the non-specific let
14 rotein-protein interaction between menin and mixed lineage leukemia 1 (MLL1) plays a critical role in
17 Menin is an essential oncogenic cofactor for mixed lineage leukemia 1 (MLL1)-mediated leukemogenesis
18 identify that the histone methyltransferase mixed lineage leukemia 1 (MLL1/KMT2A) is an important re
21 of acute leukemias arise from fusion of the mixed lineage leukemia 1 protein (MLL) N terminus to a v
22 oregulators such as histone methylases MLL1 (mixed lineage leukemia 1) and MLL3 and CREB-binding prot
24 gnificant overlap in genes regulated by MOZ, mixed lineage leukemia 1, and mixed lineage leukemia 1 c
25 down (KD) of a writer, the methyltransferase mixed-lineage leukemia 1 (Mll1) (n = 26), and an eraser,
26 We find that the histone methyltransferase Mixed-Lineage Leukemia 1 (MLL1) controls 3D cell migrati
27 tivators CREB-binding protein (CBP)/p300 and mixed-lineage leukemia 1 (MLL1) critically regulate circ
33 ity for a truncated, lacZ knock-in allele of mixed-lineage leukemia 1 (Mll1), a histone methyltransfe
35 f the H3K4-specific methyltransferase, Kmt2a/Mixed-lineage leukemia 1 (Mll1), in mouse postnatal fore
36 expression of the histone methyltransferase, mixed-lineage leukemia 1 (MLL1), which specifically trim
37 onal identity in the murine brain requires a mixed-lineage leukemia 1 (Mll1)-dependent epigenetic mem
39 he histone methyltransferases Set1 and MLL1 (mixed-lineage leukemia 1), leading to histone H3K4 trime
43 Translocations and amplifications of the mixed lineage leukemia-1 (MLL1) gene are associated with
44 q23 chromosomal translocations involving the mixed lineage leukemia-1 (MLL1) gene, a key player in hi
46 MT2A lysine methyltransferase (also known as mixed-lineage leukemia-1), and produce in-frame fusions
47 Lpt) is the N-terminal homolog of mammalian Mixed Lineage Leukemia 2 (MLL2/ALR), a core component of
48 transferases such as enhancer of zeste 2 and mixed lineage leukemia 2, histone demethylases including
49 istone-methyltransferase myeloid/lymphoid or mixed-lineage leukemia 2 (mll2/kmt2b) gene in adult fore
50 ximately 50% reduction in gene dosage of the mixed lineage leukemia 3 (MLL3) gene, located on 7q36.1,
51 and the histone monomethyltransferase, MLL3 (mixed lineage leukemia 3) form altogether a macromolecul
53 s identified were all of the subunits of the mixed-lineage leukemia 3 (Mll3) and 4 (Mll4) complexes,
54 The histone H3-lysine-4 methyltransferase mixed-lineage leukemia 3 (MLL3) and its closest homolog,
55 Although PTIP is a unique component of the mixed-lineage leukemia 3 (MLL3)/MLL4 chromatin-modifying
56 deficient in the PTIP component of the MLL3 (mixed-lineage leukemia 3)-MLL4 complex display impaired
58 e report that histone mono-methyltransferase mixed lineage leukemia 4 (MLL4), a key enhancer regulato
59 r is equipped with a 14-residue Win motif of mixed lineage leukemia 4 methyltransferase (MLL4(Win)),
65 eptor NKp44 (NKp44L), a novel isoform of the mixed-lineage leukemia-5 protein, as a cellular ligand f
66 lso suppresses proliferation of leukemogenic mixed lineage leukemia-AF9 fusion-protein-transformed my
68 mia (ALL), acute myelogenous leukemia (AML), mixed lineage leukemia, and also in therapy AML (t-AML)
69 ragile sites, and breakpoints, including the mixed-lineage leukemia breakpoint cluster region (MLL BC
70 at containing protein 5), a component of the mixed lineage leukemia complex of histone 3 lysine 4 met
71 y, although PTIP and PA1 associate with MLL (mixed lineage leukemia) complexes and participate in tra
72 effectively treats aggressive AML, including mixed-lineage leukemia-driven AML, and outperforms stand
73 f conditional transformation by an inducible mixed lineage leukemia-eleven-nineteen leukemia (MLL-ENL
74 issense and nonsense mutations targeting the mixed lineage leukemia family member 3 (MLL3, encoded by
75 A murine retroviral transduction model of mixed lineage leukemia fused to CREB binding protein suc
76 rmined that minimally, the amino terminus of mixed lineage leukemia fused to the bromodomain and hist
77 upport of this idea, we showed recently that mixed lineage leukemia fusion oncoproteins can convert c
78 ex with MLLT10, which cooperatively regulate mixed lineage leukemia fusion protein (MLL-FP) target ge
81 ort that hDOT1L interacts with AF10, an MLL (mixed lineage leukemia) fusion partner involved in acute
82 ves as a critical oncogenic cofactor of MLL (mixed lineage leukemia) fusion proteins in acute leukemi
83 in leukemogenesis driven by a subset of MLL (mixed-lineage leukemia) fusion proteins raises the possi
85 ias that harbor translocations involving the mixed lineage leukemia gene (MLL) possess unique biologi
94 adults as a result of rearrangements to the mixed-lineage leukemia gene (MLL) located on chromosome
95 atient-derived xenografts (PDX) of pediatric mixed-lineage leukemia gene (MLL)-rearranged ALL were es
97 ng a chromosomal translocation involving the mixed-lineage leukemia gene (MLL, ALL1, HRX) have a part
99 or acute myelogenous leukemia), and MLL AML (mixed-lineage leukemia gene) in comparison to control su
103 ene involved in translocations with the MLL (mixed-lineage leukemia) gene, was 631 bp away in a head-
104 to as MLL to denote the gene associated with mixed-lineage leukemia) generate MLL fusion proteins tha
106 iginally identified as a fusion partner with mixed-lineage leukemia in a patient with acute myeloid l
107 ize the biology and optimal therapy of acute mixed-lineage leukemia in children, we reviewed the path
111 ing translocation t(11;16) (q23;p13.3), MLL (mixed-lineage leukemia) is fused in frame to CBP (CREB b
112 horax family member MLL (myeloid/lymphoid or mixed-lineage leukemia) is presumed to activate Hox expr
113 tool for understanding the biologic basis of mixed lineage leukemia leukemogenesis and for developing
114 One such gene is MLL (myeloid-lymphoid or mixed lineage leukemia) located at chromosome band 11q23
115 5 (WDR5) is a common component of mammalian mixed lineage leukemia methyltransferase family members
117 in 5 (WDR5) and its various partners such as mixed lineage leukemia (MLL) and c-MYC are essential for
120 e II (TOP2)-mediated DNA cleavage within the mixed lineage leukemia (MLL) breakpoint cluster region (
121 nic fusions of the Trithorax-related protein mixed lineage leukemia (MLL) can initiate aggressive leu
122 allosteric changes that transcription factor mixed lineage leukemia (MLL) causes to the interactions
124 ated by epigenetic changes controlled by the mixed lineage leukemia (MLL) family because treatment wi
126 The oncoprotein Ash2L is a component of the mixed lineage leukemia (MLL) family members 1-4, Setd1A,
130 in, the MEN1 protein product, interacts with mixed lineage leukemia (MLL) family proteins in a histon
133 ne 79 (K79) on histone H3 and is involved in Mixed Lineage Leukemia (MLL) fusion leukemogenesis; howe
134 unctions and in leukemogenesis driven by the mixed lineage leukemia (MLL) fusion oncogene MLL-AF9.
135 ough menin acts as an oncogenic cofactor for mixed lineage leukemia (MLL) fusion protein-mediated his
136 polymerase-associated factor complex (PAFc), mixed lineage leukemia (MLL) fusion proteins activate ge
137 unctions as a critical oncogenic cofactor of mixed lineage leukemia (MLL) fusion proteins in the deve
138 The interaction between menin and oncogenic mixed lineage leukemia (MLL) fusion proteins is required
141 Chromosomal translocations involving the mixed lineage leukemia (MLL) gene are associated with ag
142 Chromosomal translocations involving the mixed lineage leukemia (MLL) gene are often observed in
143 ith chromosomal translocations involving the mixed lineage leukemia (MLL) gene are usually associated
146 o distinctive origins of human AML driven by Mixed Lineage Leukemia (MLL) gene fusions (MLL-AML).
147 first identified as a fusion partner of the mixed lineage leukemia (MLL) gene in acute myeloid leuke
150 A partial nontandem duplication (PNTD) of mixed lineage leukemia (MLL) gene is described in B-cell
153 en mutated in ALLs with rearrangement of the mixed lineage leukemia (MLL) gene on chromosome 11q23.
155 Chromosomal translocations involving the Mixed Lineage Leukemia (MLL) gene produce chimeric prote
157 of infants with ALL, particularly those with mixed lineage leukemia (MLL) gene rearrangements, is onl
158 Chromosomal translocations disrupting the Mixed lineage leukemia (Mll) gene result in leukemia, wi
159 Chromosomal translocations targeting the mixed lineage leukemia (MLL) gene result in MLL fusion p
162 kemia (B-ALL) harboring rearrangement of the mixed lineage leukemia (MLL) gene with CD19 CAR-T cells.
163 Chromosomal translocations that fuse the mixed lineage leukemia (MLL) gene with multiple partners
164 L) is characterized by rearrangements of the mixed lineage leukemia (MLL) gene with one of its >50 pa
165 lso interacts with translocation partners of Mixed Lineage Leukemia (MLL) gene, which is commonly tra
166 receptors (ERs) and ER coregulators such as mixed lineage leukemia (MLL) histone methylases (MLL2 an
167 ights into the role of the Trithorax protein mixed lineage leukemia (MLL) in maintaining cancer stem
173 plex (DotCom), which includes several of the mixed lineage leukemia (MLL) partners in leukemia such a
174 -protein interaction (PPI) between menin and mixed lineage leukemia (MLL) plays a critical role in ac
176 e Men1 gene product menin interacts with the mixed lineage leukemia (MLL) protein, a histone H3 lysin
178 WD repeat domain 5 (WDR5) and block the WDR5-mixed lineage leukemia (MLL) protein-protein interaction
180 ENL, and AF9, is recruited by HIV-1 Tat and mixed lineage leukemia (MLL) proteins to activate the ex
181 Aven stimulates the mRNA translation of the mixed lineage leukemia (MLL) proto-oncogene in an argini
183 third plant homeodomain (PHD3) finger of the mixed lineage leukemia (MLL) proto-oncoprotein and a pol
184 loid leukemias (AMLs) with the NUP98-NSD1 or mixed lineage leukemia (MLL) rearrangement (MLL-r) share
186 sents the most common leukemogenic fusion of mixed lineage leukemia (MLL) to a cytoplasmic partner pr
187 ing of activation domains from the c-Myb and mixed lineage leukemia (MLL) transcription factors to th
188 regulator in the expression of HOX genes in mixed lineage leukemia (MLL)-based hematological maligna
189 d the miRNAs are aberrantly overexpressed in mixed lineage leukemia (MLL)-rearranged acute leukemias.
190 regulator CDK6 as a promising new target in mixed lineage leukemia (MLL)-rearranged acute myeloid le
191 hylation (H3K27me3/2) and inhibits growth of mixed lineage leukemia (MLL)-rearranged leukemia cells.
192 rates for pediatric patients suffering from mixed lineage leukemia (MLL)-rearranged leukemia remain
193 ranslocations, that approximately 43% of all mixed lineage leukemia (MLL)-rearranged leukemias are EV
196 , we identify the histone-remodelling enzyme mixed lineage leukemia (MLL)3 as a clock-controlled fact
199 impaired reconstitution of stem cell-derived mixed-lineage leukemia (MLL) AML, which represents an ag
200 isordered transcription factors, such as the mixed-lineage leukemia (MLL) and c-Myb peptides, at isol
201 more, we observed that SALL4 interacted with mixed-lineage leukemia (MLL) and co-occupied the HOXA9 p
202 t multiple MLL-fusion proteins implicated in mixed-lineage leukemia (MLL) associate with AFF4, ELLs,
204 ate maintenance of target gene expression by mixed-lineage leukemia (MLL) chimeras may result from th
205 his targeting strategy does not affect other mixed-lineage leukemia (MLL) family histone methyltransf
206 as the threonine endopeptidase that cleaves mixed-lineage leukemia (MLL) for proper Hox gene express
211 ary acute myelogenous leukemia involving the mixed-lineage leukemia (MLL) gene (11q23) translocations
212 We previously identified a rearrangement of mixed-lineage leukemia (MLL) gene (also known as ALL-1,
214 hromosomal translocation that juxtaposes the mixed-lineage leukemia (MLL) gene and the AF4 gene.
216 OF REVIEW: Leukemia carrying mutation of the mixed-lineage leukemia (MLL) gene is particularly refrac
217 Chromosomal rearrangements involving the mixed-lineage leukemia (MLL) gene occur in primary and t
219 r acute lymphoblastic leukemia patients with Mixed-Lineage Leukemia (MLL) gene rearrangements (MLLr B
223 ost cell factor 1 (HCF1), a component of the mixed-lineage leukemia (MLL) histone methyltransferase c
227 Chromosomal translocations involving the mixed-lineage leukemia (MLL) locus generate potent oncog
229 t mutations such as FLT3 internal-tandem and mixed-lineage leukemia (MLL) partial-tandem duplications
230 ax binds KIX at the previously characterized mixed-lineage leukemia (MLL) protein interaction surface
232 Histone lysine methylation, mediated by mixed-lineage leukemia (MLL) proteins, is now known to b
233 determined that MSI2 directly maintains the mixed-lineage leukemia (MLL) self-renewal program by int
235 gements involving the H3K4 methyltransferase mixed-lineage leukemia (MLL) trigger aberrant gene expre
237 omal aberrations and abnormalities involving mixed-lineage leukemia (MLL), an upstream regulator of H
240 t to chromatin as an effective treatment for mixed-lineage leukemia (MLL)-fusion leukemia' by Dawson
243 alignancies, including Hodgkin, myeloma, and mixed-lineage leukemia (MLL)-translocated cell lines.
247 llite markers located at the ATM (D11S2179), mixed-lineage leukemia (MLL; D11S1356), and BCL1 (D11S98
251 ation domain associates with TRRAP/TIP60 and mixed-lineage-leukemia (MLL1/MLL2) SET1-type chromatin-m
254 h an aberrant histone methyltransferase, the mixed lineage leukemia partial tandem duplication (MLL-P
255 vation domain of the trithorax group protein mixed lineage leukemia protein (MLL), together with eith
257 Several lines of evidence suggest that the mixed lineage leukemia protein (MLL, ALL-1, HRX) plays a
258 ct the WD repeat-containing protein 5 (WDR5)-mixed lineage leukemia protein 1 (MLL1) complex across t
264 DPY-30), a complex that is part of the MLL1 (mixed lineage leukemia protein-1) core complex but that
266 he Trithorax histone H3K4 methyltransferase, mixed-lineage leukemia protein 3 (MLL3) within Complex P
267 its promoter, and p300, myeloid/lymphoid or mixed-lineage leukemia protein 4 (MLL4), and RNA polymer
268 ith the transcriptional activation domain of mixed-lineage leukemia protein leads to an enhancement o
270 lysine 4 (H3K4) methyltransferases including mixed lineage leukemia proteins to regulate homeobox (Ho
272 3 (IGF2BP3) is specifically overexpressed in mixed lineage leukemia-rearranged (MLL-rearranged) B-acu
273 nd its receptor (IL-17RB) in human and mouse mixed lineage leukemia-rearranged AML cells, which were
275 ogenesis in acute leukemias, particularly in mixed-lineage leukemia-rearranged (MLL-r) leukemia.
276 t extremely high levels in ALL patients with mixed lineage leukemia rearrangements or hyperdiploidy a
280 eport a role for Mllt11 (Myeloid/lymphoid or mixed-lineage leukemia; translocated to chromosome 11/Al
281 sented with acute myeloid leukemia, one with mixed-lineage leukemia, two with acute lymphoblastic leu