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1 DNA binding module for this novel vertebrate nuclear matrix protein.
2 was identified as matrin 3, one of the major nuclear matrix proteins.
3 ermediary factor 1 gamma, anti-MDA5 and anti-nuclear matrix protein 2, which are potentially exploita
5 rug Administration (FDA) approved the use of Nuclear matrix protein 22 (NMP22) as a monitoring tool f
7 ate dehydrogenase (LDH) isoenzymes and human nuclear matrix protein 41/7 (NMP 41/7) as potential sero
8 (such as ribosomal proteins L3, L5, and L28; nuclear matrix protein 84; matrin cyclophilin; the H3 hi
10 These proteins are distinct from the major nuclear matrix proteins and may be involved in mediating
11 ine novel protein-protein interactions among nuclear matrix proteins and suggest a potential role of
12 locytic leukemia zinc finger, nucleophosmin, nuclear matrix protein, and signal transducer and activa
15 hypothesis that fulvestrant induces specific nuclear matrix protein-ERalpha interactions that mediate
18 quence specifically interacted with isolated nuclear matrix proteins in vitro, suggesting that it may
19 This work identifies phosphorylation of the nuclear matrix protein matrin 3 as a new conserved targe
20 rupts the 3' UTR of MATR3, which encodes the nuclear matrix protein Matrin 3, and mouse Matr3 is stro
21 rostate and breast cancer have revealed that nuclear matrix protein (NMP) composition undergoes alter
23 UTP nick end labeling (TUNEL) and release of nuclear matrix protein (NMP) into the culture medium.
24 , we also show that the purified DNA-binding nuclear matrix protein (NMP) specifically represses the
25 ral scaffolding of the nucleus, and specific nuclear matrix proteins (NMPs) have been identified as a
26 member of the BTB/Kelch repeat family, is a nuclear matrix protein normally expressed in neurons but
27 ived 2 (E2)-related factor 2 (NRF2) with the nuclear matrix protein NRP/B was essential for the trans
28 in breast cancer cells, we observed that the nuclear matrix protein NRP/B was expressed and colocaliz
32 ting with both the nuclear envelope and DNA, nuclear matrix protein NuMA (Nuclear mitotic apparatus),
33 esis is accompanied by relocalization of the nuclear matrix proteins NuMA, splicing factor SRm160, an
34 he Nrf2 pathway, identifying a novel role of nuclear matrix protein(s) in oxidative stress responses.
35 elopmental Cell, Agrelo et al. show that the nuclear matrix protein SATB1 is a critical determinant o
36 l, Grosschedl and colleagues report that the nuclear matrix protein Satb2 represses Hoxa2 expression
39 Our studies indicate that NRP/B is a novel nuclear matrix protein, specifically expressed in primar
40 The results suggest that a complex of the nuclear matrix proteins SRm160 and SRm300 functions as a
41 e report the identification and cloning of a nuclear matrix protein termed matrin cyclophilin or matr
42 previously been shown to be a unique 10-kDa nuclear matrix protein that generates high affinity PR-b
43 Scaffold attachment factor-B1 (SAFB1) is a nuclear matrix protein that has been proposed to couple
44 t in part through the inhibition of SATB2, a nuclear matrix protein that is a critical determinant of
46 ractionation strategy to release the bulk of nuclear matrix proteins under conditions where the chrom
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