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1 1 substrate proteins, including histones and heterogeneous nuclear ribonucleoproteins.
2 ammalian cells, which methylates a number of heterogeneous nuclear ribonucleoproteins.
3 proteins, chaperones, elongation factor 1A, heterogeneous nuclear ribonucleoproteins, 14-3-3 protein
4 stitutive transcriptional repressor protein, heterogeneous nuclear ribonucleoprotein A/B (hnRNP A/B);
5 pendent on interactions of lincRNA-Cox2 with heterogeneous nuclear ribonucleoprotein A/B and A2/B1.
7 xtracts, HAM/TSP immunoglobulin G identified heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1) as
9 ss spectrometry, and supershift assay, human heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1) wa
11 oprecipitation experiments, we have isolated heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1), w
12 is of UP1, the N-terminal, two-RRM domain of heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1), w
13 ular distribution of the RNA-binding protein heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1).
14 ied the major RNA-binding protein species as heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1).
16 human MARs and the single mouse MAR recruit heterogeneous nuclear ribonucleoprotein A1 (hnRNP-A1) in
17 ography and mass spectrometry, we identified heterogeneous nuclear ribonucleoprotein A1 (hnRNPA1) as
18 sing purified protein, here we show that the heterogeneous nuclear ribonucleoprotein A1 (hnRNPA1) rec
20 tively associates with the mRNA that encodes heterogeneous nuclear ribonucleoprotein A1 (hnRNPA1), a
21 emia-regulated factors including RNA-binding heterogeneous nuclear ribonucleoprotein A1 and the oncog
22 l titrations indicate that the UP1 domain of heterogeneous nuclear ribonucleoprotein A1 binds the ISS
23 ptor-triggered translocation is selective as heterogeneous nuclear ribonucleoprotein A1 does not shut
24 imately 38-amino acid M9 sequence present in heterogeneous nuclear ribonucleoprotein A1 has been repo
27 of the inhibitors within the UP1 fragment of heterogeneous nuclear ribonucleoprotein A1, and docking
28 a requisite c-MYC IRES trans-acting factor, heterogeneous nuclear ribonucleoprotein A1, with its IRE
29 d that EWS/FLI, but not EWS, interfered with heterogeneous nuclear ribonucleoprotein A1-dependent spl
34 These motifs are specifically recognized by heterogeneous nuclear ribonucleoprotein A2 (hnRNP A2), a
36 includes at least two RNA binding proteins, heterogeneous nuclear ribonucleoprotein A2 and muscle bl
37 g microtubules is mediated by the cis-acting heterogeneous nuclear ribonucleoprotein A2 response elem
40 d a drastic reduction in the splicing factor heterogeneous nuclear ribonucleoprotein A2/B1 (hnRNPA2/B
41 in (TBP)-proteasome component-B1 (PSMB1) and heterogeneous nuclear ribonucleoprotein A2/B1 (HNRPA2B1)
42 nding studies, we identified human HNRPA2B1 (heterogeneous nuclear ribonucleoprotein A2/B1, also know
43 macrophage capping protein, peroxiredoxin 5, heterogeneous nuclear ribonucleoproteins A2/B, and apoli
44 howed that heat shock protein 90 (HSP90) and heterogeneous nuclear ribonucleoproteins A2/B1 (hnRNP A2
45 ive purification of VLTF-X has revealed that heterogeneous nuclear ribonucleoproteins A2/B1 and RBM3
46 athy/amyotrophic lateral sclerosis proteins, heterogeneous nuclear ribonucleoproteins A2/B1, are down
48 ermined structure of the two-RRM fragment of heterogeneous nuclear ribonucleoprotein Al, SXL displays
49 roteins that bind double-stranded RNA, novel heterogeneous nuclear ribonucleoproteins and the Ewing's
50 2 gene product but rather by multiple hnRNP (heterogeneous nuclear ribonucleoprotein) and SR (serine-
51 RAS and ILK and the roles of E2F1, c-Myc and heterogeneous nuclear ribonucleoprotein as intermediary
52 by mass spectrometry analysis, we identified heterogeneous nuclear ribonucleoprotein C (hnRNP C) as a
53 express the RALYL RNA-binding protein of the heterogeneous nuclear ribonucleoprotein C (hnRNP C) fami
54 ontains a 36-kDa protein later identified as heterogeneous nuclear ribonucleoprotein C (hnRNP C).
55 gnized by a monoclonal antibody specific for heterogeneous nuclear ribonucleoprotein C (hnRNP C).
56 ion of the acidic C-terminal domain (ACD) of heterogeneous nuclear ribonucleoprotein C (hnRNP-C), a n
57 coding RNA (lncRNA) to facilitate binding of heterogeneous nuclear ribonucleoprotein C (HNRNPC), an a
59 ious down-regulation of its target substrate heterogeneous nuclear ribonucleoprotein C and results in
60 nteraction of the translation-activating RBP heterogeneous nuclear ribonucleoprotein C with APP mRNA.
61 Nrd1, and the resulting heterodimer of these heterogeneous nuclear ribonucleoprotein-C (hnRNP)-like p
64 lly recognized as an RNA splicing regulator, heterogeneous nuclear ribonucleoprotein C1/C2 (hnRNPC1/C
65 ingerprinting, the protein was identified as heterogeneous nuclear ribonucleoprotein C1/C2, a nuclear
66 d remodeling complex (LARC) that consists of heterogeneous nuclear ribonucleoprotein C1/C2, nucleosom
70 es the role of the mRNA-binding protein AUF1/heterogeneous nuclear ribonucleoprotein D (AUF1) in VEGF
71 ein AUF1 (AU-binding factor 1, also known as heterogeneous nuclear ribonucleoprotein D [hnRNP D]) bin
72 tein-binding protein-associated factor)) and heterogeneous nuclear ribonucleoprotein D bind this regi
73 sus NF-kappaB promoter element, as well as a heterogeneous nuclear ribonucleoprotein D element and an
78 n factors: ZBP-89, YY-1, and a member of the heterogeneous nuclear ribonucleoprotein D-like protein (
80 e nucleocytoplasmic transport of each of the heterogeneous nuclear ribonucleoprotein D/AUF1 isoforms.
81 eins, namely, nucleolin and the A isoform of heterogeneous nuclear ribonucleoprotein-D0 (hnRNP-D0A),
82 o render it similar to the KH domains of the heterogeneous nuclear ribonucleoprotein E (hnRNP E) and
83 n kinase B (Akt2) induces phosphorylation of heterogeneous nuclear ribonucleoprotein E1 (hnRNP E1) at
84 actor revealed complete identity with 43-kDa heterogeneous nuclear ribonucleoprotein E1 (hnRNP E1).
85 deficiency, stimulated interactions between heterogeneous nuclear ribonucleoprotein E1 (hnRNP-E1) an
86 d to the intracellular homocysteinylation of heterogeneous nuclear ribonucleoprotein E1 (hnRNP-E1) an
87 gion of FR mRNA and a cystolic trans-factor (heterogeneous nuclear ribonucleoprotein E1 [hnRNP E1]) i
88 nd phosphorylation changes are downstream of heterogeneous nuclear ribonucleoprotein-E1 (E1), an effe
89 ilarity to creatine kinase B (CKB) isoforms, heterogeneous nuclear ribonucleoprotein F (hnRNP F) and
92 revealed that G quadruplexes are enriched in heterogeneous nuclear ribonucleoprotein F (hnRNPF)-bindi
93 , and HSP47), and nuclear proteins (lamin C, heterogeneous nuclear ribonucleoprotein F, and nucleopho
95 ffinity chromatography, three members of the heterogeneous nuclear ribonucleoprotein family (hnRNP L,
96 PR is a RNA-binding protein belonging to the heterogeneous nuclear ribonucleoprotein family, which ha
97 d to identify TDP-43 complexes not only with heterogeneous nuclear ribonucleoproteins family proteins
102 tor-1 (FGFR1), poly-A-binding protein, cAbl, heterogeneous nuclear ribonucleoprotein H', Br140, and i
103 a GGTG ins/del polymorphism influencing the heterogeneous nuclear ribonucleoprotein H-dependent incl
105 lves an increase in heavy chain ferritin and heterogeneous nuclear ribonucleoprotein H2 expression an
106 transcript contains a heavy chain ferritin, heterogeneous nuclear ribonucleoprotein H2, and CUG-bind
107 riants in the nuclear localization signal of Heterogeneous Nuclear Ribonucleoprotein H2, encoded by H
112 f E16 splicing is mediated by the binding of heterogeneous nuclear ribonucleoprotein (hnRNP) A/B prot
114 a critical protein family in RNA processing, heterogeneous nuclear ribonucleoprotein (hnRNP) A/B prot
115 UV cross-linking experiments have shown that heterogeneous nuclear ribonucleoprotein (hnRNP) A1 and a
116 teasome-dependent degradation is enhanced by heterogeneous nuclear ribonucleoprotein (hnRNP) A1 and d
117 BP-2) possessed sequence homology with human heterogeneous nuclear ribonucleoprotein (hnRNP) A1 and h
119 ype coronavirus mouse hepatitis virus (MHV), heterogeneous nuclear ribonucleoprotein (hnRNP) A1 has b
123 that the multifunctional RNA-binding protein heterogeneous nuclear ribonucleoprotein (hnRNP) A1 regul
124 eneous nuclear ribonucleoproteins, including heterogeneous nuclear ribonucleoprotein (hnRNP) A1, by b
125 nd that the PRE binds Drosophila homologs of heterogeneous nuclear ribonucleoprotein (hnRNP) A1, Hrp3
127 n signal (NLS) containing the M9 sequence of heterogeneous nuclear ribonucleoprotein (hnRNP) A1, to a
128 plicing by creating an inhibitory element, a heterogeneous nuclear ribonucleoprotein (hnRNP) A1-depen
129 these factors requires the stress-activated heterogeneous nuclear ribonucleoprotein (hnRNP) A2 as a
130 l RNA motif structures with targeting factor heterogeneous nuclear ribonucleoprotein (hnRNP) A2 form
132 transport process is the trans-acting factor heterogeneous nuclear ribonucleoprotein (hnRNP) A2 that
133 ficking element and the cognate trans-acting heterogeneous nuclear ribonucleoprotein (hnRNP) A2 traff
134 microtubule-associated protein that binds to heterogeneous nuclear ribonucleoprotein (hnRNP) A2.
135 and 16 novel mRNAs specifically bound by the heterogeneous nuclear ribonucleoprotein (hnRNP) A2.
137 proteins including TIAR, AUF1, CBF-A, RBM3, heterogeneous nuclear ribonucleoprotein (hnRNP) A3, and
138 d GM-CSF mRNA associated with YB-1, HuR, and heterogeneous nuclear ribonucleoprotein (hnRNP) C after
140 e now report the identity of this protein as heterogeneous nuclear ribonucleoprotein (hnRNP) C1/C2.
142 lly exist as tetramers (A2)(3)B1 in isolated heterogeneous nuclear ribonucleoprotein (hnRNP) complexe
143 etaARB is immunologically distinct from AUF1/heterogeneous nuclear ribonucleoprotein (hnRNP) D, anoth
144 fied proteins include MutS homolog 2 (MSH2), heterogeneous nuclear ribonucleoprotein (hnRNP) D, hnRNP
145 polypyrimidine tract-binding protein (PTB), heterogeneous nuclear ribonucleoprotein (hnRNP) F/H and
146 alternative splicing event is controlled by heterogeneous nuclear ribonucleoprotein (hnRNP) family m
148 that this factor is hnRNP H, a member of the heterogeneous nuclear ribonucleoprotein (hnRNP) family.
150 sought to investigate the mechanism by which heterogeneous nuclear ribonucleoprotein (hnRNP) H and F
151 In this study we analyzed members of the heterogeneous nuclear ribonucleoprotein (hnRNP) H protei
155 Mechanistically, Linc-RoR interacts with heterogeneous nuclear ribonucleoprotein (hnRNP) I and AU
156 ry and immunoprecipitation assays identified heterogeneous nuclear ribonucleoprotein (hnRNP) K and hn
157 nds of this tract with transcription factors heterogeneous nuclear ribonucleoprotein (hnRNP) K and nu
164 cused on the role of an RNA-binding protein, heterogeneous nuclear ribonucleoprotein (hnRNP) K, becau
167 ition to binding the CA-rich element (CARE), heterogeneous nuclear ribonucleoprotein (hnRNP) L regula
169 ch to identify Rumpelstiltskin, a Drosophila heterogeneous nuclear ribonucleoprotein (hnRNP) M homolo
171 the nonspecific H complex, which consists of heterogeneous nuclear ribonucleoprotein (hnRNP) proteins
172 llular function for the mRNA-binding protein heterogeneous nuclear ribonucleoprotein (hnRNP) Q1 in th
174 resulted from constitutive overexpression of heterogeneous nuclear ribonucleoprotein (hnRNP) that com
175 ponse DNA-binding protein (TARDBP/TDP-43), a heterogeneous nuclear ribonucleoprotein (hnRNP) with div
176 ly shown that LPS-induced S-nitrosylation of heterogeneous nuclear ribonucleoprotein (hnRNP)-A/B inhi
177 owed by MALDI/TOF-MS analysis, we identified heterogeneous nuclear ribonucleoprotein (hnRNP)-A2/B1 an
180 One gene found in several clones encoded a heterogeneous nuclear ribonucleoprotein (hnRNP)-related
181 high homology to Vicia faba AKIP1 and other heterogeneous nuclear ribonucleoprotein (hnRNP)-type RNA
182 g glucose regulated protein-78 kDa (GRP-78), heterogeneous nuclear ribonucleoprotein (hnRNP)-U, hnRNP
183 ption to translation, mRNA is complexed with heterogeneous nuclear ribonucleoproteins (hnRNP proteins
184 e used mass spectrometry to demonstrate that heterogeneous nuclear ribonucleoproteins (HNRNP) A2 and
187 endrites by the same cis/trans-determinants (heterogeneous nuclear ribonucleoprotein [hnRNP] A2 respo
189 tation in the prion-like domain of the human heterogeneous nuclear ribonucleoprotein hnRNPA2B1 increa
190 cing: serine/arginine-rich protein SRp75 and heterogeneous nuclear ribonucleoproteins hnRNPG and hnRN
192 A7 nuclear regulators, we identified several heterogeneous nuclear ribonucleoproteins (hnRNPs) (A1, A
193 ors that recognize the motifs and identified heterogeneous nuclear ribonucleoproteins (hnRNPs) A1 and
194 The recent direct implication of the human heterogeneous nuclear ribonucleoproteins (hnRNPs) A2B1 a
195 e we define pathogenic mutations in PrLDs of heterogeneous nuclear ribonucleoproteins (hnRNPs) A2B1 a
198 gical functions of poly(ADP-ribosyl)ation of heterogeneous nuclear ribonucleoproteins (hnRNPs) are no
199 hydrophobic residues of CD1 are involved in heterogeneous nuclear ribonucleoproteins (hnRNPs) bindin
202 mutations in UBQLN2 and some members of the heterogeneous nuclear ribonucleoproteins (hnRNPs) family
203 naptic activity were RNABPs and included the heterogeneous nuclear ribonucleoproteins (hnRNPs) G, A2/
204 etition assays, we also demonstrate that the heterogeneous nuclear ribonucleoproteins (hnRNPs) H and
206 se studies have implications for the role of heterogeneous nuclear ribonucleoproteins (hnRNPs) in the
211 hat changes in association between pADPr and heterogeneous nuclear ribonucleoproteins (hnRNPs) regula
212 ather, these animals have elevated levels of heterogeneous nuclear ribonucleoproteins (hnRNPs) that a
214 group of serine/arginine rich (SR) proteins, heterogeneous nuclear ribonucleoproteins (hnRNPs), and s
215 Several cellular proteins, including several heterogeneous nuclear ribonucleoproteins (hnRNPs), have
216 fied, Y box-binding protein-1 (YB-1) and the heterogeneous nuclear ribonucleoproteins (hnRNPs), hnRNP
223 the polypyrimidine tract-binding protein (or heterogeneous nuclear ribonucleoprotein I) as a candidat
224 ponents of a nuclear HDGF complex, including heterogeneous nuclear ribonucleoproteins implicated in p
225 own to mediate the nuclear import of several heterogeneous nuclear ribonucleoproteins, including hete
227 C1-interacting proteins including a group of heterogeneous nuclear ribonucleoproteins involved in WNT
229 iptional-inducer and translational-regulator heterogeneous nuclear ribonucleoprotein K (hnRNP K or HN
230 KH3 domain of the transcriptional regulator heterogeneous nuclear ribonucleoprotein K (hnRNP K) and
231 ence similarity searches in such proteins as heterogeneous nuclear ribonucleoprotein K (hnRNP K) and
233 Through differential proteomics, we identify heterogeneous nuclear ribonucleoprotein K (hnRNP K) as b
235 Instead, AURKA preferentially interacts with heterogeneous nuclear ribonucleoprotein K (hnRNP K) in t
239 ichaelis-Menten curve for the methylation of heterogeneous nuclear ribonucleoprotein K (hnRNP K) prot
241 action and bound a rapidly migrating form of heterogeneous nuclear ribonucleoprotein K (hnRNP K), a m
242 one cDNA clone were 100% identical to human heterogeneous nuclear ribonucleoprotein K (hnRNP K), a p
243 directly cleaved the DNA/RNA-binding protein heterogeneous nuclear ribonucleoprotein K (hnRNP K), des
244 hoprotein (KBBP), the mouse homolog of human heterogeneous nuclear ribonucleoprotein K (hnRNP K), whi
245 ound a direct association between TDP-43 and heterogeneous nuclear ribonucleoprotein K (hnRNP K).
246 enesis by phosphorylating a specific site on heterogeneous nuclear ribonucleoprotein K (hnRNP K).
248 identified the nucleic acid-binding protein, heterogeneous nuclear ribonucleoprotein K (hnRNP-K), by
252 e interaction of the C-terminal KH domain of heterogeneous nuclear ribonucleoprotein K (KH3) with its
253 M-2 but not the related KH domain containing heterogeneous nuclear ribonucleoprotein K are novel subs
254 oteins contain two domains homologous to the heterogeneous nuclear ribonucleoprotein K homology (KH)
255 amino acids 216 and 353, which contribute to heterogeneous nuclear ribonucleoprotein K mediated trans
260 substrates identified using this approach is heterogeneous nuclear ribonucleoprotein K, which is invo
261 us encodes several RNA-binding proteins with heterogeneous nuclear ribonucleoprotein K-type homology,
263 ne-rich C terminus classifying it with other heterogeneous nuclear ribonucleoproteins known as 2XRBD-
264 d in the 60-kDa complex and identified it as heterogeneous nuclear ribonucleoprotein L (hnRNP L) by p
266 protein (PTB) and an hnRNA binding protein, heterogeneous nuclear ribonucleoprotein L (hnRNP L), pro
268 e expression in higher eukaryotes by binding heterogeneous nuclear ribonucleoprotein L (hnRNP L).
269 the hAPE1 gene contains APE1 itself and the heterogeneous nuclear ribonucleoprotein L (hnRNP-L).
270 tivated inhibitor of translation complex and heterogeneous nuclear ribonucleoprotein L (HNRNPL, also
272 S mediates these effects by interacting with heterogeneous nuclear ribonucleoprotein L via a CANACA m
275 affinity chromatography, we have identified heterogeneous nuclear ribonucleoprotein M (hnRNP M) as a
277 In Saccharomyces cerevisiae, the shuttling heterogeneous nuclear ribonucleoprotein, Nab2, which is
280 on of this protein with other members of the heterogeneous nuclear ribonucleoprotein protein family.
281 the Caenorhabditis elegans homolog of human heterogeneous nuclear ribonucleoproteins Q and R, binds
283 two elements bound NF-kappaB p50 and p65 and heterogeneous nuclear ribonucleoprotein RNP D, respectiv
284 suggesting that IP6 was acting subsequent to heterogeneous nuclear ribonucleoprotein targeting to the
285 hnRNP A1 is a nucleocytoplasmic shuttling heterogeneous nuclear ribonucleoprotein that accompanies
286 bular domain of Mlp1p and Nab2p, a shuttling heterogeneous nuclear ribonucleoprotein that is required
287 ssociated protein 5 (E1B-AP5) is a cellular, heterogeneous nuclear ribonucleoprotein that is targeted
288 nding protein 2 (Nab2) is an essential yeast heterogeneous nuclear ribonucleoprotein that modulates b
289 ny of the putative IRES-binding proteins are heterogeneous nuclear ribonucleoproteins that have recog
290 les in human patients.SIGNIFICANCE STATEMENT Heterogeneous nuclear ribonucleoprotein U (hnRNP U) belo
292 RNA-binding protein homologous to mammalian heterogeneous nuclear ribonucleoprotein U (hnRNP U), pla
293 ein-RNA complex as HuR, TIA-1, TIAR, and the heterogeneous nuclear ribonucleoprotein U (hnRNP U).
294 tb7b recruits the brown fat lncRNA 1 (Blnc1)/heterogeneous nuclear ribonucleoprotein U (hnRNPU) ribon
295 q, and RNA-seq, we investigated roles of the Heterogeneous Nuclear Ribonucleoprotein U (HNRNPU), a nu
298 ymerase II and the transcriptional regulator heterogeneous nuclear ribonucleoprotein-U (hnRNP-U), bot
300 ly conserved across all vertebrates, whereas heterogeneous nuclear ribonucleoproteins, which bind man
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