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1 lation site, independent of the U1 snRNP (U1 small nuclear ribonucleoprotein).
2 rs such as Lsm11, a core component of the U7 small nuclear ribonucleoprotein.
3 PRP8 (R1753K), a protein component of the U5 small nuclear ribonucleoprotein.
4 of the 70-kDa subunit of U1 snRNP (U1-70kDa) small nuclear ribonucleoprotein.
5 of the 5' splice site of pre-mRNAs by the U1 small nuclear ribonucleoprotein.
6 ily, interact with the 70k protein of the U1 small nuclear ribonucleoprotein.
7 licing is mediated by the proteins of the U2 small nuclear ribonucleoprotein.
8 ding proteins (RBPs): lupus La and 70-kDa U1 small nuclear ribonucleoprotein.
9 that are suppressed, at least in part, by U1 small nuclear ribonucleoproteins.
10 which contain mostly nonoverlapping sets of small nuclear ribonucleoproteins.
11 pliceosome type resides in the U6 and U6atac small nuclear ribonucleoproteins.
12 omponent complex involved in the assembly of small nuclear ribonucleoproteins.
13 ated with the Sm core domain of spliceosomal small nuclear ribonucleoproteins.
14 ex required for the assembly of spliceosomal small nuclear ribonucleoproteins.
15 e complexes with stably bound U2, U5, and U6 small nuclear ribonucleoproteins.
17 he present study, we characterized U1-70-kDa small nuclear ribonucleoprotein (70-kDa) autoantigen-spe
18 t is characterized by high levels of anti-U1 small nuclear ribonucleoprotein 70k autoantibodies and a
20 raised against the main MCTD autoantigen U1 small nuclear ribonucleoprotein 70k were found in nearly
25 r messenger RNAs (pre-mRNAs) contains the U7 small nuclear ribonucleoprotein and shares the key cleav
26 ex functions in the assembly of spliceosomal small nuclear ribonucleoproteins and probably other ribo
27 ceosome from analysis of individual purified small nuclear ribonucleoproteins and salt-stable spliceo
28 ort of spliced mRNA, small nuclear RNAs, and small nuclear ribonucleoproteins and slow the nuclear tr
29 uclear domain important to the biogenesis of small nuclear ribonucleoproteins and telomerase, complex
30 nts, FLICE-associated huge protein, Mute, U7 small nuclear ribonucleoprotein, and MPM-2 phosphoepitop
31 ) were found in two other human proteins, U5 small nuclear ribonucleoprotein, and transcription facto
32 erved previously in myelin basic protein, Sm small nuclear ribonucleoproteins, and other polypeptides
34 evidence indicates that U1-70K and other U1 small nuclear ribonucleoproteins are Sarkosyl-insoluble
35 NAs can associate with Sm protein-containing small nuclear ribonucleoproteins, as judged by immunopre
36 ressed in metazoan cells and plays a role in small nuclear ribonucleoprotein assembly and pre-mRNA sp
37 to understand the mechanism of SMN-assisted small nuclear ribonucleoprotein assembly and the underly
38 Here we show that GEMIN2, a spliceosomal small nuclear ribonucleoprotein assembly factor conserve
39 pICln, SMN and Gemin5, which are involved in small nuclear ribonucleoprotein assembly, have an import
41 -COP protein co-immunoprecipitates with SMN, small nuclear ribonucleoprotein-associated assembly fact
43 nal transcribed allele of the imprinted gene Small nuclear ribonucleoprotein-associated polypeptide N
44 r for plasmid DNA, exon-1 from the imprinted small nuclear ribonucleoprotein-associated polypeptide N
45 at sequential addition of the U4/U6 proteins small nuclear ribonucleoprotein-associated protein 1 (Sn
46 ive, varied immune response against multiple small nuclear ribonucleoprotein autoantigens similar to
47 hanced complex A formation and binding of U2 small nuclear ribonucleoprotein auxiliary factor 65 kDa
48 d splicing regulatory proteins, including u2 small nuclear ribonucleoprotein auxiliary factor 65-kDa
51 onucleoprotein polypeptide N), and U2af1 (U2 small nuclear ribonucleoprotein auxiliary factor), remai
52 es assembled on pre-mRNA, blocking U1 snRNP (small nuclear ribonucleoprotein) binding and exon inclus
53 PID in the liberation of P-TEFb from the 7SK small nuclear ribonucleoprotein complex (7SK snPNP).
54 ibitor (PSI) and its interaction with the U1 small nuclear ribonucleoprotein complex (snRNP) control
55 luded diverse components of the U4/U6.U5 tri-small nuclear ribonucleoprotein complex and several spli
56 -B, that are physically associated in the U1-small nuclear ribonucleoprotein complex and that are fre
57 rays revealed that serum anti-Smith and anti-small nuclear ribonucleoprotein complex autoantibodies,
58 clin T1 and CDK9 are incorporated in the 7SK small nuclear ribonucleoprotein complex containing the i
60 ncode core components of the spliceosomal U6 small nuclear ribonucleoprotein complex, regulate circad
63 plicing complex Bact consisting of the three small nuclear ribonucleoprotein complexes (snRNPs) U2, U
65 ckdown of proteins associated with different small nuclear ribonucleoprotein complexes and by using t
67 osophila homologue of Prp38p (dPrp38), a tri-small nuclear ribonucleoprotein component, and is requir
68 findings imply that these two genes encoding small nuclear ribonucleoprotein components are subject t
69 tein complex with the methylosome components small nuclear ribonucleoprotein D3b (SmD3b) and protein
70 Brr2 enzyme, which is essential for U4/U6 di-small nuclear ribonucleoprotein disruption during splice
72 cts with several Sm proteins of spliceosomal small nuclear ribonucleoproteins, in particular, with Sm
74 erlying the conversion of soluble nuclear U1 small nuclear ribonucleoproteins into insoluble cytoplas
75 mammalian 70K protein, a component of the U1 small nuclear ribonucleoprotein involved in pre-mRNA spl
77 proteins found in the U1 and U2 spliceosomal small nuclear ribonucleoproteins is highly conserved.
78 ts some novel functions for Snp1p and the U1 small nuclear ribonucleoprotein late in spliceosome deve
79 of PWS carrying a paternal (p) deletion from small nuclear ribonucleoprotein N (Snrpn (S)) to ubiquit
81 and humans, the locus encoding the gene for small nuclear ribonucleoprotein N (SNRPN/Snrpn), as well
82 tends approximately 450 kb to UBE3A from the small nuclear ribonucleoprotein N (SNURF/SNRPN) promoter
84 x, SF3B3 and SF3B5, that form part of the U2 small nuclear ribonucleoprotein particle (snRNP) are als
86 snRNP and the polypyrimidine tract by the U2 small nuclear ribonucleoprotein particle (snRNP) auxilia
89 he 5' splice site, and a component of the U2 small nuclear ribonucleoprotein particle (snRNP) complex
90 k9-cyclin T modules from large, inactive 7SK small nuclear ribonucleoprotein particle (snRNP) complex
91 In this investigation, we made use of anti-small nuclear ribonucleoprotein particle (snRNP) Ig tran
92 The current model for the function of the U5 small nuclear ribonucleoprotein particle (snRNP) in the
93 t dephosphorylated SRp38 interacts with a U1 small nuclear ribonucleoprotein particle (snRNP) protein
94 s shown to promote the recruitment of the U1 small nuclear ribonucleoprotein particle (snRNP) to the
102 ) domain of spliceosomal A protein of the U1 small nuclear ribonucleoprotein particle (U1A) interacti
104 was detected in association with a subset of small nuclear ribonucleoprotein particle and Ser-Arg pro
105 esidues 885-2413) in complex with Aar2, a U5 small nuclear ribonucleoprotein particle assembly factor
108 and trans-splicing using the specialized SL2 small nuclear ribonucleoprotein particle for downstream
109 thereby promoting the dissociation of the U1 small nuclear ribonucleoprotein particle from the 5' spl
110 hat SmD1, a core component of the Drosophila small nuclear ribonucleoprotein particle implicated in s
112 the 5' splice site, cross-linking of the U5 small nuclear ribonucleoprotein particle protein, U5(200
114 l nuclear ribonucleoprotein (snRNP) is a 25S small nuclear ribonucleoprotein particle similar in size
116 which facilitates the interaction of the U2 small nuclear ribonucleoprotein particle with the branch
117 ceosome assembly within the mature U2 snRNP (small nuclear ribonucleoprotein particle), and its displ
120 IIF (TFIIF), TFIIS, splicing factors, the U7 small nuclear ribonucleoprotein particle, the stem-loop
121 nd in a manner independent of Prp16p, the U5 small nuclear ribonucleoprotein particle-associated prot
123 -B7.2 Abs expressed significantly lower anti-small nuclear ribonucleoprotein particles (snRNP) and an
124 of these introns requires a different set of small nuclear ribonucleoprotein particles (snRNPs) (U11,
125 When Prp24 is absent, unpaired U4 and U6 small nuclear ribonucleoprotein particles (snRNPs) accum
126 functions in the biogenesis of spliceosomal small nuclear ribonucleoprotein particles (snRNPs) and p
129 site for the Sm proteins, both hallmarks of small nuclear ribonucleoprotein particles (snRNPs) that
130 cipitation (ChIP) analysis of U1, U2, and U5 small nuclear ribonucleoprotein particles (snRNPs) to in
131 r messenger RNA substrate bound to U1 and U2 small nuclear ribonucleoprotein particles (snRNPs), and
133 tion as an assembly machine for spliceosomal small nuclear ribonucleoprotein particles (snRNPs), the
137 B" and is an integral component of U1 and U2 small nuclear ribonucleoprotein particles (snRNPs).
138 mplex containing U1, U2, U5 and duplex U4/U6 small nuclear ribonucleoprotein particles (snRNPs).
139 nucleotides, a method that was developed for small nuclear ribonucleoprotein particles (snRNPs).
140 of Sm core structures of spliceosomal U-rich small nuclear ribonucleoprotein particles (UsnRNPs) requ
141 strictive temperature (39.5 degrees C), both small nuclear ribonucleoprotein particles and a general
142 he U12-type spliceosomes, large complexes of small nuclear ribonucleoprotein particles and associated
143 LIP, which immunoprecipitates SmB along with small nuclear ribonucleoprotein particles and auxiliary
144 ke proteins are stable components of several small nuclear ribonucleoprotein particles that function
145 autoreactive B cells that recognize self-Ag small nuclear ribonucleoprotein particles with activated
146 important for the biogenesis of spliceosomal small nuclear ribonucleoprotein particles, but downstrea
147 tion occurred after inactivation of U1 or U2 small nuclear ribonucleoprotein particles, compatible wi
148 d the spliceosome, which is composed of five small nuclear ribonucleoprotein particles, U1, U2, U4/U6
151 l microdeletions within the 5' region of the small nuclear ribonucleoprotein polypeptide N ( SNRPN )
152 bserved at maternally methylated ICs such as small nuclear ribonucleoprotein polypeptide N (SNRPN), S
154 nscript), Sgce (epsilon-sarcoglycan), Snrpn (small nuclear ribonucleoprotein polypeptide N), and U2af
155 3), insulin-like growth factor 2 (IGF2), and small nuclear ribonucleoprotein polypeptide N, and the l
156 mplicated in the biogenesis of several other small nuclear ribonucleoproteins required for processing
157 nting stable recruitment of the U4/U5/U6 tri-small nuclear ribonucleoprotein, resulting in accumulati
158 rs include histone, a protein component of a small nuclear ribonucleoprotein, ribosomal proteins, and
159 aled that these structures contained the non-small nuclear ribonucleoprotein RNA processing factor, S
161 he CB, such as the SMN complex, spliceosomal small nuclear ribonucleoproteins (RNPs), small nucleolar
162 l domain has a protein fold similar to human small nuclear ribonucleoprotein Sm D3 and Haloarcula mar
163 ted with B7 blocking Abs exhibit strong anti-small nuclear ribonucleoprotein (snRNP) and anti-DNA aut
164 scovered an RNA motif that recognizes the U1 small nuclear ribonucleoprotein (snRNP) and is essential
165 splicing pathway through association with U1 small nuclear ribonucleoprotein (snRNP) and non-snRNP sp
166 duction, as seen in serum Ig, anti-DNA, anti-small nuclear ribonucleoprotein (snRNP) and rheumatoid f
167 pathway and involves interactions between U1 small nuclear ribonucleoprotein (snRNP) and the pre-mRNA
169 issense mutants can rescue iMEF survival and small nuclear ribonucleoprotein (snRNP) assembly, demons
175 RE consists of a single 9-nucleotide (nt) U1 small nuclear ribonucleoprotein (snRNP) base pairing sit
177 class 5' splice site and is required for U11 small nuclear ribonucleoprotein (snRNP) binding to the N
178 and Gemin4, and it plays important roles in small nuclear ribonucleoprotein (snRNP) biogenesis and i
179 N has been shown to function in spliceosomal small nuclear ribonucleoprotein (snRNP) biogenesis and p
180 tein plays an important role in spliceosomal small nuclear ribonucleoprotein (snRNP) biogenesis and t
182 urney to the spliceosome.The mechanism of U6 small nuclear ribonucleoprotein (snRNP) biogenesis is no
184 trates within Cajal bodies (CBs) and impacts small nuclear ribonucleoprotein (snRNP) biogenesis.
185 s (CBs) are subnuclear domains implicated in small nuclear ribonucleoprotein (snRNP) biogenesis.
187 stered into a transcriptionally inactive 7SK small nuclear ribonucleoprotein (snRNP) by the coordinat
188 Interestingly, canonical CB foci and coilin/small nuclear ribonucleoprotein (snRNP) co-localization
190 eoli and bound what we believe to be a novel small nuclear ribonucleoprotein (snRNP) complex composed
192 essential gene encoding a subunit of the U5 small nuclear ribonucleoprotein (snRNP) complex of the s
193 binds 7SK RNA and, as a component of the 7SK small nuclear ribonucleoprotein (snRNP) complex, is recr
197 ) complex is essential for the biogenesis of small nuclear ribonucleoprotein (snRNP) complexes in euk
198 many splicing factors, including the key U2 small nuclear ribonucleoprotein (snRNP) component SF3B1
199 spliceostatin A, sudemycin E binds to the U2 small nuclear ribonucleoprotein (snRNP) component SF3B1.
200 7, 251, 261 and 271 residues of MoSNP1, a U1 small nuclear ribonucleoprotein (snRNP) component, likel
202 otor neurons (SMN) complex for assembly into small nuclear ribonucleoprotein (snRNP) core particles.
209 licing factor Tat-SF1 associates with the U2 small nuclear ribonucleoprotein (snRNP) of the spliceoso
210 8p is a unique component of the U4/U6.U5 tri-small nuclear ribonucleoprotein (snRNP) particle and is
211 association of PSI with the spliceosomal U1 small nuclear ribonucleoprotein (snRNP) particle in soma
212 thway of subunit addition that includes both small nuclear ribonucleoprotein (snRNP) particles and no
213 In addition to La and Ro52, proteins in the small nuclear ribonucleoprotein (snRNP) particles such a
214 ous nuclear ribonucleoproteins (hnRNPs), and small nuclear ribonucleoprotein (snRNP) particles throug
216 novo motif analysis shows PAS signals and U1 small nuclear ribonucleoprotein (snRNP) recognition site
218 ing protein 1, and with several spliceosomal small nuclear ribonucleoprotein (snRNP) Sm proteins.
219 olecular recognition of tau pre-mRNA by a U1 small nuclear ribonucleoprotein (snRNP) splicing factor.
221 ds to exon 3 of the pre-mRNA and recruits U1 small nuclear ribonucleoprotein (snRNP) to the F1 pseudo
223 nisms that regulate P-TEFb involving the 7SK small nuclear ribonucleoprotein (snRNP), factors that co
224 splicing factor compartment (SFC) [e.g. the small nuclear ribonucleoprotein (snRNP), U2B, and serine
225 p80-coilin, which is colocalized with the U7 small nuclear ribonucleoprotein (snRNP), whereas the att
226 is inhibited by HEXIM1 or HEXIM2 in the 7SK small nuclear ribonucleoprotein (snRNP), which contains,
228 ctions of individual SR proteins with the U1 small nuclear ribonucleoprotein (snRNP)-associated 70-kD
230 Both the BBR and BPS interact with the U2 small nuclear ribonucleoprotein (snRNP)-associated SF3b
236 spliceosome is a complex machine composed of small nuclear ribonucleoproteins (snRNPs) and accessory
237 olyadenylation and was recognized by both U1 small nuclear ribonucleoproteins (snRNPs) and alternativ
238 clear organelles that are highly enriched in small nuclear ribonucleoproteins (snRNPs) and certain ba
239 ntial role in the production of spliceosomal small nuclear ribonucleoproteins (snRNPs) and likely oth
240 mportant role in the cytoplasmic assembly of small nuclear ribonucleoproteins (snRNPs) and likely oth
241 dynamic RNA-protein machinery consisting of small nuclear ribonucleoproteins (snRNPs) and non-snRNP
242 a key role in the biogenesis of spliceosomal small nuclear ribonucleoproteins (snRNPs) and other ribo
243 nslational modification in the biogenesis of small nuclear ribonucleoproteins (snRNPs) and pre-mRNA s
244 s a role in the assembly and regeneration of small nuclear ribonucleoproteins (snRNPs) and spliceosom
246 rine-arginine (SR) proteins, U1snRNP, and U6 small nuclear ribonucleoproteins (snRNPs) are implicated
247 tterns of autoantibody reactivities with the small nuclear ribonucleoproteins (snRNPs) are observed i
248 essential for the biogenesis of spliceosomal small nuclear ribonucleoproteins (snRNPs) as it binds to
249 splicing factors SF2/ASF and U1, U2, and U11 small nuclear ribonucleoproteins (snRNPs) bind the NRS,
250 The prespliceosome, comprising U1 and U2 small nuclear ribonucleoproteins (snRNPs) bound to the p
252 d are associated with defects in assembly of small nuclear ribonucleoproteins (snRNPs) in vitro.
254 5), which are required for the biogenesis of small nuclear ribonucleoproteins (snRNPs) involved in mR
258 machinery including SR proteins, U1 and U2, small nuclear ribonucleoproteins (snRNPs) of the major s
259 sequential recruitment and rearrangement of small nuclear ribonucleoproteins (snRNPs) on a pre-mRNA
260 rected cross-linking with in vitro assembled small nuclear ribonucleoproteins (snRNPs) or spliceosome
261 lear domains important for the biogenesis of small nuclear ribonucleoproteins (snRNPs) which function
262 ct with the Sm core proteins of spliceosomal small nuclear ribonucleoproteins (snRNPs), and they play
263 onents of the spliceosome, U1, U2, U4 and U5 small nuclear ribonucleoproteins (snRNPs), contain seven
265 N complex is essential for the biogenesis of small nuclear ribonucleoproteins (snRNPs), the major con
267 E, F, and G, shared by U1, U2, U4-6, and U5 small nuclear ribonucleoproteins (snRNPs), while anti-nu
276 clear ribonucleoprotein 70-kDa protein, a U1 small nuclear ribonucleoprotein-specific protein, has be
277 re we report that U1C, one of three human U1 small nuclear ribonucleoprotein-specific proteins, inter
279 ormation of aberrant U11- and U12-containing small nuclear ribonucleoproteins that impair the efficie
280 mic acid, which releases P-TEFb from the 7SK small nuclear ribonucleoprotein, they turned green.
283 in the assembly of spliceosomal uridine-rich small nuclear ribonucleoprotein (U snRNP) complexes coul
285 for novel peptide sequences in either p53 or small nuclear ribonucleoprotein-U (snRNP-U) and substant
286 R proteins but does not interact with the U1 small nuclear ribonucleoprotein U1-70K or the 35-kDa sub
287 he early spliceosome assembly begins with U1 small nuclear ribonucleoprotein (U1 snRNP) binding to th
288 n the disease, including U1-70K and other U1 small nuclear ribonucleoprotein (U1 snRNP) spliceosome c
289 the U1 small nuclear RNA component of the U1 small nuclear ribonucleoprotein (U1 snRNP) splicing fact
291 ng factors (SR splicing factors) with the U1-small nuclear ribonucleoprotein (U1-snRNP) and U3-small
294 me proteins associated with the uridine-rich small nuclear ribonucleoproteins U2, U5, and U6 and the
297 g in mammalian cell extracts requires the U7 small nuclear ribonucleoprotein (U7 snRNP) and an uniden
300 the latter, it is incorporated into the 7SK small nuclear ribonucleoprotein, which contains hexameth