ライフサイエンスコーパス: protein arginine methyltransferase

1 lation, and we designate the enzyme as Rmt2 (protein arginine methyltransferase).

2 nfirm its activity as the prototype type III protein arginine methyltransferase.

3 we generated an enzyme-dead knock-in of this protein arginine methyltransferase.

4 D physically interacts with PRMT1, the major protein arginine methyltransferase.

5 stone H4-specific methyltransferase PRMT1, a protein arginine methyltransferase.

6 d protein kinase, and by Hsl7, a presumptive protein-arginine methyltransferase.

7 ated arginine methyltransferase 1 (CARM1), a protein-arginine methyltransferase.

8 tification of an array of substrates for the protein arginine methyltransferases.

9 insight into the structure and catalysis of protein arginine methyltransferases.

10 nd was highly selective for CARM1 over other protein arginine methyltransferases.

11 diverse product specificity displayed by the protein-arginine methyltransferases.

12 o-hydrolase, and is derived by the action of protein-arginine-methyltransferases.

13 w that glycogen synthase kinase 3 (GSK3) and protein arginine methyltransferase 1 (PRMT-1) cooperate

14 We recently reported defects in protein arginine methyltransferase 1 (PRMT1) activity an

15 Protein arginine methyltransferase 1 (PRMT1) acts as a t

16 ion of E2F-1 by the asymmetric dimethylating protein arginine methyltransferase 1 (PRMT1) and symmetr

17 Here we identified the type I protein arginine methyltransferase 1 (PRMT1) as a restri

18 Protein arginine methyltransferase 1 (PRMT1) catalyzes t

19 Protein arginine methyltransferase 1 (PRMT1) catalyzing

20 logical activity of RIP140 was suppressed by protein arginine methyltransferase 1 (PRMT1) due to RIP1

21 and R200 of the EGFR extracellular domain by protein arginine methyltransferase 1 (PRMT1) enhances bi

22 Protein arginine methyltransferase 1 (PRMT1) is a key re

23 Protein arginine methyltransferase 1 (PRMT1) is an essen

24 Copious expression of protein arginine methyltransferase 1 (PRMT1) is associat

25 Protein arginine methyltransferase 1 (PRMT1) is involved

26 Here, we report that protein arginine methyltransferase 1 (PRMT1) is required

27 Protein Arginine methyltransferase 1 (PRMT1) is the main

28 Protein arginine methyltransferase 1 (PRMT1) is up-regul

29 , steroid receptor coactivator 1 (SRC1), and protein arginine methyltransferase 1 (PRMT1) only modest

30 As the major arginine methylation enzyme, protein arginine methyltransferase 1 (PRMT1) strictly ge

31 Here, we show protein arginine methyltransferase 1 (PRMT1), a key enzy

32 In the current study, protein arginine methyltransferase 1 (PRMT1), another ar

33 ty is potentiated by arginine methylation by protein arginine methyltransferase 1 (PRMT1), another nu

34 S by the class 1 arginine methyltransferase, protein arginine methyltransferase 1 (PRMT1), regulates

35 Protein arginine methyltransferase 1 (PRMT1), the predom

36 during Wnt signaling through the activity of protein arginine methyltransferase 1 (PRMT1), which tran

37 implementation to label substrates of human protein arginine methyltransferase 1 (PRMT1).

38 e chain of a peptide substrate by the enzyme protein arginine methyltransferase 1 (RMT1).

39 SG-nucleating protein G3BP1 is methylated by protein arginine methyltransferase 1 and 5 (PRMT1 and PR

40 deletion of the arginine methyltransferases protein arginine methyltransferase 1 and protein arginin

41 IP45 acts as an enhancer for the assembly of protein arginine methyltransferase 1 and the protein arg

42 s of protein methylation and coexpression of protein arginine methyltransferase 1 did not influence N

43 t LANA is subject to arginine methylation by protein arginine methyltransferase 1 in vitro and in viv

44 asymmetric dimethyl H4R3 catalyzed by PRMT1 (protein arginine methyltransferase 1) facilitates histon

45 asonuclin 1 physically interacts with PRMT1 (protein arginine methyltransferase 1) to activate cell c

46 overy of a novel AE9a binding partner PRMT1 (protein arginine methyltransferase 1).

47 bonucleoprotein K (hnRNP K) protein by human protein arginine methyltransferase 1, variant 1 (hPRMT1v

48 EYA1 physically interacts with protein arginine methyltransferase 1, which methylates E

49 protein arginine methyltransferase 1 and the protein arginine methyltransferase 1-linked histone 4 ar

50 FGG-amide), a highly effective substrate for protein arginine methyltransferase 1.

51 phosphatase-transcription activator EYA1 by protein arginine methyltransferase 1: mechanistic, funct

52 When protein-arginine methyltransferase 1 expression was redu

53 Protein-arginine methyltransferase 1 has much less effec

54 transferase (EC 2.1.1.23) gene "PRMT1, " for protein-arginine methyltransferase 1.

55 We found that both protein-arginine methyltransferases 1 and 5 methylate Ar

56 s used to validate the interactions of BRD4, protein arginine methyltransferase-1 (PRMT1), and Snail.

57 hydrolase protein expression was reduced and protein-arginine-methyltransferase-1 increased in alcoho

58 Protein arginine methyltransferase 10 (PRMT10) is a type

59 ed yeast two-hybrid screening and identified protein arginine methyltransferase 2 (PRMT2) as a new ER

60 Here, we uncover protein arginine methyltransferase 3 (PRMT3) as a driver

61 The mammalian protein arginine methyltransferase 3 (PRMT3) catalyzes t

62 with myocardial infarction, the PRMT3 gene (protein arginine methyltransferase 3) with stroke, and t

63 Previous studies suggested that protein arginine methyltransferase 4 (PRMT4) was incorpo

64 we report a novel regulation of pRb through protein arginine methyltransferase 4 (PRMT4)-mediated ar

65 en ASXL2 and MLL3 is negatively regulated by protein arginine methyltransferase 4 (PRMT4/CARM1), whic

66 We have identified a mutant, protein arginine methyltransferase 5 (atprmt5), that fai

67 mpairs T cell function via the inhibition of protein arginine methyltransferase 5 (PRMT5) and by aden

68 ase (MTAP) confers a selective dependence on protein arginine methyltransferase 5 (PRMT5) and its bin

69 UsnRNPs) requires assembly factors united in protein arginine methyltransferase 5 (PRMT5) and surviva

70 ion and characterization of a complex of the protein arginine methyltransferase 5 (Prmt5) and the met

71 cance of PDCD4 in breast cancer and identify protein arginine methyltransferase 5 (PRMT5) as a cofact

72 Here, we describe the identification of the protein arginine methyltransferase 5 (PRMT5) as an effec

73 rification and mass spectrometry to identify protein arginine methyltransferase 5 (PRMT5) as part of

74 Protein arginine methyltransferase 5 (PRMT5) catalyzes s

75 Here we show that protein arginine methyltransferase 5 (PRMT5) catalyzes s

76 Protein arginine methyltransferase 5 (PRMT5) catalyzes s

77 Protein arginine methyltransferase 5 (PRMT5) catalyzes t

78 Protein arginine methyltransferase 5 (PRMT5) complexed w

79 Here we demonstrate that protein arginine methyltransferase 5 (PRMT5) functions a

80 The aberrant expression of protein arginine methyltransferase 5 (PRMT5) has been as

81 Dysregulation of protein arginine methyltransferase 5 (PRMT5) has been im

82 Protein arginine methyltransferase 5 (PRMT5) has emerged

83 Protein arginine methyltransferase 5 (PRMT5) has recentl

84 a positive feedback loop between BCR-ABL and protein arginine methyltransferase 5 (PRMT5) in CML cell

85 duces a synthetic lethal phenotype involving protein arginine methyltransferase 5 (PRMT5) inhibition.

86 NS-penetrant methylthioadenosine-cooperative protein arginine methyltransferase 5 (PRMT5) inhibitor,

87 Protein arginine methyltransferase 5 (PRMT5) is a key ep

88 Protein arginine methyltransferase 5 (PRMT5) is a key sp

89 Protein arginine methyltransferase 5 (PRMT5) is a master

90 Protein arginine methyltransferase 5 (PRMT5) is a synthe

91 Protein arginine methyltransferase 5 (PRMT5) is a synthe

92 Protein arginine methyltransferase 5 (PRMT5) is a type I

93 Protein arginine methyltransferase 5 (PRMT5) is an argin

94 Protein arginine methyltransferase 5 (PRMT5) is an emerg

95 Protein arginine methyltransferase 5 (PRMT5) is implicat

96 Protein arginine methyltransferase 5 (PRMT5) is overexpr

97 evidence suggest that the methyltransferase protein arginine methyltransferase 5 (PRMT5) is responsi

98 Protein arginine methyltransferase 5 (PRMT5) is the majo

99 Protein arginine methyltransferase 5 (PRMT5) is the prim

100 cleaved kinases (M6CKs) bind subunits of the protein arginine methyltransferase 5 (PRMT5) molecular c

101 Protein arginine methyltransferase 5 (PRMT5) plays cruci

102 Protein arginine methyltransferase 5 (PRMT5) plays multi

103 tumor suppressor, but its coexpression with protein arginine methyltransferase 5 (PRMT5) promotes ac

104 transformation to document the relevance of protein arginine methyltransferase 5 (PRMT5) to regulati

105 Menin directly interacts with protein arginine methyltransferase 5 (PRMT5), a negative

106 Protein arginine methyltransferase 5 (PRMT5), a protein

107 Here, we report that protein arginine methyltransferase 5 (PRMT5), an enzyme

108 Here we report that protein arginine methyltransferase 5 (PRMT5), but not ot

109 ll nuclear ribonucleoprotein D3b (SmD3b) and protein arginine methyltransferase 5 (PRMT5), which are

110 Inhibition of protein arginine methyltransferase 5 (PRMT5), which cata

111 High levels of MTA inhibit protein arginine methyltransferase 5 (PRMT5), which sens

112 sphorylation through an association with the protein arginine methyltransferase 5 (PRMT5).

113 cted requirement for arginine methylation by protein arginine methyltransferase 5 (PRMT5).

114 ovel interaction between NF-kappaB, YBX1 and protein arginine methyltransferase 5 (PRMT5).

115 y posttranslational methylation at Arg-57 by protein arginine methyltransferase 5 (PRMT5).

116 forward genetic analysis we demonstrate that protein arginine methyltransferase 5 (PRMT5; At4g31120)

117 Protein arginine methyltransferase 5 inhibition often le

118 GSK3326595 is a first-generation protein arginine methyltransferase 5 inhibitor.

119 that E2F-1 is directly methylated by PRMT5 (protein arginine methyltransferase 5), and that arginine

120 ses protein arginine methyltransferase 1 and protein arginine methyltransferase 5, suggesting that th

121 free transcriptional system and contains the protein arginine methyltransferase 5, which acts synergi

122 ppaB is dimethylated on arginine 30 (R30) by protein-arginine methyltransferase 5 (PRMT5).

123 Protein arginine methyltransferase-5 (PRMT5) is overexpr

124 cific inhibitor of the cell-essential enzyme Protein Arginine Methyltransferase-5 (PRMT5).

125 on of the known Ajuba binding partner Prmt5 (protein arginine methyltransferase-5) inhibited the Ajub

126 ors lysine-specific demethylase 1 (LSD1) and protein arginine methyltransferase 6 (PRMT6) are overexp

127 Protein arginine methyltransferase 6 (PRMT6) catalyzes m

128 tor arginine methyltransferase 1 (CARM1) and protein arginine methyltransferase 6 (PRMT6) in vitro an

129 Protein arginine methyltransferase 6 (PRMT6) is a nuclea

130 We show here that protein arginine methyltransferase 6 (PRMT6) is a specif

131 Protein arginine methyltransferase 6 (PRMT6) plays impor

132 Here, we show that TAL1 interacts with protein-arginine-methyltransferase-6 (PRMT6) on the ID3

133 Protein arginine methyltransferase 7 (PRMT7) catalyzes t

134 Full-length human protein arginine methyltransferase 7 (PRMT7) expressed a

135 The mammalian protein arginine methyltransferase 7 (PRMT7) has been im

136 Here, we show that the protein arginine methyltransferase 7 (PRMT7) is a plurip

137 Protein arginine methyltransferase 7 (PRMT7) is an epige

138 Protein arginine methyltransferase 7 (PRMT7) methylates

139 us are associated with blunted expression of protein arginine methyltransferase 7 (Prmt7) on chromoso

140 The protein arginine methyltransferase 7 (PRMT7), but not PR

141 bstrate recognition motif specific for human protein arginine methyltransferase 7 (PRMT7).

142 We found that the selective inhibitor of protein arginine methyltransferases 7,7'-carbonylbis(aza

143 Here we use mice lacking protein arginine methyltransferase 8 (PRMT8) in the brai

144 The multifunctional protein arginine methyltransferase 8 (PRMT8) possesses b

145 Protein arginine methyltransferase 9 (PRMT9) is a recent

146 Protein arginine methyltransferase 9 (PRMT9) is part of

147 +), FDH(+/-), and FDH(-/-) mice have similar protein arginine methyltransferase activities but high,

148 lts provide an example for the regulation of protein arginine methyltransferase activity by phosphory

149 most 80% identical to human PRMT1, the major protein arginine methyltransferase activity in mammalian

150 uential recruitment of CARM1 not only adds a protein arginine methyltransferase activity to the ER-co

151 In a previous study, this protein arginine methyltransferase activity was identifi

152 ediate-early protein, was then shown to have protein arginine methyltransferase activity.

153 sferase I (PRMT1) contributes >90% of type I protein-arginine methyltransferase activity in cells and

154 Protein-arginine methyltransferases aid in the regulatio

155 nd demonstrate that the activity of PRMT5, a protein arginine methyltransferase and indirect target o

156 identify PRMT3 as the first type I ribosomal protein arginine methyltransferase and suggest that it r

157 t specificity and the catalytic mechanism of protein arginine methyltransferases and have important i

158 Multiple protein arginine methyltransferases are involved in tran

159 s study showed that the Arabidopsis thaliana protein arginine methyltransferase AtPRMT3 regulates pre

160 Recent discoveries of protein arginine methyltransferases, CARM1 and PRMT1, as

161 Type I protein arginine methyltransferases catalyze the formati

162 We have recently described a large (20 S) protein arginine methyltransferase complex, termed the m

163 Protein arginine methyltransferase enzyme 5 (PRMT5) regu

164 lude that PRMT1 contributes the major type I protein arginine methyltransferase enzyme activity prese

165 We identify the protein arginine methyltransferase enzymes that catalyze

166 Our data suggest that protein arginine methyltransferases exert key regulatory

167 s catalyzed by two families of proteins, the protein arginine methyltransferase family and the SET-do

168 Other members of the protein arginine methyltransferase family, which methyla

169 , which is highly conserved among the entire protein arginine methyltransferase family.

170 The RMT1 (protein-arginine methyltransferase), formerly ODP1, gene

171 The approach revealed protein arginine methyltransferase gene 5 (PRMT5) as an

172 tone deacetylases, BET bromodomain proteins, protein arginine methyltransferases, histone lysine meth

173 Here we demonstrate a role for the protein arginine methyltransferase Hmt1 in this process.

174 Previously, we demonstrated that the protein arginine methyltransferase Hmt1 plays a role in

175 modified within its RGG domain by the type I protein-arginine methyltransferase, Hmt1p.

176 the JCI, Liao et al. investigate the role of protein arginine methyltransferase I (PRMT1) in regulati

177 Protein-arginine methyltransferase I (PRMT1) contributes

178 ot a substrate for PRMT1, the most prominent protein-arginine methyltransferase in mammalian cells, w

179 data suggest a novel mechanism by which the protein arginine methyltransferase is involved in the co

180 Less studied than the other protein arginine methyltransferase isoforms, PRMT7 and P

181 tructure can be seen as a ternary complex of protein arginine methyltransferase (one subunit) complex

182 tion, which is catalyzed by a family of nine protein arginine methyltransferases, or PRMTs.

183 It is the first to demonstrate that protein arginine methyltransferases participate in the D

184 ated arginine methyltransferase 1 (CARM1), a protein-arginine methyltransferase previously shown to s

185 methylated on specific arginine residues by protein arginine methyltransferase (PRMT) 1 and PRMT5 in

186 Protein arginine methyltransferase (PRMT) 5 is an essent

187 Protein arginine methyltransferase (PRMT) 5 is over-expr

188 Here we report that protein arginine methyltransferase (PRMT) 6 activity is

189 Protein arginine methyltransferase (PRMT) 8 is unique am

190 Human protein arginine methyltransferase (PRMT) 9 symmetricall

191 Protein arginine methyltransferase (PRMT) activity has b

192 CARM1 contains a conserved protein arginine methyltransferase (PRMT) catalytic core

193 ttranslational modification catalyzed by the protein arginine methyltransferase (PRMT) enzyme family.

194 However, a conclusive role for the protein arginine methyltransferase (PRMT) enzymes that c

195 thyltransferase 1 (CARM1) is a member of the protein arginine methyltransferase (PRMT) family and met

196 a residue completely conserved in the type I protein arginine methyltransferase (PRMT) family of enzy

197 and HMGA1b proteins by three members of the protein arginine methyltransferase (PRMT) family: PRMT1,

198 CARM1 is a protein arginine methyltransferase (PRMT) that acts as a

199 Trypanosoma brucei PRMT7 (TbPRMT7) is a protein arginine methyltransferase (PRMT) that strictly

200 AtPRMT5 encodes a type II protein arginine methyltransferase (PRMT) that, in winte

201 Mass spectrometry identified LRP6 binding to protein arginine methyltransferase (PRMT)-1, and nuclear

202 Protein Arginine Methyltransferases (PRMT) 1 and 5 dimet

203 Bao and colleagues demonstrate that type I protein arginine methyltransferases (PRMT) are directly

204 Protein arginine methyltransferases (PRMT) are generally

205 cDNA for PRMT7, a recently discovered human protein-arginine methyltransferase (PRMT), was cloned an

206 Through an shRNA screen, we identified the protein arginine methyltransferase Prmt1 as a vulnerable

207 ceptor signaling increased expression of the protein arginine methyltransferase PRMT1, which in turn

208 emonstrate (1) the additional involvement of protein arginine methyltransferases PRMT1 and CARM1 in p

209 at SPT5 was specifically associated with the protein arginine methyltransferases PRMT1 and PRMT5 and

210 ere we show that S-HDAg can be methylated by protein arginine methyltransferase (PRMT1) in vitro and

211 The human genome encodes a family of nine protein arginine methyltransferases (PRMT1-9), whose mem

212 Here, we report that the protein arginine methyltransferase, PRMT1, methylates cG

213 n to form an extraribosomal complex with the protein arginine methyltransferase PRMT3 that is conserv

214 and mutational analysis, we demonstrate that protein arginine methyltransferase PRMT4 (CARM1) methyla

215 e report the selective overexpression of the protein arginine methyltransferase PRMT5 as a novel cand

216 body components and identify the ortholog of protein arginine methyltransferase PRMT5 as the enzyme r

217 esis, and enhanced expression of the type II protein arginine methyltransferase PRMT5 as well as the

218 The major type II protein arginine methyltransferase PRMT5 catalyzes the f

219 Here, we show that the type-II protein arginine methyltransferase PRMT5 controls H4R3me

220 Protein arginine methyltransferase PRMT5 interacts with

221 Among the target genes, we confirmed the protein arginine methyltransferase Prmt5 is a direct tar

222 The protein arginine methyltransferase PRMT5 is complexed wi

223 The type II protein arginine methyltransferase Prmt5 symmetrically d

224 cancer cells is impaired by depletion of the protein arginine methyltransferase PRMT5.

225 Epigenetic regulation by the type II protein arginine methyltransferase, PRMT5, plays an esse

226 we have functionally analyzed two different protein arginine methyltransferases, Prmt5 and Prmt4, bo

227 Human protein arginine methyltransferase PRMT8 has been recent

228 ion during flagellar dynamics, we focused on protein arginine methyltransferases (PRMTs) 1, 3, 5, and

229 Protein arginine methyltransferases (PRMTs) affect many

230 Protein arginine methyltransferases (PRMTs) aid in the r

231 hibitor library and identified inhibitors of protein arginine methyltransferases (PRMTs) among the to

232 proteins methylated on arginine residues by protein arginine methyltransferases (PRMTs) and is degra

233 Protein arginine methyltransferases (PRMTs) are (S)-aden

234 The protein arginine methyltransferases (PRMTs) are a family

235 Protein arginine methyltransferases (PRMTs) are a family

236 Protein arginine methyltransferases (PRMTs) are a group

237 Protein arginine methyltransferases (PRMTs) are enzymes

238 Protein arginine methyltransferases (PRMTs) are enzymes

239 Protein arginine methyltransferases (PRMTs) are importan

240 Protein arginine methyltransferases (PRMTs) are importan

241 Well-characterized selective inhibitors of protein arginine methyltransferases (PRMTs) are invaluab

242 Protein arginine methyltransferases (PRMTs) are proved t

243 Protein arginine methyltransferases (PRMTs) are required

244 Protein arginine methyltransferases (PRMTs) are S-adenos

245 Protein arginine methyltransferases (PRMTs) are SAM-depe

246 Protein arginine methyltransferases (PRMTs) are the driv

247 Protein arginine methyltransferases (PRMTs) catalyze arg

248 Type I protein arginine methyltransferases (PRMTs) catalyze asy

249 Misregulation of protein arginine methyltransferases (PRMTs) has been lin

250 Protein arginine methyltransferases (PRMTs) have been im

251 Protein arginine methyltransferases (PRMTs) have emerged

252 Covalent modification of histones by protein arginine methyltransferases (PRMTs) impacts geno

253 stone lysine methyltransferases (HKMTs), and protein arginine methyltransferases (PRMTs) in pancreati

254 The protein arginine methyltransferases (PRMTs) include a fa

255 Protein arginine methyltransferases (PRMTs) introduce ar

256 Malfunction of protein arginine methyltransferases (PRMTs) is correlate

257 oper epigenetic modification of chromatin by protein arginine methyltransferases (PRMTs) is crucial f

258 Protein arginine methyltransferases (PRMTs) mediate the

259 Protein arginine methyltransferases (PRMTs) mediate the

260 Protein arginine methyltransferases (PRMTs) modify diver

261 Protein arginine methyltransferases (PRMTs) play an impo

262 Protein arginine methyltransferases (PRMTs) play importa

263 Protein arginine methyltransferases (PRMTs) regulate man

264 Protein arginine methyltransferases (PRMTs) represent an

265 Protein arginine methyltransferases (PRMTs) represent pr

266 onal modification in eukaryotes catalyzed by protein arginine methyltransferases (PRMTs) that are typ

267 In the family of protein arginine methyltransferases (PRMTs) that predomi

268 Herein, we show that inhibition of type I protein arginine methyltransferases (PRMTs) with MS023 i

269 Phosphorylation of protein arginine methyltransferases (PRMTs), have been s

270 Increased arginine methylation, catalyzed by protein arginine methyltransferases (PRMTs), is increase

271 on of arginine, mediated by PRMT5 and type I protein arginine methyltransferases (PRMTs), respectivel

272 Consequently protein arginine methyltransferases (PRMTs), the writers

273 Using purified recombinant protein arginine methyltransferases (PRMTs), we showed t

274 strategies aimed at blocking the activity of protein arginine methyltransferases (PRMTs), which catal

275 we identified MS023, an inhibitor of type I protein arginine methyltransferases (PRMTs), which has a

276 in lysine methyltransferases (PKMTs) and the protein arginine methyltransferases (PRMTs).

277 ication of proteins catalyzed by a family of protein arginine methyltransferases (PRMTs).

278 posttranslational modification catalyzed by protein arginine methyltransferases (PRMTs).

279 d on multiple substrates by a family of nine protein arginine methyltransferases (PRMTs).

280 unrelated Rossman-fold enzymes that include protein arginine methyltransferases (PRMTs).

281 rotein lysine methyltransferases (PKMTs) and protein arginine methyltransferases (PRMTs).

282 an interplay between the SWI/SNF complex and protein-arginine methyltransferases (PRMTs).

283 Depletion of PRMT5, the primary protein arginine methyltransferase responsible for symme

284 ll, Wang and colleagues report that CARM1, a protein arginine methyltransferase, specifically methyla

285 The major Trypanosoma brucei protein arginine methyltransferase, TbPRMT1 enzyme (ENZ)

286 n-regulation of the major trypanosome type 1 protein arginine methyltransferase, TbPRMT1, disrupts fo

287 The protein arginine methyltransferase, TbPRMT1, interacts w

288 id not cooperate with PRMT1, a CARM1-related protein arginine methyltransferase that also functions a

289 tein arginine methyltransferase 5 (PRMT5), a protein arginine methyltransferase that catalyzes the sy

290 PRMT5 encodes a type II protein arginine methyltransferase that catalyzes the sy

291 ed arginine methyltransferase 1 (CARM1) is a protein arginine methyltransferase that methylates histo

292 CARM1 is one of nine protein arginine methyltransferases that methylate argin

293 PRMT5 is a type II protein arginine methyltransferase to symmetrically dime

294 4 substrates suggest that type I and type II protein-arginine methyltransferases use distinct molecul

295 4 have been methylated in vitro by a nuclear protein arginine methyltransferase using recombinant (un

296 electively modulates enzymatic activity of a protein arginine methyltransferase vital to abiotic stre

297 IL-4 upregulates the expression of protein arginine methyltransferases, which are essential

298 Protein arginine methyltransferases, which catalyze the

299 omolog of a recently characterized mammalian protein-arginine methyltransferase whose activity may be

300 PRMT5 is a type II protein arginine methyltransferase with roles in stem ce