ライフサイエンスコーパス: regulatory protein

1 f CsrA by sRNA in comparison with an ancient regulatory protein.

2 een SHIP2 and Mena, an Ena/VASP-family actin regulatory protein.

3 sfunction in an ion channel (or transporter) regulatory protein.

4 generic spliceosome components and splicing regulatory proteins.

5 geted by bacteriophage-encoded transcription regulatory proteins.

6 gated sepsis-induced reductions in the three regulatory proteins.

7 I, a suppression similar to that achieved by regulatory proteins.

8 eil how these flavors modulate the action of regulatory proteins.

9 ulus-specific nature of the actions of these regulatory proteins.

10 G2/M arrest and downregulation of cell cycle regulatory proteins.

11 pts, including those encoding key cell-cycle regulatory proteins.

12 ions, explaining its ability to bind diverse regulatory proteins.

13 olled by the combinatorial action of several regulatory proteins.

14 nd in hundreds of transcripts, many encoding regulatory proteins.

15 ational modifications of Cys residues in key regulatory proteins.

16 irectly through changes in interactions with regulatory proteins.

17 es are dynamically remodeled with the aid of regulatory proteins.

18 nteractions with a variety of substrates and regulatory proteins.

19 sensitive to concentration changes of single regulatory proteins.

20 nd the expression of numerous genes encoding regulatory proteins.

21 s of KRAS important for recognition of these regulatory proteins.

22 the pathway was altered by depletion of key regulatory proteins.

23 e spatiotemporal expression of actin binding/regulatory proteins.

24 h changes in the spatial expression of actin regulatory proteins.

25 a sarcomere, such as filament stiffness and regulatory proteins.

26 pression changes in key ion transporters and regulatory proteins.

27 nformation transfer between transporters and regulatory proteins.

28 teracting protein kinase 1 (RIP1) cell death regulatory proteins.

29 lants by coordinating the destabilization of regulatory proteins.

30 HBECs directly repressed epithelial splicing regulatory protein 1 (ESRP1), leading to increased expre

31 pathogenic mutations in Epithelial Splicing-Regulatory Protein 1 (ESRP1).

32 Iron-regulatory protein 1 (IRP1) belongs to a family of RNA-b

33 ockdown of ISCU enhanced the binding of iron regulatory protein 1 (IRP1), a cytosolic Fe-S protein, t

34 ted in Fe/S cluster repair of cytosolic iron regulatory protein 1 (IRP1), a key regulator of cellular

35 mammalian cytosolic aconitase, known as iron regulatory protein 1 (IRP1), led to the characterization

36 l-type-specific proteins epithelial splicing regulatory proteins 1 (ESRP1) and ESRP2 are important fo

37 Epithelial-Splicing-Regulatory-Protein 1 (Esrp1) is a cell-type specific RNA

38 olvement of reactive oxygen species and iron regulatory protein-1 in this mechanism.

39 y the antioxidant N-acetyl cysteine and iron regulatory protein-1 siRNA, suggesting involvement of re

40 verting cytosolic aconitase (ACO1) into iron regulatory protein-1 to bind iron-responsive elements pr

41 MAP2c responsible for interactions with the regulatory protein 14-3-3zeta.

42 ion studies, we identify epithelial splicing regulatory protein 2 (ESRP2) as a conserved regulatory f

43 The first is that overexpression of iron regulatory protein 2 (IRP2) recapitulates many aspects o

44 ovalently modifies cysteine residues on iron regulatory protein 2 (IRP2), rendering it unable to repr

45 egulators of iron metabolism, including iron regulatory protein 2 (IRP2).

46 or-interacting protein 1, Hemo-oxidized iron regulatory protein 2 ligase 1 (HOIL-1), HOIL-1-interacti

47 talytic core component is heme-oxidized iron regulatory protein 2 ubiquitin ligase-1-interacting prot

48 hores [3] and provides a platform to recruit regulatory proteins [4].

49 ions in TNFAIP3, which encodes the NF-kappaB regulatory protein A20, in six unrelated families with e

50 nctional relevance of genetic alterations in regulatory proteins across all samples in The Cancer Gen

51 Many eukaryotic regulatory proteins adopt distinct bound and unbound con

52 uding RBC, which, in conjunction with signal regulatory protein alpha (expressed on macrophages), pre

53 experiments from the paper "The CD47-signal regulatory protein alpha (SIRPa) interaction is a therap

54 human interleukin 15 (IL15) and human signal regulatory protein alpha (SIRPA) knock-in mouse on a Rag

55 macrophage self-recognition receptor signal regulatory protein alpha (SIRPA).

56 Thymic conventional DC (cDC) subsets signal regulatory protein alpha (SIRPalpha(+)) and CD8alpha(+)

57 Here we have shown that CD47-signal regulatory protein alpha (SIRPalpha) axis dictates the f

58 ctivating Fc receptors and inhibitory signal regulatory protein alpha (SIRPalpha) controls macrophage

59 CD47 engagement by the macrophage signal regulatory protein alpha (SIRPalpha) inhibits phagocytic

60 Signal regulatory protein alpha (SIRPalpha) is a membrane glyco

61 detection of the polymorphic molecule signal regulatory protein alpha (SIRPalpha) on donor cells.

62 t promotes immune evasion by engaging signal-regulatory protein alpha (SIRPalpha), which serves as an

63 nhibitory signal through its receptor signal regulatory protein alpha (SIRPalpha).

64 her in mice lacking the expression of signal-regulatory protein alpha (SIRPalpha).

65 acrophages upon engaging its receptor signal regulatory protein alpha (SIRPalpha).

66 nhibitory signal through the receptor signal regulatory protein alpha (SIRPalpha).

67 a ligand for the inhibitory receptor signal regulatory protein alpha and expressed on the surfaces o

68 ll surface protein CD47 to macrophage signal regulatory protein alpha receptors.

69 such as CD47, which binds macrophage signal-regulatory protein alpha to inhibit phagocytosis.

70 a ligand for the inhibitory receptor signal regulatory protein alpha, is expressed on B and T cells,

71 n transducing signals through primate signal regulatory protein alpha.

72 The inhibitory receptor signal regulatory protein-alpha (SIRPalpha) is a myeloid-specif

73 ijacking activities of endogenous complement regulatory proteins, an increasing number of uniquely ev

74 functional protein that serves as both a DNA regulatory protein and an extracellular cytokine signali

75 GpsB regulatory protein and StkP protein kinase have been pro

76 k of knowledge about the organization of the regulatory proteins and actin filaments.

77 nsitions involve collective behavior of both regulatory proteins and DNA.

78 and functional understanding of the core GSR regulatory proteins and highlights emerging data that ar

79 is motility relies on a minimal set of actin regulatory proteins and occurs in the absence of detecta

80 easome system controls the concentrations of regulatory proteins and removes damaged and misfolded pr

81 n to make actin filaments distinguishable by regulatory proteins and speculate on their possible cons

82 s involving large numbers of transcriptional regulatory proteins and their target genes.

83 tose binding protein, lysozyme, and nitrogen regulatory protein) and obtained similar results to thos

84 otein messenger RNAs and steroidogenic acute regulatory protein, and a reduction in dosage-sensitive

85 on filament stability and interactions with regulatory proteins, and analysis of single filament man

86 tem displays comparatively low levels of BBB regulatory proteins, and is unable to discriminate betwe

87 es associated with the binding of allosteric regulatory proteins, and show that the greatest variatio

88 hosphorylation of MAP kinases, translational regulatory proteins, and subunits of APC/C that validate

89 st in targeting splicing catalysis, splicing regulatory proteins, and/or specific key altered splicin

90 Many important signaling and regulatory proteins are expressed at low abundance and a

91 The functions of these viral regulatory proteins are in part interchangeable; thus, b

92 ividual biochemical activities of most actin-regulatory proteins are relatively well understood, know

93 Various regulatory proteins assist this reaction including the R

94 histone modifications and occupancy of their regulatory proteins at the specific promoters.

95 whether assembly of two different classes of regulatory proteins, beta and gamma, in BK channels is e

96 Multiple regulatory proteins bind in the SC and reprogram the cat

97 e observe a mutational cost to chromatin and regulatory protein binding, resulting in mutation hotspo

98 Conversely, the lytic cycle regulatory protein (BoHV-1 infected cell protein 0, or b

99 our epigenomic data to infer transcriptional regulatory proteins bound near these genes that likely i

100 Chemical inhibition of epigenetic regulatory proteins BrdT and Brd4 is emerging as a promi

101 cription factors (aTFs) are a major class of regulatory proteins, but few aTFs have been redesigned t

102 en the active and inactive state of nitrogen regulatory protein C (NtrC).

103 emodeling, characterized by depletion of the regulatory protein calstabin2, resulted in increased cyt

104 These results demonstrate how a single regulatory protein can maintain specificity while orches

105 ipts for regulation; ADP-ribosylation of RNA-regulatory proteins can alter their localization, activi

106 e interaction between G2019S LRRK2 and actin-regulatory proteins can be blocked by LRRK2 kinase inhib

107 Genetic defects in complement regulatory proteins can lead to severe renal diseases, i

108 y identified 27 candidate cell-cell adhesion regulatory proteins (CCARPs) whose down-regulation disru

109 nockout pigs, which express human complement regulatory protein CD46 and human thrombomodulin (GTKO.h

110 expression level of the membrane complement-regulatory proteins CD46, CD55, and CD59.

111 sponse to agents directed against the signal-regulatory protein CD47 and a potential target of anti-c

112 ed gene expression of the surface complement regulatory proteins (CD55, CD59, CD46, and CD141 [thromb

113 emolysis because of a loss of the complement regulatory proteins CD59 and CD55.

114 Z(HP) localization depends on the chemotaxis regulatory protein ChePep, and reciprocally, ChePep requ

115 y acids, and, in association with the global regulatory protein CodY, the BCAAs are key co-regulators

116 eleton and on actin filament severing by the regulatory protein cofilin.

117 The regulatory protein collybistin (CB) recruits the recepto

118 lular assembly through a membrane-associated regulatory protein complex composed of beta-Arrestin1, A

119 n proteins and also multiple scaffolding and regulatory protein components, which were assumed to be

120 Many DNA and RNA regulatory proteins contain polypeptide domains that are

121 es and that beta-catenin, a well known tumor-regulatory protein, contributes to this signaling pathwa

122 ly conserved sigma(E) , SpoIIID and sigma(K) regulatory proteins control gene expression in the mothe

123 Clostridium species and may represent a key regulatory protein controlling clostridial sporulation.

124 Transcriptional regulatory networks specify regulatory proteins controlling the context-specific exp

125 The PUF (Pumilio and FBF) family of RNA regulatory proteins controls the translation, stability,

126 Furthermore, the regulatory proteins CP110 and Cep97, which must dissocia

127 A reduction in complement negative regulatory proteins (CRPs), possibly owing to bisretinoi

128 Of the candidate enhancer-bound regulatory proteins, Ctcf, was associated with chromatin

129 We show here how the prokaryotic regulatory protein CueR both represses and activates tra

130 t human SAMHD1 interacts with the cell cycle regulatory proteins cyclin A, CDK1, and CDK2, which medi

131 te that NanR, a member of the RpiR family of regulatory proteins, decreases exosialidase activity and

132 Knocking down GRB10, another negative regulatory protein downstream of TORC1, enhanced both Ty

133 mune protein, has emerged as a critical iron regulatory protein during physiological and inflammatory

134 -dependent inhibition of steroidogenic acute regulatory protein expression and progesterone productio

135 nce has suggested that fluctuations in ER co-regulatory protein expression may facilitate resistance

136 r-mediated activation of steroidogenic acute regulatory protein expression.

137 with a known genetic basis included enzymes, regulatory proteins, extracellular matrix proteins, tran

138 Complement regulatory protein factor H (fH) binds modified host pro

139 f the central AAA(+) domain of the flagellar regulatory protein FlrC (FlrC(C)), a bEBP that controls

140 ing region and permits F-actin remodeling by regulatory proteins followed by reassociation and restab

141 APC/C-Cdh1 targets cyclin B and other regulatory proteins for degradation, whereas Cdks disabl

142 ll-cycle progression by targeting cell-cycle regulatory proteins for destruction via the ubiquitin pr

143 bF and YaaT) have been shown to be important regulatory proteins for multiple developmental fates.

144 ricate process that relies on a multitude of regulatory proteins forming complexes on chromatin.

145 functions performed by PAS-domain-containing regulatory proteins found in complex eukaryotes.

146 the very first inhibitors of a feast/famine regulatory protein from any source and set the stage for

147 Heterotrimeric guanine-nucleotide-binding regulatory proteins (G-proteins) mainly relay the inform

148 uxiliary subunit transmembrane AMPA receptor regulatory protein gamma-2 makes a substantial contribut

149 ociated with the transmembrane AMPA receptor regulatory protein, gamma-2, gating in the low- and high

150 Glucokinase regulatory protein (GCKR) inhibitors offer a novel treat

151 ly, human carriers of a loss-of-function GCK regulatory protein gene-leading to increased GCK activit

152 to a specific inhibitor protein, glucokinase regulatory protein (GKRP), and to other binding proteins

153 nel (AmtB) modulate its interaction with the regulatory protein, GlnK.

154 sylphosphatidylinositol- anchored complement regulatory proteins (GPI-AP).

155 We identified nine key regulatory proteins, guaA, guaB, rpsB, rpsI, rpsL, rpsE,

156 The combination of these two EBV regulatory proteins had a greater effect than each one i

157 hic alleles of PPP2R2A and potentially other regulatory proteins have deleterious effects and may the

158 ich is a main alternative complement pathway regulatory protein, have been well characterized in atyp

159 genic Acinetobacter spp. to identify the key regulatory proteins (hubs) in each strain.

160 mRNA) and, surprisingly, an mRNA encoding a regulatory protein (i.e., sarA mRNA).

161 ts corresponding to signature genes revealed regulatory proteins (i.e., AtMYB9 and AtMYB107) required

162 In the absence of HSV-1 regulatory protein ICP0, which counteracts the recruitme

163 ic depletion of Rho family GTPases and their regulatory proteins identified the Rac subfamily and the

164 oplasmic reticulum-localized calcium channel regulatory protein implicated in the oxidative stress re

165 spine synapse formation; however, the actin regulatory proteins important for early synaptogenesis a

166 bacterial fatty acid synthesis and is a key regulatory protein in bacterial fatty acid synthesis.

167 Complement factor H (CFH) is an important regulatory protein in the alternative pathway of the com

168 Many key regulatory proteins in bacteria are present in too low n

169 MS showed changes in the expression level of regulatory proteins in cells incubated with glaucoma ser

170 2S]-coordinating complexes in vitro and iron-regulatory proteins in fungi, but it is not clear how th

171 ression/display of AP components and surface regulatory proteins in GMVECs with and without cytokine

172 oposed that a constitutive production of HIV regulatory proteins in infected brain cells may contribu

173 findings reveal a novel role for complement-regulatory proteins in prion disease.

174 ole of the EHD family of endocytic recycling regulatory proteins in TCR-mediated T cell functions.

175 nical Galpha, this rate could be affected by regulatory proteins in the presence of specific signals,

176 constraints, possibly through the binding of regulatory proteins in the trans-Golgi network, followed

177 nd this strongly decreases their affinity to regulatory proteins including Rab GDP dissociation inhib

178 itination and degradation of several crucial regulatory proteins, including Axin and 3BP2.

179 that suppresses the translation of cellular regulatory proteins, including cyclin D1, at the elongat

180 plement activation is normally controlled by regulatory proteins, including factor H (FH) in plasma a

181 usion proteins aberrantly recruit epigenetic regulatory proteins, including histone deacetylases (HDA

182 pendent fashion with a battery of downstream regulatory proteins, including PHYTOCHROME INTERACTING F

183 body and associates with a subset of midbody regulatory proteins, including PRC1 and CYK4/MKLP1.

184 d that FAK interacted with a number of Runx1-regulatory proteins, including Sin3a and other epigeneti

185 forming alpha subunits and a multiplicity of regulatory proteins, including the cardiac-expressed and

186 temporally controlled by separase-associated regulatory proteins, including the inhibitory chaperone

187 Genetic regulatory proteins inducible by small molecules are use

188 , and increased iron-responsive element-iron regulatory protein interaction are also observed in live

189 extual specificity for TRAF6, involving both regulatory protein interactions, and messenger RNA regul

190 s orchestrated posttranscriptionally by iron-regulatory proteins (IRP)-1 and -2.

191 The RNA-binding iron regulatory proteins IRP1 and IRP2 are inactivated by eit

192 r iron homeostasis is controlled by the iron regulatory proteins (IRPs) 1 and 2 that bind cis-regulat

193 ron concentrations are modulated by the iron regulatory proteins (IRPs) IRP1 and IRP2.

194 contribute to the function of this essential regulatory protein is important in understanding the gen

195 rm heteromeric complexes in association with regulatory proteins is one mechanism to achieve diverse

196 One important class of FtsZ interacting/regulatory proteins is the Z-ring-associated proteins, Z

197 portantly, we identified K-Homology Splicing Regulatory Protein (KHSRP) as a negative regulator of th

198 In this study, we show how the integrin-regulatory protein kindlin-2 (FERMT2) promotes metastati

199 we have identified that K-homology splicing regulatory protein (KSRP), an ARE-BP, is robustly up-reg

200 d with the induction of the KH-type splicing regulatory protein (KSRP).

201 Conversely, alterations in cell cycle regulatory proteins, leading to the loss of normal cell-

202 Furthermore, down-regulation of actin regulatory proteins led to elongation of mitochondria, a

203 arrest and decrease expression of cell cycle regulatory proteins like cyclin E, cyclin D1 and decreas

204 re, anti-complement therapy using complement regulatory proteins may provide a potential clinical opt

205 ive to the interaction of C3 with complement regulatory proteins mediating cofactor activity.

206 Here, we uncover a novel role for the actin-regulatory protein Mena in the formation of a ribonucleo

207 We further report that the regulatory protein merlin (neurofibromin 2, NF2) interac

208 mitochondrial localization of calcium uptake regulatory protein MICU1.

209 c5 knockout increased phosphorylation of the regulatory protein Mob1, consistent with Hippo pathway a

210 link between changes in the conserved immune regulatory protein NF-kappaB and cnidarian symbiotic sta

211 ated by virus- or host-induced changes to MT regulatory proteins, not only play a central role in the

212 This work reveals IOS1 as a novel regulatory protein of FLS2-, EFR-, and CERK1-mediated si

213 C), encoded by MYBPC1, comprises a family of regulatory proteins of skeletal muscles that are phospho

214 issimilar alterations in the distribution of regulatory proteins of the ER-mitochondria interface, he

215 n of PKA and phosphorylation of cytoskeletal regulatory proteins of the Mena/VASP (vasodilator-stimul

216 x could be a cancer hallmark, but only a few regulatory proteins of this mechanism are currently know

217 holamban, the other well studied small SERCA-regulatory proteins, oligomerize either alone or togethe

218 = 2.24 x 10(-10)), rs1260326 in glucokinase regulatory protein (OR, 1.12; 95% CI, 1.07-1.17; P = 2.5

219 bidopsis (Arabidopsis thaliana) putative SPT regulatory proteins, orosomucoid-like proteins AtORM1 an

220 e kinase inhibitory domain of the cell cycle regulatory protein p27(Kip1) (p27) was nuclear spin hype

221 regulate the phosphorylation of mTOR and its regulatory proteins, p70S6K1 and 4E-BP1, a process essen

222 ein levels of sarcoplasmic reticulum calcium-regulatory proteins particularly in hearts from male mic

223 adaptor ClpS binds to the N terminus of the regulatory protein PhoP, resulting in PhoP degradation b

224 a-induced alternative splice mutation in the regulatory protein phosphatase 2A (PP2A) subunit PPP2R2A

225 nist-stimulated phosphorylation of the SERCA regulatory protein phospholamban was increased in cells

226 results are similar in myocytes lacking the regulatory protein, phospholemman.

227 f suppressor of cytokine signaling-1 (SOCS1) regulatory protein protects against nephropathy by suppr

228 ncogenic RAS-ERK signaling and (2) targeting regulatory protein-protein interactions, rather than cat

229 a member of the WASP family of cytoskeletal regulatory proteins required for cell migration.

230 es, lasting for tens of minutes, derive from regulatory proteins residing on chromatin for only tens

231 Similarly, measurements of regulatory proteins responsible for RLC phosphorylation

232 ling and oxidation of specific translational regulatory proteins, resulting in impaired cap-dependent

233 protein complex in Arabidopsis, and a single regulatory protein, RGS1, is one of the few known bioche

234 Here, we identify the regulatory protein RmcA and show that it links redox con

235 ing cascades is achieved through networks of regulatory proteins, segregation of pathway components i

236 Therapeutic blockade of signal regulatory protein (SIRP)-alpha, an inhibitory receptor

237 wn to be inhibited by an excess of the small regulatory protein, SlrA, and here we find that slrA mRN

238 ial membrane 22 (Tom22), steroidogenic acute regulatory protein (StAR), and 3beta-hydroxysteroid dehy

239 ocortin receptor type 2, steroidogenic acute regulatory protein (StAR), and gene coding of steroid 11

240 ARD10 is a member of the steroidogenic acute regulatory protein (StAR)-related lipid transfer protein

241 AMPARs, the prototypical transmembrane AMPAR regulatory protein stargazin, which acts as an auxiliary

242 ected for measurement of steroidogenic acute regulatory protein, steroidogenic factor 1, and dosage-s

243 evels and an increase in steroidogenic acute regulatory protein, steroidogenic factor 1, and melanoco

244 The core elements of the pathway are the regulatory protein STIM1, located in the endoplasmic ret

245 ociated with AMPARs (via transmembrane AMPAR regulatory protein subunits) or NMDARs [via glutamate io

246 compaction, resulting in steric exclusion of regulatory proteins such as RNA polymerase from the unde

247 d by a complex regulatory network connecting regulatory proteins such as transcription factors and si

248 osylase 3), as well as transcription and RNA regulatory proteins, such as TTF2 (transcription termina

249 Transmembrane AMPA receptor regulatory proteins (TARPs) are a family of scaffolding

250 STATEMENT In the brain, transmembrane AMPAR regulatory proteins (TARPs) critically determine the fun

251 In the brain, transmembrane AMPAR regulatory proteins (TARPs) critically influence the dis

252 xamined the influence of transmembrane AMPAR regulatory proteins (TARPs) on presynaptic AMPARs in cer

253 coassemble with transmembrane AMPA receptor regulatory proteins (TARPs), yielding a receptor complex

254 is tightly controlled by transmembrane AMPAR regulatory proteins (TARPs).

255 Importantly, mRNAs encoding low-abundance regulatory proteins tend to be enriched in the monosome

256 Furthermore, regulatory protein termed eIF5-mimic protein (5MP) can b

257 dant KCC2 interactor is a neuronal endocytic regulatory protein termed PACSIN1 (SYNDAPIN1).

258 tprints in their promoters left by potential regulatory proteins than do tandem duplicates (TDs).

259 s revealed that NKX2.2 is a conserved master regulatory protein that controls the acquisition and mai

260 RAF) has recently been identified as a STIM1 regulatory protein that facilitates slow Ca(2+)-dependen

261 CD59 is a membrane-bound regulatory protein that inhibits the assembly of the ter

262 Cardiac troponin C (cTnC) is the regulatory protein that initiates cardiac contraction in

263 roduction of each inhibitor is promoted by a regulatory protein that is itself inhibited by the cell-

264 edoxin (Adrx) is a recently discovered redox regulatory protein that is preferentially expressed in a

265 We identified a novel, conserved regulatory protein that is required for Apm2-dependent s

266 CsrA is a post-transcriptional regulatory protein that is widely distributed among bact

267 y in S. aureus that identifies a DNA-binding regulatory protein that senses heme to control gene expr

268 identical mutation in a gene encoding a key regulatory protein that yielded a hyperinvasive phenotyp

269 tory RNA (sRNA) interactions with mRNAs, (e) regulatory proteins that alter ribonuclease binding affi

270 the mechanism of the reaction of NO with DNA regulatory proteins that contain Fe-S clusters has been

271 ity domains are ubiquitously associated with regulatory proteins that control gene expression and RNA

272 ken together, these data highlight two novel regulatory proteins that could be therapeutically manipu

273 osphorylated pyrin bound to 14-3-3 proteins, regulatory proteins that in turn blocked the pyrin infla

274 of negative feedback loops between these two regulatory proteins that precisely modulate the level of

275 Pax genes encode developmental regulatory proteins that specify cell lineages and tissu

276 proteins, ZapA-D (Zaps), are important FtsZ regulatory proteins that stabilize FtsZ assembly and enh

277 ntify NO reaction products in WhiD and NsrR, regulatory proteins that use a [4Fe-4S] cluster to sense

278 the observation that Dig1 is one of the few regulatory proteins that were retained in the duplicated

279 , and two intracellular Ca(2+) concentration regulatory proteins, that is, sarcoplasmic/endoplasmic r

280 tural myocardial proteins, the neurohormonal regulatory proteins, the vascular proteins, and the prot

281 ently displaced to facilitate the ability of regulatory proteins to access specific DNA elements.

282 arameters governing binding and unbinding of regulatory proteins to DNA strongly influence the switch

283 istone-DNA interactions affect the access of regulatory proteins to DNA.

284 nts targeting epigenetic and transcriptional regulatory proteins to induce apoptosis in leukemic cell

285 sion is regulated by orchestrated binding of regulatory proteins to promoters and other cis-regulator

286 lose proximity, providing an opportunity for regulatory proteins to simultaneously control transcript

287 and the stalk and the correct positioning of regulatory proteins to specific cell poles.

288 can target the deployment of transcriptional regulatory proteins to specific sequences.

289 neuronal injury is that the neurotoxic HIV-1 regulatory protein trans-activator of transcription (Tat

290 ontractile proteins actin and myosin and the regulatory protein tropomyosin.

291 sin interaction controlled by Ca(2+) via the regulatory proteins troponin (Tn) and tropomyosin (Tpm),

292 molecular mechanism by which HIV-1-secreted regulatory protein Vpr regulates KSHV latency and the pa

293 Surface complement regulatory proteins were also quantified by flow cytomet

294 ignaling pathway regulator-like (TIPRL) is a regulatory protein which inhibits the catalytic subunits

295 a truncated fragment of p35, the Cdk5 kinase regulatory protein, which inhibits Cdk5/p35 and the hype

296 broad superfamily of previously studied PII regulatory proteins, which are generally involved in reg

297 A better understanding of these regulatory proteins will not only give insight into the

298 dout mechanisms have the potential to engage regulatory proteins with many more targets than might be

299 hat the maternal mRNA encoding the cell-fate regulatory protein Wnt11b is a direct target of Bicc1-me

300 The Yersinia translocation regulatory protein YopK promotes bacterial virulence by