ライフサイエンスコーパス: heterodimerization

1 e origin of stereoselectivity in this ketene heterodimerization.

2 d, due to analytical challenges in measuring heterodimerization.

3 Toll-like receptor-1/2 (TLR-1/2) and TLR-2/6 heterodimerization.

4 c was weakened, attenuating IL-2Rbeta-gammac heterodimerization.

5 tant domain Calpha is dependent on alphabeta heterodimerization.

6 deficiency, has on ZnT1, ZnT3, and ZnT4 upon heterodimerization.

7 an interfacial cavity formed through subunit heterodimerization.

8 GIT1 to activate Ras and promote B-Raf/c-Raf heterodimerization.

9 responding to a segment that is required for heterodimerization.

10 eve high transporter stability and efficient heterodimerization.

11 ithin the TM domain is necessary for p45-p75 heterodimerization.

12 the N terminus of MGAT2, is required for the heterodimerization.

13 e acetylation state of PAF49 does not affect heterodimerization.

14 R) domains of the receptors undergo homo- or heterodimerization.

15 retained in the cytosol upon wild-type DJ-1 heterodimerization.

16 ate cell survival and death through homo- or heterodimerization.

17 In Caco-2 cells, CCK enhanced CCK1R/CCK2R heterodimerization.

18 oGEFs as well as their co-recruitment due to heterodimerization.

19 binding domains (LBDs) and constitutive homo/heterodimerization.

20 the amount of ghrelin and state of receptor heterodimerization.

21 ing a Rac-1 construct via rapamycin-mediated heterodimerization.

22 ains that mediate either homodimerization or heterodimerization.

23 arrangements associated with the c-Fos/c-Jun heterodimerization.

24 s that are likely involved in their homo- or heterodimerization.

25 AK3 and PAK1 signaling may be coordinated by heterodimerization.

26 F49 were sufficient to provide the basis for heterodimerization.

27 lex and that they may serve to stabilize I-D heterodimerization.

28 and that blade I is required for CD44 MMP-14 heterodimerization.

29 cross-activation of GRPR signaling by MOR1D heterodimerization.

30 inactivating proteins with rapamycin-induced heterodimerization.

31 and PEG coimmobilized through leucine zipper heterodimerization.

32 asic helix-loop-helix domain, which mediates heterodimerization.

33 emble into complexes, through both homo- and heterodimerization.

34 of unc-10/RIM mutants deficient for C2A/RIM heterodimerization.

35 oes not identify interactions that may favor heterodimerization.

36 s of the interactions inducing CH3 interface heterodimerization.

37 mical properties, many times related to poor heterodimerization.

38 D is a dimerization domain for PHYB homo and heterodimerization.

39 by bi-specific ligands that induce receptor heterodimerization.

40 oint mutations in FGFR3 (A391E and G380R) on heterodimerization.

41 elective small molecule inhibitor of MYC-MAX heterodimerization, 10058-F4, on myeloma cell lines as w

42 This disruption of heterodimerization allows the resulting monomers of p85

43 ted by these findings, we here uncovered the heterodimerization, altered subcellular localization, an

44 These results led us to hypothesize that heterodimerization alters the intrinsic catalytic proper

45 Using type-4 BRET assays, we investigate heterodimerization among known GPCR homodimers: the CXC

46 is of (-)-communesin F based on a late-stage heterodimerization and aminal exchange is described.

47 The functional significance of rod PDE6 heterodimerization and conserved differences between PDE

48 ary zone electrophoresis to measure rates of heterodimerization and DeltaGHet for seven ALS-variant a

49 ed TLR2-lipopeptide complex, it prevents TLR heterodimerization and downstream signaling.

50 scular plant emergence, conditioned obligate heterodimerization and generated the critical function i

51 Surprisingly, we found that RTK heterodimerization and homodimerization strengths can be

52 f to CBFbeta is mutually exclusive with RUNX heterodimerization and impacts the expression of genes w

53 usion, sumoylation of Nrf2 and MafG enhances heterodimerization and increases GCLC expression, which

54 /L as was nearly complete inhibition of HER3 heterodimerization and phosphorylation, thereby preventi

55 e-linked construct to induce IL-36R.IL-1RAcP heterodimerization and predicted the binding affinity du

56 ed to the strength of homodimerization, Sox2 heterodimerization and self-renewal activity.

57 heteroallelic combinations, as well as SHELL heterodimerization and subcellular localization by yeast

58 We saw increased JAK2 heterodimerization and sustained JAK2 activation in cell

59 hen a PKA-activated Ras promotes Raf-1/B-Raf heterodimerization, and are inhibited by interfering wit

60 data imply that RAR agonist enhances RAR-RXR heterodimerization, and chromatin binding/dimerization a

61 embrane skeleton, suppression of C-RAF/B-RAF heterodimerization, and inhibition of C-RAF kinase activ

62 NA-binding domain (tandem-winged helix), the heterodimerization, and the linker domain were essential

63 PtrSND1s, making them nonproductive through heterodimerization, and thereby modulating the SND1 tran

64 Par-6 and aPKC interact via PB1 domain heterodimerization, and this interaction activates aPKC

65 uR1 and mGluR5 in a manner inconsistent with heterodimerization, and thus suggest an interaction betw

66 istic insights on Ang2 antagonism, Tie1/Tie2 heterodimerization, and Tie2 clustering.

67 o-hole interface, the molecular mechanism of heterodimerization, and to engineer Fc domains that coul

68 We also show that heterodimerization appears to disrupt homodimeric intera

69 and functional roles of homodimerization and heterodimerization are still unclear.

70 al knockout mice of all neuroligins to avoid heterodimerization artifacts, we show, in hippocampal CA

71 cally required for growth factor-induced RAF heterodimerization as well as for MEK dissociation from

72 ependent MAPK signalling by antagonizing RAF heterodimerization as well as the conformational changes

73 was important to support efficient TonB-ExbD heterodimerization at these specific regions.

74 Heterodimerization between A and B allows coimmobilizati

75 Heterodimerization between ACS isoforms from distinct su

76 reactivation of JAK-STAT signalling and with heterodimerization between activated JAK2 and JAK1 or TY

77 te from a dominant-negative effect caused by heterodimerization between AQP4 and AQP4-Delta4, which w

78 Paradoxically, SARAH domain-mediated heterodimerization between Hippo and Salvador enhances H

79 Intermolecular FRET studies confirmed heterodimerization between PAR(2) and PAR(4).

80 Protein-protein interaction assays reveal heterodimerization between PpSMF1 and PpSCRM1, which, to

81 imaging model system by detecting changes in heterodimerization between RXRalpha and one of its partn

82 Mechanically stable specific heterodimerization between small protein domains have a

83 -terminal domain (NTD) of the GluN1 promotes heterodimerization between the NTDs of GluN1 and GluN2,

84 n of PDGFRA by EGFR and EGF-induced receptor heterodimerization, both of which are abolished by EGFR

85 uggests a possible structural basis for Her2 heterodimerization, but all available structures for dim

86 olecules designed to inhibit HIF-2alpha-ARNT heterodimerization by binding an internal cavity of the

87 s that allows the quantification of receptor heterodimerization by dual-color fluorescence cross-corr

88 main with an alpha-helical cap that mediates heterodimerization by forming an intermolecular helix bu

89 that the temporal regulation of Neurog2-E47 heterodimerization by GSK3 is a central component of the

90 ns are similar and compatible with Tie2/Tie1 heterodimerization by the same mechanism.

91 By heterodimerization, CCRL2 could regulate membrane expres

92 Heterodimerization creates V-shaped molecules with a hin

93 ion, pertuzumab-mediated inhibition of ErbB2 heterodimerization decreased AKT phosphorylation, cell g

94 a Nab3 self-association defect, a Nab3-Nrd1 heterodimerization defect, a Nrd1-polymerase II binding

95 The rate, mechanism, and DeltaG of heterodimerization (DeltaGHet) all remain undetermined,

96 Rates of heterodimerization did not correlate with survival time

97 us substitutions affecting the extracellular heterodimerization domain (HD).

98 long intra-molecular coiled-coil arms with a heterodimerization domain at one end and an ABC-like nuc

99 NOTCH1 heterodimerization domain mutations were associated with

100 fibroblasts with mutations in the alpha/beta heterodimerization domain seems to be associated with a

101 ng mutations outside the alpha/beta spectrin heterodimerization domain, four had normal brain imaging

102 antibody fragments and blue-light inducible heterodimerization domains.

103 constituent LNR (Lin12-Notch repeat) and HD (heterodimerization) domains, at forces similar to those

104 nts can be physiologically important through heterodimerization, even when inactive alone, and can co

105 erbB3 homo- and heterodimerization events were captured in real time on

106 Using a similar approach, ALX/FPR1 heterodimerization evoked using the panagonist peptide A

107 A unique GPCR that is known to require heterodimerization for function(2-6), the GABA(B) recept

108 Despite the significance of TF heterodimerization for gene regulation, a quantitative u

109 as a signaling molecule, or if it depends on heterodimerization for secretion.

110 Heterodimerization generates a compound collection with

111 form homodimers; however, a few examples of heterodimerization have also been reported.

112 The structural basis for Her2 heterodimerization, however, remains poorly understood.

113 Braf35-iBraf heterodimerization impairs Braf35 interaction with the L

114 d in an inverted orientation or capture only heterodimerization in a single assay.

115 Yet heterodimerization in achondroplasia has not been charac

116 While methods exist for studying receptor heterodimerization in cell membranes, they are limited t

117 Efficient heterodimerization in mammalian cell transient transfect

118 The in vivo significance of Mdm2-Mdm4 heterodimerization in regulation of p53 function is unkn

119 This suggests a role for NHERF2/NHERF3 heterodimerization in the regulation of NHE3 activity.

120 Y1009, rationalizing LsdA and LsdB homo- and heterodimerization in vivo A structure of an LsdA.phenyl

121 he physiological relevance of 5-HT2 receptor heterodimerization in vivo Accordingly, exogenous expres

122 t 2.47 A resolution, revealed a mechanism of heterodimerization in which UL50 clamps onto helices of

123 sion, yet increased glomerular VEGF receptor heterodimerization, indicating differential signaling by

124 age RNA homodimerization or to encourage RNA heterodimerization, indicating that HIV-1 and HIV-2 RNA

125 In addition, we demonstrate that heterodimerization influences the stability of ACS prote

126 biology assays revealed that PD-L1:CD80 cis-heterodimerization inhibited both PD-L1:PD-1 and CD80:CT

127 HER2 antibody pertuzumab, which blocks HER2 heterodimerization, inhibited growth induced by hereguli

128 trengths and weaknesses of all of the PA-PB1 heterodimerization inhibitors, we analyze their hypothes

129 cellular sites within CaV1.2-alpha1C permits heterodimerization-initiated channel inhibition with rap

130 have high binding affinity for the ERCC1-XPF heterodimerization interface by interacting with the XPF

131 to surface residues in the characterized M50 heterodimerization interface substantially decreased UL5

132 ined asymmetric architecture, with extensive heterodimerization interfaces and AHR interdomain intera

133 Mechanistically, Mdm2-Mdm4 heterodimerization is critical for inhibiting lethal p53

134 cificity in receptor homodimerization versus heterodimerization is essential in determining the role

135 NHERF2/NHERF3 heterodimerization is mediated by PDZ domains of NHERF2

136 C- and E-class protein heterodimerization is predicted by the floral quartet mo

137 Mst1/Mst2 heterodimerization is strongly promoted by oncogenic H-r

138 FSHR heterodimerization is unique to the ovary because in the

139 biology, and receptor dimerization (homo- or heterodimerization) is central to signal transduction.

140 dividual K8, K18, or K19 but is limited upon heterodimerization (K8/K18 or K8/K19) in the absence of

141 ired in unc-10 mutants deficient for C2A/RIM heterodimerization, leading to decreased release probabi

142 ucines abolished protein disulfide isomerase heterodimerization, lipid transfer, and apoB secretion,

143 of common target promoters, suggesting that heterodimerization may be required for the full regulati

144 dorsal root ganglion neurons indicating that heterodimerization may provide greater diversity of leak

145 family III(a + c)1 members, which suggests a heterodimerization mechanism conserved in angiosperms.

146 regulation of MST1/2 includes both homo- and heterodimerization, mediated by helical SARAH domains, t

147 ults demonstrate that Pi-regulated PiT1-PiT2 heterodimerization mediates Pi sensing independently of

148 This study suggests that NHERF2/NHERF3 heterodimerization mediates the formation of NHE3 macroc

149 at substrate dimerization (homo- or possibly heterodimerization) might represent a general principle

150 amic range, we employed improved optogenetic heterodimerization modules and engineered a photosensiti

151 Mutation of the heterodimerization motif that interferes with DNMT3A(R88

152 ether, our results provide evidence that the heterodimerization of 6TM-MOR with beta2-AR underlies a

153 AM1 and AM2 receptors formed by the obligate heterodimerization of a G protein-coupled receptor, the

154 protease also cleaves the iPQM relevant for heterodimerization of a subgroup of neurotoxins.

155 hat controls ACS protein stability through a heterodimerization of ACS isoforms.

156 reveal the molecular basis for the homo- and heterodimerization of AFF proteins and implicate the AFF

157 Recent development suggests that homo- and heterodimerization of APP and APP-like proteins (APLPs),

158 NPD1 also enhanced the heterodimerization of Bcl-x(L) with its counterpart, pro

159 Heterodimerization of both proteins with the NXT (NTF2-r

160 eir spatial colocalization via light-induced heterodimerization of cryptochrome 2 and a dCas9-CIBN fu

161 Finally, we explored a possible heterodimerization of Cul3 and Cul5 and indeed discovere

162 These data demonstrate that heterodimerization of erbB2/erbB3 is a prerequisite for

163 Heterodimerization of G protein-coupled receptors has an

164 al and can be applied to study the homo- and heterodimerization of GPCRs and other transmembrane prot

165 Heterodimerization of human epidermal growth factor rece

166 close a computational study on the homo- and heterodimerization of isocyanides, in particular on the

167 hat mutations within either interface weaken heterodimerization of isolated half hinges in vitro but

168 Catalytic heterodimerization of ketenes can lead to important four

169 scribe an unprecedented catalytic asymmetric heterodimerization of ketenes of wide substrate scope.

170 xtensive studies of the catalytic asymmetric heterodimerization of ketenes to give ketene heterodimer

171 been shown to be extremely important for the heterodimerization of many TFIID subunits.

172 M2 and MDMX by inhibitor-driven homo- and/or heterodimerization of MDM2 and MDMX proteins.

173 Our results suggest a model by which heterodimerization of monoubiquitinated FANCD2 and FANCI

174 of unsymmetrical cyclobutanes by controlled heterodimerization of olefins remains a substantial chal

175 Heterodimerization of RAF kinases as well as dephosphory

176 Heterodimerization of RcsB with various auxiliary regula

177 pendent TGF-beta signaling by disrupting the heterodimerization of TbetaRI and TbetaRII receptors.

178 cubane 4Fe-4S cluster, which is crucial for heterodimerization of TFEalpha/beta and its engagement w

179 Homodimerization or heterodimerization of TFs are required for DNA binding a

180 ltiple Fc variant pairs that drive efficient heterodimerization of the antibody heavy chains.

181 restricted to the receptor itself, allowing heterodimerization of the four EGFR family members witho

182 ligand-mediated co-internalization following heterodimerization of the GHS-R1a receptor with the dopa

183 t the first demonstration of agonist-induced heterodimerization of the H1R and H2R.

184 tes lymphocyte function by signaling through heterodimerization of the IL-2Rbeta and gammac receptor

185 Binding of CHOP prevented heterodimerization of the receptor subunits GABAB1 and G

186 To evaluate potential heterodimerization of the receptors, sensitized emission

187 The interaction is also required for proper heterodimerization of the transporter.

188 sAbs) having two unique Fab domains requires heterodimerization of the two heavy chains and pairing o

189 of the NC, ND and NE sequences and directed heterodimerization of these photosensory regions with th

190 ltaneous measurement of homodimerization and heterodimerization of type I receptor domains in their n

191 To study the consequences of homo- and heterodimerization of wild-type and mutant PTEN in vivo,

192 This likely resulted from the heterodimerization of wild-type and mutant TRESK subunit

193 Although homo- and heterodimerizations of G protein-coupled receptors (GPCR

194 gth among all possible homodimerizations and heterodimerizations of these three NHERF proteins by pul

195 ults demonstrate that the impact of receptor heterodimerization on endocytic recruitment is controlle

196 here, we investigate the impact of receptor heterodimerization on endocytic recruitment using a fami

197 AHR and its heterodimerization partner aryl hydrocarbon receptor nuc

198 )) and the marked-box domains of E2F and its heterodimerization partner DP.

199 We found that TAL1 and its heterodimerization partner E47 regulate miR-17-92 transc

200 Id4 sequesters Ascl1 heterodimerization partner E47, promoting Ascl1 protein

201 tional regulator and serves as an obligatory heterodimerization partner for at least 20 other nuclear

202 Among the top hits was MAX, the obligate heterodimerization partner for MYC family proteins that

203 ncur with RXRalpha functioning as obligatory heterodimerization partner for several nuclear receptors

204 determination in a manner beyond that of its heterodimerization partner MEIS2.

205 on of Notch-1, ErbB4, pErbB4, and pEGFR, the heterodimerization partner of ErbB4, suggesting increase

206 targeted via bexarotene, a ligand of Nurr1's heterodimerization partner retinoid X receptor (RXR).

207 sponse element (XRE) in association with the heterodimerization partner, the AhR nuclear translocator

208 taining loosely organized domains, while its heterodimerization partners use a surface patch on their

209 Candidate heterodimerization partners were identified, and interac

210 Ligand binding, heterodimerization, phosphorylation of ERBB3, and AKT si

211 and tetrasubstituted cyclobutanes through a heterodimerization process involving two different alken

212 e map dimerization determinants and define a heterodimerization profile.

213 We found that ATP-binding and Smc1-Smc3 heterodimerization promote conformational changes within

214 Thus, heterodimerization provides a means for diversifying fun

215 This heterodimerization provides a potential mechanism for cr

216 significantly and consistently improved the heterodimerization rate of this format (>=95%) by induci

217 ny TALE either using effector molecules or a heterodimerization reaction.

218 ivity studies show that the competitive HER4 heterodimerization reactions have a profound impact on t

219 complexes, the specificity and mechanism of heterodimerization remain unclear.

220 ither AR-V7 homodimerization nor AR-V7/AR-FL heterodimerization requires cofactors or DNA binding.

221 tatic interactions that facilitate efficient heterodimerization, resulting in bispecific antibodies w

222 Broadly, these observations indicate that heterodimerization results from the divergence of homodi

223 Furthermore, KSR2-BRAF heterodimerization results in an increase of BRAF-induce

224 r receptor Nurr1 can be activated by RXR via heterodimerization (RXR-Nurr1) and is a promising target

225 engineered is by creating "knob" and "hole" heterodimerization sites in the CH3 domains of two antib

226 Structural determinants responsible for heterodimerization specificity of bZIP53 are poorly unde

227 tions that modulate the homodimerization and heterodimerization states to define additional roles of

228 d DAF-38 form heterodimers, and we show that heterodimerization strongly increases cAMP inhibition in

229 Moreover, we used constant heavy domain 3 heterodimerization substitutions to create TTR-mediated

230 Here, we show that the protein heterodimerization switches FKBP-rapalog-FRB can be harn

231 hydrolysis, and the CRY2-CIBN light-mediated heterodimerization system to create an optogenetic PLD (

232 We use a small molecule-regulated heterodimerization system to rapidly control the localiz

233 Here, we explore the possibility to develop heterodimerization system with a range of mechanical sta

234 ibitor GRK2ct (GRK2ct-KERE) and the FRB/FKBP heterodimerization system.

235 ted by recruitment of a 4-phosphatase with a heterodimerization system.

236 of-of-principle by generating nanobody-based heterodimerization systems induced by cannabidiol with h

237 or a variety of regulatory possibilities via heterodimerization that could impact song behavior in ze

238 of Mycobacterium tuberculosis induces TLR1/2 heterodimerization to elicit proinflammatory-type respon

239 successfully drive human IgG1 CH3 or IgM CH4 heterodimerization to levels similar to or above those o

240 the molecular basis of TLR1 and TLR6-driven heterodimerization upon LPA binding underlines the highl

241 Light-induced heterodimerization using the phytochrome system has prev

242 incipally reliant on ligand-induced Fzd/LRP6 heterodimerization, versus the allosteric mechanisms see

243 ated with an increased receptor binding, and heterodimerization was associated with a decreased recep

244 In vivo NHERF2/NHERF3 heterodimerization was confirmed by FRET and FRAP (fluor

245 ligation assays demonstrated that BRAF-CRAF heterodimerization was increased in fixed tumor samples

246 were substituted with alanine, the PiT1-PiT2 heterodimerization was no longer regulated by extracellu

247 pendent Pi transport activity, the PiT1-PiT2 heterodimerization was still regulated by extracellular

248 ent subunits were linked together to enforce heterodimerization), we characterized the biophysical an

249 NMT3A(R882mut) relied on a motif involved in heterodimerization, whereas its various chromatin-bindin

250 pical DR1 sequence favors PPARalpha/RXRalpha heterodimerization, whereas the switch from RXRalpha to

251 y interacts with VDR and RXR promoting their heterodimerization, which is critical for VDR:RXR target

252 the cytostatic activity of C/EBPbeta through heterodimerization, which prevents senescence and suppre

253 Although heterodimerization with 5-HT2C receptors does not alter

254 and receptor tyrosine kinases, suggests that heterodimerization with a strongly recruited receptor ca

255 1 cytoplasmic tail and does not entail beta1 heterodimerization with an alpha-subunit or its localiza

256 tidylinositol 3-kinase/Akt signaling through heterodimerization with and activation by other ErbB rec

257 A dimerization leads us to propose a mode of heterodimerization with ARNT that is supported by both b

258 f Bcl-xL in mitochondria, increase in Bcl-xL heterodimerization with Bax in mitochondria, and reduced

259 lation of the alpha3 precursor prevented its heterodimerization with beta1, whereas CD151 association

260 We show that heterodimerization with c-Jun increases c-Fos half-life.

261 to wild-type B-Raf kinase domain leading to heterodimerization with C-Raf causing a paradoxical hype

262 eased C/EBPbeta homodimer formation, whereas heterodimerization with C/EBPgamma was relatively unaffe

263 merization, whereas blade I was required for heterodimerization with CD44.

264 Parp9 undergoes heterodimerization with Dtx3L, a histone E3 ligase invol

265 the widest repertoire of PAMPs owing to its heterodimerization with either TLR1 or TLR6, broadening

266 or via a ligand-independent process through heterodimerization with ErbB2 overexpressed in breast tu

267 s the dynamics of ErbB3 homodimerization and heterodimerization with ErbB2.

268 een shown to acquire membrane association by heterodimerization with GAD65.

269 Although heterodimerization with Gdf1 did not increase binding of

270 ction for the HIF-2alpha PAS-B domain beyond heterodimerization with HIF-1beta.

271 lls with NO increased the level of ITGalpha6 heterodimerization with ITGbeta1 but not with ITGbeta4.

272 tivates the receptor kinase BRI1 by inducing heterodimerization with its co-receptor kinase BAK1; how

273 inal domain of PRG, which is responsible for heterodimerization with LARG, strongly inhibited Ca(2+)-

274 MO-1, which promoted Nrf2 binding to ARE and heterodimerization with MafG.

275 n signals and the bHLHZ domain essential for heterodimerization with Max and DNA binding.

276 is responsible for ubiquitination of p53 and heterodimerization with MDM4.

277 to produce bispecific antibodies by driving heterodimerization with mutations in the CH3 domain of e

278 d cell entry, nectin-4 homodimerization, and heterodimerization with nectin-1.

279 The NHERF3-4A mutant is defective in heterodimerization with NHERF2 and does not support the

280 the nuclear portion was inactive because of heterodimerization with NPM1.

281 "knob-into-hole" technology for heavy chain heterodimerization with one heavy chain consisting of a

282 y identified regions in Ostbeta required for heterodimerization with Ostalpha, trafficking of the Ost

283 ot bind EGF-like ligands, relying instead on heterodimerization with other (ligand-bound) EGFR-family

284 essential for protein stability and possible heterodimerization with other isoforms of RGP.

285 Transcriptional activation by CHOP involves heterodimerization with other members of the basic leuci

286 These modifications include competitive HER4 heterodimerization with other members of the ErbB family

287 ons of CXCR4 dimerization and studying CXCR4 heterodimerization with other receptors.

288 at mediate their homodimerization as well as heterodimerization with other SARAH domain-containing pr

289 competent itself as it requires aPC-induced heterodimerization with PAR-2 (human podocytes) or PAR-1

290 is controlled by the activating protease and heterodimerization with PAR2 or PAR3.

291 Dtx3L heterodimerization with Parp9 enables NAD(+) and poly(AD

292 Heterodimerization with prozyme displaces this sequence

293 Heterodimerization with R2 reduced the rate of internali

294 Thus, coiled-coil heterodimerization with Stepping stone normally recruits

295 hrough homodimerization of MMP-14 as well as heterodimerization with the cell surface adhesion molecu

296 PIF1 is also degraded in the dark by direct heterodimerization with the positively acting factor HFR

297 lation of MMP7 transcription did not require heterodimerization with the retinoid X receptor (RXR), i

298 LR expressed on human monocytes, by inducing heterodimerization with TLR1 in an NADPH oxidase-depende

299 Its location in the nucleus and heterodimerization with WC-2, together with the presence

300 Furthermore, upon heterodimerization with ZnT1, the zinc transporters ZnT2