ライフサイエンスコーパス: adapter

1 a molecular clamp and as a microtubule-cargo adapter.

2 g" of gold nanorods decorated by the surface adapter.

3 oxic stress and autophagy involving the Doa1 adapter.

4 2), in which TRAF3 serves as the NIK-binding adapter.

5 r preferred orientations shift away from the adapter.

6 ays is adapter ligation using pre-adenylated adapters.

7 , possibly, cdc20 homolog 1 (Cdh1) E3 ligase adapters.

8 of nanoparticles using programmable surface adapters.

9 ALs adapters compared to presbyopic PALs non-adapters.

10 rs compared to incipient presbyopic PALs non-adapters.

11 via ligation of double-stranded DNA (dsDNA) adapters.

12 efficient, template- and purification-free, adapter adenylation method using T4 RNA ligase 1.

13 proteins provide docking sites for distinct adapter and effector proteins important for regulating d

14 proteins that can interact with a variety of adapter and signaling molecules.

15 via a canonical pathway involving the MyD88 adapter and the interleukin-1 receptor-associated kinase

16 Fremont, CA) using an anterior segment lens adapter and the split-spectrum amplitude decorrelation a

17 l intradermal devices, including intradermal adapters and disposable-syringe jet injectors, have also

18 n by membrane-localized Src homology 3 (SH3) adapters and N-WASP, resulting in the assembly of dynami

19 related with the chemistry of the sequencing-adapters and the length of the DNA fragments.

20 ul whole-body point-light displays (PLDs) as adapters and were then asked to perform an explicit cate

21 Inflammasomes consist of a sensor, an adapter, and the effector caspase-1, which interact thro

22 ts; explore the various reported designs for adapters; and consider future opportunities for this tec

23 Although FRS adapters are dispensable for ERK-1/2 activation, they ar

24 ite mutant of Fgfr1, we established that FRS adapters are necessary for mediating most or all FGFR1 s

25 In Db-PCR, 5'- and 3'-stem-loop adapters are specifically hybridized and ligated to the

26 Alternatively, the adapter ASC may regulate inflammasome activity by expres

27 h interact with the PYD- and CARD-containing adapter ASC through homotypic PYD interactions.

28 requires the effector caspases 1 and 11, the adapter ASC, and NLRP1, the sensor previously described

29 vation, NLRP3 forms an inflammasome with the adapter ASC, resulting in caspase-1 activation, release

30 A fiber adapter assembly and gas filling setup was designed for

31 d is capable of adenylating large amounts of adapter at ~100% efficiency and can efficiently adenylat

32 h a model in which Ltn1 uses 60S subunits as adapters, at least in part via its NTD, to target stalle

33 Resultant cDNAs are amplified by adapter-based PCR and subjected to high-throughput seque

34 sidates the viral genome and functions as an adapter between the virus and the host cell machinery.

35 , suggesting that TRAM can act as a bridging adapter between these two molecules.

36 results in the sequestration of MyD88 (TLR2 adapter) by Act1/CIKS (IL17R adapter), thereby turning o

37 While pre-adenylated adapters can be chemically or enzymatically prepared, en

38 Here we used the parallel adapter capture (PAC) proteomics approach to study betaT

39 During normal signaling, the multidomain adapter CARD11 transitions from a closed, inactive state

40 or adapter to initiate a different cytosolic adapter cascade with double-stranded RNA agonists.

41 ater (p < 0.03) in incipient presbyopic PALs adapters compared to incipient presbyopic PALs non-adapt

42 cantly greater (p < 0.03) in presbyopic PALs adapters compared to presbyopic PALs non-adapters.

43 DLBCL), engages the CARD11-MALT1-BCL10 (CBM) adapter complex to activate IkappaB kinase (IKK) and the

44 Furthermore, oligomerization of LAT by adapter complexes enhances intracellular signaling and i

45 extraction probe was built into a luer lock adapter connected to a HTC PAL autosampler syringe.

46 es downstream signaling cascades through the adapter DAP12.

47 The structure suggests that the DUF is an adapter domain that stabilizes the aldehyde substrate bi

48 engagement of FRS and non-FRS intracellular adapters downstream of FGFRs could therefore in principl

49 Talin, a force-bearing cytoplasmic adapter essential for integrin-mediated cell adhesion, l

50 lopment as an example, we show here that FRS adapters exhibit some selectivity in their requirement f

51 ecifically, parkin targets the SCF substrate adapter Fbw7beta for proteasomal degradation.

52 family protein TULP3 functions as a general adapter for ciliary trafficking of structurally diverse

53 DAP12, a signaling adapter for multiple pattern recognition receptors in my

54 ated protein 4 family-interacting protein 1) adapter for the ubiquitin ligase ITCH is genetically lin

55 Several organelle-bound adapters for kinesin-1 and dynein have been reported tha

56 codes for computational error correction and adapters for library preparation and sequencing.

57 Even though several known adapters for the export factor NXF1 become part of BR mR

58 n as an example to study the role of the FRS adapters FRS2 and FRS3 in mediating the functions of FGF

59 domain of VE-cadherin mediates an essential adapter function by binding directly to the transmembran

60 In summary, this study identifies a novel adapter function for VE-cadherin mediated by transmembra

61 a role for tRNA distinct from its canonical adapter function in translation, as cleavage of tRNAs by

62 This complex requires the adapter GRB2, which bridges SHP to THEMIS in a Tyr-phosp

63 BL1, via phosphorylated Tyr177, recruits the adapter GRB2-associated binding protein 2 (GAB2) as part

64 We previously found that the scaffold adapter GRB2-associated binding protein 2 (GAB2) is ampl

65 The molecular adapter growth factor receptor binding protein 14 (Grb14

66 method relies on the ligation of sequencing adapters harboring random yet complementary double-stran

67 the early endosome association of the cargo adapter HookA (Hook in A. nidulans).

68 97 or siRNA-mediated depletion of p97 or its adapters impairs Ku80 removal after non-homologous end j

69 tail and kindlin-2, a member of a family of adapters implicated in human disease pathogenesis, is ma

70 Only MyD88- and TIR-domain containing adapter inducing IFN beta (TRIF) double deficient NOD mi

71 in (MyD88), and Toll-IL-1R domain-containing adapter inducing IFN-beta (TRIF)-dependent cytokine gene

72 daptor molecule Toll/IL-1R domain-containing adapter inducing IFN-beta and downstream production of t

73 pression of the Toll-IL-1R domain-containing adapter inducing IFN-beta in epithelial cells.

74 required in the Toll/IL-1R domain-containing adapter inducing IFN-beta pathway.

75 to proapoptotic Toll-IL-1R domain-containing adapter inducing IFN-beta signaling, but was also trigge

76 MyD88, but not Toll/IL-1R domain-containing adapter inducing IFN-beta, dependent.

77 ivated the TLR4/Toll/IL-1R domain-containing adapter inducing IFN-beta-dependent signaling pathway co

78 D88-independent Toll/IL-1R domain-containing adapter inducing IFN-beta-IFN regulatory factor 3 pathwa

79 g the TLR4/MD-2/Toll/IL-1R domain-containing adapter inducing IFN-beta-mediated signaling, whereby PT

80 immunity are linked by TIR domain-containing adapter-inducing beta interferon (TRIF) during establish

81 volving Toll-IL-1-receptor domain-containing adapter-inducing IFN-alpha (TRIF) and nuclear factor kap

82 al for both MyD88- and TIR-domain-containing adapter-inducing IFN-beta (TRIF)-mediated signaling path

83 cules MyD88 and Toll/IL-IR domain-containing adapter-inducing IFN-beta (TRIF)-related adaptor molecul

84 ation with TLR4/Toll/IL-1R domain-containing adapter-inducing IFN-beta activation is an efficient str

85 adapter protein TRIF (TIR domain-containing adapter-inducing IFN-beta adapter protein) was also abla

86 protein Toll/IL-1 receptor domain-containing adapter-inducing IFN-beta and responded poorly to TLR ag

87 hrough the TLR4/Toll/IL-1R domain-containing adapter-inducing IFN-beta pathway, independent of the pr

88 uced IFN-1 in a Toll/IL-1R domain-containing adapter-inducing IFN-beta-dependent manner.

89 Toll/IL-1 resistance (TIR) domain-containing adapter-inducing interferon beta) and activation of the

90 nduced endosomal TRIF (TIR domain-containing adapter-inducing interferon beta) signaling pathways.

91 like receptor 3 (-/-), TIR-domain-containing adapter-inducing interferon-beta (-/-), and wild-type mi

92 like receptor 3 (-/-), TIR-domain-containing adapter-inducing interferon-beta (-/-), and wild-type mi

93 y Toll-like receptor 4-TIR-domain-containing adapter-inducing interferon-beta (TLR4-TRIF).

94 tein kinase 3 (RIPK3), TIR-domain-containing adapter-inducing interferon-beta (TRIF) and Z-DNA-bindin

95 a Toll/IL-1 receptor (TIR) domain-containing adapter-inducing interferon-beta (TRIF) but less so for

96 tion factor 88 (MyD88)/TIR-domain-containing adapter-inducing interferon-beta (TRIF) double knockout

97 well as Toll-dependent TIR-domain-containing adapter-inducing interferon-beta (TRIF), which function

98 Toll/Interleukin-1R (TIR) domain-containing adapter-inducing interferon-beta (TRIF)-, TRIF-related a

99 8 adapter-like), TRAM (TIR domain-containing adapter-inducing interferon-beta (TRIF)-related adaptor

100 he pretreatment of WT, TIR domain-containing adapter-inducing interferon-beta knockout, and MyD88 ada

101 adaptor protein TRIF (TIR-domain-containing adapter-inducing interferon-beta) is essential for GN, b

102 terleukin-1 receptor (TIR) domain-containing adapter-inducing interferon-beta-dependent response that

103 lated adaptor molecule/TIR domain-containing adapter-inducing interferon-beta-dependent signaling pat

104 nocytes by enhancing a TIR domain-containing adapter-inducing interferon-dependent response and favor

105 CD38, via Src family kinases and adapters, interacts with a MAPK signalling axis that pro

106 tion chemistry between an integrin and a key adapter involved in integrin signaling.

107 at signalling complexes nucleated at the key adapter LAT show a hierarchical topology.

108 Since the cloning of the critical adapter, LAT (linker for activation of T cells), more th

109 mily kinase Fgr and shifted signals from the adapter LAT1 to the related adapter LAT2.

110 signals from the adapter LAT1 to the related adapter LAT2.

111 es (Ldb1 complexes) that include the nuclear adapters Ldb1 and Lmo2.

112 tured by oligo-dT primers and processed into adapter-ligated cDNA libraries that were sequenced using

113 We report the development of Y-shaped Adapter-ligated MAture TRNA sequencing (YAMAT-seq), an e

114 ter phosphatase treatment; hence, subsequent adapter ligation and cDNA amplification steps are exclus

115 -containing RNAs because the cP inhibits the adapter ligation reaction.

116 al step in many microRNA profiling assays is adapter ligation using pre-adenylated adapters.

117 MAT-seq circumvents the issue of inefficient adapter ligation, a characteristic of conventional RNA s

118 ves fragmentation of genomic DNA followed by adapter ligation, bisulfite conversion and limited ampli

119 A method using adapter-ligation and PCR amplification was successfully

120 inducing interferon-beta knockout, and MyD88 adapter-like knockout macrophages with gedunin (10 micro

121 ion primary response gene 88) and Mal (MyD88 adapter-like) for its signal transduction.

122 nd intracellular adaptors such as MAL (MyD88 adapter-like), TRAM (TIR domain-containing adapter-induc

123 The selective effect of gedunin on MyD88-adapter-like/myeloid differentiation primary response 88

124 ion in glial cells depends on TLR2 and MyD88 adapter-like/TIRAP.

125 immunological synapse via the transmembrane adapter linker for activation of T cells (LAT) and for T

126 CD45, and preassociation with the signaling adapters linker for activation of T cells and growth fac

127 between the monocyte populations is that the adapter Mal (encoded by TIRAP) has appeared crucial for

128 ng data files by trimming reads and removing adapters, mapping reads to a reference, counting gene fe

129 sphorylation does not occur by the canonical adapter mechanism demonstrated for other substrates, as

130 t also in cell survival, implying that other adapters mediate at least in part the signaling from FGF

131 itro in the absence or presence of the cargo adapter melanophilin (Mlph), which links myoVa to Rab27a

132 t both the myosin motor domain and the cargo adapter Mlph, which has an actin-binding domain that act

133 ith the adapter protein Rap1-GTP-interacting adapter molecule (RIAM) followed by the recruitment of t

134 AMSH interacts with signal transducing adapter molecule (STAM) 1 or 2, which enhances the activ

135 rve injury increased ionized calcium binding adapter molecule 1 (Iba1) and phosphorylated p38 MAPK im

136 signaling, levels of ionized calcium-binding adapter molecule 1 and glial fibrillary acidic protein,

137 panmicroglial marker ionized calcium-binding adapter molecule 1 was decreased in all AD cases and the

138 not differ regarding ionized calcium-binding adapter molecule 1+ immunoreactivity for microglia, sugg

139 hocyte expression of ionized calcium-binding adapter molecule 1, toll-like receptor 2, and toll-like

140 NZB gene encoding the SLAM signaling pathway adapter molecule EWS-activated transcript 2 (EAT-2) is p

141 protein 2 (Grb2) is a ubiquitously expressed adapter molecule involved in signaling processes of nume

142 mice and mice lacking the Toll-like receptor adapter molecule MyD88 were infected with a pool of infe

143 m in cancer, with a focus on complement, the adapter molecule Stimulator of Interferon Genes, natural

144 ely TLR independent, but is dependent on the adapter molecule STING, suggesting that the type I IFN s

145 s an oxidative stress-responsive cytoplasmic adapter molecule that is an upstream regulator of both I

146 ase (IKK) subunit NEMO/IKKgamma (NEMO) is an adapter molecule that is critical for canonical activati

147 riched in lymphoid tissues; Rap1-interacting adapter molecule).

148 complexes (Ldb1 complexes) that include the adapter molecules Lmo2 and Ldb1.

149 The adapter molecules Src-like adapter proteins (SLAP and SL

150 In animals, these proteins serve as adapter molecules to mediate signal transduction from Tu

151 his receptor interacts with mTOR via the TLR adapter MyD88.

152 For all TLRs except TLR3, recruitment of the adapter, myeloid differentiation primary response gene 8

153 Efl1 and Sdo1 and the release of the export adapter, Nmd3, by the GTPase Lsg1.

154 he subcellular distribution of the organizer/adapter NOX p47(phox) subunit is altered in PVN dendrite

155 e demonstrate that Grp170 binds to Sel1L, an adapter of the transmembrane Hrd1 E3 ubiquitin ligase po

156 ry response protein 88 (MyD88), a downstream adapter of TLRs including TLR7, abolished the RNA-induce

157 ferentiation 88 (MyD88) is the key signaling adapter of Toll-like and interleukin-1 receptors.

158 of proteins that are best known as signaling adapters of TNFRs.

159 ion, revealing Hook protein as general motor adapters on early endosomes.

160 blocks cell-surface recruitment of the MyD88 adapter, one of the earliest events in TLR signaling.

161 In this mechanism, the autophagic adapter p62/SQSTM1/Sequestosome-1 is an N-recognin that

162 ed significantly increased expression of the adapter PI3Kgamma subunits Pik3r5 (p101) and Pik3r6 (p84

163 Barcoded adapter primers are designed with an oligonucleotide hai

164 chnology-specific factors, such as choice of adapters/primers and sample amplification methods.

165 ole for adhesion and degranulation-promoting adapter protein (ADAP) in CD8 T cell function.

166 ole of adhesion- and degranulation-promoting adapter protein (ADAP) in promoting CD8 T cell responses

167 Adhesion and degranulation promoting adapter protein (ADAP) is a multifunctional adapter that

168 g protein 2 (SH3BP2) gene, which encodes the adapter protein 3BP2.

169 pansion by MSC EVs is mediated via the MyD88 adapter protein and is partially blocked by treatment wi

170 ngage caspase-1, in most cases requiring the adapter protein apoptosis-associated speck-like protein

171 dramatic relocalization of the inflammasome adapter protein apoptosis-associated speck-like protein

172 Many inflammasome receptors require the adapter protein ASC [apoptosis-associated speck-like pro

173 ion lies CrK-like (CRKL), a gene encoding an adapter protein belonging to the Crk family that is invo

174 a had greatest effects on recruitment of the adapter protein beta-arrestin 2.

175 t also signaling through the multifunctional adapter protein beta-arrestin.

176 Here, we report that the dynein adapter protein bicaudal D2 (BICD2) is able to interact

177 ion significantly increased the proximal BCR adapter protein BLNK.

178 Toll/IL-1 adapter protein cascades are induced by an activated Tol

179 expanding the life span of mice lacking the adapter protein CD2AP.

180 been suggested that the kinase CheA and the adapter protein CheW are integral for receptor connectiv

181 lular localization of human UNC93B1 via both adapter protein complex (AP)1- and AP2-dependent traffic

182 have identified the beta subunit of the AP-3 adapter protein complex, AP3B1, as a binding partner for

183 nduced an increase in the association of the adapter protein cortactin with Pfn-1 in smooth muscle ce

184 tively, these results identify a microtubule adapter protein critical for trafficking of HIV-1 in the

185 nd genetic approaches revealed that the ShcA adapter protein critically influences proliferation and

186 terminal Src homology 3 domain of the murine adapter protein Crk-II.

187 olecular level, Siglec-15 interacts with the adapter protein DAP12 and can induce Akt activation when

188 At this time, IL-13 and the adapter protein DAP12 promote TREM-2 cleavage to sTREM-2

189 cantly dependent on type I IFN and IPS-1 (an adapter protein downstream of the RIG-I pathway) signali

190 Our results indicate that the adapter protein Ecm29 is the main proteasome-interacting

191 eceptor bound protein 10 (Grb10) is a signal adapter protein encoded by an imprinted gene that has ro

192 ShcA is an adapter protein expressed in thymocytes, and it is requi

193 As CRKL is a member of the CRK adapter protein family that contains an SH2 and two SH3

194 vitro Macrophages deficient in Mincle or its adapter protein Fc receptor gamma chain (FcRgamma) produ

195 betaII-Spectrin (SPTBN1) is an adapter protein for Smad3/Smad4 complex formation during

196 ort that the c-Src kinase functions as a key adapter protein for the estrogen receptor (ER, ESR1) in

197 When mPyTK was introduced into the adapter protein Grb2, it enabled the photocapture of EGF

198 tested the hypothesis that Grb2 is a crucial adapter protein in (hem)immunoreceptor tyrosine-based ac

199 ological application we demonstrate that the adapter protein Inscuteable (mInsc) can actively promote

200 he PI3K, through tyrosine phosphorylation of adapter protein insulin receptor substrate (IRS1).

201 ates that Toll-like receptor (TLR) signaling adapter protein interactions with Toll/Interleukin-1 Rec

202 e myeloid differentiation protein 88 (MyD88) adapter protein is an important mediator of kidney allog

203 The adapter protein linker for activation of T cells (LAT) i

204 The Mig10/RIAM/Lpd (MRL) adapter protein Lpd regulates actin dynamics through int

205 ing, the type 1 IL1 receptor or the receptor adapter protein MyD88, were not protected from tumor-ind

206 cle, we report that C57BL/6 mice lacking the adapter protein MyD88, which mediates signaling by TLRs

207 volves caspase-dependent cleavage of the TLR adapter protein MyD88.

208 PP2A and increased its association with the adapter protein neuroblast differentiation-associated pr

209 Mst50 is an adapter protein of the Mst11-Mst7-Pmk1 cascade that is e

210 this modulation was dependent on DAP12, the adapter protein of TREM2.

211 roteins adhesion and degranulation promoting adapter protein or CT10 regulator of kinase/CT10 regulat

212 TRIP13 recognizes MAD2 with the help of the adapter protein p31(comet) We show that p31(comet) bindi

213 We find that TRIP13, aided by the adapter protein p31(comet), converts the HORMA-family sp

214 usly we reported that Jak3 interactions with adapter protein p52ShcA (Shc) facilitate mucosal homeost

215 association with the cellular focal adhesion adapter protein paxillin contributes to cell transformat

216 integrins competent to recruit the signaling adapter protein paxillin.

217 -bound Ras-related protein 1 (Rap1) with the adapter protein Rap1-GTP-interacting adapter molecule (R

218 Merlin and Kibra together recruit the adapter protein Salvador, which in turn recruits the cor

219 hese data identify an important role for the adapter protein ShcA in later stages of thymic T cell de

220 f PD-1 was associated with expression of the adapter protein SHP-2, which signals to NF-kappaB; howev

221 uitinated proteins, and the multi-functional adapter protein SQSTM1/p62.

222 of CaV1.1 in tsA201 cells is promoted by the adapter protein Stac3, because recent work has shown tha

223 ts intracellular DNA and signals through the adapter protein STING to initiate the antiviral response

224 mRNAs through the activity of the viral Rev adapter protein that forms a multimeric complex on these

225 at RANKL controls the expression of 3BP2, an adapter protein that is required for activation of SRC t

226 tor (TNFR)-associated factor 6 (TRAF6) is an adapter protein that mediates a wide array of protein-pr

227 ADAP is a hematopoietic-restricted adapter protein that promotes integrin activation and is

228 otein A repetitions predominant [GARP]), the adapter protein that tethers TGF-beta to the membrane.

229 C57BL/6 mice, nor when signaling through the adapter protein TRIF (TIR domain-containing adapter-indu

230 The signaling adapter protein tumor necrosis factor receptor (TNFR)-as

231 lasmic capping complex assembles on Nck1, an adapter protein with functions in translation and tyrosi

232 domain-containing adapter-inducing IFN-beta adapter protein) was also ablated.

233 We report here that an adapter protein, ArgBP2, is a component of alpha-actinin

234 ect binding to AtDCP1 rather than through an adapter protein, as known for membrane-coated organelles

235 ay have been facilitated by the bifunctional adapter protein, PSD-95, which associated with LRP1 sele

236 of the E. coli stress response, RpoS, by its adapter protein, SprE (RssB).

237 zinc finger-expressing, SLAM family receptor adapter protein-dependent thymocyte population that is e

238 c-CrkII is a central signal adapter protein.

239 reases with increasing levels of CheW, a key adapter protein.

240 I recognition motif and to a well-structured adapter protein.

241 The adapter molecules Src-like adapter proteins (SLAP and SLAP2) are involved in the re

242 ctive in the cytoplasm and that a variety of adapter proteins activate processive motility by linking

243 Although these adapter proteins bound readily to wild-type EGF receptor

244 Multiple SH3 domain-containing adapter proteins can bind and possibly activate N-WASP,

245 yotic cells require IQGAP family multidomain adapter proteins for cytokinesis, but many questions rem

246 This was attributed to the absence of both adapter proteins in platelets, as demonstrated by adopti

247 ink membrane subdomains, clathrin, and other adapter proteins involved in early steps of clathrin coa

248 TNF receptor-associated factor (TRAF)-family adapter proteins involved in TLR and TNFR pathways.

249 in of Nv-TLR can interact with the human TLR adapter proteins MAL and MYD88.

250 ractions between the tail and regions of the adapter proteins outside of the SH2/PTB domains are impo

251 CRK and CRKL adapter proteins play essential roles in development and

252 ns (betaarrs) are versatile, multifunctional adapter proteins that are best known for their ability t

253 Arrestins function as adapter proteins that mediate G protein-coupled receptor

254 asmic reticulum (ER) is organized in part by adapter proteins that nucleate the formation of large pr

255 Importin-alphas are essential adapter proteins that recruit cytoplasmic proteins desti

256 ling and facilitate recruitment of signaling adapter proteins to the intracytoplasmic domain.

257 prime example is binding of the rigid 14-3-3 adapter proteins to their numerous partner proteins, who

258 ses occurred in macrophages deficient in the adapter proteins TRIF or MyD88 but not in macrophages de

259 ctivation, Toll-like receptor 4 (TLR4) binds adapter proteins, including MyD88 (myeloid differentiati

260 tegrin activation and is a carrier for other adapter proteins, Src kinase-associated phosphoprotein 1

261 tin and one of four different cargo-specific adapter proteins, the motor became ultraprocessive, movi

262 747) motif, to induce spreading and paxillin adapter recruitment to substrate- and talin-bound integr

263 We show that EPS8, a signaling adapter regulating actin dynamics, is a novel partner of

264 al. (2014) report that degradation of cargo adapters releases yeast vacuoles and peroxisomes from my

265 w sequence evaluation, (2) read trimming and adapter removal, (3) read mapping and quality filtering,

266 ation sequencing reads, PALEOMIX carries out adapter removal, mapping against reference genomes, PCR

267 function, whereas double deficiency of both adapters resulted in markedly increased signal transduct

268 ssociated gene-9 (mda-9/syntenin) encodes an adapter scaffold protein whose expression correlates wit

269 as it was congruent with the emotion in the adapter sequence.

270 data and differentiate them from artificial adapter sequences added in the sequencing process.

271 tion-based strategy that leaves behind 38-bp adapter sequences, which must be computationally removed

272 n molecule family receptors and the specific adapter signaling lymphocytic activation molecule-associ

273 ull use of the sequence on both sides of the adapter site to build 'virtual libraries' of mate pairs,

274 o the centre of LAT-based complexes, and the adapter SLP-76 and actin molecules localize to the perip

275 e conversion and limited amplification using adapter-specific PCR primers in preparation for sequenci

276 signaling or the endoplasmic reticulum (ER) adapter, stimulator of interferon genes (STING).

277 M-PCR and unidirectionally ligated to bridge adapters; subsequent PCR steps amplify the single-strand

278 provide a detailed protocol for efficient DS adapter synthesis, library preparation and target enrich

279 Among six SH3 adapters tested, Nck was the most potent activator of N-

280 Here, we present a versatile DNA surface adapter that can programmably self-assemble into various

281 adapter protein (ADAP) is a multifunctional adapter that regulates "inside-out" signaling from the T

282 gene, which encodes gigaxonin, an E3 ligase adapter that targets intermediate filament (IF) proteins

283 main containing proteins (BET) are chromatin adapters that bind acetylated histone marks via two tand

284 k and Crk-like (CrkL), are broadly expressed adapters that interact with a variety of proteins to ful

285 binding proteins (PCBPs) are multifunctional adapters that mediate interactions between nucleic acids

286 ependent association with 14-3-3, a group of adapters that modulate dimerization and association betw

287 of MyD88 (TLR2 adapter) by Act1/CIKS (IL17R adapter), thereby turning off TLR2 signaling to restore

288 aining protein 4 (NLRC4) as the inflammasome adapter to activate innate immunity.

289 uses the toll receptor 3/4 induction factor adapter to initiate a different cytosolic adapter cascad

290 efficient and specific ligation of Y-shaped adapter to mature tRNAs using T4 RNA Ligase 2.

291 Rs, with the exception of TLR3, use an MyD88 adapter to Toll/IL-1 to initiate a proinflammatory casca

292 While 'adapter trimming' is a well-studied area of bioinformati

293 and by implementing different approaches in adapter trimming, mapping and quantification.

294 miseq does this by automating the process of adapter trimming, quality filtering, error correction, c

295 universal electromagnetic energy conversion adapter (UEECA) based on MA.

296 and the assembly vector is encoded by 'VEGAS adapter' (VA) sequences, which are orthogonal in sequenc

297 osin V motor Myo2 binds the vacuole-specific adapter Vac17 to attach to the vacuole/lysosome and init

298 ich SQSTM1/p62 plays a major role as a cargo adapter, we also were able to confirm that p62 binds to

299 photographers using the low-cost smartphone adapter were able to acquire optic nerve images at a sta

300 and while simultaneously attaching a DNA-seq adapter without end repair, tailing, or ligation.