ライフサイエンスコーパス: adapter

1 uto-disable syringe with a Helms intradermal adapter).

2 ona discharge device in a novel setup via an adapter.

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

4 r preferred orientations shift away from the adapter.

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

6 oxic stress and autophagy involving the Doa1 adapter.

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

8 viral protein is also required to act as an adapter.

9 of nanoparticles using programmable surface adapters.

10 ALs adapters compared to presbyopic PALs non-adapters.

11 rs compared to incipient presbyopic PALs non-adapters.

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

13 ays is adapter ligation using pre-adenylated adapters.

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

15 randomized splint ligation with a cleavable adapter, a design which resolves previous challenges ass

16 ell as the optimization of this activity for adapter addition in RNA- and DNA-Seq protocols.

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

18 ing the concentration and dosing schedule of adapter administration, we document two methods that can

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

20 le of the Toll/interleukin 1 (IL-1) receptor adapter and major inflammatory mediator myeloid differen

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

22 ce, implying that arrestins, multifunctional adapter and signaling proteins, play a vital role in med

23 of the activity during the interval between adapter and test stimuli.

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

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

26 als from many receptors and involves diverse adapters and kinases.

27 le-stranded excised oligomers are ligated to adapters and re-immunoprecipitated with damage-specific

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

29 complex or cyclosome (activated by the Cdh1 adapter), and the deubiquitinating enzyme USP35.

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

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

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

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

34 of synaptic cargo via the lysosomal kinesin adapter Arl8 regulates AZ abundance to modulate global s

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

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

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

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

39 with APP tail-1 (PAT1) as a potential direct adapter between zipcode-binding protein 1 (ZBP1, a beta-

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

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

42 is found in an autism patient and loses its adapter capacity for binding kinesin-1 motors.

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

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

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

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

47 We show that the optimization of adapter concentrations along with the addition of nucleo

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

49 y, we conclude that proper use of bispecific adapters could potentially avoid a life-threatening CRS

50 es downstream signaling cascades through the adapter DAP12.

51 Presentation of a visual adapter did not change the response to subsequent photo-

52 This process dramatically reduces adapter dimer and targeted smRNA sequences, can be multi

53 lly designing RNA-seq adapters that minimize adapter dimer formation.

54 oaches for remediating biases and decreasing adapter dimer formation.

55 However, this method does not deplete adapter dimer ligation products that, unless removed by

56 ed with single guide RNAs (sgRNAs) targeting adapter dimer ligation products, alongside highly expres

57 g studies, highly abundant molecules such as adapter dimer products and tissue-specific microRNAs (mi

58 to smRNA-seq, which we have termed miRNA and Adapter Dimer-DASH (MAD-DASH).

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

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

61 arises during the ligation of single-strand adapters during library preparation, and that this ligat

62 cocktail of low-molecular-weight bispecific adapters, each comprised of fluorescein linked to a diff

63 Rsp5 ubiquitin ligase and its transmembrane adapters, Ear1 and Ssh4, which localize to endosome and

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

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

66 levels of the MuvB core subunit LIN52, a key adapter for assembly of both the DREAM and MMB complexes

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

68 re kinesin light chains, which are a typical adapter for kinesin-dependent cargo transport.

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

70 macrophage transition is dictated by B-cell adapter for PI3K (BCAP).

71 D) promotes 26S assembly and functions as an adapter for proteasome transport in axons.

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

73 avage of chromosomal DNA with Cas9 to ligate adapters for nanopore sequencing.

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

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

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

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

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

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

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

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

82 A cocktail of tumor-targeted bispecific adapters greatly augments CAR T-cell therapies against h

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

84 Furthermore, the dynein adapter histone deacetylase 6 (HDAC6) is indispensable f

85 ce of either PTPN21 FERM domain or the cargo adapter Hook3 that binds the same region of KIF1C tail.

86 cifically, we found that overexpressed cargo adapter HookA (Hook in A. nidulans) missing its cargo-bi

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

88 97 or siRNA-mediated depletion of p97 or its adapters impairs Ku80 removal after non-homologous end j

89 a carefully designed cocktail of bispecific adapters in combination with antifluorescein CAR T cells

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

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

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

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

94 growth factor beta 1, TIR-domain containing adapter inducing interferon-beta (TRIF), TRIF-related ad

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

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

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

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

99 of TLR4 with MyD88 and TIR domain-containing adapter-inducing IFN-beta, thereby dampening the activat

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

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

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

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

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

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

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

107 response 88 (MyD88) or TIR-domain-containing adapter-inducing interferon-beta (TRIF) signaling pathwa

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

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

110 receptor 3 (TLR3)- and TIR domain-containing adapter-inducing interferon-beta (TRIF)-dependent type I

111 led DAI and DLM1), and TIR domain-containing adapter-inducing interferon-beta (TRIF).

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

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

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

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

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

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

118 , whereby Tn5 transposase inserts sequencing adapters into accessible DNA ('tagmentation').

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

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

121 ription complex that includes the ubiquitous adapter Ldb1 along with b-HLH and/or GATA family transcr

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

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

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

125 vailable to address important issues such as adapter ligation bias, PCR amplification artefacts or to

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

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

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

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

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

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

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

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

134 sly revealed that syntabulin acts as a motor adapter linking kinesin-1 motor and presynaptic cargos.

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

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

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

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

139 Here, we revealed its function in cargo-adapter-mediated dynein activation in the model organism

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

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

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

143 RAP1-interacting adapter molecule (RIAM) mediates RAP1-induced integrin a

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

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

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

147 ein) and microglial (ionized calcium-binding adapter molecule 1) markers was performed to investigate

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

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

150 staining showed more ionized calcium-binding adapter molecule 1-positive cells in the ischemic cortex

151 r results suggest that the NHERF1 acts as an adapter molecule and promotes IgE/Ag-induced mast cell a

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

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

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

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

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

157 obility group box 1, IFN-gamma, TRIF-related adapter molecule, IRF-3, HIF-1, nucleotide-binding oligo

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

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

160 DDB-kinesin-1 complexes, formed using a DNA adapter, moved slowly and persistently, and blocking p15

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

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

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

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

165 , ultimately suggesting Jip3 is a retrograde adapter of active Ret51.

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

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

168 ansmembrane signaling polypeptide and direct adapter of TREM2, as the most robust key driver gene in

169 with RNA productive factors as well as with adapters of the degradative RNA exosome.

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

171 First, biotinylated adapter oligonucleotides are hybridized to the DNA fragm

172 low-cost mobile fundus examination using an adapter on a smartphone; however, key aspects such as im

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

174 al enzyme L, and the oligomeric multimodular adapter P of Mononegavirales We outline the structural a

175 ting this process by silencing the mitophagy adapter p62/sequestosome-1 (SQSTM1) might mitigate myoto

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

177 L1 binding to optineurin (OPTN), a ubiquitin-adapter platforming TBK1 kinase.

178 Barcoded adapter primers are designed with an oligonucleotide hai

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

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

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

182 T cell kinase (ITK) with the T cell-specific adapter protein (TSAD) promotes LCK-mediated phosphoryla

183 between two different PPI interfaces of the adapter protein 14-3-3.

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

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

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

187 The adapter protein ASC assembles inflammasome components by

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

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

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

191 The adapter protein beta-arrestin2 inhibits Mrgprb2 and Fcep

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

193 ion significantly increased the proximal BCR adapter protein BLNK.

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

195 SDCBP is an adapter protein containing two tandem PDZ domains mediat

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

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

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

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

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

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

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

203 port proteins with the membrane-cytoskeleton adapter protein ezrin.

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

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

206 acetyl lysine) to N-terminal SH3 domain from adapter protein Grb2.

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

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

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

210 that tyrosine phosphorylation of the T cell adapter protein LAT at position Y132 is a critical kinet

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

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

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

214 ST2 signals through the adapter protein MyD88.

215 ell receptor (TCR) results in binding of the adapter protein Nck (noncatalytic region of tyrosine kin

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

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

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

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

220 autophagosomal membranes and the autophagic adapter protein p62.IMPORTANCE Although the mechanisms b

221 While the focal adhesion adapter protein paxillin is a well-characterized regulat

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

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

224 ocytes is mediated by the Toll-like receptor adapter protein SCIMP.

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

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

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

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

229 bitory regulation of the integrin-associated adapter protein talin coordinates cell-ECM adhesion duri

230 Rapsn is an adapter protein that bridges AChRs to the cytoskeleton a

231 Abi1 (Abelson interactor 1) is an adapter protein that has been implicated in nonmuscle ce

232 SH2B1 is an adapter protein that is recruited to the receptors of mu

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

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

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

236 l mitochondrial GTPases RHOT1 and RHOT2, the adapter protein TRAK2, the anterograde motor Kif5B, and

237 protein trafficking (NMT1), and the membrane adapter protein TSK5.

238 TRAF3 is a versatile intracellular adapter protein with multiple context-specific roles.

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

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

241 The postsynaptic adapter protein-coding gene, SHANK2, located on Chromoso

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

243 vep3, a zinc finger transcription factor and adapter protein.

244 c-CrkII is a central signal adapter protein.

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

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

247 xample, multifunctional beta-arrestin (ARRB) adapter proteins are best known as regulators of G prote

248 The epsin family of endocytic adapter proteins are widely expressed, and interact with

249 s previously shown that extracellular 14-3-3 adapter proteins bind to APN and thereby induce the tran

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

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

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

253 protein-tyrosine kinases, phosphatases, and adapter proteins interact to transmit signals from the T

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

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

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

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

258 mall Src homology domain 2 (SH2) and 3 (SH3) adapter proteins regulate cell fate and behavior by medi

259 Binding of the intracellular adapter proteins talin and its cofactor, kindlin, to the

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

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

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

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

264 ptic vesicles, ion channels, scaffolding and adapter proteins, and membrane receptors.

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

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

267 e the quality control process with automatic adapter removal.

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

269 lation of EC phenotype via an unconventional adapter role, assembling and anchoring a multifunctional

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

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

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

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

274 naling loop whereby N-WASP and the endocytic adapter SNX18 promote lysophosphatidic acid-induced RhoA

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 nsposase simultaneously cleaves DNA and adds adapters ('tagmentation') for paired-end DNA sequencing.

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

280 0) is a PSD-95, disc large, zona occludens-1 adapter that acts as a scaffold for signaling complexes

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

282 adjusting the dose of a low molecular weight adapter that must bridge between the CAR T cell and canc

283 The complex acts as a cargo adapter that recognizes signaling proteins such as GPCRs

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

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

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

287 me profiling by rationally designing RNA-seq adapters that minimize adapter dimer formation.

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

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

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

291 or was connected through a coaxial-waveguide adapter to the S parameter meter, by means of which the

292 Pipette tips were designed and 3D printed as adapters to fit most commercial 50-200 muL pipettes.

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

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

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

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

297 In neurons whose response to the visual adapter was inhibited by simultaneous photo-stimulation,

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.