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1 corticothalamic and inhibitory tectothalamic terminals.
2 es of action other than the primary afferent terminals.
3 or capsaicin-induced ablation of nociceptive terminals.
4 es large and rapid acid loads in presynaptic terminals.
5 g in axons and APP processing at presynaptic terminals.
6 t the evolutionarily conserved human CDC73 N-terminal 111 residues form a globularly folded domain (h
7 nal intermembrane space (IMS) domain and a C-terminal 16-stranded beta-barrel domain.
8 es, while the median (2n = 24) presents four terminal 35S sites and three interstitial 5S sites.
9    The ancestral karyotype (2n = 16) has two terminal 35S sites and two interstitial 5S sites, while
10  acid substitution mutations within a PMS2 C-terminal (721)QRLIAP motif attenuate or abolish human Mu
11 -acetyltransferase D (NatD) mediates N-alpha-terminal acetylation (Nt-acetylation) of histone H4 know
12  p53 residence times on chromatin requires C-terminal acetylation-a classical mark for transcriptiona
13 s recently identified as an unconventional N-terminal acetyltransferase (NAT) because it localizes to
14 Lysine 1016 and Phenylalanine1037 with the N-terminal acidic domain of the telomere shelterin protein
15 he presence of Ng13-49 by showing that the N-terminal acidic region of Ng peptide pries open the beta
16 nt ubiquitination and Rqc2p-mediated Carboxy-terminal Alanine and Threonine (CAT) tail elongation-can
17 I) ligands catalyze the cycloaddition of two terminal alkynes and one cyanamide.
18 certain deoxygenated derivatives with either terminal alkynes or borylated alkenes.
19                              The addition of terminal alkynes to racemic beta-stereogenic alpha-keto
20 talyzed intermolecular aminosulfonylation of terminal alkynes with sodium sulfinates and TMSN3 is rep
21 respectively, which differ solely in their N-terminal amino acid sequences.
22 ng site residue Y745 and, essentially, the N-terminal amino acids 1-800.
23 tive region(s) of Ov-GRN-1, four truncated N-terminal analogues were synthesized and characterized st
24 made as precursors with positively charged N-terminal anchors, whose cleavage via the prepilin peptid
25                                        The N-terminal and C-terminal domains of CA (NTD and CTD, resp
26                                 Effects of N-terminal and C-terminal STIM1 antibodies on TRPC1-based
27 antioselective addition of N-heteroarenes to terminal and internal 1,3-dienes is reported.
28 or Toll-like receptor 4 (TLR4) through its N terminal and modulates STAT3 and TBK1 signaling, trigger
29  an unexpected allosteric site between the C-terminal and the N-terminal helicase cassettes, while 12
30 not disrupt the morphogenesis of presynaptic terminals and dendritic spines, suggesting that glutamat
31  Simulations show frequent exchanges between terminal aquo groups and adsorbed water in locations and
32                                The tecto-IOC terminals are delicate and divergent, unlike the promine
33 nd female mice, we show that pulvinocortical terminals are densely distributed in the extrastriate co
34              An Ala mutation of the distal C-terminal Arg-354 or Ser-357, which forms a consensus pho
35    Binding of the intrinsically disordered C-terminal arm of CcdA to the toxin CcdB prevents CcdB fro
36 ed' together is stabilized via a conserved C-terminal arm, which may interact with the portal protein
37                     We identify a distinct C-terminal autoinhibitory four-residue sequence in CNAbeta
38 ty troponin T, creatine kinase, myoglobin, N-terminal B-type natriuretic peptide, C-reactive protein,
39 ry glycans could be obtained by removal of a terminal beta-GlcNAc moiety by treatment with beta-N-ace
40 ontracts, resulting in a shortening of the C-terminal beta-strand.
41 ecombinant alpha-syn protein containing an N-terminal bicysteine tag (C2-alpha-syn).
42 nscriptional repressors via recruitment of C-terminal Binding Proteins.
43 tative scaffold interactions involving the N-terminal BRCT domains 1 to 4 of Brc1 have remained obscu
44              Finally, we observed that the N-terminal, but not the C-terminal, moiety of MF6p/HDMs ha
45 factor neuronal pentraxin 1 from presynaptic terminals by signaling through presynaptic protein tyros
46 le 12 binds an RNA-binding site inside the N-terminal cassette.
47    BoNTs are dichain toxins, comprising an N-terminal catalytic domain (LC) disulfide bond linked to
48 revious structural studies showed that the C-terminal catalytic domain of human A3B has a tightly clo
49                        Overexcitation of the terminal causes Ca(2+) accumulation and swelling that ca
50 e with beta-arrestins for interaction with C-terminal CB1R domains that could affect agonist-driven,
51  correlated to the br-CF3's proximity to the terminal CF3.
52                              Moreover, two C-terminal charges impact CRY2 homo-oligomerization, with
53                             By engineering C-terminal charges, we develop CRY2high and CRY2low with e
54 F2, whereas IGF1 displayed homogeneous amino-terminal cleavage with complete removal of the bombyxin
55  footprint extends 13 nucleotides into the N-terminal coding region and, when a mRNA structure overla
56 eration of anaphylatoxins (C3a, C5a) and the terminal complement complex (TCC) that together contribu
57 t activation independent of formation of the terminal complement complex and provide in vivo evidence
58                                 Formation of terminal complement complex on other complement-activati
59 PV-IR synapses from putative thalamocortical terminals comprised the remaining approximately 40% of P
60  disordered C-terminal linker (CTL), and a C-terminal conserved peptide (CTC).
61 sequence of the phosphorylated CTD via its N-terminal CTD-interacting domain.
62 otropes express a TET1 isoform lacking the N-terminal CXXC-domain, which represses Lhb gene expressio
63  also found that, after addition of a single-terminal Cys residue, a CdtB homologue from cytolethal d
64                        In viruses with the N-terminal Cys residues mutated, TF is much less efficient
65 s (classical, alternative, and lectin) and a terminal cytolytic pathway common to all.
66 formational change unveils a region of the N-terminal cytosolic tail targeted by the Art1 alpha-arres
67 The design of the peptides is based on the C-terminal D4 domain of the Escherichia coli polysaccharid
68                  Lon recognizes HspQ via a C-terminal degron, whose precise presentation, in synergy
69 critical determinant, Ser5 mutants bearing C-terminal deletions were created.
70                                              Terminal deoxynucleotidyl transferase dUTP nick end labe
71 ining of occludin, Ki-67, NF-kappaB-p65, and terminal deoxynucleotidyl transferase-mediated dUTP nick
72 tosis of LX-2 cells, as was confirmed by the terminal deoxynucleotidyl transferase-mediated dUTP-biot
73  bi-lobal architecture, with the catalytic N-terminal DHH domain linked to the substrate binding C-te
74 DHH domain linked to the substrate binding C-terminal DHHA1 domain via an extended linker.
75 , it induced expression of a large number of terminal differentiation genes.
76  of Corti and the vestibular organ, impaired terminal differentiation manifests as immature stereocil
77  genome become open for transcription during terminal differentiation, blocking the action of a promi
78 nodules in which bacterial symbionts undergo terminal differentiation.
79 nslational modifications on the RNA pol II C-terminal domain (CTD) and the chromatin template.
80 es the catalytic core domain (CCD) and the C-terminal domain (CTD) of the integrase.
81 (CDK9) recruitment and phospho-Ser 2 carboxy-terminal domain (CTD) RNA polymerase (Pol) II formation
82 ere, we investigate the impact of the PHF1 N-terminal domain (NTD) on the Tudor domain interaction wi
83                  Here, we show that Cet1's N-terminal domain (NTD) promotes the recruitment of FACT (
84 , electron density was missing for the p59 N-terminal domain and for the linker connecting it to the
85 apZ at 3.40 A and 3.25 A, and its isolated C-terminal domain at 1.17 A resolution.
86                     In addition, the GSDMB N-terminal domain binds liposomes containing sulfatide.
87  the absence of coiled-coil formation, the C-terminal domain bound liposomes and ProP concentrated at
88 lipoxygenases, the topologically conserved C-terminal domain catalyzes the oxidation of polyunsaturat
89              Overexpression of NRP2 or its N-terminal domain enhances VSV-LUJV infection, and cells l
90 ta1-6A2V, which supports a role of Abeta's N-terminal domain in amyloid fibril formation.
91  on the face of the beta-helix whereas the C-terminal domain is likely involved in carbohydrates bind
92                               The FliG amino-terminal domain is organized in a regular array with dim
93 ssed by CO2 in a manner dependent on a key C-terminal domain located in its transactivation domain.
94       Here, we report that the hydrophilic N-terminal domain of Brassica napus DGAT1 (BnaDGAT11-113)
95 nteracts with a novel binding motif in the N-terminal domain of CaV1 LTCC alpha1 subunits that is not
96 endent conformational rearrangement of the C-terminal domain of heme binding protein (PhuS) is requir
97 prevents the specific interaction with the N-terminal domain of Hsp90 required for catalysis.
98  suggested that POA binds within the carboxy-terminal domain of ribosomal protein S1 (RpsA) and inhib
99 nding with TATA-box DNA, and also with the N-terminal domain of TAF1 previously implicated in TATA-bo
100 e variants identified in the intracellular C-terminal domain of the GluN2B NMDAR subunit.
101                                        The C-terminal domain of the human Ino80 subunit (Ino80CTD) bi
102 and a higher-order form that adopts carboxyl-terminal domain rearrangements.
103                                    The amino-terminal domain with a fold distinct among known TRP str
104 ing isoform (LIG3beta) that differs in the C-terminal domain.
105 portant differences in how the Rb and p107 C-terminal domains (CTDs) associate with the coiled-coil a
106                         The N-terminal and C-terminal domains of CA (NTD and CTD, respectively) engag
107 ere we solve the crystal structures of the N-terminal domains of PHF1 and MTF2 with bound CpG-contain
108                                          The terminal domains of suprabasal keratins of the skin epit
109               We find that both the N- and C-terminal domains of TTP are involved in an interaction w
110                                        The C-terminal DSP domain induced phosphorylation of occludin
111 g differentiation resulted in acquisition of terminal effector cell characteristics, whereas enhancem
112 slational suppression was more pronounced in terminal effector cells than in memory precursor cells a
113 teps controlling postinfection CD8(+) T cell terminal effector versus memory differentiation are inco
114 ormate and facilitate the use of oxygen as a terminal electron acceptor, respectively.
115  activity of cytochrome c oxidase (COX), the terminal electron-accepting complex of the mitochondrial
116 tail that is rich in basic residues at the C-terminal end is responsible for the interaction with RNA
117 C database, confirms that mutations in the N-terminal end of the kinase domain are more disruptive of
118 own for both species that mutations at the C-terminal end of this epitope dramatically improve presen
119 d hydrophobic and polar amino acids at the C-terminal end.
120 enomic characteristics of the regions at the terminal ends of two frequent types of large structural
121  where it truncates core histones at their N-terminal ends.
122 r confirm this function of chloroplasts, the terminal enzyme for melatonin synthesis, N-acetylseroton
123 H from the culture medium completely blocked terminal erythroid differentiation and enucleation.
124 er time with mortality acting as a dependent terminal event.
125            Bacteria encoding L27 with this N-terminal extension also encode a sequence-specific cyste
126 lack TMBS2 and half of ABS1, and present a C-terminal extension containing a proline-rich domain and
127 them to open the F pocket and expose their C-terminal extension into the solvent.
128                                        The C-terminal extension of capsid protein VP3 folds into a gl
129         Finally, we find that deleting the C-terminal extension of Lmod1 and Lmod2 results in an appr
130    This binding was not affected by cry1's C-terminal extension, which is important for signal transd
131 F loop of VP2, the GH loop of VP3, and the N-terminal extensions of VP1 and VP2, which, in retrospect
132 ation sites to the otherwise divergent amino-terminal extensions on these pollen sPPases.
133 with the crystal structure of the isolated N-terminal extracellular domain of the GLP-1R in complex w
134 ts the normal age-dependent "pruning" of all terminal fields, which could lead to alterations in sens
135 f ubiquitin, two interhelical loops of the C-terminal four-helix bundle appear to penetrate the membr
136                            We show that an N-terminal fragment comprising the catalytic domain can in
137 n2 TM2 leads to the appearance of a carboxyl-terminal fragment consistent with intramembrane proteoly
138 d for a mixture of Abeta1-28WT and a short N-terminal fragment, Abeta1-6A2V, which supports a role of
139 n can interact both with itself and with a C-terminal fragment.
140 studies have shown that the aggregation of N-terminal fragments (encoded by HTT exon 1) underlies the
141 ously characterized viruses expressing amino-terminal fusions, this virus expresses more VP26 fusion
142 nts, including high mannose, sialylated, and terminal galactosylated species were studied in detail.
143 g properties of 40 CBMs, in fusion with an N-terminal GFP domain, revealed that type A CBMs possess t
144 sting a similar expansion of cells that lack terminal glial differentiation.
145 can-binding proteins uncovered that not only terminal glycoepitopes but also complex architectures of
146 o cleave the N-terminal prodomain from the C-terminal growth factor (GF) domain in each monomer, pro-
147 sphorylation-dependent (40E8 and p396) and C-terminal half (4E4) tau antibodies also reduced tau upta
148 we determined the crystal structure of the N-terminal half of a conserved tegument protein, UL37, fro
149 tic domain (LC) disulfide bond linked to a C-terminal heavy chain (HC) which includes a translocation
150 steric site between the C-terminal and the N-terminal helicase cassettes, while 12 binds an RNA-bindi
151 ich the small molecule stabilizes a mobile C-terminal helix inside a hydrophobic crevice of NCS-1 to
152 permits positively charged residues in the C-terminal helix to engage in DNA binding, triggering a ma
153                                        The C-terminal homology domain (CHD) of Af4 was sufficient to
154         Using the endocytic protein epsin1 N-terminal homology domain (ENTH), previously thought to d
155 e demonstrate an essential role of TH during terminal human erythroid cell differentiation; specific
156                           In contrast, the N-terminal hydrophobic core showed extremely slow solvent
157 n associated with DSD activity and a novel C-terminal hydroxyphenylpyruvate dioxygenase-like domain.
158         Optogenetic inhibition of PBel(CGRP) terminals identified a network of forebrain sites under
159 ere we report the crystal structure of the N-terminal IMS domain of Toc75 from Arabidopsis thaliana,
160                                        The C-terminal in-frame green fluorescent protein fusion may s
161 t, unlike the prominent convergent tecto-ION terminals in Neognathae.
162 both GABA and GABA-A receptors to their axon terminals in the EB, and optogenetic stimulation coupled
163 l activity when ATP consumption within nerve terminals increases drastically.
164 erminal "thumb" and a disulfide-stabilized C-terminal "index finger," yet how these binding events tr
165 sonance spectroscopy demonstrated that the N-terminal inhibitory domain (NID) is intrinsically disord
166 o have a beta-barrel fold consisting of an N-terminal intermembrane space (IMS) domain and a C-termin
167 ous neurological diseases, its role at nerve terminals is poorly understood.
168 e ER-Golgi-cycling FKBP proteins contain a C-terminal KDEL-like sequence, bind ST-FRB in the Golgi, a
169 inflammatory skin disease, is driven by both terminal keratinocyte differentiation defects and strong
170 re TBI elicits neuroinflammation and c-Jun-N-terminal kinase (JNK) activation, which is associated wi
171  show that ATZ induces activation of c-Jun N-terminal kinase (JNK) and c-Jun and that genetic ablatio
172                            Moreover, c-Jun N-terminal kinase (JNK) has been implicated in regulation
173      Because islet amyloid increases c-Jun N-terminal kinase (JNK) pathway activation, we investigate
174                                      c-Jun N-terminal kinase (JNK) plays a vital role in malignant tr
175 tor of both IkappaB kinase (IKK) and c-Jun N-terminal kinase (JNK), and an important mediator of auto
176 sor function for KIND1, and identify c-Jun N-terminal kinase and NF-kappaB as potential therapeutic t
177 optosis and recently a specific JNK (c-Jun N-terminal kinase)-dependent S574 phosphorylated form (p-F
178      Abnormal accumulation of Abeta at nerve terminals leads to synaptic pathology and ultimately to
179 GTPase domain, an intrinsically disordered C-terminal linker (CTL), and a C-terminal conserved peptid
180 rectly destabilize the complex through the N-terminal linker.
181 nt on both the presence of a 22-amino-acid N-terminal 'loop' region and its catalytic activity.
182 on of K29-linked ubiquitin chains with two N-terminal loops of Ufd2p.
183 reactivity against recombinantly expressed N-terminal LRP2 fragments on Western blots and immunopreci
184 ta contains a specific NLS sequence in the N-terminal lyase domain that promotes transport of the pro
185                  An APP mutant lacking all C-terminal lysines underwent the most pronounced increase
186     Here, we show that substitution of APP C-terminal lysines with arginine disrupts APP ubiquitinati
187 n a primary binding site and the nonreducing terminal mannose residue occupying an adjacent secondary
188 on of cell migration as a feature of NK cell terminal maturation in this system.
189 rrier is established through the coordinated terminal maturation of the retinal pigment epithelium (R
190  modes of migration that are associated with terminal maturation.
191 and that limiting Ca(2+) accumulation in the terminal may protect against hearing loss.
192 hyltransferase activity of MEPCE through a C-terminal MEPCE interaction domain (MID).
193                               Truncations, N-terminal methionine excision, signal peptide removal, an
194 Furthermore, it is shown that this type of C-terminal modification may be combined with a second peri
195 otein and the peptide corresponding to the N-terminal moiety of MF6p/FhHDM-1 interact in vitro with c
196  observed that the N-terminal, but not the C-terminal, moiety of MF6p/HDMs has a predicted structural
197 d that the use of allosterically regulated C-terminal motifs could be a common mechanism for PilZ ada
198 vised road map emphazises close parallels of terminal mTEC development with that of skin, undergoing
199  The first complex featuring an unsupported, terminal multiple bond between a Ce(IV) ion and a ligand
200 hydrogen atom abstraction and synthesis of a terminal nitride from coordinated ammonia, a key step in
201             The molecular basis of how the N-terminal non-catalytic CD1 regulates the catalytic activ
202 N-terminal nuclear localization signal and C-terminal nuclear export signal (NES).
203 istic activities of both a peptide-encoded N-terminal nuclear localization signal and C-terminal nucl
204  isoforms were full length, containing the N-terminal nuclear localization signal.
205 e between the transmembrane domain and the C-terminal nucleotide binding domain.
206 h amphipathic peptide sequence attached to N-terminal of bZIP53 leucine zipper.
207                                        The N-terminal of MyRF, which contains a proline-rich region a
208  alpha-synuclein is found at the presynaptic terminals of dementia with Lewy bodies cases mainly in t
209 e performed live Ca(2+) imaging in the nerve terminals of gonadotropin-releasing hormone neurons.
210 umulation of intermediate filaments in nerve terminals of the neuromuscular synapse and improves the
211 t abundant being transcripts containing a 5' terminal oligopyrimidine (5' TOP) motif.
212 erse late transition metal catalysts convert terminal or internal alkynes into transient allylmetal s
213  DP4+ methodology in the stereoassignment of terminal or spiroepoxides bearing a wide variety of mole
214 n partners interact via association of the C-terminal or transmembrane segments, with consequences fo
215         Mutation of the start codon of two C-terminal ORFs in an infectious clone reduced virus yield
216  a periplasmic formate dehydrogenase and two terminal oxidases, which serve to metabolize formate and
217                                        The C-terminal pair of BRCT domains in Brc1 were previously sh
218  alpha-synuclein levels sufficient to induce terminal pathology without significant loss of nigral ne
219  CRIP1a, but that a phosphorylated central C-terminal peptide competed for association with beta-arre
220 d replacements on lipid association of the C-terminal peptide fully recapitulated their effects on th
221 nce, the protein was identified as a carboxy-terminal peptide of the acute phase protein serum amyloi
222 in 1, and phosphorylated central or distal C-terminal peptides competed for association with beta-arr
223 plexes demonstrated that central or distal C-terminal peptides competed for the CB1R association with
224 ternal metal nodes of MOF nanoparticles with terminal phosphate-modified oligonucleotides.
225         We explored the functionality of two terminal PKS modules that produce the 16-membered tylosi
226  of the antiviral drug, amantadine, at the N-terminal pore at low pH did not convert all histidines t
227 e change in 6-minute walk distance, plasma N-terminal pro-B-type natriuretic peptide (NT-proBNP) leve
228 high-dose spironolactone and usual care on N-terminal pro-B-type natriuretic peptide (NT-proBNP) leve
229 ailure score (48 versus 40), higher median N-terminal pro-B-type natriuretic peptide concentration (4
230  congestion, worse quality of life, higher N-terminal pro-B-type natriuretic peptide levels, and a po
231  mL [517-768 mL]; P<0.0001), despite lower N-terminal pro-B-type natriuretic peptide levels.
232  serial measurement of soluble ST2 and amino-terminal pro-B-type natriuretic peptide to clinical para
233 n class III/IV, RVESRI, and log NT-proBNP (N-Terminal Pro-B-Type Natriuretic Peptide) were retained (
234 entation index, (4) circulating NT-proBNP (N-terminal pro-B-type natriuretic peptide), TNF-alpha, IL-
235 fter processing in the Golgi to cleave the N-terminal prodomain from the C-terminal growth factor (GF
236  bridges with Cys-158 of the very flexible N-terminal propeptide being covalently linked to Cys-319 a
237                                            N-terminal propeptide of type I procollagen (PINP) and C-t
238 phosphorylation of residues in alpha1C and C-terminal proteolytic cleavage of the alpha1C subunit.
239 ines cationic, unambiguously demonstrating C-terminal protonation of H37 in the mutant.
240 the bacterial chemotaxis protein CheY, the N-terminal receiver domain of the nitrogen regulation prot
241 ing question concerns the structure of the C-terminal region of CA and the peptide SP1 (CA-SP1), whic
242 non-synonymous substitution (A120G) in the N-terminal region of eIF2Bbeta was responsible for the TuM
243  sugar modifications and revealed that the C-terminal region of FUS is sufficient to retain ASOs in c
244 noprecipitated the recombinantly expressed N-terminal region of LRP2.
245                           TFAM tethers the N-terminal region of mtRNAP to recruit the polymerase to t
246       The interaction occurred through the C-terminal region of RING1B (C-RING1B), with an affinity i
247 d versions of SS4 and a fusion between the N-terminal region of SS4 and GS in the Arabidopsis ss4 mut
248 caused by a polyglutamine expansion in the N-terminal region of the huntingtin protein (N17).
249 O homooligomerization, mediated by the amino-terminal region of the protein, and carboxyl-terminal ta
250  mediated by the coiled-coil domain at the N-terminal region of the protein.
251                            An unstructured N-terminal region of Tim10 is necessary and sufficient to
252 actions of the central part of Tm with the C-terminal region of TnI.
253  cyclin F-specific amino acid motif in the C-terminal region of Vif indicated rescue of the protein f
254 n TRP structures, together with the carboxyl-terminal region, forms a large two-layered cytosolic rin
255 ith deletion of residues 338 to 347 in the C-terminal region, has been an enigma, because the basis f
256 m the presence of an acidic residue at its N-terminal region.
257 estigated the specific roles of the N- and C-terminal regions of SS4 by expressing truncated versions
258 e transcriptional activity of the viral long terminal repeat (LTR) from Vpr-deficient proviruses was
259  recombination with specific classes of long terminal repeat (LTR) retrotransposons and organize into
260 ter phenotypically resembles endogenous long terminal repeat (LTR) sequences, pointing to a select ro
261 ons in the regulatory elements in their long terminal repeats and differed in a helical segment of en
262          Here, we show that the regulatory N-terminal residues and the EH domain keep the EHD2 dimer
263 on the formation of hydrogen bonds between C-terminal residues of lentil peptides and residues of the
264 ec72, even though it lacks the TPR-binding C-terminal residues of Ssa1.
265 expressing DAT selectively in DA neurons and terminals, resulting in the rescue of aberrant striatal
266  the effect of three enhanced strategies for terminal room disinfection (disinfection of a room betwe
267 e versa during development, which affect the terminal seam cell number in opposing directions.
268 by the SCI's B and C domains encircles the C-terminal segment of the IR alpha-subunit.
269 f the permeation of the lethal factor (LF) N-terminal segment through the anthrax channel.
270 we ectopically expressed C. elegans CHE-1, a terminal selector of ASE sensory neuron identity.
271                       The conserved COE-type terminal selector UNC-3 not only controls the expression
272 d by its collaboration with non-sex-specific terminal selector-type transcription factors, whereas th
273                        Manipulation of the N-terminal sequence affected the amount of Polbeta in the
274 cifically recognize a four-amino acid CAAX C-terminal sequence within their substrates.
275  its relative molecular mass of 7287 and NH2-terminal sequence, the protein was identified as a carbo
276 F region; however, a specific role for the C-terminal set of five ZFs remains to be elucidated.
277  uptake of tau species, whereas the distal C-terminal-specific antibody (Tau46) had little effect.
278                  Effects of N-terminal and C-terminal STIM1 antibodies on TRPC1-based SOCs and STIM1
279 ngs demonstrate that the occurrence of amino-terminal structural homogeneity may be associated with t
280 rase component, which contains a conserved C-terminal structural loop, preferentially binds to and fi
281 in is a fusion of two distinct modules: an N-terminal sugar phosphate isomerase-like domain associate
282                                       This C-terminal tail displays the binding site for partner prot
283 terminal region of the protein, and carboxyl-terminal tail identity both contribute to MLO activity d
284  by hyperphosphorylation of the inhibitory C-terminal tail of Lck.
285 ylation of several Ser/Thr residues in the N-terminal tail.
286 d to extend the Ser65 loop and shorten the C-terminal tail.
287 r phosphorylation, often at the receptor's C-terminal tail.
288  that contained only one tyrosine in their C-terminal tail.
289 tau uptake in an epitope-dependent manner: N-terminal (Tau13) and middomain (6C5 and HT7) antibodies
290  suppression of bone turnover (assessed by C-terminal telopeptide levels).
291 as shown a maximum rectification of 10.9% at terminals' temperatures of 375 and 530 K.
292 ASK1 kinase domain in conjunction with its N-terminal thioredoxin-binding domain, along with a centra
293 with high affinity through a palmitoylated N-terminal "thumb" and a disulfide-stabilized C-terminal "
294  expressing the target protein with SpyTag C-terminal to the SrtA recognition motif, it can be covale
295               We found different levels of C-terminal truncation, soluble protein aggregates, and gly
296 t to be transported to axons and presynaptic terminals where they signal via ErbB3/4 receptors in par
297 xocytosis from a subset of cortical synaptic terminals within the EC and in this way, constrain non-a
298 une evasion protein, E3, which contains an N-terminal Z-nucleic acid binding (Zalpha) domain that is
299 d for its conserved methylated DNA binding N-terminal ZF region; however, a specific role for the C-t
300 and a polarity reversal at the center of the terminal zone.

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