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1 vel of the 130-kDa form of beta(1) integrin (mature form).
2 nally (accelerating primiR processing to the mature form).
3 ilitates processing of precursor GILT to the mature form.
4 retion signal sequence that is absent in the mature form.
5 essing of precursor cytochrome b mRNA to the mature form.
6 a precursor form and 189 amino acids in the mature form.
7 site and the 3' terminal stem-loop into the mature form.
8 ctA) and posttranslationally modified to its mature form.
9 ro, resulting in a rapid conversion into the mature form.
10 of MT6-MMP converts proMMP-2 into mostly the mature form.
11 s responsible for cleaving pro-sigmaK to its mature form.
12 opeptides are cleaved to generate the 30-kDa mature form.
13 SREBP-1 is proteolytically processed to the mature form.
14 utation of Cys-200, which is retained in the mature form.
15 mal processing into the enzymatically active mature form.
16 as an integral membrane protein to yield its mature form.
17 the conversion of the IL-18 precursor to the mature form.
18 sis of pro-ICA512 and the degradation of its mature form.
19 necessary for the biosynthesis of the final mature form.
20 t is C-terminally processed into a 64-66-kDa mature form.
21 nverted the intermediate form of Yfh1 to the mature form.
22 e of IL-1alpha by calpain to the more active mature form.
23 lyhedral capsids but can be converted to the mature form.
24 d autocatalytic processing of zymogen to the mature form.
25 whereas bFGF-Short induced only the 17.8 kDa mature form.
26 of pro-a-factor, a mating pheromone, to its mature form.
27 he trans-Golgi network to yield a 35-residue mature form.
28 to process the 40-kDa molecule to the 28-kDa mature form.
29 d, purified, and cleaved by ICE into a 18-kD mature form.
30 tracellular matrix (ECM) proteins into their mature form.
31 and impairs conversion of precursors to the mature form.
32 he Cas system to process CRISPR RNA into its mature form.
33 n stems from their resistance to taking on a mature form.
34 F, that is cleaved to release its C-terminal mature form.
35 n post-Golgi compartments to yield a 3.7-kDa mature form.
36 rm that is distinct from the function of its mature form.
37 mitochondria faster than their corresponding mature forms.
38 zymogen activation and inhibits activity of mature forms.
39 tivating prochymase and protryptase to their mature forms.
40 L-33 through the generation of highly active mature forms.
41 e that processes microRNAs (miRNAs) to their mature forms.
42 a-glutamyl carboxylated, propeptide-cleaved (mature) form.
44 otein (66 kDa) and an N-terminally truncated mature form (55 kDa) have been described in human brain.
45 s, GEC1 expression enhanced the level of the mature form (55-kDa band) of FLAG-hKOR at 4, 8, and 22 h
47 cessed the 40-kDa mutant zymogen to a 28-kDa mature form, a result suggesting that the derivative pro
48 whereas gp120 preferentially recognized the mature form, a result that underscores a role for posttr
49 syncytial virus (RSV) is synthesized as two mature forms: a membrane-anchored form and a smaller sec
50 syncytial virus (RSV) is synthesized as two mature forms: a membrane-anchored form and a smaller sec
51 y activating p75NTR to mediate apoptosis and mature forms activating Trk receptors to promote surviva
53 t these basal body proteins are FliP (in its mature form after signal peptide cleavage) and FliR resp
54 riations and processing of pre-miRNAs to the mature form also may account for various differences in
56 y: (1) processing of full-length SUMO to its mature form and (2) deconjugation of SUMO from targeted
57 o a reproducible ratio of two sequences, the mature form and a form starting at Ala3, by adjustment o
59 ity converting the proNEDD8 precursor to its mature form and an isopeptidase activity deconjugating N
60 fic protease NEDP1 processes preNEDD8 to its mature form and deconjugates NEDD8 from substrates such
61 cifically cleaves precursor TNF-alpha to its mature form and is involved in the ectodomain shedding o
62 less stable in the matrix space than is the mature form and provides an explanation for why the lead
63 in flexibility between the germ line and the mature form and the differences in structure between TSA
64 d in Escherichia coli BL21(DE3) cells in its mature form and with the R. sphaeroides or E. coli N-ter
65 n endonuclease that trims pre-rRNAs to their mature forms and a sentinel that partners with RnaseR to
67 ions of IL-1 alpha, IL-1 beta (precursor and mature forms), and IL-1 receptor antagonist (IL-1Ra) wer
68 ng the proteolytic processing of SUMO to its mature form, and negatively, by catalyzing SUMO deconjug
69 ignal peptide, a molecular mass of 22 kDa in mature form, and the highest homology to cardiotrophin-1
71 ired for efficient processing of AtlA to its mature form, and treatment of the thmA mutant strain wit
74 ent processing of the miRNA precursor to its mature form as well as diminished capacity to regulate t
75 Rescue of the defect, i.e., increase in the mature form at the bile canaliculi, was obtained by cell
77 -fibers in early prometaphase to their fully matured form at metaphase, just before anaphase onset.
78 Pichia pastoris, was processed to its active mature form autocatalytically or by incubation with peps
79 ing along the axon and the expression of the mature form (BFA insensitive, P/Q type Ca2+ channel medi
80 ses, subtilisin is kinetically stable in the mature form but unable to fold without assistance from i
82 ecause pro-IL-16 is cleaved to its bioactive mature form by caspase-3, and caspase-3 is also the pivo
83 imported by mitochondria and processed to a mature form by cleavage of the NH2-terminal mitochondria
84 pro-IL-1beta, and following cleavage to its mature form by IFN-gamma-activated ICE, IL-1 then initia
85 olecule and proteolytically processed to the mature form by members of the family of the proprotein c
86 ce the isomerization of the Cdk into a fully mature form by promoting the exposure of the T-loop for
88 f prointerleukin-1beta (pro-IL-1beta) to its mature form by the cysteine protease caspase-1 are not w
89 ong to Type II LTP characterized under their mature forms by a molecular weight of around 7.3 kDa, a
90 ociates with their precursors as well as the mature forms by binding to regions in addition to the IA
92 ismatch) lead to increased expression of the mature form compared to the unedited version in cell cul
93 s a progression from initial attachment to a mature form composed of pillar-like multicellular struct
94 led by precursor Gag (PrGag) proteins; and a mature form, composed of proteins processed from PrGag.
96 umor suppressor gene that, by utilizing both mature forms, coordinately controls the key cancer hallm
98 inflammatory responses were higher with the mature form, demonstrating that the cysteine protease ac
99 interfering RNA precursors into their short mature forms, enabling them to regulate gene expression.
104 om their initial unstructured state to their mature form has long been known to be promoted by other
105 full-length human IL-33(1-270) and generate mature forms IL-33(95-270), IL-33(99-270), and IL-33(109
106 The Y212C precursor was activated to its mature form in a manner similar to that of the wild-type
109 A portion of the IL-1beta is shed in its mature form in membrane microvesicles, and induces adhes
113 Defective processing of let-7a precursors to mature forms, in part, explained the discrepancies obser
115 S.cerevisiae, the mitochondrially generated mature form is separated by gel filtration into monomer
117 process from the pro-silicatein state to the mature form is the crucial step during which silicatein
118 eltaF508 has substantial accumulation in its mature form, leading to higher level of processing at th
119 lated in both heterologous systems is in its mature form, localizes in the chloroplast thylakoid memb
120 orted into chloroplasts and processed to the mature form located in the thylakoid lumen, as shown by
121 Failure of SREBP-1 to be processed to the mature form <18 days postpartum correlates with low hepa
123 recursors that are poorly converted to their mature forms may be polyadenylated and subsequently degr
124 n normal samples (P = 3.52E-05), whereas the mature form modified for secretion (sCLU) was not signif
125 ng protein 1 (SREBP1), when presented in its mature form (mSREBP1), enhances lipogenesis by increasin
129 genesis and cancer, but the structure of the mature form of ADAM12 is not known, and its localization
131 rsican at the Glu(441)-Ala(442) bond and the mature form of ADAMTS-4 was detected by Western analysis
132 k regulatory mechanism that functions on the mature form of ALAS-1 protein through the activity of a
137 analyses showed that exercise increased the mature form of BDNF, synapsin I and cyclic-AMP response-
142 hat involves the extracellular region of the mature form of cell surface ADAM17 and not its intracell
144 Here, we report the crystal structure of the mature form of Der f 1, which was isolated from its natu
157 IK(IR) and the development of IK(Ca) and the mature form of ICa are all prevented by transcription bl
172 asts (MEFs) produce primarily the processed, mature form of OGN, MEFs homozygous null for genes encod
174 w PAP accesses ribosomes and showed that the mature form of PAP is targeted to the cytosol from the e
177 rometry analysis, we show that the in planta mature form of proGrCLE1, a multidomain CLE effector sec
182 g protein 1c), nor the nuclear levels of the mature form of SREBP-1 protein were elevated in apoB/BAT
185 shows that inordinately slow folding of the mature form of subtilisin results from the accrued effec
186 er, the addition of Cat B generated a 25-kDa mature form of TGF-beta1 in Cat B siRNA-pretreated lysat
189 e various complexes that they form, only the mature form of the complex was detectable at the infecte
192 583 amino acid residues corresponding to the mature form of the enzyme, whereas the monomer consists
194 ell signalling precedes the formation of the mature form of the immunological synapse, but that full
195 ned for proteins differentially bound to the mature form of the miR-1 or miR-133 miRNA families.
197 NLRP3 inflammasome-mediated secretion of the mature form of the proinflammatory cytokine IL-1beta.
208 aled that inhibition of DGK reduced only the mature form of tyrosinase, and the decrease of tyrosinas
209 The capacity of an adenovirus encoding the mature form of vascular endothelial growth factor (VEGF)
215 risingly, the stability of both immature and mature forms of APP is dramatically elevated in cells ex
216 The N-terminal amino acid sequences of the mature forms of both UspA1 and UspA2 from strain O35E we
218 ed, pulse-chase analysis suggests that these mature forms of CatL are degraded by endocytic proteases
219 The 2D7 antibody recognized immature and mature forms of CCR5 equally, whereas gp120 preferential
222 n to the previously identified precursor and mature forms of ExoR (designated ExoR(p) and ExoR(m), re
224 mutants 277, 291, and 348 bound gI, produced mature forms of gE that reached the cell surface, and we
225 rminal sequencing revealed that the cellular mature forms of hADAM19 started at (204)EDLNSMK, demonst
226 ileostomy fluid contained both precursor and mature forms of HD-5, with the majority present in a com
228 ly active form of MIF co-immunopurified with mature forms of HLA DP2/15, and a peptide derived from t
229 tein amounts of IL-1alpha, the precursor and mature forms of IL-1beta, IL-1 receptor antagonist (IL-1
230 d mast cells (chymase and tryptase) generate mature forms of IL-33 with potent activity on ILC2s.
231 provide concrete evidence that there are two mature forms of mammalian MRPL12 that are generated by a
232 wn reduced the expression of the primary and mature forms of miR-205 and the miR-205 "host" gene (miR
237 ng confirmed that the predicted immature and mature forms of Psd2(C2Delta)p, Psd2(GRDelta)p, and wild
240 s leading to five mature forms of S6 and two mature forms of S10, C-terminal and/or internal modifica
241 f S9, N-terminal processings leading to five mature forms of S6 and two mature forms of S10, C-termin
242 f BRUCE to antagonize both the precursor and mature forms of Smac and caspase-9 is an important mecha
246 rgies of hapten binding to the germ line and mature forms of the 48G7 antibody Fab fragments by apply
247 The striking thermodynamic stability of mature forms of the ALS mutant SOD1 (Tm>70 degrees C) is
248 dependent signaling through intermediate and mature forms of the BCR has been postulated to regulate
250 -III and processes precursors to produce the mature forms of the cross-linking enzyme prolysyl oxidas
253 uctural biology of both the immature and the mature forms of the HIV capsid have made it possible to
254 y, stenotic lesions, but not AAAs, contained mature forms of the interferon-gamma-inducing cytokines
256 ength zymogen and a truncated zymogen, three mature forms of the SprE proteinase, Leu1-Ala237, Ser-1-
257 depletion of the cells or by coexpression of mature forms of the SRE-binding proteins (SREBP) 1a and
261 found that TACI interacts with the cleaved, mature forms of TLR7 and TLR9 and plays an important rol
264 he conversion of an iron-only precursor to a matured form of the M cluster before delivering the latt
266 ssays showed that the precursor, but not the mature form, of AtFKBP13 interacted with Rieske protein,
271 zyme that processes PACAP's precursor to the mature form, peptidylglycine alpha-amidating monooxygena
274 f growth factors and ECM proteins into their mature forms, resulting in TM stiffness and resistance t
275 are reduced 35-65% by cleavages making their mature form similar (26-31 kDa), while their precursors
276 : an abundant TMG-capped 124-nucleotide (nt) mature form (snR13F) and two less abundant RNAs, includi
277 in precursor to the intermediate but not the mature form, suggesting that a different peptidase might
278 d the conversion of TPP I proenzyme into the mature form, suggesting that this process takes place in
279 erived by alternative splicing of RNA into a mature form that either includes or excludes exon 4.
281 N-methyl-D-aspartate receptors (NMDARs) with mature forms that differ in subunit composition, electro
282 esults in initiation of fibrillation of more mature forms that have an intact Cys-57-Cys-146 disulfid
284 in polypeptides, not corresponding to pro or mature forms, that increased in accumulation in betaVPE
285 ess than 7 months of age, including the more mature forms; the visual status of these patients may be
286 Defining the constituent elements of its mature form, their organization within the particle, and
287 proMMP-9 can be irreversibly converted to a mature form through cleavage of the N-terminal propeptid
289 ized as inactive zymogens and convert to the mature form upon activation by specific enzymes, often a
290 suggest that the complex is processed to the mature form via the Golgi network prior to secretion.
291 leavage of intracellular pro-IL-1beta to the mature form was found to occur independently of NLRP3, i
292 g of human host cell factor 1 (HCF-1) to its mature form was recently shown, unexpectedly, to occur i
293 wed that SpeB expression and processing to a mature form was unaffected by either deletion mutation.
295 n L (CatL) and CatB into their fully active, mature forms was reduced in pancreatitis, as were their
297 rate constants (ke) of the intermediate and mature forms were approximately 3 times those of the wil
299 the endoplasmic reticulum (ER), whereas the mature forms were present in non-ER fractions in culture
300 pol gammaB proteins were expressed in their mature forms, without their apparent mitochondrial local
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