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1                                              TTC documents dating from 1989 to 2004/5 were retrieved
2                                              TTC influenced survival outcomes in the overall study co
3                                              TTC stain was used to mark infarct areas, which were siz
4                                             (TTC)n repeat in both expansions and contractions drastic
5                                              TTC-derived infarct volumes were not significantly diffe
6                                              TTCs did not, however, make SLT investments until 2002,
7                                              TTCs' efforts to undermine the FCTC were comprehensive,
8 les were from 11-100, 101-1,000, and > 1,000 TTC/100 mL, respectively compared to < 1 TTC/100 mL.
9 000 TTC/100 mL, respectively compared to < 1 TTC/100 mL.
10 effectively bound and internalized the IGF-1-TTC in vitro.
11                             Similarly, IGF-1-TTC injected into skeletal muscles was taken up and retr
12                          Three monthly IGF-1-TTC injections into muscles of ageing mice did not incre
13                                        IGF-1-TTC retains IGF-1 activity as indicated by [(3)H]thymidi
14 complex in muscle fibres injected with IGF-1-TTC, compared to the other groups, suggesting preservati
15                                        IGF-1:TTC exhibited IGF-1 and TTC activity in vitro; it increa
16 ular- or intrathecal administration of IGF-1:TTC had no significant effect on disease progression or
17 tein resulted in substantial levels of IGF-1:TTC in spinal cord tissue extracts.
18                                        IGF-1:TTC may prove to be neuroprotective in other animal mode
19              Like rhIGF-1, infusion of IGF-1:TTC reduced levels of IGF-1 receptor immunoreactivity in
20 mbar spinal cords of mice infused with IGF-1:TTC were estimated to be approximately 500-fold higher t
21 tanus toxin fragment C fusion protein (IGF-1:TTC) as a secreted product from insect cells.
22  diarrhea with contamination levels below 11 TTC/100 mL, either in adults or children.
23  that HCN3(+) cells coexpress T-type Ca(2+) (TTC) channels and that TTC channel inhibition with R(-)e
24 rved for the destabilization of the (GAA)2T4(TTC)2T4(CTT)2 triplex to the corresponding Watson-Crick
25 (3-)) or 5,10,15-tris(4-tolyl)corrolate (H(3)TTC(3-))) leads to NO labilization.
26 ropean mutational spectrum, 5'-TCC-3' --> 5'-TTC-3' is known to be the most common somatic mutation p
27 enriched for the transition 5'-TCC-3' --> 5'-TTC-3'.
28 d recognises the symmetrical sequence GAAN(7)TTC.
29       Our results demonstrate that ShcV is a TTC for the HopPtoV effector.
30                                          All TTCs have now invested in snus (and recently in pure nic
31                IGF-1:TTC exhibited IGF-1 and TTC activity in vitro; it increased levels of immunoreac
32   The oligonucleotides TA(C)TAT, AATTTT, and TTC are located approximately (+/- 1 nucleotide) 29, 19,
33 ermeability of the BBB to Evans blue dye and TTC as detected by augmented concentrations of these sub
34 eks the extent of extracellular enhanced and TTC regions were smaller (13.2 +/- 1.4% and 12.0 +/- 1.5
35 rct size determined by (99m)Tc-glucarate and TTC staining (r = 0.96; slope = 0.87).
36 icity in 2 distinct muscle types, as HCN and TTC channels also mediate cardiac pacemaker activity.
37 R imaging (6.6% +/- 0.5 of the LV mass), and TTC staining (7.0% +/- 0.6 of the LV mass).
38        Hemodynamic values were recorded, and TTC staining was used to assess necrosis.
39 nd the second (B), based around the RILs and TTC families, involved marker-based QTL analysis.From (A
40 in 200 mM sodium (pH 5.0) repeats of TCC and TTC have half-lives of approximately 20 min, while the t
41 istochemistry demonstrated that both TTC and TTC-SOD-1 were distributed in a punctate perineuronal an
42 entrality of evidence to debates over SP and TTCs' history of denying harms and manufacturing uncerta
43 7-Anthraquinone stabilizes (TC)n (CCT)n and (TTC)n, although it has the greatest effect on the latter
44 iplexes that are formed at (TC)n (CCT)n and (TTC)n.
45 t analyses with anti-SMN, anti-DTx, and anti-TTC antibodies.
46 unolabeling of SDT-treated neurons with anti-TTC and anti-SMN antibodies showed staining restricted t
47                                           At TTC analysis, seven dogs had evidence of myocardial infa
48 t was similar to that of infarcted tissue at TTC staining (mean, 13.6% +/- 6.0; range, 7.8%-30.9%).
49                                          ATC/TTC haplotype cells significantly increased transmigrati
50           When stimulated with Poly I:C, ATC/TTC haplotype, cells significantly up-regulated the IL-8
51 a provides evidence that carriage of the ATC/TTC haplotype in itself may increase the influx of neutr
52                          To test whether ATC/TTC haplotype is functional, we used a trans-well assay
53         We evaluated the association between TTC and survival according to breast cancer subtype and
54      We investigated the association between TTC in drinking water and diarrhea using data from seven
55  intramuscular injection, and exhibited both TTC- and IGF-1 activity in the CNS following intrathecal
56  Immunohistochemistry demonstrated that both TTC and TTC-SOD-1 were distributed in a punctate perineu
57 +/-1.8% of LV mass by MRI and 27.5+/-1.7% by TTC (P=NS).
58 rons in amounts similar to those achieved by TTC.
59 nd correlated with infarct volume defined by TTC staining at 24 h after MCAO.
60 ld exist naturally if Phe-508 was encoded by TTC, has wild type-like mRNA structure, and enhanced exp
61        Cerebral infarction was visualized by TTC staining on day 3 post-surgery.
62 or neurone loss, a tetanus toxin fragment-C (TTC) fusion protein was created to target IGF-1 to motor
63  of tetanus toxin (tetanus toxin fragment C, TTC) has been used as a vector to enhance delivery of po
64 exogenous protein (tetanus toxin fragment C; TTC), and a viral vector (recombinant adeno-associated v
65  alleles of HLA-C and CDSN (HLA-Cw6 and CDSN*TTC) were genotyped in 678 families with early-onset pso
66 aplotypes retaining HLA-Cw6 but lacking CDSN*TTC were significantly associated with psoriasis, wherea
67 oriasis, whereas recombinants retaining CDSN*TTC but lacking HLA-Cw6 were not associated, despite goo
68  531 (TCG-->TTG or TTC), and 526 (CAC-->CGC, TTC, AAC, or CAA) demonstrated an association with highe
69 tion next to a candidate type III chaperone (TTC) gene, shcV, and within a pathogenicity island in th
70 cessory proteins called type III chaperones (TTCs) to be secreted via the TTSS.
71 time to initiation of adjuvant chemotherapy (TTC) after definitive surgery is unknown.
72 on via 2,3,5-triphenyl tetrazolium chloride (TTC) staining.
73 sed by 2,3,5-triphenyl tetrazolium chloride (TTC).
74 d using 2,3,5-triphenyltetrazolium chloride (TTC) or hematoxylin and eosin (H&E) stains.
75 assessed with triphenyltetrazolium chloride (TTC) staining and a transmission electron microscope (TE
76  with 2, 3, 5-triphenyltetrazolium chloride (TTC) staining for stroke volume measurement.
77               Triphenyltetrazolium chloride (TTC) staining indicated that pretreatment with MANF sign
78 determined by triphenyltetrazolium chloride (TTC) staining versus (99m)Tc-glucarate imaging ex vivo.
79 ized by 2,3,5-triphenyltetrazolium chloride (TTC) staining, hematoxylin-eosin (H&E) staining, the ter
80 ents by 2,3,5-triphenyltetrazolium chloride (TTC) staining.
81 analysis, and triphenyltetrazolium chloride (TTC) staining.
82 staining with triphenyltetrazolium chloride (TTC) was used to confirm and quantify heterogeneous micr
83               Triphenyltetrazolium chloride (TTC) was used to delineate infarctions at postmortem.
84 lood flow and triphenyltetrazolium chloride (TTC)-stained tissue samples for infarct assessment by us
85  with 2, 3, 5-triphenyltetrazolium chloride (TTC).
86 arly as measured by thermotolerant coliform (TTC) bacteria, a WHO-approved indicator of drinking wate
87 scherichia coli or thermotolerant coliforms (TTC) were included provided they associated results with
88 er was assayed for thermotolerant coliforms (TTC), an indicator of faecal contamination.
89 isease-free survival, and time to colostomy (TTC) with pretreatment and treatment variables.
90  opposed by transnational tobacco companies (TTCs) whose responses to the UK government's public cons
91 r examines transnational tobacco companies' (TTCs') efforts to influence policy there, paying particu
92 ms to explore transnational tobacco company (TTC) interests in SLT and pure nicotine in Europe from t
93 sing the threshold of toxicological concern (TTC) approach.
94 rm daily threshold of toxicological concern (TTC) of 1.5 mug/g and the potential for quantitative ana
95 s (SML) and threshold toxicological concern (TTC) recommended values according to the Cramer classifi
96 CT)n, but stabilizes triplexes that contain (TTC)n.
97 iated by transnational tobacco corporations (TTCs) to try to undermine the proposed convention.
98 inbred lines (RILs) and a triple test cross (TTC), the latter produced by crossing the RILs to Col, L
99 n repeat expansion during replication of a d(TTC)n repeat template.
100                                      Delayed TTC was particularly detrimental among patients with tri
101  the first dose of chemotherapy, and delayed TTC was defined as 91 or more days from surgery to the f
102 FS) estimates were similar for the different TTC categories.
103 C linked to the enzyme superoxide dismutase (TTC-SOD-1).
104 HopO1-1 secretion and translocation and each TTC was able to bind the other's cognate effectors in ye
105 highly profitable) cigarettes while ensuring TTCs' long-term future should cigarette sales decline fu
106 e tumor diameter independently predicted for TTC (P = .008).
107 ft ventricle was sectioned into 4 slices for TTC staining.
108 bilize the (TTC)6.(GAA)6 composite function (TTC)6 triplex.
109 analyses of (TTC)6.(GAA)6 composite function(TTC)6 triplex detected ions due to both triplex and sing
110 and formation of triplex DNA at expanded GAA TTC repeats have been shown to regulate the FXN gene sil
111  of heterochromatin at the long expanded GAA TTC repeats, which is enriched in hypoacetylated histone
112 to the pUC control DNA) and that the GAA GAA TTC triplex further lowers the nucleosome assembly effic
113 ylation on the GAA TTC duplex or the GAA GAA TTC triplex has been measured in vitro.
114 ments for the GAA TTC duplex and the GAA GAA TTC triplex, and on the effect of histone acetylation, t
115 ved from the human FXN gene, and the GAA GAA TTC triplex, were examined for their ability to assemble
116 ng the formation of nucleosome arrays on GAA TTC-containing plasmids, the triplex structure was shown
117                           In this study, GAA TTC repeating DNAs derived from the human FXN gene, and
118 irst direct binding measurements for the GAA TTC duplex and the GAA GAA TTC triplex, and on the effec
119 onstitution assays demonstrated that the GAA TTC duplex excludes nucleosomes (53% decrease compared t
120 the effect of histone acetylation on the GAA TTC duplex or the GAA GAA TTC triplex has been measured
121                         Expansion of a GAA . TTC repeat in the first intron of the frataxin (FXN) gen
122 molecular model of FRDA by inserting 560 GAA*TTC repeats into an intron of a GFP reporter minigene.
123 s and number of tracts (one or two) of a GAA*TTC repeat in Escherichia coli to evaluate the in vivo r
124 of FRDA mutations involve expansion of a GAA*TTC-repeat tract in intron 1, which leads to an FXN mRNA
125 eletions as observed for the CTG*CAG and GAA*TTC repeats.
126 prior work demonstrated that CTG*CAG and GAA*TTC triplet repeats (responsible for DM1 and Friedreich'
127        We previously showed that cloned (GAA*TTC)n sequences replicated in Escherichia coli are more
128                             The expanded GAA*TTC repeat sequence associated with Friedreich's ataxia
129         Most FRDA patients have expanded GAA*TTC repeats (up to 1700 triplets), which inhibit the tra
130 We examined instability of the expanded (GAA*TTC)(n) sequence in mammalian cells by analyzing individ
131 ion in Friedreich ataxia is an expanded (GAA*TTC)n sequence, which is highly unstable in human somati
132 edreich ataxia is caused by an expanded (GAA*TTC)n sequence, which is unstable during intergeneration
133                                 The GFP_(GAA*TTC)(560) minigene recapitulates the molecular hallmarks
134 ion, increase the expression of the GFP_(GAA*TTC)(560) reporter.
135 quence unaffected and (iii) heterozygous GAA*TTC expansion carriers with approximately 50% decrease o
136  plasmids by the association of two long GAA*TTC tracts at lengths that are found in the sequence of
137 ia (FRDA) is caused by hyperexpansion of GAA*TTC repeats located in the first intron of the FXN gene,
138                          Replication of (GAA*TTC)n sequences (9-105 triplets) in plasmids propagated
139 othesized that genetic stability of the (GAA*TTC)n sequence may require efficient RecA-dependent reco
140 eplication is known to occur within the (GAA*TTC)n sequence when GAA is the lagging strand template,
141 ect of DSB repair on instability of the (GAA*TTC)n sequence.
142 echanism for genetic instability of the (GAA*TTC)n sequence.
143 echanism for genetic instability of the (GAA*TTC)n sequence.
144 ents is the unstable hyperexpansion of a GAA.TTC triplet repeat in the first intron of the frataxin g
145 as evaluated following replication of a (GAA.TTC)115 sequence in transfected COS1 cells under the con
146 eating tracts of CTG.CAG, CCTG.CAGG, and GAA.TTC are integral to the etiology of myotonic dystrophy t
147          The capacity of (CTG.CAG)n and (GAA.TTC)n repeat tracts in plasmids to induce mutations in D
148 us, intramolecular recombination between GAA.TTC tracts and GAAGGA.TCCTTC repeats also occurred with
149 linked pyrrole-imidazole polyamides bind GAA.TTC tracts with high affinity and disrupt the intramolec
150 diseases caused by expansion of CTG.CAG, GAA.TTC, or CGG.CCG repeat tracts.
151                                 Expanded GAA.TTC repeats result in decreased transcription and reduce
152  the Friedreich's ataxia (FRDA) expanded GAA.TTC sequence, which forms sticky DNA, are prone to form
153 edreich ataxia is caused by an expanded (GAA.TTC)n sequence in intron 1 of the FXN gene.
154  yeast and reporter construct models for GAA.TTC triplet-repeat expansion have been reported, studies
155      These studies suggest that in FRDA, GAA.TTC triplet-repeat instability occurs in embryonic cells
156          Sticky DNA is a single long GAA.GAA.TTC triplex formed in plasmids harboring a pair of long
157  locus-specific differences for genomic (GAA.TTC)n sequences.
158                                 However, GAA.TTC triplet repeats were stable in FRDA fibroblasts and
159 shRNA silencing of MSH2 and MSH6 impeded GAA.TTC triplet-repeat expansion.
160 er characterized the role of MutSbeta in GAA.TTC expansion using a functional assay in primary FRDA p
161      Thus, despite its essential role in GAA.TTC expansion, MSH2 is not an attractive therapeutic tar
162 RNA.DNA hybrids have a potential role in GAA.TTC tract instability and in the mechanism underlying re
163 opic expression of MSH2 and MSH3 induced GAA.TTC repeat expansion in the native FXN gene.
164 d ataxia caused primarily by an intronic GAA.TTC triplet repeat expansion in the frataxin (FXN) gene.
165         During propagation of the iPSCs, GAA.TTC triplet repeats expanded at a rate of about two GAA.
166 med in plasmids harboring a pair of long GAA.TTC repeat tracts in the direct repeat orientation.
167   The recombinational properties of long GAA.TTC repeating sequences were analyzed in Escherichia col
168 DNA conformation of genes harboring long GAA.TTC repeats or by chromatin opening.
169 e sticky-DNA conformation formed by long GAA.TTC repeats.
170 c property of transcription through long GAA.TTC tracts.
171 ity on the genetic instabilities of long GAA.TTC, CGG.CCG, and CTG.CAG repeat sequences was studied i
172                           In this model, GAA.TTC repeats expand incrementally and continuously.
173 rapeutic target to slow the expansion of GAA.TTC repeats in the future.
174                Interestingly, tracts of (GAA.TTC)(n) (where n = 176 or 80) readily formed sticky DNA
175 ard cross-linking studies on a family of GAA.TTC-containing plasmids showed the presence of sticky DN
176 es extensive RNA.DNA hybrid formation on GAA.TTC templates in bacteria as well as in defined transcri
177 mall pool PCR analysis showed that pure (GAA.TTC)44+ sequences at the FXN locus are unstable in somat
178 fied three other genomic loci with pure (GAA.TTC)44+ sequences.
179  DNAs containing a pair of direct repeat GAA.TTC sequences.
180 expansion of the triplet-repeat sequence GAA.TTC within the first intron of the FXN gene.
181 pansions of the triplet-repeat sequence (GAA.TTC) cause transcriptional repression of the Frataxin ge
182                  DNAs harboring a single GAA.TTC repeat are unable to form this type of triplex confo
183 n smaller, so-called 'pre-mutation' size GAA.TTC repeats, that do not cause disease, but are prone to
184  knockdown of either MSH2 or MSH3 slowed GAA.TTC expansion in our system.
185 ic pyrrole-imidazole polyamide targeting GAA.TTC triplet-repeat DNA partially blocked repeat expansio
186 AG.CTG repeat expansion, its role in the GAA.TTC expansion of Friedreich ataxia (FRDA) is less clear.
187 asurements are as follows: length of the GAA.TTC insert; the extent of periodic interruptions within
188 sis is that structures formed within the GAA.TTC repeat during transcription attract DNA repair enzym
189             Increasing the length of the GAA.TTC repeats decreased the intramolecular recombination f
190 ated the expansions and deletions of the GAA.TTC repeats.
191 rrests in the promoter distal end of the GAA.TTC tract and an extensive RNA.DNA hybrid is tightly lin
192 ve correlation between the length of the GAA.TTC tracts and the frequency of intramolecular recombina
193  was found between the propensity of the GAA.TTC tracts to adopt the sticky DNA conformation and the
194 e frequency of recombination between the GAA.TTC tracts was as much as 15 times higher than the non-r
195 that the recombination properties of the GAA.TTC tracts were unique, compared with CTG.CAG repeats, b
196 tudy the mechanism of instability of the GAA.TTC triplet repeats in the human genome.
197  essentially inert, as observed for the (GAA.TTC)176-containing plasmid.
198 tion of the SV40 origin relative to the (GAA.TTC)n sequence, we noted either no instability, predomin
199  repeats expanded at a rate of about two GAA.TTC triplet repeats/replication.
200                 Expansion of an unstable GAA.TTC repeat in the first intron of the FXN gene causes Fr
201 ee of frataxin reduction correlates with GAA.TTC tract length, but the mechanism of reduction remains
202                       The formation of a GAA/TTC DNA triplex has been implicated in Friedreich's atax
203 the discovery of agents that destabilize GAA/TTC triplexes and as general methods for the characteriz
204 del system, we demonstrate that expanded GAA/TTC repeats represent a threat to eukaryotic genome inte
205             Expansion of triplex-forming GAA/TTC repeats in the first intron of FXN gene results in F
206                Triplex structure-forming GAA/TTC repeats pose a dual threat to the eukaryotic genome
207                   In model systems, long GAA/TTC tracts also act as chromosomal fragile sites that ca
208                   The destabilization of GAA/TTC DNA triplexes either by pH or by binding to appropri
209 chanisms that regulate the metabolism of GAA/TTC repeats are poorly understood.
210 ms can mediate detrimental metabolism of GAA/TTC tracts in human cells.
211         We suggest that the mechanism of GAA/TTC-induced chromosomal aberrations defined in yeast can
212  there are a number of other polymorphic GAA/TTC loci in the human genome where the size variations t
213                  Like GDNF, addition of GDNF:TTC to culture media of neuroblastoma cells expressing G
214 intramuscular injection, mice receiving GDNF:TTC revealed intense GDNF immunostaining associated with
215 esent in the purified conjugate sample, GDNF:TTC, had a molecular weight of approximately 80 kDa as d
216                                    That GDNF:TTC provided neuroprotection of axotomized motor neurons
217 xamination of one signal, an increased TCC--&gt;TTC mutation rate in Europeans, indicates a burst of mut
218 ctively, these data demonstrate that HCN3(+)/TTC(+) cells are the pacemakers that set the origin and
219 C3000; these operons encode three homologous TTCs, ShcO1, ShcS1, and ShcS2.
220 ion provides insights into the nature of how TTCs function.
221            Factors associated with delays in TTC included low socioeconomic status, breast reconstruc
222 iarrhea increased for each log10 increase in TTC/100 mL by 18% (95% CI: 11, 26%) for children < 5 yea
223 ave failed, and little evidence was found in TTCs' corporate materials that snus is central to their
224 gs with contemporary documentation including TTC investor presentations.
225 uorescence microscopy revealed that injected TTC was not retained solely in a restricted deposit alon
226  (sum of areas with lacking and intermediate TTC staining) was similar among all six groups.
227 distribution was confirmed using HRP-labeled TTC with electron microscopy along with localization wit
228 ntitative fluorimetry, we found that labeled TTC showed vastly superior retention within brain tissue
229 Neurological evaluation and ischemic lesion (TTC stain) were assessed at 24 hours of reperfusion.
230 bgroup analysis according to subtype, longer TTC caused patients with triple-negative breast cancer t
231                                      Maximum TTC and TBC were up to 25.5 and 16.6 mug/g (fresh weight
232 ion households than controls (geometric mean TTC count of 50 [95% CI 44-57] per 100 ml compared to 12
233 a from available field studies that measured TTC levels in household-drinking water and reported prev
234                    Expansions of a (GAA)(n)/(TTC)(n) repeat tract during its transmission from parent
235  in the Friedreich ataxia-associated (GAA)n*(TTC)n repeats from the FRDA gene that were cloned with f
236             To follow the effects of (GAA)n*(TTC)n repeats on gene expression, we have chosen E. coli
237                                      (GAA)n*(TTC)n repeats were cloned into bacterial plasmids in bot
238 sm seems less likely for the AT-rich (GAA)n*(TTC)n repeats.
239 , and were decreased by cholesterol; neutral TTC partitioned into membranes more strongly than the pr
240 by investing in snus, and recently nicotine, TTCs have eliminated competition between cigarettes and
241                     Instead, a 3-nucleotide (TTC) deletion in the MLH1 3'-UTR was found in the patien
242 nd tax structures are an important aspect of TTC competitiveness.
243 of a recombinant fusion protein comprised of TTC linked to the enzyme superoxide dismutase (TTC-SOD-1
244 pport for health-based targets for levels of TTC in drinking water and for interventions to improve d
245 d risk of diarrhea with increasing levels of TTC in drinking water.
246  resulted in a substantial overestimation of TTC-defined infarct volume and a lower inter-observer re
247  nodal status and sex were not predictive of TTC.
248        In contrast, triplets with repeats of TTC, TCC and CTCT melt at 67, 72 and 76 degrees C, respe
249 ch to examine the conceptual significance of TTC critiques.
250                             The existence of TTCs that can bind to dissimilar effectors and that can
251          The mass spectrometric analyses of (TTC)6.(GAA)6 composite function(TTC)6 triplex detected i
252              Volumetric calculation based on TTC-derived infarct also correlated significantly strong
253 nfarct size of the left ventricle (% IAR) on TTC staining was smaller in IR30 (49.2 +/- 4.3) than in
254 depicted with MTET imaging with that seen on TTC-stained tissue.
255 9% +/- 3.9% infarct in the left ventricle on TTC staining.
256  There is clear evidence of past and ongoing TTC influence over tobacco advertising and excise policy
257 ged controls injected with saline, IGF-1, or TTC.
258  tetanus toxin (tetanus toxin fragment C, or TTC).
259 in codons 523 (GGG-->GCG), 531 (TCG-->TTG or TTC), and 526 (CAC-->CGC, TTC, AAC, or CAA) demonstrated
260                                    A Phe377 (TTC(1130-1132)) deletion in exon 9 of the pyrophosphate
261 ependent pretreatment variable that predicts TTC and 5-year colostomy rate in patients with anal carc
262  two spectrally distinct isomers, presumably TTC and TTT cis-trans isomers, for the open-ring merocya
263               We hypothesized that prolonged TTC would be associated with adverse outcomes.
264 ly, positioning of normal- and carrier-size (TTC)n repeats into the sense strand for transcription le
265 from short priming sequences such as 3'-TCC, TTC, and TTT, and the consensus sequence is 3'-Pu(Py)2-3
266 ence intensity of membrane-bound tetracaine (TTC) on solution pH.
267 he complexation of Fe(II) with tetracycline (TTC), oxytetracycline (OTC), or chlorotetracycline (CTC)
268 xpress T-type Ca(2+) (TTC) channels and that TTC channel inhibition with R(-)efonidipine or NNC55-039
269                             We conclude that TTC may be a useful vector to enhance neuronal delivery
270                  These results indicate that TTC can serve as a non-viral vehicle to substantially im
271 came more affordable post-accession and that TTCs have taken advantage of low excise duties by raisin
272                  Interview data suggest that TTCs enjoy high-level political support and continue to
273 ating the global application of tactics that TTCs have previously been found to have employed nationa
274 in edible organs at concentrations above the TTC value should be categorized as contaminants of emerg
275                                 Although the TTC technique was negative for infarct, histopathologica
276 ot be useful for SMA therapy, the use of the TTC:DTx fusion construct to deliver other passenger prot
277                       Our data show that the TTC value of lamotrigine can be reached for a child at a
278                                          The TTCs' claim that SP will not lead to public health benef
279 ting ligand acridine orange destabilize the (TTC)6.(GAA)6 composite function (TTC)6 triplex.
280                                       Third, TTCs engaged in 'evidential landscaping', promoting a pa
281 mes were estimated and compared according to TTC and by BC subtype.
282 e categorized into three groups according to TTC: </= 30, 31 to 60, and >/= 61 days.
283              A single point mutation (TCC to TTC; Ser to Phe) was identified in Lec23 Gcs1 cDNA and g
284 Tx) followed by fragment C of tetanus toxin (TTC).
285 cent to areas of 2,3,5-triphenyltetrazolium (TTC)-negative tissue, normally associated with infarcted
286  24 hour 2,3,5-triphenyltetrazoliumchloride (TTC)-derived infarct volumes.
287  third strands consisting of repeats of TTT, TTC, TCC and TCTC.
288     We purposively selected and analysed two TTC submissions using a verification-oriented cross-docu
289 cted for infarct size (IS) measurement using TTC staining.
290 rm the haplotype-I (Hap-I), whereas variants TTC constitute Hap-II.
291  MTET infarct volume correlated with ex vivo TTC analysis data (y = 1.01x + 0.00, R = 0.98, standard
292 ge at diagnosis was 53 years, and median was TTC was 46 days.
293                         Unlike the case with TTC, however, immunolabeling of SDT-treated neurons with
294                   Analogous to the case with TTC, intrathecal infusion of the fusion protein resulted
295 ately assess infarct size when compared with TTC staining.
296 ution produced an excellent correlation with TTC-defined infarct volume and inter-observer reliabilit
297 ions showed similar robust correlations with TTC-defined infarct volumes for both groups using previo
298 vidence of adverse outcomes among those with TTC of 31 to 60 or 60 to 90 days.
299 he 1970s to the present, comparing them with TTCs' public claims of support for harm reduction.
300                   The expansion of the GAA x TTC tract in intron 1 to as many as 1700 repeats elicits

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