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1                                              TX had significant VO2max deficits that were not capture
2                                              TX had significantly lower height Z-scores (P<0.001) and
3                                              TX phosphorylated the cAMP response element-binding prot
4                                              TX WT-infected DCs displayed higher viral replication th
5  in sequence to A/chicken/Texas/167280-4/02 (TX/02), a low-pathogenicity AIV isolate recovered from c
6         Additionally, 38 of 81 (46.9%) NC/02-TX/96 reassortants contained all NC/02 polymerase gene s
7 esentative virus (A/chicken/Texas/298313/04 [TX/04]) was not virulent for experimentally inoculated c
8                  Seventy-seven of 81 (95.1%) TX/96-NC/02 reassortants contained at least one polymera
9 m that TRAF2 translocates to a Triton X-100 (TX)-insoluble compartment upon TNF-R2 engagement.
10  by intranasal irrigation with Triton X-100 (TX).
11                          Using Triton X-100 (TX-100) as a representative HA, we found that the mtrCDE
12                          Using Triton X-100 (TX-100) detergent treatment of membrane fractions and fl
13 , the newly synthesized M1 was Triton X-100 (TX-100) extractable but became resistant to TX-100 extra
14 action with the mild detergent Triton X-100 (TX-100) followed by a sucrose gradient flotation assay.
15  association, as determined by Triton X-100 (TX-100) resistance.
16 re MOG is not raft associated [Triton X-100 (TX-100) soluble, 4 degrees C].
17 olubilization by the detergent Triton X-100 (TX-100), a property commonly attributed to association w
18 ACAMs were solubilized by cold Triton X-100 (TX-100), indicating their absence from lipid rafts.
19  was resistant to removal with Triton X-100 (TX-100), whereas it was lost nearly completely when cell
20  that Gs alpha migrates from a Triton X-100 (TX-100)-insoluble membrane domain (lipid raft) to a TX-1
21 on by Western blot analysis of Triton X-100 (TX-100)-soluble and TX-100-insoluble cell lysates using
22  when exposed to the detergent Triton X-100 (TX-100).
23       In the cerebellum, the ratio of TX-100/TX-114-soluble Gs alpha is approximately 2:1 for control
24 r dichroism (CD) spectroscopy, Triton X-114 (TX-114) phase partitioning, and liposome incorporation d
25  Five CPE factors, surfactant (Triton X-114 (TX-114)) concentration, pH, ionic strength, incubation t
26 ldren were evaluated (5 patients with KD; 12 TX recipients).
27 ium-, and long-chain length (e.g., n = 1-16) TX-series nonionic surfactants.
28 nd a seasonal human H3N2 virus, A/TX/6/1996 (TX/96), to measure in vitro reassortment and growth pote
29                              KBO 55636 (2002 TX(300)) is a member of the water-ice-rich Haumea KBO co
30 egg-grown H3 vaccine strain A/Texas/50/2012 (TX/12e).
31 rgy X-ray absorptiometry were obtained in 50 TX and 70 controls, ages 8 to 21 years.
32 ed from the human isolate influenza A/TX/91 (TX WT, where WT is wild type) to study the functions of
33  virulent wild-type A/Swine/Texas/4199-2/98 (TX/98) virus and various mutants encoding carboxy-trunca
34 erase gene segments, while none of the MN/99-TX/96 reassortants contained all MN/99 polymerase genes.
35 m NC/02, whereas only 34 of 61 (55.7%) MN/99-TX/96 reassortants contained at least one polymerase gen
36 -insoluble membrane domain (lipid raft) to a TX-100-soluble nonraft membrane domain in response to ch
37 s derived from the human isolate influenza A/TX/91 (TX WT, where WT is wild type) to study the functi
38  (NC/02), and a seasonal human H3N2 virus, A/TX/6/1996 (TX/96), to measure in vitro reassortment and
39 epressing miRNAs or Ago2 knockdown abrogates TX's ability to suppress HIF-1alpha translation.
40 a obtained using proteinase K accessibility, TX-114 phase partitioning, and cell fractionation reveal
41                      M1 also did not acquire TX-100 insolubility in ts 56 (a temperature-sensitive mu
42              NP, on the other hand, acquired TX-100 resistance immediately after synthesis.
43 d, late in the infectious cycle, M1 acquired TX-100 resistance when chased in either the presence or
44 ower serum lipids and ACEI in patients after TX.
45  time of harvest, the amount remaining after TX-100 treatment increased markedly as the time of harve
46 was independently associated with time after TX, hypertension, nonuse of ACEI, donor age, and changes
47 40 months after cardiac allotransplantation (TX).
48                     In exploratory analyses, TX/CEX improved breast cancer-specific survival (HR, 0.6
49 to only 17 H3 reassortants between NC/02 and TX/96.
50                        Sequential TX-100 and TX-114 detergent extractions were performed on the brain
51 re were 21 H3 reassortants between MN/99 and TX/96, compared to only 17 H3 reassortants between NC/02
52 PEPCK, activities were similar in intact and TX fetuses; however, hepatic PEPCK was increased by TX.
53                         Patients with KD and TX recipients were evaluated between December 2012 and O
54 erefore tested combinations of COT, NBA, and TX; the combinations altered the fluorescence quench rat
55 nalysis of Triton X-100 (TX-100)-soluble and TX-100-insoluble cell lysates using antibodies to N-term
56 igrees of Hispanic descent from San Antonio, TX (SA) and San Luis Valley, CO (SLV).
57 Institute of South Texas (RIST, San Antonio, TX) and The University of Texas Health Science Center Sa
58 o receive either a V.A.C. (KCI, San Antonio, TX) or a standard dry dressing over their incision at th
59 ional Swimming Pool Foundation (San Antonio, TX).
60 y transmitted disease clinic in San Antonio, TX, by use of diagnostic real-time PCR.
61 ak of respiratory infections in San Antonio, TX.
62 dation for Biomedical Research, San Antonio, TX.
63 n-American ancestry residing in San Antonio, TX.
64  both rain and air of Houston and Arlington, TX, confirmed by tandem MS) takes just over 5 min with r
65                             In 2006, Austin, TX, became the first jurisdiction in the U.S. to ban the
66 A) expression analysis using Ambion (Austin, TX, USA) arrays showed that three miRNAs were overexpres
67 s were immersed in RNAlater (Ambion, Austin, TX) at 5, 12, 24, or 48 hours.
68 ltiplex bead analysis (Luminex Inc., Austin, TX).
69 R assays: EraGen Multicode (Luminex, Austin, TX), Focus Simplexa (Focus Diagnostics, Cypress, CA), El
70 can 2000ED (Mirabel Medical Systems, Austin, TX).
71                NP, on the other hand, became TX-100 insoluble as in the virus-infected cells.
72 an injection of 3 mg/kg MCTP 4 months before TX.
73  RV performance adapts acutely after bicaval TX with significant increases in power and contractility
74 t not EGFR, were not sensitive to either BTC-TX form.
75 ata indicate that despite the ability of BTC-TX to bind and phosphorylate HER4, it was only cytotoxic
76                         The inability of BTC-TX to kill cells was likely due to its failure to intern
77 ses; however, hepatic PEPCK was increased by TX.
78 iginal vesicle and completely solubilized by TX-100.
79  three cycles of docetaxel and capecitabine (TX) followed by three cycles of cyclophosphamide, epirub
80 lophosphamide, epirubicin, and capecitabine (TX+CEX).
81                                        CARDS TX binds to human surfactant protein A and annexin A2 on
82       Here we present the structure of CARDS TX, a triangular molecule in which N-terminal mART and C
83                    We demonstrate that CARDS TX binds phosphatidylcholine and sphingomyelin specifica
84 d Respiratory Distress Syndrome Toxin (CARDS TX).
85 iversity of Texas MD Anderson Cancer Center, TX, USA.
86 re challenging separation of very long chain TX-series with a large number (n = 30-70) of ethoxy unit
87 as mostly soluble when extracted by ice-cold TX-100 and stayed at the bottom of the gradients.
88 cyclodextrin before extraction with ice-cold TX-100 or when treated with ice-cold octyl-beta-glucosid
89 e MuLV Env protein was resistant to ice-cold TX-100 treatment and floated to the top of the gradients
90 dogs were used for 10 successfully completed TX experiments.
91  TNL proteins were demonstrated in conifers; TX and TN genes are present in very low numbers in grass
92                                 In contrast, TX, a popular detergent used to isolate raft membranes i
93 pulation in Galveston and Chambers counties, TX.
94 19th Judicial District Court, Collin County, TX, 2009), which provided evidence that direction can be
95  (TB) cases were collected in Harris County, TX, in 2007 to 2008.
96 ies from a cohort collected in Starr County, TX (1,890 samples).
97 senting Mexican Americans from Starr County, TX, and Mexicans from Mexico City.
98 York, NY, and Baylor Medical Center, Dallas, TX) were randomized to same-day (n=150) or next-day (n=1
99 f Texas Southwestern Medical Center, Dallas, TX; Dr. Elizabeth H. Blackburn, University of California
100  with interstitial lung disease from Dallas, TX (primary cohort), and from Chicago, IL, and San Franc
101 sive care unit at Parkland Hospital, Dallas, TX, USA.
102 s from unrelated healthy controls in Dallas, TX, and spouses of patients were also enrolled as an ind
103 ED) at Parkland Memorial Hospital in Dallas, TX.
104 examinations at the Cooper Clinic in Dallas, TX.
105 p (University of Texas Southwestern [Dallas, TX], Baylor College of Medicine [Houston, TX], Johns Hop
106 red (local or distant recurrences or deaths; TX/CEX, n = 96; T/CEF, n = 118).
107                                      Delayed TX/96 infection was fully excluded by both swine viruses
108 ofiling system (Luminex Corporation, DeSoto, TX).
109 SUS, Gibbs sampler, MEME, SPLASH and DIALIGN-TX).
110 nding site (TN) and TIR-unknown site/domain (TX) families.
111 s it partitioned to the aqueous phase during TX-114 partitioning.
112                                     Elevated TX-M persisted in diabetic patients taking low-dose aspi
113                               Genes encoding TX, TN and TNL proteins were demonstrated in conifers; T
114  mutations that encode merlins with enhanced TX-100 solubility have been explained previously in term
115  mutations that encode merlins with enhanced TX-100 solubility.
116             Transient overexpression of five TX and TN genes in tobacco (Nicotiana benthamiana) induc
117 M-1 s-1 for CPP32 to 1.0 x 10(3) M-1 s-1 for TX.
118 .60 to 1.04; P = .087; 5-year RFS, 86.6% for TX/CEX v 84.1% for T/CEF).
119 crog m(-3) for PM2.5, and +1.7 degrees C for TX.
120 erminus of the NA TMD were also critical for TX-100 resistance.
121 7 microg/mL total octylphenol ethoxylate for TX-45; acceptable precision of migration time (<1% RSD,
122                                 Furthermore, TX recruited the NF-kappaB subunits p65 and p50 to the N
123 rine sediment sample collected in Galveston, TX.
124 e and implicate a unique sequence motif (GGS/TX(5)GXNXLE) in Kdo binding.
125 ature form by ICE and three of its homologs, TX, CPP-32, and CMH-1.
126 tatectomy at the Methodist Hospital, Houston TX.
127 of Texas MD Anderson Cancer Center (Houston, TX) and 293 cases from the Mayo Clinic (Rochester, MN).
128  Texas M.D. Anderson Cancer Center (Houston, TX) and a series of 137 patients identified through the
129  Texas M.D. Anderson Cancer Center (Houston, TX) between 1985 and 2005.
130  Texas M.D. Anderson Cancer Center (Houston, TX) between January 1975 and June 2005 was performed, an
131  Texas M.D. Anderson Cancer Center (Houston, TX) from February 1999 to August 2004 and observed throu
132             Anderson Cancer Center (Houston, TX) with post-orchiectomy megavoltage XRT between 1951 a
133             Anderson Cancer Center (Houston, TX).
134 Texas M. D. Anderson Cancer Center (Houston, TX).
135 olled at MD Anderson Cancer Center (Houston, TX, USA) between Sept 15, 2014, and Sept 20, 2015.
136 eated at MD Anderson Cancer Center (Houston, TX, USA) from 1997 to 2015.
137 of Texas MD Anderson Cancer Center (Houston, TX, USA).
138 of Texas MD Anderson Cancer Center (Houston, TX, USA).
139 L at the MD Anderson Cancer Center (Houston, TX, USA).
140 of Texas MD Anderson Cancer Center (Houston, TX, USA).
141  Texas M.D. Anderson Cancer Center, Houston, TX (n = 42).
142  Texas M.D. Anderson Cancer Center, Houston, TX, between December 1997 and June 1998.
143 of Texas MD Anderson Cancer Center, Houston, TX, from 2002 to 2014.
144 ong 735 (MD Anderson Cancer Center, Houston, TX, USA) and 253 (Harvard University, Boston, MA, USA) n
145 s at the MD Anderson Cancer Center, Houston, TX, USA, between June, 2010, and March, 2011.
146 Texas M. D. Anderson Cancer Center, Houston, TX.
147 iously sequenced USA300 strain from Houston, TX).
148 referred to The Methodist Hospital (Houston, TX) between August 1, 2010 and July 31, 2011 for latent
149 ndemic wave, March to July 2009, in Houston, TX, Milwaukee, WI, and New York State.
150  food companies with restaurants in Houston, TX, with complete publicly available data.
151 infall and catastrophic flooding in Houston, TX.
152 Center, a tertiary care hospital in Houston, TX.
153 cruited from Head Start settings in Houston, TX.
154 g system (Bacterial BarCodes, Inc., Houston, TX) (rep-PCR) to that of PFGE for typing MRSA isolates f
155 tudy at Baylor College of Medicine (Houston, TX).
156 s, TX], Baylor College of Medicine [Houston, TX], Johns Hopkins University [Baltimore, MD]) carried o
157 dustrialized ship channel region of Houston, TX over a 2-month period.
158 r ground-based sites located in the Houston, TX (September 21-28, 2013) and were analyzed for 12 orga
159 inical Center for Targeted Therapy (Houston, TX, USA).
160 rlying the relationship among hyperglycemia, TX generation, and platelet hyperactivity remains unclea
161 mbers Ice, CPP32 (Yama, apopain), ICErel-II (TX, Ich-2), Mch-3 (ICE-LAP3, CMH-1), Mch-4, and Mch-5 (M
162 ludes caspase-1 (ICE), caspase-4 (ICErel-II, TX, ICH-2), and caspase-5 (ICErel-III, TY).
163 is a proteolytically processed, immunogenic, TX-114 detergent-phase protein which appears to have ant
164                                           In TX recipients, angiography was normal; however, intimal
165 max was 13% lower (95% CI 18, 8; P<0.001) in TX, compared with controls, adjusted for FM, FFM, sex, a
166 145 days, tissue G6P and PEPCK activities in TX fetuses were lower than in intact fetuses.
167                             Lower fitness in TX may be related to sirolimus effects on skeletal muscl
168 identify risk factors for reduced fitness in TX.
169 reated in the same way; (ii) the tegument in TX-100-treated extracellular virions was asymmetrically
170 ssess maximal oxygen consumption (VO2max) in TX and controls, adjusted for body composition, and to i
171 antibody-mediated repartitioning of MOG into TX-100-insoluble glycosphingolipid-cholesterol-rich micr
172 thology database (Caris Diagnostics, Irving, TX) was used to identify EE cases from a cohort of upper
173 rom $31 175 (Salem, MA) to $61 895 (McAllen, TX).
174 her insight into the mechanisms that mediate TX-induced up-regulation of GLT-1 (EAAT2 in humans), we
175 e [Cr], P < .05) and thromboxane metabolite (TX-M; 1.4 +/- 0.3 vs 0.9 +/- 0.1 pmol/mg Cr, P < .01) le
176 ation of cells with an ERBB1 inhibitor, NAC, TX, CsA, or BKA.
177 an E(a)/C varies by 6-36% among selected NC, TX, and NYC domains, and 15-34% among four seasons, as a
178 ive) and HER2 status (positive vs negative), TX+CEX was more effective than T+CEF in the subset of pa
179 The expression, prevalence, and diversity of TX and TN genes suggests that these genes encode functio
180                                The effect of TX on astrocytic GLT-1 was attenuated by the inhibition
181                   In addition, the effect of TX on GLT-1 promoter activity was abolished by the inhib
182 ed to a complete abrogation of the effect of TX on GLT-1 promoter activity.
183 flammatory ATL opposite to the inhibition of TX.
184 ith ice-cold octyl-beta-glucoside instead of TX-100.
185    Stable overexpression transgenic lines of TX and TN genes in Arabidopsis produced a variety of phe
186 ry levels of a major enzymatic metabolite of TX (11-dehydro-TXB2 [TX-M]) were substantially increased
187 ication events have increased the numbers of TX and TN genes in Arabidopsis.
188 ation of phase separation in the presence of TX.
189                         Growth properties of TX/98 viruses with mutated NS1, induction of IFN in tiss
190              In the cerebellum, the ratio of TX-100/TX-114-soluble Gs alpha is approximately 2:1 for
191 iency (87.3%) was obtained at 0.25% (w/v) of TX-114, pH = 10, salt content of 15 mM NaCl, incubation
192   This work provides direct visualization of TX-100-induced domain formation followed by selective (L
193 romyces cerevisiae) two-hybrid screen; other TX and TN proteins interacted with nucleotide binding-le
194 ical centers in Las Cruces, NM, and El Paso, TX, revealed the presence of spa types 2 and 24 (clone U
195 ary aneurysms because of KD and in pediatric TX recipients.
196 mice despite virtual elimination of platelet TX production.
197         These data demonstrate that platelet TX production does not aggravate early atherosclerotic l
198   After coinfection with NC/02 or MN/99 plus TX/96, H1/H3 double-positive cells were identified.
199 lly relevant millimolar concentration range, TX, NBA, and pNBA, caused comparable increases in gA cha
200 women received T+CEF, and 753 women received TX+CEX.
201 ss in pediatric renal transplant recipients (TX) has not been established.
202  (Scalopus aquaticus) collected in Rockport, TX, in 1986.
203 earing sediments from an ISR site at Rosita, TX, USA.
204  U mobility at an ISR mining site at Rosita, TX, USA.
205 ptides sharing the common consensus sequence TX(2)CXXthetaPXLLGCPhiXE (theta represents a hydrophobic
206                                   Sequential TX-100 and TX-114 detergent extractions were performed o
207 e from the University of Texas Southwestern, TX, USA (UTSW).
208 rformed using STATA/MP v10 (College Station, TX).
209 s using the STATA software (College Station, TX).
210 sing STATA 12.1 (StataCorp, College Station, TX).
211                                   Tamoxifen (TX), a selective estrogen receptor modulator, exerts ant
212           Microtubule perturbation by taxol (TX) and other microtubule-targeting drugs stalls HIF-1al
213 ate matter (PM2.5), and maximum temperature (TX) over the eastern United States and Canada to constru
214 ion and stimulated naive T-cells better than TX WT virus-infected DCs.
215  Taken together, our findings establish that TX regulates GLT-1 via the CREB and NF-kappaB pathways.
216                  We reported previously that TX enhanced the expression and function of glutamate tra
217                         We clearly show that TX-100 has a restructuring action on biomembranes.
218                 Further analysis showed that TX increased membrane thickness of the DPPC phase to a g
219                                          The TX/04 isolate also had a stalk deletion in the NA gene,
220                                          The TX/04 isolate was similar in sequence to TX/02 isolate i
221                                In Col-0, the TX family is encoded by 27 genes and three pseudogenes;
222  but neither mutant completely abolished the TX-induced GLT-1 promoter activity.
223                                 However, the TX/04 isolate had one additional basic amino acid at the
224 tioning of approximately 95% of MOG into the TX-100-insoluble fraction.
225 ); both forms, however, partitioned into the TX-114 detergent-enriched phase.
226               The ZnO NPs extracted into the TX-114-rich phase were characterized by transmission ele
227 s detected for only approximately 40% of the TX-encoding genes, again at low levels.
228           The hemagglutinin (HA) gene of the TX/04 isolate was similar in sequence to A/chicken/Texas
229  genetic and biologic characteristics of the TX/04 isolate, which highlight the complexity of the pol
230 tics, we found that the pathogenicity of the TX/04 virus could be increased in vitro and in vivo by t
231  the NS1 protein decrease the ability of the TX/98 virus to prevent IFN-alpha/beta synthesis in pig c
232    Confocal microscopy demonstrated that the TX-insoluble compartment is perinuclear and co-localizes
233                                        These TX and TN proteins could be plant analogues of small TIR
234                                 Thromboxane (TX) A2 is released from multiple cell types and is a pri
235                                 Thromboxane (TX) A2 is released from multiple cell types and is a pri
236 e inhibition of COX-1-dependent thromboxane (TX) A2.
237  to long-lasting suppression of thromboxane (TX) A2 production and TXA2-mediated platelet activation
238 coupled with enhanced levels of thromboxane (TX), an eicosanoid that facilitates platelet aggregation
239                          Plasma thromboxane (TX)B2, an indicator of platelet reactivity, and ATL were
240         COX-1-mediated platelet thromboxane (TX) production has been proposed to promote both early a
241                             The thromboxane (TX) A(2) receptor (TP) encompasses two alternatively spl
242 ic agonist phenylephrine or the thromboxane (TX) A2 analog U-46619 were similar between eNOS(-/-) and
243         We investigated in vivo thromboxane (TX) and prostacyclin (PGI2) biosynthesis and their deter
244 ndin (PG) I2 synthesis, whereas thromboxane (TX) A2 production and COX-2 protein expression were unaf
245 iators CD40 ligand (CD40L) and thromboxanes (TXs).
246 tisol, was prevented by fetal thyroidectomy (TX).
247 e-winged teal/Texas/Sg-00079/2007 (H3N8) (tl/TX/079/07) wt virus and the six internal protein gene se
248 antibody response against the homologous (tl/TX/079/07) and two heterologous influenza viruses, inclu
249 fety, immunogenicity, and efficacy of the tl/TX/079/07 ca vaccine in mice and ferrets support further
250                           One dose of the tl/TX/079/07 ca vaccine induced a robust neutralizing antib
251   We also analyzed human sera against the tl/TX/079/07 H3N8 avian influenza virus and observed low bu
252               Fifty-six patients assigned to TX/CEX died during the follow-up compared with 75 of pat
253 nents that connect high levels of glucose to TX generation and to examine their clinical relevance.
254 ver, the enhanced resistance of gonococci to TX-100 was dependent on the expression of a previously u
255 plex glycosylation, also became resistant to TX-100 extraction but was sensitive to octylglucoside de
256 (TX-100) extractable but became resistant to TX-100 extraction during the chase with a t1/2 of 20 min
257 pressed with NP, did not become resistant to TX-100 extraction even after a long chase.
258 The TX/04 isolate was similar in sequence to TX/02 isolate in several internal genes (NP, M, and NS),
259 with heterologous Sendai virus F was totally TX-100 soluble but the membrane-bound M1 protein express
260 disease (KD) and pediatric heart transplant (TX) recipients.
261 ne model of bicaval cardiac transplantation (TX) and monocrotaline pyrrole (MCTP)-induced CPH.
262 avengers N-acetyl cysteine (NAC) and Trolox (TX), as well as by cyclosporin A (CsA) and bongkrekic ac
263 mely beta-mercaptoethanol (beta-ME), Trolox (TX), n-propyl gallate (n-PG), and ascorbic acid (AA).
264 OT), para-nitrobenzyl alcohol (NBA), Trolox (TX), 1,4-diazabicyclo[2.2.2]octane (DABCO), para-nitrobe
265 enzymatic metabolite of TX (11-dehydro-TXB2 [TX-M]) were substantially increased.
266 mpared to those of the recombinant wild-type TX/98 virus.
267 ubjects, with females showing higher urinary TX metabolite (TXM) excretion than male subjects with T1
268                                        Using TX-114 extraction, we find that accumulated 5-HT remains
269 of Texas Southwestern Medical Center (UTSW), TX, USA, between 1998 and 2011.
270  220 were obtained with 0.25 and 0.05% (w/v) TX-114, respectively.
271 pera stent, IDEV Technologies, Inc, Webster, TX) to confer greater radial strength, flexibility, and
272 (61.3 +/- 19.9 pmol/mg Cr, P < .05), whereas TX-M levels did not change.
273 ns, PGD-M levels remained unchanged, whereas TX-M levels (0.7 +/- 0.1 pmol/mg Cr, P = .07) tended to
274 ith body mass index Z-scores comparable with TX.
275 ibody-binding sites A and B as compared with TX/12e.
276                                 Contact with TX-100 readily induces domain formation on the previousl
277      We also compared infections of DCs with TX WT and our previously characterized laboratory strain
278 nized around the capsid and extractable with TX-100 to a state where it is asymmetrically arranged an
279 rms of PC3 were resistant to extraction with TX-100, were floated to low-density fractions in sucrose
280 at HA, unlike M1 or NP, was interacting with TX-100-insoluble lipids and not with cytoskeletal elemen
281 hosphatidylinositol anchors partitioned with TX-100-resistant lipid rafts, but cells bearing these ra
282 ME and efficient geminate recombination with TX.
283                                       Within TX, hemoglobin levels were positively associated with VO
284  structural and nonstructural regions of WNV-TX contribute to the control of type I interferon defens
285 ) [PQ], Alcon Laboratories, Inc; Fort Worth, TX) for 12 weeks.
286 e (Tobradex; Alcon Laboratories, Fort Worth, TX) ophthalmic suspension, and balanced salt solution (B
287 AcrySof SA60AT lens (Alcon, Inc, Fort Worth, TX) or the low-cost Tecsoft Flex lens (Fred Hollows Foun
288 femtosecond laser (LenSx, Alcon, Fort Worth, TX), or an automated PPC device (Zepto, Mynosys Inc., Fr
289 MA60AC (Alcon Laboratories Inc., Fort Worth, TX).
290 plant (Alcon Laboratories, Inc., Fort Worth, TX).
291  pIOL (Alcon Laboratories, Inc., Fort Worth, TX).
292  in June 2011 downwind of Dallas-Fort Worth, TX, and evaluate the role of stabilized Criegee radicals
293 d with an Acrysof SA60AT (Alcon, Fort Worth, TX, USA) monofocal IOL.
294  February 27 to March 2, 2010 in Fort Worth, TX.
295 h (including ExPRESS [Alcon Inc, Fort Worth, TX]) increased 116% from 2718 in 2009 to 5870 in 2012.
296 toptic; Alcon Laboratories Inc., Fort Worth, TX], brinzolamide/brimonidine [Simbrinza; Alcon Laborato
297 ogic saline solution (BSS; Alcon, Ft. Worth, TX) was injected into the left eye of each rabbit as a c
298                                   The TIR-X (TX) family of proteins lacks both the nucleotide-binding
299                                The Triton X (TX)-series are alkylphenol polyethoxylates -type nonioni
300 lipid amphiphiles, vitamin E (VE), Triton-X (TX)-100, and benzyl alcohol (BA).

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