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1 TX attenuates ABI by converting inhibitory, protein-bind
2 TX had significant VO2max deficits that were not capture
3 TX had significantly lower height Z-scores (P<0.001) and
4 TX phosphorylated the cAMP response element-binding prot
5 TX WT-infected DCs displayed higher viral replication th
6 in sequence to A/chicken/Texas/167280-4/02 (TX/02), a low-pathogenicity AIV isolate recovered from c
8 esentative virus (A/chicken/Texas/298313/04 [TX/04]) was not virulent for experimentally inoculated c
10 enuation by additives, such as Triton X-100 (TX) and human serum albumin (HSA), are not fully underst
13 action with the mild detergent Triton X-100 (TX-100) followed by a sucrose gradient flotation assay.
15 olubilization by the detergent Triton X-100 (TX-100), a property commonly attributed to association w
17 was resistant to removal with Triton X-100 (TX-100), whereas it was lost nearly completely when cell
18 that Gs alpha migrates from a Triton X-100 (TX-100)-insoluble membrane domain (lipid raft) to a TX-1
19 on by Western blot analysis of Triton X-100 (TX-100)-soluble and TX-100-insoluble cell lysates using
22 r dichroism (CD) spectroscopy, Triton X-114 (TX-114) phase partitioning, and liposome incorporation d
23 Five CPE factors, surfactant (Triton X-114 (TX-114)) concentration, pH, ionic strength, incubation t
26 nd a seasonal human H3N2 virus, A/TX/6/1996 (TX/96), to measure in vitro reassortment and growth pote
30 ed from the human isolate influenza A/TX/91 (TX WT, where WT is wild type) to study the functions of
31 virulent wild-type A/Swine/Texas/4199-2/98 (TX/98) virus and various mutants encoding carboxy-trunca
32 erase gene segments, while none of the MN/99-TX/96 reassortants contained all MN/99 polymerase genes.
33 m NC/02, whereas only 34 of 61 (55.7%) MN/99-TX/96 reassortants contained at least one polymerase gen
34 -insoluble membrane domain (lipid raft) to a TX-100-soluble nonraft membrane domain in response to ch
35 s derived from the human isolate influenza A/TX/91 (TX WT, where WT is wild type) to study the functi
36 (NC/02), and a seasonal human H3N2 virus, A/TX/6/1996 (TX/96), to measure in vitro reassortment and
38 a obtained using proteinase K accessibility, TX-114 phase partitioning, and cell fractionation reveal
40 time of harvest, the amount remaining after TX-100 treatment increased markedly as the time of harve
41 was independently associated with time after TX, hypertension, nonuse of ACEI, donor age, and changes
46 re were 21 H3 reassortants between MN/99 and TX/96, compared to only 17 H3 reassortants between NC/02
47 PEPCK, activities were similar in intact and TX fetuses; however, hepatic PEPCK was increased by TX.
49 erefore tested combinations of COT, NBA, and TX; the combinations altered the fluorescence quench rat
50 nalysis of Triton X-100 (TX-100)-soluble and TX-100-insoluble cell lysates using antibodies to N-term
51 ent flanking dinucleotide sites, i.e. XT and TX (X = A, C, or G), and assessed how these lesions impa
53 Institute of South Texas (RIST, San Antonio, TX) and The University of Texas Health Science Center Sa
54 o receive either a V.A.C. (KCI, San Antonio, TX) or a standard dry dressing over their incision at th
58 both rain and air of Houston and Arlington, TX, confirmed by tandem MS) takes just over 5 min with r
62 A) expression analysis using Ambion (Austin, TX, USA) arrays showed that three miRNAs were overexpres
65 Group A Strep (GAS) assay (Luminex, Austin, TX) is a fully automated PCR assay for direct detection
67 R assays: EraGen Multicode (Luminex, Austin, TX), Focus Simplexa (Focus Diagnostics, Cypress, CA), El
73 three cycles of docetaxel and capecitabine (TX) followed by three cycles of cyclophosphamide, epirub
81 re challenging separation of very long chain TX-series with a large number (n = 30-70) of ethoxy unit
82 cyclodextrin before extraction with ice-cold TX-100 or when treated with ice-cold octyl-beta-glucosid
83 e MuLV Env protein was resistant to ice-cold TX-100 treatment and floated to the top of the gradients
84 TNL proteins were demonstrated in conifers; TX and TN genes are present in very low numbers in grass
87 19th Judicial District Court, Collin County, TX, 2009), which provided evidence that direction can be
92 York, NY, and Baylor Medical Center, Dallas, TX) were randomized to same-day (n=150) or next-day (n=1
93 f Texas Southwestern Medical Center, Dallas, TX; Dr. Elizabeth H. Blackburn, University of California
94 with interstitial lung disease from Dallas, TX (primary cohort), and from Chicago, IL, and San Franc
96 s from unrelated healthy controls in Dallas, TX, and spouses of patients were also enrolled as an ind
99 p (University of Texas Southwestern [Dallas, TX], Baylor College of Medicine [Houston, TX], Johns Hop
109 mutations that encode merlins with enhanced TX-100 solubility have been explained previously in term
114 7 microg/mL total octylphenol ethoxylate for TX-45; acceptable precision of migration time (<1% RSD,
115 Using standards synthesized in our lab, four TX transformation products (GM: 34.8 ng/g) were also det
117 edical centres-in Baltimore (MD), Galveston (TX), New York (NY), St Louis (MO), San Diego (C92A), and
119 ntrol Panel; Radix Biosolutions, Georgetown, TX) can determine the level of nonspecific binding on a
122 Brooklyn-Manhattan, NY; Dallas and Houston, TX; and Washington, DC), we recruited people living with
123 of Texas MD Anderson Cancer Center (Houston, TX) and 293 cases from the Mayo Clinic (Rochester, MN).
124 Texas M.D. Anderson Cancer Center (Houston, TX) and a series of 137 patients identified through the
126 Texas M.D. Anderson Cancer Center (Houston, TX) between January 1975 and June 2005 was performed, an
127 Texas M.D. Anderson Cancer Center (Houston, TX) from February 1999 to August 2004 and observed throu
133 f Texas, MD Anderson Cancer Center (Houston, TX, USA) in February, 2019, to evaluate the available ev
134 of Texas MD Anderson Cancer Center (Houston, TX, USA), who fulfilled the diagnostic criteria of the I
135 of Texas MD Anderson Cancer Center (Houston, TX, USA), with refractory agitation, despite low-dose ha
145 ong 735 (MD Anderson Cancer Center, Houston, TX, USA) and 253 (Harvard University, Boston, MA, USA) n
149 referred to The Methodist Hospital (Houston, TX) between August 1, 2010 and July 31, 2011 for latent
155 g system (Bacterial BarCodes, Inc., Houston, TX) (rep-PCR) to that of PFGE for typing MRSA isolates f
157 s, TX], Baylor College of Medicine [Houston, TX], Johns Hopkins University [Baltimore, MD]) carried o
159 r ground-based sites located in the Houston, TX (September 21-28, 2013) and were analyzed for 12 orga
161 rlying the relationship among hyperglycemia, TX generation, and platelet hyperactivity remains unclea
162 is a proteolytically processed, immunogenic, TX-114 detergent-phase protein which appears to have ant
164 max was 13% lower (95% CI 18, 8; P<0.001) in TX, compared with controls, adjusted for FM, FFM, sex, a
168 reated in the same way; (ii) the tegument in TX-100-treated extracellular virions was asymmetrically
169 ssess maximal oxygen consumption (VO2max) in TX and controls, adjusted for body composition, and to i
170 antibody-mediated repartitioning of MOG into TX-100-insoluble glycosphingolipid-cholesterol-rich micr
171 thology database (Caris Diagnostics, Irving, TX) was used to identify EE cases from a cohort of upper
173 her insight into the mechanisms that mediate TX-induced up-regulation of GLT-1 (EAAT2 in humans), we
174 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 an E(a)/C varies by 6-36% among selected NC, TX, and NYC domains, and 15-34% among four seasons, as a
177 ive) and HER2 status (positive vs negative), TX+CEX was more effective than T+CEF in the subset of pa
178 The expression, prevalence, and diversity of TX and TN genes suggests that these genes encode functio
184 Stable overexpression transgenic lines of TX and TN genes in Arabidopsis produced a variety of phe
185 ry levels of a major enzymatic metabolite of TX (11-dehydro-TXB2 [TX-M]) were substantially increased
190 iency (87.3%) was obtained at 0.25% (w/v) of TX-114, pH = 10, salt content of 15 mM NaCl, incubation
191 This work provides direct visualization of TX-100-induced domain formation followed by selective (L
192 romyces cerevisiae) two-hybrid screen; other TX and TN proteins interacted with nucleotide binding-le
193 ical centers in Las Cruces, NM, and El Paso, TX, revealed the presence of spa types 2 and 24 (clone U
198 lly relevant millimolar concentration range, TX, NBA, and pNBA, caused comparable increases in gA cha
201 .001) and 0.5% Tetravisc (Ocusoft, Richmond, TX; OR, 3.95; 95% CI, 1.15-13.50; P = 0.03) use were ind
205 ptides sharing the common consensus sequence TX(2)CXXthetaPXLLGCPhiXE (theta represents a hydrophobic
212 n 14 IC; Stata Corporation, College Station, TX, USA), Meta-DiSc (version 1.4 for Windows; Cochrane C
215 ate matter (PM2.5), and maximum temperature (TX) over the eastern United States and Canada to constru
217 Taken together, our findings establish that TX regulates GLT-1 via the CREB and NF-kappaB pathways.
230 genetic and biologic characteristics of the TX/04 isolate, which highlight the complexity of the pol
231 tics, we found that the pathogenicity of the TX/04 virus could be increased in vitro and in vivo by t
232 the NS1 protein decrease the ability of the TX/98 virus to prevent IFN-alpha/beta synthesis in pig c
233 Confocal microscopy demonstrated that the TX-insoluble compartment is perinuclear and co-localizes
234 include benzophenones (BZPs), thioxanthones (TXs), amine co-initiators (ACIs), and novel phosphine ox
238 to long-lasting suppression of thromboxane (TX) A2 production and TXA2-mediated platelet activation
239 coupled with enhanced levels of thromboxane (TX), an eicosanoid that facilitates platelet aggregation
243 ic agonist phenylephrine or the thromboxane (TX) A2 analog U-46619 were similar between eNOS(-/-) and
245 ndin (PG) I2 synthesis, whereas thromboxane (TX) A2 production and COX-2 protein expression were unaf
248 e-winged teal/Texas/Sg-00079/2007 (H3N8) (tl/TX/079/07) wt virus and the six internal protein gene se
249 antibody response against the homologous (tl/TX/079/07) and two heterologous influenza viruses, inclu
250 fety, immunogenicity, and efficacy of the tl/TX/079/07 ca vaccine in mice and ferrets support further
252 We also analyzed human sera against the tl/TX/079/07 H3N8 avian influenza virus and observed low bu
254 nents that connect high levels of glucose to TX generation and to examine their clinical relevance.
255 The TX/04 isolate was similar in sequence to TX/02 isolate in several internal genes (NP, M, and NS),
256 further studies exploring human exposure to TXs should include these transformation products to avoi
258 avengers N-acetyl cysteine (NAC) and Trolox (TX), as well as by cyclosporin A (CsA) and bongkrekic ac
259 mely beta-mercaptoethanol (beta-ME), Trolox (TX), n-propyl gallate (n-PG), and ascorbic acid (AA).
260 OT), para-nitrobenzyl alcohol (NBA), Trolox (TX), 1,4-diazabicyclo[2.2.2]octane (DABCO), para-nitrobe
264 ubjects, with females showing higher urinary TX metabolite (TXM) excretion than male subjects with T1
268 pera stent, IDEV Technologies, Inc, Webster, TX) to confer greater radial strength, flexibility, and
270 ns, PGD-M levels remained unchanged, whereas TX-M levels (0.7 +/- 0.1 pmol/mg Cr, P = .07) tended to
274 We also compared infections of DCs with TX WT and our previously characterized laboratory strain
275 nized around the capsid and extractable with TX-100 to a state where it is asymmetrically arranged an
276 rms of PC3 were resistant to extraction with TX-100, were floated to low-density fractions in sucrose
277 hosphatidylinositol anchors partitioned with TX-100-resistant lipid rafts, but cells bearing these ra
280 structural and nonstructural regions of WNV-TX contribute to the control of type I interferon defens
283 n 23 eyes and the CZ70BD (Alcon, Fort Worth, TX) in 8 eyes, and all lenses were sutured 3 mm behind t
285 e (Tobradex; Alcon Laboratories, Fort Worth, TX) ophthalmic suspension, and balanced salt solution (B
286 IOL; SA60AT; Alcon Laboratories, Fort Worth, TX) or a 3-piece acrylic IOL (MA60AS; Alcon Laboratories
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 osing of Systane Balance (Alcon, Fort Worth, TX), patients were randomized to the respective treatmen
293 in June 2011 downwind of Dallas-Fort Worth, TX, and evaluate the role of stabilized Criegee radicals
296 h (including ExPRESS [Alcon Inc, Fort Worth, TX]) increased 116% from 2718 in 2009 to 5870 in 2012.
297 toptic; Alcon Laboratories Inc., Fort Worth, TX], brinzolamide/brimonidine [Simbrinza; Alcon Laborato
298 ogic saline solution (BSS; Alcon, Ft. Worth, TX) was injected into the left eye of each rabbit as a c