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1                                              TM cells were more prone to ER stress from ECM accumulat
2                                              TM has long been hypothesized to play a role in aging, c
3                                              TMs have been associated with the capacity of glioma cel
4 r) was observed, from 37.2% (TM-2) to 18.1% (TM-3).This study shows that tea consumed simultaneously
5  in parental genotypes of 'Texas Marker-1' ('TM-1'), 'Pima 3-79' and their F1 hybrids.
6 relative to water) was observed, from 37.2% (TM-2) to 18.1% (TM-3).This study shows that tea consumed
7 ion was 5.7% +/- 8.5% (TM-1), 3.6% +/- 4.2% (TM-2), and 5.7% +/- 5.4% (TM-3).
8 n authentic TM helix; supporting VKOR is a 3-TM protein, which is different from VKORL.
9 1), 3.6% +/- 4.2% (TM-2), and 5.7% +/- 5.4% (TM-3).
10 with arms consisting of repeated arrays of 4-TM structural units surrounding a pore.
11  that the second TM domain in the proposed 4-TM model of VKOR does not function as an authentic TM he
12 t biophysical evidence that Death Receptor 5 TM-dimers open in response to ligand binding.
13 on method.Iron absorption was 5.7% +/- 8.5% (TM-1), 3.6% +/- 4.2% (TM-2), and 5.7% +/- 5.4% (TM-3).
14 ogous copies of a six-transmembrane-helix (6-TM) domain, which has no sequence homology to the canoni
15 cteria and archaea, contains only a single 6-TM domain and functions as a tetramer.
16 copies of a Shaker-like six-transmembrane (6-TM) domain in each subunit and are ubiquitously expresse
17 extra interactions in seven-transmembrane (7-TM) domain of Smo due to an additional 2-pyridylmethyl g
18 orption of TE-polarised light--and acts as a TM-pass waveguide polariser.
19                 In this paper, we identify a TM that goes beyond the above paradigms.
20 he finding that hydrogen bond strengths in a TM helix can vary widely has implications for membrane p
21  that being more than just membrane anchors, TM helices could play an important role in the clusterin
22 a-ray emission mappings and of the color and TM element speciation by optical absorption spectroscopy
23 e region at the interface between the EC and TM domains, near the interlobe groove of NCT, emerges as
24 endothelial resistance of SC endothelial and TM cell monolayers and reduced monolayer permeability wh
25 ver concordance of diagnoses between WSI and TM methods and interobserver variance from GTC, followin
26 an intraobserver concordance between WSI and TM was 94%.
27 dermatopathologists who diagnosed by WSI and TM with a minimum 30-day washout between methodologies.
28 evaluate workflow efficiency between WSI and TM.
29 rtant because the identification of TNTs and TMs fills the gap in our knowledge of how cancer cells c
30 el of VKOR does not function as an authentic TM helix; supporting VKOR is a 3-TM protein, which is di
31 cytosolic domain (TM/CT) with a tilted beta3 TM/CT that leads to activation when disrupted.
32 performed to assess the relationship between TM height and glaucoma subtype.
33 and lowered perfusate pressure in biomimetic TM scaffolds populated with primary hTM cells.
34  the TGF-beta-induced collagen expression by TM cells.
35 26 experimental dimeric structures formed by TM alpha-helices of 21 single-pass membrane proteins (in
36              During storage at 40 degrees C, TM displayed remarkably lower tocotrienols loss (50.8%)
37 5 and TM7, prior to entry into the canonical TM bundle orthosteric site.
38      Molecular modeling indicates that CD16A TM residues F(202), D(205), and T(206) form the core of
39 d network previously identified in the CD247 TM dimer solution NMR structure.
40 o the enhanced functionality of human CD8(+) TM and their prominent role in protection and auto-immun
41                 In contrast, those in CD8(+) TM were significantly enriched for immune-response-assoc
42                              By casting CD8+ TM populations within the temporal framework of their sl
43                 Notably, the process of CD8+ TM aging is characterized by a progressive harmonization
44 e sequence of APP and possibly other cleaved TM helices may be designed, in part, to make their backb
45 d multivariate linear mixed models comparing TM height and glaucoma type were performed to assess the
46 t room temperature in the bottles containing TM.
47 ain of wild-type hCNT1 and the corresponding TMs of cysteine-less NupC(C-) yielded results that valid
48 s, only two, Abisco((R))-100 and CoVaccineHT(TM), enhanced vaccine efficacy and sterile protection fo
49                              The CoVaccineHT(TM) adjuvanted vaccine induced significantly higher prop
50 xpressing supporting cells or by Atoh1-CreER(TM)-expressing type II hair cells.
51 nlasered TM from eyes with ExGl demonstrated TM thinning with collapse of Schlemm's canal; and proteo
52 lar heterogeneity of the recently discovered TMs with potential implications for future TM-targeting
53 regarding formation and function of distinct TM subtypes, with multiple parallels to neuronal develop
54 nally mobile regions within transport-domain TMs, identified pore-lining residues of functional impor
55 alphaIIb transmembrane and cytosolic domain (TM/CT) with a tilted beta3 TM/CT that leads to activatio
56 2, hairpin 1, putative transmembrane domain (TM) 7, and TM8), as well as TM9 of the scaffold domain o
57 eric structure for the transmembrane domain (TM) also was modeled and supported by experimental data.
58 tion of the quantitative redox state of each TM in each color shows that the contents of Fe, Cu, and
59                          The Biolog EcoPlate(TM) technique was utilized to examine microbial metaboli
60          The TM domain of Lnt contains eight TM helices which form a membrane-embedded cavity with a
61 ociated with insufficiency of the endogenous TM/APC pathway, such as sepsis.
62             Therefore, similar to endogenous TM, RBC-anchored scFv/TM activates several protective pa
63 as found, and analysis of the Hendra virus F TM domain revealed a heptad repeat leucine-isoleucine zi
64 cificity: protective (Influenza-induced, Flu-TM) and non-protective (peptide-induced, TIM) spleen mem
65 cordance was 94% for WSI and GTC and 94% for TM and GTC.
66 nd identified novel molecular candidates for TM formation and function.
67 sis versus no change or better prognosis for TM, based on the postscan assessment.
68                   Clots formed in blood from TM-AC cases had the same viscoelastic strength as contro
69 oses from WSI were noninferior to those from TM.
70                                 Furthermore, TM significantly increased hepatic LDLR expression and r
71 d TMs with potential implications for future TM-targeting strategies.
72 accumulation in mouse and human glaucomatous TM tissues.
73 s observed in human post-mortem glaucomatous TM tissues.
74  whereas mutations in transmembrane helices (TM), alphaTM2 and alphaTM4, abolish the stimulation of a
75 hanism, in particular transmembrane helices (TMs) 1a and 7 as well as extracellular loops (ELs) 2 and
76 ented with 0 (NTM), low (LTM) and high (HTM) TM levels in the same basal diet.
77 s9-mediated genome editing in cultured human TM cells and in a MYOC mouse model of POAG to knock down
78 rticoid (GC)-induced glaucoma, primary human TM cells and human post-mortem TM tissues, we show that
79                                Primary human TM cells grown on ECM derived from Dex-treated TM cells
80 o induced chronic ER stress in primary human TM cells.
81 ctorial fluid are significantly increased if TM thickness is decreased.
82 al fluid can cause small (<20%) decreases in TM wave decay constants.
83 tachment can cause small (<20%) increases in TM wavelength, and that viscous loss in the subtectorial
84  stress injury was confirmed by reduction in TM-induced cell death when CHOP was depleted in Parkin k
85   Herein, we report a novel finding that, in TM cells, TGF-beta-induced increase in collagen expressi
86                      In contrast, increasing TM thickness above its physiological range has little ef
87 usly reported performance of each individual TM.
88  Primary and Preschool Scale of Intelligence(TM)-III (WPPSI-III) and two scales of the Behavior Ratin
89 increased network formation by intercellular TMs, suggesting a functional and molecular heterogeneity
90 mor cells, however, had more interconnecting TMs, which were associated with increased radioresistanc
91 ectively inhibited the formation of invasive TMs and glioma growth, but increased network formation b
92       At the surface, transition metal ions (TM ions) are in a lower valence state than in the bulk,
93 on was utilized to demonstrate that isolated TM domains of Hendra virus F protein associate in a mono
94 lecular dynamics simulations of the isolated TM domain in explicit lipid bilayers coupled to thermody
95 two residues at the external end of the KCNE TM segments underlie differences in the effects of the d
96 as led to the dramatic acceleration of known TM-catalyzed reactions, as well as to the discovery of u
97  It has been well-established that the known TMs can be classified by the dimensionality of the topol
98 ltisensor radar and optical imagery (Landsat TM/PALSAR/RADARSAT-1/TPI image stack) for detecting peat
99  control can be maintained by replacing lost TM cells, we transplanted TM-like cells derived from ind
100  refractive indices the transverse magnetic (TM) and transverse electric (TE) polarized modes were ca
101                           A transfer matrix (TM) treatment is used to derive the reflectivity profile
102 a 14-d time interval between each test meal (TM).
103 s administered simultaneously with the meal (TM-2) (P = 0.046).
104                                         Mean TM heights in the POAG and PACG groups were 812 +/- 13 m
105 e cartridge was filled with transport media (TM) (sealed at its funnel and back entrance with a stopp
106 that wave motions of the tectorial membrane (TM) play a critical role in determining the frequency se
107 r the center of certain FliP trans-membrane (TM) segments are accessible to polar reagents.
108  pathway comprising the trabecular meshwork (TM) and Schlemm's canal (SC).
109 e previously shown that trabecular meshwork (TM) cells might detect aqueous humor fluid shear stress
110 cilin expression in the trabecular meshwork (TM) has been suggested to play an important role in GC-i
111         To determine if trabecular meshwork (TM) height differs between primary open-angle glaucoma (
112 x (ECM) proteins in the trabecular meshwork (TM) is associated with TM dysfunction and intraocular pr
113 e unlasered portions of trabecular meshwork (TM) of laser-treated primate eyes are understudied.
114                         Trabecular meshwork (TM) tissue in the eye is under constant mechanical stres
115 ulum (ER) stress in the trabecular meshwork (TM), the tissue that regulates IOP.
116 ts drainage through the trabecular meshwork (TM).
117       Employment of simple transition metal (TM = Co, Fe, Cu, Pd, Pt, Au)-based photocatalyst (PC) ha
118 l glasses arise from their transition metal (TM) impurities and capture information about ancient gla
119 coordination of first-row transition metals (TMs) to {P8W48} typically yields frameworks which extend
120  approach that combines Phenotype MicroArray(TM) and SSR genotyping appeared useful to assess the per
121 nt metabolic profile by Phenotype MicroArray(TM).
122                   Tocotrienol microcapsules (TM) were formed by firstly preparing Pickering emulsion
123 of glass slides from traditional microscopy (TM) in a large cohort of dermatopathology cases with att
124 ment, as a potent driver of tumor microtube (TM)-mediated brain colonization by glioma cells.
125  related extensions called tumor microtubes (TMs) reported in gliomas in vivo, has propelled this fie
126 ons) membrane protrusions [tumor microtubes (TMs)] extended by glioma cells.
127                              Trace minerals (TM) play a role in skin integrity and wound healing.
128 s metastasis [POM]; or treatment monitoring [TM]) and type of cancer (prostate, lung, breast, or othe
129                                    Moreover, TMs are also used by some tumor cells to interconnect to
130 primary human TM cells and human post-mortem TM tissues, we show that increased ECM accumulation lead
131 ghting the functional importance of the MPER/TM-FL interaction in EBOV entry and fusion.
132                 Transcriptional mutagenesis (TM) due to misincorporation during RNA transcription can
133  of the novel form of band crossing, the new TM cannot be described by the established results that c
134 confirmed to be a potent regulator of normal TM morphology and of TM-mediated tumor-cell invasion and
135 e continuous remodeling of ECM in the normal TM.
136  yields frameworks which extend through {W-O-TM-O-W} bridges in one, two, or three dimensions.
137                              The addition of TM into yogurt caused minimal changes in the yogurt's co
138 ent regulator of normal TM morphology and of TM-mediated tumor-cell invasion and proliferation.
139 ates actin dynamics and the contractility of TM cells, consistent with its regulation of actin-relate
140                                The degree of TM softening was consistent, regardless of pre-mortem cl
141 ry protein load of ECM proteins in the ER of TM cells, inducing ER stress.
142 tic potential to alleviating the fibrosis of TM in POAG patients.
143 ueous humor is the main cause of fibrosis of TM in POAG patients.
144     Recombinant APC and soluble fragments of TM (sTM) have been tested in settings associated with in
145           This study evaluated the impact of TM on FPD and consisted of 3 treatments supplemented wit
146                          Direct injection of TM should be avoided because of the presence of bovine s
147 onally generated three-dimensional models of TM alpha-helices positioned in membranes; (iv) amino aci
148 cal motions and slower collective motions of TM helices and of structured loops, and used the simple
149 se primary hepatocytes, and in the plasma of TM-treated C57BL/6 mice.
150   We previously designed a fusion protein of TM [single-chain variable fragment antibody (scFv)/TM] t
151  In this study, we examined the stability of TM during storage and when applied into a model food sys
152 approximation method that calculates TFEs of TM residues in TMBs accurately, with which depth-depende
153                    A better understanding of TM coordination to the {P8W48} ring may allow the target
154 rsity of such compounds, the coordination of TMs to the {P8W48} ring is poorly understood, and theref
155  which was highly expressed in a fraction of TMs in mice and patients.
156 highest in tests related to the outgrowth of TMs was tweety-homolog 1 (TTYH1), which was highly expre
157     The single mutants had a small effect on TM domain separation and cell death, whereas the double
158 t hair bundle stiffness has little effect on TM traveling waves calculated with physiological paramet
159 cts of this loss and other cochlear loads on TM traveling waves.
160 o probe the importance of the closed-to-open TM domain transition in the overall energetics of recept
161         However, the fate of the cleaved p75 TM domain is unknown.
162 receptor is necessary for the ability of p75 TM to induce TrkB phosphorylation.
163 ts indicated that a peptide representing p75 TM increases TrkB phosphorylation in a dose- and time-de
164 emical fractionation data suggested that p75 TM stimulates TrkB phosphorylation at the cell membrane.
165                 Here, we report that the p75 TM can stimulate the phosphorylation of TrkB (tyrosine k
166 nylalanine) in the predicted, tightly packed TM domain dimer interface.
167 .2%) when tea was administered 1 h postmeal (TM-3) than when tea was administered simultaneously with
168 -2), and with tea administered 1 h postmeal (TM-3).
169 his association, 140 paramyxovirus F protein TM domain sequences were analyzed.
170 be a promising target to specifically reduce TM-associated brain colonization by glioma cells in pati
171 ith alanine resulted in dramatically reduced TM-TM association.
172 r ring resonators, but to date NRPS requires TM-modes, so the TE-modes normally produced by integrate
173 e of the sterol rings apposed to methyl-rich TM residues.
174 urate marker for LC presence than these same TMs considered individually.
175 (BASC-2) and the Social Responsiveness Scale(TM)-2 (SRS-2).
176 ngle-chain variable fragment antibody (scFv)/TM] targeted to red blood cells (RBCs) to improve pharma
177                                         scFv/TM provided protection when injected after endotoxin, wh
178  similar to endogenous TM, RBC-anchored scFv/TM activates several protective pathways.
179 concomitantly with or before endotoxin, scFv/TM provided more potent protection against liver injury
180                                Finally, scFv/TM was more effective at reducing cerebral infarct volum
181                                   Here, scFv/TM was studied in mouse models of systemic inflammation
182                                However, scFv/TM injected after endotoxin did not reduce thrombin/anti
183 rophylactic anti-inflammatory effect of scFv/TM.
184 hese results indicate that RBC-targeted scFv/TM exerts multifaceted cytoprotective effects and may fi
185 arable to Modeller in terms of GDT-TS score, TM-score, and GDT-HA score, while the average RMSD was i
186 mbrane (TM) regions revealed that the second TM domain in the proposed 4-TM model of VKOR does not fu
187 fects of mutations at transmembrane segment (TM) 6 and 12 helices in HEK293 cells.
188           Topological metals and semimetals (TMs) have recently drawn significant interest.
189  combined assessment of a panel of six serum TMs is a more accurate marker for LC presence than these
190 nthetic methods used for the formation of Si-TM complexes, Section 3 provides an extended discussion
191 le of finding 93+/-2% of all highly similar (TM-score>0.7) structures in the PDB for each query struc
192 TM-1), with tea administered simultaneously (TM-2), and with tea administered 1 h postmeal (TM-3).
193 ect analysis in real time mass spectrometry (TM-DART-MS).
194 hase microextraction-transmission mode (SPME-TM) device made of poly(etheretherketone) (PEEK) mesh th
195 ase Micro Extraction-Transmission Mode (SPME-TM) is a technology conceived as an effective synergy be
196                                    PEEK SPME-TM devices proved to be robust and were therefore used t
197        This research highlights plastic SPME-TM's potential usefulness as a method for rapidly screen
198               In this study, we present SPME-TM as a novel tool for the ultrafast enrichment of pesti
199 tes according to the scheme (SU-TM)3 --> (SU-TM)2TM --> (SU-TM)TM2 --> TM3 This was the case both whe
200 o the scheme (SU-TM)3 --> (SU-TM)2TM --> (SU-TM)TM2 --> TM3 This was the case both when activation wa
201 er intermediates according to the scheme (SU-TM)3 --> (SU-TM)2TM --> (SU-TM)TM2 --> TM3 This was the
202      We followed the isomerization of the SU-TM disulfide and subsequent SU release from Env with bio
203  event in the transformation via a substrate-TM interaction, an aspect that is uncommon for conventio
204 ) and a fusion active transmembrane subunit (TM).
205  such as aerobic glycolysis, while memory T (TM) cells engage catabolic pathways, like fatty acid oxi
206  by at least a factor of 60, confirming that TM helix motions are linked to the citrate-binding event
207 (15)N NMR relaxation data and RDCs show that TM is highly ordered and uninterrupted for a total lengt
208                     Our findings showed that TM not only improved growth performance but also reduced
209                                          The TM domain of Lnt contains eight TM helices which form a
210                                          The TM was administered with water (TM-1), with tea administ
211 mposed of only a fluorescent protein and the TM helices of Tar to demonstrate that interactions betwe
212                 This is possible because the TM coordination sites of the {P8W48} ring are found, onc
213            Due to the difference between the TM and TE light propagation associated with the diffract
214  length of 250 mum was achieved for both the TM and TE guided modes at telecom wavelengths.
215   Beyond the glass chemical composition, the TM redox is also a key factor in the glass color, but it
216 trength might be necessary to facilitate the TM helix breaking and bending that is often needed to sa
217 in transmembrane (TM) domains implicated the TM domain in the fusion process, but the structural and
218  that equivalent F, D, and T residues in the TM domain of FcepsilonR1alpha markedly influence the bio
219 nerally, the tocotrienols were stable in the TM form and showed highest stability when these TM were
220 sure backbone hydrogen bond strengths in the TM helix of the amyloid precursor protein (APP).
221 agen I, and alpha-smooth muscle actin in the TM in mouse eyes.
222  showed increased myocilin expression in the TM on DEX-Ac treatment.
223 es of 20 amino acids at all positions in the TM region of OmpLA.
224  to endoplasmic reticulum (ER) stress in the TM.
225 he double mutant significantly increased the TM domain separation and more than doubled the sensitivi
226 ected and compensatory changes involving the TM in the NHP model of ExGl.
227 ive ECM remodeling can cause fibrosis of the TM as in primary open-angle glaucoma (POAG) patients, an
228 ion at i, i+4 positions at the center of the TM domain dimer eliminates the barrier and stabilizes th
229 nd aromatic residues along the length of the TM domain.
230 ity connected to the periplasmic exit of the TM domain.
231  obtained in the presence and absence of the TM electrical potential.
232 de of motions on the cytoplasmic side of the TM helices correlates with the ability of ASR to undergo
233 ter depends on the sequence or length of the TM helices, implying that certain conformations of these
234 d are dominant in the middle portions of the TM helices.
235 ionally, the N- and C-terminal halves of the TM helix form trimeric cores of opposite nature (hydroph
236 nce of an arginine R696 in the middle of the TM helix.
237 enough to maximize the spatial extent of the TM traveling wave.
238 ttle effect on the wave, suggesting that the TM is just thick enough to maximize the spatial extent o
239 imal external region (MPER) connected to the TM domain: i.e., the missing parts of the EBOV GP2 struc
240 e photoexcitation/catalytic cycle, where the TM complex plays a "double duty" role by harvesting ligh
241 tion of the P1 domain dipole moment with the TM electrical field considerably lowers the free-energy
242 bilized by hydrophobic interactions with the TM helix and polar and aromatic interactions with neighb
243 g between native E. coli receptors, with the TM sequence of better-clustering high-abundance receptor
244 relies on a conformational change within the TM domain of PhoQ induced by a perturbation in cell memb
245 otrienols were incorporated into yogurt, the TM and bulk oil forms showed a loss of 23.5% and 81.0%,
246                                  Also, these TM photocatalysts participate in the bond-forming/breaki
247 sment of dimerization heterogeneity of these TM domains demonstrated that 7 of them have a unique dim
248 form and showed highest stability when these TM were added into yogurt.
249         In addition, nine novel thiomarinol (TM) derivatives with different oxidation patterns decora
250                  Endothelial thrombomodulin (TM) regulates coagulation and inflammation via several m
251        Here we discuss the concept that TNTs/TMs fill an important niche in the ever-changing microen
252 e approximately 3 kcal/mol energy barrier to TM domain opening and the approximately 2 kcal/mol energ
253   Importantly, this softening is contrary to TM stiffening reported in glaucomatous human eyes.
254 st that the heptad repeat LIZ contributed to TM-TM association and is important for F protein functio
255 not understood how ECM accumulation leads to TM dysfunction and IOP elevation.
256 d CHOP levels and enhanced susceptibility to TM-induced cell death.
257 mation, in vitro assay data (including Tox21(TM)/ToxCast high-throughput screening data), and in sili
258  strategies to search for mediators of trans-TM transport.
259 e nitrilase domain fused to a transmembrane (TM) domain.
260 tein that results in Abeta, a transmembrane (TM) peptide.
261 between the lipid bilayer and transmembrane (TM) helices of Escherichia coli chemoreceptors alone are
262 ling of single-pass (bitopic) transmembrane (TM) proteins and their complexes by providing structural
263 parallel homodimers formed by transmembrane (TM) alpha-helices.
264 acid residues in the disputed transmembrane (TM) regions revealed that the second TM domain in the pr
265 l dynamics of a seven-helical transmembrane (TM) protein, Anabaena Sensory Rhodopsin (ASR) reconstitu
266 gh backbone hydrogen bonds in transmembrane (TM) helices have the potential to be very strong due to
267 ening of the disulfide-linked transmembrane (TM) dimer.
268 p (ECL) and adjacent parts of transmembrane (TM) segments.
269  dissected its four predicted transmembrane (TM) segments.
270        Mutations in F protein transmembrane (TM) domains implicated the TM domain in the fusion proce
271        We find that the seven-transmembrane (TM) receptor conserved disulfide bridge (7TM bridge) lin
272 lesterol binds the C-terminal transmembrane (TM) residues, near an amphipathic helix, without requiri
273 ough current models place the transmembrane (TM) and FL domains of GP2 in close proximity at critical
274  presenilin enhancer 2 in the transmembrane (TM) domain.
275 the signal transmitted to the transmembrane (TM) helices in a CitA construct in liposomes.
276 affected by the length of the transmembrane (TM) helix as well as by membrane lateral pressure.
277 the membrane, maintaining the transmembrane (TM) potential, and facilitating the ATP-independent stag
278 ies (TFEs) of residues in the transmembrane (TM) region provides fundamental quantifications of therm
279 mutation in the middle of the transmembrane (TM) segment of KCNE3 introduces KCNE1-like effects on th
280 pressive domain (ISD), in the transmembrane (TM) subunit of the envelope glycoprotein and identified
281 partic acid residues in their transmembrane (TM) domains that mediate assembly, via interaction with
282  by replacing lost TM cells, we transplanted TM-like cells derived from induced pluripotent stem cell
283  cells grown on ECM derived from Dex-treated TM cells induced ER stress markers.
284 tructure, prevented ER stress in Dex-treated TM cells.
285 dia from both thapsigargin- and tunicamycin (TM)-treated HuH7 cells, mouse primary hepatocytes, and i
286 load or in response to systemic tunicamycin (TM) developed adverse ventricular remodeling with excess
287                 Glioma cells with one or two TMs were mainly responsible for effective brain coloniza
288 rthermore, microscopic analysis of unlasered TM from eyes with ExGl demonstrated TM thinning with col
289                       Softening of unlasered TM in ExGl eyes compared to untreated controls was obser
290 the reconstructed models are evaluated using TM-score.
291                            Experiments using TM domains from other receptors, EGFR and FGFR1, failed
292 ivalent to diagnosis from glass slides using TM in this statistically powerful study of 499 dermatopa
293 rimental structures of bitopic proteins; (v) TM topology and intracellular localization, (vi) physica
294          The TM was administered with water (TM-1), with tea administered simultaneously (TM-2), and
295 e derived from the same base glass, to which TMs were deliberately added.
296 ot hold true for receptors like CD16A, whose TM domains do not contain basic residues.
297  trabecular meshwork (TM) is associated with TM dysfunction and intraocular pressure (IOP) elevation
298 the workflow efficiency of WSI compared with TM.
299 e with WSI experience, achieving parity with TM by the most experienced user.
300  Mean interobserver concordance between WSI, TM, and GTC was 91%.
301                            Intraobserver WSI/TM diagnoses were compared, followed by interobserver co

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