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1 nicking the DNA at multiple sites around the mismatch.
2 e mobile clamp that no longer recognizes the mismatch.
3 L MMR initiation complexes localize near the mismatch.
4 -FLAIR mismatch, and 54 (13%) only a PWI-DWI mismatch.
5 ting a correct nucleotide over a single-base mismatch.
6 -cognate recognition pairs with at least one mismatch.
7  a transplant from a donor with a >1 antigen mismatch.
8 licenses the MutS mobile clamp to rebind the mismatch.
9 tion then accelerated, but could not prevent mismatch.
10 paced seeds, which are capable of tolerating mismatches.
11  15-21 are largely intolerant of target site mismatches.
12 f the specific base composition of crRNA-DNA mismatches.
13 on in species' niches and niche-distribution mismatches.
14 B ranges between 10(-4)-10(-9) for different mismatches.
15 VHD increased with increasing numbers of HLA mismatches.
16 al dynamic motions associated with base pair mismatches.
17 vely distinguish and reject single base-pair mismatches.
18  HLA-A, HLA-B, HLA-C, HLA-DRB1, and HLA-DQB1 mismatching.
19 longer than the dynamic motions of base pair mismatches (0.1-10 ns).
20 , van der Waals force(13), thermal expansion mismatch(14), and heat-induced substrate phase transitio
21              Of these, 57 (13%) had a double mismatch, 151 (35%) only a DWI-FLAIR mismatch, and 54 (1
22 D for the following reasons: cytomegalovirus mismatch (18.5% [10/54]), Epstein-Barr virus (EBV) misma
23 ellent selectivity towards one- and two-base mismatches (1MM, 2MM) or scrambled (SCR) sequences was h
24  reasons for inappropriate use were bug-drug mismatch (27.7%), surgical prophylaxis > 24 hours (17.7%
25 AIR mismatch was more prevalent than PWI-DWI mismatch (48%, 95% confidence interval [CI] = 43-53% vs
26 (EBV) mismatch (EBV) (9.3% [5/54]), age/size mismatch (51.9% [28/54]), or altruistic reasons (20.3% [
27  exposure, potentially creating phenological mismatches(7).
28 SW utilization was 20.4%, with more zero HLA mismatch (8% vs 4%), living donors (26% vs 20%), and lym
29     The provoking mechanism of supply/demand mismatch affects long-term survival.
30  to understanding of how the identity of the mismatch affects the substrate channeling of the repair
31 ation of MutS such that it can recognize the mismatch again instead of bypassing it; thus, ATP hydrol
32 ered to be as important as the leader of the mismatched allotype for GVHD.
33  ecological rates of change, seeks to reduce mismatch among climate and ecological rates of change, a
34 lance gradient and found high variability in mismatches among species and among performance measures,
35                                    Molecular mismatch analysis for assessment of histocompatibility i
36      Recipients who entered KPD for age/size mismatch and altruistic reasons received kidneys from do
37  pDC viability, immaturity, and class II MHC mismatch and blocked by MEK/ERK and NFkappaB inhibition.
38 plementary, single-base mismatch, three base-mismatch and non-complementary oligonucleotides.
39 ggest MutSalpha localizes MutLalpha near the mismatch and promotes DNA configurations that could enha
40 ncorporation step and those that accommodate mismatches and lesions during the extension reaction.
41  chronic changes are not associated with HLA mismatches and may be due to non-immunologic causes (hyp
42 PPO)]Cl(2) (Rh-PPO), specifically target DNA mismatches and selectively induce cytotoxicity within MM
43 erize position-dependent effects of sequence mismatches and show how DNA supercoiling modulates the e
44 sts lack consensus on the prevalence of such mismatches and their underlying mechanisms.
45  double mismatch, 151 (35%) only a DWI-FLAIR mismatch, and 54 (13%) only a PWI-DWI mismatch.
46 nge in the impact of climate-induced trophic mismatch, and evidence that shags are tracking long-term
47 eas, percentage of severe prosthesis-patient mismatch, and left ventricular mass regression were simi
48 his phase 1 and 2 trial, we administered HLA-mismatched anti-CD19 CAR-NK cells derived from cord bloo
49 nclear how relevant these niche-distribution mismatches are for biodiversity dynamics and how they de
50 d, the regulatory factors that underlie such mismatches are poorly understood.
51 age by electron transfer and identifies size-mismatch as an important concept in control of electroni
52 atory bird species to encounter phenological mismatches as vegetation phenology responds to climate c
53  The percentage of severe prosthesis-patient mismatch at 30 days was low and similar between TAVR and
54 e spectrum range due to tremendous impedance mismatch at stable air/water interfaces, viz., the Cassi
55 The results suggest that the tissue property mismatch at the gray-white matter interface places axons
56 pSGN system was sensitive to the single base mismatch at the position next to the hairpin both in vit
57  unrelated donor (fully matched or one-locus mismatched at HLA-A, HLA-B, HLA-C, or DRB1 loci) graft f
58 nce of transfused semiallogeneic donor cells mismatched at major histocompatibility class I can enhan
59 d waves suffer from absorption and impedance mismatches at biological interfaces.
60                                   By placing mismatches away from duplex ends, the thermodynamic driv
61 e of efficiency for incorporation of various mismatched base pairs and have uncovered a mechanism in
62                                    In SaMBA, mismatched base pairs are introduced to pre-induce struc
63 cal-mechanical theory to study the effect of mismatched base pairs on DNA supercoiling.
64  WIF confidences can be used to evaluate the mismatch between computational models and imaging data,
65 of the Dot/Icm T4SS that includes a symmetry mismatch between distinct structural features of the out
66  niche, while also suggesting a recalcitrant mismatch between E. coli physiology and growth on citrat
67 -Benard instability, these rely on a density mismatch between layers of the fluids.
68 ures initiated in layer 2/3 due to a dynamic mismatch between local PNs and inhibitory INs, and only
69 esent a conceptual framework to quantify the mismatch between optimal conditions for species occurren
70 ulated closed-loop performance was robust to mismatch between plant and controller.
71 icates how this flexibility accommodates the mismatch between the 3- and 10-fold symmetries of the F(
72  scarcity of high-quality annotated data and mismatch between the development dataset and the target
73                                 We show that mismatch between the nature of the generating (i.e. biol
74 ain away' connections occurs when there is a mismatch between the true network dynamics and the model
75                                 An antigenic mismatch between the vaccine and circulating H3N2 strain
76 as raised concern that 2020 would also see a mismatch between the winner of the popular vote and the
77 h the OMC and the PR and bridge the symmetry mismatch between these regions.
78  quantify the magnitude of resultant trophic mismatches between aphids and their plant hosts and para
79                                              Mismatches between generating and analytical equations c
80 ogical trap is contributing significantly to mismatches between habitat selection and demographic pro
81 nd understanding the consequences of thermal mismatches between host and parasites.
82                     Identifying such habitat mismatches between selection and survival facilitates de
83                         Higher number of HLA mismatches between the VA donor and the recipient, and d
84 oughput assay that we term SaMBA (saturation mismatch-binding assay) to investigate the role of DNA c
85       Study of the neural deficits caused by mismatched binocular vision in early childhood has predo
86 t evolution can help correct cue-environment mismatches but not in the same way under all conditions.
87                        While large impedance mismatch can be readily realized in an air environment,
88                            However, symmetry mismatch can prohibit vaccine nanoassembly.
89  revealing an all-or-nothing mechanism where mismatches can be bound, but not cleaved.
90      Finally, ASOs with strategically placed mismatches can be used to reduce unwanted off-target spl
91 recognition, and reveals mechanisms by which mismatches can recruit transcription factors and thus mo
92 ) but not wild-type mice receiving fully MHC-mismatched cardiac transplants became tolerant and showe
93                                      Trophic mismatches caused by changes in consumer energetics duri
94 itive and negative signs of the linear phase mismatch close to the phase-matching condition.
95  ClpP rings, it remains unknown how symmetry mismatched ClpX and ClpP work in tandem for processive s
96 progress in the development of HLA molecular mismatch computational scores as a potential prognostic
97 rget miRNA-21 from its single- and four-base-mismatched counterparts and another non-complementary mi
98 es its residence time in the vicinity of the mismatch, coupled with MutL's ability to trap MutS, shou
99 rejection and BKVAN, human leukocyte antigen mismatch, cyclosporine therapy, and indication biopsy fo
100 es in southern populations show the greatest mismatch despite possessing exaggerated traits, with som
101 ocessing of Perfusion and Diffusion software mismatch determination).
102 sitoids, and then model the impacts of these mismatches, direct weather effects and density dependenc
103                                   Damaged or mismatched DNA bases result in the formation of physical
104 a high selectivity that discriminates single-mismatched DNA from fully matched target DNA under optim
105 tch in a sensitized patient is attributed to mismatched donor HLA.
106 r-specific antibodies (DSA) directed against mismatched donor human leukocyte antigen (HLA) is a majo
107                          The preferred HLA-B-mismatched donor is leader-matched and shares a T leader
108         On univariate analysis, pre-HCT AIC, mismatched donor, alemtuzumab, anti-thymocyte antiglobul
109 % versus 14.8%, P<0.01), and 67.4% were size mismatched (donor weight >130% of recipient).
110                             Use of 1-antigen-mismatched donors was associated with reduced OS and EFS
111 ch (18.5% [10/54]), Epstein-Barr virus (EBV) mismatch (EBV) (9.3% [5/54]), age/size mismatch (51.9% [
112 ge, owing to the absence of suitable lattice-mismatched epitaxial substrates.
113  fundamentally unavoidable in highly lattice-mismatched epitaxy(9-11).
114 ry based on point-by-point assessment with a mismatch error of 7.0%.
115    Our data provide contemporary data on sex mismatch for recipient counseling and reassurance with r
116                          We quantified these mismatches for 59 tree species in the western US along a
117  of portal morphs to compensate for symmetry-mismatch, forming similar interactions in different caps
118 lated HCT and differentiates high-risk HLA-B mismatches from those with lower risk.
119                                       Single mismatches generally reduce knockdown to a modest degree
120 uating environments can give rise to trophic mismatches governing the emergent effects of global chan
121   Older patients and recipients of 1-antigen-mismatched grafts had a less favorable outcome.
122 ion where early rejection of immunologically mismatched grafts is driven by the recipient's natural k
123             Unexpectedly, only minor antigen-mismatched grafts were rejected at the same time points
124       We suggest that this nutrition-related mismatch has contributed to the widespread, ~50% decline
125                                 SA due to RI mismatches has many deleterious effects on imaging.
126 g center effects identified four or more HLA mismatches (hazard ratio [HR], 2.06; P <= 0.01) as assoc
127 ould be reduced to <70% in HLA class I or II mismatched HCT.
128 oablative conditioning for HLA class I or II mismatched hematopoietic cell transplantation (HCT).
129                        Whether reexposure to mismatched HLA antigens (RMM) in the setting of a negati
130                                    The match-mismatch hypothesis (MMH) suggests that trophic asynchro
131  on our results, we introduce the Inactivity Mismatch Hypothesis and propose that human physiology is
132 e context of trophic interactions, the match-mismatch hypothesis postulates that differential shifts
133 s, respectively, as predicted by the thermal mismatch hypothesis.
134 nator systems may be susceptible to temporal mismatch if bees and flowering plants differ in their ph
135 americ ClpP surface with the empty, symmetry-mismatched IGL pocket maintained at the seam.
136 T across an major histocompatibility class I mismatch in an unmanipulated B6 host.
137 iodic reaction norm has compensated for this mismatch in Colias eurytheme.
138 eved through the introduction of a base-pair mismatch in the duplex of the hairpins.
139 tes existing shunt and ventilation-perfusion mismatch in the model, the reported hypoxemia severity i
140 bute to male reproductive aging but reveal a mismatch in their aging patterns.
141 -fluid-attenuated inversion recovery (FLAIR) mismatch in WAKE-UP who underwent PWI.
142 ne conjugate (Z1) functions by targeting T:T mismatches in CTG trinucleotide repeats that are respons
143                                              Mismatches in other loci seem to have less effect.
144             Interhomolog polymorphism causes mismatches in recombining molecules, which can be detect
145 isingly ambiguous, and there are predictable mismatches in risk perception between laypeople and expe
146  has been consistently underestimated due to mismatches in space, scale, time, and weather variable t
147 tion are important mechanisms when involving mismatches in the displacement process.
148 we use field surveys to demonstrate seasonal mismatches in the exposure of marine consumers to low pH
149                            We speculate that mismatches in the opposing actions on dendritic excitabi
150 n of new sequence-specific ligands targeting mismatches in the repeat-associated structures.
151 A signal as a strategy to indicate potential mismatches in the target sequence.
152 of pulmonary embolism, ventilation-perfusion mismatching in the noninjured lung, and normal perfusion
153                Notably, approximately 10% of mismatches increased transcription factor binding, and f
154 is consistent with computational accounts of mismatch-induced memory updating.
155  replication errors (i.e. ribonucleotide and mismatch insertions).
156  products for over 10,000 targets containing mismatches, insertions and deletions relative to the gui
157 between portal and capsid, across a symmetry-mismatched interface.
158 ch as lithium polysulfide shuttling effects, mismatched interfaces, Li dendrite growth, and the gap b
159  time of onset with a DWI-FLAIR or perfusion mismatch, intravenous alteplase resulted in better funct
160                          The effect of eplet mismatch is well documented in renal and lung transplant
161 ition of a genome while allowing for up to e mismatches is computationally challenging.
162 D20 antibody, prior to receiving MHC class I-mismatched (K(d) ) skin.
163  airway inflammatory cells isolated from sex-mismatched lung transplant recipients.
164 observations support the notion that PPR-RNA mismatches may be essential for proper function of editi
165                                         This mismatch might be because current theory is not clear ab
166 acids of the HLA molecule-instead of antigen mismatches might offer a better approach to assessing do
167 ze the dynamics of OX40 expression in an MHC-mismatch mouse model of acute GvHD using OX40-immunoPET.
168 s possibility, we utilized a full allogeneic mismatch murine transplant model and T follicular helper
169  association between functional outcomes and mismatch negativity (MMN) activity in participants with
170 ry speech discrimination ability [indexed by mismatch negativity (MMN) responses].
171         Among the measures studied, P300 and mismatch negativity are notable because deficits predict
172 ce processing was associated with the visual mismatch negativity independently of consciousness and t
173 rontotemporal networks, including an evoked 'mismatch negativity' response and transiently induced os
174 0.50, -0.29), automatic auditory processing (mismatch negativity), g = -0.44, 95% CI (-0.66, -0.22),
175 easures include task-based fMRI (RISE task), mismatch negativity, the Scale for the Assessment of Neg
176 hese disruptions on auditory discrimination (mismatch negativity; MMN) responses to phoneme and tone
177 the capacity of CoVs to proofread and remove mismatched nucleotides during genome replication and tra
178 s in blood type compatibility, degree of HLA mismatch, number of veins/arteries, cold ischemia, and t
179 uid metal eliminates the issue of compliance mismatch observed in soft polymers with solid fillers.
180 sease (PD) in the context of an evolutionary mismatch of central nervous system functions.
181 ction and tissue pathology can result from a mismatch of oxygen supply and demand.
182 emains elusive due to insufficient impedance mismatch of state-of-the-art metamaterials.
183                 It is observed that the size mismatch of the mixed "A" site composition films and dev
184 or genomic searching with DNA/RNA bulges and mismatches of arbitrary size as specified by the user as
185        In kidney transplantation, evaluating mismatches of HLA eplets-small patches of surface-expose
186 ave a better distinction against single-base mismatch oligonucleotide sequences compared to the compe
187  comprising three to eight proteins around a mismatch on DNA.
188             To better evaluate the impact of mismatches on DNA target recognition and binding, we dev
189 ariate regression models for the role of HLA mismatching on outcome.
190 rast, the local destabilization induced by a mismatch or an abasic site restores a strong dependence
191 ld-type and Mdr2(-/-) mice were treated with mismatch or H2HR vivo-morpholino by tail vein injection
192                 We found that TERT inserts a mismatch or ribonucleotide ~1 in 10,000 and ~1 in 14,000
193 fusion defects, severe ventilation-perfusion mismatch, or hyperperfusion of nonoxygenated regions.
194 pairing discrimination between C:G and other mismatched pairs like C:A, C:T and C:C.
195 ally correctable (e.g., lack of transport or mismatched patient expectations).
196 ment modes and affine gap and quality-scaled mismatch penalties, it can implement the scoring functio
197 nterspecific variation in niche-distribution mismatches: poorer dispersers are absent from larger par
198 n the sub-sequence feature length, number of mismatch positions, and the task's alphabet size.
199 endent counting operations over the possible mismatch positions.
200                    Using competing match and mismatch probes, Zombie can accurately discriminate sing
201                        To eliminate the feed mismatch problem, the quasi-conformal transformation opt
202 ional cerebral blood flow (<30%) < 70ml with mismatch ratio >= 1.2 and mismatch volume >= 10ml).
203 ion event, MutS undergoes frequent cycles of mismatch rebinding and mobile clamp reformation without
204 tion into ABO-compatible, nonsensitized, MHC-mismatched recipients.
205         Dominant MMR models posit that after mismatch recognition, ATP converts MutS to a hydrolysis-
206 he activity of 24,460 gRNAs with and without mismatches relative to the target sequences.
207 minase activity (COSMIC signature 2) and DNA mismatch repair (COSMIC signature 6).
208                                Deficient DNA mismatch repair (dMMR) induces a hypermutator phenotype
209                                          DNA mismatch repair (MMR) corrects errors that occur during
210 aberrations, most notably BRCA1/2 mutations, mismatch repair (MMR) deficiencies or NTRK1-3 fusions, h
211  Lynch syndrome is caused by variants in DNA mismatch repair (MMR) genes and associated with an incre
212  in strains lacking Poldelta proofreading or mismatch repair (MMR).
213 essing POLE tumor variants, with and without mismatch repair (MMR).
214  repeat expansion without impeding canonical mismatch repair activity.
215 s are low-fidelity replication, insufficient mismatch repair and increased double-strand breaks.
216 ith consideration in HOXB13, BRCA1, ATM, and mismatch repair carriers.
217 pair complex, Rad10-Rad1(ERCC1-XPF), and the mismatch repair complex, Msh2-Msh3, are required for Z-D
218 neoantigens in hypermutated cancers with DNA mismatch repair deficiency (dMMR) are proposed as the ma
219  should be offered somatic tumor testing for mismatch repair deficiency (dMMR).
220                                              Mismatch repair deficient (dMMR) gastro-oesophageal aden
221 computed tomography (CE-CT) can identify DNA mismatch repair deficient (MMR-D) and/or tumor mutationa
222 and 1 expression, microsatellite-high and/or mismatch repair deficient (MSI-H/MMR-D) status, and soma
223 of-function missense variants in the key DNA mismatch repair factor MSH2.
224   Recent genetic evidence indicates that the mismatch repair factor MutSbeta (Msh2-Msh3 complex) and
225 nts with pathogenic germline variants in DNA mismatch repair genes.
226                          Inactivation of DNA mismatch repair propels colorectal cancer (CRC) tumorige
227 bust lymphocytic infiltrate, such as loss of mismatch repair protein expression or expression of Epst
228  which can be detected by MutS homolog (MSH) mismatch repair protein heterodimers.
229                                     POLE and mismatch repair protein-encoding genes were mutated at l
230 orectal tumors that had normal expression of mismatch repair proteins (validation cohort).
231 r programmed cell death ligand 1 (PD-L1) and mismatch repair proteins MutL homolog 1 (MLH1), MutS hom
232 gender, age, tumor location, tumor grade, or mismatch repair status in any cancer stage.
233 tS homolog 2 (MSH2), MSH6, and PMS1 homolog, mismatch repair system component 2 (PMS2) was performed.
234 e frequently in isolates with defects in DNA mismatch repair that confer an elevated mutation rate.
235 r resolution and the initiation steps of DNA mismatch repair(12,13) and evoke a novel model for cross
236 otide excision repair, base excision repair, mismatch repair, and DNA double-strand break repair.
237 tly contribute to genetic instability in DNA mismatch repair-defective human tumors.
238 esting for microsatellite instability and/or mismatch repair-deficiency (MSI/IHC) and clinical predic
239 charomyces cerevisiae that are deficient for mismatch repair.
240 ndreds of randomly selected clones from both mismatch-repair-deficient and -proficient populations.
241 ts to explain the fitness difference between mismatch-repair-deficient and -proficient strains.
242                 Although PD-1 inhibitors for mismatch-repair-deficient tumours and NTRK inhibitors fo
243 ication and to inactivation of genes such as mismatch-repair-related genes.
244 implemented in C++ to compute supermaximal k-mismatch repeats directly, and show that these elements
245 as 0.84 and 0.82 for HLA-DR and HLA-DQ eplet mismatches, respectively.
246  switching among diverse strains, phenotypic mismatches resulting from divergence of secondary symbio
247                              Relative to sex-mismatched scores, sex-matched polygenic hazard scores s
248 tients with suspected CTEPH, the presence of mismatched segmental defects being consistent with the d
249  motor areas, presumably reflecting an early mismatch signal and subsequent top-down influences inclu
250 ulations show that plectoneme pinning at the mismatch site is deterministic under conditions of relat
251 d the pinning probability increases with the mismatch size.
252 over the patterned substrate/crystal lattice mismatch, something not yet realized for any epitaxy pro
253 of 208 randomized patients with PWI, PWI-DWI mismatch status did not modify the treatment response (p
254                            However, a strong mismatch still exists between our expectations and the r
255 se diagrams dependence on the film-substrate mismatch strain, concentration of defects, and Vegard co
256  predetermined angles of the ligands and the mismatched structural tensions created from the multi-la
257 th syngenic MHC-matched and in allogenic MHC-mismatched studies as C57BL/6 (H-2(b)) and BALB/cBy (H-2
258 hrough an interface of refractive index (RI)-mismatched substances (i.e., a discrepancy between the R
259  time, conventional heteroepitaxy of lattice-mismatched systems produces dislocations above a critica
260 ound that xCas9 has the lowest tolerance for mismatched target sequences and that SpCas9-NG has the b
261 ctural analyses, showed that many of the DNA mismatches that increase binding induce distortions that
262 dent on whether the TMS frequency matched or mismatched the expected underlying task-driven oscillati
263 e spatial distribution of healthcare demands mismatches the post-earthquake capacities of hospitals,
264            Overall, the large variability in mismatches, their costs and the relationship with functi
265 Overall, our results are compatible with the mismatch theory for ADHD but suggest a much older time f
266 analyte over full complementary, single-base mismatch, three base-mismatch and non-complementary olig
267                           Previously defined mismatch thresholds stratified recipients into low- (N =
268 ystem in which MHC-matched but minor antigen-mismatched tissue (skin) grafts were transplanted into M
269 which has low sensitivity, probably due to a mismatch to circulating SARS-CoV-2 in the reverse primer
270  waveguiding, which requires large impedance mismatches to realize total side reflection with negligi
271 -adapted system via sequence specialization, mismatch tolerance, and selective regulation to avoid to
272                         When considering HLA-mismatched transplantation for Hodgkin or non-Hodgkin ly
273  were not detected only in the minor antigen-mismatched transplantation.
274 roembolic type 1 MI (T1MI) and supply-demand mismatch type 2 MI (T2MI).
275 y and long-term outcome in matched (MUD) and mismatched unrelated donor (mMUD) setting is not well de
276 ny age with a haploidentical relative or HLA-mismatched unrelated donor and patients age 13 years or
277 e HLA-B leader informs GVHD risk after HLA-B-mismatched unrelated HCT and differentiates high-risk HL
278 of the leader dimorphism in GVHD after HLA-B-mismatched unrelated HCT.
279                         However, the mean of mismatches VerEp in locus C (VerEpC) was significantly i
280 (<30%) < 70ml with mismatch ratio >= 1.2 and mismatch volume >= 10ml).
281                    The accuracy of DWI-FLAIR mismatch was 68.8% (95% confidence interval [CI] = 53.7-
282                    The ventilation-perfusion mismatch was elevated (median, 34% [32-45%] of lung unit
283 ion factors that were examined, at least one mismatch was found that increased the binding affinity.
284 in the diet, as would be expected if trophic mismatch was increasing.
285                                    DWI-FLAIR mismatch was more prevalent than PWI-DWI mismatch (48%,
286 fication of antibody-verified eplets (VerEp) mismatch was performed with HLA-matchmaker 2.1 version.
287  association with DQ antibody-verified eplet mismatches was linear, without a safe threshold at which
288                           To understand this mismatch, we conducted a large-scale predation experimen
289                      Cytomegalovirus and EBV mismatch were avoided in 90% (9/10) and 100% (5/5) of ca
290 id attenuated inversion recovery (DWI-FLAIR) mismatch were eligible.
291 ear whereas AR and severe prosthesis-patient mismatch were not.
292 te to severe AR or severe prosthesis-patient mismatch, were associated with increased risk of the com
293 stic energy of the dopant due to cation size mismatch, which also promotes the reaction of the dopant
294             MutS's frequent rebinding of the mismatch, which increases its residence time in the vici
295 ion in NiTi to accommodate stress and strain mismatch with deformation.
296 ave behind it a string of "wrong" spins that mismatch with the antiferromagnetic background.
297 fficacy of LAIV is affected by the degree of mismatch with the currently circulating influenza strain
298  Migrating deer did not experience a trophic mismatch with the green wave during drought.
299  were adversely impacted by the magnitude of mismatch with their host plants or parasitoids, or direc
300  forward reaction rates: the introduction of mismatches within the initial duplex.

 
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