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1 e to hypoxia, with these events conferring a selective advantage.
2 viruses that acquire these mutations have a selective advantage.
3 lls with more robust SMAD5 expression have a selective advantage.
4 er periods of starvation, providing a strong selective advantage.
5 when retaining memory of the past provides a selective advantage.
6 CTL recognition, providing the virus with a selective advantage.
7 energy as fat between famines would be at a selective advantage.
8 y arise early during tumorigenesis or confer selective advantage.
9 ul conditions specific aneuploidies confer a selective advantage.
10 reduction in bicarbonate demand may confer a selective advantage.
11 ean populations, suggesting that they confer selective advantage.
12 ispensable residue that appears to confer no selective advantage.
13 aptation is due to new mutations of definite selective advantage.
14 y, a limited number of mutations that confer selective advantage.
15 or other properties of this motif, provide a selective advantage.
16 hancers in CRC tumor epigenomes to provide a selective advantage.
17 ility, whereby the PNH clone does not have a selective advantage.
18 iolent intrasexual competition giving them a selective advantage.
19 nments where biofilm formation may provide a selective advantage.
20 f the substrate that previously conferred no selective advantage.
21 sR mutant, loss of flagella did not confer a selective advantage.
22 in vivo, demonstrating tumor PD-L1 confers a selective advantage.
23 erved, suggesting that the process confers a selective advantage.
24 s were most frequently mutated, suggesting a selective advantage.
25 oss of chromosomes by cancer cells confers a selective advantage.
26 in the altered tumor environment, suggesting selective advantage.
27 y some treatment while some subclones gained selective advantage.
28 ether it may result from or confer an innate selective advantage.
29 f-function or regulatory mutations may be of selective advantage.
30 ns, suggesting that the P53 mutations confer selective advantage.
31 lative to 614D in a manner consistent with a selective advantage.
32 ier hypotheses that such diversity confers a selective advantage.
33 ge is minimal, faster growing fibrils have a selective advantage.
34 maintaining biological fitness and gaining a selective advantage?
35 might be driven by a cell-envelope mediated selective advantage across diverse chemical compounds.
36 how that, in addition, mecA provides a broad selective advantage across diverse chemical environments
37 of the Nebraska Sand Hills provides a strong selective advantage against visually hunting predators.
39 tion and progression, cancer cells acquire a selective advantage, allowing them to outcompete their n
40 a model that virulent X. nematophila have a selective advantage and accumulate in aging IJs in advan
41 e persistent IL-15Ralpha expression are at a selective advantage and become founder cells, outgrow ot
42 The cells were isolated regardless of their selective advantage and differed only by the site of HPV
43 alled alginate provides P. aeruginosa with a selective advantage and facilitates survival in the CF l
44 We propose that this effect is linked to selective advantage and identify potential driver genes.
45 se "new" substitutions that enhance both the selective advantage and kinetic constants are positioned
47 tein, mediated by binding to GAGs, determine selective advantage and plaque size in BHK-21 cells, lev
48 Deletion of Trp53 in gastric cells confers a selective advantage and promotes the development of dysp
51 in which transgenes are predicted to confer selective advantages and disadvantages to recipient host
52 d fitnesses of clone variants, measure their selective advantages and order of appearance by fitting
53 ive to those that invoke external factors or selective advantage, and represents a null hypothesis fo
55 ate of the hypermutators was governed by the selective advantage arising from a reduced mutation rate
56 molecular mimicry (1) shows a key potential selective advantage arising from the partitioning of aaR
57 hat the new viral strains gained a potential selective advantage as a consequence of the acquired tra
58 rld to the New World and may have provided a selective advantage as begomoviruses adapted to a differ
59 Such chromosomal clustering may confer a selective advantage as it enables coordinated gene regul
61 We found that serotinous individuals have a selective advantage at high fire frequencies and low pre
62 New antigenic variants have a substantial selective advantage at the population level, but these v
63 (2) WASp(+) murine B cells exhibit a marked selective advantage beginning at the late transitional B
64 genetic and epigenetic changes that confer a selective advantage but also need strategies to avoid im
65 ke protein variant D614G are suggestive of a selective advantage but may also be due to a random foun
66 e case of variants conferring a heterozygous selective advantage, but a homozygous disadvantage, as i
67 ns that exist in larger numbers experience a selective advantage by being more stochastically robust
69 that a "synthetic" genetic code can confer a selective advantage by increasing the number of function
70 tibiotic-producing microorganisms can gain a selective advantage by inhibiting nearby competing speci
71 this interaction might explain the mutant's selective advantage by means of repression of stem cell
73 lon carcinoma, may confer tumor cells with a selective advantage by providing a mechanism for blockad
75 codon reassignments would have a significant selective advantage compared to hosts utilizing the univ
76 gly, spirochetes containing lp28-3 were at a selective advantage compared to lp28-3-deficient spiroch
78 multiple spindles coupled with a subsequent selective advantage conferred by at least some aneuploid
79 enged with WT vs. H28-A2 escape mutants, the selective advantage conferred by glycan-mediated global
80 AKT are downstream effectors of RAS, and the selective advantage conferred by mutation of two genes i
81 uestions remain regarding the mechanisms and selective advantages conferred by both of these symplast
82 fundamental trade-off between the short-term selective advantages (Cope's rule) and long-term selecti
84 g antigen stimulation-a mechanism conferring selective advantage during B-cell lymphoma development.
86 suggests that some porin sequences confer a selective advantage during infection and/or transmission
90 enhanced functional responses in vitro or to selective advantages during in vivo responses to cytomeg
91 ted hematologic defects that lack an in vivo selective advantage following gene correction may benefi
94 flow cytometry-selected cells, demonstrating selective advantage for cells with multiple transposon i
95 penias that characterize AP syndrome and the selective advantage for clones that have lost the mutant
96 TrkC silencing by promoter methylation is a selective advantage for colorectal cell lines to limit t
97 uch of the low-latitude oceans, generating a selective advantage for diazotrophic organisms capable o
99 at inhibit rumen protozoa may provide such a selective advantage for EcO157 to proliferate in lagoons
100 ocytes, we obtained suggestive evidence of a selective advantage for increased GNAQ(Q209L) expression
101 d disruptions of F-pilus dynamics provides a selective advantage for infecting phages and thus may be
102 pression of XPC protein might also provide a selective advantage for initiation and progression of si
103 t during skin carcinogenesis that provides a selective advantage for initiation and progression of sq
104 o rewarding and aversive events, providing a selective advantage for maximizing the former while mini
105 ant-associated microbes, and thus provides a selective advantage for microbes such as P. syringae tha
106 model also successfully predicted a stronger selective advantage for more strongly activating gain-of
109 accelerated evolution may be due to a larger selective advantage for resistance mutations in synergis
110 ation of a more robust biofilm may provide a selective advantage for strains that cause systemic dise
111 of HREs does not always provide an ultimate selective advantage for TEs, but may increase the probab
112 of a B cell for antigen is translated into a selective advantage for that B cell in immune responses
113 ed in the Wiskott-Aldrich syndrome, provides selective advantage for the development of naturally occ
114 ould be beneficial to therapy by providing a selective advantage for the expansion of stem cells.
115 end of the proto-spacer, suggesting a strong selective advantage for the phage that mutated in this r
119 he hypothesis that small body size confers a selective advantage for tropical rainforest hunter-gathe
121 ed RNA editing in cancer cells may provide a selective advantage for tumor growth and resistance to a
122 gous female WASp mice revealed a substantial selective advantage for WASp(+) vs WASp(-) iNKT cells.
123 munized individuals, identifying a potential selective advantage for wcjE inactivation and serotype 9
127 at strategy A fixates in a B-population with selective advantage if the fitness of A is greater than
129 Although these adaptations may confer some selective advantage, if they are not appropriately regul
130 in vivo or ex vivo but confers a significant selective advantage in competitive mosquito infections i
131 n truncated LEC1 proteins may have been of a selective advantage in creating somatic propagules, beca
132 rain-specific genes may provide an isolate a selective advantage in environments and contribute to th
134 an increased degree of placentation offers a selective advantage in high predation environments.
137 s, such as nirS and cNor, appear to confer a selective advantage in microbial communities experiencin
138 osis-like death in pneumococci and confers a selective advantage in nasopharyngeal cocolonization.
139 ured environments, and thus likely confers a selective advantage in natural habitats of magnetotactic
143 .IMPORTANCE Genetic alterations conferring a selective advantage in protecting from life-threating pa
145 panded "synthetic" genetic code can confer a selective advantage in the directed evolution of protein
146 no acid p-boronophenylalanine (BF) confers a selective advantage in the evolution of glycan-binding p
147 alizing antibodies did not bind, conferred a selective advantage in the immune systems of infected ho
148 TssM deubiquitinase may provide B. mallei a selective advantage in the intracellular environment dur
149 ll antigen receptor signaling and an in vivo selective advantage in the peripheral versus central B-c
150 table, amyloid-like aggregates that confer a selective advantage in the presence of specific antifung
151 hat grant spermatogonial stem cells (SSCs) a selective advantage in the testes of the father, but hav
153 ical domain mutations in PIK3CA may confer a selective advantage in the urothelium in vivo by overcom
156 ation of the PTAP motif in p6(Gag) confers a selective advantage in viral replication by increasing G
157 se immunodeficiencies corrected cells have a selective advantage in vivo, and low numbers of gene-mod
163 ost significant determinant of the threshold selective advantage is compartment size, with the thresh
164 explanation for these findings, whereby the selective advantage is driven by the competing risks of
165 onal B-cell stage; and (3) a similar in vivo selective advantage is manifest by mature WASp(+) human
170 of a lipid droplet, which despite the clear selective advantage it confers is also a harbinger of ce
171 us consequences, possibly as a result of the selective advantage it originally provided to either a h
172 ive evidence supports two hypotheses for the selective advantages leading to the origin of vocal lear
173 tations that provide the mutant cells with a selective advantage, leading to the clonal expansions re
174 ond distinct cell population that may have a selective advantage, leading to variation of LOI in norm
176 ed with low Igmu-chain and can eliminate the selective advantage of "double-producers" that achieve h
178 es are used to quantify the magnitude of the selective advantage of a monogenic heterozygous variant
180 e disequilibrium generated by migration; the selective advantage of an inversion is dependent on the
182 other diseases, is confounded by the strong selective advantage of cells in which shRNA expression i
183 been the subject of much speculation, and a selective advantage of clusters of functionally related
186 ropose that CsrD evolution was driven by the selective advantage of decoupling Csr sRNA decay from Cs
191 s can ensure correlated gene expression, the selective advantage of maintaining adjacent gene pairs r
192 tes mitochondrial DNA (mtDNA), can alter the selective advantage of one mtDNA type over another.
194 ips among species in order to understand the selective advantage of producing milk with specific nutr
197 ufficient for symbiosis, thus explaining the selective advantage of this allele at the mechanistic le
203 -dependent hematopoiesis consistent with the selective advantage of WASP-positive hematopoietic cells
204 nsion of a dominant homozygous subclone, the selective advantage of which is likely to reflect additi
207 evolutionary selection, including potential selective advantages of mutation carriers in genes affec
210 suggests that Myc heterogeneity confers some selective advantage on breast tumor growth and progressi
211 et, known as driver mutations, confer clonal selective advantage on cancer cells and are causally imp
212 elegans with metabolic plasticity and thus a selective advantage on different diets in the wild.
215 sults suggest that type IV pili may confer a selective advantage on K. kingae early in infection and
218 d and heterogeneous conditions influence the selective advantage or disadvantage of antibiotic resist
220 duals that do not contribute socially have a selective advantage over altruists if both types receive
221 ssume that modern humans benefited from some selective advantage over Neanderthals, which led to the
222 ssary mutations the transformed cell gains a selective advantage over normal cells, and the mutation
223 e ribosome biogenesis and provide pre-LSCs a selective advantage over normal hematopoietic cells thro
224 ning elevated levels of plasticity acquire a selective advantage over other clonal populations within
225 he surfactant provides L. pneumophila with a selective advantage over other legionellae in the natura
226 talytic transformations would have enjoyed a selective advantage over other protocells in high Mg(2+)
227 bial pressure, 6 out of 11 mutants carried a selective advantage over the antimicrobial-sensitive par
229 t that the HBeAg-negative variant may have a selective advantage over wild-type HBV within the livers
232 he molecular (sequence) pathway by which the selective advantage provided by this protein can be impr
233 the model allows us to calculate the actual selective advantage provided by typical somatic mutation
234 s paper, we build on our recent work on the "selective advantage" relation among driver mutations in
235 ple cognitive abilities (each with their own selective advantage) requires no additional evolutionary
236 fraction exceeded 50%, suggesting additional selective advantage resulting from the loss of heterozyg
237 lthough the mechanisms of regulation and the selective advantage(s) of regulating cellular shape are
238 how that viruses with these mutations have a selective advantage since they are preferentially locate
239 expression of particular genes may provide a selective advantage such that it is conserved across spe
240 ge transaldolase may be a tradeoff for other selective advantages such as reduced gene size: we show
241 tion, we predict that revertant cells have a selective advantage that allows their clonal expansion a
242 e latter case, heterogeneity should confer a selective advantage that benefits the entire population.
243 kinase gene, which conferred an exceptional selective advantage that could be demonstrated through b
244 l chromosomes(1,2,5,6,9), but the sources of selective advantage that drive the expansion of most clo
245 thelium plays a unique function, providing a selective advantage that gives rise to transgene-positiv
246 er or not this exclusion activity provides a selective advantage through maintenance of Stk activity
248 investigate whether aneuploidy may confer a selective advantage to cancer cells, we employed a contr
249 pression of light-inducible genes provides a selective advantage to cavefish at the expense of a damp
252 s do not have the necessary proliferative or selective advantage to evolve into a disease-relevant re
255 , the DNE of p53 missense variants confers a selective advantage to hematopoietic cells on DNA damage
256 of heterozygotes, may result in an apparent selective advantage to heterozygotes at the neutral locu
257 common MHC alleles, which in turn provides a selective advantage to hosts carrying rare MHC alleles.
258 ll, our data show that aneuploidy can confer selective advantage to human cells cultured under non-st
259 iversity acts as a mechanism that provides a selective advantage to individual cells within otherwise
260 ated nuclear antigen (LANA/orf73) provides a selective advantage to infected B cells by driving proli
261 sure to inflammatory cytokines can provide a selective advantage to infiltrating CD8(+) T cells by tr
262 n this model, each genetic polymer imparts a selective advantage to its protocell by, for example, co
264 age or death of their host offers no obvious selective advantage to microbial growth or survival.
265 ive virulence determinants may both confer a selective advantage to mucA mutant strains of P. aerugin
266 mutations and biological processes that give selective advantage to mutant clones, we analysed genoty
267 ic mutations in a single HSC that provides a selective advantage to mutant HSC over normal HSC and pr
268 owever, very high seed predation shifted the selective advantage to nonserotinous individuals even at
269 ations on space and/or growth factors gave a selective advantage to phenotypes derived from tumorigen
270 clock, acting with hormone signals, provides selective advantage to plants through anticipation of an
273 lution, our findings suggest that there is a selective advantage to retaining polar, uncharged residu
274 d corresponding stress resistance provides a selective advantage to Runx1-deficient HSPCs, allowing t
275 ly unrecognized role in providing a germline-selective advantage to spermatogonia for the recurrent m
278 at support conjugation, exclusion provides a selective advantage to the element and its host cells.
279 housekeeping genes suggests that they offer selective advantage to the genomes and ecosystems they i
281 lly, the resistance gene must confer a large selective advantage to the vector to surmount the effect
282 us-encoded miRNAs are likely to be of little selective advantage to the virus, and our approach provi
284 ype p53 in glioblastoma cells could confer a selective advantage to these cells under the adverse con
286 inherent to viral populations may provide a selective advantage to viruses that can be fully exploit
289 a unique family of retroelements that confer selective advantages to their hosts by facilitating loca
290 onse to specific challenges and can confer a selective advantage under certain environmental stresses
291 ncoded by TP53) provides cancer cells with a selective advantage under conditions of hypoxia, but lit
292 de that LeuRS-I may have evolved to confer a selective advantage under the extreme and fluctuating en
294 changes in amino acid function provided the selective advantage underlying the expansion of the gene
297 t certain environment-altering traits have a selective advantage when those traits also contribute to
298 equence of behaviors that evolved to provide selective advantages when elicited by tall trees, but ar
299 ing development might offer dosage-dependent selective advantage, whereas rapid expression divergence
300 ) Initially, the two linked mutations have a selective advantage while rare and will increase in freq