戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ote operons in Wolbachia-induced cytoplasmic incompatibility.
2 nses to mtDNA damage and mito-nuclear genome incompatibility.
3  focusing on the presence or absence of self-incompatibility.
4  does not harbor loci contributing to hybrid incompatibility.
5 ne to circumvent hisn6a lethality and hybrid incompatibility.
6 in wMel recapitulate and enhance cytoplasmic incompatibility.
7 the hybrids and is therefore named as hybrid incompatibility.
8 rbidities, including one case of blood group incompatibility.
9 geographic patterns in the frequency of self-incompatibility.
10  involvement of a silent epiallele in hybrid incompatibility.
11  and biome in predicting outcrossing or self-incompatibility.
12 sperm-egg incompatibility called cytoplasmic incompatibility.
13 external forcing or as a result of geometric incompatibility.
14  the SRK/SCR haplotype is functional in self-incompatibility.
15 t crosses and in the presence of cytonuclear incompatibility.
16 sites infecting another and/or host-parasite incompatibility.
17 ristic properties of quantum theory based on incompatibility.
18 ave evolved specifically to function in self-incompatibility.
19 de a molecular explainable example of hybrid incompatibility.
20  enzyme are not tolerated, implying sequence incompatibility.
21 cus on recent strategies to address catalyst incompatibility.
22 covered a two-locus Dobzhansky-Muller hybrid incompatibility.
23 f functional graft loss independently of HLA incompatibility.
24 compatible with the phenotype of cytoplasmic incompatibility.
25 under-utilized due to linkage drag and cross-incompatibility.
26 n, particularly male killing and cytoplasmic incompatibility.
27 o prevent genomic conflicts that may lead to incompatibilities.
28 lementary action of CI and asymmetric hybrid incompatibilities.
29 we found no strong support for such X-linked incompatibilities.
30 g, selection, recombination and differential incompatibilities.
31 s evolved reproductive isolation via genetic incompatibilities.
32 become increasingly isolated by reproductive incompatibilities.
33  host speciation rates by generating genetic incompatibilities.
34 in outbreeding depression because of genetic incompatibilities.
35 ndscape, of two allopatric lineages leads to incompatibilities.
36 ifying individual genes that underlie hybrid incompatibilities.
37 for this purpose suffer severely from buffer incompatibilities.
38 igation of the evolutionary history of these incompatibilities, a reckoning of how the reproductive b
39 mented here conform to the view that genetic incompatibilities accumulating with divergence generate
40 rize the variation in self and interspecific incompatibility across 29 populations of Phlox drummondi
41 orrelated strength of self and interspecific incompatibility across the range of P. drummondii and th
42 s two strong candidate genes for the genetic incompatibility, agt and Taf1 Both encode unrelated DNA-
43 ls in preventing clinically significant drug incompatibilities, aiming at the reduction of adverse re
44                                       Steric incompatibility also allows FBXL5 to physically dislodge
45            One of the genes involved in this incompatibility also causes melanoma in hybrids between
46                                 Mito-nuclear incompatibility also resulted in aberrant egg morphology
47  identify conditions under which cytoplasmic incompatibilities and Allee effects successfully interac
48 ctions might contribute to Dobzhansky-Muller incompatibilities and be important in speciation.
49 nt regulatory elements might underlie hybrid incompatibilities and contribute to reproductive isolati
50                           For example, genic incompatibilities and differences in chromosome numbers
51                     Our results preclude X-X incompatibilities and instead support an interchromosoma
52 tant candidates for Dobzhansky-Muller hybrid incompatibilities and may contribute to hybrid dysfuncti
53        Unique disease symptoms such as graft incompatibilities and stem pitting cause considerable cr
54 ts, and animals, where they underlie genetic incompatibilities and sterility in crosses between wild
55  analyzed the effects of the KIR/HLA genetic incompatibilities and studied cord blood cells at both t
56 henomena such as small RNAs, symbiosis, self-incompatibility and circadian rhythms.
57 ive explanations for the association between incompatibility and colouration, such as fine-scale link
58                  This study documents hybrid incompatibility and genome instability triggered by the
59 er approach to assessing donor-recipient HLA incompatibility and improve risk assessment and predicti
60  is extensive quantitative variation in self-incompatibility and interspecific-incompatibility with i
61 that parallel those of wild-type cytoplasmic incompatibility and is notably rescued by wMel-infected
62                  The new bounds capture both incompatibility and mutually exclusiveness, and are tigh
63 ntifies genes underlying a vertebrate hybrid incompatibility and provides a glimpse into the action o
64 data have significantly higher interspecific incompatibility and self-incompatibility than geographic
65 monstrate that Wolbachia-induced cytoplasmic incompatibility and the Allee effect act independently f
66 e combination of adaptive evolution, species incompatibilities, and ongoing gene flow.
67 o the waiting times for mutations that cause incompatibilities, and permit ecological differentiation
68 ing polyploidy, multisomic inheritance, self-incompatibility, and high levels of heterozygosity.
69 weakest selection contribute to the earliest incompatibilities; and 3) pair-wise incompatibilities do
70                                          MLV incompatibility appeared to be caused by lack of incorpo
71                             The MLV particle incompatibility appeared to be caused in part by fusogen
72                                         Drug incompatibilities are considered as one of the most crit
73  that involve positive selection and genetic incompatibilities are plausible alternative explanations
74 lectrical properties due to their structural incompatibility, are formed into harmonious states by th
75 nt to a general mechanistic principle of how incompatibilities arise the under stabilising selection
76 utions are required in either lineage before incompatibilities arise.
77 ically and phenotypically but before genetic incompatibilities arise.
78                          It is possible that incompatibilities at one or more of these genes played a
79         However, the chemical and mechanical incompatibilities at the interfaces of dissimilar materi
80 ritories and mates, rather than from genetic incompatibilities at Z-linked loci.
81           Host range breaches are limited by incompatibilities between avian virus components and the
82                It is therefore unlikely that incompatibilities between cis-trans regulatory changes e
83  a likely mechanism for the origin of hybrid incompatibilities between closely related species.
84 e context of kidney transplantation, genomic incompatibilities between donor and recipient may lead t
85 ocomposites have remained elusive because of incompatibilities between fillers and polymers that are
86 ages, might be an important source of hybrid incompatibilities between flowering plant species.
87                   We conclude that epistatic incompatibilities between human and archaic alleles are
88  challenging because of fundamental chemical incompatibilities between lanthanides and most intermedi
89 e to understand the mechanism that generates incompatibilities between morphs.
90 udies showed remarkable pre- and postzygotic incompatibilities between sympatric colour morphs of the
91 s with organ failure-is limited by molecular incompatibilities between the immune systems of pigs and
92  in non-permissive species may be limited by incompatibilities between the viral replication machiner
93 MERS-CoV cannot infect wild-type mice due to incompatibilities between the virus spike and the mouse
94                The perceived differences and incompatibilities between these subsystems have led to t
95 ere the detailed mechanistic basis of hybrid incompatibilities between two allopatric lineages, for a
96 d QTL analysis, as well as studies of hybrid incompatibilities between worm species.
97 y source of this morphological complexity-an incompatibility between an elastically favored "microstr
98 lt concentration can effectively resolve the incompatibility between aqueous environments and quinone
99  and its chaperone CAL1 accounts for species incompatibility between centromeric histones in Drosophi
100 moving organic solvent, solving the inherent incompatibility between CNM and polymers of interest, an
101 mammal speciation gene causes only transient incompatibility between diverging species.
102 ntibodies after transplantation and red cell incompatibility between donors and recipients.
103 lear implantation has been restricted due to incompatibility between established neuroimaging techniq
104 cuadorian case study analysis, where spatial incompatibility between exposed populations and rain gau
105 actions less positively due to the perceived incompatibility between financial incentives and intrins
106                        However, the apparent incompatibility between fluidity and permanent porosity
107  better and should be employed when there is incompatibility between imputation and analysis models.
108 ubin ("Rubin's rules" (RR)) is biased due to incompatibility between imputation and analysis models.
109 tant unresolved issue is the extent to which incompatibility between mitochondrial and nuclear genome
110 mic rearrangements, chimeric gene formation, incompatibility between nucleus and cytoplasm, and horiz
111 tial neutral theory was published showing an incompatibility between regional and local scale fits wh
112 truncatula-Sinorhizobium meliloti symbiosis, incompatibility between symbiotic partners frequently oc
113 ess considerations rooted in a psychological incompatibility between the allocation of harms, which i
114                                          The incompatibility between the anode and the cathode chemis
115 stence of a G186V mutation, revealing strong incompatibility between these mutations.
116                   In such materials, lattice incompatibility between transformed and parent phases of
117 in latency, primarily because of the general incompatibility between virus production and cell surviv
118 nt challenging and most frequently cite the "incompatibility" between the solvent systems used in the
119  molecular level to previously characterized incompatibilities, but also raised new questions about c
120 processes owing to their high volatility and incompatibility, but have low abundances in most geologi
121                  Here, we tackle this mutual incompatibility by recognizing that the 8-oxo-purines sh
122 lanaceae occurs via direct breakdown of self-incompatibility by whole genome duplication, rather than
123 d through the populations due to a sperm-egg incompatibility called cytoplasmic incompatibility.
124 ole of conflict in the evolution of a hybrid incompatibility can be proven beyond reasonable doubt.
125                This solvent strength related incompatibility can lead to severe peak distortion and l
126                Therefore, the origins of ACP incompatibility can reside in either helix I or in helix
127                                  Cytonuclear incompatibilities caused hybrid anther sterility, confou
128 tion occurs due to conformational/structural incompatibility caused by the 19-AA insertions.
129         Here, we show that this mito-nuclear incompatibility causes a severe temperature-sensitive fe
130                                  Cytoplasmic incompatibility (CI) generated by Wolbachia is central t
131                                  Cytoplasmic incompatibility (CI) is the most common symbiont-induced
132    The most common alteration is cytoplasmic incompatibility (CI)(3-5), where eggs from uninfected fe
133 , infected by Cardinium inducing cytoplasmic incompatibility (CI), and its sibling species E. gennaro
134    The most prevalent mechanism, cytoplasmic incompatibility (CI), traces to a Wolbachia deubiquityla
135                                  Cytoplasmic incompatibility (CI), whereby the symbiont makes itself
136 sis induction; male killing; and cytoplasmic incompatibility (CI).
137 t commonly by a mechanism called cytoplasmic incompatibility (CI).
138                            Compatibility and incompatibility coincided with reduced and enhanced accu
139  ways to reach it; thus, not only should BDM incompatibilities commonly arise during parallel evoluti
140 sequences; moreover, structure compatibility/incompatibility constraints have been expanded.
141                           The HIV-1 particle incompatibility correlated with less efficient cleavage
142 earliest incompatibilities; and 3) pair-wise incompatibilities dominate over higher order, contrary t
143 Our findings show that maternal mito-nuclear incompatibility during Drosophila oogenesis has severe c
144 oblems for in-line processes such as solvent incompatibilities, e.g., for a multistep synthesis or th
145 eneral approach to create engineered genetic incompatibilities (EGIs) in the model insect Drosophila
146 , where it showed high levels of cytoplasmic incompatibility, enabling rapid invasion of laboratory p
147 phorus one of the only two vertebrate hybrid incompatibility examples in which interacting genes have
148                 The discovery of cytoplasmic incompatibility factor genes cifA and cifB pioneers gene
149 nd is linked to adaptive evolution of hybrid incompatibility genes.
150  disequilibrium between the colour locus and incompatibility genes.
151                            Plasmids from the incompatibility group A/C were detected at low levels in
152                                    The IncP (Incompatibility group P) plasmids are important carriers
153 s applicable to nine plasmids from six major incompatibility groups and mixed populations carrying mu
154 er of plasmids and distribution of different incompatibility groups did not differ between generic fe
155 uding three clades with fidelity for plasmid incompatibility groups H, F or X.
156 nstrate that the presence or absence of self-incompatibility has strong explanatory power for plant g
157 he pollen-pistil interaction, suggests these incompatibilities have an overlapping molecular mechanis
158                                         MICA incompatibilities have been associated with an increased
159    Recent molecular investigations of hybrid incompatibilities have revealed fascinating patterns of
160                                       Hybrid incompatibility (HI) prevents gene flow between species,
161 r-generation hybrids, we suggest cytonuclear incompatibilities, hybrid breakdown, and purifying selec
162 arized vessels, issues such as biomechanical incompatibility, immunogenicity risks and the hazards of
163            Here we test the role of X-linked incompatibilities in a rare exception to Haldane's rule
164 t accounts for Wolbachia-induced cytoplasmic incompatibilities in addition to an Allee effect arising
165 the ability of nanomaterials to prevent drug incompatibilities in clinical settings has been investig
166                          Because of material incompatibilities in conventional approaches based on th
167       We find a broad continuum of intrinsic incompatibilities in hybrid males that increase in stren
168 ted with Wolbachia, which causes cytoplasmic incompatibilities in its host population, into a populat
169 tibility, with a greater persistence of weak incompatibilities in later generations.
170                    Instead of framing hybrid incompatibilities in light of genetic conflict, we advoc
171 rphisms (nsSNPs) were calculated to identify incompatibilities in transmembrane and secreted proteins
172 egulators of muscle metabolism to explain an incompatibility in adaptation between endurance and resi
173 mmodate stress and strain and satisfy strain incompatibility in addition to the existing internal str
174 tween biparental inheritance and cytonuclear incompatibility in Campanulastrum americanum, a plant sp
175  a plausible explanation for plastome-genome incompatibility in Geraniaceae.
176                                         Self-incompatibility in Petunia is controlled by the polymorp
177      Here, we explored potential mitonuclear incompatibility in six admixed human populations from th
178 tle is known regarding the effect of KIR/HLA incompatibilities (inc.) in the setting of T-replete hap
179                     Moreover, other chemical incompatibilities, including products of aborted ligatio
180      We investigated the influence of gender incompatibility, including H-Y incompatibility, on corne
181 he geographical distribution of variation in incompatibilities indicates that this mechanistic link b
182  present an approach to understand geometric-incompatibility-induced rigidity in underconstrained mat
183 act the evolutionary dynamics of cytonuclear incompatibility, interactions between nuclear and organe
184 d among individuals and the strength of both incompatibilities is explained by the success of pollen
185 t; by contrast, neither pollen size nor male incompatibility is affected by GLO2 activity.
186                                              Incompatibility is associated with major TAL effectors t
187                            This mito-nuclear incompatibility is between alleles of the nuclear-encode
188                                              Incompatibility is defeated by transfer of pthXo1 to oth
189                                         This incompatibility is environment dependent, such that the
190 ies show that while recognition of rhizobium incompatibility is root driven, bacterial exclusion requ
191       The strength of self and interspecific incompatibility is significantly correlated among indivi
192 al inheritance helps to mitigate cytonuclear incompatibility, leading to increased fitness of F1 hybr
193 on, as occurs in sex chromosomes, plant self-incompatibility loci and fungal mating-type loci.
194 e highly polygenic, indicating that multiple incompatibility loci have accumulated rapidly between th
195 ng of foreign alleles more tightly linked to incompatibility loci.
196                       The Leavenworthia self-incompatibility locus (S locus) consists of paralogs (La
197 g because of limitations such as calendering incompatibility, low mass loading, and excessive usage o
198 indicates that this mechanistic link between incompatibilities may affect the evolution of mate choic
199 ns, known as Bateson-Dobzhansky-Muller (BDM) incompatibilities, may arise when the two populations fa
200                        The gametophytic self-incompatibility mechanism enables the pistil of a plant
201                                We propose an incompatibility mechanism involving TsYUC6 and TsBAHD.
202 ns, and are potentially involved in the self-incompatibility mechanism.
203    Further, we find longer sequences develop incompatibilities more quickly at small population sizes
204 tion that smaller populations should develop incompatibilities more quickly.
205  commensal strains, and (ii) because of this incompatibility, multidrug-resistant strains sharing fea
206 t their limitations include functional group incompatibility, narrow scope of application, high cost
207 ions, yet this has been challenging owing to incompatibilities of fabrication methods.
208 ively young nature of the field and inherent incompatibility of CNM with most man-made materials in u
209 nally, we use this method to correct for the incompatibility of data as used in current species sensi
210 fundamental crystal chemistry and mechanical incompatibility of dissimilar interfaces.
211  containing E. coli AcpP helix II was due to incompatibility of L. lactis AcpA helix I with the downs
212 cellular RNA are limited, largely due to the incompatibility of modified nucleobases and nucleosides
213      Refuting the conventional wisdom of the incompatibility of organolithium reagents with air and m
214 males, the indicine PRDM9 variant may induce incompatibility of recombination hotspots and male infer
215 ction is documented, possibly because of the incompatibility of the generated thiol with typical hydr
216                                              Incompatibility of the human platelet antigen-1 (HPA-1)
217 PEEM) for such purposes has been hampered by incompatibility of the liquid samples with ultrahigh vac
218 n of several factors, including the inherent incompatibility of the mesh material with some applicati
219 PT sequence: RNase H sequence preference and incompatibility of the poly(rA/dT) tract of the PPT with
220          It comprises another example of the incompatibility of the reduced cytoplasms of microbes wi
221                                          The incompatibility of the two blocks makes the final coupli
222 ere, we demonstrate that there is in fact no incompatibility of these results and, indeed, that the v
223 generation of nonclassicality and the mutual incompatibility of two states connected by time evolutio
224 nce of gender incompatibility, including H-Y incompatibility, on corneal transplant graft rejection a
225 olbachia invasion threshold, and cytoplasmic incompatibilities only have a marginal effect on the All
226      Several loci contributing to unilateral incompatibility or hybrid necrosis were mapped with the
227 ate egg laying but do not induce cytoplasmic incompatibility or sex-ratio distortion, two parasitic r
228 n opportunity to expand LDLT in cases of ABO incompatibility or when nondirected donors arise.
229 g capabilities, sterilization by cytoplasmic incompatibility, or both; the release of Aedes carrying
230 rs including, bacterial density, cytoplasmic incompatibility, or resistance to infection with Zika vi
231 elf-recognition model for S-RNase-based self-incompatibility predicts that multiple S-locus F-box pro
232            Although the existence of genetic incompatibilities preventing the cross-species transfer
233  we describe a novel approach to address the incompatibility problem, which we refer to as Active Sol
234 gh frequency on red blood cells, transfusion incompatibility problems, due to the absence of undefine
235           Considering the ontogeny of hybrid incompatibilities provides a profitable connection betwe
236  metabolites playing crucial roles in sexual incompatibility reactions in apricot (Prunus armeniaca L
237 s and avoid growth arrest involved in sexual incompatibility reactions of apricot.
238 lites with significant influence on the self-incompatibility reactions.
239 ropagated in vitro and that, despite species incompatibility, recombinant TR3 vectors elicit high fre
240   Exclusion criteria were age <18 years, ABO incompatibility, redo or multivisceral transplants, part
241 , the bacterial genes underlying cytoplasmic incompatibility remain unknown.
242 ward flowing offshore current and endogenous incompatibilities restricting integration of certain reg
243 th chimeric transgenes imply that the hybrid incompatibilities result from interactions among nucleot
244                                       Hybrid incompatibility resulting from deleterious gene combinat
245 onuclear compatibility, reducing cytonuclear incompatibility's contribution to reproductive isolation
246                The genetic breakdown of self-incompatibility (SI) and subsequent mating system shifts
247                                         Self-incompatibility (SI) is a major genetically controlled s
248                    In the Brassicaceae, self-incompatibility (SI) is a spectacular example of a diver
249                                         Self-incompatibility (SI) is an important mechanism to preven
250                                         Self-incompatibility (SI) is used by many angiosperms to prev
251                                         Self-incompatibility (SI) is used by many angiosperms to reje
252 nisms are less well understood than the self-incompatibility (SI) mechanisms plants use to reject pol
253  of SRK and thus facilitate analysis of self-incompatibility (SI) signaling, we coexpressed an Arabid
254 e pollen S-Locus F-box protein controls self-incompatibility (SI).
255 comparison with RPP1 loci involved in hybrid incompatibility suggests that these functions evolved in
256 tudy, the Papaver rhoeas (poppy family) self-incompatibility system has been transferred into Arabido
257                        The simple poppy self-incompatibility system may finally make it possible to i
258                                    The RCD-1 incompatibility system was reconstituted in human 293T c
259  highly conserved eukaryotic invention, self-incompatibility systems such as mating types or sexes ap
260 cipants (n = 33) completed the Simon Spatial Incompatibility Task during high-resolution, multiband f
261 igher interspecific incompatibility and self-incompatibility than geographically isolated P. drummond
262  overcome a severe bottleneck of male hybrid incompatibilities that enabled us to experimentally puri
263 of niosomes to prevent physical and chemical incompatibilities that occur upon mixing acyclovir and v
264 p the genes that drive the development of an incompatibility that causes melanoma in swordtail fish h
265 ution of irreversible reproductive barriers (incompatibilities) that complete the speciation process(
266 cluding the factors that contribute to graft incompatibility, the prevalence of genetic and epigeneti
267 ed to be among the earliest types of genetic incompatibility to arise in speciation.
268                Amongst a total of 13 plasmid incompatibility types, the IncI2, IncX4 and IncHI2 plasm
269 fer dominated by a limited number of plasmid incompatibility types.
270                     Unilateral interspecific incompatibility (UI) is a postpollination, prezygotic re
271 e evolution and may also reveal reproductive incompatibilities unique to hybrids.
272 irus-restricting allorecognition [vegetative incompatibility (vic)] loci were disrupted in the chestn
273                    However, the MLV particle incompatibility was more nuanced.
274 her the factors affecting virus-specific Env incompatibility, we characterized Env incorporation, mat
275                Four candidate genes for self-incompatibility were linked in F153, but were not functi
276 ted, indicating some degree of host-pathogen incompatibility when barriers to encounter are overcome.
277 lock co-evolution has produced cross-species incompatibilities, which may contribute to reproductive
278 mon reproductive manipulation is cytoplasmic incompatibility, which results in embryonic lethality in
279 ng Paniceae Rubisco are identified; however, incompatibilities with Paniceae Rubisco biogenesis in to
280 cols, 1) in situ cyclization of products, 2) incompatibility with alpha-H-containing substrates, and
281       Unfortunately, DIA methods suffer from incompatibility with common multiplexed quantification m
282 vo studies in Drosophila is limited by their incompatibility with existing GAL4 lines and side effect
283                                          Its incompatibility with high conductivity media and limited
284 aqueous solubility and poor partitioning and incompatibility with insoluble polymers make long-term r
285 on in self-incompatibility and interspecific-incompatibility with its close congener P. cuspidata.
286 pitous collapse of the neuronal networks and incompatibility with life within days.
287 e iron salts include chemical reactivity and incompatibility with other components.
288 ed in vitro assays has been limited by their incompatibility with packaging or form factors necessary
289 s, often based on mistaken ideas about their incompatibility with prison security.
290 ty, toxic and hazardous organic solvent, and incompatibility with scalable fabrication process.
291 roduction, which was further enhanced by the incompatibility with simw(501) mitochondria.
292  processed for a variety of reasons, such as incompatibility with spin coating, electron beam lithogr
293                            Pregnancy-induced incompatibility with spouse donors was limiting given th
294 lost during vector library production due to incompatibility with the cognate AAP.
295 trange or bad metallic transport, defined by incompatibility with the conventional quasiparticle pict
296  NFS1 gene that regulates the fixation-level incompatibility with the microsymbiont Sinorhizobium mel
297   The Ag(90) nanocluster solves the apparent incompatibility with the most symmetric arrangement of 2
298                               We demonstrate incompatibility with weak-scattering theory and key char
299 cacy of rescue depended upon the strength of incompatibility, with a greater persistence of weak inco
300 raphical variation in self and interspecific incompatibilities within a species can reveal if and how

 
Page Top