ライフサイエンスコーパス: incompatibility

1 focusing on the presence or absence of self-incompatibility.

2 ristic properties of quantum theory based on incompatibility.

3 ave evolved specifically to function in self-incompatibility.

4 enzyme are not tolerated, implying sequence incompatibility.

5 cus on recent strategies to address catalyst incompatibility.

6 covered a two-locus Dobzhansky-Muller hybrid incompatibility.

7 s an integral part of their function in self-incompatibility.

8 does not harbor loci contributing to hybrid incompatibility.

9 he obstacles of shear degradation and engine incompatibility.

10 ver the series of S-alleles controlling self-incompatibility.

11 gy, a key component of heterostyly type self-incompatibility.

12 h a mechanism of heterotypic claudin-binding incompatibility.

13 t that results in inter-species reproductive incompatibility.

14 n C24 hybrids, consistent with the degree of incompatibility.

15 ne to circumvent hisn6a lethality and hybrid incompatibility.

16 onse and restricting pathogen ingress during incompatibility.

17 radiation modes--that is not due to symmetry incompatibility.

18 ability to induce high levels of cytoplasmic incompatibility.

19 to evaluate the impact of maternal/fetal KEL incompatibility.

20 erian mimicry and with known Z-linked hybrid incompatibility.

21 nsfusion practices allowing for platelet ABO incompatibility.

22 in wMel recapitulate and enhance cytoplasmic incompatibility.

23 rbidities, including one case of blood group incompatibility.

24 geographic patterns in the frequency of self-incompatibility.

25 involvement of a silent epiallele in hybrid incompatibility.

26 and biome in predicting outcrossing or self-incompatibility.

27 sperm-egg incompatibility called cytoplasmic incompatibility.

28 external forcing or as a result of geometric incompatibility.

29 the SRK/SCR haplotype is functional in self-incompatibility.

30 t crosses and in the presence of cytonuclear incompatibility.

31 sites infecting another and/or host-parasite incompatibility.

32 s evolved reproductive isolation via genetic incompatibilities.

33 become increasingly isolated by reproductive incompatibilities.

34 host speciation rates by generating genetic incompatibilities.

35 in outbreeding depression because of genetic incompatibilities.

36 ndscape, of two allopatric lineages leads to incompatibilities.

37 ergence is an important source of regulatory incompatibilities.

38 terotypic transgenes due to packaging signal incompatibilities.

39 which imprinting could contribute to hybrid incompatibilities.

40 lementary action of CI and asymmetric hybrid incompatibilities.

41 rms races in driving the evolution of hybrid incompatibilities.

42 to ecological adaptations also cause hybrid incompatibilities.

43 we found no strong support for such X-linked incompatibilities.

44 Consistent with the snowball theory of incompatibility accumulation, we found that trigenic int

45 s two strong candidate genes for the genetic incompatibility, agt and Taf1 Both encode unrelated DNA-

46 ls in preventing clinically significant drug incompatibilities, aiming at the reduction of adverse re

47 tolerance locus indirectly caused the hybrid incompatibility allele to go to high frequency in the co

48 Mito-nuclear incompatibility also resulted in aberrant egg morphology

49 tibility in sexual eukaryotes and linguistic incompatibility among human cultures, the commonality be

50 Many flowering plants show self-incompatibility, an intra-specific reproductive barrier

51 identify conditions under which cytoplasmic incompatibilities and Allee effects successfully interac

52 ctions might contribute to Dobzhansky-Muller incompatibilities and be important in speciation.

53 nt regulatory elements might underlie hybrid incompatibilities and contribute to reproductive isolati

54 For example, genic incompatibilities and differences in chromosome numbers

55 However, genic incompatibilities and ecological divergence may also be

56 Our results preclude X-X incompatibilities and instead support an interchromosoma

57 Unique disease symptoms such as graft incompatibilities and stem pitting cause considerable cr

58 analyzed the effects of the KIR/HLA genetic incompatibilities and studied cord blood cells at both t

59 The number of incompatibilities and their type significantly impact su

60 henomena such as small RNAs, symbiosis, self-incompatibility and circadian rhythms.

61 ive explanations for the association between incompatibility and colouration, such as fine-scale link

62 ch nonlinear phenomena, thereby defining the incompatibility and cooperativity between all pairs of s

63 that parallel those of wild-type cytoplasmic incompatibility and is notably rescued by wMel-infected

64 The new bounds capture both incompatibility and mutually exclusiveness, and are tigh

65 ese include the well-referenced case of self-incompatibility and recent evidence from species with nu

66 hese recognition factors interact to trigger incompatibility and restrict virus transmission.

67 monstrate that Wolbachia-induced cytoplasmic incompatibility and the Allee effect act independently f

68 ar operons of two related plasmids can cause incompatibility and the reduced transmission of one or b

69 nt in the context of the maintenance of self-incompatibility and understanding the evolutionary dynam

70 he confusion between species that show 'self-incompatibility' and those that possess one of the 'conv

71 ing polyploidy, multisomic inheritance, self-incompatibility, and high levels of heterozygosity.

72 Drug incompatibilities are considered as one of the most crit

73 Many of these incompatibilities are likely the result of natural or se

74 ns of linkage disequilibrium, homoplasy, and incompatibility are difficult to interpret because they

75 Does incompatibility arise as a limitation, to avoid the requ

76 eliminated from males most likely represent incompatibilities arising from hybridization.

77 an increase in the probability of character incompatibility (as well as the maximum homoplasy measur

78 HLA incompatibilities at >1 locus showed additive detrimenta

79 It is possible that incompatibilities at one or more of these genes played a

80 However, the chemical and mechanical incompatibilities at the interfaces of dissimilar materi

81 s were probably not a cause of interspecific incompatibility at the scale that could be examined with

82 SsPV1 can overcome vegetative incompatibility barriers and can be transmitted horizont

83 Host range breaches are limited by incompatibilities between avian virus components and the

84 ages, might be an important source of hybrid incompatibilities between flowering plant species.

85 challenging because of fundamental chemical incompatibilities between lanthanides and most intermedi

86 e to understand the mechanism that generates incompatibilities between morphs.

87 udies showed remarkable pre- and postzygotic incompatibilities between sympatric colour morphs of the

88 MERS-CoV cannot infect wild-type mice due to incompatibilities between the virus spike and the mouse

89 The perceived differences and incompatibilities between these subsystems have led to t

90 d QTL analysis, as well as studies of hybrid incompatibilities between worm species.

91 and its chaperone CAL1 accounts for species incompatibility between centromeric histones in Drosophi

92 rmal process not only solves the interfacial incompatibility between CNTs and titanate sol and contro

93 mammal speciation gene causes only transient incompatibility between diverging species.

94 ntibodies after transplantation and red cell incompatibility between donors and recipients.

95 lear implantation has been restricted due to incompatibility between established neuroimaging techniq

96 However, the apparent incompatibility between fluidity and permanent porosity

97 tant unresolved issue is the extent to which incompatibility between mitochondrial and nuclear genome

98 Intrinsic genomic incompatibility between S. aethnensis and S. chrysanthem

99 Our data suggest that KIR/HLA incompatibility between sexual partners confers protecti

100 truncatula-Sinorhizobium meliloti symbiosis, incompatibility between symbiotic partners frequently oc

101 rics that residual strains are caused due to incompatibility between the electric-field-induced strai

102 ave identified segregation-dependent plasmid incompatibility between the highly divergent Par operons

103 Incompatibility between the microbiota and Wolbachia may

104 linkage groups detected, indicating genomic incompatibility between the species.

105 nt challenging and most frequently cite the "incompatibility" between the solvent systems used in the

106 molecular level to previously characterized incompatibilities, but also raised new questions about c

107 processes owing to their high volatility and incompatibility, but have low abundances in most geologi

108 Here, we tackle this mutual incompatibility by recognizing that the 8-oxo-purines sh

109 Petunia possesses self-incompatibility, by which pistils reject self-pollen but

110 d through the populations due to a sperm-egg incompatibility called cytoplasmic incompatibility.

111 yxococcus xanthus to show that colony-merger incompatibilities can be strong barriers to social inter

112 In contrast, ABO incompatibility can be crossed with outcomes equivalent

113 onal assessment should be made of how immune incompatibility can best be managed and how a network of

114 This solvent strength related incompatibility can lead to severe peak distortion and l

115 Therefore, the origins of ACP incompatibility can reside in either helix I or in helix

116 h population-specific adaptations or genetic incompatibilities, can cause net gene flow to vary acros

117 Cytonuclear incompatibilities caused hybrid anther sterility, confou

118 Here, we show that this mito-nuclear incompatibility causes a severe temperature-sensitive fe

119 cted spiders demonstrated strong cytoplasmic incompatibility (CI) induced by a different strain of Wo

120 The most common alteration is cytoplasmic incompatibility (CI)(3-5), where eggs from uninfected fe

121 , infected by Cardinium inducing cytoplasmic incompatibility (CI), and its sibling species E. gennaro

122 ways to reach it; thus, not only should BDM incompatibilities commonly arise during parallel evoluti

123 ltodextrins was followed under thermodynamic incompatibility conditions.

124 sequences; moreover, structure compatibility/incompatibility constraints have been expanded.

125 suggesting multiple, non-independent genetic incompatibilities contribute to barriers to gene flow in

126 Additional tests revealed that cytonuclear incompatibility contributed to TRD at five loci, Bateson

127 Incompatibility due to DSA accounted for 86% of the list

128 Our findings show that maternal mito-nuclear incompatibility during Drosophila oogenesis has severe c

129 oblems for in-line processes such as solvent incompatibilities, e.g., for a multistep synthesis or th

130 We propose that incompatibility (electrostatic repulsion) between this p

131 ychology, such as the uncertainty principle, incompatibility, entanglement, and superposition.

132 on Darwin's original supposition that hybrid incompatibilities evolve as an incidental by-product of

133 The model implies that the incompatibilities evolve randomly, unless a particular g

134 The discovery of cytoplasmic incompatibility factor genes cifA and cifB pioneers gene

135 when expressed with two other A. lyrata self-incompatibility factors.

136 s in part because of potential finger-finger incompatibility generated on assembly of modules into zi

137 s to accelerate the identification of hybrid incompatibility genes in other model and nonmodel system

138 However, identifying hybrid incompatibility genes remains a key obstacle in understa

139 disequilibrium between the colour locus and incompatibility genes.

140 nd is linked to adaptive evolution of hybrid incompatibility genes.

141 Plasmids from the incompatibility group A/C were detected at low levels in

142 The IncP (Incompatibility group P) plasmids are important carriers

143 s applicable to nine plasmids from six major incompatibility groups and mixed populations carrying mu

144 In different groups of mammals, hybrid incompatibility has indeed been linked to loss of imprin

145 nstrate that the presence or absence of self-incompatibility has strong explanatory power for plant g

146 MICA incompatibilities have been associated with an increased

147 Although several genes causing hybrid incompatibilities have been identified, there is intense

148 Hybrid incompatibility (HI) prevents gene flow between species,

149 Pre-zygotic interspecific incompatibility (II) involves an active inhibition mecha

150 arized vessels, issues such as biomechanical incompatibility, immunogenicity risks and the hazards of

151 Here we test the role of X-linked incompatibilities in a rare exception to Haldane's rule

152 t accounts for Wolbachia-induced cytoplasmic incompatibilities in addition to an Allee effect arising

153 the ability of nanomaterials to prevent drug incompatibilities in clinical settings has been investig

154 Because of material incompatibilities in conventional approaches based on th

155 We find a broad continuum of intrinsic incompatibilities in hybrid males that increase in stren

156 ted with Wolbachia, which causes cytoplasmic incompatibilities in its host population, into a populat

157 tibility, with a greater persistence of weak incompatibilities in later generations.

158 elements, including the role of cytonuclear incompatibilities in maintaining polymorphism.

159 Hybrid incompatibilities in the context of phylosymbiosis are r

160 rtants can be attributed at least in part to incompatibilities in the virus-specific packaging signal

161 d ARC1's requirement for reconstituting self-incompatibility in A. thaliana and uncovered an importan

162 osed standardized strategy for studying self-incompatibility in A. thaliana, we offer our perspective

163 egulators of muscle metabolism to explain an incompatibility in adaptation between endurance and resi

164 of the evolution of self-compatibility/self-incompatibility in almond and other Prunus species, and

165 tween biparental inheritance and cytonuclear incompatibility in Campanulastrum americanum, a plant sp

166 a plausible explanation for plastome-genome incompatibility in Geraniaceae.

167 r self-incompatibility) locus regulates self-incompatibility in Petunia inflata; the S-RNase regulate

168 us to the indirect evolution of reproductive incompatibility in sexual eukaryotes and linguistic inco

169 eptor kinase [SRK]) factors controlling self-incompatibility in the Brassicaceae, research in this fi

170 that the ARC1 E3 ligase is required for self-incompatibility in two diverse Brassicaceae species, Bra

171 Moreover, other chemical incompatibilities, including products of aborted ligatio

172 We investigated the influence of gender incompatibility, including H-Y incompatibility, on corne

173 an the distinction between compatibility and incompatibility inform our understanding of differences

174 act the evolutionary dynamics of cytonuclear incompatibility, interactions between nuclear and organe

175 t five loci, Bateson-Dobzhansky-Muller (BDM) incompatibilities involving epistatic interactions betwe

176 Loss of self-incompatibility is also associated with the evolution of

177 Incompatibility is associated with major TAL effectors t

178 This mito-nuclear incompatibility is between alleles of the nuclear-encode

179 Incompatibility is defeated by transfer of pthXo1 to oth

180 ic and biochemical studies revealed that the incompatibility is due to the functional promiscuity of

181 This incompatibility is environment dependent, such that the

182 al inheritance helps to mitigate cytonuclear incompatibility, leading to increased fitness of F1 hybr

183 e highly polygenic, indicating that multiple incompatibility loci have accumulated rapidly between th

184 tions from D. melanogaster to map two hybrid incompatibility loci in F(1) hybrids with its sister spe

185 ompatibility complex in vertebrates and self-incompatibility loci in plants.

186 The Leavenworthia self-incompatibility locus (S locus) consists of paralogs (La

187 The highly polymorphic S (for self-incompatibility) locus regulates self-incompatibility in

188 ovules, a phenomenon called late-acting self-incompatibility (LSI).

189 ns, known as Bateson-Dobzhansky-Muller (BDM) incompatibilities, may arise when the two populations fa

190 The gametophytic self-incompatibility mechanism enables the pistil of a plant

191 ns, and are potentially involved in the self-incompatibility mechanism.

192 Maternal-fetal genotype incompatibility (MFGI) is increasingly reported to influ

193 majority of the isolates exhibited mycelial incompatibility, minimizing the possibility of heterokar

194 netic variants can vary, and to use a single incompatibility model for all circumstances would cause

195 ice, it is challenging to identify the ideal incompatibility model for analysis, since the true MFGI

196 Further, we find longer sequences develop incompatibilities more quickly at small population sizes

197 tion that smaller populations should develop incompatibilities more quickly.

198 commensal strains, and (ii) because of this incompatibility, multidrug-resistant strains sharing fea

199 t their limitations include functional group incompatibility, narrow scope of application, high cost

200 nidirectional transition from ancestral self-incompatibility (obligate outcrossing) to self-compatibi

201 fundamental crystal chemistry and mechanical incompatibility of dissimilar interfaces.

202 ium results in low yields due to the solvent incompatibility of DNA and hydrophobic compounds.

203 containing E. coli AcpP helix II was due to incompatibility of L. lactis AcpA helix I with the downs

204 e fluorescence signal, thus establishing the incompatibility of nitrobenzofurazan-based thiol labelin

205 Incompatibility of the human platelet antigen-1 (HPA-1)

206 PEEM) for such purposes has been hampered by incompatibility of the liquid samples with ultrahigh vac

207 PT sequence: RNase H sequence preference and incompatibility of the poly(rA/dT) tract of the PPT with

208 Steric incompatibility of the RS domain and RanGTP engagement b

209 The incompatibility of the two blocks makes the final coupli

210 ere, we demonstrate that there is in fact no incompatibility of these results and, indeed, that the v

211 generation of nonclassicality and the mutual incompatibility of two states connected by time evolutio

212 e of variables such as anticoagulant and ABO incompatibility on post-transfusion platelet recovery.

213 nce of gender incompatibility, including H-Y incompatibility, on corneal transplant graft rejection a

214 olbachia invasion threshold, and cytoplasmic incompatibilities only have a marginal effect on the All

215 ate egg laying but do not induce cytoplasmic incompatibility or sex-ratio distortion, two parasitic r

216 ut cross-species transgenic assays uncovered incompatibility, or 'unintelligibility', of orthologous

217 g capabilities, sterilization by cytoplasmic incompatibility, or both; the release of Aedes carrying

218 rs including, bacterial density, cytoplasmic incompatibility, or resistance to infection with Zika vi

219 on what constitutes a strong and stable self-incompatibility phenotype in A. thaliana and how this sh

220 strain associated with a strong cytoplasmic incompatibility phenotype in its native host, Laodelphax

221 ructing a strong and stable A. thaliana self-incompatibility phenotype, in the context of the putativ

222 Strong incompatibility phenotypes emerged abruptly in some popu

223 vergence at these regions imply that genetic incompatibilities play a significant role in limiting ge

224 elf-recognition model for S-RNase-based self-incompatibility predicts that multiple S-locus F-box pro

225 Although the existence of genetic incompatibilities preventing the cross-species transfer

226 we describe a novel approach to address the incompatibility problem, which we refer to as Active Sol

227 mall secreted peptides in plants (e.g., self-incompatibility protein homologues) as well as non-secre

228 ates and avoids many of the functional group incompatibilities, regioselectivity issues, and high-ene

229 , the bacterial genes underlying cytoplasmic incompatibility remain unknown.

230 matory responses and cross-species molecular incompatibilities represents a major obstacle to success

231 ndidates for multigenic orchestration of the incompatibility response through disruption of endosperm

232 to the S-locus that are crucial to the self-incompatibility response.

233 e generated, and they exhibited reduced self-incompatibility responses resulting in successful fertil

234 ward flowing offshore current and endogenous incompatibilities restricting integration of certain reg

235 th chimeric transgenes imply that the hybrid incompatibilities result from interactions among nucleot

236 Hybrid incompatibility resulting from deleterious gene combinat

237 In Solanaceae, the self-incompatibility S-RNase and S-locus F-box interactions d

238 onuclear compatibility, reducing cytonuclear incompatibility's contribution to reproductive isolation

239 mber and genome-wide distribution of genetic incompatibilities separating species.

240 The genetic breakdown of self-incompatibility (SI) and subsequent mating system shifts

241 Self-incompatibility (SI) is a major genetically controlled s

242 Self-incompatibility (SI) is an important genetically control

243 Self-incompatibility (SI) is an important mechanism to preven

244 Self-incompatibility (SI) is the primary determinant of the o

245 nisms are less well understood than the self-incompatibility (SI) mechanisms plants use to reject pol

246 The self-incompatibility (SI) response of the Brassicaceae is med

247 of SRK and thus facilitate analysis of self-incompatibility (SI) signaling, we coexpressed an Arabid

248 both of the two genes that comprise the self-incompatibility (SI) specificity-determining S-locus hap

249 of all species of flowering plants show self-incompatibility (SI).

250 e pollen S-Locus F-box protein controls self-incompatibility (SI).

251 oes ecological adaptation cause reproductive incompatibilities such as hybrid sterility or lethality?

252 e protein but abolished its function in self-incompatibility, suggesting that dynamic cycling of SLF

253 comparison with RPP1 loci involved in hybrid incompatibility suggests that these functions evolved in

254 tudy, the Papaver rhoeas (poppy family) self-incompatibility system has been transferred into Arabido

255 The simple poppy self-incompatibility system may finally make it possible to i

256 A leaky self-incompatibility system was found, with self pollen havin

257 highly conserved eukaryotic invention, self-incompatibility systems such as mating types or sexes ap

258 bjects during performance of a Simon Spatial Incompatibility task.

259 his functional mismatch might lead to hybrid incompatibilities that are analogous to those underlying

260 overcome a severe bottleneck of male hybrid incompatibilities that enabled us to experimentally puri

261 of niosomes to prevent physical and chemical incompatibilities that occur upon mixing acyclovir and v

262 In several examples of plant self-incompatibility, the functional role of multiple element

263 s a suitable conception for examining hybrid incompatibilities, their account of the evidence is fact

264 speciation models find the strongest genetic incompatibilities to be nuclear-nuclear (specifically X

265 ed to be among the earliest types of genetic incompatibility to arise in speciation.

266 outcrossing mode of mating enforced by self-incompatibility to self-fertility in the Arabidopsis tha

267 transplantation including a death due to ABO incompatibility, two HIV transmissions and two hepatitis

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 This study models the probability of incompatibility versus compatibility for binary or unord

273 irus-restricting allorecognition [vegetative incompatibility (vic)] loci were disrupted in the chestn

274 performed with and without acceptance of ABO incompatibility was analyzed.

275 In adjusted models, ABO incompatibility was associated with twice the risk of pn

276 size discrepancy and human leukocyte antigen incompatibility were common reasons for declining offers

277 ted, indicating some degree of host-pathogen incompatibility when barriers to encounter are overcome.

278 lock co-evolution has produced cross-species incompatibilities, which may contribute to reproductive

279 inear effect on the probability of character incompatibility, which is also affected by the number of

280 mon reproductive manipulation is cytoplasmic incompatibility, which results in embryonic lethality in

281 the association of HLA-A, -B, -C, and -DRB1 incompatibilities with adverse outcome in hematopoietic

282 ng Paniceae Rubisco are identified; however, incompatibilities with Paniceae Rubisco biogenesis in to

283 Unfortunately, DIA methods suffer from incompatibility with common multiplexed quantification m

284 Associations of ABO incompatibility with complications were assessed by mult

285 vo studies in Drosophila is limited by their incompatibility with existing GAL4 lines and side effect

286 Its incompatibility with high conductivity media and limited

287 aqueous solubility and poor partitioning and incompatibility with insoluble polymers make long-term r

288 pitous collapse of the neuronal networks and incompatibility with life within days.

289 compounds has been limited by their general incompatibility with native enzymes.

290 e iron salts include chemical reactivity and incompatibility with other components.

291 s, often based on mistaken ideas about their incompatibility with prison security.

292 ble data is frequently under-utilized due to incompatibility with quantitative model tuning technique

293 Insufficient length and flexibility cause incompatibility with saturation kinetics.

294 ty, toxic and hazardous organic solvent, and incompatibility with scalable fabrication process.

295 roduction, which was further enhanced by the incompatibility with simw(501) mitochondria.

296 processed for a variety of reasons, such as incompatibility with spin coating, electron beam lithogr

297 Pregnancy-induced incompatibility with spouse donors was limiting given th

298 NFS1 gene that regulates the fixation-level incompatibility with the microsymbiont Sinorhizobium mel

299 cacy of rescue depended upon the strength of incompatibility, with a greater persistence of weak inco

300 basis to adaptive evolution and reproductive incompatibility; yet, the genomic scope and timing of po