ライフサイエンスコーパス: hybrid

1 female rats of six inbred strains and six F1 hybrids.

2 formance of ZIFs and their derived materials/hybrids.

3 polyketides, nonribosomal peptides and their hybrids.

4 Motion correction of hybrid (18)F-fluoride PET markedly improves SNR, resulti

5 Furthermore, the hybrid 3D additive printing strategy for biosensors faci

6 Herein, a hybrid adsorption-periphyton reactor (HAPR), combining a

7 GranSim is a hybrid agent-based computational model that simulates gr

8 e prospective European registry adopting the hybrid algorithm for CTO percutaneous coronary intervent

9 hase transition from nematic to smectic A in hybrid-aligned liquid crystal droplets on water substrat

10 Two-hybrid analysis revealed that the dynamins are part of t

11 , VNII, and VNB), some haploid isolates show hybrid ancestry including some that appear to have recen

12 cetylase subunits were observed in yeast two-hybrid and bimolecular fluorescence assays, consistent w

13 Two-hybrid and pulldown assays demonstrated that UL20, but n

14 ite, red and pink grape, as 28 interspecific hybrids and 2 Vitis vinifera L. popularly grown in Polan

15 tibility, leading to increased fitness of F1 hybrids and recovery in the F2 generation.

16 nces the association of RNaseH1 with RNA:DNA hybrids and stimulates the activity of RNaseH1 on R loop

17 oeologous gene pairs in the allopolyploid F1 hybrids and suggest that high-parental expression-level

18 opy, we studied four amphiphilic PEG-dendron hybrids and their self-assembled micelles in order to de

19 d scalable reaction to synthesize TiO2-S/rGO hybrid, and its excellent photocatalytic performance, su

20 nthesis of this graphene foam/TiO2 nanosheet hybrid, and its excellent water treatment performance an

21 markers between cultivated and interspecific hybrids, and 15 897 polymorphic markers within A. hypoga

22 We present a hybrid approach for modelling invasions of populations w

23 A hybrid approach integrating structural scaling factors d

24 ting uncertainty from the literature using a hybrid approach that combines rule induction and machine

25 en-Vacancy centers; our method is based on a hybrid approach that exploits ingredients in both digita

26 A-pIII complex, we developed a bacterial two-hybrid approach, named Oxi-BTH, suited for studying the

27 d and the potential for new applications and hybrid approaches are discussed.

28 multilayer MXenes and MXene/carbon nanotube hybrid architectures in terms of capacity, rate capabili

29 These results demonstrate that PAH-porphyrin hybrids are easily accessible, and this strategy may all

30 photocatalytic performance, such TiO2-S/rGO hybrids are expect to find practical applications in env

31 ylation changes induced in the interspecific hybrids are largely maintained in the allotetraploids.

32 s made by proteoliposomes bearing CesA8 from hybrid aspen.

33 ne-centered approach utilizing the yeast one-hybrid assay to generate a network of protein-DNA intera

34 and proteomics data together with yeast two-hybrid assays suggest that MS23 along with MS32, bHLH122

35 Using ChIP and one-hybrid assays, we find evidence for direct interaction b

36 ays, fluorescence Job plots, and yeast three-hybrid assays, we investigate the interactions of rProte

37 These hybrid assemblies are shown to be potentially attractive

38 nally, the formation of this three-component hybrid assembly from one-pot procedure, in water and usi

39 hat lateral gating of the BamA barrel and/or hybrid barrel formation is not required, at least for th

40 It involved the fabrication of nano-hybrid based electrochemical micro fluidic paper-based a

41 The analysis favours a hybrid between "enhanceosome" and "smorgasbord" models o

42 A hybrid biomarker developed using a stepwise feature sele

43 of cis and trans steroid-fulleropyrrolidines hybrids by reaction of N-metalated azomethine ylides [Cu

44 ggest that Hsp70 inhibitors as well as their hybrids can serve as potential anti-leukemia agents.

45 tion of this technology, we have developed a hybrid capture method to determine the exact triplet rep

46 The computational model is based on a hybrid cellular Potts and finite-element simulation fram

47 first demonstration of a functional 3D CMOL hybrid circuit.

48 emonstrate the applicability of such 3D CMOL hybrid circuits as a multiply-add engine.

49 Hybrid classification models were developed that could p

50 e aimed to investigate whether day-and-night hybrid closed-loop insulin delivery can improve glucose

51 mble copper-nanowires/reduced-graphene-oxide hybrid coatings onto inorganic and organic supports.

52 Importantly, the hybrids composed of Az and geldanamycin, which have high

53 These hybrid conductive composite hydrogels showed bi-stable s

54 The light transmittance of the hybrid construct after perforation was approximately 15-

55 an keratocytes (HKs) cultured on the optimal hybrid construct both demonstrated that the cells adhere

56 Centromeres are also stable in multiple F1 hybrid contexts.

57 A hybrid control model based on integrated motion cues sim

58 Notably, the hybrid CPT-Cap prodrug showed a synergistic effect and s

59 Thus, the novel IL233 hybrid cytokine, which utilizes the cooperation of IL-2

60 These include a novel hybrid data acquisition strategy to sequence cross-links

61 s revealed substantial changes rendering the hybrid de facto nonreactive with patients' serum IgE.

62 Such hybrids demonstrated effectiveness in two of the most wi

63 a proof-of-concept biobattery/supercapacitor hybrid device.

64 Our hybrid dielectric-loaded nanoridge plasmonic platform ma

65 In this study, we employed a hybrid diffuse optical system consisting of diffuse corr

66 hat the synthetic alkylated piperazine-azole hybrids do not function by fungal membrane disruption, b

67 ion of probe (single stranded DNA-ssDNA) and hybrid (double stranded DNA-dsDNA) both via 3-NT reducti

68 avithri, Tellahamsa, Triguna, Varalu and one hybrid DRRH-3, having wide agronomical and grain morphol

69 te evidence for misregulation as a source of hybrid dysfunction.

70 ls can be stably halted en route to EMT in a hybrid E/M phenotype.

71 mechanism is consistent with observations of hybrid earthquakes.

72 sing and contactless conductivity detection (hybrid EC-CE-C(4)D) is herein described.

73 Finally, the hybrid electrode was used for the determination of GSH a

74 to traditional chromatographic approaches, a hybrid electrophoresis device with electrochemical prepr

75 ancer landscape in X. tropicalis x X. laevis hybrid embryos.

76 nsposons are derepressed and recruit p300 in hybrid embryos.

77 Novel food-grade hybrid encapsulation structures based on the entrapment

78 ignaling, medullary AVR exhibited an unusual hybrid endothelial phenotype, expressing lymphatic marke

79 light irradiation, the presence of MoS2-rGO hybrids enhanced the hydrogen production rate of CZTS by

80 frequency (LF) events, whereas intermediate "Hybrid" events, have HF onsets followed by LF ringing.

81 a consequence, the number of active genes in hybrids exceeded the number of active genes in the paren

82 The Regent hybrid exhibited the highest total phenolics content (27

83 RNA-DNA hybrid exists at the repressed loci but is unrelated to

84 Two-hybrid experiments demonstrate self-interaction of the d

85 This supernova shows hybrid features of different supernova subclasses, namel

86 Ps are seamlessly grown on the CNTs, and the hybrid foam exhibits excellent EMI shielding effectivene

87 Supramolecular nanoparticle hybrids for biosensing of analytes have been a major foc

88 revealed that the coastal region harbours a hybrid form characterised by an A. gambiae-like sex chro

89 mainly co-transcriptional, abundant RNA/DNA hybrids, form naturally and can indeed be beneficial for

90 structures, noncoding RNA associated DNA/RNA hybrid formation, and promote collisions of transcriptio

91 ve a secondary structure that favors RNA:DNA hybrid formation.

92 An R-loop is a DNA:RNA hybrid formed during transcription when a DNA duplex is

93 can be created either by configuring RNA-DNA hybrid four-way junctions or by template-directed synthe

94 D methods, making it a valuable new tool for hybrid fragmentation approaches.

95 was designed and successfully installed in a hybrid FT-ICR instrument in place of the standard gas co

96 ilored biomimetic nanoparticles with varying hybrid functionalities, which may be used to overcome th

97 ving the loss of GYPB and gain of two GYPB-A hybrid genes, which encode a serologically distinct bloo

98 Using a yeast two-hybrid genome-wide screen, we identified novel interacti

99 ed as a bare active material or component in hybrids, graphene has been the subject of numerous studi

100 Using yeast two-hybrid, GST pull-down, co-immunoprecipitation and bimole

101 Organic-inorganic hybrid halide perovskites (e.g., MAPbI3 ) have recently

102 Two-dimensional (2D) hybrid halide perovskites come as a family (B)2(A)n-1Pbn

103 The phenolic profiles of these hybrids have not yet been reported.

104 However, the Az and imatinib hybrids have weak inhibitory activities towards Hsp70 an

105 the development of III-V/graphene functional hybrid heterostructures.

106 Hybrid hierarchical clustering of these six factors iden

107 sh, and parasite size was intermediate in F1 hybrid hosts.

108 This self-healing polymer-beta-sheet peptide hybrid hydrogel with tailorable mechanical properties is

109 e and exists in a dynamic equilibrium with a hybrid i-motif/hairpin species and an unfolded hairpin s

110 1, an enzyme that cleaves the RNA of RNA/DNA hybrids in B cells.

111 Hybrids in this population formed separate genetic clust

112 Hybrid incompatibility resulting from deleterious gene c

113 omosome does not harbor loci contributing to hybrid incompatibility.

114 indirectly trigger heterosis in Arabidopsis hybrids independent of genetic changes.

115 Thus we show a route by which simple hybrid inorganic-organic monomers, such as compound 1, c

116 Hybrid inorganic-organic superlattice with an electron-t

117 t one of them, the optical fiber/micropillar hybrid, into a soft optical contact sensor.

118 ZTS) photocatalysts, indicating the MoS2-rGO hybrid is a better co-catalyst for photocatalytic hydrog

119 nt performance and recycle stability, such a hybrid is promising for large scale production for pract

120 t the EPEC and ETEC virulence genes of these hybrid isolates were differentially-expressed under viru

121 In addition, these novel hybrid-layered membranes exhibit better chlorine resista

122 These results show that HISN6-dependent hybrid lethality is a revertible epigenetic phenomenon a

123 Magnon-polaritons are hybrid light-matter quasiparticles originating from the

124 Hybrid lipids show no enrichment at the boundary, but de

125 This opens new research paths in hybrid magneto-molecular optoelectronics, and the optica

126 here, but altered the soil communities where hybrid maize was grown.

127 By combining hybrid mass spectrometry with cryo-EM, computational and

128 ther to give a three-component, well-ordered hybrid material derived either as a supramolecular hydro

129 Protonation of all basic sites of the hybrid material nearly doubles its conformational space

130 quenching capabilities of a graphene-related hybrid material, is truly new and may have broad interes

131 bserve 'quantum cutting' in 0D metal-organic hybrid materials based on methylammonium bismuth halide

132 ature has evolved hierarchical structures of hybrid materials with excellent mechanical properties.

133 ptides is a promising route for synthesizing hybrid materials with the economy and efficiency of livi

134 f excitons in zero-dimensional metal-organic hybrid materials, a highly orientated film of (CH3NH3)3B

135 ent blends, supramolecular assemblies, novel hybrid materials, and large cross-linked or nonionizable

136 We found that human subjects employed a hybrid MB/MF strategy on the task, corroborating the par

137 ses function with Ub E2s through a RING/HECT hybrid mechanism to conjugate Ub to target proteins.

138 te that contiguous cell walls indeed exhibit hybrid mechanochemical properties.

139 This unique property provides the hybrid membrane with switchable oil/water separation fun

140 The resulting particles, termed RBC-platelet hybrid membrane-coated nanoparticles ([RBC-P]NPs), are t

141 Free-standing and flexible WS2 /WO2.9 /C hybrid membranes are synthesized and used as catalytic e

142 A hybrid metamaterial/graphene device is implemented into

143 Hybrid metamaterials that exhibit reconfigurable respons

144 shape variation in the first upper molar of hybrid mice between Mus musculus musculus and M. m.

145 ing of these mice generated animals that had hybrid microbiotas and displayed intermediate susceptibi

146 s in parental mouse strains and in mice with hybrid microbiotas identified the bacterial family Lachn

147 Compared with the paper-free non-hybrid microfluidic biochip over a period of three month

148 c biochip over a period of three months, the hybrid microfluidic biochip was found to have a much lon

149 Here we report Y-shp-MOF-5, a hybrid microporous highly connected rare-earth-based met

150 ostructures is then triggered to form stable hybrid microtoroids.

151 24 and 8 from Ler were present in all of the hybrid mimic lines, whereas in the F6 small phenotype li

152 The hybrid mimics are almost completely homozygous with chro

153 fic data on cation reorientation dynamics in hybrid mixed-cation formamidinium (FA)/methylammonium (M

154 nfinement and attenuation of the fundamental hybrid mode, and we demonstrate the tolerance of its pro

155 To this purpose, the cost-sensitive hybrid model (CSHM) and five conventional machine learni

156 distribution of exciton-polaritons along the hybrid modes by a thermodynamic model, which yields a ve

157 Here we disclose an efficacious hybrid molecule 4-(5-Amino-1,2,3-oxadiazol-3-yl)-2,2,6,6

158 rts on each of the 3 parental allergens, the hybrid molecule was designed to cover relevant epitopes

159 of the charge carriers through the resulting hybrid molecule/metal spinterface in a single-molecule e

160 pped carbon nanotubes are a class of bionano hybrid molecules that have enabled carbon nanotube sorti

161 This hybrid MS(3) strategy affords the lipid's sum compositio

162 r also contribute to this process, forming a hybrid myocardial zone that is composed of cells derived

163 f current biosensing structures created from hybrid nanomaterials are reviewed, with a distinct empha

164 We developed core shell lipid-polymer hybrid nanoparticles (CSLPHNPs) with poly (lactic-co-gly

165 DNA circuit (CHDC) in cationic lipid-polymer hybrid nanoparticles (LPHNs) that are tethered on a chip

166 w that immunization with these lipid-polymer hybrid nanoparticles (LPNs) coated with the mucoadhesive

167 Magnetic-plasmonic hybrid nanoparticles (MPHNs) have attracted great intere

168 On the other hand, metal-semiconductor hybrid nanostructures are found to be very promising for

169 optimization of functional organic/inorganic hybrid nanostructures for diverse optoelectronic applica

170 their practical utilization in NRET-coupled hybrid nanostructures.

171 the two categories mentioned above, that of hybrid NHC ligands in which the functionality associated

172 mplantable sensors, or prosthetic devices in hybrids of living and non-living systems.

173 yanins in two the most popular interspecific hybrids of red grapes, Rondo and Regent, nowadays very p

174 e, Davanco et al. stride toward this goal by hybrid on-chip integration of Si3N4 waveguides and GaAs

175 on of pre- and post-synaptic spikes within a hybrid one-transistor/one-resistor (1T1R) memristive syn

176 ase in recombination observed in recq4 figl1 hybrids opens the possibility of manipulating recombinat

177 In hybrid optomechanical systems, light and matter are stro

178 on the ground state and does not generate a hybrid orbital.

179 The occurrence of proton tunneling in MAPbI3 hybrid organic inorganic perovskites is demonstrated thr

180 The performance of bulk organic and hybrid organic-inorganic heterojunction photovoltaics is

181 For hybrid organic-inorganic nanomaterials, here we show tha

182 Hybrid (organic-inorganic) multication lead halide perov

183 ialization of thin-film solar cells based on hybrid organohalide lead perovskites is interface loss i

184 After evaluating the assay system in the hybrid paper-SPCE cell, the three-electrode system consi

185 This transformation operates via a hybrid Pd-radical mechanism, which synergistically combi

186 changes in DNA methylation and small RNAs in hybrid performance; however, it remains unclear whether

187 A combination of hybrid periodic density functional theory calculations a

188 This pressure-induced comminution of hybrid perovskite NCs and a subsequent amorphization-rec

189 We report the metallization of the hybrid perovskite semiconductor (MA)PbI3 (MA = CH3NH3(+)

190 efficiency demonstrated in organic-inorganic hybrid perovskite solar cells (PVSCs), critical concerns

191 h has led to the realization of single-phase hybrid perovskites of (FAPbI3 )1-x (CsSnI3 )x (0<x<1) co

192 and injected carrier densities.Mixed halide hybrid perovskites possess tunable band gaps, however, u

193 pportunities for solar water splitting using hybrid perovskites with solar-to-hydrogen efficiencies b

194 he possibilities of engineering the advanced hybrid perovskites with specific properties.

195 rrier thermalization times of 10 to 85 fs in hybrid perovskites.

196 : 1, high-grade: 1) were investigated with a hybrid PET/MR scanner.

197 We propose that the hybrid phenotype contributes to metabolic plasticity, al

198 raphy, whereby the selected ethylene-bridged hybrid phenyl ultra-high-performance liquid chromatograp

199 Hybrid plants lacking CML38 and having high accumulation

200 we report a guiding approach that integrates hybrid plasmon polariton with dielectric-loaded plasmoni

201 Here, we describe a hybrid platform combining common analysis pathways with

202 Increasing the efficiency of TET in this hybrid platform will increase both the up- and down-conv

203 The formation of hybrid polariton modes is evidenced in momentum resolved

204 upling regime, resulting in the formation of hybrid polariton modes.

205 ROAMP followed by RAFT polymerization yields hybrid poly-(o-phenylene ethynylene)-block-poly-(methyl

206 Through the construction of hybrid PorB types and PorB molecular dynamics simulation

207 monstrate the excellent performance of these hybrid porous materials in removing low-concentration SO

208 Successfully assembled cell-particle hybrids presented here comprised either melanoma cells o

209 nary intervention (Registry of CrossBoss and Hybrid Procedures in France, the Netherlands, Belgium an

210 ion mechanisms into a single self-assembling hybrid prodrug to construct self-deliverable nanomedicin

211 d cytotoxicity evaluation of self-assembling hybrid prodrugs containing both camptothecin (CPT) and a

212 d lines B73 and Mo17 and their reciprocal F1 hybrid progeny in primary roots under control and water

213 nder fluctuating environmental conditions in hybrid progeny of the inbred lines B73 and Mo17.

214 heterosis) between Dura, Pisifera and their hybrid progeny Tenera has not yet been well understood.

215 n is now complete because of sterility of F1 hybrid progeny, prezygotic isolation is still incipient.

216 els than the commonly used Hsp70A-RBCS2 (AR) hybrid promoter/terminator sequences.

217 content imaging and a mammalian membrane two-hybrid protein-protein interaction method, we identified

218 ention procedures performed according to the hybrid protocol in 17 European centers, comparing fTRA (

219 report herein a computational study based on hybrid QM/MM umbrella sampling simulations that allow th

220 and peptide identifications to rival modern hybrid quadrupole orbitrap systems.

221 tion with gas chromatography (GC) coupled to hybrid quadrupole time-of-flight (QTOF) mass spectrometr

222 We use classical molecular dynamics and hybrid quantum mechanics/molecular mechanics calculation

223 Hybrid quantum networks rely on efficient interfacing of

224 odel Accuracy (EMA), which uses a pioneering hybrid quasi-single model approach.

225 rA27(aa 21-84)-FND, rDA27(aa 33-84)-FND, and hybrid rA27(aa 21-84)/rDA27(aa 33-84)-FND.

226 ReFOLD is a novel hybrid refinement server with integrated high performanc

227 se genes are significantly altered in the F1 hybrids relative to the parental lines.

228 uggests the potential for creating VO2 based hybrid resonators that operate at THz frequencies.

229 Xieyou9308 is one of the most famous super hybrid rice varieties.

230 In vivo assays show that this hybrid RNA-cDNA molecule is required for mutagenic trans

231 eraction between two inequivalent spins in a hybrid rotaxane molecule.

232 The sensor-regulator hybrid SagS plays a central role in biofilm development

233 Furthermore, using a yeast two-hybrid screen, we identified the motor protein Kif15 as

234 The multi-billion-dollar maize hybrid seed business, however, is supported by industria

235 ctical pipelines for recurrent selection and hybrid seed production in wheat.

236 ne and discuss its potential for large-scale hybrid seed production in wheat.

237 Such hybrid SEIs composed of Si-interlinked OOCOR molecules t

238 We report on the design and fabrication of a hybrid sensor that integrates transmission-mode localize

239 different stationary phases were evaluated (hybrid silica and a solid-core-based C18 column).

240 The formation of hybrid silicon-gold NPs as a result of the laser action

241 This algorithm, the Hybrid Similarity Search, generates a similarity score b

242 Three-dimensional hybrid simulations corroborate our experimental observat

243 radiation hydrodynamic and three-dimensional hybrid simulations shows the control of the deflection a

244 roach is quite limited because very few such hybrid solar cells can simultaneously show high short-ci

245 ent, organic, photovoltaics (OPV)/perovskite hybrid solar cells.

246 equipped with parallel hole collimators, and hybrid SPECT/CT images were acquired using a dedicated c

247 nd 8.0% for tilapia, catfish, trout, salmon, hybrid striped bass and yellow perch, respectively.

248 We propose a Hybrid Structural variant Assembly (HySA) approach that

249 ge can be extended to tens of microns in the hybrid structure mediated by an exciton-surface plasmon

250 e limit, we consider the emergent physics in hybrid structures comprised of a conventional s-wave sup

251 age in part through the formation of RNA:DNA hybrid structures, leading to motor neuron death.

252 ub-gap conductance) is demonstrated in these hybrid superconductor-semiconductor nanowires, highlight

253 SPCH represents a class of hybrid supramolecular composites, opening a window into

254 crosses, and then associate inheritance with hybrid survival across multiple generations.

255 wild rice populations should be considered a hybrid swarm, connected to domesticated rice by continuo

256 e report on a three-component supramolecular hybrid system built from specific recognition processes

257 A Bacterial Two Hybrid system indicates that DauA and the sensor complex

258 nsional chiral Majorana fermion modes in the hybrid system of a quantum anomalous Hall insulator thin

259 Not only does our hybrid system represent the first example of a reversibl

260 The use of hybrid systems for which the change in properties of one

261 ing initial interactions at the interface of hybrid systems under humid conditions has the potential

262 al to understand the long-term durability of hybrid systems.

263 Nevertheless, hybrid terahertz (THz) metamaterials whose spectral perf

264 robust, and biocompatible hydrogel-elastomer hybrids that host various types of genetically engineere

265 tubes to penetrate to the ovary and produce hybrids that, otherwise, would be difficult to obtain.

266 s, M. galloprovincialis, M. edulis and their hybrids through clearly-distinguishable melting curves.

267 iver glycogen of triplicate groups of 20 red hybrid tilapia (Orecohromis sp.).

268 A new hybrid time stepping approach, which couples the Runge-K

269 to achieve topological phase and to realize hybrid topological superconducting devices.

270 rthermore, recombinant strains co-expressing Hybrid toxin and AaIT (Na(+) channel blocker) produced s

271 The hybrid transcription factor SS18:SSX alters SWItch/Sucro

272 Hybrid, transhiatal, and emergency procedures were exclu

273 lish this using two-dimensional (2D) layered hybrid trihalide perovskites that are deposited onto sil

274 alphaPEG, long-type cells; 293T/SL-alphaPEG, hybrid-type cells) to improve the binding capacity and d

275 The connection of two of these hybrid units together, using a flexible spacer, facilita

276 Here, we exposed F2 hybrids, used to separate Eda genotype from genetic back

277 oited as a useful approach for production of hybrid varieties to harness the benefits of hybrid vigou

278 moter of rice for facilitating production of hybrid varieties.

279 AVRs as Tie2 signaling-dependent specialized hybrid vessels and provide genetic evidence of the criti

280 for EgWRI1 as an important gene contributing hybrid vigor in lipid biosynthesis in oil palm.

281 genes may be critical for the generation of hybrid vigor.

282 However, the molecular mechanisms of hybrids vigor (or heterosis) between Dura, Pisifera and

283 hybrid varieties to harness the benefits of hybrid vigour.

284 ave generated a mouse line with an optimized hybrid voltage sensor (hVOS) probe within a locus design

285 The hybrid was evaluated for both chromium (VI) and organic

286 d during the synthesis of flavone-amino acid hybrids, was successfully prevented in most cases.

287 lower propagation loss than its conventional hybrid waveguiding counterpart, while maintaining strong

288 lele-specific transcript abundance in the F1 hybrids, we were able to measure the abundance of cis- a

289 Novel mupirocin-thiomarinol hybrids were also synthesized by mutasynthesis.

290 , we designed a graphene foam/TiO2 nanosheet hybrid, which is able to effectively remove both chromiu

291 plex and the formation of cellular:viral RNA hybrids, which are essential RNA intermediates that lice

292 ocess to produce DNA-wrapped carbon nanotube hybrids with nanotubes of broad diameter range and DNA o

293 s mechanisms of these two different types of hybrid ZIFs are unknown.

294 ted the extent, causes and consequences of a hybrid zone between Anopheles coluzzii and Anopheles gam

295 the relationship between climate change and hybrid zone dynamics remains tenuous [5].

296 fferentials in survival, which in turn drive hybrid zone movement for two woodrat species (Neotoma fu

297 period, matched the spatial dynamics of the hybrid zone, which moved steadily north into N. fuscipes

298 nge expansions are expected to result in new hybrid zones between closely related species.

299 e dictating the location and extent of their hybrid zones, and that runaway introgression between the

300 to both climatic conditions and movement of hybrid zones, such that the relationship between climate