ライフサイエンスコーパス: winged

1 ts with a descending order of worker> alate (winged adult) female> alate (winged adult) male> larvae>

2 worker> alate (winged adult) female> alate (winged adult) male> larvae> worker pupae approximately a

3 insects metamorphose from aquatic larvae to winged adults, and recent surveys indicate that adults m

4 m the generic flight circuitry of their four-winged ancestors.

5 We measured fecundity of winged and unwinged aphids challenged with a heat-inacti

6 12 miRNAs were significantly up-regulated in winged and wingless S. avenae small RNA libraries, respe

7 ults, queens and workers, and female alates (winged) and queens (wingless), AK cDNA was obtained from

8 pared the safety of a new tampon with a four-winged apertured film cover over its nonwoven cover to i

9 We found that winged aphids are less resistant and mount a weaker immu

10 Winged aphids have the advantage of being able to migrat

11 nse than unwinged aphids, demonstrating that winged aphids pay higher costs for a less effective immu

12 nticipation of higher disease risk, and that winged aphids would be more resistant due to a stronger

13 , and found that immune costs are limited to winged aphids.

14 Our study focused on the disc-winged bat Thyroptera tricolor, a species highly morphol

15 tor genes (WCI2 and WCI5) were isolated from winged bean (Psophocarpus tetragonolobus (L.) DC).

16 WCI5 was exclusively expressed in winged bean seeds.

17 Winged bean, Psophocarpus tetragonolobus (L.) DC., is si

18 z trypsin inhibitor (KTI) gene family within winged bean.

19 o infer relationships of four species of net-winged beetles characterised by female neoteny.

20 n avian host-parasite system: adult male red-winged blackbirds (Agelaius phoeniceus) infected with ha

21 We studied free-living male red-winged blackbirds (Agelaius phoeniceus) to test whether

22 dual aspects of hybridization in the golden-winged/blue-winged warbler complex, two phenotypically d

23 r classic small, lightweight, feathered, and winged body plan was pieced together gradually over tens

24 ages after disturbance comprised smaller and winged carabids, and smaller plants with wind-dispersed

25 performance electrocatalysts based on unique winged carbon nanotubes.

26 etween them, most notably in the absence of 'winged' cilia morphology in P. pacificus.

27 screaming cowbird) and one nonparasite (bay-winged cowbird).

28 nd smallest in the nonparasitic species (bay-winged cowbird).

29 Microraptor gui, a four-winged dromaeosaur from the Early Cretaceous of China, p

30 homeotic transformation of the normally two-winged Drosophila into a four-winged mutant fly.

31 closely related allopatric Hawaiian picture-winged Drosophila that produce sterile F1 males but fert

32 It is thus possible to increase winged female parasitoid production for the purposes of

33 The percentage of winged female parasitoid progeny increased exponentially

34 The percentage of winged female progeny was not significantly influenced b

35 favourable conditions for the production of winged females in this bethylid wasp.

36 ly nutritionally determined) short- and long-winged females.

37 and wing morphology (that is, either a long-winged flight-capable phenotype or a short-winged flight

38 g-winged flight-capable phenotype or a short-winged flightless phenotype) to predict phenotypic chang

39 ht contributed to the success of insects and winged forms are present in most orders.

40 cally reasonable configuration for this four-winged gliding animal.

41 ., herring gull (Larus argentatus), glaucous-winged gull (L. glaucescens), and California gull (L. ca

42 lta(13)C) evidence from feathers of Glaucous-winged Gulls (Larus glaucescens) has shown that over the

43 c change in the relative orientations of the winged helical DNA binding domains within the dimer.

44 l sensors that appear to conform to the same winged helical, homodimeric fold, that collectively "sen

45 We have localized the position of the TFE winged helix (WH) and Zinc ribbon (ZR) domains on the RN

46 FIIE-like factors, which is characterised by winged helix (WH) domain expansion in eukaryotes and los

47 we identify and determine the structure of a winged helix (WH) domain from human MUS81, which binds D

48 The C-terminal winged helix (WH) domains of Tfg1 and Tfg2 are mobile, b

49 Deleting or mutating K99 of the N-terminal winged helix (WH) motif in ASH2L abrogates H2Bub-depende

50 cription initiation and binds the mobile C34 winged helix 2 domain, sealing off the active site.

51 ic residue predicted to be at the tip of the winged helix beta-hairpin), showed a decrease in DNA bin

52 are critical for the development of forkhead-winged helix box transcription factor 3(+) regulatory T

53 FoxA, the paradigm pioneer TF, has a winged helix DBD that resembles linker histone and there

54 AphA is a dimer with an N-terminal winged helix DNA binding domain that is architecturally

55 -mediated phosphorylation of a serine in the winged helix DNA binding motif curtails FoxO1 nucleosome

56 family of TFs, defined by a highly conserved winged helix DNA-binding domain (DBD), has diverged into

57 U_0916 protein identified two domains, one a winged helix DNA-binding domain common for transcription

58 tion of mouse HOP2, which contains a typical winged helix DNA-binding domain.

59 AphA is a winged helix DNA-binding protein that enhances the abili

60 We show that Cac1C forms a winged helix domain (WHD) and binds DNA in a sequence-in

61 domains in Uaf30 that include an N-terminal winged helix domain and a disordered tethering domain as

62 C-terminus of Cac1, including the structured winged helix domain and glutamate/aspartate-rich domain,

63 uch a region consists of a zinc domain and a winged helix domain and plays an important role in enzym

64 unds binding to a protein pocket between the winged helix domain and topoisomerase-primase domain, re

65 tsK interacts with KOPS through a C-terminal winged helix domain gamma.

66 binding to a H3-H4 dimer activates the Cac1 winged helix domain interaction with DNA.

67 NA in a manner similar to RecQ1, whereas the winged helix domain may assume alternative conformations

68 erminal domain near Pol I wall or the tandem winged helix domain of A49 at a partially overlapping lo

69 of these complexes were mapped to the second winged helix domain of human ESCRT-II subunit VPS25 and

70 merization domain on the Pol II lobe and the winged helix domain of the TFIIF small subunit Tfg2 abov

71 ding is mediated principally by a C-terminal winged helix domain that inserts deeply into the major a

72 ithin the ATPase, Topoisomerase/Primase, and Winged helix domains, including four that encode protein

73 We recently demonstrated that the winged helix factor forkhead box protein A3 (Foxa3) regu

74 es and show here for the first time that the winged helix factor Foxa3 promotes adipocyte differentia

75 e result of increase binding of the forkhead winged helix factor FoxD1 to a TGF-beta-responsive eleme

76 The winged helix factors Foxa1 and Foxa2 are essential membe

77 hat the Foxk1 gene, a member of the forkhead/winged helix family of transcription factors, is express

78 and that the C-terminal domain might have a winged helix motif.

79 m the IGFBP1 promoter via a highly conserved winged helix motif.

80 We map binding to the winged helix of H1 and determine that citrulline 53 repr

81 e data suggest that the winged region of the winged helix protein participates in DNA binding and act

82 or the nuclear transcription factor Forkhead winged helix protein-3 and able to inhibit naive T cell

83 ution x-ray crystal structure of the dimeric winged helix SarA protein, which differs from the publis

84 action is direct and is mediated by the RecQ winged helix subdomain and the C terminus of SSB.

85 etween these repeats and the more C-terminal winged helix subdomain.

86 Binding of the winged helix to the protrusion is PIC specific.

87 ro, as demonstrated by cytokine and forkhead/winged helix transcription factor (FoxP3) gene and prote

88 beta induce naive T cells to become forkhead/winged helix transcription factor (Foxp3) positive regul

89 of the T(reg) cell lineage factor, Forkhead/winged helix transcription factor (Foxp3), and tolerance

90 Additionally, CD4+ forkhead/winged helix transcription factor 3+ T cells were also d

91 Foxc1 encodes a forkhead/winged helix transcription factor expressed in many embr

92 Two members of the forkhead/winged helix transcription factor family, Foxa1 and Foxa

93 ted motility and is a putative member of the winged helix transcription factor family.

94 e X-linked Foxp3 is a member of the forkhead/winged helix transcription factor family.

95 a 35,000-fold higher expression of forkhead/winged helix transcription factor forkhead box (FOXF1) n

96 ed genome-wide binding sites of the forkhead/winged helix transcription factor Foxa1, which functions

97 l YAC-based Foxa3Cre transgene to delete the winged helix transcription factor Foxa2 (formerly HNF-3b

98 The variant histone H2A.Z and the winged helix transcription factor Foxa2 both act to regu

99 nd cell type-specific gene ablation that the winged helix transcription factor Foxa2 is required for

100 We show in both mouse and zebrafish that the winged helix transcription factor Foxg1 is expressed in

101 The winged helix transcription factor Foxl1 is a marker for

102 The winged helix transcription factor Foxl1 localizes to mes

103 cell-specific transcription factor forkhead/winged helix transcription factor gene (FOXP3) in CD4+CD

104 tabolite NAD induce death in murine forkhead/winged helix transcription factor gene-expressing CD4+CD

105 khead Box C1 (FOXC1) gene encodes a forkhead/winged helix transcription factor involved in embryonic

106 generation of allospecific CD4CD25 forkhead/winged helix transcription factor P3 (FOXP3) T-regulator

107 L, however, significantly increased forkhead/winged helix transcription factor P3 (FOXP3) Tregs, wher

108 In this study we find that the winged helix transcription factor Rfx2 is expressed in m

109 ances is restrained by CD4(+)CD25(+)forkhead/winged helix transcription factor(+) regulatory T cells.

110 hymic mice depleted of CD4(+)CD25(+)forkhead/winged helix transcription factor(+) regulatory T cells.

111 D25+ glucocorticoid-inducible TNFR+-Forkhead/winged helix transcription factor+ populations and effic

112 Members of the Foxa family of forkhead/winged helix transcription factor, Foxa1 and Foxa2, have

113 We identified a forkhead/winged helix transcription factor, Foxj3, which was expr

114 opulation does acquire the X-linked forkhead/winged helix transcription factor, FoxP3, which is assoc

115 The winged helix transcription factors Foxa1 and Foxa2 are e

116 we demonstrate novel roles for the forkhead/winged helix transcription factors Foxa1 and Foxa2 in th

117 -beta and -gamma) constitute a sub-family of winged helix transcription factors with multiple roles i

118 The initiator belongs to the family of winged helix type of proteins.

119 nnovation that involve founder 'p-loop' and 'winged helix' domain structures.

120 t the C-terminal, DNA-binding domain (tandem-winged helix), the heterodimerization, and the linker do

121 In comparison, weaker interaction of FOXA1 winged helix, and the NH(2)-terminal domains was documen

122 Foxe3 encodes a winged helix-forkhead transcription factor that is initi

123 The C-terminal, winged helix-loop-helix, protein-protein interaction dom

124 Although the RepA and DnaD NTD both contain winged helix-turn-helices, the DnaD NTD self-assembles i

125 ture consists of an intertwined dimer with a winged helix-turn-helix (HTH) motif.

126 n1 (Stn1C) was found to comprise two related winged helix-turn-helix (WH) motifs, one of which is mos

127 n factor complexes and contain an N terminal winged helix-turn-helix (wHTH) DNA binding domain (DBD).

128 form a dimer, with each monomer harboring a winged helix-turn-helix (WHTH) DNA-binding motif.

129 yclases, FhlA) domain that binds BCAAs and a winged helix-turn-helix (wHTH) domain that binds to DNA,

130 in ligase of Escherichia coli belongs to the winged helix-turn-helix (wHTH) family of transcriptional

131 TFs with winged helix-turn-helix (wHTH) motifs use an alpha helix

132 PF0610 is a novel winged helix-turn-helix (wHTH) protein with a rubredoxin

133 To bind DNA, OhrR employs a chimeric winged helix-turn-helix DNA binding motif, which is comp

134 d binding site, partially overlapping with a winged helix-turn-helix DNA binding site.

135 -terminal regulatory domain and a C-terminal winged helix-turn-helix DNA-binding domain, with phospho

136 ding, while the N-terminal domains contain a winged helix-turn-helix DNA-binding motif and are arrang

137 is composed of three domains: an N-terminal winged helix-turn-helix domain (WH), a GAF-like domain,

138 R on a conserved arginine residue within the winged helix-turn-helix domain is necessary for modulati

139 al domain is fused to a C-terminal MarR-like winged helix-turn-helix domain that is expected to be in

140 family nucleases, are replaced by an unusual winged helix-turn-helix domain, where the "wing" is cont

141 s overall fold resembles closely that of the winged helix-turn-helix family of DNA-binding proteins.

142 the 28 degrees rigid body rotations of each winged helix-turn-helix motif and DNA dissociation.

143 (chxR), whose amino acid sequence contains a winged helix-turn-helix motif similar to the DNA-binding

144 t with the DNA in the classical fashion of a winged helix-turn-helix motif.

145 Z adopts a unique fold in which three tandem winged helix-turn-helix motifs scaffold a positively cha

146 onal changes needed to allow the DNA-binding winged helix-turn-helix motifs to interact with the cons

147 ected residues map to the wing domain of the winged helix-turn-helix of ToxR.

148 of the yeast transcription factor Mbp1 is a winged helix-turn-helix structure, with an extended DNA

149 PhoPC exhibits a typical fold of the winged helix-turn-helix subfamily of response regulators

150 posed of an N-terminal DNA binding domain of winged helix-turn-helix topology and a C-terminal dimeri

151 ffector domain, and a C-terminal DNA-binding winged helix-turn-helix-like domain.

152 e riboflavin kinase domain and a DNA-binding winged helix-turn-helix-like domain.

153 ovel 7 kDa T7 protein, Gp5.7, which adopts a winged helix-turn-helix-like structure and specifically

154 OmpR is a winged helix-turnhelix DNA-binding protein that function

155 Deletion of the Foxa2 gene, encoding a winged helix/forkhead box transcription factor that is s

156 foxd3 encodes a winged helix/forkhead class transcription factor express

157 involves the first FF motif of p190A and the winged helix/PCI domain of eIF3A, is enhanced by serum s

158 on factors, binds DNA via a highly conserved winged-helix "forkhead box" motif used by other regulato

159 at both the DNA substrate and the C-terminal winged-helix (WH) domain influence the orientation but t

160 Helicase activity, as well as the conserved winged-helix (WH) motif and the helicase and RNase D C-t

161 d-forming N-terminal domain, which reveals a winged-helix architecture, with additional structural el

162 itself to one Cul3 molecule and binds to the winged-helix B domain at the C terminus of the second Cu

163 third of the polypeptide, just distal to its winged-helix DNA binding domain.

164 (Fox) proteins share the Forkhead domain, a winged-helix DNA binding module, which is conserved amon

165 Xis is a winged-helix DNA binding protein that cooperatively bind

166 mpletely different manner from the canonical winged-helix DNA recognition motif.

167 monomer comprises two domains: an N-terminal winged-helix DNA-binding domain and a C-terminal PLP-bin

168 hich are located within wings 1 and 2 of its winged-helix DNA-binding domain.

169 of Sso10a and show that it is a homodimer of winged-helix DNA-binding domains.

170 crystal structure of Vfr shows that it is a winged-helix DNA-binding protein like its homologue cycl

171 an N-terminal AAA(+) domain and a C-terminal winged-helix domain (WHD), but use remarkably few base-s

172 This region folds into a winged-helix domain and an extended coiled-coil domain t

173 cQ has evolved an SSB-Ct binding site on its winged-helix domain as an adaptation that aids its cellu

174 The winged-helix domain contains putative DNA-binding residu

175 s indicate that ORC encircles DNA, using its winged-helix domain face to engage the mini-chromosome m

176 in the RecQ variants indicate a role for the winged-helix domain in helicase activity beyond SSB prot

177 Furthermore, the winged-helix domain of LEM2 activates the ESCRT-II/ESCRT

178 th tubulin monomers via the carboxy-terminal winged-helix domain of Ska1, providing the structural ba

179 e conserved aromatic residue in the extended winged-helix domain of TFEalpha interacts with promoter

180 A-dependent conformational rearrangements: a winged-helix domain pivots approximately 90 degrees to c

181 alpha/beta fold, a short helical motif and a winged-helix domain, resulting in the burial of the casp

182 s, a RecQ-specific zinc-binding domain and a winged-helix domain, the latter implicated in DNA strand

183 between RecQ and SSB is mediated by the RecQ winged-helix domain, which binds the nine C-terminal-mos

184 to the NTR and to the N-terminal half of the winged-helix domain.

185 nct from the previously described C-terminal winged-helix domain.

186 AAA+-like domains forming one layer, and the winged-helix domains (WHDs) forming a top layer.

187 CHMP7's N terminus comprises tandem Winged-Helix domains [6], and, by using homology modelin

188 wo-layered notched ring in which a collar of winged-helix domains from the Orc1-5 subunits sits atop

189 stallography, we show that Cdt1 contains two winged-helix domains in the C-terminal half of the prote

190 th the N-terminal OB fold and the C-terminal winged-helix domains of Stn1 can bind to the Pol12 subun

191 The wings and helices of the winged-helix domains remain exposed on the surface of th

192 dynamic movements of the ORC1 AAA+ and ORC2 winged-helix domains that likely impact DNA incorporatio

193 site in the ORC ring and cooperate with the winged-helix domains to stabilize DNA bending.

194 Although the forkhead/winged-helix family member FOXP3 is critical for Treg di

195 FOXO1A, a member of the forkhead winged-helix family of proteins is a transcription facto

196 Foxp3, a member of the forkhead/winged-helix family of transcription factors, acts as th

197 jI gene, which encodes a novel member of the winged-helix family of transcriptional regulators and al

198 Foxp3, a winged-helix family transcription factor, serves as the

199 vitro, and reveals how subtle changes in the winged-helix fold can modulate the functional properties

200 The FOXC2-DBD adopts the winged-helix fold with helix H3 contributing to all the

201 ted domain-swapping interactions between the winged-helix folds and AAA+ modules of neighbouring prot

202 nucleic acid binding surfaces of the RRM and winged-helix motifs, although present in the RNA binding

203 nd a concomitant down-regulation of Forkhead/winged-helix protein 3 (Foxp3), TGFbeta, and IL-10 expre

204 criptional regulator SarA protein family are winged-helix proteins that are involved in gene regulati

205 otic homeodomain proteins and the "wings" of winged-helix proteins, but structurally distinct.

206 The predicted Cdc6 domain III winged-helix structure may well be responsible for dimer

207 ologous regions of both proteins fold into a winged-helix structure, which specifically binds to the

208 whose structure is remarkably similar to the winged-helix structures of histones H1 and H5.

209 is and (lambda)Xis adopt related prokaryotic winged-helix structures.

210 ors, namely Kite dimers (Kleisin interacting winged-helix tandem elements), interact with Smc-kleisin

211 However, some DNA-BPs, such as the winged-helix transcription factor FOXO1, are difficult t

212 Forkhead winged-helix transcription factor Foxp3 serves as the de

213 Foxg1, a winged-helix transcription factor, promotes the developm

214 of the foxd3 gene, which encodes a conserved winged-helix transcription factor.

215 We demonstrate here that the winged-helix transcription factors Foxa1 and Foxa2 co-oc

216 y unrecognized domains in ASXL1: a forkhead (winged-helix) DNA-binding domain and a deubiquitinase ad

217 ain, and the C-terminal part, which includes winged-helix, ratchet, and oligonucleotide/oligosacchari

218 Here, we truncated the C-terminal winged-helix-domain (WHD) of Mcm6 to slow down the loadi

219 ix hydrolase-like domain and the DNA-binding winged-helix-turn-helix (wHTH) domain.

220 AbiEi has an N-terminal winged-helix-turn-helix domain that is required for repr

221 domain and a C-terminal circularly permuted winged-helix-turn-helix domain.

222 tudies show that RacA contains an N-terminal winged-helix-turn-helix module connected by a disordered

223 RctB contains at least three DNA binding winged-helix-turn-helix motifs, and mutations within any

224 a C2H2 zinc finger, a leucine zipper, and a winged-helix/forkhead (FKH) domain.

225 whether NKX2.1 interacts with members of the winged-helix/forkhead family of FOXA transcription facto

226 ell phenotypes, suppressor ability, forkhead winged/helix transcription factor box P3 (FOXP3) gene, a

227 esents the addition of another branch to the winged HTH protein family and could contribute to our un

228 which unexpectedly mediates dimerization, a winged-HTH and a Walker-box containing C-domain.

229 Zbeta maintains a winged-HTH fold with the addition of a C-terminal helix.

230 e further investigation include the earliest winged insects (Palaeoptera) and Polyneoptera (orthopter

231 This is the first record of Collembola using winged insects for dispersal.

232 The evolution of winged insects revolutionized terrestrial ecosystems and

233 Among two-winged insects such as houseflies and their relatives, t

234 Winged insects underwent an unparalleled evolutionary ra

235 ect Drosophila melanogaster, suggesting that winged insects use the same regulatory mechanism to prom

236 are characteristic of ancestral pterygotes (winged insects) have often undergone evolutionary modifi

237 es, as one of the sister groups of all other winged insects, are key to understanding this radiation.

238 In winged insects, metamorphic changes either are limited t

239 from the formation of cellular components to winged insects.

240 atter representing the most basal lineage of winged insects.

241 during flight in hawk moths, which are four-winged insects.

242 key evolutionary adaptations in mayflies and winged insects.

243 ng living and fossil Neuroptera, even across winged insects.

244 model was established among all lineages of winged insects.

245 s-wanderer (Pedionomus torquatus) and letter-winged kite (Elanus scriptus), that suggest the evolutio

246 dings of the courtship displays of male Club-winged Manakins, Machaeropterus deliciosus, reveal that

247 Here we describe a new 'four-winged' microraptorine, Changyuraptor yangi, from the Ea

248 (Akt) signalling cascade, leads to the long-winged morph if active and the short-winged morph if ina

249 he long-winged morph if active and the short-winged morph if inactive.

250 We discovered that the production of the winged morph in asexual clones of the rosy apple aphid,

251 pple aphid virus (RAAV), did not produce the winged morph in response to crowding and poor plant qual

252 In the winged morph, energy needed for wing maintenance may lea

253 uction rate, but such aphids can produce the winged morph, even at low insect density, which can fly

254 n of InR2 results in development of the long-winged morph.

255 and track changing resources, whereas short-winged morphs are flightless, but usually possess higher

256 Long-winged morphs can fly, which allows them to escape adver

257 Winged morphs of aphids are essential for their dispersa

258 ut usually possess higher fecundity than the winged morphs.

259 ted ligand Ilp3 triggers development of long-winged morphs.

260 ental fate of their embryos from wingless to winged morphs.

261 lso significantly induced the development of winged morphs.

262 e normally two-winged Drosophila into a four-winged mutant fly.

263 This introgression of wdw from large-winged N. giraulti into small-winged N. vitripennis incr

264 wdw from large-winged N. giraulti into small-winged N. vitripennis increases male but not female fore

265 After doping with nitrogen, the winged nanotubes exhibited outstanding activity toward c

266 ple aphids and causes their hosts to produce winged offspring [3].

267 tressors resulted in increased production of winged offspring and shifts in fecundity rates.

268 asticity: the pea aphid's ability to produce winged offspring in response to crowding.

269 ea aphids are typically unwinged but produce winged offspring in response to high population densitie

270 role in the regulation of the proportion of winged offspring produced in response to crowding in thi

271 no correlation between immune challenge and winged offspring production, suggesting that this mechan

272 We induced production of winged offspring through distinct environmental stressor

273 analog resulted in a decreased production of winged offspring.

274 RNAi resulted in an increased production of winged offspring.

275 uced ecdysone signaling would result in more winged offspring.

276 pathway being involved in the production of winged offspring.

277 Here we show that the Early Cretaceous five-winged paravian Microraptor is most stable when gliding

278 wingless maternal parasitoids produced more winged progeny.

279 nique to ants is a marked divergence between winged queens and wingless workers, but morphological sp

280 ids exhibit phenotypic plasticity, producing winged (rather than wingless) progeny that may be better

281 hin the DNA-binding helix-turn-helix and the winged region as well as within the metal-binding pocket

282 These data suggest that the winged region of the winged helix protein participates i

283 licate basic residues R84 and R90 within the winged region to be critical in DNA binding, whereas aci

284 sp. nov., comprising the worker/pseudergate, winged reproductive, and soldier, and a second species,

285 om the Cretaceous have, until now, only been winged reproductives (alates and dealates); the earliest

286 e weakness, 6.7% display minor signs such as winged scapula or hyperCKemia, without functional motor

287 Winged sexuals of social insects (ants, honey bees, and

288 ckroach (Periplaneta americana) and the pink winged stick insect (Sipyloidea sipylus).

289 hic analyses of full-length H6N6-NS1 (A/blue-winged teal/MN/993/1980) and an LR deletion mutant, comb

290 linker region mutant of the H6N6 NS1 (A/blue-winged teal/MN/993/1980), which together with the previo

291 and neuraminidase (NA) genes from the A/blue-winged teal/Texas/Sg-00079/2007 (H3N8) (tl/TX/079/07) wt

292 To test this, we monitored the ratio of winged to unwinged offspring produced by adult mothers o

293 lden-winged (Vermivora chrysoptera) and blue-winged (V. cyanoptera) warblers to identify a single gen

294 leverage the genomic similarity among golden-winged (Vermivora chrysoptera) and blue-winged (V. cyano

295 s of hybridization in the golden-winged/blue-winged warbler complex, two phenotypically divergent war

296 cultative migration, wherein breeding golden-winged warblers (Vermivora chrysoptera) carrying light-l

297 -throated phenotype characteristic of golden-winged warblers.

298 ntal stressors drive shifts in fecundity and winged/wingless offspring production, and how secondary

299 entropus and Dualula lineages are small, two-winged, with unique siphonate mouthparts for imbibing po

300 bility and differentiation in a panel of 100 winged-yam (Dioscorea alata) accessions using 24 phenoty