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

5 12 miRNAs were significantly up-regulated in winged and wingless S. avenae small RNA libraries, respe

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

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

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

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

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

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

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

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

14 WCI5 was exclusively expressed in winged bean seeds.

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

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

17 times in 10 h) in the mite-infested, normal-winged bees to levels similar to those found in mite-inf

18 times higher than varroa-infested but normal-winged bees).

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

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

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

24 performance electrocatalysts based on unique winged carbon nanotubes.

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

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

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

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

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

30 The percentage of winged female parasitoid progeny increased exponentially

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

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

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

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

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

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

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

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

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

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

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

42 of the protein extends from the core of the winged helices into the coiled coil.

43 ed by an unidentified member of the forkhead/winged helix (Fox) family of transcription factors.

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

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

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

47 e present a model for the interaction of the winged helix (WH) domain of ORC2 with DNA that differs f

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

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

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

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

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

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

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

57 The 95 amino acid residue protein contains a winged helix DNA-binding domain with an extended C-termi

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

59 monomeric subunits are predicted to adopt a winged helix DNA-binding motif which dimerizes through f

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

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

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 In this structural model, a single winged helix domain binds to both DNA and other proteins

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

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

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

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

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

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

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

73 The winged helix domains are at opposite ends of the extende

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

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

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

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

78 The winged helix factors Foxa1 and Foxa2 are essential membe

79 Foxa1 is a member of the winged helix family of transcription factors and is expr

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

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

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

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

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

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

86 scussed on the basis of comparisons to other winged helix proteins.

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

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

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

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

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

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

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

94 essage for the transcription factor forkhead/winged helix transcription factor (FOXP3).

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

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

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

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

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

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

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

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

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

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

105 The winged helix transcription factor Foxd1 (previously know

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

107 The winged helix transcription factor Foxl1 is a marker for

108 The winged helix transcription factor Foxl1 localizes to mes

109 The winged helix transcription factor FoxO1 is a growth-atte

110 duction in the CD4(+)CD25(+)CD62L(+)forkhead/winged helix transcription factor gene (Foxp3(+)) compar

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

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

113 ed mice possess increased levels of forkhead/winged helix transcription factor gene-expressing CD4+CD

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

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

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

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

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

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

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

121 The winged helix transcription factor, FOXA2, is expressed i

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

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

124 The winged helix transcription factors Foxa1 and Foxa2 are e

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

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

127 Members of the MarR family of winged helix transcriptional regulators have been shown

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

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

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

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

132 DPBD consists of a winged helix-like motif and an unstructured C-terminal r

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

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

135 domains represent a growing subfamily of the winged helix-turn-helix (HTH) domain family whose member

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

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

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

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

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

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

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

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

144 The La motif adopts a winged helix-turn-helix architecture that has a highly c

145 at least two receiver domains, an OmpR-class winged helix-turn-helix DNA binding domain, and a histid

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

161 eet is a unique feature of the OmpR group of winged helix-turn-helix proteins.

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

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

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

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

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

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

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

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

170 We show here that the Foxn4 winged helix/forkhead transcription factor is coexpresse

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

210 Xis forms a unique winged-helix motif that interacts with the major and min

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

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

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

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

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

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

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

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

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

220 ES1; FOXN3) encodes a member of the forkhead/winged-helix transcription factor family.

221 In this study, we elucidate the roles of the winged-helix transcription factor Foxa2 in ventral CNS d

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

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

224 FOXP1 (Forkhead box-P1) is a winged-helix transcription factor that is differentially

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

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

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

228 ist), a novel member of the Foxi-subclass of winged-helix transcription factors that is involved in t

229 RovA, a member of the MarR/SlyA family of winged-helix transcription factors, regulates expression

230 The forkhead/winged-helix transcription factors, XFast-1/XFoxH1a and

231 family of prokaryotic metalloregulators are winged-helix transcriptional repressors that collectivel

232 Both structures show the "winged-helix" fold typical of GH1 and GH5 and are very s

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

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

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

236 The structure reveals the presence of a winged-helix-turn-helix DNA binding motif, but the locat

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

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

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

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

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

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

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

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

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

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

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

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

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

250 Winged insects underwent an unparalleled evolutionary ra

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

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

253 In winged insects, metamorphic changes either are limited t

254 niognatha has derived characters shared with winged insects, suggesting that the origin of wings may

255 atter representing the most basal lineage of winged insects.

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

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

258 model was established among all lineages of winged insects.

259 from the formation of cellular components to winged insects.

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

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

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

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

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

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

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

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

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

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

270 Winged morphs of aphids are essential for their dispersa

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

272 lso significantly induced the development of winged morphs.

273 ut usually possess higher fecundity than the winged morphs.

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

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

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

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

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

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

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

281 RNAi resulted in an increased production of winged offspring.

282 uced ecdysone signaling would result in more winged offspring.

283 pathway being involved in the production of winged offspring.

284 analog resulted in a decreased production of winged offspring.

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

286 wingless maternal parasitoids produced more winged progeny.

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

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

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

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

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

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

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

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

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

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

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

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

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

300 -throated phenotype characteristic of golden-winged warblers.