ライフサイエンスコーパス: head-to-tail

1 t-like arrangement with Xis monomers aligned head to tail.

2 ody axis mediolaterally and elongate it from head to tail.

3 and generate traveling waves that decay from head to tail.

4 ely transferred along the helicene skeleton, head to tail.

5 while extension movements elongate them from head to tail.

6 e sheet to scan an unfolded biomolecule from head to tail.

7 ng faces, six have such DAD vectors arranged head-to-tail.

8 The dimerization of methyl acrylate to the head-to-tail 2-methylene-pentanedioic acid dimethyl este

9 ty and regioselectivity (head-to-head versus head-to-tail adducts) is required for the synthesis of b

10 Although most duplications are positioned head-to-tail adjacent to the original locus, those that

11 merization driven by the C terminus, and the head-to-tail alignment of adjacent molecules.

12 The Tpm coiled coil polymerizes head to tail along the long-pitch helix of F-actin to fo

13 pomyosin is a coiled-coil protein that binds head-to-tail along the length of actin filaments in euka

14 CntA exists in a head-to-tail alpha(3) trimeric structure.

15 inity and likely further disrupt the tubulin head-to-tail alpha/beta dimer-dimer interaction by virtu

16 by a cohesive primordium that migrates from head to tail and deposits future neuromasts at intervals

17 ation, contains two GAGGC sequences arranged head to tail and separated by a 7-bp AT-rich sequence.

18 ences, which allowed the polymers to connect head-to-tail and form supramolecular nanostructures.

19 nd monomer to bind in multiple orientations (head-to-tail and head-to-head), depending on the specifi

20 ked via K6, K11, K27, K29, or K33, or linked head-to-tail), and no structural information on these ch

21 A distribution of head-to-head, head-to-tail, and tail-to-tail regiochemistries was dete

22 hains linked via K29, K33, or K63, or linked head-to-tail are unable to form such a contact due to st

23 am distance and orientation (head-to-head or head-to-tail) are important for the promoter architectur

24 This head-to-tail arrangement along the c-direction places th

25 Within each trimer, a head-to-tail arrangement causes the RFK and FMNAT cataly

26 se data is that UL9 dimers are oriented in a head-to-tail arrangement in which the N terminus is in c

27 nds of the heptamer, our findings indicate a head-to-tail arrangement of elongated Nup84 complexes in

28 -sheet arrangement along the b-direction and head-to-tail arrangement of such beta-sheets along the c

29 Diffraction studies elucidated the head-to-tail arrangement of the coiled-coil linear stran

30 f the two protomers rather than the expected head-to-tail arrangement seen in nuclear receptors bound

31 The head-to-tail arrangement was disfavored by adding site-d

32 n-protein contacts to stack along dsRNA in a head-to-tail arrangement, and that the signaling domain

33 The duplications are typically in a head-to-tail arrangement, and they vary in size and gene

34 iation of the two NBDs, forming a dimer in a head-to-tail arrangement, with two nucleotides "sandwich

35 binds both CaM lobes, which adopt a distinct head-to-tail arrangement.

36 The relative "head-to-tail" arrangement of the N-substituents in Bn(4)

37 likely accompanies complex formation on the head-to-tail array of binding sites in oriCII.

38 AAV genomes were arranged predominantly in a head-to-tail array, with deletions and extensive rearran

39 es, but the adjacent downstream element in a head-to-tail array.

40 rs of different gene families, arranged in a head-to-tail array.

41 anspositions to chromosome ends produce long head to tail arrays of these elements.

42 and presumably involved in the formation of head-to-tail arrays of migrating cells.

43 complicated due to multilayer formations and head-to-tail assemblies resulting from the strong fuller

44 mplications due to multilayer formations and head-to-tail assemblies were revealed.

45 A head-to-tail association has also been reported for EBP5

46 oelectric ordering, including a tendency for head-to-tail association into polar, chain-like assembli

47 rms of the monomer; second, they mediate the head-to-tail association of monomers to form the elongat

48 Likewise, head-to-tail association of tropomyosin molecules must b

49 decorated with an anti-FLAG antibody reveals head-to-tail association with mean distances between the

50 olecules overlap via tropomyosin-tropomyosin head-to-tail associations, forming a continuous strand a

51 anslocation, with IgH Cmu and Pvt-1 oriented head to tail at the breakpoint, resulting in an elevated

52 cation, resulting in multiple genomes linked head to tail at the cos site.

53 renyl tail polymerization, 4-hydroxybenzoate head-to-tail attachment, and head modification, resultin

54 l data for mammalian myosin V suggest that a head-to-tail autoinhibitory interaction is a primary mea

55 nts displayed a pronounced shortening of the head-to-tail axis as well as compression, flattening, an

56 arized cell rearrangements that elongate the head-to-tail axis.

57 d the subsequent formation of the embryonic (head to tail) axis.

58 llowed the assignment of the rostral/caudal (head-to-tail) axis for the first time.

59 The rostrocaudal (head-to-tail) axis is supplied by populations of progeni

60 suggesting that the mutation interferes with head-to-tail beta-tropomyosin polymerization and with ov

61 cis,syndiotactic microstructure with minimal head-to-tail bias was observed.

62 Elongation of the head-to-tail body axis by convergent extension is a cons

63 bound dodecanethiolate ligands as well as of head-to-tail bound R-S-R molecules.

64 s, or pinocytosis, inhibits the formation of head-to-tail cell streams during cAMP-induced aggregatio

65 i) There is an increasing cranial-to-caudal (head-to-tail) cell-autonomous motility gradient, with ca

66 cked streams in which cells are organized in head-to-tail chains.

67 gamma di- and triterpene synthases; the zeta head-to-tail cis-prenyl transferases that produce the ci

68 rmed during re-replication are the result of head-to-tail collisions and collapse of adjacent replica

69 neous recombinant allele, V99A(T)/V99A(T), a head-to-tail concatemer of three V99A targeting construc

70 mplification of loci 3, 4, 6, and 8 produced head-to-tail concatemeric intermediates; loci 1, 2, and

71 e (nt) sequence found at the junction of the head-to-tail concatemers of T7 genomic DNA generated dur

72 ate (FPP) synthase catalyzes the consecutive head-to-tail condensations of isopentenyl diphosphate (I

73 demonstrate that NBD1 and NBD2 interact in a head-to-tail configuration analogous to that in homodime

74 equence homology, the genes are aligned in a head-to-tail configuration and joined by chromosomal rea

75 s that the tandem ZF motifs adopt a flexible head-to-tail configuration well-suited for binding to mu

76 and rat-human chimeric PXR cDNAs in a tandem head-to-tail configuration were created using a random c

77 binds to the Cascade complex as a dimer in a head-to-tail configuration, at the interface formed by C

78 The NBDs dimerize in a head-to-tail configuration, forming two ATP binding pock

79 This novel head-to-tail conformation masked the interaction of both

80 otion of the cohesin ring is able to adopt a head-to-tail conformation, in agreement with experimenta

81 pothesis that EL is active as a homodimer in head-to-tail conformation.

82 yrazole with an oxalyl spacer and a trimeric head-to-tail connected aminopyrazole, of nine similar am

83 n whether EPs are made of one (4, 5) or two "head-to-tail"-connected pyridinium rings (6-10), the nat

84 nd CO(2), yielding iso-enriched PPC with 94% head-to-tail connectivity.

85 0 A-long helical tail structure to reach the head-to-tail connector.

86 amagnetic in the solid due to close (3.26 A) head-to-tail contact between Ru pyridine planes of neigh

87 Adjacent, horizontally oriented MDs form head-to-tail contacts and repress ClpB activity by preve

88 , methyl 3,4-epoxybutanoate, displayed 91.8% head-to-tail content and a lower Tg of 18 degrees C.

89 ely debond from a surface by stimuli-induced head-to-tail continuous depolymerization of poly(benzyl

90 ence of a SWNT, followed by the formation of head-to-tail covalent bonds, yielding closed rings on th

91 ilar three-helix-junction elements associate head-to-tail, creating a trough that cradles two c-di-AM

92 acids in size and are characterized by their head-to-tail cyclic backbone and cystine knot motif, whi

93 e disulfide bond, respectively, within their head-to-tail cyclic backbones.

94 MCoTI-II is a head-to-tail cyclic peptide with potent trypsin inhibito

95 ree different synthetic strategies including head-to-tail cyclization (C1), side-chain-to-tail cycliz

96 date, the most commonly used method for the head-to-tail cyclization of peptides has been native che

97 Head-to-tail cyclization of the mu opioid receptor (MOR)

98 idases are crucial in the final stage of the head-to-tail cyclization reaction, but the enzyme(s) inv

99 angement mechanism is thought to be due to a head-to-tail cyclization reaction, where the N-terminal

100 Circular proteins, defined as head-to-tail cyclized polypeptides originating from ribo

101 om the decapeptide tyrocidine synthetase, 13 head-to-tail cyclized tyrocidine derivatives were obtain

102 e a class of cyclic peptides that are small, head-to-tail cyclized, composed of proteinogenic amino a

103 Head-to-tail cyclodimerization of resin-bound oligopepti

104 Since Rings with head-to-tail DADs would be unlikely to self-assemble or

105 Continuous head-to-tail depolymerization provides faster rates of r

106 The polymers in these networks undergo a head-to-tail depolymerization upon removal of the trigge

107 how that a geometric constraint-exclusion of head-to-tail dihedral angle discrepancies (DADs)-explain

108 ticle, we proposed that fullerene cages with head-to-tail dihedral angle discrepancies do not self-as

109 symmetry-related actin-actin contacts form a head to tail dimer that is strikingly similar to the lon

110 Models of Itk suggest either a head to tail dimer, with the SH2 domain interacting with

111 al structure of MAP-1, which also contains a head-to-tail dimer approximately 146 A long.

112 NK1, which is a Met agonist, forms a head-to-tail dimer complex in crystal structures and mut

113 For most substrates, hydrolysis and head-to-tail dimer formation are avoided.

114 C222 and has a structure very similar to the head-to-tail dimer in the P2(1) unit cell.

115 e ligand-receptor fusion forms a reciprocal, head-to-tail dimer that provides a reservoir of inactive

116 rate, showing that two FAN1 molecules form a head-to-tail dimer to locate the lesion, orient the DNA

117 NK1 crystallizes as a head-to-tail dimer with an extensive inter-protomeric in

118 )7B89 reveals a tightly associated, extended head-to-tail dimer, which is stabilized via pair-wise sh

119 olved in protein/protein interactions in its head-to-tail dimer.

120 t the CvaB CTD formed a nucleotide-dependent head-to-tail dimer.

121 ead stacked dimer, and the third as a single head-to-tail dimer.

122 A "head-to-tail" dimer ([M + H]+ at m/z 217) was exhibited

123 sphocholine (PC) groups forms a macrocyclic "head-to-tail" dimer stabilized by NH(urea)...OP(PC) hydr

124 he nucleotide-binding domains (NBDs) form a "head-to-tail" dimer upon binding ATP; and the cytoplasmi

125 Lipoprotein lipase (LPL) is a 448-amino-acid head-to-tail dimeric enzyme that hydrolyzes triglyceride

126 l in which EcoPrrC toxicity is contingent on head-to-tail dimerization of the NTPase domains to form

127 A reversible head-to-tail dimerization of the O-nitrooxide to the 1,2

128 sertion of ED-B appears to stabilize overall head-to-tail dimerization of two separate Fn chains, whi

129 Spontaneous "head-to-tail" dimerization of these dyes via the formati

130 In contrast to the antiparallel (head-to-tail) dimerization reported previously for the o

131 cyclopentenone, forming their respective exo head-to-tail dimers in high conversion.

132 o suppress the influence of the attractive, 'head-to-tail', dipolar interactions.

133 id-state NMR not only confirms that there is head-to-tail disorder of the C identical withN groups pr

134 led, which assembles signalosomes by dynamic head-to-tail DIX domain polymerization.

135 The quaternary structure of GabR is a head-to-tail domain-swap homodimer.

136 hat differ in the overall orientation of the head to tail domains.

137 ents, respectively, allows a head-to-head or head-to-tail double helix to be generated.

138 oposed that the ori DNA is first melted by a head-to-tail double trimer of E1 that evolves into two h

139 coordinating rhythmic undulatory waves from head to tail during forward movement.

140 pase structures suggests a structure for the head-to-tail EL homodimer that is consistent with the ex

141 etal-catalyzed dimerization are the branched head-to-tail enynes.

142 Because the head-to-tail exclusion rule is an implicit geometric con

143 gon pairs, we prove that for all n > 60, the head-to-tail exclusion rule permits only (and all) fulle

144 elf-assemble, we proposed a hypothesis, the "head-to-tail exclusion rule" (the "Rule").

145 y that obeys the IPR may be explained by the head-to-tail exclusion rule, a geometric constraint.

146 wer, we described a geometric constraint-the head-to-tail exclusion rule-that permits self-assembly o

147 opose that peptide helices are arranged in a head to tail fashion to cover the edge of the disc.

148 ber is formed by PitB monomers associated in head-to-tail fashion and that short, flexible fibers can

149 assemble trimeric coiled-coil peptides in a head-to-tail fashion into linear strands with interstran

150 structure revealed two molecules bound in a head-to-tail fashion on opposite sides of the DNA.

151 bp-long arrays of tandem repeats arranged in head-to-tail fashion separated by an intergenic spacer (

152 ers built of tubulin dimers that attach in a head-to-tail fashion to form protofilaments, which furth

153 mer composed of multiple genomes linked in a head-to-tail fashion, and terminase enzymes perform two

154 determinant of their ability to migrate in a head-to-tail fashion, requires vesicular trafficking.

155 interlocking interfaces with G5 domains in a head-to-tail fashion, resulting in a contiguous, elongat

156 ophobicity of the (iPr)Th group, occurs in a head-to-tail fashion, the formyl headgroups being locate

157 tein composites by fusion of polypeptides in head-to-tail fashion.

158 with neighboring molecules interacting in a head-to-tail fashion.

159 ng composed of eight heptamers arranged in a head-to-tail fashion.

160 FtsZ monomers polymerize head to tail forming tubulin-like dynamic protofilaments

161 ms such as mammals, only a small fraction of head-to-tail genes have retained a short upstream distan

162 eosomes that flank the core promoter than do head-to-tail genes.

163 most cpDNA in genome-sized linear molecules, head-to-tail genomic concatemers, and complex branched f

164 e, with the dimerized anthracenes assuming a head-to-tail geometry, as evidenced by NMR spectroscopy

165 (t1/2 approximately 10(7) y),(5) of the 1-4 "head-to-tail" glycosidic linkages that join the common g

166 ind a diverse array of neurons responding to head-to-tail (h-t) flow, tail-to-head (t-h) flow, or bot

167 A construct encoding a covalent head-to-tail homodimer of EL (EL-EL) was expressed and h

168 whereas i-PrLi/(+)-sparteine surrogate is a head-to-tail homodimer.

169 Chd(T) forms a "head-to-tail" homodimer, formed between two alpha-helice

170 Remarkably, despite the head-to-tail homology shared with several fungal and bac

171 ed by biomimetic heterocycle-hydroxycarbonyl head-to-tail hydrogen-bonding.

172 form sensory structures, that migrates from head to tail in the zebrafish embryo.

173 atic poly(carbamates) that depolymerize from head-to-tail in low dielectric constant environments whe

174 of alphabeta-tubulin heterodimers that align head-to-tail in the MT wall, forming linear protofilamen

175 V Myo2p to reveal that it is regulated by a head-to-tail interaction and that loss of regulation ren

176 pact ring-shaped tetramer featuring a unique head-to-tail interaction at its center that replicates t

177 n which protocadherin cis-dimers engage in a head-to-tail interaction between EC1-EC4 domains from ap

178 temporal regulation of myosin V in vivo by a head-to-tail interaction is critical for the normal deli

179 a7, beta6, and beta8), revealing a canonical head-to-tail interaction mode for homophilic trans dimer

180 of the two halves of the Venus molecule, the head-to-tail interaction of NC-Venus-ICP27 locks ICP27 i

181 at occurs in vivo and likely disrupts NHERF1 head-to-tail interaction.

182 the assembly of the dodecamer occurs through head-to-tail interactions of the bipolar monomers.

183 ent structure, most likely requiring unusual head-to-tail interactions.

184 pha motif (SAM) domains, revealing versatile head-to-tail interactions.

185 Head-to-tail interchain disulfide bonds link subunits wi

186 ceptor photobleaching that ICP27 undergoes a head-to-tail intramolecular interaction but not head-to-

187 the N and C termini of ICP27 could undergo a head-to-tail intramolecular interaction that exists in o

188 tion, branching, or cyclobutanation have non-head-to-tail (irregular) skeletons.

189 n), the 4,1'-dipyridinium isomer (so-called "head-to-tail" isomer) undergoes two electron transfers a

190 or PSPP ionization; and the observation that head-to-tail isoprenoid synthases as well as terpene cyc

191 en described as card-packed H-aggregates and head-to-tail J-aggregates, respectively.

192 tation disrupts the four-helix bundle at the head-to-tail junction, leading to weaker tropomyosin-tro

193 Here, using RT-PCR and sequence analyses of head-to-tail-ligated (-) strands, we show that after tra

194 c peptides whose backbones are cyclized from head to tail, like the membrane permeable and orally bio

195 ficiency of dual-vector gene expression from head-to-tail linear and/or circular heterodimers.

196 on origins on linear molecules to generate a head-to-tail linear concatemer, followed by recombinatio

197 Although the "head-to-tail" linear complexes display classic J-aggrega

198 ry can be captured by a free subunit through head-to-tail linkage of juxtaposed amino (N)- and carbox

199 licative intermediates that are comprised of head-to-tail linked genomes.

200 erial cells we reveal the predicted chain of head-to-tail linked subunits in the transit channel of f

201 d by the known structures of K48-, K63-, and head-to-tail-linked chains.

202 information on the crystal structure of the head-to-tail-linked diubiquitin (Ub(2)).

203 licative intermediates that are comprised of head-to-tail-linked genomes.

204 Head-to-tail-linked polyubiquitins (Ubq1-11) were used t

205 role in the assembly and/or stabilization of head-to-tail lipase homodimers.

206 ed and larger fragments an isomerization to "head-to-tail" macrocycles is observed (see picture).

207 eport that peptoids undergo highly efficient head-to-tail macrocyclization reactions.

208 We analyze the relevance of the CaFADS head-to-tail macromolecular interfaces to stabilization

209 to group migration in which cells align in a head-to-tail manner to form streams.

210 ial cytoskeletal protein FtsZ assembles in a head-to-tail manner, forming dynamic filaments that are

211 moted by pentanucleotide pairs arranged in a head-to-tail manner.

212 omposed of repeating monomers assembled in a head-to-tail manner.

213 ster of three intronless genes arranged in a head-to-tail manner.

214 ntrast to the previously proposed asymmetric head-to-tail model.

215 d in its processing of water flow simulating head-to-tail motion but rudimentary in processing flow i

216 pening of the split channels, firmly linking head-to-tail NBD1-NBD2 association to channel opening.

217 monomer-dimer sigmoidal transitions, or as a head-to-tail noncentrosymmetric columnar polymer, exhibi

218 of target site orientation (head-to-head or head-to-tail) on the TPM behavior of synapsed DNA molecu

219 ongation is a conserved process in which the head-to-tail or anterior-posterior (AP) axis of an embry

220 limited, the cycloadditions proceed to give head-to-tail or head-to-head regioisomers, depending on

221 d-to-tail intramolecular interaction but not head-to-tail or tail-to-tail intermolecular interactions

222 d, to yield mixtures of dimers 4 and 5 (anti-head-to-tail), or exclusively 5 in the triplet-sensitize

223 presence of two genes that are arranged in a head to tail orientation.

224 rs confirmed that they packed in the desired head-to-tail orientation and within a viable distance fo

225 Xis binds DNA in a head-to-tail orientation to generate a micronucleoprotei

226 ene consisting of a partial duplication in a head-to-tail orientation without altering the NSP3 open

227 P(exsD), P(exoT), and P(pcrG) promoters in a head-to-tail orientation.

228 arrayed at their endogenous locus in direct head-to-tail orientation.

229 lar DNA harboring two recombination sites in head-to-tail orientation.

230 D1 homodimerizes in solution in the expected head-to-tail orientation.

231 ng RNA polymerases in either head-to-head or head-to-tail orientations, as well as EcoRI(E111Q), lac

232 ation between sites in both head-to-head and head-to-tail orientations, we could show that motor acti

233 rly exclusive products from head-to-head and head-to-tail oriented "non-homologous" FRT partners are

234 bilizing elements, favoring the formation of head-to-tail overlap complexes in four of five crystallo

235 aments on actin dominated by stereo-specific head-to-tail overlap linkage.

236 es are joined together by a 9- to 10-residue head-to-tail overlapping domain to form a continuous cab

237 significance of the molecular swivel at the head-to-tail overlapping ends of contiguous tropomyosin

238 f Hcp1 contains rings stacked in a repeating head-to-tail pattern.

239 Unrelated genes establish head-to-tail polarity in embryos of different fly specie

240 and the molecular mechanism for establishing head-to-tail polarity is poorly understood.

241 en by a single gene, bicoid, which generates head-to-tail polarity of the main embryonic axis.

242 We have identified a gene that establishes head-to-tail polarity of the mosquito-like midge, Chiron

243 fragment in vitro, self-associates to form a head-to-tail polymer.

244 around actin of thin filaments features both head-to-tail polymeric interactions and local twisting,

245 h is assembled by Dishevelled via reversible head-to-tail polymerization by its DIX domain.

246 opomyosin and other molecules and to disturb head-to-tail polymerization of beta-tropomyosin dimers.

247 phase transitions in cells is the reversible head-to-tail polymerization of hub proteins into filamen

248 rization appears to proceed via the addition/head-to-tail polymerization of short-lived free phosphin

249 These complexes are assembled by dynamic head-to-tail polymerization of the DIX domains of Axin o

250 y depends on its DIX domain, which undergoes head-to-tail polymerization to assemble signalosomes.

251 mains have been discovered so far to undergo head-to-tail polymerization, though these are widespread

252 Ph SAM forms helical head to tail polymers, and SAM-SAM interactions between

253 ripts were fused in phase such that covalent head-to-tail protein multimers were translated.

254 cing efficiently generates mRNAs that encode head-to-tail protein multimers.

255 Both kinds of homodimers adopt a head-to-tail quaternary structure and thus do not contai

256 generate the corresponding dimer with a syn-head-to-tail regio- and diastereoselectivity.

257 ed greater than 99% carbonate linkages, 100% head-to-tail regioselectivity, and a glass-transition te

258 molecules produced by chain elongation have head-to-tail (regular) carbon skeletons, while those fro

259 nt; single sites or pairs in tail-to-tail or head-to-tail repeat only supported a DNA nicking activit

260 meric polyubiquitin arranged as five tandem, head-to-tail repeats of 76 aa.

261 All but one of these mutants carried tandem head-to-tail repeats of a chromosomal segment (amplicon)

262 mal RNAs (rDNA) are clustered in long tandem head-to-tail repeats.

263 hydroxyurea, supporting a model of increased head-to-tail replication fork collisions due to over-ini

264 to extensive DNA damage, potentially due to head-to-tail replication fork collisions that ultimately

265 Directed head-to-tail self-assembly was driven by genetically enc

266 ent coimmunoprecipitation experiments, and a head-to-tail self-interaction of hmwBP was also observed

267 p-dinaphthoporphyrins were synthesized by a "head-to-tail" self-condensation of a dipyrrylmethane ald

268 the rearrangement originates from a partial head-to-tail sequence duplication that initiates after t

269 tterning of the vertebrate embryo occur in a head-to-tail sequence.

270 lls: Head-to-head signaling is stronger than head-to-tail signaling.

271 n negatively supercoiled plasmids containing head-to-tail sites, the reaction produces a series of kn

272 ptide is an 18-residue chimera formed by the head-to-tail splicing of nonapeptides derived from two s

273 the macrocyclic -defensins are formed by the head-to-tail splicing of nonapeptides excised from a pai

274 ensins (BTD-1 to BTD-10) produced by binary, head-to-tail splicing of nonapeptides excised from paire

275 ated to form circRNAs through back-splicing (head-to-tail splicing).

276 cked aggregates, which show a preference for head-to-tail stacking and antiparallel dipole order.

277 ead-to-head stacking geometry (orange) for a head-to-tail stacking geometry (yellow).

278 Results identified a unique head-to-tail stacking pattern for 3,8-diphenyldeuteropor

279 As a result, not only is the head-to-tail structure of amino acid columns confirmed b

280 interacted in a rotational (N- to C-terminal/head-to-tail) symmetry.

281 le relative orientation of dipoles including head-to-tail, tail-to-tail pairs, and antiparallel chain

282 Using the accepted head-to-tail tandem-binding model as a guide, we set out

283 bstitution (R168C) results in a high rate of head-to-tail (tandem) short sequence duplications, which

284 or p1 allele, P1-wr, is composed of multiple head-to-tail tandemly arranged copies of the complete ge

285 ses for these recombinases, action of Cre on head-to-tail target sites produces mainly unlinked circl

286 formation of tandem pairs of cells connected head to tail to which other cells subsequently adhere.

287 the Abeta25-35 dimer features unusual helix head-to-tail topology supported by a parallel off-regist

288 these enzymes: the alphaalpha and alphadelta head-to-tail trans-prenyl transferases that produce tran

289 nactis occipitalis, which uses a stereotyped head-to-tail traveling wave to move quickly on homogeneo

290 Their anti-parallel head-to-head-to-tail 'triplex' strand arrangement creates an amp

291 the G-tetrad core; in the second structure (head-to-tail), two loops are located on opposite ends of

292 ence of Oct-1-binding element and a putative head-to-tail-type p53-binding site.

293 ubiquitin-like protein containing two tandem head-to-tail ubiquitin-like domains.

294 disassemble in a domino-like mechanism from head-to-tail upon a triggering event induced by an exter

295 so show that linking two identical fragments head-to-tail using diglycine increases the proportion of

296 The lipid head-to-tail vector field is examined and shows strong o

297 uaramide bolaamphiphiles self-assemble into "head-to-tail" versus "stacked" arrangements, respectivel

298 erization reaction reveals that the branched head-to-tail vinyl cation is energetically more stable t

299 As) are single-stranded RNAs that are joined head to tail with largely unknown functions.

300 GPO), as pairs of triple helices interacting head-to-tail, yielded stabilization energies in the orde