ライフサイエンスコーパス: tetrad

1 ifferent postsynaptic cells at each synapse (tetrad).

2 ns (i.e. hilate monads, dyads, and permanent tetrads).

3 ating populations derived from gametes (half-tetrads).

4 localization and shuttling through the His37 tetrad.

5 repair than did adducts located in the inner tetrad.

6 e first crystal structure observation of a C-tetrad.

7 ing to identify spores derived from the same tetrad.

8 ates of the pH sensor located at the His(37) tetrad.

9 BMVC-base plane stacking over the external G-tetrad.

10 ed by two or three charged His residues in a tetrad.

11 from different protonation states of the H37 tetrad.

12 nal Hoogsteen hydrogen bonds to complete a G-tetrad.

13 de-chain conformational change of the His-37 tetrad.

14 bserved in the minor groove side of the base tetrad.

15 ted interaction (N3(G) and N3(U)) with the G tetrad.

16 e adenine stacking very well with the bottom tetrad.

17 ics of charge migration along the tryptophan tetrad.

18 rom about 3 ns in each dyad to 850 ns in the tetrad.

19 how a mimic of the Z-scheme with a molecular tetrad.

20 m two nonplanar minor-groove-aligned G.C.G.C tetrads.

21 distances, MLH1 foci, and fluorescent pollen tetrads.

22 prophase I progression to the first labeled tetrads.

23 igher order structures by the formation of G tetrads.

24 on of L1 and L2 postsynaptic elements at all tetrads.

25 rather than intercalated between adjacent G-tetrads.

26 g more stable with the addition of further G-tetrads.

27 intramolecular structure containing three G-tetrads.

28 king of adenine residues from the terminal G-tetrads.

29 main fused and pollen grains are released as tetrads.

30 time further promoted formation of stable G-tetrads.

31 lls, no callose wall separated the resulting tetrads.

32 ultistranded structure stabilized by guanine tetrads.

33 to isolate a complete series of six meiotic tetrads.

34 junctional DHPRs into groups of four termed tetrads.

35 of fluorescent protein in Arabidopsis pollen tetrads.

36 ures having G-C base pairs in place of the G-tetrads.

37 rnative structures observed contain only two tetrads.

38 ed presynaptic densities, mostly arranged as tetrads.

39 ly stabilized by G*C*G*C-tetrads and C*C*C*C-tetrads.

40 condary structures forming stacks of guanine tetrads.

41 This catalytic tetrad accounts for the tremendous rate acceleration obs

42 n-reversal and V-shaped loops, triads, mixed tetrads, adenine-mediated pentads and hexads and snap-ba

43 -mediated pentads and hexads and snap-back G-tetrad alignments.

44 G.G.G) pentad sandwiched between two G.G.G.G tetrads, all G-stretches are parallel, and all guanines

45 otide polymorphisms, we showed that, in most tetrads, all three pairs of homologs recombined.

46 tacts between the divalent cations and the C-tetrad, allowing Ba(2+) ions to occupy adjacent steps in

47 resequenced the four products of 13 meiotic tetrads along with 10 doubled haploids derived from Arab

48 ll to incorporate into the same postsynaptic tetrad, altering the specificity of photoreceptor transm

49 Tetrad analyses in the quartet1-2 background revealed th

50 n attempted in C. neoformans in the style of tetrad analyses performed in other fungal species.

51 Tetrad analyses showed that all small ascospore-derived

52 (or more) observable events were defined by tetrad analysis and compared with those predicted by dif

53 Thus, mouse tetrad analysis demonstrates how unique aspects of mamma

54 Tetrad analysis has been a gold-standard genetic techniq

55 A new method for tetrad analysis in mammals provides valuable insights in

56 In Arabidopsis, tetrad analysis in qrt mutants has been used to map all

57 We used tetrad analysis in Saccharomyces cerevisiae to examine t

58 Meiotic tetrad analysis is a powerful tool for analyzing all fou

59 From tetrad analysis of S288C/Sigma1278b hybrid strains and w

60 Tetrad analysis performed using the Arabidopsis quartet

61 g-based image recognition package for pollen tetrad analysis that enables high-throughput measurement

62 eiotic recombination, representing the first tetrad analysis with whole-genome sequencing in a nonfun

63 Tetrad analysis, which examines the four chromatids resu

64 ain physically attached thereby facilitating tetrad analysis.

65 centromeres (functional in meiosis) by half-tetrad analysis.

66 d physical mapping of centromeres using half-tetrad analysis.

67 Comparison with both G tetrad and adenine tetrad indicates that lack of NH2 in

68 MpPR-1i lacks the conserved CAP tetrad and is incapable of binding divalent cations.

69 otonation states of the proton-gating His-37 tetrad and their effects on proton transport for this lo

70 n oleosin-like protein (oleolike) in zygotes-tetrads and a transcript encoding oleosin in vegetative

71 by varying the sequence and the number of G-tetrads and by using small, G4-stabilizing molecules.

72 d quadruplexes, likely stabilized by G*C*G*C-tetrads and C*C*C*C-tetrads.

73 ructure of Hoogsteen hydrogen-bonded guanine tetrads and diverse loop structures.

74 own, dramatically enhanced the formation of tetrads and EC coupling rescue by constructs that otherw

75 We identified tetrads and reconstructed parental haplotypes, which rev

76 ue the resolution, but not the formation, of tetrads and rosettes in Fgfr2 mutant limb-bud ectoderm.

77 gulates both the formation and resolution of tetrads and rosettes in the mouse embryo, possibly in pa

78 lves dynamic multicellular structures called tetrads and rosettes.

79 ucture containing two central antiparallel G-tetrads and six i-motif C-C+ base pairs.

80 o discuss the roles of amino group in purine tetrads and the inter-quadruplex interactions in RNA mol

81 The interaction between the minor groove tetrads and the nearby C:C(+) base pairs affords a stron

82 d quadruplex conformation with three guanine tetrads and three side loops, including two single-nucle

83 G-quadruplexes by automatically detecting G-tetrads and treating them as large square blocks.

84 ide covers a terminal guanine base tetrad (G-tetrad), and clamps the G-quadruplex using three-anchor-

85 wiched between a G-tetrad surface and a TATA tetrad, and held in the site by networks of water molecu

86 to the duplex-quadruplex junction, the mixed tetrad, and the duplex region of the RNA through shape c

87 ridges during mitosis, micronuclei in pollen tetrads, and 30% seed abortion.

88 gh self-recognition of guanines into stacked tetrads, and considerable biophysical and structural evi

89 DHPR triad expression, assembly of DHPRs in tetrads, and elicitation of DHPRalpha1S charge movement-

90 The two subunits are stacked at their 5'-end tetrads, and multiple stacking rotamers may be present d

91 internal G4 unit predominantly coexist in 2-tetrad antiparallel basket and hybrid-2 structures that

92 physiological conditions and identify the 2-tetrad antiparallel basket and hybrid-2 topologies as th

93 This DNA fragment formed a stable two G-tetrad antiparallel G4 with an additional Watson-Crick C

94 This tetrad appears in a C-terminal sequence pattern that is

95 is approach, including in species where half-tetrads are currently difficult to isolate.

96 lta mutant can be constructed by mating when tetrads are dissected on plates with a nonfermentable ca

97 RyR1 residues 1-1681 restored wild-type DHPR tetrad arrays and, in part, skeletal-type excitation-con

98 DHPRs) and for the organization of DHPR into tetrad arrays by expressing RyR1-RyR3 chimerae in dysped

99 s targeting the K61-D146-K180-E216 enzymatic tetrad as well as residues lining the RNA binding groove

100 data reveals that CB2Rs are involved in the tetrad assay induced by cannabinoids which had been asso

101 al report of a stabilized individual thymine tetrad assembly is presented here.

102 ructure of an RNA quadruplex containing an I tetrad at 1.4 A resolution.

103 hydrogen-bonding geometries in the histidine tetrad at low pH, thus validating the proton conduction

104 n Na(+) solution but close enough in a two G-tetrad basket-like form 3 conformation that can form in

105 Ru), leading to the energy efficiency of the tetrad being 47% of the sum of the photon threshold ener

106 method, called barcode-enabled sequencing of tetrads (BEST), that uses (i) a meiosis-specific GFP fus

107 The tetrad Bodipy-NDI-TAPD-Ru is composed of two different d

108 ed spectrum of amino protons from a specific tetrad-bound guanine can be extracted from the nuclear O

109 intramolecular G-quadruplex with only two G-tetrads but multiple-layer capping structures formed by

110 iosis-specific GFP fusion protein to isolate tetrads by FACS and (ii) molecular barcodes that are rea

111 NA G-quadruplex structures possessing 2-to-4 tetrads by means of femtosecond and nanosecond transient

112 e constriction at W23 increases with the H19 tetrad charge but is independent of the H27A mutation.

113 lanthanide ions are distributed in arrays of tetrad clusters.

114 that the esterase activity is derived from a tetrad composed of Ser(44), His(273), Glu(194), and Asp(

115 esidues, our results suggest that this two-G-tetrad conformation is likely to be an intermediate form

116 Unlike G*G*G*G-tetrads, some G*C*G*C-tetrad conformations do not require the N7-Guanine posit

117 ure composed of three G-quartets and a mixed tetrad connected to an RNA duplex.

118 l/antiparallel structure consisting of three tetrads connected by loops of one, seven, and three base

119 Mutagenesis of a K(61)-D(146)-K(182)-E(218) tetrad conserved in other cellular and viral MTases sugg

120 ted toward the pi tautomer and less cationic tetrads, consistent with faster forward deprotonation to

121 kingly, an isolated guanine is involved in G-tetrad core formation, despite the presence of four thre

122 structural details at the two ends of the G-tetrad core in the context of natural sequences and info

123 symmetric dimeric quadruplex, in which the G-tetrad core involves all three G-tracts of one strand an

124 Both structures contain the (3 + 1) G-tetrad core with one double-chain-reversal and two edgew

125 anines participate in the formation of the G-tetrad core, despite the interruption between the first

126 The two structures contain the (3+1) G-tetrad core, in which three G-tracts are oriented in one

127 -residue bulge and is projected out of the G-tetrad core.

128 Previously published, and some unpublished, tetrad data from budding yeast (Saccharomyces cerevisiae

129 cell toxicity, induction of the cannabinoid tetrad, depressive- and anxiety-like behaviors.

130 We genotyped populations of half-tetrad-derived individuals (from Brassica interspecific

131 Spore tetrads develop in spore mother cell walls within a muci

132 d haploid was crossed with its ancestor, and tetrad dissections were used to isolate a complete serie

133 usual pore structures, and had problems with tetrad dissociation.

134 or the formation of a stable, antiparallel G-tetrad DNA structures.

135 s are based on the stacking of two or more G-tetrads; each tetrad is a planar association of four gua

136 ualization of inheritance patterns in intact tetrads, eliminating the need for microdissection and pe

137 I-MS are different than those observed for G-tetrad end-stacking binding ligands.

138 hich is similar to the effect observed for G-tetrad end-stacking ligands.

139 omain mediates an interaction with a guanine tetrad face of quadruplexes.

140 In tetrad fluorescence microscopy, double mutants of for3 d

141 ormation to a contracted form to match the G-tetrad for an optimal stacking interaction.

142 ion of L-type Ca(2+) currents, and a lack of tetrad formation as evaluated by freeze-fracture analysi

143 hate protecting groups (pro-D ODN) reduces G-tetrad formation in solution, while allowing tetrad form

144 tetrad formation in solution, while allowing tetrad formation inside the cell where the potassium con

145 nce and a 3' end poly(G) track that favors G-tetrad formation leading to multimerization.

146 suggest that the orthograde signal and DHPR tetrad formation require the contributions of numerous R

147 hough incapable of supporting EC coupling or tetrad formation, restored a significant level of Ca(2+)

148 thanol for emergent properties of nucleobase tetrad formation.

149 t even an isolated guanine was involved in G-tetrad formation.

150 13 of the other monomer, to complete G.G.G.G tetrad formation.

151 effect (>85% reduction) on the percentage of tetrad-forming cells compared with the wild type strain.

152 horus removal (EBPR), Defluviicoccus-related tetrad-forming organisms (DTFO) were observed to predomi

153 to C(60) is witnessed in the supramolecular tetrad from the femtosecond transient absorption spectra

154 he rate constants for binding to the His(37) tetrad from the two sides of the membrane and the corres

155 this site can fold into an anti-parallel two-tetrad G-quadruplex.

156 The peptide covers a terminal guanine base tetrad (G-tetrad), and clamps the G-quadruplex using thr

157 Even though it is sandwiched by guanine tetrads (G tetrads), the I tetrad is buckled towards the

158 As UCSF Tetrad graduates with diverse careers in academia, medic

159 hosphate (dCMP) insertion opposite the first tetrad-guanine by hRev1 is approximately 56% as fast as

160 sic sites replacing loop adenines (A/AP) and tetrad guanines (G/AP) in quadruplexes formed by the hum

161 romote fork progression by either dislodging tetrad guanines to unfold the G4 DNA, which could assist

162 At lower pH values the His37 tetrad has a larger total charge that increases the chan

163 The I tetrad has one cyclic hydrogen bond N1...O6 with the bon

164 ll chromatids from a single meiosis in yeast tetrads has been indispensable for defining the mechanis

165 need to manually isolate, disrupt and space tetrads has relegated its application to small-scale stu

166 ucture but its basic unit, inosine tetrad (I tetrad), has not been determined at the atomic level.

167 rangement (anti:anti:syn:anti) and the top G-tetrad having the reversed G-arrangement (syn:syn:anti:s

168 ntiparallel G-strands, with the bottom two G-tetrads having the same G-arrangement (anti:anti:syn:ant

169 H:T) G-quadruplex structures by stacking two tetrad:heptad G-quadruplexes formed by two of the three

170 demonstrate that the element is able to form tetrad:heptad:heptad:tetrad (T:H:H:T) G-quadruplex struc

171 t one residue in the conserved AKR catalytic tetrad, His(120) (AKR1D1 numbering), is substituted by a

172 with Mg(2+) coordinated to the conserved CAP tetrad (His208, Glu215, Glu233 and His250) in spacegroup

173 elical structure but its basic unit, inosine tetrad (I tetrad), has not been determined at the atomic

174 yields polymers highly enriched in isotactic tetrads (iii).

175 hypothesis that mutation of the hydrophobic tetrad ILLV to AAAA leads to the ab initio misfolding an

176 Here we identify a hydrophobic amino acid tetrad (ILLV) close to the C terminus of the secretory N

177 panied by pronounced upfield shifts of the G-tetrad imino proton resonances in the NMR, which is simi

178 e of azaBODIPY and fullerene entities of the tetrad improved the overall light energy conversion effi

179 emplated an analogous methanolic monomeric G-tetrad in comparison to the thymine species.

180 o isolate the four microspores from a single tetrad in maize for the purpose of whole-genome sequenci

181 etermined the four pK(a) values of the His37 tetrad in the viral membrane.

182 ould confirm a previously proposed catalytic tetrad in this selenoprotein.

183 erization of all 256 variants of the central tetrad in this structure indicates that certain mutation

184 ystems have been complemented by a molecular tetrad in which pyrene residues replace the fluorine ato

185 earcher was able to isolate over 3,000 yeast tetrads in 3 h, an output equivalent to that of almost 1

186 three loop regions interact with the core G-tetrads in a specific way that defines and stabilizes th

187 The three loops interact with the core G-tetrads in a specific way that defines and stabilizes th

188 L2 were tetrads, revealing the emergence of tetrads in an arthropod group present 200 million years

189 elf-assemble into discrete helically stacked tetrads in hydrocarbon solvents.

190 G-quadruplexes stabilized by stacked G*G*G*G tetrads in monovalent cation solution.

191 G-quadruplexes stabilized by stacked G-G-G-G tetrads in monovalent cation-containing solution.

192 tations can compensate for canonical G-G-G-G tetrads in the context of both GTP-binding and peroxidas

193 oth markers occurred rarely, and many of the tetrads in which both markers converted were the product

194 ns events were originally identified only in tetrads in which the non-Mendelian segregations were not

195 ations and structural variations in the 3' U tetrad, including one that leads to the formation of a h

196 Comparison with both G tetrad and adenine tetrad indicates that lack of NH2 in the C2 position mak

197 Sporogenesis always produced either dyads or tetrads, indicating strict genetic control.

198 distribution of heterozygosity in these half-tetrad individuals allowed the genetic mapping of all 19

199 Maintaining tetrad information allows accurate inference of missing

200 the ribose-2'-O-methyltransferase catalytic tetrad, interact with S-adenosyl-l-methionine, and contr

201 Moreover, the His-37 tetrad interrupts the otherwise continuous hydrogen-bond

202 The His37 tetrad is a pH sensor in the center of the M2 TM helix t

203 the stacking of two or more G-tetrads; each tetrad is a planar association of four guanines held tog

204 wiched by guanine tetrads (G tetrads), the I tetrad is buckled towards the 3' side of the tetrad plan

205 k, where the C8 of guanine in the external G-tetrad is covalently linked with the C5 of its adjacent

206 The conserved K-D-K-E catalytic tetrad is identified in ronivirus 2'-O-MTase.

207 d(G(2)ACGTAGTG(2))(2), with only two core G-tetrads, is less stable and forms a heterogeneous mixtur

208 kit2 promoter strands span a pair of three-G-tetrad-layer-containing all-parallel-stranded G-quadrupl

209 amolecular RG4 structures consisting of five tetrad layers formed by 5'-terminal oligoguanine motifs

210 back parallel-stranded scaffold with three G-tetrad layers, three double-chain-reversal loops, and a

211 lel-stranded G-quadruplex containing three G-tetrad layers, three double-chain-reversal loops, and a

212 4n - 1) guanines, n denoting the number of G-tetrad layers, was previously reported.

213 rent loop lengths and different numbers of G-tetrad layers.

214 ed state (oxidized Bodipy/reduced Ru) in the tetrad lies higher than that in the reference dyads (Bod

215 e telomeric G-quadruplex consists of three G-tetrads linked with mixed parallel-antiparallel G-strand

216 Thus, DHPRs in tetrads may be arranged such that the N and C termini of

217 ns with the highest expression in meiocytes, tetrads, microspores and mature pollen.

218 iency of up to 17% has been achieved for the tetrad modified electrode.

219 tudies have found that the conserved K-D-K-E tetrad motif in the L protein is related to the methyltr

220 In contrast, tetrad nests, created by boron extraction from B-SSZ-70

221 r cell entry into meiosis and formation of a tetrad of haploid megaspores.

222 p of dipolar-dephased (15)N signals from the tetrad of His37 side chains have been observed as a func

223 ma should be considered if a patient has the tetrad of pancreatitis, biliary obstruction, gastric out

224 rs (cladologs) and further corroborated on a tetrad of pochonicine stereoisomers, obtaining the corre

225 X-ray structures of MIPs indicate that a tetrad of residues (the ar/R region) form a narrow pore

226 This methodology was applied on a tetrad of synthesized cladosporin stereoisomers (cladolo

227 ruple alanine substitutions in the catalytic tetrad of the 2'-O-MTase using a virulent infectious cDN

228 ne residues, A21, A3 and A9, capping the top tetrad of the hybrid-type telomeric G-quadruplex.

229 be highly relevant for other homologs with a tetrad of tryptophans and tyrosines as electron donors.

230 matic core designed to stack on the terminal tetrads of a G-quadruplex, these compounds are neither p

231 eneral, adducts located in the top or bottom tetrads of a quadruplex stack exhibited more rapid-phase

232 uble chain reversal loops linking juxtaposed tetrads of a quadruplex stem may facilitate formation of

233 from G-rich sequences that are built around tetrads of hydrogen-bonded guanine bases.

234 G-quadruplex structure where multiple planar tetrads of hydrogen-bound guanines stack on top of each

235 nded G-quadruplex structure contains three G-tetrads of mixed G-arrangements, which are connected wit

236 red by laser microdissection from 19 matched tetrads of unaffected comparison subjects and subjects w

237 nti.syn.syn.syn and two syn.anti.anti.anti G-tetrads; one double-chain reversal and two edgewise loop

238 w that robust analyses of interactions using tetrads or disease-discordant sibling pairs are equivale

239 rved symmetrically repeating hydrogen-bonded tetrad, or located at the top face of the beta-propeller

240 tetrad is buckled towards the 3' side of the tetrad plane, which results from the different interacti

241 ion strength with K ions on two sides of the tetrad plane.

242 Stacking of the ligand to the G-tetrad planes changes the conformation of the G-quadrupl

243 a squeezed balloon effect strengthens the G-tetrad planes, but dislocates and weakens the loops in t

244 binomial distribution with no evidence of a tetrad-pollen effect.

245 and science historians have appealed to the tetrad-pollen model as an explanation of the bias toward

246 d once two charges are absorbed by the His37 tetrad prior to activation of this proton channel.

247 duate students over the past 20 years in the Tetrad program at the University of California at San Fr

248 t lack of NH2 in the C2 position makes the I tetrad prone to buckle for interactions with ligands.

249 lope, (15)N NMR spectra show that the His-27 tetrad protonates with higher pKa values than His-19, in

250 The intercalated base tetrads provide the basic repeat unit for constructing a

251 ne ring of actinomycin D is stacked on the G-tetrad rather than intercalated between adjacent G-tetra

252 means that animal cryptochromes that have a tetrad (rather than a triad) of tryptophan electron dono

253 Binding to an exposed G-tetrad represents a simple and efficient way to specific

254 etry to closely match that of the terminal G-tetrad required for efficient pi-pi stacking.

255 C(+) base pairs, flanked by two minor groove tetrads resulting from the association of G:C or G:T bas

256 ous PNAs can hybridize by the formation of G tetrads, resulting in hybrid PNA-RNA quadruplexes.

257 ust R cell synapses onto both L1 and L2 were tetrads, revealing the emergence of tetrads in an arthro

258 y activated long-range hopping between multi-tetrad segments of DNA.

259 are significantly different, indicating that tetrad sequence plays a role in determining the biochemi

260 Unlike G*G*G*G-tetrads, some G*C*G*C-tetrad conformations do not requir

261 eat stress on maize (Zea mays) plants at the tetrad stage of pollen development.

262 te heat stress during the highly susceptible tetrad stage strongly affects basic metabolic pathways a

263 ed on the surface of microspores at the late tetrad stage, is hypothesized to play a key role.

264 otein highly expressed in tapetum during the tetrad stage.

265 d(GpG) consists of long columns of stacked G-tetrad structures and carry a net negative charge.

266 value the sincere intentions behind the UCSF Tetrad study.

267 -folded quadruplexes, sandwiched between a G-tetrad surface and a TATA tetrad, and held in the site b

268 ts in accessible external 5' and 3' planar G-tetrad surfaces for ligand stacking.

269 ternal TTA loop nucleotides and stack onto G-tetrad surfaces.

270 The base-tetrad swapping results in a dimer of quadruplexes with

271 ucture of an RNA quadruplex containing "base-tetrad swapping" and bulged nucleotide at 2.1-Angstroms

272 In Drosophila, photoreceptor terminals form tetrad synapses that incorporate an invariable pair of p

273 element is able to form tetrad:heptad:heptad:tetrad (T:H:H:T) G-quadruplex structures by stacking two

274 at this agent exhibits broad activity in the tetrad test for CB1 agonism, causing analgesia, hypomoti

275 H, the mutant channel contains more cationic tetrads than the WT channel, consistent with faster reve

276 88 of AChRalpha is part of an interdependent tetrad that contributes to rearrangement of the C-loop d

277 that catalysis depends on a Lys-Tyr-Asn-Tyr tetrad that emerged adjacent to a computationally design

278 viral 2'-O-MTase harbors a catalytic K-D-K-E tetrad that is conserved among 2'-O-MTases and can targe

279 hough it is sandwiched by guanine tetrads (G tetrads), the I tetrad is buckled towards the 3' side of

280 (ii) Using each basidium as an unordered tetrad, the ADE2 and URA5 genes are linked to their cent

281 Heat treatment of rODNs disrupted G tetrads, the high m.w. aggregates, and the HLA-DR inhibi

282 sults confirm the stability of the central G-tetrads, the individual quadruplexes, and the resulting

283 completes a universally conserved catalytic tetrad, thereby activating Argonaute for RNA cleavage.

284 ix bundles to secure the capsid via cysteine tetrad-to-SCP interactions.

285 entral ions and observe distortions from the tetrad topology in their absence.

286 yn.syn.syn.anti and two anti.anti.anti.syn G-tetrads, two edgewise loops, three G-tracts oriented in

287 A supramolecular tetrad was formed by assembling bis-pyridine functionali

288 ed for the conducting pKa value of the His37 tetrad, we believe that this inter-helical motion accomp

289 of the fluorescent alleles in 92,489 pollen tetrads, we demonstrate (i) a correlation between develo

290 G tetrads were detected by circular dichroism in active rO

291 Tetrads were linked to the evolution of aerial agility.

292 The long-held consensus that tetrads were the archetypal condition in land plants is

293 urther, the supramolecular polyads (triad or tetrad) were utilized to build photoelectrochemical cell

294 free-energy barrier to diffuse to the His37 tetrad, where it is stabilized in a deep minimum reflect

295 are transmitted in only approximately 25% of tetrads, whereas the PS- genomes are faithfully inherite

296 ostatic constraints on opposite sides of the tetrads, which determine their preferred relative orient

297 show that deletion of MSH4 reduces crossover tetrads with 6:2 or normal 4:4 segregation more than it

298 In most tetrads with four viable spores, two of the spores had t

299 eric G-quadruplex structure contains three G-tetrads with mixed G-arrangements, which are connected c

300 onsonance of all possible dyads, triads, and tetrads within a single octave.