ライフサイエンスコーパス: homologue

1 in csq-1 (CASQ2 homologue) and unc-68 (RyR2 homologue).

2 2) and cross react with PfHRP3, a structural homologue.

3 the engineering must be replicated for each homologue.

4 creased expression of phosphatase and tensin homologue.

5 ytosis, identifying it as an Ede1 functional homologue.

6 on, causing a reductional segregation of one homologue.

7 st a comparative model based on a eukaryotic homologue.

8 medial nucleus, but not the lateral nucleus homologue.

9 d residues found in NapA and other bacterial homologues.

10 d in artificial supramolecular and colloidal homologues.

11 scriptional regulation through TCP15 and its homologues.

12 nisms of enzyme-membrane interaction for the homologues.

13 level of GenX also contained two C2nH2nF2nO2 homologues.

14 re strongly reminiscent of eukaryotic pepsin homologues.

15 he infralimbic cortex and area 25 are likely homologues.

16 meric protein has no identifiable structural homologues.

17 made with the previously described arylimido homologues.

18 en the functional capacities of the two AURK homologues.

19 ion of the dimeric, trimeric, and tetrameric homologues.

20 ongest between cognate partners in cidA-cidB homologues.

21 erstitial synapsis between the corresponding homologues.

22 e shown that the transcription factor Atonal homologue 1 (Atoh1) is required for Shh-type medulloblas

23 Liver receptor homologue 1 (LRH-1) is an orphan nuclear receptor that h

24 MR pathway through its interaction with MutL homologue 1 (MLH1).

25 in kidney fibrosis involving a RBP, Musashi homologue 1 (Msi1), which is expressed in tubular epithe

26 CircANRIL binds to pescadillo homologue 1 (PES1), an essential 60S-preribosomal assemb

27 TRANSFERASE 2 (DRM2) and SAWADEE HOMEODOMAIN HOMOLOGUE 1 (SHH1).

28 Silent mating type information regulation 2 homologue 1 (SIRT1) activity and content increased signi

29 silent mating type information regulation 2 homologue 1 (SIRT1) content and activity (P < 0.001).

30 ting of the iron donor, Yfh1 (yeast frataxin homologue 1), and the Fe-S cluster scaffold, Isu1, with

31 ssed for expression of the MMR proteins mutL homologue 1, mutS homologue 2, mutS homologue 6, and PMS

32 ly, exon-skipping event in Enhancer of Zeste Homologue 2 (EZH2) along with expression changes showed

33 Enhancer of Zeste homologue 2 (EZH2) methylates histone 3 at lysine 27 (H3

34 keletal muscle progenitors Enhancer of zeste homologue 2 (EZH2), the catalytic subunit of Polycomb Re

35 end processing similar to that found in MutS homologue 2 (Msh2)- and Mlh1-deficient B cells.

36 osine-1-phosphate (S1P) transporter spinster homologue 2 (Spns2)-deficient mice.

37 Here we report that tribbles homologue 2 (TRIB2) ablates forkhead box O activation an

38 n of the MMR proteins mutL homologue 1, mutS homologue 2, mutS homologue 6, and PMS1 homologue 2.

39 mutS homologue 2, mutS homologue 6, and PMS1 homologue 2.

40 dium falciparum reticulocyte-binding protein homologue 2b (PfRh2b) is an invasion ligand that is a po

41 We show that Tribbles homologue 3 (Trib3) binds to SNRK, and downregulates UCP

42 ins mutL homologue 1, mutS homologue 2, mutS homologue 6, and PMS1 homologue 2.

43 h molecular complex in which a diverged Orc4 homologue and one replicative helicase subunit can also

44 obtained evidence that the link between LFY homologues and B-genes is also conserved in two other gy

45 Meteorin and Cometin are homologues and contain ten evolutionarily conserved Cys

46 markers associated with rubber related gene homologues and differentially expressed genes, provides

47 can also repress expression of RD26 and its homologues and inhibit drought responses.

48 ained for TETs in two evolutionarily distant homologues and posit that this mode of function allows t

49 ctable diatom silicic acid transporter (SIT) homologues and study their structure and function in vit

50 formation as well as of derived hydrocarbon homologues and their ions (carbocations and carbanions)

51 ding five determinants without characterized homologues and three mechanisms not previously shown to

52 , we characterized mutations in csq-1 (CASQ2 homologue) and unc-68 (RyR2 homologue).

53 d to be conserved with the Bacillus subtilis homologue, and resistance to oxidative stress required t

54 ired limbs, paired fins are purported serial homologues, and the advent of pelvic fins has been hypot

55 able in any peanut sample, while the Bet v 1 homologue Ara h 8 and the lipid transfer protein allerge

56 e describe the structures of two prokaryotic homologues, archaeal SaTRIC and bacterial CpTRIC, showin

57 to determine whether Flowering Locus T (FT) homologues are associated with the Ku locus.

58 F1 (TCP) transcription factors TCP15 and its homologues are mediators of MOS1 function in the immune

59 argo is released by Arl3 and its non-ciliary homologue Arl2.

60 nd Rab G-protein families in regulating WASP homologue associated with actin, membranes, and microtub

61 conserved protein family that includes human homologues associated with neurodegenerative and develop

62 Disc large homologue-associated protein 5 (HURP/DLGAP5), required f

63 egree to which each PRDM9 variant binds both homologues at the DSB sites it controls.

64 as endogenously replaced with that of atonal homologues (ATHs) at key phylogenetic positions, non-ATH

65 of the Arabidopsis respiratory burst oxidase homologue AtrbohD and the SA biosynthesis gene ISOCHORIS

66 e spirochetes possess a single HtrA protease homologue, Borrelia burgdorferi HtrA (BbHtrA).

67 case DNA-binding protein 9 (CHD9) and Brahma homologue (BRM, a product of the SMARCA2 gene) are requi

68 tor antagonist (IL1RN), which is an IL-1beta homologue but has no agonistic activity.

69 In contrast, access to subunits of the homologue C70 remains challenging.

70 Drosophila has an NG2 homologue called kon-tiki (kon), of unknown CNS function

71 (human, mouse and Arabidopsis) Oxs1 and Pap1-homologues can bind interchangeably with each other in v

72 he fission yeast, heterologous Oxs1 and Pap1-homologues can substitute for S. pombe Oxs1 and Pap1 to

73 he activity of CPR-4 is regulated by the p53 homologue CEP-1 in response to radiation, and CPR-4 seem

74 e that despite conservation among eukaryotic homologues, chaperone holdase activity is not an obligat

75 that the Forkhead TFs Checkpoint suppressor homologue (CHES-1-like) and Jumeau (Jumu), which govern

76 c RNA-binding protein clustered mitochondria homologue (CLUH) regulates the expression of a mitochond

77 experimental characterization of its distant homologue CorA magnesium channel.

78 stronger activation of their left functional homologues correlated with better spatial processing in

79 geometry from its hypothesized Streptomyces homologue CprB, which is a gamma-butyrolactone regulator

80 guration in comparison with the Catharanthus homologue CrISY.

81 n measure the localization of MreB, an actin homologue crucial to cell wall synthesis, inside confine

82 displays selectivity over the mycobacterial homologues CysK1 and CysK2.

83 without affecting the phosphatase and tensin homologue deleted on chromosome 10 (PTEN) loss regulated

84 nts of triacetone triperoxide (TATP) and its homologue diacetone diperoxide (DADP) from surfaces.

85 The diaphanous homologue Diaph3 (aka mDia2) is a major regulator of act

86 ion constants but does not inhibit close FAP homologues dipeptidyl peptidase IV, dipeptidyl peptidase

87 n Mek1 persists on closely paired (synapsed) homologues, DNA repair is severely delayed, suggesting t

88 iP that distinguishes BiP from its bacterial homologue DnaK.

89 ipeptidyl peptidase 4 (DPP4), the mouse DPP4 homologue does not allow virus entry into cells.

90 Recent studies have suggested that Ras homologue enriched in brain (Rheb), a direct activator o

91 1 is activated by the small GTPase RHEB (Ras homologue enriched in brain) and inhibited by PRAS40.

92 ose that once pairing or synapsis juxtaposes homologues, exclusion of Mek1 is necessary to avoid supp

93 ARABIDILLO homologues exist throughout land plants, including early

94 substrate specificity of FXIIa and its close homologue factor Xa and used these data, together with i

95 The mouse homologue, Fndc1, is expressed in middle ear tissue and

96 Recently, a microcin C homologue from Bacillus amyloliquefaciens containing a l

97 ion of a single-terminal Cys residue, a CdtB homologue from cytolethal distending toxin can form a fu

98 (CDs) of TET2 and TET1 from mouse and their homologue from Naegleria gruberi, the full-length protei

99 cation of PfVIT, a vacuolar iron transporter homologue from the human malaria-causing parasite Plasmo

100 Here we study the VIT homologue from the malaria parasites Plasmodium falcipar

101 Mic60 homologues from alpha-proteobacteria display the same me

102 Early-diverging ARABIDILLO homologues from both P. patens and the lycophyte Selagin

103 The ability of RcCDI1 and its homologues from different fungal species to induce cell

104 RcCDI1 and its homologues from different fungal species, including Zymo

105 ion is co-ordinated by the essential tubulin homologue FtsZ and represents an attractive but as yet u

106 Recently a fungi-derived sphingosine homologue, FTY720, has been approved for treatment of mu

107 ermined the crystal structure of yeast ChaC2 homologue, GCG1, at 1.34 A resolution, which represents

108 ith consequent loss of function, whereas its homologue GDE2 fails to attack uPAR.

109 lated C3 botulinum toxin substrate 1 and Ras homologue gene family, member A (RhoA) guanine nucleotid

110 Octachlorodibenzofuran is the most abundant homologue group detected in all experiments.

111 anifestation of PTEN (phosphatase and tensin homologue) hamartoma-tumor syndrome.

112 emical studies of the monomeric archaeal XPD homologues have aided a mechanistic understanding of thi

113 in highly variable regions, improving remote homologue identification.

114 ructure prediction server focusing on remote homologue identification.

115 We discovered the first FXYD homologue in sea lamprey, a basal jawless vertebrate, wh

116 biochemistry to characterize a putative NsrR homologue in Streptomyces venezuelae.

117 of the hypothetical protein Slr1270, a TolC homologue in Synechocystis sp. PCC 6803.

118 metallic toxicity, as the Hemotin functional homologue in vertebrates, showing that this novel regula

119 virus 1 (HSV-1), pUL7 and pUL51, which have homologues in all other herpesviruses.

120 nger (CAX) as part of a widespread family of homologues in animals.

121 The function of FusA and the presence of homologues in clinically important pathogens suggests th

122 absence of a F. succinogenes genetic system, homologues in Escherichia coli were mutated and compleme

123 With significant numbers of dsyB homologues in marine metagenomes, we propose that bacter

124 LamA has no known homologues in other organisms, but is highly conserved a

125 1 of this virus was more divergent from its homologues in other Picobirnaviridae species than segmen

126 ntal Salmonella isolates, we identified EspJ homologues in S. bongori, S. enterica subsp. salamae, an

127 We demonstrate that ARABIDILLO homologues in the moss Physcomitrella patens regulate a

128 With 47 homologues in tomato (Solanum lycopersicum) were reporte

129 of bacterial, eukaryotic and archaeal PNPase homologues in vitro.

130 Accordingly, Mek1 is excluded from synapsed homologues in wild-type cells.

131 w a function of Pten (phosphatase and tensin homologue) in quiescent SCs.

132 ethyl analogue 2 and four isomeric methylene homologues (including the natural product itself) were o

133 hemisphere posterior dorsal stream language homologues independently contributes to language product

134 structure, the server automatically collects homologues, infers their multiple sequence alignment and

135 ghly conserved MutS (MSH) and MutL (MLH/PMS) homologues initiate mismatch repair and, in higher eukar

136 genetic changes of gene regulation and trans-homologue interactions.

137 CD4(+) T cells, few have focused on the IRF4 homologue, IRF8.

138 ne protein complexes, screening of complex I homologues is limited to large mammals reared for human

139 We show that Meru, a RASSF9/RASSF10 homologue, is expressed specifically in SOPs, recruited

140 sent from mammalian oral epithelium, a close homologue, Klf4, is expressed in this tissue and is requ

141 In analogy with a bacterial homologue, LRRK2 was proposed to act as a GTPase activat

142 f eukaryotic Lyp1 to that of the prokaryotic homologue LysP and find that LysP has a similar KM for t

143 lective inhibitors induce high levels of its homologue MDM4, prompt us to identify, through a recepto

144 nstrate that in yeast, deficiency of the ATR homologue Mec1 or of any among several other proteins in

145 RN) and in Modulator of retrovirus infection homologue (MRI).

146 fication and functional analysis of a Dorsal homologue (MsDorsal) and two Relish short isoforms (MsRe

147 Drosophila has corresponding homologues named Ime4 and KAR4 (Inducer of meiosis 4 and

148 otinylated derivative of the small ubiquitin homologue, NEDD8.

149 ter NhaA from Escherichia coli and the human homologue NHA2.

150 lyses have relied on homology modelling of a homologue (nhTMEM16) from the fungus Nectria haematococc

151 ription start site and akin to its bacterial homologue NusG.

152 iable gene of Campylobacter jejuni encodes a homologue of an unusual Type IIG restriction-modificatio

153 notype of yeast deficient in Vms1, the yeast homologue of ANKZF1.

154 verexpression of the N terminus of mammalian homologue of Drosophila Pins (LGN), which blocks the mic

155 tudy we examine Prickle3 (Pk3), a vertebrate homologue of Drosophila Prickle, in Xenopus gastrocoel r

156 Furthermore, the mosquito homologue of ERI3 is required for DENV-2 replication in

157 VAT, the Thermoplasma acidophilum homologue of eukaryotic CDC48/p97, works in conjunction

158 FtsZ, the bacterial homologue of eukaryotic tubulin, plays a central role in

159 and identify the cysteine protease CPR-4, a homologue of human cathepsin B, as the first RIBE factor

160 se and mouse mast cell protease-4 (the mouse homologue of human chymase) had the ability to reduce FX

161 cell protease (MCPT) 4, the mouse functional homologue of human chymase, were used.

162 Chicken NK-lysin (cNK-lysin), the chicken homologue of human granulysin, is a cationic amphiphilic

163 ochondrial matrix protease Ste23 in yeast, a homologue of human insulin-degrading enzyme, which is re

164 eported that mice lacking Spink3, the murine homologue of human SPINK1, die perinatally due to massiv

165 unconnected (target 2, control) with a human homologue of infralimbic cortex in the ventromedial pref

166 trate that postsynaptic knockdown of the fly homologue of LRRK2 thwarts retrograde, homeostatic synap

167 Finally, a homologue of lymphostatin from E. coli O157:H7 (ToxB; L7

168 point mutations in pfcpsf3, which encodes a homologue of mammalian cleavage and polyadenylation spec

169 Here, we characterized a unique T. gondii homologue of mammalian lecithin:cholesterol acyltransfer

170 the fission yeast Schizosaccharomyces pombe homologue of mammalian SUV39H H3K9 methyltransferases, w

171 Two of these proteins, Clf, a homologue of Mst11, which corresponds to MAP kinase kina

172 eceptor for octopamine (OA, the invertebrate homologue of norepinephrine), plays a major role in cont

173 via splicing factor 1 (SFA-1; the C. elegans homologue of SF1, also known as branchpoint binding prot

174 One gene BoLCVIG2 is a homologue of the alternative-splicing regulator (AtPTB1)

175 One of these proteins is a homologue of the bacterial ribosome-silencing factor (Rs

176 NOPE1 encodes a functional homologue of the Candida albicans N-acetylglucosamine (G

177 Helicobacter pylori lacks a gene encoding a homologue of the known pimeloyl-ACP methyl ester cleavag

178 tive, fibers densely innervating the lamprey homologue of the mammalian medial nucleus, but not the l

179 quent investigations on the Yvc1p channel, a homologue of the mammalian TRP channels, revealed that t

180 Yet, for one gene (a distant homologue of the merC gene implicated in metal resistanc

181 In each case, both the beta(3) homologue of the natural alpha residue and a cyclic beta

182 Here we show that the AnkB homologue of the Paris strain has a frame shift mutation

183 tic nerve despite the presence of Rtn4b, the homologue of the rat neurite growth inhibitor RTN4-A/Nog

184 ate that pneumococcal MltG is the functional homologue of the recently reported MltG endo-lytic trans

185 The pwi gene encodes a homologue of the yeast Get1 and human tryptophan-rich ba

186 The mesopallium of birds then is the homologue of this ventrolateral dorsal pallial part, not

187 We demonstrate that a T. gondii homologue of Tom22 (TgTom22), a central component of the

188 e also identify and characterize a T. gondii homologue of Tom7 (TgTom7) that is important for parasit

189 tassium channels with a non-hydrogen bonding homologue of tryptophan, Ind.

190 , the gene Synpcc7942_2071 encodes an ATPase homologue of type II/type IV systems.

191 Hyp mice, a murine homologue of XLH, are characterized by hypophosphatemia,

192 iles indicated Ac45 as the long-sought human homologue of yeast V-ATPase assembly factor Voa1.

193 he nature of electronic transition in higher homologues of (R2N)PPn(+*) (n >/= 4).

194 le-to-kinetochore contact has been made, the homologues of a 4-mum-long bivalent begin to separate.

195 sex combs-like (ASXL) proteins are mammalian homologues of additional sex combs (Asx), a regulator of

196 propose that fungal pathogens use functional homologues of alkalinizing peptides found in their host

197 ifferentially expressed transcripts included homologues of ASP-like proteins, proteases, or excretory

198 Notably, thorarchaeal genomes encode several homologues of eukaryotic membrane-trafficking machinery

199 confirmed multiple bacterial proteins to be homologues of eukaryotic tubulin and actin.

200 ng evolution, makes it difficult to identify homologues of pallial divisions in different amniotes.

201 The genome of M. perniciosa encodes 11 homologues of plant PR-1 proteins, designated MpPR-1 pro

202 We find that ArtA and ArtB, homologues of PltA and PltB, can form a functional compl

203 Human homologues of profibrotic genes expressed by mouse monoc

204 t the apicomplexan Toxoplasma gondii harbors homologues of proteins from all the major mitochondrial

205 romatic amino acids through 20 herpesviruses homologues of pUL56 suggests an involvement of this shor

206 dentify the rhgf-1 and rga-5 genes, encoding homologues of RhoGEF and RhoGAP, respectively, as regula

207 y is conserved between humans and yeast, and homologues of several components are widely distributed

208 ral strategy to diversely substituted higher homologues of the dendralenes.

209 soybean: FT2a, FT2b, FT2c and FT2d that are homologues of the floral inducer FLOWERING LOCUS T (FT).

210 Mycobacterium tuberculosis genome possesses homologues of the ruvC and yqgF genes that encode putati

211 We have prepared and characterised several homologues of this compound, with each material subjecte

212 cing polyketide synthase clusters containing homologues of TpcK and TpcL (a putative anthrone oxidase

213 rks the 25th anniversary of the discovery of homologues of tubulin and actin in prokaryotes.

214 The functional homologues of vertebrate natriuretic peptides (NPs), the

215 Naturally occurring enzyme homologues often display highly divergent activity with

216 tered IRS-1 and PTEN (phosphatase and tensin homologue on chromosome 10) activities.

217 tural soils, and the persistence of the POEA homologues on agricultural soils into the following grow

218 Ser269 is highly conserved in vertebrate CSL homologues, opening the possibility of a general and nov

219 Similar results were observed for the NleE homologue OspZ from Shigella flexneri 6 that also bound

220 After proper homologue pairing has been established, the synaptonemal

221 nstant distance from the portal plane in all homologues, pointing at a strong attractive interaction

222 ptides is performed by Cym1 in yeast and its homologue, PreP, in humans.

223 One of four FT homologues present in the narrow-leafed lupin genome, La

224 he absolute concentrations of the individual homologues present in the sample formulation.

225 he sister template is distinguished from the homologue primarily by its closer proximity to inhibitor

226 roduced advantageous mutations in vertebrate homologues, promoting elaboration of NC traits.

227 the basis of three independent templates of homologue proteins of Cry1A(a) and Cry1A(c) using an int

228 Loss of function of TOC1 and its close homologue PRR5 restores thermosensitivity in the evening

229 hogens deploy deamidases or enzyme-deficient homologues (pseudoenzymes) to induce deamidation of key

230 the tumor-suppressor phosphatase and tensin homologue (PTEN) and overexpression of prostate-specific

231 The phosphatase and tensin homologue (PTEN) gene is frequently mutated or lost in h

232 vation resulting from phosphatase and tensin homologue (PTEN) loss and EGFR-dependent PI3K activation

233 Phosphatase and tensin homologue (PTEN) protein levels are critical for tumor s

234 eceptor 3 (FGFR3) and phosphatase and tensin homologue (PTEN) signalling pathway components (for exam

235 in part to defective phosphatase and tensin homologue (PTEN).

236 Zebrafish with a mutation in the SCN1A homologue recapitulate spontaneous seizure activity and

237 equence similarities and to identify distant homologues, regardless of the structure class.

238 rly recruitment of contralesional functional homologues represented specific features of favorable re

239 osophila melanogaster riboflavin transporter homologue revealed reduced levels of riboflavin, downstr

240 the gene neighbourhood of the alginate lyase homologues revealed distinct patterns depending on the p

241 PRPH2 oligomerizes with its homologue rod outer segment (OS) membrane protein 1 (ROM

242 tunistic pathogen Aspergillus fumigatus Sch9 homologue (SchA).

243 rticotropin-releasing factor receptor family homologue SEB-3.

244 BioV homologues seem the sole pimeloyl-ACP methyl ester ester

245 show that PccA forms a complex with the Sco1-homologue SenC.

246 H2nF2nO2, C2nH2n+2F2nSO4 or C2n+1H2nF2n+4SO4 homologue series were detected, but only in downstream w

247 Recently, the human homologue, SETD2, was found to be recurrently mutated in

248 udy, we demonstrate that both Smurf1 and its homologue Smurf2 carry a non-covalent Nedd8-binding site

249 Also, the AMP kinase homologue, Snf1, and 14-3-3 proteins have been shown to

250 emal complex (SC) assembles along the paired homologues, stabilizing their interaction and allowing f

251 Other homologues, such as Z-d-Phe, are less effective but may

252 Retention of the C-terminal NLS in anillin homologues suggests that this is a conserved mechanism f

253 Comparison of peptide 1a to homologues suggests that this toxicity results from nons

254 ifs conserved across a broad range of PNPase homologues, suggests that this regulatory mechanism may

255 eading to neglect, contralesional functional homologues support recovery by modulating the preserved

256 Ubiquitin and some of its homologues target proteins to the proteasome for degrada

257 nction of alphaE-catenin through YAP and its homologue TAZ, as opposed to its adhesive function, and

258 ently regulated in comparison to its closest homologues TC10 and Cdc42.

259 Its closest homologue tetranectin binds to the kringle 4 domain of p

260 the previously reported structure of a close homologue that binds to a distinct target, LlaBIII.

261 a surface glycan-binding protein and a SusD homologue that delivers glycans to the outer membrane tr

262 We have demonstrated that SAV6 is an FEN1 homologue that shows double-flap endonuclease and gap-de

263 uncharged isostere citrulline gives peptide homologues that assemble to form tetramers in both the c

264 ld near Lawrence, Kansas, but with a loss of homologues that contain alkenes.

265 Bacteria express a variable number of HtrA homologues that contribute to the virulence and pathogen

266 The optic tectum in birds and its homologue the superior colliculus in mammals both send m

267 n through its structure in contrast with its homologue, the [(L)Cu(II)](2-) water oxidation catalyst,

268 As reported for B. amyloliquefaciens homologue, the initially synthesized compound contains a

269 In contrast to its other Gram negative homologues, the MtDapE was insensitive to inhibition by

270 riguingly the site is also conserved in SNX5 homologues throughout evolution, suggesting that IncE ca

271 gamma1 appears to be the closest functional homologue to alpha-syn.

272 ns, non-ATH proneural genes, and the closest homologue to ancestral proneural genes.

273 cies revealed a pronounced role of the human homologue to support HBV and HDV infection.

274 nduced nuclear protein, is the nearest human homologue to the mouse Ipr1 protein that has been shown

275 re, but the contributions of individual ORAI homologues to CRAC channel function are not well underst

276 Homologues to genes encoding these SSPs are present in t

277 MoGsk1 is functionally homologues to the Saccharomyces cerevisiae GSK3 homolog

278 d the actin-remodelling protein flightless-1 homologue, to modulate cell contraction in a RhoA-ROCK-i

279 Mechanistically, we identify foxo and mTOR homologue, Tor as important regulators of GSC quiescence

280 ncoded (TSPY), on the Y chromosome and its X-homologue, TSPX, are cell cycle regulators and function

281 like proteins present in C. sativa and their homologues, ubiquitously distributed throughout plant ki

282 (indolines, tetrahydroquinolines, and their homologues) undergo migratory ring expansion through dep

283 and for its heavier germanium, tin, and lead homologues uniformly electronic structures of carbene an

284 e complex diseases, most of which have human homologues, using far fewer samples than required in hum

285 previously demonstrated that the dystrophin homologue utrophin neither binds microtubules in vitro n

286 Ten VAP homologues (VAP27-1 to 27-10) can be identified in the A

287 ed by computational studies of the bacterial homologue vSGLT.

288 The Bib homologue was enriched in embryos, exclusively expressed

289 richloroethene reductive dehalogenase (TceA) homologue was the most consistently expressed of four de

290 he Wiskott-Aldrich syndrome protein and SCAR homologue (WASH) complex.

291 Screening yeast TA proteins with mammalian homologues, we show that the particular sensitivity of S

292 Individual parent and C1-5 alkyl homologues were easily separated (GC x GC/MS), allowing

293 GPCAT homologues were found in the major eukaryotic organism g

294 Porewater concentrations of all PCB homologues were reduced 94-97% for bioaugmented treatmen

295 the composition C15H8O2 and four methylated homologues were shown to accumulate as a result of biore

296 ertebrates (Cyclostomata), expresses an FXYD homologue, which strongly suggests that FXYDs predate th

297 transcription factor (forkhead box O (FOXO) homologue), whose global targets were identified in Caen

298 benzodiazepines, benzodiazocines, and their homologues, with ring sizes of 8-12.

299 Unlike XTRPM6's close homologue XTRPM7, whose loss interferes with mediolatera

300 APPII is a bona fide GEF for the yeast Rab11 homologues Ypt31/32.