ライフサイエンスコーパス: homologue

1 conserved among pneumococci and has no human homologue.

2 ma-tocopherol was the predominant tocopherol homologue.

3 arily distant Schizosaccharomyces pombe Num1 homologue.

4 ic and a eukaryotic sodium/proton antiporter homologue.

5 have coevolved in the same region on MADBUB homologues.

6 e the resultant motif to identify wider DslA homologues.

7 currents and a net outflow of shorter-chain homologues.

8 y of GTAs in other species that possess gafA homologues.

9 n-centric network of sequence and structural homologues.

10 at they may be as common in bacteria as LigE homologues.

11 dependence of other organisms with DNA clamp homologues.

12 drolases are still widely used as structural homologues.

13 made with the previously described arylimido homologues.

14 tissues qualify as potential crustacean wing homologues.

15 nene-derived carboxylic acid and dimer ester homologues.

16 s and RdRp with respect to other coronavirus homologues.

17 thetic peptide and the full-length Luk toxin homologues.

18 key transcription regulators: achaete-scute homologue 1 (ASCL1; also known as ASH1), neurogenic diff

19 allows binding with two APC adaptors, CDC20-homologue 1 (CDH1) and cell division cycle 20 (CDC20).

20 MutT homologue 1 (MTH1) removes oxidized nucleotides from the

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

22 Fragile-X mental retardation autosomal homologue-1 (FXR1) is a muscle-enriched RNA-binding prot

23 ecific suppression of phosphatase and tensin homologue 10 (PTEN), a negative regulator of insulin sig

24 Bioinformatics identified enhancer of zeste homologue 2 (EZH2) as an epigenetic regulator of the cho

25 ethyltransferases (DNMTs), enhancer of zeste homologue 2 (EZH2), bromodomain and extra-terminal domai

26 repressive complex member enhancer of zeste homologue 2 (EZH2).

27 t and activation, and disruption of the MutS homologue 2 (MSH2)-ATR module.

28 histone methyltransferase, enhancer of zeste homologue 2 [Ezh2]) showed that this phenotype was assoc

29 al introgressed reticulocyte-binding protein homologue 5 (RH5) sequence and used quantitative protein

30 cs analyses revealed the presence of RgNanOx homologues across Gram-negative and Gram-positive bacter

31 but not digestion products of nonallergenic homologues, activate FPR3 signaling.

32 Canoe's mammalian homologue Afadin plays similar roles in cultured cells,

33 g pneumococcal strains and the lack of human homologue, all suggest that rTF can be considered as a f

34 Ps were in, or close to, genes with putative homologues already known to be involved in pathogen resp

35 0.34 kV/cm) is lower than that for the n = 1 homologue (AMP)PbI(4) (DJP(n=1),0.4 kV/cm).

36 a 5mC-modifying enzyme (CMD1) that is a TET homologue and catalyses the conjugation of a glyceryl mo

37 the gene expression of Cxcl2, the mouse IL-8 homologue and increased the expression of its receptor,

38 ication that is catalysed by a divergent TET homologue and unexpectedly derived from vitamin C, and d

39 In nuclei with fully synapsed homologues and crossover precursors, removing different

40 o such heteromerization using a structurally homologue apolipoprotein fragment of apoA-I (4F) complex

41 Pkd2p, whose human homologues are associated with autosomal polycystic kidn

42 gnaling via RM CD200R.IMPORTANCE Viral CD200 homologues are encoded by KSHV and the closely related R

43 Agd3 homologues are encoded in previously unidentified putati

44 AMT1 homologues are generally found in protists and basal fun

45 DivIVA proteins and their GpsB homologues are late cell division proteins found in Gram

46 e divergence from ancestral genes, such that homologues are not readily detectable; and de novo emerg

47 other differentiating cyanobacteria as HetL homologues are spread across the phylum.

48 gst restriction enzymes, McrBC and its close homologues are unique in employing the AAA+ domain for G

49 biosynthetic gene clusters that encode SznF homologues are widely distributed among bacteria-includi

50 plasma membrane-binding domains of the Num1 homologues, as well as the membrane features these domai

51 Human ANP32A and ANP32B homologues both support function of human-adapted influe

52 that paired fins evolved as gill arch serial homologues, but this hypothesis is now widely discounted

53 AAT degradation process that involves a DnaJ homologue chaperone bound to ZAAT.

54 wrapping of terminal DNA, in contrast to its homologue Chd1, which functions in gene activation.

55 ctroscopy experiments show that the XDoc-Coh homologue complex withstands forces up to 1 nN at loadin

56 ined a large number of high molecular weight homologues containing sulfur and nitrogen, suggesting th

57 umor suppressor PTEN (phosphatase and tensin homologue deleted on chromosome 10) levels are frequentl

58 Phosphatase and tensin homologue deleted on chromosome ten (PTEN), one of the m

59 orders of magnitude compared to their human homologue, demonstrating a route to the selective chemic

60 Additionally, the homologue-dependant transfer resulted in a change of pat

61 iP that distinguishes BiP from its bacterial homologue DnaK.

62 nd PHLOEM EARLY DOF 2 (PEAR2)-and their four homologues (DOF6, TMO6, OBP2 and HCA2), which we collect

63 e (PmAldolase), but not its Escherichia coli homologue (EcAldolase), was found to catalyze the format

64 ompounds with human DMT1 and its prokaryotic homologue EcoDMT.

65 Strikingly, the PPARgamma-homologue Eip75B drives ISC daughter cells towards absor

66 ermidine/spermine N-acetyltransferase (SSAT) homologues encoded by S. aureus USA300 and E. faecalis a

67 Here we reveal functional STING homologues encoded within prokaryotic defence islands, a

68 tin immunoprecipitation identified RHEB (Ras homologue enriched in brain) as an ATF6 target gene in t

69 C1 that acts through modulation of RHEB (Ras homologue enriched in brain).

70 Here, we demonstrate that the separase homologue Esp1p in the ascomycete Candida albicans, an i

71 tituted cccDNA formation with purified human homologues, establishing these as a minimal set of facto

72 PHD homologues exist in other types of eukaryotes and prokar

73 Architecture Project are explored to show a homologue exists in marmoset.

74 We have mutated the second mammalian menorin homologue, Fam151a, and homozygous mutant mice have no d

75 we show that the sine oculis homeobox (SIX) homologue family transcription factors SIX1 and SIX2 are

76 P51 and excellent selectivity over the close homologue FKBP52.

77 Here, we show that the FemA/FemB homologues FmhA and FmhC pair with FemA and FemB to inco

78 s a nervous system but possesses single gene homologues for Ca(V)1-Ca(V)3 channels.

79 In contrast, a homologue from Escherichia coli, DtpA (dipeptide and tri

80 The perA homologue from M. rileyi (MR_perA) is shown to encode a

81 est case, we studied a previously unreported homologue from Ruminococcus flavefaciens called X-module

82 logues that are potent inhibitors of the APN homologue from the malarial parasite Plasmodium falcipar

83 mulations demonstrate how MalC and PhqE (its homologue from the paraherquamide pathway) catalyse dias

84 at 1.9 angstrom resolution and compare it to homologues from A. baumannii strains ACICU and BIDMC57,

85 f the four mitochondrial complexes and their homologues from bacterial respiratory chains using O(2)

86 ified differences in the response of RNase E homologues from different species to the same inhibitory

87 N6-methyl-dATP activity is present in MTH1 homologues from distantly related vertebrates, suggestin

88 Cyclin B3 homologues from frog, zebrafish, and fruit fly rescue me

89 analysis of DdPhyA enables comparisons with homologues from humans, Trichoplax adhaerens, and prokar

90 aracterised, far less is known about RNase E homologues from other bacterial species.

91 We also show that BaeAB homologues from other sphingomonads can cleave beta(R)-M

92 head-associated (FHA) fold, like that of its homologues from other T3SS.

93 t biochemical and biophysical studies on PHD homologues from the cellular slime mold, Dictyostelium d

94 cteria require RodA for growth; however, its homologue, FtsW, is a core member of the divisome comple

95 membrane protein ZipA, binds to the tubulin homologue FtsZ, in the early stage of cell division.

96 formed by the polymerization of the tubulin homologue FtsZ.

97 rom ancestral non-genic sequences, such that homologues genuinely do not exist.

98 of the archaeal model glutamate transporter homologue Glt(Ph) from Pyrococcus horikoshii suggested t

99 All homologue groups decreased in bioamended sediment and po

100 s of the sample matrix, the most abundant CP homologue groups were hepta- and octa-chlorinated undeca

101 The human Msp1 homologue has been implicated in neurodegenerative disea

102 generation of homoenolates and their higher homologues has been a long-standing challenge.

103 ple; woodchuck hepatitis virus (WHV), an HBV homologue, has been an important model system for drug d

104 cies-specific sequences that lack detectable homologues, has remained mysterious since the dawn of th

105 own how the transcriptional circuits of MqsA homologues have changed in bacteria over evolutionary ti

106 mbined results support the proposal that PHD homologues have evolved kinetic and structural features

107 l chemistries, homoenolates and their higher homologues have much potential, albeit largely unrealize

108 Structures of bacterial homologues have provided valuable information on the bin

109 noglobulin heavy chain-binding protein (BiP) homologue Heat-Shock Protein 4 (HSP-4), is selectively i

110 biota-Faecalibaculum rodentium and its human homologue, Holdemanella biformis-that are strongly under

111 ned with mutations in the fission yeast Ensa homologue, Igo1.

112 kinase TBK1 (TANK-binding kinase 1) and its homologue IKKepsilon are noncanonical members of the inh

113 ipitation assays confirmed that Me10 and its homologue in Aphis gossypii, Ag10k, interact with TFT7 i

114 ction as Pseudomonas aeruginosa lacks a pelX homologue in its pel gene cluster.

115 kdown strain of the BCG2529 gene, the Rv2509 homologue in Mycobacterium bovis BCG, was unable to grow

116 Similarly, ForT, the PyfQ homologue in the formycin pathway, can catalyze the coup

117 Knockout of the cytoplasmic UBA1 isoform homologue in zebrafish caused systemic inflammation.

118 Finally, we show that TRPT1 and MACROD homologues in bacteria possess activities equivalent to

119 ral homeotic gene AGAMOUS (AG) and its close homologues in development of anemophilous, unisexual cat

120 Here we show that while SurA homologues in early proteobacteria typically contain one

121 Caspase-11 in mice and its homologues in humans (caspase-4/5) belong to caspase-1 f

122 or MTB viability and it has highly conserved homologues in many eubacteria.

123 Phylogenetic analyses identified TcyP homologues in many pathogenic species, implying that thi

124 Thus, the activity of SpoT (or its homologues in other bacterial species) can likely influe

125 , the enzymatic activity and function of TET homologues in other eukaryotes remains largely unexplore

126 We identified six TTBK homologues in the genome of the planarian Schmidtea medi

127 In addition, we identify functional poxin homologues in the genomes of moths and butterflies and t

128 d but the Zn-fingernail appears only in VARP homologues in the lineage directly giving rise to animal

129 Although the ORM homologues in yeast are well-known inhibitors of sphingo

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

131 volutionarily conserved property of Ena/VASP homologues, including human VASP and Caenorhabditis eleg

132 Studies of bacterial NSS homologues-including LeuT-have shown how their transmemb

133 similar, heterozygous mutations in mammalian homologues initiate genetic instability in cancer.

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

135 elded a CDK called Pef1, whose closest human homologue is CDK5.

136 This fat homologue is shown to be the most widely expressed in th

137 f nickel-bound homoenolates and their higher homologues is demonstrated by cross-coupling with unacti

138 Knock-down of the zebrafish homologue klhl24a results in heart defects similar to th

139 Finally, loss of the Drosophila homologue Lasp from a subset of commissural neurons in t

140 B-BACK domain-containing ubiquitin E3 ligase homologue, leading to its rapid turnover.

141 rrelated with the upregulation of the lesion homologue, likely reflecting compensation.

142 Drosophila Lgl and its mammalian homologues, LLGL1 and LLGL2, are scaffolding proteins th

143 dently at least twice in GSTs and that BaeAB homologues may be important for cleaving the beta(R)-ary

144 These results suggest that serial homologues may diverge evolutionarily through replacemen

145 Thus, Prp40 homologues may regulate the assembly or function of dyne

146 alphaalpha, distinguishing it from its human homologue MHC class I antigen E (HLA-E).

147 t body cells that is anchored by the Nesprin homologue Msp300 at the cytoplasmic surface of the nucle

148 MCV ST recruits the MYC homologue MYCL (L-Myc) to the EP400 chromatin remodeler

149 or other methyltransferases and even for its homologue NTMT2.

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

151 the localization of amphiphysin (Amph), the homologue of another AD risk factor BIN1, and that Amph

152 te complex-like ( ASCL) gene family and is a homologue of ASCL5.

153 Furthermore, we showed that DWL2, the homologue of DWT1, is also able to interact with OsPIP5K

154 Utrophin is a fetal homologue of dystrophin that can subserve many dystrophi

155 orated into position 13 of MreB, a bacterial homologue of eukaryotic cytoskeletal protein actin F.

156 argophyllus (probably through deletion of a homologue of FLOWERING LOCUS T (FT)), and are associated

157 Loss of mcp-1, the single homologue of GDPGP1 in C. elegans, leads to increased de

158 ormation completely by re-expressing Asense (homologue of human ASCL1), which we show is a direct tar

159 cterized the synaptic role of the Drosophila homologue of human DCAF12, a putative cofactor of Cullin

160 itatory amino acid carrier 1 (EAAC1; the rat homologue of human excitatory amino acid transporter 3 (

161 ame peptides to Mamu-E, the nonhuman primate homologue of human HLA-E, and to the HLA-E-like molecule

162 We demonstrated that AN, a plant homologue of mammalian C-TERMINAL BINDING PROTEIN (CtBP)

163 The arcopallium is also considered the avian homologue of mammalian deep cortical layers and/or amygd

164 In Caenorhabditis elegans, MET-2, the homologue of mammalian SETDB1, catalyzes H3K9me1 and me2

165 mutant Drosophila that are deficient in the homologue of MEGF10 (Drpr) and megf10 mutant zebrafish.

166 In obese patients, the hepatic CIDEC2 (human homologue of mouse FSP27beta) expression strongly correl

167 in flies harboring a mutation in Cyfip, the homologue of one of the genes within the deletion.

168 We further showed that PIR2, the closest homologue of PIR1.2, also interacted with PP2CA.

169 sterior nucleus (LP) of thalamus, the rodent homologue of primate pulvinar, projects extensively to s

170 fied the prp40A(L438*) mutation in Prp40A, a homologue of Prp40, an essential RNA-splicing factor in

171 confirmed to exist as C53-C181 in rTvCyP2, a homologue of rTvCyP1.

172 However, C. albicans lacks a sequence homologue of securins found in model ascomycetes.

173 These data indicate that VTL8, the closest homologue of SEN1 in Lotus japonicus, is the main route

174 The mammalian homologue of SIR2 is SIRT1, an NAD-dependent histone dea

175 e (SPD) and norspermidine (NSPD), a chemical homologue of SPD, on the structure of DNA and gene expre

176 d that partial loss function of Ik2, the fly homologue of TBK1 also known as I-kappaB kinase epsilon

177 m of the D14L receptor, corresponding to the homologue of the Arabidopsis thaliana Suppressor of MAX2

178 Fam151b is a mammalian homologue of the C. elegans menorin gene, which is invol

179 and colocalizes with Bsg25D, the Drosophila homologue of the centrosomal protein Ninein.

180 Here we report that a homologue of the claustrum, identified by single-cell tr

181 transporter of hydrophobic amino acids and a homologue of the eukaryotic SLC6 family of Na(+) -depend

182 y-modulated photodetector based on the n = 2 homologue of the ferroelectric two-dimensional DJ-OIHP (

183 .32 serotype vector was evaluated in the cat homologue of the human lysosomal storage disease alpha-m

184 A homologue of the mammalian sterol regulatory element-bin

185 MATIN PROTEIN1 (LHP1) encodes the only plant homologue of the metazoan HETEROCHROMATIN PROTEIN1 (HP1)

186 lateral entorhinal cortex (alEC) - the human homologue of the rodent lateral entorhinal cortex - spec

187 , the gold standard adds a single structural homologue of the target compound at a known concentratio

188 e nucleotide polymorphism (SNP) located in a homologue of the VEG2 gene from pea, associated with flo

189 ins encoded by myxoma virus, M013 is a viral homologue of the viral pyrin domain-only protein (vPOP)

190 and characterized the function of FolVam7, a homologue of the yeast SNARE protein Vam7p in Fusarium o

191 Mammals possess a functional homologue of yeast SCoR, an aldo-keto reductase family m

192 Here, we identify a role for the mammalian homologue of yeast SFI1, involved in the duplication of

193 Homologues of 5alpha-reductase genes have been identifie

194 as analogues of perfluorosulfonic acids and homologues of alkyl ether sulfates (C(8)- and C(10)/EO(n

195 Removal of mouse homologues of atrial fibrillation-associated regions in

196 rbon receptor-mediated toxic potencies among homologues of chrysene with structural modifications suc

197 are synthesized as a mixture of four or more homologues of different length with one or two predomina

198 The broad expression of homologues of floral ABCE genes in N. colorata might sup

199 tion of variants between the two chromosomal homologues of genes must be known.

200 ained from this whole-genome duplication are homologues of genes that regulate flowering transition a

201 thelial, and fibroblast cells.IMPORTANCE All homologues of herpesvirus gH studied to date have been i

202 ynteny to guide loss-of-function analysis of homologues of human enhancers in mice, we show that the

203 Knockout of AFF2/FMR2 (one of four mammalian homologues of Lilli) with CRISPR-Cas9 decreases the expr

204 nonapeptides arginine-vasotocin or isotocin, homologues of mammalian arginine vasopressin and oxytoci

205 usands of publicly available metagenomes for homologues of methyl-coenzyme M reductase complex (MCR),

206 ons, we further demonstrate that the heavier homologues of phosphine-stabilized borylenes and carbon(

207 NA) are PNAs with two faces and are designed homologues of PNAs in which each aminoethylglycine (aeg)

208 We show that interaction between homologues of pUL7 and pUL51 is conserved across human h

209 Odd and even homologues of some n-alkane-based systems are known to e

210 ca napus), we have characterized four canola homologues of the Arabidopsis (Arabidopsis thaliana) ROD

211 ocystine to initially characterize S. aureus homologues of the Bacillus subtilis cystine transporters

212 s-reactive allergens as Der f 15 in HDM, two homologues of the Periplaneta americana cockroach allerg

213 ins, DotU and IcmF, that, interestingly, are homologues of the T6SS membrane complex components TssL

214 Both proteins are homologues of the yeast ARP2/3 complex activator, Pan1p.

215 The phenotypic homologues of these centers across Panarthropoda support

216 Homologues of this enzyme (named Crn2) exist in type III

217 Defects in mammal and algal homologues of this gene coincide with a loss of fertilit

218 In a search for homologues of this protein, we identified and characteri

219 We find that the fission yeast homologues of Tristetraprolin/TTP and Pumilio/Puf (Zfs1

220 cyte invasion associated gene, PfEBA165, the homologues of which are intact in all ape-infective Lave

221 10 out of 57 genes with orthologues or close homologues) of the targets we identified have homologous

222 ect of lipocalin allergens and nonallergenic homologues on human monocyte-derived dendritic cells (DC

223 The Kaposi's sarcoma-associated herpesvirus homologue, ORF61, also bound APOBEC3B and mediated reloc

224 atota genomes/MAGs found no evidence of mcrA homologues outside of the Methanomassiliicoccales.

225 Although the SC is essential for stable homologue pairing and crossover recombination in diverse

226 mmed DNA double-strand breaks (DSBs) promote homologue pairing and initiate recombination at meiosis

227 ns known as pairing centers to ensure proper homologue pairing and synapsis.

228 trolled termination of these events when all homologue pairs achieve synapsis and form crossover prec

229 y interacting with the p21-activating kinase homologue PAK-1 and acting in this pathway, thereby iden

230 P-ribose) polymerase 1 (PARP1) and its close homologue, PARP2, are early responders to DNA damage in

231 mic acid (Y102E) or to the nonphosphorylated homologue phenylalanine (Y102F) remain nuclear; however,

232 lained by a parallel role played by the ZO-1 homologue Polychaetoid.

233 We find that the zebrafish Hook2 homologue promotes dynein-dynactin association and was e

234 ipids in annular positions on the presenilin homologue protease are subject to constant exchange with

235 shed interactome data that a mammalian Prp40 homologue PRPF40A interacts with Arp1.

236 example, by targeting phosphatase and tensin homologue (PTEN) for proteasomal degradation.

237 ients with pathogenic phosphatase and tensin homologue (PTEN) variants, but the frequency of cortical

238 In orthotopic phosphatase and tensin homologue (PTEN)-deficient glioma mouse models, mRNA-con

239 velop T cells restricted by the murine MHC-E homologue, Qa-1b.

240 Expression of Rad or its homologue Rem in HEK293T cells also imparts stimulation

241 APP N-terminus and compensatory APP-homologues remain intact, with no apparent effects on ne

242 However, it failed to interact with ETO-homologues, repress RUNX1 targets, and transform progeni

243 Baculovirus and insect host poxin homologues retain selective 2',3'-cGAMP degradation acti

244 binding antigens (EBA), reticulocyte binding homologues (RH), surface associated interspersed protein

245 assessed the circRNAome of the interspecies homologue rhesus macaque lymphocryptovirus (rLCV) in a n

246 In mammalian cells, the Tip20 homologue RINT1 associates with ERES, indicating possibl

247 functions in oligomers with and without its homologue ROM1.

248 However, the MAPKKK homologue SepA contributes substantially-sepA mutants ha

249 Analysis of identical test mixtures of homologue series and pharmaceutical samples revealed tha

250 demonstrated and illustrated by a potential homologue series with C(12)H (x)Br (y)Cl (z)O(2) as a pu

251 on, enzymatic transformations of the heavier homologue silicon are rare.

252 Here, we use the yeast VAMP2 homologue Snc1 to investigate the pathways and signals r

253 SNX14 homologues Snz (Drosophila) and Mdm1 (yeast) have also b

254 he DNA-binding domains of SOX2 and its close homologue SOX11 bound to nucleosomes.

255 In Streptococcus mutans, two Spx homologues, SpxA1 and SpxA2, were identified as mediator

256 active-site conservation among distant EanB homologues suggests that the oxidative sulfurization of

257 Knockout of the homologue TabZIP28 in common wheat resulted in declines

258 show that high levels of the Drosophila TLX homologue, Tailless, initiate tumourigenesis by revertin

259 There are nine NPR1 homologues (TaNPR1) in wheat, but little research has be

260 During meiotic recombination, homologue-templated repair of programmed DNA double-stra

261 vealing that PRDM9 also functions to promote homologue-templated repair.

262 trated that RRV vCD200 is a functional CD200 homologue that is capable of affecting immune responses

263 highly conserved, but to a smaller degree in homologues that perform different reactions or are nonen

264 ession is most similar to that of its serial homologue, the mesonotum.

265 We sought a functional homologue through identifying Esp1p interacting factors.

266 terleukin-6 (vIL-6) was the first viral IL-6 homologue to be identified.

267 MC001 is homologue to lipid A deacylase enzyme (LpxR), and to our

268 expressed in Escherichia coli, which lacks a homologue to SmvAR, resistance to chlorhexidine increase

269 its composition of areas make it a candidate homologue to the human default network.

270 that the L*-cluster represents a structural homologue to the l-cluster except for the missing belt s

271 Trypanosomes lack homologues to most of the involved proteins and their nu

272 Homologues to these proteins are found in the brain, and

273 the lack of the Caenorhabditis elegans Msp1 homologue triggers an import stress response in the worm

274 and PARP15 as well as a highly diverged PARP homologue TRPT1, ADP-ribosylate phosphorylated ends of R

275 The TRPV1 homologues TRPV2 and TRPV3 are also activated by heat, b

276 over other TRP channels, including its close homologue TRPV6.

277 e show that the VACV epidermal growth factor homologue, VGF, promotes infected cell motility and the

278 Downregulation of all the TaNPR1 homologues via virus-induced gene co-silencing resulted

279 generation of homoenolates, and their higher homologues, via decarbonylation of readily available cyc

280 of genus Epichloe; however, a putative perA homologue was recently identified in the genome of the i

281 mation; however, a decrease in the number of homologues was observed, as well as loss of molecules at

282 the C2C12 cell line, and unlike other ferlin homologues, we found Fer1l6 expression was independent o

283 Hypercapnia-responsive Wnt pathway homologues were similarly observed in secondary analysis

284 y.IMPORTANCE Human herpesvirus 8-encoded IRF homologues were the first to be identified in a virus.

285 We also show that unlike the M. smegmatis homologue which was not essential for growth, Rv2509 was

286 gulated spectrin-associated protein (CAMSAP) homologue, which functions redundantly with Ninein to fu

287 ERdj3 is an ER luminal DnaJ homologue, which, along with calreticulin, directly inte

288 ide groups bestowed water solubility for all homologues, which allowed their use as a model for study

289 Examples of higher homologues, which are sparsely investigated, will also b

290 fall into two distinct GST subclasses: LigE homologues, which cleave the beta(R) stereoisomer of the

291 e beta(R) stereoisomer of the bond, and LigF homologues, which cleave the beta(S) stereoisomer.

292 bility that both tissues are crustacean wing homologues, which supports a dual evolutionary origin of

293 cs analysis demonstrates that Apd6 and their homologues, widely distributed within several bacterial

294 between the periplasmic domains of two YejM homologues with hydrolases like arylsulfatases, no enzym

295 e conserved nudiviral genes (sharing 57 gene homologues with other crustacean-infecting nudiviruses)

296 ne-reconstituted Glt(Ph), a prokaryotic EAAT homologue, with millisecond temporal resolution.

297 tures, either of the same protein or related homologues, with similar or functionally different terti

298 We hypothesized that some, but not all, SMN homologues would rescue the SMA phenotype in mouse model

299 onization spray MS that the Escherichia coli homologue YjhC displayed activity against 2,7-anhydro-Ne

300 ession protein 39 (BRP-39) in mice and human homologue YKL-40, plays important roles in Th2 inflammat