ライフサイエンスコーパス: paralogous

1 Here, we report the identification of four paralogous 2-oxoglutarate/Fe(II)-dependent oxygenases in

2 This analysis identified two highly paralogous 24.5 kb blocks within the FCGR2C/FCGR3B/FCGR2

3 In the paralogous 4.1B gene, we identified approximately 120 kb

4 use tolC transcription is activated by three paralogous activators, MarA, SoxS, and Rob, we examined

5 Two paralogous alpha/beta hydrolases, KAI2 and D14, are resp

6 s a result of functional redundancy with the paralogous Alx4 gene.

7 The paralogous and functionally redundant GATA transcription

8 lternative splicing, among a large number of paralogous and orthologous genes.

9 observed, and it tends to occur in pairs of paralogous and redundant proteins.

10 Three paralogous Arabidopsis basic helix-loop-helix proteins,

11 Using the paralogous Arabidopsis thaliana inositol transporters IN

12 a Site 2 like CadC or has no Site 2 like the paralogous ArsR and implies that acquisition of regulato

13 Based on the paralogous aspartate-beta-semialdehyde dehydrogenase str

14 te that Archaeal AMP-Acs and ADP-Acs contain paralogous ATPase motifs previously identified in Ack, w

15 stigator data indicated that AtXTH31 and the paralogous AtXTH32 were abundantly expressed in expandin

16 Inpp5b and INPP5B, paralogous autosomal genes that encode another type II p

17 te the physiological significance of the two paralogous BCCP-coding genes, CAC1A (At5g16390, codes fo

18 matodes and planaria, however, have a set of paralogous beta-catenins; for example, C. elegans HMP-2

19 e dicot species, Arabidopsis, in which three paralogous bHLH transcription factors, FAMA, MUTE and SP

20 ing of haplotype blocks between these highly paralogous blocks that most likely arose from sequential

21 Interestingly, the paralogous BoxR and BzdR regulators act synergistically

22 r particularly frequently within families of paralogous C(2)H(2) zinc-finger genes, suggesting the po

23 The recurrent evolution of paralogous, catalytically dead enzyme-based activating m

24 perties of CaV1.3 in a manner similar to the paralogous CaV1.2.

25 n a disaggregation mechanism whereby the two paralogous chaperones alternatively activate the release

26 Mutation in three paralogous class III homeodomain leucine zipper (HD-ZIPI

27 locus was identified on chromosome 1, and a paralogous ClpP5 gene was isolated and confirmed as the

28 However, these genes are located in distinct paralogous clusters in the genome apart from the classic

29 e genomic arrangement of Hox genes into four paralogous clusters is a primitive feature of jawed vert

30 Future, functional tests of homologous and paralogous CMTs will uncover novel roles and consequence

31 A paralogous complex, tMAC, controls expression of at leas

32 al gene duplications drive the expansions of paralogous copies and the expansions occur in independen

33 odular peptidases regularly found in several paralogous copies in animals and plants, where they have

34 nce several biologically important loci have paralogous copies that interfere with genotyping, and wh

35 C-B1 is a NAC transcription factor and has a paralogous copy on chromosome 2B in wheat, GPC-B2.

36 systems are orthologous and the origin of a paralogous CRZ-type signalling system can be traced to t

37 nown activator of disA encoding one of three paralogous diadenylate cyclases (DAC).

38 Truncation of the paralogous domain from the Nedd8 activating enzyme has n

39 ered both alternatively spliced and putative paralogous dsx transcripts from several orders of hexapo

40 originating in the luminal layer exploit the paralogous EMT-TFs Slug and Snail, respectively, which i

41 ical function of VKORC1-like 1 (VKORC1L1), a paralogous enzyme sharing about 50% protein identity wit

42 ion, while the physiological function of its paralogous enzyme VKOR-like (VKORL) is yet unknown.

43 e for ethanolamine over choline, whereas two paralogous enzymes from Loxosceles arizonica either pref

44 In particular, they suggest how paralogous enzymes with similar catalytic properties cou

45 cDNA expression screening, we identified two paralogous epithelial cell-type-specific RNA-binding pro

46 es (tissue-specific, alternative splicing of paralogous exons of a single gene) and vertebrates (tiss

47 -specific, alternative splicing of a pair of paralogous exons.

48 derive from the segment corresponding to the paralogous exons.

49 A significant paralogous expansion of key gene families--families enco

50 We found that within paralogous families the expression pattern of individual

51 among the present-day receptors, allowing a paralogous family of transcription factors to control di

52 B transcription factors (TFs), MYB88 and the paralogous FLP (MYB124), in cold stress in apple and Ara

53 ultiple paralogs of Spx, suggesting that two paralogous forms of Spx could simultaneously contact RNA

54 le that gene duplication events discriminate paralogous from orthologous genes, QuartetS has been sho

55 rence of duplication events and discriminate paralogous from orthologous genes.

56 ectable AdoMetDC activity; however, when two paralogous fusion proteins are mixed, AdoMetDC activity

57 Here, we show that the two paralogous GATA transcription factors GATA, NITRATE-INDU

58 the Bmal1-knockout mice by expression of the paralogous gene Bmal2, insulin action and activity patte

59 r than tandem gene duplication can result in paralogous gene clustering during genome evolution.

60 the developmental origin, oncogenic drivers, paralogous gene expression pattern, and chromosomal stru

61 Borrelia burgdorferi genome harbors several paralogous gene families (pgf) that can encode immunogen

62 tified four pathways/gene networks and eight paralogous gene families affected by Microcystis .

63 enes, of which six are fragmented, and seven paralogous gene families are present.

64 regulation of the ribosome, including three paralogous gene families encoding 40S, 60S, and mitochon

65 ray to identify pathways, gene networks, and paralogous gene families responsive to Microcystis stres

66 tentially mediating expression divergence in paralogous gene families under specific conditions.

67 ion (49.1%) of these CDSs are organized into paralogous gene families, which can now be further explo

68 oxidoreductase gene family) and the trypsin paralogous gene family (a major component of the digesti

69 ein 2 [Msp2(P44)] is encoded by members of a paralogous gene family and is speculated to play roles i

70 PFam54 is the largest paralogous gene family in the genomes of Borrelia burgdo

71 thirteen novel genes that belong to the L1L paralogous gene family of Solanum lycopersicum.

72 rthologous genes from diverse genomes and of paralogous gene family sizes, and the negative correlati

73 and are grouped into the same B. burgdorferi paralogous gene family.

74 Loss of Hox11 paralogous gene function results in dramatic malformatio

75 A paralogous gene in humans, SMN2, produces low, insuffici

76 Orthologs of bm4 include at least one paralogous gene in maize and various homologs in other g

77 hat developmental mutations in the zebrafish paralogous gene otpa but not otpb affect both stress res

78 Direct comparison of paralogous gene pairs all duplicated simultaneously reve

79 stitutions per synonymous site (Ks ) between paralogous gene pairs and reconciliation of 578 gene tre

80 n studies of duplicated dps genes shows that paralogous gene pairs are expressed differentially and t

81 ted to the dominant expression of individual paralogous gene pairs.

82 Although it is well established that the paralogous gene product Phox2b is widely expressed in ad

83 t modify the alternative splicing of SMN2, a paralogous gene to SMN1, restoring the survival motor ne

84 SMN2, a paralogous gene to SMN1, undergoes alternative splicing

85 This paralogous gene was previously identified only in the el

86 Previously, it was shown that the CTCF paralogous gene, BORIS (brother of the regulator of impr

87 A paralogous gene, germ-cell expressed (gce), possesses ho

88 e regulation of Samd9L in the context of its paralogous gene, SAMD9, which harbors mutations in NFTC.

89 ethod of differentiating between allelic and paralogous (gene copy) sequence variants, allowing ident

90 dopsis thaliana Ms-0 includes two functional paralogous genes (RPW8.1 and RPW8.2) and confers broad-s

91 nids have seven primary subunits (encoded by paralogous genes a-g), which combine to form a 24-mer (4

92 key information and links to orthologous and paralogous genes are now included to further facilitate

93 In Arabidopsis (Arabidopsis thaliana), these paralogous genes are positioned in tandem within a clust

94 ee joints of mouse embryos lacking all Hox11 paralogous genes are specifically remodeled and reorgani

95 yanobacterial strains, there are one to four paralogous genes coding for homologs to the NTD of the O

96 Several features of paralogous genes correlate with gene conversion, such as

97 n and generated independent mutations in the paralogous genes DCL4a and DCL4b.

98 r expression patterns diverged from those of paralogous genes elsewhere in the genome.

99 s (Arabidopsis thaliana) genome contains two paralogous genes encoding stomatin-like proteins (SLPs;

100 ces of P. aeruginosa reveal it to have three paralogous genes for this protease, designated as ampD,

101 all RNA targeting, relating to the multicopy paralogous genes generated from whole genome triplicatio

102 lant 26S proteasome and suggest that its two paralogous genes in Arabidopsis have both redundant and

103 ndition-specific expression divergence among paralogous genes in Saccharomyces cerevisiae.

104 is genetically downstream of both the Hox11 paralogous genes in the developing mammalian kidney and

105 single crossover chimeras between duplicated paralogous genes is a known process for increasing diver

106 unidirectional redundancy between these two paralogous genes is that whereas the BCCP1 protein can c

107 hat functional redundancy between duplicated paralogous genes is the molecular mechanism for the inte

108 The local regulators are the products of two paralogous genes mapping at positions adjacent to the co

109 d by single-subunit enzymes encoded by three paralogous genes of which TbSTT3B and TbSTT3C can comple

110 epeat (OPR) proteins encoded in a cluster of paralogous genes on chromosome 15.

111 which predicted functional divergence in the paralogous genes per clade.

112 The seven families of paralogous genes recognized in EEHV1 are also represente

113 Analyses of paralogous genes suggest a whole-genome duplication shar

114 tromeres, TET/JBP transposons, and multicopy paralogous genes that are not expressed, but rarely mark

115 Psc) and Suppressor 2 of zeste [Su(z)2], two paralogous genes that likely arose by gene duplication.

116 ying this metric, the authors concluded that paralogous genes within the mouse genome or the human ge

117 cleotide diversity, copy number variation of paralogous genes, and long repetitive sequences.

118 Two highly similar paralogous genes, clag 3.1 and clag 3.2, are mutually ex

119 s of several proteasome subunits, encoded by paralogous genes, have been discovered, and in some case

120 ly as fetal gamma-globin expression from two paralogous genes, hemoglobin subunit gamma 1 (HBG1) and

121 y of target genes to the loss of one or both paralogous genes, including preferential effects on spec

122 The paralogous genes, jamb2 and jamc2, were not detected in

123 d CyHV3 have five, six, and five families of paralogous genes, respectively.

124 (SMN), a protein expressed in humans by two paralogous genes, SMN1 and SMN2.

125 ssociated with such mutations are functional paralogous genes, suggesting that epistatic interactions

126 Two paralogous genes, tomosyn-1 and -2, occur in mammals and

127 Humans have two paralogous genes, TWIST1 and TWIST2, and mutations in ea

128 Here we show that Hox11 paralogous genes, which developmentally pattern the zeug

129 ous genes are functionally more similar than paralogous genes.

130 major force in homogenizing the sequences of paralogous genes.

131 me are represented in the genome by multiple paralogous genes.

132 echanisms control differential expression of paralogous genes.

133 tions in homologous positions across sets of paralogous genes.

134 tribution of TEs between flanking regions of paralogous genes.

135 s more to the higher expressing gene copy of paralogous genes.

136 h convergent subgenome parallel selection of paralogous genes.

137 , a high coding density, and a low number of paralogous genes.

138 2/FCGR3 genes are arranged across two highly paralogous genomic segments on chromosome 1q23.

139 r heterozygous missense substitutions in the paralogous glutamic acid residue in TWIST2 (p.Glu75Ala,

140 Several invertebrate deuterostomes have two paralogous glycine carrier genes, with one gene in the p

141 ny fishes, one leading to a newly identified paralogous group (we have termed CHIO).

142 We then identified a paralogous group of secreted chaperone proteins in the H

143 ing the high level of redundancy in this Hox paralogous group.

144 owever, to what extent members of individual paralogous groups can undergo functional changes during

145 diverse cyanobacteria, occurring as multiple paralogous groups, with two representatives exhibiting s

146 IsdG and IsdI are paralogous heme degrading enzymes from the bacterium Sta

147 Most species encode numerous paralogous histidine kinases that exhibit significant st

148 nundrum, it is necessary to directly compare paralogous (horizontal) evolution of repeats within prot

149 on of Hox function across species, and among paralogous Hox genes within a species, supports a model

150 We then tested whether three putative, paralogous inner membrane efflux pumps, HefC, HefF, or H

151 The paralogous iron-responsive transcription factors Aft1 an

152 etabolic vulnerability upon targeting of its paralogous isoform ME3.

153 e auxotrophy in a leuB(-) strain lacking the paralogous isopropylmalate dehydrogenase enzyme.

154 Mice and humans possess three paralogous KDEL receptors, but little is known about the

155 Two paralogous kinases phosphorylate subsets of thylakoid me

156 anslocation to 24 bp within interchromosomal paralogous LCRs of approximately 130 kb in length and 94

157 cis-abienol synthase (AbCAS), along with the paralogous levopimaradiene/abietadiene synthase and isop

158 The paralogous loci encode maize CRABS CLAW co-orthologs in

159 errors in locus reconstruction, distinguish paralogous loci, rarify raw reads originating from the s

160 elic homologous recombination (NAHR) between paralogous long interspersed nuclear element (LINE) or h

161 We delineated and analyzed directly oriented paralogous low-copy repeats (DP-LCRs) in the most recent

162 r site-specific positive selection acting on paralogous main olfactory receptor genes.

163 The paralogous maize (Zea mays) LBD (Lateral Organ Boundarie

164 for disaccharides that are transported by a paralogous maltose transport operon present in T. thermo

165 CTCF and BORIS (CTCFL), two paralogous mammalian proteins sharing nearly identical D

166 ort an example of cooptive convergence where paralogous members of the globin gene superfamily indepe

167 RNase II and RNase R are paralogous members of the RNR superfamily of nonspecific

168 tutions, as well as analysis of variation at paralogous miR390-generating loci (MIR390a and MIR390b),

169 r development or viability and proposed that paralogous miRNAs might often function redundantly.

170 The miR-183 cluster, which is comprised of paralogous miRs-183, -96 and -182, is overexpressed in m

171 In vertebrates, the paralogous MLL2 and MLL3 contain multiple domains requir

172 module (CBM6), and F. succinogenes-specific paralogous module 1 (FPm-1).

173 designated Fibrobacter succinogenes-specific paralogous module 1 (FPm-1).

174 In contrast, paralogous multicopy genes are found in the highly recom

175 The paralogous multifunctional adaptor proteins YAP and TAZ

176 sh, prps1a and prps1b and characterized each paralogous mutant individually as well as the double mut

177 The existence of paralogous NL1/Tsh1/TRD-like genes in the grasses indica

178 a new candidate Aft1 target-gene (LSO1) and paralogous non-target (LSO2), plus nine putative Cth2 ta

179 logenomic analysis, we have revealed two new paralogous OCP families, each distributed among taxonomi

180 A paralogous operon involves a putative nuclease (CinB) ra

181 ity-coverage metrics, tailored solutions for paralogous or low-complexity areas of the genome, and th

182 ifferent fungal lineages and formed distinct paralogous/orthologous clades.

183 me of Mycobacterium tuberculosis encodes two paralogous P1 B 4 -ATPases, CtpD (Rv1469) and CtpJ (Rv37

184 X-linked mouse gene Atp11c, which encodes a paralogous P4-type ATPase, precludes B-cell development

185 eterogeneous set of particles assembled with paralogous pairs for most subunits.

186 the underlying evolutionary forces of these paralogous pairs through conducting neutrality tests wit

187 Similar paralogous pairs were detected throughout terrestrial pl

188 nctional complex with its catalytically dead paralogous partner, prozyme.

189 ive, enabling PhoR to avoid crosstalk with a paralogous pathway that arose specifically in alpha-prot

190 psdA that ensure the insulation of these two paralogous pathways at the RR-promoter interface.

191 e original method by extending the theory to paralogous phenotypes.

192 uld be restored by ectopic expression of the paralogous pilA gene.

193 cosylation on pilus assembly and function of paralogous pilins.

194 Two paralogous plasma membrane-associated protein kinases, P

195 Mechanistically, miRNAs derived from these paralogous pri-miRNAs (miR-18a, miR-19b, and miR-20b) ta

196 of miRNAs derived from the processing of the paralogous primary transcripts (pri-) mir-17-92 and mir-

197 Six distinct but paralogous proteasome ATPase proteins, Rpt1 to -6, form

198 ow that strains lacking Edc2, as well as the paralogous protein Edc1, are compromised for growth unde

199 ication of toxin-antitoxin systems and other paralogous protein families during evolution.

200 ay help explain the apparent ease with which paralogous protein families expanded in all organisms.

201 In addition, RevB, a paralogous protein found in a subset of B. burgdorferi s

202 tion in Escherichia coli is regulated by two paralogous proteins (GlnB and GlnK), which orchestrate i

203 NA encoding YapV or each of three individual paralogous proteins (YapK, YapJ, and YapX) was present a

204 iation between the gene profile for the four paralogous proteins and the geographic location of the c

205 ne duplication influence the extent to which paralogous proteins are functionally repurposed.

206 These paralogous proteins bind to Rgt1 and enable it to repres

207 Toc75 and OEP80 are paralogous proteins found in the Viridiplantae lineages,

208 e most conserved residues of orthologous and paralogous proteins likely define those most important.

209 he combination of mutations suggest that the paralogous proteins perform redundant functions in motil

210 FslE (FTT0025) and FupA (FTT0918) are paralogous proteins that are predicted to form beta-barr

211 relies on interactions with Met31 and Met32, paralogous proteins that bind the same cis-regulatory el

212 interfaces) are investigated and compared to paralogous proteins that bind the same protein ligand (f

213 Thus, we identify three distinct but paralogous proteins that donate electrons to NirK.

214 The evolutionary events that cause paralogous proteins to bind different protein ligands (f

215 In this study, we compared these paralogous proteins to identify characteristics correlat

216 our studies indicate that BmpA and its three paralogous proteins, BmpB, BmpC, and BmpD, all bind to m

217 he ring of Fungi, which is composed of three paralogous proteins, evolved from a more ancient two-par

218 be (BHD) syndrome, which associates with two paralogous proteins, folliculin-interacting protein (FNI

219 Here we report a group of LRRC26 paralogous proteins, LRRC52, LRRC55, and LRRC38 that pot

220 P. sojae, however, secretes a paralogous PsXEG1-like protein, PsXLP1, that has lost en

221 sis that zebrafish tlr4a and tlr4b genes are paralogous rather than orthologous to human TLR4.

222 MiST carefully handles paralogous reads that map ambiguously to the genome and

223 ferentiation-associated protein 5 (MDA5) are paralogous receptors for viral double-stranded RNA (dsRN

224 These paralogous receptors share redundant function during dev

225 NPs, while 26% of SNPs might be derived from paralogous regions.

226 cificities toward effectors and DNA sites in paralogous regulators is a fundamental question in biolo

227 tions, and the concept of orthologous versus paralogous relationships at different levels, including

228 regulatory proteins revealed orthologous and paralogous relationships from species divergences and an

229 erminal regions to determine orthologous and paralogous relationships, as well as the influence of se

230 = 26), short inserted sequences (n = 8), or paralogous repeats (n = 3) at the junctions, indicating

231 of molecular function, including hotspots at paralogous residues of Ras-related small GTPases RAC1 an

232 The paralogous ribonucleases J1 and J2, recently identified

233 cts of its own antibiotics by expressing two paralogous rRNA methylase genes pikR1 and pikR2 with see

234 d core eudicot species Antirrhinum majus L., paralogous SBP-box proteins SBP1 and SBP2 have likewise

235 Rcr3 and Pip1 are paralogous secreted papain-like proteases of tomato.

236 e high degree of sequence similarity between paralogous segments has prevented precise definition of

237 in single-nucleotide polymorphisms (SNPs) or paralogous sequence variants (PSVs) separated by several

238 sequencing across MAP2K3 identified several paralogous sequence variants indicating that the region

239 r inversion probes designed to target unique paralogous sequence variants.

240 s to establish a detailed map of allelic and paralogous sequence variation across the FCGR2/FCGR3 loc

241 GR2B locus that are devoid of nonpolymorphic paralogous sequence variations and that define the limit

242 ies to allow traversal among orthologous and paralogous sequences across the legumes.

243 sequence was also used to recover additional paralogous sequences from genomic DNA, one of which (PtA

244 to aspects of strand exchange events between paralogous sequences in the human genome.

245 ithin high-identity, copy-number polymorphic paralogous sequences that cannot be specifically assayed

246 ces that are not in allelic positions (i.e., paralogous sequences) can result in recurrent deletions

247 y nonreciprocal recombination events between paralogous sequences, a phenomenon known as interlocus g

248 ct genotyping include copy-number-variation, paralogous sequences, library preparation, sequencing er

249 indicated that PnSERK1 and PnSERK2 represent paralogous sequences.

250 e obtained, even in the presence of captured paralogous sequences.

251 Here we describe two paralogous single Myb domain genes, MYB-RELATED PROTEIN

252 In addition, the results of analysis of the paralogous small transmembrane protein AppX show that th

253 nts indicated that Arabidopsis possesses two paralogous solanesyl-diphosphate synthases, AtSPS1 (At1g

254 ic, consisting of two stacked rings of eight paralogous subunits each.

255 mapped within 55 bp in approximately 7.8-kb paralogous subunits of 95.3% sequence identity located i

256 ion breakpoints within the directly oriented paralogous subunits of the flanking LCR clusters, demons

257 contain a conserved set of 17 genes encoding paralogous subunits of the three major photosynthetic co

258 family member unveils critical dependence on paralogous subunits.

259 ther tumor suppressor lesions/complexes with paralogous subunits.

260 chromosome I, encodes one of two V-ATPase B paralogous subunits.

261 Comparison of the structure of GALNS to paralogous sulfatases shows a wide variety of active-sit

262 Esx-3, a paralogous system present in all mycobacterial species,

263 Transcription of these paralogous TA systems is differentially regulated under

264 dominant human fungal pathogen, contains two paralogous TAF12 genes, CaTAF12L and CaTAF12, encoding H

265 Members of paralogous TF families typically recognize similar DNA s

266 ion models, we show that even in the case of paralogous TF with highly similar position weight matric

267 However, many paralogous TFs (i.e. members of the same TF family) perf

268 for studying the genomic binding profiles of paralogous TFs and identifying their putative co-factors

269 r determinants of protein-DNA recognition by paralogous TFs is of central importance for understandin

270 s input two sets of genomic regions bound by paralogous TFs, and it identifies a small set of putativ

271 co-factors that might provide specificity to paralogous TFs.

272 ns as a bona fide cleavage factor, while the paralogous TFS4 evolved into a potent RNA polymerase inh

273 rkably, the E17K mutation in AKT3 is exactly paralogous to E17K mutations in AKT1 and AKT2 recently d

274 -stranded telomere DNA-binding protein Teb1, paralogous to heterotrimeric replication protein A (RPA)

275 of two partially redundant proteins that are paralogous to IDN2 and that form a stable complex with I

276 ncluding two ribosomal proteins (r-proteins) paralogous to L31 and S14.

277 F169, an uncharacterized E3 ubiquitin ligase paralogous to RNF168, accumulated in DSB repair foci thr

278 sulting in part from deletion of an srg gene paralogous to srg-36 and srg-37.

279 poorly polymorphic HLA-DQA2/HLA-DQB2 genes, paralogous to the HLA-DQA1/HLA-DQB1 genes, has never bee

280 Teb1 is paralogous to the large subunit of the general single-st

281 d archaea encode varying numbers of proteins paralogous to their main recombinase.

282 notated genes, including PAK2 and DLG1, both paralogous to X-linked ID genes and now strong candidate

283 Phylogenetic analyses indicate that they are paralogous to, but quite distinct from, classical dynami

284 Using microarray analysis, we found that the paralogous tomato WRKY genes SlWRKY72a and b are transcr

285 on, protein interactions, and DNA binding of paralogous transcription factors ("TF parameters") are t

286 ngly, we show that different combinations of paralogous transcription factors (Sox8, Pea3 and cMyb ve

287 To understand how paralogous transcription factors evolve divergent DNA sp

288 ly conserved function for the combination of paralogous transcription factors in these tissues of dis

289 Three paralogous transcriptional activators MarA, SoxS, and Ro

290 Paralogous transcriptional regulators MarA, Rob, and Sox

291 s, and EST-supported loci with convergent or paralogous transcripts.

292 afish, as a model for teleost fish, have two paralogous troponin C (TnC) genes that are expressed in

293 we survey the role of neuronally expressed, paralogous tumor necrosis factor receptor super family (

294 BceRS and PsdRS are paralogous two-component systems in Bacillus subtilis co

295 IFs (QYE motif), we tested the effect of the paralogous Tyr in glial fibrillary acidic protein (GFAP)

296 le PDZ protein harmonin is not involved, its paralogous USH2 proteins, PDZD7 and whirlin, function sy

297 S cells markedly decreases expression of the paralogous UTY gene encoded by Y chromosome, but has no

298 Comparison of paralogous vitellogenins in 10 insect species representi

299 The paralogous yeast proteins Lsb1 and Lsb2 bind the actin a

300 g of ZF DNA binding and provide evidence for paralogous ZFs utilizing alternate modes of DNA binding