ライフサイエンスコーパス: multigene family

1 rved in the Diptera and may be a member of a multigene family.

2 a heteromer of MSP1a and MSP1b, encoded by a multigene family.

3 ot is the COBRA (COB) gene that belongs to a multigene family.

4 -18,159 Da; these are probably products of a multigene family.

5 ression of one odorant receptor from a large multigene family.

6 s) of Ehrlichia chaffeensis are encoded by a multigene family.

7 ytophilum are encoded by the p44 polymorphic multigene family.

8 cytoplasmic actin proteins are encoded by a multigene family.

9 re surface-exposed proteins encoded by a p44 multigene family.

10 specifically altering a single gene within a multigene family.

11 have a large impact on the evolution of this multigene family.

12 E2F-independent activation of the histone H4 multigene family.

13 ns of A. phagocytophila are encoded by a p44 multigene family.

14 P1b is expressed by members of the msp1 beta multigene family.

15 fluence the expression of members of the p44 multigene family.

16 nt degrees of gene amplification in the zein multigene family.

17 outer membrane proteins (P44s) encoded by a multigene family.

18 c ehrlichiosis agent) are encoded by the p44 multigene family.

19 the prototypic member of a novel B7-related multigene family.

20 eded to disrupt the compensation within this multigene family.

21 e members of the major surface protein (MSP) multigene family.

22 8) of Ehrlichia chaffeensis are encoded by a multigene family.

23 ighly conserved protein that is encoded by a multigene family.

24 ing antibiotic drugs to several members of a multigene family.

25 to reflect functional specification of this multigene family.

26 It is highly conserved and encoded by a multigene family.

27 mylase (BAM) activity, which is encoded by a multigene family.

28 luding Arabidopsis and rice, contains a CAF1 multigene family.

29 f the surface-associated interspersed (surf) multigene family.

30 use of the difficulty in deleting this large multigene family.

31 ins of gap junctions are the products of two multigene families.

32 origination, diversification and loss within multigene families.

33 he japonica genome, 38 (76%) fell into eight multigene families.

34 ry receptor (Or) and gustatory receptor (Gr) multigene families.

35 ch step is executed by components encoded by multigene families.

36 mes, many of which are encoded by members of multigene families.

37 e evolution and expression dynamics of these multigene families.

38 n of gene expression, are usually members of multigene families.

39 certain members of both the LeACS and LeIAA multigene families.

40 ariation and linkage disequilibrium in small multigene families.

41 r the control of gene expression of unlinked multigene families.

42 ones and for establishing contigs of several multigene families.

43 of transcripts derived from the GRP and HRGP multigene families.

44 sophila members of developmentally important multigene families.

45 nce diversity, such as that seen in variable multigene families.

46 In plants, profilins are encoded by multigene families.

47 ar structures and are encoded by polymorphic multigene families.

48 proteins of A. marginale encode polymorphic multigene families.

49 everal E3s have expanded in their genomes as multigene families.

50 ed by at least four evolutionarily unrelated multigene families.

51 ter GA biosynthetic stages being governed by multigene families.

52 lenging when the target genes are members of multigene families.

53 d to gene-rich regions that harbor clustered multigene families.

54 roles of the different members of these OMP multigene families.

55 to characterize a large number of eukaryotic multigene families.

56 eletions in the region containing members of multigene family 360 (MGF 360) and MGF530.

57 ain Georgia (ASFV-G) lacking only six of the multigene family 360 (MGF360) and MGF505 genes (ASFV-G-D

58 Multigene family 360 (MGF360) and MGF505 represent a gro

59 African swine fever virus (ASFV) multigene family 360 and 530 (MGF360/530) genes affect v

60 sine, (2) determination of when members of a multigene family acquire distinct activities, (3) applic

61 e selected to present many peptides, through multigene families, allelic polymorphism, and peptide-bi

62 f the sarcomere, is encoded by a four-member multigene family: alpha-TM, beta-TM, TPM 3, and TPM 4.

63 egration site), respectively, are encoded by multigene families and are present in multimeric complex

64 id transfer proteins (nsLTPs) are encoded by multigene families and possess physiological functions t

65 along with novel strategies to characterize multigene families and redundant biochemical pathways.

66 s an inherent property of highly polymorphic multigene families and that it cannot be taken as eviden

67 ombardment method for functional genomics of multigene families and the modification of the nutritive

68 Transcription factors often belong to multigene families and their individual contribution in

69 Many Drosophila genes exist as members of multigene families and within each family the members ca

70 These genes are members of a multigene family and are expressed at moderate levels in

71 shock protein 70s (Hsp70s) are encoded by a multigene family and are located in different cellular c

72 othelial PDI further extends this increasing multigene family and EndoPDI, unlike archetypal PDI, may

73 s a member of the ATP-binding cassette (ABC) multigene family and is composed of two nucleotide bindi

74 Poplar BSPs are encoded by a multigene family and one member, bspA, has been cloned a

75 IL-1beta regulates expression of the claudin multigene family and that gap and tight junction protein

76 Variant antigens, encoded by multigene families, and expressed at the surface of eryt

77 generally to examine expression profiles of multigene families, and in particular to refine informat

78 ral differences between divergent members of multigene families are functionally important.

79 Major repeat sequences and multigene families are largely free of DNA methylation.

80 The members of this multigene family are found in all cellular organisms, mo

81 hown that subfamily 1 receptors encoded by a multigene family are present in all charophytes examined

82 Procyclins, the products of a small multigene family, are glycosyl phosphatidylinositol-anch

83 Phylogenetic analysis revealed multigene family associations and faster evolution of ea

84 interesting opportunity to study a dispersed multigene family because invertebrates possess a single

85 ress expression of the Rubisco small subunit multigene family by placing an IR, homologous to the con

86 However, the expression of genes in multigene families can diverge rapidly between related s

87 e changes between closely related members of multigene families can generate novel specificities for

88 known gene family members, new members of a multigene family can be identified.

89 Like PRF and SPF, PMF is produced by a multigene family characterized by gene duplication and h

90 ity-related factor prediction, orthology and multigene family classification, transcriptome analyses,

91 Phylogenetic analyses assigned the vap multigene family complement from pVAPN, pVAPA, and pVAPB

92 bidopsis ENOD-like proteins are encoded by a multigene family composed of several types of structural

93 ycobacterium tuberculosis identified a novel multigene family composed of two closely related subfami

94 RIFIN proteins are products of a polymorphic multigene family comprising approximately 150-200 genes

95 rabidopsis thaliana, AUX1 belongs to a small multigene family comprising four highly conserved genes

96 s are thought to be represented by two large multigene families, comprising the V1r and V2r genes, wh

97 ycopersicum), cryptochromes are encoded by a multigene family, comprising CRY1a, CRY1b, CRY2, and CRY

98 ome sequence indicated that COB belongs to a multigene family consisting of 12 members, all predicted

99 lin 3-oxidase in Arabidopsis is encoded by a multigene family consisting of at least four members, de

100 TbPT0 belongs to a clustered multigene family consisting of five members, whose expre

101 In angiosperms, CAD is encoded by a multigene family consisting of members thought to have d

102 mbrane proteins are encoded by a polymorphic multigene family consisting of more than 20 paralogs.

103 o)genes that belong to a newly characterised multigene family containing a hot spot of insertion for

104 d variable regions, and is also encoded by a multigene family containing some truncated gene copies.

105 erefore, the Sperm dynein intermediate chain multigene family contributes to the differential reprodu

106 econstruct the tree of life and histories of multigene families demand the inference of phylogenies c

107 uberculosis revealed the presence of a novel multigene family designated PE/PE_PGRS that encodes nume

108 protein expression from many members of the multigene family, despite primary high-level expression

109 s of an extremely large, globally regulated, multigene family, each member of this family resides wit

110 These analyses suggest that the FKBP multigene family emerged early in the evolutionary histo

111 ors (ORs), encoded by the largest vertebrate multigene family, enable the detection of thousands of u

112 Multigene families encode enzymes of the hydrogenosome o

113 Several multigene families encode RNA binding proteins (RNABPs)

114 hicken Ig-like receptors (CHIRs) represent a multigene family encoded by the leukocyte receptor compl

115 In Arabidopsis, a multigene family encodes six SUS (SUS1-6) isoforms.

116 Multigene families encoding class XI myosins are conserv

117 These findings suggest that novel multigene families encoding diversified immune receptors

118 ls large-scale duplication and divergence of multigene families encoding molecules that effect innate

119 ocyte Membrane Protein 1 (PfEMP1), two other multigene families encoding STEVOR and RIFIN are express

120 able expression of individual members of the multigene families encoding these genes also occurs duri

121 transcribe multiple SRCR genes from among a multigene family encoding an estimated number of 1,200 S

122 The current study analyzed the pleomorphic multigene family encoding approximately 30-kDa major out

123 A heretofore-unrecognized multigene family encoding diverse immunoglobulin (Ig) do

124 analysis of the Chlamydiaceae has revealed a multigene family encoding large, putatively autotranspor

125 lar neurons and coexpression with a distinct multigene family encoding neural receptors.

126 4 in Col-0 as a member of the clustered RPP5 multigene family encoding nucleotide-binding leucine-ric

127 Certain genes in the Jonah multigene family encoding serine proteases have been imp

128 The multigene family encoding the five classes of replicatio

129 The vir multigene family, encoding a very large number of varian

130 e recruitment is a common phenomenon in tRNA multigene family evolution and should be taken into cons

131 The birth-and-death model of multigene family evolution describes patterns of gene or

132 According to this model of multigene family evolution, some genes are maintained in

133 Various members of the Ets multigene family exhibit diverse roles in development, c

134 eplication-dependent histones are encoded by multigene families found in several large clusters in th

135 Our phylogenetic analyses of 11 multigene families from five species belonging to distin

136 pose that similar systematic analyses of all multigene families from human and other mammalian genome

137 e of evolutionary conservation of the Ikaros multigene family from cartilaginous fish through mammals

138 In mammals, small multigene families generate spliceosomal U snRNAs that a

139 ns from Argentina to Mexico showed that this multigene family has expanded significantly during evolu

140 Duplication of genes, giving rise to multigene families, has been a characteristic feature of

141 Two multigene families have been identified that encode prot

142 functions of the individual members of this multigene family have been difficult to ascertain becaus

143 the Rsl genes, like members of certain other multigene families, have diversified in a species-specif

144 opsis thaliana), both enzymes are encoded by multigene families, having distinctive expression patter

145 ants, the CslA genes are members of extended multigene families; however, it is not known whether all

146 es encoding PP2A subunits have expanded into multigene families in both flowering plants and mammals,

147 specific opportunities to target members of multigene families in crops.

148 the analysis of homeodomain repertoires and multigene families in general.

149 ying genetic variation in homologous loci or multigene families in general.

150 ergent tissue specificities and targeting of multigene families in IVs.

151 Although present as multigene families in most species, the functional relev

152 teine protease genes (cbls) constitute large multigene families in parasitic and nonparasitic nematod

153 Primary ion pumps and antiporters exist as multigene families in the Synechocystis sp. PCC 6803 gen

154 unctional characterization of members of the multigene families in this model insect.

155 mb repressive complexes (PRC) are encoded by multigene families in vertebrates.

156 Here we show that E2Fs are a multigene family in Arabidopsis, and report isolation of

157 te the contribution of specific members of a multigene family in complex regulatory pathways.

158 developed and applied to the data of the Amy multigene family in Drosophila melanogaster.

159 he involvement of a member of this conserved multigene family in eukaryotic development and viability

160 factory receptor (OR) genes form the largest multigene family in mammalian genomes.

161 ositol monophosphates, is encoded by a small multigene family in many organisms.

162 rsed repeat (pir) genes comprise the largest multigene family in many Plasmodium spp.

163 ent of microtubules, alpha-tubulin is also a multigene family in many species.

164 s related-10 (PR-10) proteins are present as multigene family in most of the higher plants.

165 ar matrix (ECM) component encoded by a large multigene family in multicellular animals.

166 nt a detailed molecular analysis of the PpcK multigene family in nodulated soybeans.

167 g our understanding of the evolution of this multigene family in nonmodel avian groups.

168 GS1 is encoded by a small multigene family in soybean (Glycine max), and cDNA clon

169 y receptor (OR) genes form the largest known multigene family in the human genome.

170 Members of a multigene family in the rodent malaria parasite Plasmodi

171 represent the majority of members of the GST multigene family in these species.

172 mation for understanding the role of the p44 multigene family in transmission of the HGE agent betwee

173 used on the role of [the var genes and other multigene families] in pathogenesis of malaria".

174 he organization of most virulence-associated multigene families, including the hypervariable var gene

175 ng numerous signaling molecules from several multigene families, including Wnts, have been implicated

176 f tetrapods and bony fish and diversified as multigene families independently in the two lineages.

177 nctional dissection of different isoforms of multigene families involved in beta-oxidation.

178 remarkable Laverania-specific expansion of a multigene family involved in erythrocyte remodelling, an

179 bility of statistical tests of neutrality to multigene families is considered.

180 mulating patterns of polymorphism in a small multigene family is developed.

181 The MASP multigene family is specific to T. cruzi, accounting for

182 IV, a secreted protein and member of the Reg multigene family, is up-regulated in malignancies of the

183 known as PfEMP1 and encoded by the multicopy multigene family known as the var genes.

184 bers of cellular homologues together with 10 multigene families largely account for the marked size d

185 There were 21 members of the p28 multigene family located in a 23kb DNA fragment in the g

186 nome, we determined that CLM-1 was part of a multigene family located on a small segment of mouse chr

187 est that representatives of the FcR and FCRL multigene families may have independently evolved to eng

188 Some members of this multigene family may function in cell signaling and/or c

189 oducts suggest that the members of this FcRH multigene family may serve important regulatory roles in

190 er protection in a mouse model and to be the multigene family member primarily expressed in mammalian

191 Rhodococcus sp. NS1 and harbors six new vap multigene family members (vapN to vapS) in a vap pathoge

192 egions of shared sequence identity in Ikaros multigene family members found in mammals and several ot

193 tified a 20-kb fragment, encoding members of multigene families (MGF) 360 and 530, as being capable o

194 ported that African swine fever virus (ASFV) multigene family (MGF) 360 and 530 genes are significant

195 To date, certain members of this multigene family occur only in mycobacteria that cause d

196 Flowering plants have evolved multigene families of the class XI myosin motors, the fu

197 Reiterative database searches revealed a multigene family of 48 members that includes eight proba

198 dorant-binding proteins (OBPs), encoded by a multigene family of 51 genes.

199 ences patterned after conserved regions in a multigene family of 56 subtilisin-related proteolytic en

200 APOBEC3 proteins comprise a multigene family of antiviral cytidine deaminases that a

201 hat black cherry PH is encoded by a putative multigene family of at least five members.

202 Protein kinase C (PKC) is a multigene family of at least ten isoforms, nine of which

203 Annexins comprise a multigene family of Ca2+ and phospholipid- binding prote

204 The human kallikreins are a large multigene family of closely related serine-type protease

205 in vivo expression of the members of the p28 multigene family of E. chaffeensis, sera from two beagle

206 Proteins expressed from the map1 multigene family of Ehrlichia ruminantium are strongly r

207 proteins in plants and each is encoded by a multigene family of five members in Arabidopsis thaliana

208 rabidopsis thaliana) aldehyde oxidases are a multigene family of four oxidases (AAO1-AAO4) that oxidi

209 In plants, a large multigene family of glycosyltransferases is involved in

210 An analysis of the multigene family of Group 1 glucosyltransferases (UGTs)

211 the context of functional redundancy of the multigene family of GTs in Arabidopsis.

212 Here we report that a multigene family of KCNQ-like channels is present in the

213 e-type receptor (NITR) genes encode a unique multigene family of leukocyte regulatory receptors, whic

214 E. chaffeensis has a multigene family of major outer membrane proteins with p

215 The PE multigene family of Mycobacterium tuberculosis is remark

216 An extensive, highly diversified multigene family of novel immune-type receptor (nitr) ge

217 urvival of mammals, is controlled by a large multigene family of olfactory receptor (OR) genes.

218 Expansins comprise a multigene family of proteins in maize (Zea mays).

219 different protein cargoes including the MASP multigene family of proteins MASPs are specific to this

220 e growth factor binding proteins (IGFBPs), a multigene family of proteins that are thought to mediate

221 Glutathione transferases are a multigene family of proteins that catalyze the conjugati

222 cid sequence similar to those of the claudin multigene family of proteins that constitute tight junct

223 rgonaute (AGO) proteins are a well-conserved multigene family of regulators mediating gene silencing

224 A novel multigene family of such K+ channels has recently been i

225 The isolation and characterization of a multigene family of the first class of dirigent proteins

226 Connexins comprise a multigene family of transmembrane proteins that form gap

227 nition may be mediated by a complex germline multigene family of V structures resembling those that a

228 Members of the Ikaros multigene family of zinc finger proteins are expressed i

229 Killer Ig-like receptor (KIR) genes are a multigene family on human chromosome 19.

230 Although alpha-zeins are encoded by large multigene families, only a few of these genes are transc

231 sis of homologous gene sequences either from multigene families or from different species with a spec

232 birth-and-death evolution within a bacterial multigene family, our results indicate that the extent o

233 A polymorphic multigene family (p44) of Anaplasma phagocytophilum enco

234 rs performed the best at aligning genes from multigene families-perhaps the most challenging test for

235 Plasmodium multigene families play a central role in the pathogenes

236 A multigene family produces tubulin isotypes that are expr

237 Our work suggests that the wtf multigene family proliferated due to meiotic drive and h

238 Claudin-8 (CLDN8), a multigene family protein that constitutes the backbone o

239 of these chromosomally proximal members of a multigene family provides a mechanism for both immune ev

240 However, Naip5 is a member of a small multigene family, raising the possibility of redundancy

241 squito D7 salivary proteins are encoded by a multigene family related to the arthropod odorant-bindin

242 t species, the functional relevance of these multigene families remains largely undefined.

243 p, a member of the Arabidopsis thaliana PABP multigene family, rescues the lethal phenotype associate

244 We deleted all the members of this multigene family resident on the X chromosome of D. mela

245 MSP2 is encoded by a multigene family, resulting in the expression of variant

246 Ets1 is a member of a multigene family, several members of which are expressed

247 The majority of the 10 largest conserved multigene families share similar copy numbers in tomato

248 the extent of lateral transfer in bacterial multigene families should be re-examined in the light of

249 These studies show that multigene family-specific antibodies can be applied to t

250 e vast majority (>95%) of DPs in these large multigene families still await discovery of their bioche

251 anisms that cause the concerted evolution of multigene families such as rDNA.

252 s linked to the variant expression of clonal multigene families such as the var genes.

253 sed in a given culture condition in expanded multigene families, suggesting that family expansi on co

254 t neurons of the basal layer express another multigene family, termed H2-Mv, representing nonclassica

255 t of mammalian T and B lymphocytes belong to multigene families that are represented by members in th

256 s in TUBA1A and TUBB2B, each a member of the multigene families that encode alpha- and beta-tubulins,

257 However, many plant genes are organised in multigene families that exhibit variation in expression

258 Intriguingly, actinoporins appear as multigene families that give rise to many protein isofor

259 These receptors are encoded by a multigene family that can be divided into subfamilies 1

260 te immune type receptors (LITRs) represent a multigene family that encodes Ig superfamily proteins th

261 Pax5 is a member of the multigene family that encodes the paired box transcripti

262 One multigene family that has served as a paradigm for the s

263 pressed in skeletal muscles are encoded by a multigene family that is clustered on syntenic regions o

264 ells, and that UNC-93 is a member of a novel multigene family that is conserved among C. elegans, Dro

265 erged in primitive land plants and founded a multigene family that is conserved in all flowering plan

266 so called psoriasin, is a member of the S100 multigene family that is encoded in the epidermal differ

267 Vertebrate tubulin is encoded by a multigene family that produces distinct gene products, o

268 RL representatives are members of an ancient multigene family that share a common ancestor with the c

269 er, we report for the first time a bacterial multigene family that undergoes birth-and-death evolutio

270 One such multigene family, the acyl-CoA desaturases, is composed

271 udin and members of a recently characterized multigene family, the claudins.

272 ate that although poplar BSP is encoded by a multigene family, transcriptional activation of bspA per

273 Encoded by a multigene family, ubiquitin is expressed in the form of

274 An alternative approach to characterizing multigene families utilizes the fact that genes within t

275 lasmodium falciparum harbors three extensive multigene families, var, rif, and stevor (for subtelomer

276 This three-exon gene, a member of a multigene family (ves), encodes a polypeptide with no cl

277 ibed, and identify a novel branch of the ves multigene family, ves1beta.

278 oteins, including members of three different multigene families (VIR, Pv-FAM-A, Pv-FAM-D), one membra

279 Patterns of network connection of members of multigene families were examined for two biological netw

280 A total of 10 putative multigene families were found.

281 Until around 1990, most multigene families were thought to be subject to concert

282 iant proteins pertaining to VIR and Pv-FAM-D multigene families were used.

283 es provided evidence that all members of the multigene family were co-ordinately expressed and placed

284 he FKBP65 gene and other members of the FKBP multigene family were therefore investigated from a taxo

285 dicated that 16 of the 22 members of the p28 multigene family were transcribed.

286 Homology extends to multigene families, where the distinction between orthol

287 The Sperm dynein intermediate chain multigene family, which encodes a Sperm dynein intermedi

288 usly, we identified the conserved obstructor multigene-family, which encodes chitin-binding proteins.

289 t plant membrane transporters are encoded by multigene families whose members often exhibit overlappi

290 er Ig-like receptor (KIR) genes constitute a multigene family whose genomic diversity is achieved thr

291 species suggests divergent evolution of this multigene family with a birth-and-death process of membe

292 lase2 and that these genes belong to a novel multigene family with members in animals, plants, fungi,

293 InlF, a member of the internalin multigene family with no known function, was identified

294 The protein tyrosine kinases are a large multigene family with particular relevance to many human

295 The infinite-site model of a small multigene family with two duplicated genes is studied.

296 ch, are part of one of the largest mammalian multigene families, with an estimated copy number of up

297 any metazoan splicing factors are members of multigene families, with each member having different fu

298 SSX is a multigene family, with 9 complete genes on chromosome Xp

299 5S rRNA genes exist as a large and dispersed multigene family, with between 50 and 100 copies per gen

300 inding 14-3-3 proteins are the products of a multigene family, with many organisms having 10 or more