ライフサイエンスコーパス: rename

1 ubstantia nigra pars reticulata and was also renamed accordingly.

2 alian substantia nigra pars compacta and was renamed accordingly; a group of gamma-aminobutyric acid

3 of previously unknown function that we have renamed acpH.

4 Acute renal failure (ARF), recently renamed acute kidney injury (AKI), is a relatively frequ

5 Therefore, elk4 was renamed agb1.

6 findings indicated an association of BHA128, renamed Alp, with the tick environment: (i) Alp was prod

7 homology with AmpD, we recognized YbjR, now renamed AmiD, as a possible second 1,6-anhydro-N-acetylm

8 this unique substrate profile, the enzyme is renamed aminoglycoside 2''-phosphotransferase type IIIa.

9 ivator of the ant genes and was subsequently renamed antR.

10 to L-arabinose metabolism, and this gene was renamed araD1.

11 into 10m and 10r, and area 10o (orbital) was renamed area 10p (polar).

12 PmrI (renamed ArnA) was overexpressed using a T7 construct, an

13 PmrM and PmrL, now renamed ArnE and ArnF because of their involvement in L-

14 The enzyme, renamed ArnT, consists of 548 amino acid residues in S.

15 BPH was mapped by Jirapong Jairin et al. and renamed as "Bph32".

16 reported the NMR structures of Ac-18A-NH(2) (renamed as 2F because of two phenylalanines), the base-l

17 role in acid-resistance in E. coli, has been renamed as AriR for regulator of acid resistance influen

18 We propose that GPR2 be renamed as CCR10.

19 ne losses, zebrafish retained six cry genes, renamed as cry1aa (zcry1a in the old nomenclature), cry1

20 riatal parts of mammalian basal ganglia were renamed as part of the pallium, using prefixes that reta

21 ide homologue of PGC-1, PGC-1beta (PGC-1 was renamed as PGC-1alpha), first identified through searche

22 n splicing regulation; consequently, N13 was renamed as PN_LNC_N13.

23 this toxin of previously unknown function be renamed as RatA (Ribosome association toxin A).

24 Finally 13d, renamed as SAR197, was characterized in vitro and by in

25 ologous to the mammalian globus pallidus and renamed as such.

26 Hence, yjhX is renamed as the gene for the TopA inhibitor (the topAI ge

27 striatal part of the basal ganglia and were renamed as the medial and lateral striatum.

28 e, we report that in Escherichia coli, yaeB (renamed as trmO) encodes a tRNA methyltransferase respon

29 accessory secretion system, these genes were renamed asp1-3 (for accessory secretory protein).

30 AtcpFHy1 was renamed AtcpFHy/PyrP1, At4g11570 and At4g25840 were name

31 h high similarity to katanin (hence FRA2 was renamed AtKTN1), a protein shown to be involved in regul

32 ed NK cells expressing B220, which were thus renamed B220+ NK cells.

33 this study, 36 TCP genes were identified and renamed based on cassava whole-genome sequence and their

34 As such, we have renamed bbe16 a gene encoding borrelial persistence in t

35 These data demonstrate that CT1063, renamed bciA, encodes a C-8 divinyl reductase in C. tepi

36 d a gene, originally annotated as "fruA" and renamed "bepA," putatively encoding a carbohydrate phosp

37 We show that this technique, which we rename betalue-betalau technique, can be used to detect

38 elated transcription factor Bhlhb5 (recently renamed Bhlhe22) plays two central roles in this process

39 fine mutations in a single gene that we have renamed BIG.

40 ects, and DNA sequence alterations of sepI1 (renamed bimA10) and two other ts lethal bimA(APC3) allel

41 uence of the null mutant phenotype, whiK was renamed bldM.

42 " phenotype) and, as a consequence, whiN was renamed bldN.

43 division superfamily (vexB and vexD [herein renamed breB]) that were induced in response to bile.

44 al serotype (Bt1) or newly emerged Vsp (n=1, renamed Bt3) or Vlp serotypes.

45 ake in SALMONELLA: The E. coli yadT product, renamed BtuF, is shown here to participate in CN-Cbl upt

46 phage inflammatory protein-3 alpha, recently renamed CCL20, and its receptor CCR6 are markedly up-reg

47 ation of a chemokine (CTACK), which has been renamed CCL27 according to a new systematic chemokine no

48 aciens, originally designated Urr14 and here renamed CCMB1, was found to grow at wild-type rates on e

49 We therefore suggest that ndhR be renamed ccmR to better represent its broader regulatory

50 hey support the emerging role of C1qRp (here renamed CD93) in functions relevant to intercellular adh

51 t the plasma membrane-localized transporter (renamed CDR6/ROA1 for consistency with C. albicans nomen

52 Rv2393 (renamed che1) resides in the sulfur reduction operon and

53 ogous expression of the psbA4 gene, which we rename chlF, enables Chl f biosynthesis in Synechococcus

54 all peptide encoded within the ciaRH operon (renamed ciaX) mediates this regulation.

55 e mutant, we propose that C. jejuni CydAB be renamed CioAB (cyanide-insensitive oxidase), as in Pseud

56 In E. coli, the cls and ybhO genes (renamed clsA and clsB, respectively) each encode a CL sy

57 We identified a third Cls encoded by ymdC (renamed clsC).

58 at the protein encoded by the dfp gene, here renamed coaBC, also has phosphopantothenoylcysteine synt

59 cally and functionally coordinated via YbgF, renamed CpoB (Coordinator of PG synthesis and OM constri

60 ed that open reading frame SynPCC7002_A2032, renamed cruF, encodes a 1',2'-hydroxylase [corrected] an

61 nd that open reading frame SynPCC7002_A2031, renamed cruG, encodes a 2'-O-glycosyltransferase.

62 similar enzymes, we suggest that METTL12 be renamed CS-KMT (gene name CSKMT).

63 We propose that, together, CrgA and Rv0008c, renamed CwsA for cell wall synthesis and cell shape prot

64 zation of a null mutant of CG14939, which we rename Cyclin Y (CycY).

65 ic Pol of low-GC gram-positive organisms, be renamed DNA polymerase III C (Pol III C) to denote its o

66 primary structure, it is proposed that it be renamed DNA polymerase III E (Pol III E) to accurately r

67 ide-bond A oxidoreductase (DsbA) and is thus renamed DsbA-like protein (DsbA-L).

68 hat HMW-DSP is the proteoglycan form of DSP (renamed "DSP-PG").

69 We identify ef1090 (renamed ebpR) and show its importance for the transcript

70 sing c-di-GMP phosphodiesterase Ec Dos (here renamed Ec DosP) follows and is translationally coupled

71 ence corresponds to the product of the yagZ (renamed ecpA) gene present in all E. coli genomes sequen

72 2P]lipid A as the acceptor showed that YhjW (renamed EptB) utilizes phosphatidylethanolamine in the p

73 osphoethanolamine (pEtN) transferase Cj0256, renamed EptC, that serves a dual role in modifying the f

74 we localized it to the ER, we propose it be renamed ER-aminopeptidase 1 (ERAP1).

75 TpiA2 (D-3-tetrulose-4-phosphate isomerase; renamed EryH), and RpiB (D-erythrose-4-phosphate isomera

76 and RpiB (D-erythrose-4-phosphate isomerase; renamed EryI), a pathway fully consistent with the isoto

77 h Orf29/30 of E. tarda strain EIB202, and is renamed EseJ.

78 e secretion system 2 (ETT2) locus and herein renamed EtrB, plays an important role in EHEC pathogenes

79 V) confirming thatEu3 encodes UreG, which is renamed Eu3.

80 YBR163w (DEM1) gene, and this gene has been renamed EXO5.

81 YgaA was renamed FabL to denote the discovery of a new family of

82 The yfcYX operon (renamed fadIJ) encodes enzymes required for hydration, o

83 ncodes a putative acyl-CoA synthetase, ydiD (renamed fadK), as well as putative electron transport ch

84 ferric citrate and that a protein, BC_3466 [renamed FctC (ferric citrate-binding protein C)], binds

85 ere we demonstrate that eukaryotic homologs [renamed FEX (fluoride exporter)] function in fluoride ex

86 fhy1 and pat3 (renamed fhy1-3) are independently isolated alleles of a

87 s observed upon disruption of just T14G12.4 (renamed fkh-2) gene function, simultaneous disruption of

88 ced by formaldehyde, and the genes have been renamed frmR, frmA, and frmB, respectively.

89 us Fusarium solani f. sp. glycines, recently renamed Fusarium virguliforme (Fv).

90 rain ATCC 25586, gene FN1704) that we hereby rename Fusobacterium phospholipase autotransporter (FplA

91 Because G6Pase (renamed G6Pase-alpha) is primarily expressed only in the

92 the only RmlD homologue from GAS, previously renamed GacA, functions in a novel monomeric manner.

93 Therefore, yhiX was renamed gadX.

94 ponse genes reported here, this RNA has been renamed GadY.

95 majority of which lack the canonical GCYH-I (renamed GCYH-IA).

96 Expression of wild-type MIR16 (renamed GDE1), but not two catalytic domain mutants (E97

97 A chromosome-located locus (BMQ_1820, renamed gerWB) is shown to encode a receptor B-protein s

98 We therefore propose renaming gguAB as mmsAB, for multiple monosaccharide tra

99 (bHLH) DNA-binding transcription factor now renamed Glycine max bHLH membrane 1 (GmbHLHm1).

100 etion, the glycosylated form of AcaC, hereby renamed GspA, was accumulated in the membrane.

101 cation as Helitron-like transposons and were renamed Helitron1_BM.

102 Escherichia coli, leading to the gene being renamed hemQ.

103 ntified the hypothetical lipoprotein HD0192, renamed here "fibrinogen binder A" (FgbA), as being pref

104 locus genes eipB, eipC, eipD, eicA and eaeX (renamed here air), as well as glyU ETT2 genes eivF and e

105 nclude that this conserved PCD-like protein, renamed here alpha-carboxysome RuBisCO assembly factor (

106 ype HEAT domains, previously termed BZW2 and renamed here as eIF5-mimic protein 1 (5MP1).

107 onstrating that biallelic mutations in SLX4 (renamed here as FANCP) cause a new subtype of Fanconi an

108 TMEM149 (renamed here as IGFLR1) is an uncharacterized gene with

109 stin/human guanylate-binding protein-3 gene (renamed here atlastin-1), which codes for a 64-kDa membe

110 srtC (renamed here bps for biofilm and pilus-associated sortas

111 pressed G6Pase-related protein, PAP2.8/UGRP, renamed here G6Pase-beta, is an acid-labile, vanadate-se

112 previously uncharacterized gene, SCE59.12c, renamed here rsuA.

113 located immediately downstream of SCE59.13c, renamed here sigU, whose product is inferred to be a mem

114 Sm-hPAF, or lectinolysin (LLY) as renamed herein, is most closely related to CDCs from Str

115 nicum genome identified two paralogous genes renamed hmuQ (bll7075) and hmuD (bll7423) that encode pr

116 etion mutants of the latter candidate genes, renamed hopX1(Ea) and hopAK1(Ea), respectively, did not

117 On the basis of this phenotype, we renamed HP0289 ImaA for immunomodulatory autotransporter

118 e present evidence that one of them, HP1228 (renamed HpRppH), is an RNA pyrophosphohydrolase that tri

119 rity in sequences, we proposed that hPTTG be renamed hPTTG1 and the new genes be named hPTTG2 and hPT

120 According to its function, YjiE is now renamed HypT (hypochlorite-responsive transcription fact

121 t, we show that human IFIT1 and mouse IFIT1 (renamed IFIT1B) are not orthologs, but are paralogs that

122 rectional traffic of IFT particles (recently renamed IFT trains) within the flagellum.

123 onal role of IL-1 family member 10, recently renamed IL-38, remains unknown.

124 r activity of human IL-1 homologue 4(IL-1H4; renamed IL-F7) by adenovirus-mediated gene transfer (AdI

125 ly designated CDC coryneform group 1 and was renamed in 1994.

126 ially to RNA/DNA hybrids by over 25-fold and rename it as hybrid binding domain (HBD).

127 for Izumo1 on the mouse egg, and propose to rename it Juno.

128 e containing the cld mutation as Tmem112 and rename it Lmf1 (Lipase maturation factor 1).

129 molecular weight of atToc75-V is 80 kDa and renamed it (AtOEP80) Arabidopsis thalianaouter envelope

130 C4.1 as a C. elegans CS-sulfotransferase and renamed it chst-1 (CarboHydrate SulfoTransferase) based

131 iosynthesis in Escherichia coli, and we have renamed it ubiI.

132 We have, therefore, renamed it XXYLT1 (xyloside xylosyltransferase 1).

133 olving the long-standing naming conundrum by renaming it Peptoclostridium difficile.

134 Here we show that JMJD5 (now renamed KDM8), a JmjC family member, demethylates H3K36m

135 ations were identified in the FLJ20116 gene (renamed "KIND1" [encoding kindlin-1]).

136 cific for insertion sites and is accordingly renamed KREN2 (kinetoplastid RNA editing endonuclease 2)

137 ified function, we propose that this gene be renamed lhgO.

138 atabase searching revealed a candidate gene (renamed lmtA) in L. interrogans showing distant homology

139 opose that these two proteins, which we have renamed LptF and LptG, respectively, are the missing tra

140 genetic analyses are consistent with lmo0422-renamed lstR (for lineage-specific thermal regulator)-an

141 ously uncharacterized yvfV-yvfW-yvbY (herein renamed lutABC) operon, which is inferred to encode thre

142 AOF1, now renamed lysine demethylase 1B (KDM1B) following a new no

143 ins [AIP-1 (atrophin interacting protein 1), renamed MAGI-2 (membrane associated guanylate kinase inv

144 coli, the gene for the sRNA IS061/IsrA, here renamed McaS, was predicted to reside in an intergenic r

145 the misnamed genes cysK(Hp) and metB(Hp) be renamed mccA (methionine-to-cysteine-conversion gene A)

146 The rgl genes were renamed mcrA and mcrBC (modified cytosine restriction).

147 We propose that MA3736 be renamed mdrA (methanosarcina disulfide reductase).

148 ne (previously called Mgat3(neo), but herein renamed Mgat3(T37) because the allele generates inactive

149 mpC expression; thus, the small RNA has been renamed MicC.

150 i strain 297, designated 2.9 LP and recently renamed mlp, was found on circular and linear plasmids i

151 pneumococcal YceG-domain protein, Spd_1346 (renamed MltG), remove the requirement for PBP2b.

152 ron uptake, we demonstrate that yqhN (herein renamed mntR) encodes a manganese modulated regulator of

153 the E. coli mntH promoter and hence has been renamed MntR.

154 t transcriptional repressor and is therefore renamed MntR.

155 ng hypoxia; hence, we propose that Rv0348 be renamed mosR for regulator of mycobacterial operons of s

156 lyze the function of this protein, which was renamed MTase1, it was overexpressed in Escherichia coli

157 d the essential inner-membrane protein MviN (renamed MurJ) as a likely candidate for the peptidoglyca

158 lticopper oxidase of M. tuberculosis and was renamed mycobacterial multicopper oxidase (MmcO).

159 logues of MGA0674, the gene product has been renamed "Mycoplasma-specific lipoprotein A" (MslA).

160 ed into four transcripts, and the genes were renamed nanE, nanR, nanK, nanA, and nanT.

161 abeled Abeta tracer, (18)F-AZD4694 (recently renamed NAV4694), with (11)C-PiB in the same subjects.

162 We propose to rename NCBE as the second electroneutral Na/HCO(3) cotra

163 econd protein, originally named NEH2 and now renamed NEIL2 (Nei-like).

164 cently, a previously named Nek8 sequence was renamed Nek9/Nercc1 in Genbank due to its lack of homolo

165 Two nuclear loci, A and B (renamed NIC1 and NIC2) have been identified that mediate

166 We also show that the renamed NO-associated protein 1 (AtNOA1) is a member of

167 inactive at the cloned NPR-1, we propose to rename NPR-1 and refer to it as an AF9 receptor, AF9-R1.

168 we propose that the yjeB gene of E. coli be renamed nsrR.

169 Thus we renamed Nss as glucosyltransferase 3 (Gtf3).

170 ify the metazoan ortholog of Spo7p, TMEM188, renamed nuclear envelope phosphatase 1-regulatory subuni

171 us naming of similar enzymes, we suggest the renaming of human METTL20 to ETFbeta-KMT.

172 but our characterization of TP0796 prompts a renaming of this superfamily as a periplasmic flavin-tra

173 Therefore, RygA and RygB were renamed OmrA and OmrB respectively (for OmpR-regulated s

174 functions as the CTXphi pIII, we propose to rename OrfU as pIII(CTX).

175 a repressor of cif gene expression, we have renamed PA2931 as CifR.

176 Thus, we have renamed PA2983 and PA2982, pocA and pocB, respectively,

177 allervorden-Spatz syndrome, the disorder was renamed pantothenate kinase-associated neurodegeneration

178 enicillin, so the gene and gene product were renamed pbpG and PBP2d, respectively.

179 C19orf79 was recently renamed PET100 and predicted to encode a complex IV biog

180 Ypl112p, renamed Pex25p, is a novel peroxin required for the regu

181 we show that the protein encoded by YCL056c, renamed Pex34p, is a peroxisomal integral membrane prote

182 Deletion of cjj81176_0915 (renamed pgp2) resulted in straight morphology, represent

183 atase gene (previously annotated as yfhB but renamed pgpC) using an expression cloning strategy.

184 fate monoester 1 and then the reassigned and renamed phosphate monoester 2, relied on diagnostic (1)H

185 xygenase or the chloroplastic lipocalin, now renamed plastid lipocalin (LCNP).

186 ith its M. pneumoniae counterpart, MGA_1199 (renamed PlpA) was demonstrated to be surface exposed, de

187 CG12108 has been appropriately renamed Ppt1.

188 ation scheme is arbitrary and we have simply renamed previously identified interneuron types.

189 s specifying homologs of a fungal lactamase (renamed prokaryotic 5-oxoprolinase A, pxpA) and homologs

190 d the functionally unassigned paralog DIOX2, renamed protopine O-dealkylase, showed novel and efficie

191 in rank order they are as follows: YKL116c (renamed PRR1) = YDL214c (renamed PRR2) > YJL141c (YAK1,

192 s follows: YKL116c (renamed PRR1) = YDL214c (renamed PRR2) > YJL141c (YAK1, SRA1) > YNR047w = YCR091w

193 that PsChR1 is an anion conducting ChR, now renamed PsACR1, with a red-shifted absorption suited for

194 I-like signal transduction protein, which we renamed PstA, as c-di-AMP binding proteins.

195 This protein set includes Ylr414cp, herein renamed Pun1p, a previously uncharacterized protein loca

196 he GLOB blood group system (ISBT 028) and is renamed PX2 (GLOB2).

197 homologs of allophanate hydrolase subunits (renamed pxpB and pxpC).

198 f this signaling cascade, an LTTR heretofore renamed QseD (quorum-sensing E. coli regulator D).

199 This gene was renamed qseG, and it was shown to encode an outer membra

200 r queuosine biosynthesis, and the genes were renamed queCDEF.

201 TBC1D15 was thus renamed Rab7-GAP.

202 We propose that yejH be renamed radD, reflecting its role in the DNA repair of r

203 The original rag allele found in W50 was renamed rag-1, while three novel alleles, rag-2 to rag-4

204 Keoxifene was renamed raloxifene and became the first SERM for the tre

205 identified, we propose that the elaC gene be renamed rbn.

206 RcsD, the product of the yojN gene, now renamed rcsD, acts as a phosphorelay between RcsC and Rc

207 observe immediately that suppressor T cells, renamed 'regulatory T cells' (Tregs) have become a centr

208 ere we report that down-regulation of Hel61 [renamed REH1 (RNA editing helicase 1)] expression in Try

209 neostriatum, and the archistriatum have been renamed (respectively) the hyperpallium (hypertrophied p

210 tumour viruses in which it was detected were renamed retroviruses.

211 YjgF is renamed RidA (reactive intermediate/imine deaminase A) t

212 The Mcap0476 methyltransferase (renamed RlmFO) represents the first folate-dependent fla

213 ' exoribonuclease activity and was therefore renamed RNA editing exonuclease 1 (REX1).

214 Here, this gene (renamed ropA1) is shown to be required for infection by

215 gC and lrhA or within dam, setB and STM4463 (renamed rosE) resulted in expression of StdA and its ass

216 family of four co-antagonist proteins, here renamed RsbRA, RsbRB, RsbRC, and RsbRD, each with a carb

217 these data, we propose that the yhiQ gene be renamed rsmJ.

218 mutation greatly diminished AML-1 (recently renamed RUNX1) binding in gel shift assays with a mutant

219 The AML1 gene (recently renamed Runx1), which encodes the DNA-binding subunit of

220 Hence, we renamed rv0990c heat shock protein 22.5 (hsp22.5), refle

221 stone methyltransferase SDG8 in this mutant (renamed sdg8-5), which provides a unique opportunity to

222 racterized proteins, YgfY (a DUF339 protein, renamed SdhE; succinate dehydrogenase protein E) and Ygf

223 translocated effector protein, we propose to rename SepZ as EspZ.

224 The open reading frame YOR165W (renamed SEY1 for synthetic enhancement of YOP1) was iden

225 The ryaA gene was renamed sgrS, for sugar transport-related sRNA.

226 These repeats, herein renamed SIB, are conserved in closely related bacteria,

227 persicum linalool synthase (SlMTS1, recently renamed SlTPS5) gene in glandular trichomes, we function

228 allele encoding the Smc6 subunit, rad18-74 (renamed smc6-74), is suppressed by mild overexpression o

229 utation proved to be an epigenetic mutation (renamed smp(epi)) that defined a single locus, SMP1, but

230 uncharacterized protein (C11orf84), which we renamed SPIN1 docking protein (SPIN.DOC), that directly

231 lung, and nasal epithelium clone (Plunc, now renamed Splunc1) is a small secreted protein expressed i

232 he early 1900s to dark glasses, subsequently renamed sunglasses.

233 e third would refer to SPC earlier if it was renamed supportive care.

234 expression of the TFIID subunit TAF(II)105 (renamed TAF4b) in the ovary is essential for proper foll

235 The gene has recently been renamed TDP2 because it plays a critical role for the re

236 This led us to rename the genes of the S.

237 volvement in homogentisic acid transport, we rename the genes of this operon hatABCDE.

238 Based on our results, we propose to rename the two major eukaryotic groups Unikonta and Biko

239 Based on these results we propose to rename the ylqF gene rbgA (ribosome biogenesis GTPase A)

240 reviously uncharacterized orphan riboswitch, renamed the "M-box," is a divalent metal-sensing RNA inv

241 tal sulcus (previously known as "TOS"), here renamed the "occipital place area" (OPA).

242 n accordance with GPCR nomenclature, we have renamed the cDNA clone, KIAA0001, and its orthologs GPR1

243 l and pseudopneumococcal pherotypes, we have renamed the competence pherotype CSP6.1, formerly report

244 fined crystal structure of M. hyorhinis p37, renamed the extracytoplasmic thiamine-binding lipoprotei

245 ficient transport, and based on this we have renamed the family Occ, for outer membrane carboxylate c

246 Given these results, we have renamed the gene CHRONO (computationally highlighted rep

247 s a repressor of oxyS, and therefore we have renamed the gene roxY.

248 We have renamed the genes kdhA for keto-deoxyoctulosonate hydrol

249 In 2005, the center housing this work was renamed the George W.

250 metal-binding residues, this family has been renamed the IZH gene family (Implicated in Zinc Homeosta

251 ion on the Accreditation of Hospitals (later renamed the Joint Commission on Accreditation of Healthc

252 products encoded by the mnh operon, we have renamed the locus sno (S. aureus nuo orthologue).

253 es QseBC and motility; hence, b3022 has been renamed the motility quorum-sensing regulator gene (the

254 ably, the lamina medularis dorsalis has been renamed the pallial-subpallial lamina.

255 Based on this we have renamed the Pfam families representing the two domains f

256 posterior part of the archistriatum has been renamed the posterior pallial amygdala, the nucleus taen

257 in V. cholerae, which we named OxyR2, and we renamed the previous OxyR OxyR1.

258 wship for radiology attending physicians was renamed the RSNA William R.

259 a lenticularis in the avian diencephalon was renamed the subthalamic nucleus, both for their evident

260 We therefore renamed the sucB product dihydrolipoamide acyltransferas

261 Thus, we have renamed the two genes snm9 and snm10 respectively.

262 We propose renaming the three genes chbA, chbB, and chbC, since the

263 that these three complexes are identical and rename them the conserved oligomeric Golgi (COG) complex

264 nzH are bona fide coat proteins, and we have renamed them CotI, CotQ, and CotU, respectively.

265 bed murine decoy receptors for TRAIL, and we renamed them mDcTrailr1 and -r2, respectively.

266 sis and attachment of L-Ara4N to lipid A and renamed these genes arn-BCADT, respectively.

267 We now rename this cellular protein as Vpr-binding protein, or

268 rgument is presented that it is necessary to rename this parasite, and that H. bakeri is the correct

269 ype III secretion chaperone for EspF, and we rename this protein CesF, the chaperone for EPEC secrete

270 ause of this embryological activity, we have renamed this clone Coco, after the Spanish word meaning

271 Therefore, we renamed this gene as hypoxia-induced mitogenic factor (H

272 8543 is the haplo-insufficient gene and have renamed this gene matrimony (mtrm).

273 ts effect on olfactory neurogenesis, we have renamed this gene Rossy, in homage to the Spanish actres

274 Based on these phenotypes, we have renamed this locus rstA, for regulator of sporulation an

275 We renamed this ORF YNO1 (yeast NADPH oxidase 1).

276 alyzing the degradation of heme, and we have renamed this protein IruO.

277 212 was secreted by the S. flexneri T3SS and renamed this protein OspZ.

278 We renamed this receptor CCR10.

279 sensing by using transcriptional fusions and renamed this regulator quorum-sensing E. coli regulator

280 We have renamed this sRNA MicX as, like the Escherichia coli sRN

281 AGPAT6 is a microsomal GPAT, and we propose renaming this enzyme GPAT4.

282 We propose to rename Tlp11 as CcrG, Campylobacter ChemoReceptor for Ga

283 DTA1 corresponds to AtGA2ox6 and was renamed to indicate this identity.

284 , the NCK-interacting kinase (NIK) (recently renamed to mitogen-activated protein kinase kinase kinas

285 We thus rename Tp0655 as TpPotD.

286 sense mutation in a predicted gene, C9orf75, renamed TPRN.

287 ics, and divalent cations, and was therefore renamed TriABC.

288 PA2374 (which we have renamed TseF) appears to be secreted by H3-T6SS and is i

289 efficient UQ biosynthesis, and which we have renamed ubiK Using several methods, we demonstrated that

290 se-polarity channels, which we propose to be renamed "unconventional" mechanically sensitive channels

291 be converted to a Drosophila model simply by renaming variables.

292 We show that Ydr049 (renamed VCP/Cdc48-associated mitochondrial stress-respon

293 n Tcv and the white-eye mutation white, here renamed vermilion(white) (v(w)).

294 , we identified a gene, CXXC5, which we have renamed WID (WT1-induced Inhibitor of Dishevelled), as a

295 Here we propose to rename YeeU as CbeA for cytoskeleton bundling-enhancing

296 We accordingly propose to rename yegMNOB as mdtABCD (mdt for multidrug transporter

297 Therefore we propose to rename YehU/YehT as BtsS/BtsR, after "Brenztraubensaure"

298 Thus, we propose renaming yhcS, yhcR, yhcQ, and yhcP, to reflect their ro

299 ibosome are alleviated by YNL260c, hence, we rename YNL260c as LTO1; required for biogenesis of the l

300 of the spore germination process, we propose renaming ywdL as a spore germination gene, gerQ.