ライフサイエンスコーパス: mammalian homolog

1 e approximately 30% larger than those of the mammalian homolog.

2 on, and that sd activity is conserved in its mammalian homolog.

3 ganogenesis, similar to the functions of its mammalian homologs.

4 control genes identified in C. elegans have mammalian homologs.

5 h amino acid identity and structure with the mammalian homologs.

6 e of SNARE interaction within both yeast and mammalian homologs.

7 ly 140-fold), as well as in combination with mammalian homologs.

8 may act less specifically than their fly and mammalian homologs.

9 re conserved, particularly between yeast and mammalian homologs.

10 shown to be highly conserved with chick and mammalian homologs.

11 ficient frameshifting are identical to their mammalian homologs.

12 ntical, respectively, to their corresponding mammalian homologs.

13 l regulation comes from studies of yeast and mammalian homologs.

14 Its mammalian homolog Acinus has been implicated in RNA proc

15 This activity is conserved in mammalian homologs; additionally, mtClpX depletion impai

16 which activate the yeast kinase SNF1 and its mammalian homolog AMPK, respectively.

17 he Manduca genes are highly similar to their mammalian homologs and show similar biochemical properti

18 Because this transporter and its mammalian homologs are functionally similar, we suggest

19 Because some mammalian homologs are strongly induced by glucocorticoi

20 yeast SWI/SNF complex and its Drosophila and mammalian homologs are thought to control gene expressio

21 Drosophila Sema-5c and the mammalian homologs are transmembrane proteins with extra

22 ring Drosophila development, and some of its mammalian homologs are tumor suppressors, highlighting i

23 parisons of arginine vasotocin (AVT) and its mammalian homolog arginine vasopressin (AVP) demonstrate

24 The mammalian homolog B1 of Unc-93 Caenorhabditis elegans kn

25 Here CED-9 and its mammalian homolog Bcl-xL (a member of the Bcl-2 family o

26 The Sgs1 DNA helicase and its mammalian homolog BLM control crossover formation in mit

27 Like its mammalian homolog, budding yeast Polymerase eta itself i

28 ssues, comparable to the expression of other mammalian homologs, but less restricted than the express

29 posing interactions between their respective mammalian homologs CAAT Displacement Protein (CDP; now C

30 t dELL is a nuclear protein, which, like its mammalian homologs, can increase the catalytic rate of t

31 Mutation of the mammalian homolog causes significant neurological pathol

32 y conserved regions of Hap5p, Php5p, and the mammalian homolog CBF-C revealed two essential domains w

33 Rad9) is required for activation of scRad53 (mammalian homolog Chk2) and transduction of the signal f

34 Analysis of the mammalian homologs CK1delta/epsilon suggests a conserved

35 chicken brain is very similar to that of the mammalian homologs, consistent with the view that the ex

36 ions for understanding how disruption of its mammalian homolog contributes to cancer and metastasis.

37 elial apical membrane protein Crumbs and its mammalian homolog CRB1 in photoreceptor cell morphogenes

38 their molecular functions, including how the mammalian homologs Cripto-1 and Cryptic recognize and re

39 ns genes ced-2, ced-5, and ced-10, and their mammalian homologs crkII, dock180, and rac1, mediate cyt

40 nction reminiscent of the role of one of its mammalian homologs, Crx, in eye development.

41 cal substrates, the Drosophila NinaA and its mammalian homolog, cyclophilin-B, impair opsin biogenesi

42 show that both the yeast PNG1 enzyme and its mammalian homolog display N-glycanase activity towards i

43 Here, we report that their mammalian homolog, Dom3Z (referred to as DXO), possesses

44 approximately 10 years ago that Dot1 and its mammalian homolog, DOT1L (DOT1-Like), possess histone me

45 1 (disruptor of telomeric silencing) and its mammalian homolog, DOT1L.

46 calponin homology domain (CH) protein, whose mammalian homolog Ehbp1 was previously shown to function

47 r of this signaling pathway, ced-12, and its mammalian homologs, elmo1 and elmo2.

48 orced expression of fly eya or of one of its mammalian homologs, Eya2, triggers rapid apoptosis in in

49 We report that the mammalian homologs Ezh1 and Ezh2 form similar PRC2 compl

50 te (Ezh) constituent, of which there are two mammalian homologs: Ezh1 and Ezh2.

51 bution of DAF-16 as previously shown for its mammalian homologs FKHR and FKHRL1.

52 In HepG2 cells, DAF-16 and its mammalian homologs, FKHR, FKHRL1, and AFX, activate tran

53 sms and stability by supplying better stable mammalian homologs for structural biology and other biop

54 inase (DRK) and daughter of sevenless (DOS) (mammalian homologs, Grb2 and Gab2, respectively) and the

55 The bacterial MutT protein and its mammalian homolog have been shown to catalyze in vitro t

56 up genes have been cloned in Drosophila, and mammalian homologs have been identified for most of thes

57 Although mammalian homologs have been identified in mouse and man

58 Since CYCLINL, CDKG, and their mammalian homologs have been previously shown to affect

59 neural, suggesting that the functions of the mammalian homologs have diverged and diversified.

60 We show here that DSP1 as well as its mammalian homolog hHMG2 bind to the mammalian protein SP

61 With its highly conserved mammalian homologs, human p42 and ground squirrel CADp44

62 One of its mammalian homologs, Ikaros, was recently reported to pla

63 ranching, whereas overexpression of Cut or a mammalian homolog in lower-level neurons resulted in tra

64 Conversely, misexpression of Dar1 or its mammalian homolog in unipolar and bipolar neurons causes

65 es underscore the importance of Caf1 and its mammalian homologs in development and disease.

66 In contrast to its mammalian homologs, in situ hybridization detected dFKBP

67 is regulated by a series of genes that have mammalian homologs, including rad1, rad9, hus1, and rad1

68 eported on the recombinase activities of the mammalian homologs, including the human protein, denoted

69 Trithorax-group proteins and their mammalian homologs, including those in BAF (mSWI/SNF) co

70 Chip and its mammalian homologs interact with and promote dimerizatio

71 Northern analysis reveals that the mammalian homolog is highly expressed in several tissues

72 he Caenorhabditis elegans unc-6 locus, whose mammalian homolog is Netrin, is perhaps the best known o

73 Similar to its mammalian homolog, Jhd1-catalyzed histone demethylation

74 MALS-1, -2, and -3 are mammalian homologs LIN-7, a Caenorhabditis elegans prote

75 ctively) and the GEF son of sevenless (SOS) (mammalian homolog, mSOS) are required for efficient acti

76 The Drosophila protein frequenin and its mammalian homolog neuronal Ca2+ sensor-1 (NCS-1) belong

77 e in Drosophila melanogaster that have known mammalian homologs, Numb is the best candidate to have a

78 6 family members, Nup145N, Nup100 and to the mammalian homolog, Nup98.

79 ce that the GMEBs contact Ubc9, which is the mammalian homolog of a yeast E2 ubiquitin-conjugating en

80 brid screen, SCNM1 interacted with LUC7L2, a mammalian homolog of a yeast protein involved in recogni

81 The mammalian homolog of AcbA is processed to diazepam bindi

82 This is the first report of a mammalian homolog of ACE and has implications for our un

83 series for WD40 repeat protein 1 (Wdr1), the mammalian homolog of Aip1, and report that reductions in

84 r adhesion molecule beta-catenin, which is a mammalian homolog of ARMADILLO, a component of the WINGL

85 NaBC1, the mammalian homolog of AtBor1, is a borate transporter.

86 Mice deficient in Pms2, a mammalian homolog of bacterial mutL, develop cancer and

87 Recent work demonstrating a function for the mammalian homolog of BRK1 (HSPC300) in activation of Arp

88 roper subcellular localization of mPar3, the mammalian homolog of C. elegans polarity protein Par3.

89 The function of MEX3C, the mammalian homolog of Caenorhabditis elegans RNA-binding

90 In other cell types, Munc13 (mammalian homolog of Caenorhabditis elegans uncoordinate

91 Cbl-b, a mammalian homolog of Cbl, consists of an N-terminal regi

92 Apaf-1 is a mammalian homolog of CED-4 that regulates cell death by

93 Here we show that a mammalian homolog of CED-4, Apaf-1, can associate with s

94 mutation of the transcription factor Gli2, a mammalian homolog of Ci, results in severe skeletal abno

95 A mammalian homolog of CTR1 was previously reported to be

96 We studied the signaling controlled by the mammalian homolog of DAF-16, FOXO3a, in model systems of

97 (GTP)-binding protein Rho and its effector, mammalian homolog of Diaphanous (mDia), in migrating cel

98 Lastly, mice in which SAP97, the mammalian homolog of DlgS97, was conditionally deleted i

99 A mammalian homolog of dLMO is expressed in the developing

100 nduced stress fiber formation caused by RhoB/mammalian homolog of Drosophila diaphanous-induced actin

101 mmalian sterile 20-like kinase 1 (Mst1) is a mammalian homolog of Drosophila Hippo, the master regula

102 The present study found that CIAP1, a major mammalian homolog of Drosophila IAPs, is irreversibly in

103 Here we have cloned a cDNA encoding a mammalian homolog of Drosophila Nkd, mNkd, and demonstra

104 We have isolated a highly conserved mammalian homolog of Drosophila numb, m-numb.

105 ciation inhibitor (GDI) proteins like LGN, a mammalian homolog of Drosophila Partner of Inscuteable (

106 SCML2 is a mammalian homolog of Drosophila SCM, a Polycomb-group pr

107 oR protein levels are regulated by mSiah2, a mammalian homolog of Drosophila Seven in absentia that t

108 and found to be identical to RBPJkappa, the mammalian homolog of Drosophila Suppressor of Hairless (

109 CBF1/RBP-Jkappa, the mammalian homolog of Drosophila Suppressor of Hairless [

110 trated that one of the CIF components is the mammalian homolog of Drosophila TAF(II)150, which is not

111 Here we show that TRB3, a mammalian homolog of Drosophila tribbles, functions as a

112 Trb3, a mammalian homolog of Drosophila tribbles, was proposed a

113 tes its effects via the pseudokinase TRB3, a mammalian homolog of Drosophila Tribbles.

114 glycogen synthase kinase 3beta (GSK3beta), a mammalian homolog of Drosophila ZESTE WHITE 3.

115 The mammalian homolog of EOL-1, Dom3Z, which regulates quali

116 ter paralog of ESC, ESC-like (ESCL), and the mammalian homolog of ESC, EED, also interact with histon

117 MYH, a mammalian homolog of Escherichia coli MutY, is a DNA gly

118 Furthermore, the localization of MAP1B, the mammalian homolog of Futsch, is altered in ALS spinal co

119 otein of the peroxisomal membrane 22PMP, the mammalian homolog of geranylgeranyl pyrophosphate syntha

120 The mammalian homolog of HIB, SPOP, can functionally substit

121 interaction with proapoptotic kinase MST1, a mammalian homolog of Hippo.

122 nterestingly, reduction of expression of the mammalian homolog of HNT, RREB1, by siRNA inhibited coll

123 kinase 1 and 2 (ERK1/2), as well as p38, the mammalian homolog of HOG1 in yeast which is a major kina

124 Deletion of the mammalian homolog of Indy (mIndy, Slc13a5) encoding for

125 Herein, we characterize a mammalian homolog of l(2)gl, called Mlgl, in the epithel

126 have been identified, including HSPC300, the mammalian homolog of maize BRICK1 (BRK1).

127 DOCK180, the mammalian homolog of Mbc, associates with Rac, but not C

128 In addition, we show that the mammalian homolog of mRNA-cap, RNGTT, can replace mRNA-c

129 A mammalian homolog of Msn, Nck interacting kinase, intera

130 e extended some of these observations to the mammalian homolog of Msn, Nck-interacting kinase (NIK),

131 A mammalian homolog of msn, the NCK-interacting kinase (NI

132 Expression of SIRT1, a mammalian homolog of NAD-dependent protein deacetylase s

133 The mammalian homolog of one Drosophila gene identified in t

134 no role has been established for KIF17, the mammalian homolog of OSM-3.

135 ently it has been shown to interact with the mammalian homolog of PAR-6.

136 ke kinase/IL-1R-associated kinase protein, a mammalian homolog of pelle.

137 The mammalian homolog of PHO36 is a receptor for the hormone

138 We speculate that Naip5 is a functional mammalian homolog of plant "resistance" proteins that mo

139 Mutations in GATA4, the mammalian homolog of pnr, have also been implicated in c

140 In vitro studies of the mammalian homolog of Rbl2p, cofactor A, have suggested t

141 Sirtuin1 (Sirt1; mammalian homolog of Saccharomyces cerevisiae enzyme Sir

142 Here, we identify Syk, the mammalian homolog of Shark, as a signal transducer for b

143 The mammalian homolog of SID-3, activated cdc-42-associated

144 th heart-specific overexpression of Sirt1, a mammalian homolog of Sir2.

145 Intriguingly, lynx1, a mammalian homolog of SSS, can partially restore normal s

146 ave isolated a human cDNA clone encoding the mammalian homolog of stanniocalcin (STC), a calcium- and

147 We conclude that FZA-B is the mammalian homolog of SUG1 (mSug1) and that it is present

148 its ability to activate CBF1/RBP-Jkappa, the mammalian homolog of Suppressor of Hairless, a protein t

149 shown to bind to HSP60, the highly conserved mammalian homolog of the bacterial protein, and it was f

150 The protein kinase Chk2, the mammalian homolog of the budding yeast Rad53 and fission

151 The serine/threonine kinase Mst1, a mammalian homolog of the budding yeast Ste20 kinase, is

152 sphorylation-dependent interaction between a mammalian homolog of the C. elegans polarity protein Par

153 n by differential display PCR of Munc13-3, a mammalian homolog of the Caenorhabditis elegans "uncoord

154 Caspase 3 (CPP32/Yama/apopain), a mammalian homolog of the Caenorhabditis elegans pro-cell

155 taining protein hDlg/SAP97 (DLG), which is a mammalian homolog of the Drosophila discs large tumor su

156 0- and 140-kDa isoforms encoded by Mena, the mammalian homolog of the Drosophila Enabled gene.

157 to 200-amino-acid N-terminal fragment of the mammalian homolog of the Drosophila Enhancer of zeste [E

158 ion factor genes whose archetype is TFCP2, a mammalian homolog of the Drosophila gene grainyhead.

159 We show that Pf1 interacts with a mammalian homolog of the Drosophila Groucho corepressor,

160 these modifications, we examined ASH1L, the mammalian homolog of the Drosophila melanogaster Trithor

161 and characterized the mouse cDNA of a third mammalian homolog of the Drosophila period gene and desi

162 We have characterized a mammalian homolog of the Drosophila period gene and desi

163 n could activate the cation channel TRPC3, a mammalian homolog of the Drosophila phototransduction ch

164 (embryonic ectoderm development) protein, a mammalian homolog of the Drosophila Polycomb group prote

165 We cloned the mouse cDNA of a mammalian homolog of the Drosophila timeless (tim) gene

166 n, Lrp4 (a co-receptor of agrin) or with the mammalian homolog of the Drosophila tumorous imaginal di

167 Here we show that Schnurri-3 (Shn3), a mammalian homolog of the Drosophila zinc finger adapter

168 The mammalian homolog of the Escherichia coli MutY DNA glyco

169 the first evidence for elevation of MYH, the mammalian homolog of the Escherichia coli MutY DNA glyco

170 s type 9 E4-ORF1, evolved to target the Dlg1 mammalian homolog of the membrane-associated Drosophila

171 linker histone H1oo (1) constitutes a novel mammalian homolog of the oocyte-specific linker histone

172 SIRT1 is a mammalian homolog of the Saccharomyces cerevisiae chroma

173 We identified Chk2, the mammalian homolog of the Saccharomyces cerevisiae Rad53

174 P)-target 1 (RAFT1, also known as FRAP) is a mammalian homolog of the Saccharomyces cerevisiae target

175 The mammalian homolog of the Schizosaccharomyces pombe Rad9

176 show that c-Abl binds constitutively to the mammalian homolog of the Schizosaccharomyces pombe Rad9

177 TEP1 is the mammalian homolog of the Tetrahymena p80 telomerase prot

178 with hsp90 and a 50-kDa protein that is the mammalian homolog of the yeast cell cycle control protei

179 ere maintenance component 1, a member of the mammalian homolog of the yeast heterotrimeric CST telome

180 Here we report that the mammalian homolog of the yeast mitochondrial disulfide r

181 mber of these complexes as class II mMOB1, a mammalian homolog of the yeast protein MOB1, and show th

182 be involved in vesicle trafficking, and the mammalian homolog of the yeast septin protein cdc10, whi

183 Sirtuin 6 (SIRT6) is a mammalian homolog of the yeast Sir2 deacetylase.

184 We have observed that Munc18c, a mammalian homolog of the yeast syntaxin-binding protein

185 We recently identified the mammalian homolog of this molecule to be highly up-regul

186 A mammalian homolog of THRUMIN1, GRXCR1, has been implicat

187 We have examined the developmental role of a mammalian homolog of trx and putative oncogene, Mll.

188 ole in yeast, TIP does not interact with the mammalian homolog of type 2A-associated protein of 42 kD

189 protein Mig-2 (mitogen inducible gene-2), a mammalian homolog of UNC-112, and the actin binding prot

190 Given the interaction of FEZ1, the mammalian homolog of UNC-76, with protein kinase Czeta,

191 As retinoid X receptor (RXR) is the mammalian homolog of USP, we also solved the 2.60 A crys

192 cently, Golgi phosphoprotein 3 (GOLPH3), the mammalian homolog of Vps74, has been shown to control th

193 ation correlates with phosphorylation of the mammalian homolog of yeast GCN2 eIF2 alpha kinase.

194 also contains Nup160, Nup133, Nup96, and the mammalian homolog of yeast Sec13p.

195 Interestingly, SIRT1, a mammalian homolog of yeast Sir2, bound to and deacetylat

196 part of the 19S cap, we identified USP14, a mammalian homolog of yeast Ubp6p, as being bound to the

197 We have thus identified the first mammalian homolog of yeast UPF1, a protein that regulate

198 Notably, the mammalian homolog of yeast vacuole segregation mutant (V

199 We now find that the mammalian homolog of yeast VPS41, a member of the homoty

200 DNA replication and repair in yeast, and the mammalian homolog of yFEN-1 (DNase IV, FEN-1, or MF1) pa

201 for an activator protein predicted to be the mammalian homolog of yHac1, the activity of which can be

202 ulminates in the phosphorylation of YAP, the mammalian homolog of Yki.

203 Yes-associated protein (YAP), the mammalian homolog of Yorkie, promotes cardiomyocyte grow

204 Mammalian homologs of Atg8 are unmodified in Atg7(-/-) e

205 LanC-like (LanCL) proteins are mammalian homologs of bacterial LanC enzymes, which cata

206 However, although mammalian homologs of C. elegans cell death gene product

207 phenotypes, propose the hypothesis that the mammalian homologs of Cx36.7 and Nkx2.5 lie in a pathway

208 Naked (NKD)1 and NKD2 are mammalian homologs of Drosophila Naked Cuticle, which ne

209 especially dependent upon the expression of mammalian homologs of Drosophila segmentation genes.

210 catenin degradation was discovered involving mammalian homologs of Drosophila Sina (Siah), which bind

211 Finally we show that mammalian homologs of Ey and Da can functionally replace

212 The Mst1 and Mst2 protein kinases are the mammalian homologs of hippo, a major inhibitor of cell p

213 Mammalian homologs of hus1+ were recently identified, an

214 LIN28A and LIN28B, the mammalian homologs of lin-28, are implicated in malignan

215 Although mammalian homologs of nanos3 are expressed in early sper

216 Mammalian homologs of nematode sex determination genes h

217 There are three mammalian homologs of Orai1, and in expression experimen

218 Clock together with the recent discovery of mammalian homologs of per indicate that there is high st

219 To identify mammalian homologs of Sec7p and its interacting proteins

220 To examine the functional similarity of mammalian homologs of SID-1 (SIDT1 and SIDT2), we expres

221 RB-like, E2F, and MuvB (DREAM) that contains mammalian homologs of synMuvB proteins LIN-9, LIN-37, LI

222 tudies of mouse recently have implicated the mammalian homologs of the C. elegans heterochronic gene

223 The mammalian homologs of the C. elegans partitioning-defect

224 Two mammalian homologs of the Caenorhabditis elegans protein

225 Mammalian homologs of the components of this pathway are

226 The mammalian homologs of the D. melanogaster Grainyhead gen

227 Dlx homeobox genes are mammalian homologs of the Drosophila Distal-less (Dll) g

228 Osr1 and Osr2 are the only mammalian homologs of the Drosophila odd-skipped family

229 Vangl2, one of two mammalian homologs of the Drosophila planar cell polarit

230 oplasmic domain binds to proteins encoded by mammalian homologs of the Drosophila seven in absentia (

231 ransmembrane domain receptor family that are mammalian homologs of the Drosophila tissue polarity gen

232 ereditary colon cancer and is one of several mammalian homologs of the Escherichia coli mutL DNA mism

233 Here we report that Osr1 and Osr2, the mammalian homologs of the odd-skipped family of zinc fin

234 hBRG1 and hBRM are mammalian homologs of the SNF2/SW12 yeast transcriptiona

235 ytosine (5mC), we identified TET proteins as mammalian homologs of the trypanosome proteins JBP1 and

236 We generated mice lacking Cks2, one of two mammalian homologs of the yeast Cdk1-binding proteins, S

237 Mammalian homologs of the yeast protein kinase, Sterile

238 SUMOylation is reversible, and several mammalian homologs of the yeast SUMO-specific protease U

239 es the possibility of as yet uncharacterized mammalian homologs of these new amphibian peptides.

240 Mammalian homologs of these proteins have been shown to

241 Trib1, Trib2, and Trib3 are mammalian homologs of Tribbles, an evolutionarily conser

242 Mammalian homologs of TRP and TRPL recently have been is

243 Mammalian homologs of two of these genes, ced-9 and ced-

244 The existence of mammalian homologs of UNC-4 and UNC-37 indicates that a

245 cell death and inhibits cell proliferation, mammalian homologs of Warts, termed Lats1 and Lats2, may

246 zinc finger transcription factor PAG-3, the mammalian homologs of which are coexpressed in olfactory

247 ganic solute transporter alpha-like protein, mammalian homologs of which have been implicated in memb

248 Ulk1, one of the mammalian homologs of yeast Atg1, is a serine-threonine

249 Mammalian homologs of yeast IRE1, which activate chapero

250 f class III histone deacetylases such as the mammalian homologs of yeast Silent Information Regulator

251 BRG1 and BAF155, mammalian homologs of yeast SWI2 and SWI3, respectively,

252 Mammalian homologs of YiiP play critical roles in zinc h

253 the ATPase site motifs is a feature of many mammalian homologs, our proposed model has broad implica

254 Contrary to the observations made for its mammalian homologs, overexpression of dTIS11 does not pr

255 a different role in APA regulation than its mammalian homolog, PABPN1.

256 quired to complete mitosis, and Ess1 and its mammalian homolog, Pin1, interact directly with RNA poly

257 family of proteins (RBF1 and RBF2) and their mammalian homologs (pRB, p130, and p107) are best known

258 2 is stably associated with KHT-1, while its mammalian homolog, prostatic acid phosphatase (PAP; also

259 The Rab GTPase Ypt1 and its mammalian homolog Rab1 regulate macroautophagy and two o

260 Unlike these mammalian homologs, Relish is endoproteolytically cleave

261 phila p90 ribosomal S6 kinase (S6KII) or its mammalian homolog RSK has not been performed in the cont

262 only 3-fold, whereas analogous studies using mammalian homologs show >30-fold stimulation.

263 g analysis carried out on homology models of mammalian homologs shows that these family members also

264 Like its mammalian homolog, sterol regulatory element-binding pro

265 in Drosophila cells, and their corresponding mammalian homologs STIM1 and Orai1 in T cells, as essent

266 s upward of 85% amino acid identity with its mammalian homologs (termed Siahs), but the function of t

267 The Snf1 kinase and its mammalian homolog, the AMP-activated protein kinase, are

268 Different from mammalian homologs, the amino-terminal part of almost al

269 ein, band 3, that are not conserved in other mammalian homologs, the question arose whether GEs can o

270 ith the recent biochemical analysis of their mammalian homologs, these results simultaneously identif

271 80% of these Drosophila glial genes have mammalian homologs; these are now excellent candidates f

272 st in Xenopus laevis where, similar to their mammalian homologs, they form functional heterodimers.

273 and because the majority of these genes have mammalian homologs, this approach provides an avenue for

274 In the search for a mammalian homolog, three proteins in the human data base

275 s and some saturated pyrimidines is NEIL1, a mammalian homolog to Escherichia coli endonuclease VIII.

276 identified were: a Y-box protein (MSY2), the mammalian homolog to the Xenopus oocyte masking protein

277 is sufficient to recruit Groucho or the TLE mammalian homologs to target gene promoters.

278 y the patterns of conserved sequences in the mammalian homologs to the beta-globin LCR, we determined

279 he S. pombe telomeric protein Tpz1, like its mammalian homolog TPP1, increases the affinity of Pot1 f

280 Atg1 serine/threonine protein kinase and its mammalian homologs ULK1 and ULK2 play critical roles dur

281 Spry1, among the four mammalian homologs, was specifically induced by TCR sign

282 Its mammalian homolog, WASP, has also been studied extensive

283 as been cloned, but this N-glycanase and its mammalian homolog were reported to be incapable of degly

284 The presence of mammalian homologs with circadian expression features (D

285 The two tomato MMPs were found to resemble mammalian homologs with respect to gelatinolytic activit

286 Similar to its mammalian homolog working as an integral part of the tra

287 The Drosophila Yorkie (Yki) protein and its mammalian homolog Yes-associated protein (YAP) are poten

288 s, investigations of the role of Yki and its mammalian homolog Yes-associated protein (YAP) in develo