ライフサイエンスコーパス: mammalian homolog

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

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

3 this interaction is conserved in Salvador's mammalian homolog.

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

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

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

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

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

9 may act less specifically than their fly 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 re conserved, particularly between yeast and mammalian homologs.

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

15 Its mammalian homolog Acinus has been implicated in RNA proc

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

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

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

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

20 Because some mammalian homologs are strongly induced by glucocorticoi

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

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

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

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

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

26 d they provide a framework to understand the mammalian homologs BAF/PBAF and the Sfh1 ortholog INI1/B

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

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

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

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

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

32 In contrast to the mammalian homologs, CALX is inhibited by Ca(2+) binding

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

34 Mutation of the mammalian homolog causes significant neurological pathol

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

36 osophila fizzy-related protein (Fzr) and its mammalian homolog Cdh1 function as key regulators of end

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

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

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

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

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

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

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

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

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

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

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

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

49 1 (disruptor of telomeric silencing) and its mammalian homolog, DOT1L.

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

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

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

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

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

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

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

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

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

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

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

61 Although mammalian homologs have been identified in mouse and man

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

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

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

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

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

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

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

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

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

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

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

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

74 Chip and its mammalian homologs interact with and promote dimerizatio

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

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

77 While overall similarity to mammalian homologs is high, we found notable differences

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

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

80 The molecular function of Mask, or its mammalian homologs Mask1 (ANKHD1) and Mask2 (ANKRD17), r

81 ncer H3K4 mono-methyltransferase Trr and its mammalian homologs, MLL3/4, cause only minor changes in

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

83 ible enzyme in Escherichia coli MutT and its mammalian homolog MTH1.

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

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

86 6 family members, Nup145N, Nup100 and to the mammalian homolog, Nup98.

87 Rix7's mammalian homolog, NVL2 has been linked to cancer and me

88 gement of domains between UNC-89 and its two mammalian homologs, obscurin and SPEG: kinase, a non-dom

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

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

91 The mammalian homolog of AcbA is processed to diazepam bindi

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

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

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

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

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

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

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

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

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

101 cells this process is controlled by Munc18 (mammalian homolog of Caenorhabditis elegans uncoordinate

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

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

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

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

106 A mammalian homolog of CTR1 was previously reported to be

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

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

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

110 A mammalian homolog of dLMO is expressed in the developing

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

143 The mammalian homolog of one Drosophila gene identified in t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

166 0- and 140-kDa isoforms encoded by Mena, the mammalian homolog of the Drosophila Enabled gene.

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

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

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

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

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

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

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

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

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

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

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

178 The mammalian homolog of the Escherichia coli MutY DNA glyco

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

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

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

182 SIRT1 is a mammalian homolog of the Saccharomyces cerevisiae chroma

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

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

185 The mammalian homolog of the Schizosaccharomyces pombe Rad9

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

223 Mammalian homologs of hus1+ were recently identified, an

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

225 Although mammalian homologs of nanos3 are expressed in early sper

226 Mammalian homologs of nematode sex determination genes h

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

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

229 To identify mammalian homologs of Sec7p and its interacting proteins

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

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

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

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

234 Two mammalian homologs of the Caenorhabditis elegans protein

235 Mammalian homologs of the components of this pathway are

236 The mammalian homologs of the D. melanogaster Grainyhead gen

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

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

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

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

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

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

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

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

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

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

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

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

249 Mammalian homologs of these proteins have been shown to

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

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

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

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

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

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

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

257 Mammalian homologs of yeast Atg8 protein (mAtg8s) are im

258 Mammalian homologs of yeast IRE1, which activate chapero

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

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

261 Mammalian homologs of YiiP play critical roles in zinc h

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

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

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

265 Conditional knockout of its mammalian homolog Piezo1 in vivo accelerates regeneratio

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

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

268 2 is stably associated with KHT-1, while its mammalian homolog, prostatic acid phosphatase (PAP; also

269 The mammalian homolog, PUF60, also displays anti-inflammator

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

271 Unlike these mammalian homologs, Relish is endoproteolytically cleave

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

273 function appears to be conserved because its mammalian homolog, SEC24C, was also required for ER-phag

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

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

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

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

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

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

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

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

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

283 80% of these Drosophila glial genes have mammalian homologs; these are now excellent candidates f

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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