ライフサイエンスコーパス: human homolog

1 The sequence is 91% identical to that of a human homolog.

2 shares only 30% amino acid identity with its human homolog.

3 644) may also mediate multimerization in the human homolog.

4 the motion area known as MT in monkey or its human homolog.

5 recombinant protein, ATX1 is similar to the human homolog.

6 RhoGAP shares 86% sequence identity with the human homolog.

7 uence homology to murine SPP1, we cloned the human homolog.

8 electivity for the bacterial enzyme over the human homolog.

9 replaced the gene encoding mouse TPO by its human homolog.

10 this interaction is conserved between their human homologs.

11 trons occupy positions identical to those in human homologs.

12 substrate preferences of AlkB and its three human homologs.

13 functional prediction for medically relevant human homologs.

14 hosphoethanolamine methyltransferase with no human homologs.

15 are potential drug targets because they lack human homologs.

16 le control; 88% of these genes have putative human homologs.

17 , consistent with data on the interaction of human homologs.

18 4 and cloned cDNAs for the chick, mouse, and human homologs.

19 th Homo sapiens proteins to sort out the non-human homologs.

20 se of its zebrafish, mouse, rat, bovine, and human homologs.

21 zeta (Rev3/7), and Pol eta (Rad30), all with human homologs.

22 tified a ubiquitin-like protein, hPLIC1 (for human homolog 1 of protein linking intergrin-associated

23 ised of 53 miRNAs on mouse chromosome 12qF1 (human homolog 14q32).

24 al 454 miRNAs identified so far in rhesus to human homologs, 173 miRNA genes showed 100% homology in

25 144 of these genes have human homologs, 60 of which are associated with disease

26 Three human homologs, ABH1, ABH2 and ABH3, have been identifie

27 The Escherichia coli AlkB protein, and two human homologs ABH2 and ABH3, directly demethylate 1-met

28 of the currently approved bacterial drugs by human homologs aiming at the elimination of adverse effe

29 link seven proteins including Hfd1p and its human homolog ALDH3A1 to mitochondrial coenzyme Q (CoQ)

30 and other RNAs in vitro; the putative 29 kDa human homolog also displays this decapping activity.

31 mp53) has similar apoptotic functions as its human homolog and is therefore an attractive model syste

32 nociception, which suggests the dpIns is its human homolog and, as such, a potential therapeutic targ

33 In this study, we have identified its human homolog, and demonstrated that RPS23RG1 regulates

34 sly uncharacterized loci, many of which have human homologs, and we anticipate that this collection w

35 l differences between trypanosomal TyrRS and human homologs are promising for the design of inhibitor

36 The highly conserved human homologs are well-established drug targets.

37 hylogenic analysis of human CD109 with other human homologs as well as orthologs from other mammalian

38 stability in Saccharomyces cerevisiae whose human homologs BLM, WRN, and RECQL4 are mutated in Bloom

39 Here, we identify the human homolog (C1orf176; EXO5) that functions in the rep

40 and virus maintenance, and that the closest human homolog can fully complement these defects.

41 ding how other H3-like proteins, such as the human homolog CENP-A, function in kinetochore assembly a

42 However, placing these residues in the human homolog confers only partial binding, indicating t

43 of the interaction of RNA with LAF-1 and its human homolog, DDX3X.

44 A human homolog (DEGS-1) of the Drosophila melanogaster de

45 Yeast Dis3 and its human homologs, DIS3 and DIS3L1, have exoribonuclease ac

46 tes, 11 of which are similar to those of its human homolog, DNA polymerase kappa.

47 as the gene encoding DOHH and identified the human homolog DOHH gene, HLRC1.

48 Dachsous, the receptor protein Fat, and its human homolog FAT4.

49 haromyces cerevisiae Ydr109c protein and its human homolog FGGY, both of which belong to the broadly

50 so used to generate a homology model for the human homolog hASNase1 and to help explain its vastly di

51 we report the identification of a functional human homolog, hBRE1, of the yeast BRE1 E3 ubiquitin lig

52 lity to apoptosis, can be deregulated by the human homolog Hdm2 (Mdm2) E3 ligase.

53 The Rad23 family of proteins, including the human homologs hHR23a and hHR23b, stimulates nucleotide

54 richia coli adenine glycosylase MutY and its human homolog (hMYH) play an important role in the preve

55 ns fuse a homeobox DNA-binding domain to the human homolog (hNup98) of a transcriptionally active com

56 loned canine P2Y11 receptor (cP2Y11) and its human homolog (hP2Y11) were stably expressed in Chinese

57 shows substrate specificities similar to its human homolog hPEPT1.

58 A putative human homolog (hPot1) was previously identified, based o

59 The assembly of bacterial RecA, and its human homolog hRAD51, into an operational ADP/ATP-regula

60 functional conservation between AMP1 and its human homolog HsGCPII, a tumor marker of medical interes

61 ely probe the functional significance of the human homologs, i.e., area hMT and hMST, on motion perce

62 carcinogenesis model and then evaluate their human homologs in breast cancer case-control association

63 cient survey of the wealth of information on human homologs in model organisms across numerous databa

64 ate the TMA proteins and, potentially, their human homologs, in translation related processes.

65 H3 lysine 4 (H3K4) methyltransferases, whose human homologs include the MLL and hSet1 complexes.

66 have been identified in other animals, and a human homolog is implicated in the genetic disease Cat-E

67 in (VCP), a ubiquitin-dependent ATPase whose human homolog is linked to neurodegenerative disease, le

68 ptor nontransgenic) Tregs, and (iii) the B29 human homolog is presented by HLA class II, we are neari

69 man D-2HG dehydrogenase: Dld2, which, as its human homolog, is a mitochondrial protein, and the cytos

70 cific co-factor Earthbound 1 (Ebd1), and its human homolog jerky, promote interaction between the Wnt

71 Similar mutations in the human homolog L3MBTL1 correlate with some cancers.

72 We previously demonstrated that the human homolog, Las1L, is required for efficient ITS2 rRN

73 sfection with the yeast gene Lag1 Sc and the human homolog LASS1 increased ceramide levels and partia

74 Drosophila Lft, and its human homologs LIX1 and LIX1-like, bind to the cytoplasm

75 nd breast cancer models, but the role of its human homologs Ly6K and Ly6E in breast cancer are not es

76 Nelfinavir and its analogs inhibit human homolog M. jannaschii S2P cleavage of an artificia

77 Virus capsid protein has no human homolog, making its assembly a promising but undev

78 re essential for bacterial growth and lack a human homolog, making them attractive targets for the de

79 plore the relationship between sut-2 and its human homolog, mammalian SUT-2 (MSUT2) and find both pro

80 Variation in activity of their human homologs may also affect vinorelbine pharmacokinet

81 that parasite enzymes with highly conserved human homologs may represent a promising reservoir of ne

82 ouse liver specific Oatp is Oatp1b2, and the human homologs most closely related are OATP1B1 and 1B3.

83 genesis to replace mouse ZP2 and/or ZP3 with human homologs, mouse lines with human-mouse chimeric zo

84 The DNA repair factor Rad60 and its human homolog NIP45, which contain SLDs, are candidate S

85 l stretches, similar to the structure of its human homolog, NUP98.

86 Mutations in the human homolog of a Drosophila gene, patched, underlie Go

87 ional candidates at this locus was ANKH, the human homolog of a gene that is responsible for the phen

88 rting enzyme 2 (ACE2), a recently identified human homolog of ACE, is a novel metallocarboxypeptidase

89 As the only known human homolog of ACE, the demonstration that ACE2 is ins

90 We isolated the human homolog of B(0)AT1, called SLC6A19, and determined

91 Tid1 is a human homolog of bacterial DnaJ and the Drosophila tumor

92 ons with expressed sequence tags (ESTs), the human homolog of bwd is predicted to reside in the chrom

93 purification strategy, we have identified a human homolog of Caenorhabditis elegans Egl9 as a HIF pr

94 whether casein kinase 2alpha (CK2alpha), the human homolog of Cka1p, regulates MRP1 by phosphorylatio

95 In this study, we have shown that the human homolog of Claspin is required for resistance to m

96 bacteria but are also present in ATP7B, the human homolog of copA, and direct ribosomal frameshiftin

97 In addition, we found that SNIP1, the human homolog of DDL, is involved in miRNA biogenesis an

98 Mutations in CRB1, the human homolog of Drosophila Crumbs, cause autosomal rece

99 PORCN encodes the human homolog of Drosophila melanogaster porcupine, an e

100 e stem cell markers p21(CIP1) and Msi-1, the human homolog of Drosophila Musashi.

101 Siah-1, the human homolog of Drosophila seven in absentia, is a p53-

102 a yeast two-hybrid screen, we identified the human homolog of Drosophila Tribbles 3, TRIB3, as an int

103 MLL, the human homolog of Drosophila trithorax, maintains Hox gen

104 cose production were dependent on TIP60, the human homolog of ESA1.

105 find any evidence of an effect of Pin1, the human homolog of ESS1, on transcription by RNA polymeras

106 This study and studies showing that the human homolog of EVI24 is located in a region of 19q13 f

107 A mutation in the human homolog of gkt causes the neurodegenerative diseas

108 A human homolog of hpo completely rescues the overgrowth p

109 ant, light ear (le), which suggests that the human homolog of le is a possible human HPS locus.

110 We now show that human LSD2/KDM1b/AOF1, the human homolog of LSD1, is an H3K4me1/2 demethylase that

111 The HGAL gene is the human homolog of M17, a mouse gene expressed specificall

112 poral cortex, including the motion-selective human homolog of macaque area MT (hMT), object-form-sele

113 n identified as occurring in area V1 and the human homolog of macaque MT/V5, respectively.

114 show that SETDB1 tightly associates with the human homolog of mAM, a murine ATFa-associated factor.

115 Mutations in the human homolog of MeaB, MMAA, lead to methylmalonic acidu

116 Here we show that the human homolog of MMS21 is also a SUMO ligase.

117 cleotide polymorphism in the promoter of the human homolog of mouse double minute 2 (MDM2) gene was c

118 vers OspC3 to inhibit caspase-4, a potential human homolog of murine caspase-11.

119 caused a decrease in p53 and an increase in human homolog of murine double minute 2 (Hdm2) and phosp

120 , triggers an interaction between Rb and the human homolog of murine double minute 2 (Hdm2), leading

121 rized family member termed Stk10, which is a human homolog of murine Lok, a serine/threonine kinase h

122 d the expression levels of p53 and HDM2 (the human homolog of murine MDM2) in various human diploid f

123 Analysis of the human homolog of mutY, MYH, showed that the siblings wer

124 hearing in humans requires myosin IIIA, the human homolog of NINAC.

125 yndrome, which is caused by mutations in the human homolog of Nipped-B.

126 The human homolog of peptide deformylase (HsPDF) resides in

127 The human homolog of PKK has over 90% identity to its murine

128 We also found that the human homolog of Psf2p, PSF2, was required for proper ch

129 Knockdown of the human homolog of Psid reduced the speed and directionali

130 r demonstrate that expression of PTPRZ1, the human homolog of Ptprz, is induced in multiple sclerosis

131 Here, we show that PUM2, a human homolog of Pumilio, a protein required to maintain

132 lls specific for Hsp60sp bound to HLA-E (the human homolog of Qa-1) exist and play an important role

133 UbL-UBA proteins, including human homolog of Rad23 (hHR23) proteins, may regulate pr

134 We investigated whether within the human homolog of RHS7, functional polymorphisms exist, w

135 level engages the anterior hippocampus, the human homolog of rodent ventral hippocampus.

136 This gene is the human homolog of Rp8, a rat gene associated with program

137 e, RPD3, suppressed neurodegeneration, and a human homolog of RPD3, histone deacetylase 2, bound ATM

138 In this study, we identified a human homolog of RVS161, termed BIN3 (bridging integrato

139 he isolation of a cDNA encoding h-mtTFB, the human homolog of Saccharomyces cerevisiae mitochondrial

140 Treslin, the human homolog of Sld3, stimulates human DDK phosphorylat

141 .3 locus in breast cancer cells, wherein the human homolog of SMAR1 (BANP) has been mapped, enhances

142 We show that a human homolog of SPT4 (HsSPT4) complements Scspt4-silenc

143 ecific recognition protein 1 (SSRP1) and the human homolog of suppressor of Ty 16 (hSpt16).

144 We reported that hBG1, the human homolog of the acyl-CoA synthetase mutated in the

145 onent of the ATR/CHK1 signaling pathway, the human homolog of the Caenorhabditis elegans biological c

146 Kindlin-1 is a human homolog of the Caenorhabditis elegans protein UNC-

147 ing p53 degradation, E6AP binding, and hDlg (human homolog of the Drosophila discs large tumor suppre

148 hDlg is the human homolog of the Drosophila Discs-large tumor suppre

149 AP54alpha/beta, actin-like proteins, and the human homolog of the Drosophila Enhancer of Polycomb pro

150 L3MBTL1, the human homolog of the Drosophila L(3)MBT polycomb group t

151 H-L(3)MBT, the human homolog of the Drosophila lethal(3)malignant brain

152 Moreover, we identified magoh, a human homolog of the Drosophila mago nashi gene product,

153 d protein-truncating mutations in NIPBL, the human homolog of the Drosophila melanogaster Nipped-B ge

154 The human homolog of the Drosophila Patched gene (PTCH), loc

155 The human homolog of the Drosophila patched gene, has been s

156 L3MBTL1 is a human homolog of the Drosophila polycomb L(3)MBT tumor s

157 This protein, Bicd2, is a human homolog of the Drosophila protein Bicaudal D, a co

158 We show here that the human homolog of the Drosophila Scribble (Vartul) (hScri

159 Mutations in SALL1, the human homolog of the Drosophila spalt gene, result in To

160 r 10 (TLR10) is the most recently identified human homolog of the Drosophila TOLL protein.

161 LL denoted MLL2, which represents the second human homolog of the Drosophila trithorax gene, was char

162 hTid-1, a human homolog of the Drosophila tumor suppressor l(2)Tid

163 hTid-1, a human homolog of the Drosophila tumor suppressor protein

164 ell extracts containing His-tagged rpl3, the human homolog of the E. coli 50 S subunit rplC.

165 corresponding to exon 12, is present in the human homolog of the gene, ATP11B.

166 tant role in vertebrate development and is a human homolog of the HIF asparaginyl-hydroxylase.

167 or precentral sulcus (thought to contain the human homolog of the macaque frontal eye fields).

168 EPG5 is the human homolog of the metazoan-specific autophagy gene ep

169 rophin-1-interacting protein 4 (AIP4) is the human homolog of the mouse Itch protein (hItch), an E3 l

170 Leptin (LEP), the human homolog of the mouse obesity (ob) gene, is positio

171 escence in situ hybridization, we placed the human homolog of the mouse protocadherin Pcdh15 in the l

172 Inhibition of the p53 E3 ligase human homolog of the murine double minute protein-2 (HDM

173 ANKH, the human homolog of the mutated gene in the ank/ank mouse,

174 ear autoantigenic sperm protein (sNASP) is a human homolog of the N1/N2 family of histone chaperones.

175 Germline mutations in the human homolog of the patched1 (PTCH1) are associated wit

176 A strong candidate gene (hPer2), a human homolog of the period gene in Drosophila, maps to

177 We have demonstrated that the human homolog of the rat inositol phosphate multikinase

178 RHBDL2, a human homolog of the rhomboids, belongs to a unique clas

179 A human homolog of the RPA2 subunit, called RPA4, was prev

180 rotein product of the gene hSIR2(SIRT1), the human homolog of the S. cerevisiae Sir2 protein known to

181 Chk2/hcds1, the human homolog of the Saccharomyces cerevisiae RAD53/SPK1

182 at a S20 kinase activity copurifies with the human homolog of the Schizosaccharomyces pombe checkpoin

183 In this report, we identify the human homolog of the Schizosaccharomyces pombe EME1 gene

184 Here, we show that human homolog of the ScPSO4/PRP19 (hPso4) forms a stable

185 ck cognate protein 20 (hHSC20), the putative human homolog of the specialized DnaJ type co-chaperones

186 se genetics, we recently identified VentX, a human homolog of the vertebrate Xenopus Vent family of h

187 We identified that ZNF143, the human homolog of the Xenopus transcriptional activator S

188 The hCHK2 gene encodes the human homolog of the yeast Cds1 and Rad53 G2 checkpoint

189 The human homolog of the yeast DNA repair protein RAD23, hHR

190 We show here that DLP1, the human homolog of the yeast DNM1 and VPS1 genes, plays an

191 Here we identified a human homolog of the yeast p24 family of proteins, named

192 PD2 is the human homolog of the yeast RNA polymerase II-associated

193 ythology Hera controlled Artemis) (K-H), the human homolog of the yeast transcription termination fac

194 The identification of a human homolog of this conserved gene suggests a potentia

195 The human homolog of this gene (LARGE) maps to chromosome 22

196 The human homolog of this gene was cloned and characterized.

197 The human homolog of TIM-1 is the hepatitis A virus (HAV) re

198 ke its fungal counterpart but similar to the human homolog of Tim50, recombinant TbTim50 possesses a

199 a (MLL; also known as myeloid/lymphoid), the human homolog of trithorax in Drosophila, is a transcrip

200 atients with de novo mutations in TUBA3, the human homolog of Tuba1.

201 E2-25K, a human homolog of Ubc1, also promotes APC-dependent chain

202 The human homolog of Ubp10, USP36, also has IDRs flanking it

203 Depletion of the human homolog of UBP3, USP10, is detrimental to the fitn

204 A human homolog of very long-chain acyl-CoA synthetase, hV

205 and subcellular distribution of hCAP-H, the human homolog of XCAP-H, in order to better understand i

206 Response Element (EpRE) and a novel protein, human homolog of Xenopus gene which Prevents Mitotic Cat

207 We probed the mitotic function of TOGp (human homolog of XMAP215/Dis1) using siRNA.

208 H2B monoubiquitination was attributed to the human homolog of yeast Bre1 (RNF20/40).

209 hSPC25 interacted with HEC1 (human homolog of yeast Ndc80) throughout the cell cycle

210 transcripts, we cloned and characterized the human homolog of yeast NOP5/NOP58, whose gene product ha

211 report the identification and sequence of a human homolog of yeast REV1.

212 Previously, we described the isolation of a human homolog of yeast REV3, the catalytic subunit of po

213 The hSEP1 gene is the human homolog of yeast SEP1.

214 The human homolog of yeast Sir2, SIRT1, was found to interac

215 d that RBM25 associated selectively with the human homolog of yeast U1 snRNP-associated factor hLuc7A

216 9 (TMEM199, previously called C17orf32) as a human homolog of yeast V-ATPase assembly factor Vph2p (a

217 The TB2 gene is the human homolog of Yop1p.

218 Using the human homologs of Bre2 and Sdc1, ASH2L and DPY-30, respe

219 We identify putative human homologs of Bye1, the proteins PHD finger protein

220 Among the human homologs of candidate genes, knockdown of PPP2R1A,

221 Herein, we have analyzed the two human homologs of Cdc14p, hCdc14A and hCdc14B.

222 Townes-Brocks Syndrome, which are linked to human homologs of Distal-less and spalt, respectively.

223 bind to several PDZ proteins, including the human homologs of Dlg and Scrib, is dependent on E6's ab

224 ancer of split (TLE) proteins, which are the human homologs of Drosophila Groucho, directly associate

225 Overexpression of human homologs of egl-5 modulated NF-kappaB-dependent TL

226 sequence allowed the identification of three human homologs of Escherichia coli Nei.

227 We confirmed centriolar localization for the human homologs of four candidate proteins.

228 Each of the three human homologs of HP1 includes a chromoshadow domain (CS

229 K-related kinase/intestinal cell kinase) are human homologs of Ime2p in Saccharomyces cerevisiae and

230 Centroids of the human homologs of JvA genes showed that JH tumors were m

231 o of interest because of the interactions of human homologs of lanthipeptide cyclases with kinases su

232 Our work suggests that human homologs of multiple C. elegans heterochronic gene

233 alian farnesyl transferases, suggesting that human homologs of NisC posttranslationally modify a cyst

234 evaluated currents induced by expression of human homologs of Orai together with STIM1 in human embr

235 xpression for endogenous STIM1 and all three human homologs of Orai was up-regulated, accompanied by

236 ause of this phenotype is not known, but the human homologs of PRC2 subunits have been shown to play

237 The human homologs of prokaryotic mismatch repair have been

238 Human homologs of several of these genes have well-estab

239 In addition to the previously reported human homologs of Srb10 and 11, we have identified TRAP2

240 ied TRAP230/ARC240 and TRAP240/ARC250 as the human homologs of Srb8 and Srb9, showing the entire Srb8

241 that contain ORs with known odor ligands or human homologs of such ORs.

242 We characterized human SirT1, one of the human homologs of the budding yeast Sir2p, an NAD+-depen

243 RAD51 is one of six mitotic human homologs of the E. coli RecA protein (RAD51-Paralo

244 We have cloned and expressed the human homologs of the ORC subunits as recombinant protei

245 Drosophila and human homologs of the Rps0 proteins physically interact

246 rganization of hSNM1B, one of at least three human homologs of the Saccharomyces cerevisiae PSO2 gene

247 All the human homologs of the six subunits of Saccharomyces cere

248 Here we show that two human homologs of the yeast ubiquitin-like Dsk2 protein,

249 The murine and human homologs of the zebrafish pescadillo protein (Pes1

250 None of the closest human homologs of these carriers had any detectable effe

251 the sequence and expression pattern of four human homologs of these genes.

252 lass III myosin, cause retinal degeneration, human homologs of this gene are potential candidates for

253 Human homologs of top-ranked hits protected against alph

254 PV E6 proteins induce the degradation of the human homologs of two Drosophila PDZ domain-containing t

255 omplex containing hCcr4d and hCaf1z, distant human homologs of yeast Ccr4p and Caf1p/Pop2p, respectiv

256 As part of a strategy to identify human homologs of yeast proteins that are known to be in

257 Lin et al. describe how HLTF and SHPRH, the human homologs of yeast Rad5, can discriminate between M

258 Two closely related human homologs of yeast Rad6 have been identified as HHR

259 and-independent activation compared with its human homologs or murine orthologs.

260 onal complementation of yeast deletions with human homologs, our technique could be readily applied t

261 s highly conserved DNA binding domain or the human homolog PC4 is sufficient to suppress G4-associate

262 Ess1 and its human homolog, Pin1, bind to phospho-Ser-Pro sites withi

263 homolog, as well as a more distantly related human homolog, provide a more complete understanding of

264 ulating Mmp2 and Oamb can be replaced by its human homolog Ras-responsive element-binding protein 1 (

265 Dhh1p, and its human homolog, RCK/p54, repress translation in vitro, an

266 expressed in humans, and the identity of its human homolog remains elusive.

267 no acid sequence identity with its mouse and human homologs, respectively, and with several polymorph

268 d the beta-strand (beta7) where mutations in human homologs result in inherited disease.

269 Consistent with the screening result, the human homolog, RSPH3, interacts with and is a substrate

270 e homologs were discovered; among these, the human homolog Sprouty 2 (hSpry2) contains the highest de

271 ocity of pyrophosphate:ATP exchange than its human homolog, suggesting different kinetics of ubiquiti

272 pressors Drosophila melanogaster Yan and its human homolog TEL/ETV6, can polymerize.

273 s sequenced and the primary structure of the human homolog (termed TFIIIA-intP for TFIIIA-interacting

274 y efficient at CPT-11 metabolism; however, a human homolog that was more than 81% identical to this p

275 Several crn genes have human homologs that are important for RNA processing, pr

276 The 430 kDa Tra1 subunit and its human homolog the transformation/transcription domain-as

277 ifferent modalities is unknown, although its human homolog, the inferior frontal gyrus, is known to b

278 Like their human homologs, the genomic order of the mouse Muc genes

279 tions and the role of Drosophila Trr and its human homologs, the MLL3 and MLL4/COMPASS-like complexes

280 All 68 Fugu receptors had a clear human homolog, thus defining no new nuclear receptor sub

281 s Ath1 in mice and that polymorphisms in its human homolog TNFSF4 increase the risk of myocardial inf

282 SALL4, a human homolog to Drosophila spalt, is a novel zinc finge

283 IRAK-4 is the closest human homolog to Pelle.

284 (RPA1, RPA2, and RPA3); however, there is a human homolog to the RPA2 subunit, called RPA4, that can

285 reover, MtTrxR sufficiently differs from its human homologs to suggest the possibility of selective i

286 We also identified a human homolog, TRMO, indicating that m(6)t(6)A plays a g

287 iquilin (Ubqn), the ubiquitin receptor whose human homolog ubiquilin 2 is associated with familial am

288 ro was inhibited by S. enterica YjgF and the human homolog UK114.

289 port that mutations in the gene encoding the human homolog VMA21 cause the disease X-linked myopathy

290 The human homolog was also isolated and later proved to be h

291 -1R with the corresponding sequence from the human homolog was sufficient to confer high T-0632 affin

292 Its human homolog, WBSCR1, maps on 7q11.23, inside the 1.6 M

293 Its human homolog, WDR79, associates with C/D, H/ACA, and mi

294 hat are essential in flies and have multiple human homologs were found to be likely to be associated

295 xRTS can be replaced in extracts by its human homolog, while RECQL4 depletion from mammalian cel

296 o a previously reported NMR structure of the human homolog with 96% sequence identity (PDB 1TGQ), whi

297 n lung epithelial cells and polymorphisms in human homolog XRN2 are associated with human lung cancer

298 ising one-quarter of microbial PKLs and five human homologs, yet its biochemical activities remain ob

299 Similar to its human homolog, zebrafish Arhgef11 stimulated actin stres

300 tantly, these functions are conserved in the human homolog, ZMPSTE24, although disease-associated mut