ライフサイエンスコーパス: homolog

1 europeptide F, the Drosophila neuropeptide Y homolog.

2 about the function of NRG2, the closest NRG1 homolog.

3 BPR (TAP-binding protein-related), a tapasin homolog.

4 cy with UTY, a Y-chromosome demethylase-dead homolog.

5 aligning short reads that are part of remote homologs.

6 ct functional properties in different enzyme homologs.

7 t in cells dependent on other anti-apoptotic homologs.

8 junctions (dHJs) that primarily include both homologs.

9 markedly different from the regulons of its homologs.

10 icting secondary structures for multiple RNA homologs.

11 ific sequence that was mapped but also other homologs.

12 g of function in functionally diverse enzyme homologs.

13 Arabidopsis contains two OsMYBS1 homologs.

14 t the cochaperone, activator of Hsp90 ATPase homolog 1 (Aha1), dramatically increased the production

15 e kinase V-Akt murine thymoma viral oncogene homolog 1 (AKT1), and the protease cathepsin H (CTSH), f

16 The Achaete-scute homolog 1 (Ascl1) protein regulates a large subset of ge

17 IFICANCE STATEMENT The discovery that Atonal homolog 1 (Atoh1) governs the development of the sensory

18 Atonal homolog 1 (Atoh1) is a basic helix-loop-helix (bHLH) tra

19 Dachshund homolog 1 (DACH1), a key cell fate determination factor,

20 lood cells preferentially recruit Disc large homolog 1 (Dlgh1) and exclude protein kinase C (PKC)-the

21 ype I receptor inhibition using dorsomorphin homolog 1 (DMH1) or CRISPR/Cas9 activin A receptor type

22 the zinc finger transcription factor Kruppel homolog 1 (Kr-h1), one of the key players in juvenile ho

23 PGC1alpha binding partners is liver receptor homolog 1 (LRH-1; NR5A2), an orphan nuclear hormone rece

24 lorectal tumors with epigenetic loss of MutL homolog 1 (MLH1) had lost or had lower levels of HES1 th

25 er, Msh2-Msh6 or Msh2-Msh3 activate the MutL homolog 1 (Mlh1)-postmeiotic segregation 1 (Pms1) endonu

26 silent mating type information regulation 2 homolog 1 (SIRT1), which deacetylates forkhead box o3 (F

27 s related to the outgrowth of TMs was tweety-homolog 1 (TTYH1), which was highly expressed in a fract

28 creased levels of glioma-associated oncogene homolog 1 and 2 (GLI1/GLI2) compared with naive cells.

29 FXR1 (fragile X mental retardation autosomal homolog 1), an RNA-binding protein, are critical to main

30 Enhancer of zeste homolog 2 (EZH2) has been characterized as a critical on

31 Meg3 relied on functional enhancer of zeste homolog 2 (EZH2), a component of polycomb repressive com

32 eraction between Snail and enhancer of zeste homolog 2 (EZH2), an enzymatic subunit of the polycomb-r

33 Here, we show enhancer of zeste homolog 2 (EZH2), an enzyme that catalyzes H3 lysine tri

34 histone methyltransferase enhancer of zeste homolog 2 (EZH2).

35 Loss of MutS homolog 2 (MSH2), a mismatch repair (MMR) protein, abrog

36 e methyl transferase EZH2 (Enhancer of Zeste Homolog 2) is generally associated with H3K27 methylatio

37 ore subunit of PRC2 (Ezh2 [enhancer of zeste homolog 2]) at the cell membrane, preventing its nuclear

38 Chromobox homolog 3 (Cbx3/heterochromatin protein 1gamma [HP1gamma

39 ere associated with upregulation of tribbles homolog 3 (Trib3) that suppressed adipogenic differentia

40 Discs Large Homolog 5 (DLG5) plays an important role in the maintena

41 centrin-binding site within H. sapiens Prp40 homolog A (HsPrp40A), which contains a hydrophobic triad

42 ABCD1 and its homolog ABCD2 are peroxisomal ATP-binding cassette (ABC)

43 Loss-of-function mutations of KIB1 and its homologs abolished BR-induced BIN2 degradation and cause

44 e, we report on two potent ClpG disaggregase homologs acquired through horizontal gene transfer by th

45 on of alpha-ketoglutarate, inhibits the AlkB homolog (ALKBH) enzymes activity and induces DNA alkylat

46 We found that human, fly, and yeast profilin homologs all directly enhance microtubule growth rate by

47 at in addition to a conserved function, UL37 homologs also have divergent virus-specific functions.

48 These results solidify Hrq1 as a true RecQ4 homolog and position it as the premier model to determin

49 th the trimming ability of the fungal Hsp104 homolog and the strength of the [PSI(+)] variant: the gr

50 Gram-positive S. aureus lacks an RMF homolog and the structural basis for its 100S formation

51 greater the trimming activity of the Hsp104 homolog and the weaker the variant, the greater the curi

52 Therefore, we cloned the maize Tel2 and Tti1 homologs and showed that TEL2 can interact with both TTI

53 However, PN_LNC_N13-like homologs and/or its derived sRNAs showed overall a highe

54 ), RAB5A, VPS35 (vacuolar protein sorting 35 homolog), and M6PR (mannose 6-phosphate receptor) blocke

55 genes, including 292 disease resistance gene homologs, and nine genes determining essential oil chara

56 Y5 in monocots; however, AtHYH (HY5 homolog) homologs are absent in the monocots analyzed.

57 t prediction regardless of how many sequence homologs are available for proteins in question.

58 Whether IPSE homologs are expressed in other schistosome species has

59 All three GLXI homologs are functional in vivo, as they complemented a

60 e sought to determine if KSHV and MHV68 LANA homologs are functionally interchangeable.

61 d motif analyses indicated that XND1 and its homologs are present only in angiosperms and possess a h

62 while their Saccharomyces cerevisiae (yeast) homologs are stable components of U1 snRNP.

63 superfamily of methyltransferases, and Trm10 homologs are widely conserved throughout Eukarya and Arc

64 suppressor gene PTEN (phosphatase and tensin homolog) are frequent events and are associated with the

65 Deficiency in its homolog ARID1B is synthetically lethal with ARID1A mutat

66 a murine model of MS, thus implicating both homologs as copathogenic contributors.

67 e identified jun-1 (JUN transcription factor homolog) as a novel target of cel-mir-237.

68 tol phosphatase PTEN (phosphatase and tensin homolog) as primarily responsible for defects in B lymph

69 romophore rapidly deprotonates to the Asp-85 homolog, as in BR.

70 WASP homolog associated with actin, membranes, and microtubul

71 e kinase v-RAF murine sarcoma viral oncogene homolog B (BRAF(V600E)), oncogenic signaling enhances gl

72 The closely related homolog beta-synuclein (betaS) is essentially fibril-res

73 t betaCAs and includes the identification of homologs between species using phylogenetic approaches,

74 In contrast to previously characterized homologs, both of these proteins show closed pores at bo

75 of the GtCCR2 SB occurs not from the Asp-96 homolog, but by proton return from the earlier protonate

76 nhances covalent flavinylation of Complex II homologs, but the mechanisms underlying the covalent att

77 questered outside the nucleus by the IkappaB homolog Cactus.

78 At the same time, HSV and PRV homologs cannot be swapped, which suggests that in addit

79 itionally, gymnosperms and ferns share a CMT homolog closely related to CMT2 and 3.

80 Mammalian autophagy-related 8 (Atg8) homologs consist of LC3 proteins and GABARAPs, all of wh

81 cular functions, including how the mammalian homologs Cripto-1 and Cryptic recognize and regulate TGF

82 xpression level of RESPIRATORY BURST OXIDASE HOMOLOG D (RbohD).

83 phage migration inhibitory factor (MIF), its homolog D-dopachrome tautomerase (D-DT), and their commo

84 vely regulated by the phosphatase and tensin homolog DAF-18/PTEN.

85 rate that depletion of the single Drosophila homolog dBRWD3 results in altered gene expression and ab

86 the loss of LKB1 and phosphatase and tensin homolog deleted on chromosome 10 (PTEN) induces activati

87 the tumor suppressor, phosphatase and tensin homolog deleted on chromosome 10 (PTEN), alters the inva

88 one-helix proteins and their cyanobacterial homologs designated high-light-inducible proteins.

89 y and functionally closely related GalNAc-T3 homolog did not show compensatory functionality for effe

90 one of the miRNA mutants on the NF-kappaBeta homolog Dif.

91 ison of the two structures reveals that UL37 homologs differ in their overall shapes, distributions o

92 by the phylogenetically conserved Doublesex homolog dmd-3, which is both required and sufficient for

93 mpletion of crossover (CO) formation between homologs during meiosis I.

94 Here we show that knockdown of EAF2 or its homolog EAF1 sensitized prostate cancer cells to DNA dam

95 or (HER3/ERBB3) and its catalytically active homologs EGFR and HER2 are essential for their signaling

96 angiogenic potential of EMC10 and its mouse homolog (Emc10) in cultured endothelial cells and infarc

97 to the evolutionary functional divergence of homolog-encoded proteins.

98 cific to eutherian mammals because no direct homologs exist at the syntenic genomic locus in metather

99 ripts encoding the Respiratory Burst Oxidase Homolog F, signaling components involved in ethylene and

100 romotes the expression and activation of Ras homolog family member A (RhoA) and subsequent activation

101 ed to the activation of the small GTPase Ras homolog family member A (RhoA) by the Galpha12/13 pathwa

102 Here, we show that knocking out the Ras homolog family member A (RhoA) gene in normal fibroblast

103 FASTK, the founding member and its homologs FASTKD1-5 are architecturally related RNA-bindi

104 mponents (PotA, PotB, PotC, and PotD), while homologs for polyamine biosynthesis were conspicuously a

105 ing conformations of a glutamate transporter homolog from archaebacterium Pyrococcus horikoshii, sodi

106 We purified R.PabI homologs from Campylobacter coli (R.CcoLI) and Helicobac

107 es in their DNA-binding domains (DBDs), LANA homologs from Kaposi sarcoma-associated herpesvirus (KSH

108 Studies of UL37 homologs from two alphaherpesviruses, herpes simplex vir

109 etic Z-rings formed by the bacterial tubulin homolog FtsZ, and the stabilization of the newly formed

110 sion correlates with increased levels of Ras homolog gene family, member A (RhoA), a KCTD13/CUL3 ubiq

111 s, we created domain swaps between the close homologs Gpa2 and Rx1, which confer resistance in potato

112 c Hsp90 homologs, whereas organellular Hsp90 homologs (Grp94 and TRAP1) are relatively insensitive to

113 While TRC35 and its fungal homolog, guided entry of tail-anchored protein 4 (Get4),

114 Furthermore, only one beta-glucosidase 12 homolog has been characterized so far.

115 ously found in eukaryotes but no prokaryotic homolog has been characterized.

116 r, the functional relationship between these homologs has not been explored.

117 LeuT, a thermostable eubacterial NSS homolog, has been exploited as a model protein for NSS m

118 We find that Esrp homologs have been independently recruited for the devel

119 mmalian cells to show that these two EGF-CFC homologs have distinct, highly specific ligand binding a

120 s and functional analyses of the human H2-Ob homolog, HLA-DOB, revealed both loss- and gain-of-functi

121 gs of AtHY5 in monocots; however, AtHYH (HY5 homolog) homologs are absent in the monocots analyzed.

122 t that overexpression of cel-mir-237 and its homolog, hsa-miR-125b, functions as sensitizers to gamma

123 teasome itself, these include the proteasome homolog HslV, which functions together with the AAA+ Hsl

124 Out of the three homologs identified in rice (Oryza sativa), we have func

125 nown tumor necrosis factor (TNF) superfamily homolog in Drosophila, Coxiella-infected flies exhibit r

126 The Pik1 homolog in mammals, PI4KIIIbeta, interacted preferential

127 Deletion of the homolog in the filamentous ascomycete Neurospora crassa

128 In this study, we identified another OxyR homolog in V. cholerae, which we named OxyR2, and we ren

129 h a potential role in root development, DRO1 homologs in Arabidopsis and peach showed root-specific e

130 the SM regulator laeA, and deletion of mcrA homologs in Aspergillus terreus and Penicillum canescens

131 is of exons regulated by ancient CELF family homologs in chicken, Drosophila, and Caenorhabditis eleg

132 We have identified and characterized new ACR homologs in different cryptophyte species, showing that

133 evealed five glutamine amidotransferase-QueC homologs in Enterobacteria and Pseudomonas phage, and di

134 We further identified CISD3 homologs in fungi that were previously reported not to c

135 survey of the wealth of information on human homologs in model organisms across numerous databases.

136 obacteria and Pseudomonas phage, and distant homologs in other phage and bacterial genomes, suggestin

137 not manifest the in vitro phenotypes of its homologs in other streptococcal species.

138 0% of the viral genes do not have detectable homologs in public databases.

139 ly conserved and divergent functions of LANA homologs in Rhadinovirus infection and disease.

140 rd targets that lack sequence and structural homologs in the databases.

141 (rRNA) and 34 proteins, including 14 without homologs in the evolutionarily related bacterial ribosom

142 protein interacts with P. blakesleeanus Ras homologs in yeast two-hybrid assays, indicating that Mad

143 Antisense knockdown of NR4A2 and NR4A3 homologs in zebrafish larvae significantly reduces the a

144 and large body size associated with 16p11.2 homologs in zebrafish.

145 and mechanics of the pectoral fins, forelimb homologs, in the fish family Labridae.

146 w fold and only 0.3L-2.3L effective sequence homologs, including one beta protein of 182 residues, on

147 Trithorax-group proteins and their mammalian homologs, including those in BAF (mSWI/SNF) complexes, a

148 efect caused by mutation of the nematode RD3 homolog is suppressed in vivo by mutation of key compone

149 contacts for proteins without many sequence homologs is still of low quality and not very useful for

150 hemotaxis by c-di-GMP through MapZ orthologs/homologs is widespread in proteobacteria and that the us

151 K-Ras (Kirsten-rat sarcoma viral oncogene homolog) is a prominent oncogene that has been proven to

152 This asymmetry, unobserved in other Hsp90 homologs, is due to buckling of one of the protomers and

153 es proteins in the nucleus and cytoplasm, in homolog juxtaposition and crossing over.

154 compared Kirsten rat sarcoma viral oncogene homolog (KRAS) mutations in pancreatic CTC and correspon

155 ether the Kirsten rat sarcoma viral oncogene homolog (KRAS)-variant, a germline mutation in a microRN

156 dimeric structure resolved for the bacterial homolog, LeuT, presumably because of a kink at TM12 prev

157 ir (Ant-21) increased phosphatase and tensin homolog levels.

158 cell differentiation and, together with its homolog LRF, supports CD4(+) T cell helper effector resp

159 ologues to the Saccharomyces cerevisiae GSK3 homolog MCK1.

160 Here we show that the YcgR homolog MotI (formerly DgrA) of Bacillus subtilis inhibi

161 ue to single amino acid changes in the actin homolog MreB.

162 tes the human receptor MRGPRX1 and the mouse homolog MrgprC11, implicated previously in itch.

163 Compared to its homolog, Ndt80, MyRF has a smaller and less complex DBD

164 imordial germ cells (PGCs) lacking the nanos homologs nos-1 and nos-2 in C. elegans.

165 of succinyl-CoA, which is a close structural homolog of (2S)-methylsuccinyl-CoA and an essential inte

166 falciparum and Toxoplasma gondii is FtsH1, a homolog of a bacterial membrane AAA+ metalloprotease.

167 Plants with mutations in a homolog of an Arabidopsis (Arabidopsis thaliana) boron e

168 we investigated whether Appl, the Drosophila homolog of App, could influence sleep-wake regulation wh

169 ifically, we show that CUA-1, the C. elegans homolog of ATP7A/B, localizes to lysosome-like organelle

170 In other cell types, Munc13 (mammalian homolog of Caenorhabditis elegans uncoordinated gene 13)

171 In this study, we focus on a close homolog of Cdc42, TC10 (also known as RhoQ), and investi

172 The vaccinia virus B1 protein is a homolog of cellular vaccinia virus-related kinases (VRKs

173 We demonstrate that CKS1 is a functional homolog of CKS1/SUC1 and can physically interact with th

174 ria but are also present in ATP7B, the human homolog of copA, and direct ribosomal frameshifting in v

175 d NGO0176), a two-component system that is a homolog of CpxRA.

176 domain 5 with a synthesized exon encoding a homolog of hCD163L1 SRCR domain 8.

177 P. aeruginosa GroEL, a homolog of heat shock protein 60, was identified as one

178 se data strongly suggest that MRV is a mouse homolog of HHV-6A, HHV-6B, and HHV-7.IMPORTANCE Herein w

179 As miR-237 is the homolog of human miR-125, we validated our findings in M

180 Deletion of the mammalian homolog of Indy (mIndy, Slc13a5) encoding for a plasma m

181 ng potential new biomarkers, a P. falciparum homolog of insulin-degrading enzyme (PfIDEh) met our sea

182 y up-regulating expression of the Drosophila homolog of lactate dehydrogenase (dLdh).

183 study shows that mutations of HRPU-2, a worm homolog of mammalian hnRNP U, result in dysfunction of a

184 Here we show that Drosophila Kenny, the homolog of mammalian IKKgamma, is a selective autophagy

185 ole in regulating the expression of SLO-2 (a homolog of mammalian Slo2) in Caenorhabditis elegans Los

186 Because mutations of MIB1, the homolog of MIB2, have been found in patients with left v

187 In addition, we show that the mammalian homolog of mRNA-cap, RNGTT, can replace mRNA-cap to play

188 e show that Myoglianin (MYO), the Drosophila homolog of myostatin and GDF11, regulates not only body

189 Octopamine (OA), the insect homolog of NE, is known to promote both arousal and aggr

190 Dorsal, a Drosophila homolog of NF-kappaB, patterns the dorsal-ventral axis i

191 of this motif with critical residues in the homolog of other Helicobacter gastric pathogens.

192 A homolog of PEX5, tetratricopeptide repeat-containing Rab

193 the ETS domain of Ets-1, a close structural homolog of PU.1, 2:1 complex formation may represent an

194 F element-encoded protein TraR is a distant homolog of the chromosome-encoded transcription factor D

195 E. histolytica encodes a homolog of the human cytokine macrophage migration inhib

196 in more detail, we focused on Cindr, the fly homolog of the human NS gene CD2AP.

197 Here, we show that a homolog of the human retinal dystrophy gene Retinal Dege

198 lateral tuberal nucleus (NLT), the putative homolog of the mammalian arcuate nucleus.

199 Here, we identify Fft3, a fission yeast homolog of the mammalian SMARCAD1 SNF2 chromatin remodel

200 a pseudoenzyme PDX1.2 that is a noncatalytic homolog of the PDX1 subunit of the vitamin B6 biosynthes

201 They can therefore be viewed as the rat homolog of the primate anterior limb of the internal cap

202 tors, we identified RPAP2 IYO Mate (RIMA), a homolog of yeast and human proteins linked to nuclear im

203 eins, whereas CBH-2 depends on the N. crassa homolog of yeast Erv29p.

204 work (TGN) depends on ECHIDNA (ECH), a plant homolog of yeast Triacylglycerol lipase (TLG2/SYP4) inte

205 Here we show in mouse that ZFP804A, the homolog of ZNF804A, is required for normal progenitor pr

206 Two homologs of APP exist in mammals: the APP like proteins

207 Homologs of Aquifex RNase P (HARP) were identified in ma

208 functional analysis of two maize (Zea mays) homologs of At-NPF6.3 (Zm-NPF6.6 and Zm-NPF6.4) showed t

209 d phylogenetic analysis, we identified three homologs of AtHY5 in monocots; however, AtHYH (HY5 homol

210 LanC-like (LanCL) proteins are mammalian homologs of bacterial LanC enzymes, which catalyze the a

211 While the AR9 nvRNAP does not contain homologs of bacterial RNAP alpha subunits, it contains,

212 both in shared expression patterns of wheat homologs of Brachypodium genes and functional overlap re

213 We examined the roles of 2 homologs of Calcineurin A, CanA14F, and Pp2B in the Dros

214 We identified homologs of DICER-LIKE (DCL), ARGONAUTE (AGO), and other

215 e found that three pathways that include the homologs of Drosophila Dys, Trio, and Shot were downregu

216 Homologs of each gene have been implicated in pollen dev

217 thaliana, the GLX system is encoded by three homologs of GLXI and three homologs of GLXII, from which

218 encoded by three homologs of GLXI and three homologs of GLXII, from which several predicted GLXI and

219 Each of the three human homologs of HP1 includes a chromoshadow domain (CSD).

220 We identified homologs of key RNAi genes in the genomes of some of the

221 because its genome encodes a single TLR and homologs of many downstream signaling components, includ

222 Importantly, in vivo analyses of the homologs of RBPJ and L3MBTL3 in Drosophila melanogaster

223 lants, we have characterized the Arabidopsis homologs of SEIPIN proteins, which are crucial factors f

224 (SLs) that are predicted to form in MYB33/65 homologs of species as evolutionary distant as gymnosper

225 dopsis (Arabidopsis thaliana) genome encodes homologs of the Guided Entry of Tail (GET)-anchored prot

226 these loci colocalize with the B. distachyon homologs of the major flowering pathway genes VRN2 and F

227 carbohydrate binding module (CBM48) and are homologs of the PROTEIN TARGETING TO STARCH (PTST) prote

228 elated sequence has been added to the model, homologs of the unrelated sequence will also produce hig

229 tion of wheat, we functionally characterized homologs of the VACUOLAR IRON TRANSPORTER (VIT).

230 endent 5-oxoprolinase; most prokaryotes lack homologs of this enzyme (and the gamma-glutamyl cycle) b

231 haracterization of novel phages that possess homologs of this GTA's structural and regulatory genes h

232 to possess the RNase A superfamily fold, and homologs of this toxin are associated with secretion sys

233 Human homologs of top-ranked hits protected against alphaSyn-i

234 This pseudogene was flanked by C. porcellus homologs of two genes, FBXO3 and ORF91, a relationship a

235 ve transfer of rabbit IgG against the murine homologs of two immunodominant fragments in adult C57BL/

236 Homologs of Xpp1 are found among a broad range of fungi,

237 No structural homologs or high-resolution structure exists for the TP

238 omozygous diploids, the presence of multiple homologs or homeologs in polyploids affords greater tole

239 light, suggesting redundancy with other ELF3 homologs or possibly an alternative mode of action for t

240 h is regulated to ensure at least one CO per homolog pair.

241 n this well-studied model, it is unclear how homolog pairing in diploids or environmental conditions

242 Of note, we observed that GacI homologs perform a similar function in Streptococcus aga

243 Meiotic synapsis and recombination between homologs permits the formation of cross-overs that are e

244 9 residue encoded by hlh-8, the single Twist homolog present in Caenorhabditis elegans.

245 sing a polymer model, we observe significant homolog proximity that increases in saturated culture co

246 Loss of phosphatase and tensin homolog (PTEN) and activation of the PI3K/AKT signaling

247 th phosphorylation of phosphatase and tensin homolog (PTEN) at residues Ser380/Thr382/383.

248 Phosphatase and tensin homolog (PTEN) negatively regulates downstream protein k

249 find here, using the phosphatase and tensin homolog (PTEN) pseudogene as a model system, that antise

250 ion, higher levels of phosphatase and tensin homolog (PTEN), and diminished Akt phosphorylation.

251 umor-suppressor genes phosphatase and tensin homolog (PTEN), cyclin dependent kinase inhibitor 2A (CD

252 diated degradation of phosphatase and tensin homolog (PTEN), which impaired intercellular junction fo

253 ndrial damage induces Phosphatase and Tensin Homolog (PTEN)-induced Putative Kinase 1 (PINK1) and Par

254 lization, we define a phosphatase and tensin homolog (PTEN)-regulated checkpoint that retains deltaR

255 The Escherichia coli Complex II homolog quinol:fumarate reductase (QFR, FrdABCD) catalyz

256 Here, we show that Akt activation by a Ras homolog, R-Ras, stabilizes the microtubule cytoskeleton

257 ion (GHaPrP) and its less susceptible rabbit homolog (RaPrP).

258 g Mmp2 and Oamb can be replaced by its human homolog Ras-responsive element-binding protein 1 (RREB-1

259 known function included transcription factor homologs related to oxidative stress by 3D-homology mode

260 ein Imd leads to activation of the NF-kappaB homolog Relish and robust antimicrobial peptide gene exp

261 he Arabidopsis uORF and its maize (Zea mays) homolog repressed the translation of the main open readi

262 s2t6A and ct6A by depletion of tcdA and mtaB homologs, respectively, demonstrating that TcdA and MtaB

263 face, enabling activation of mTOR by the Ras homolog Rheb.

264 NEET proteins, and revealed that plants lack homolog(s) of CISD3.

265 ain specificity of antibodies was studied by homolog-scanning mutagenesis (HSM) with single human dom

266 n is released on the chromatid arms when the homologs segregate at anaphase I.

267 ly crossovers, which are critical for proper homolog segregation in Meiosis I.

268 which creates genetic diversity and balances homolog segregation.

269 Although the two homologs share the same three-dimensional structure and

270 The least characterized homolog, ShcD, is robustly expressed in the developing a

271 Characterization of a dozen PriA homologs shows that these enzymes adapt from bifunctiona

272 n, Mer2 is required for pairing by mediating homolog spatial juxtaposition, with implications for cro

273 Clip domain serine protease homologs (SPHs) are positive and negative regulators of

274 cient oocytes that are severely defective in homolog synapsis.

275 velopment and is less characterized than its homolog Tau, which has various roles in neurodegeneratio

276 rs Drosophila melanogaster Yan and its human homolog TEL/ETV6, can polymerize.

277 ein we show that mftE encodes a creatininase homolog that catalyzes cleavage of the oxidatively decar

278 tal structures of BjaI, a CoA-dependent LuxI homolog that represent views of enzyme complexes that ex

279 lost, resulting in an elevated frequency of homologs that do not receive a crossover, which in turn

280 of plant R-proteins, animal NLRs, and their homologs that represent the NB-ARC (nucleotide-binding a

281 N-terminal domain homologs, the helical carotenoid proteins (HCPs), have b

282 HFR-TS3) operates as an inhibitor of its two homologs, thus regulating DHFR and TS activities and, as

283 nel to cations in GtCCR2 requires the Asp-96 homolog to be unprotonated, as has been proposed for the

284 n (Ubqn), the ubiquitin receptor whose human homolog ubiquilin 2 is associated with familial amyotrop

285 Drosophila, amorphic mutations in the KIF1A homolog unc-104 disrupt the formation of mature boutons.

286 VASH1 and its homolog VASH2, when complexed with SVBP, exhibited robus

287 Here we show that the C. elegans VAP homolog VPR-1 is essential for gonad development.

288 reted MSPds derived from the C. elegans VAPB homolog VPR-1 promote mitochondrial localization to acti

289 DANT1 (TBA1) to TBA3; a less abundant fourth homolog was named TBA-LIKE (TBAL).

290 of the miR-21 target phosphatase and tensin homolog was reduced.

291 language region extended to right-hemisphere homologs was positively associated with the time elapsed

292 While induction of FLOWERING LOCUS T homologs was very early in ICCV 96029, an analysis of ci

293 ls between use-dependent and use-independent homologs, we have determined the molecular basis that un

294 Using a dataset that only contains remote homologs, we have shown that WSeqKernel performs remarka

295 PstSCR1 homologs were found to be conserved in Pst, and in its c

296 g ATPase inhibitor of cytosol-specific Hsp90 homologs, whereas organellular Hsp90 homologs (Grp94 and

297 r secondary structure prediction of multiple homologs, whereby the mapping data benefits not only the

298 c pathways dependent on the C. elegans PINK1 homolog, which is necessary for cellular resistance to c

299 modifiers have functionally-similar X-linked homologs whose deficiency is involved in ccRCC progressi

300 ariation at sector positions can distinguish homologs with a conserved dynamic pattern and optimal ca