ライフサイエンスコーパス: homolog

1 structural information obtained from a SLC16 homolog.

2 raction is conserved in Salvador's mammalian homolog.

3 e first known alphaherpesvirus-encoded Bcl-2 homolog.

4 by a null mutation in the single worm lamin homolog.

5 d to the dynamic behavior of FtsZ, a tubulin homolog.

6 eukaryotic enzymes but absent in the E. coli homolog.

7 ity among a sampling of plant pathogen Cdc14 homologs.

8 ry conservation and variant frequency across homologs.

9 while EcLsi2 and EcLsi3 form another pair of homologs.

10 ed to the localization of the other two BADC homologs.

11 model and two acetylcholine-binding protein homologs.

12 system that has both eukaryotic and archaea homologs.

13 ediction using conservation information from homologs.

14 of the rapidly growing number of identified homologs.

15 e structural flexibility than nonmetamorphic homologs.

16 els of crossovers and non-crossovers between homologs.

17 of FIT in concert with ILR3 and its closest homologs.

18 family zinc finger 1 (Gli1) or achaete-scute homolog 1 (Ascl1).

19 itotic exit mediated by APC/C bound to CDC20 homolog 1 (CDH1).

20 ice, and found that miRNAs of the delta-like homolog 1 (Dlk1)-deiodinase iodothyronine type III (Dio3

21 e frontal cortex, derived from Homer protein homolog 1 (HOMER1), is significantly reduced in both the

22 investigated the role of protein diaphanous homolog 1 (known as Diaph1 or mDia1) for the myofibrobla

23 1 (PD-L1) and mismatch repair proteins MutL homolog 1 (MLH1), MutS homolog 2 (MSH2), MSH6, and PMS1

24 s via inhibition of DNA repair protein RAD51 homolog 1 (RAD51).

25 to the promoter of RESPIRATORY BURST OXIDASE HOMOLOG 1 (RBOH1), and that RBOH1-mediated ROS promote p

26 Whether truncated glioma-associated oncogene homolog 1 (TGLI1), a transcription factor known to promo

27 r hairy and enhancer of split 1:mouse atonal homolog 1 ratio in ilea from Msi1-overexpressing mice im

28 ma signaling protein, SOS1 (Son of sevenless homolog 1), in DCM pathogenesis.

29 with the BMP-mothers against decapentaplegic homolog 1/5/8 (SMAD1/5/8) pathway.

30 nist of the nuclear receptors liver receptor homolog-1 (LRH-1) and steroidogenic factor-1 (SF-1).

31 d histone methyltransferase enhancer of zest homolog 2 (EZH2) and specifically causes EZH2 degradatio

32 Enhancer of zeste homolog 2 (EZH2) is the catalytic subunit of polycomb re

33 tumor and immune cells of enhancer of zeste homolog 2 (EZH2), the catalytic subunit of polycomb repr

34 repair proteins MutL homolog 1 (MLH1), MutS homolog 2 (MSH2), MSH6, and PMS1 homolog, mismatch repai

35 outer membrane protein mitochondrial carrier homolog 2 (MTCH2).

36 1 (HDAC11) and suppressor of variegation 3-9 homolog 2 (SUV39H2), key histone-modifying enzymes invol

37 that in OCSC, the tumor suppressor disabled homolog 2-interacting protein (DAB2IP) is silenced by EZ

38 osphorylated mothers against decapentaplegic homolog 2/SMAD2, suggesting transforming growth factor-b

39 avian erythroblastic leukemia viral oncogene homolog 3 (ERBB3) receptor kinase.

40 de repeats (EMAST) show reduced nuclear MutS homolog 3 (MSH3) expression with surrounding inflammatio

41 P5-125 (dPspCas13b) to m6A demethylase AlkB homolog 5 (ALKBH5).

42 Alkb homolog 7 (ALKBH7) is a mitochondrial alpha-ketoglutarat

43 RL increased mothers against decapentaplegic homolog 7 (SMAD7) in CD34(+)PRLR(+) myeloid cells, which

44 binding site for two COPII components, SEC31 homolog A COPII coat complex component (SEC31) and SEC23

45 e migration inhibitory factor (MIF) cytokine homolog, a virulence factor linked to severe disease.

46 ost native genes but contains intact foreign homologs acquired from legume host plants.

47 The serine/threonine protein kinase v-AKT homologs (AKTs), are implicated in typical and atypical

48 e determined the structure of a close BotCYP homolog and used our data to conduct the first large-sca

49 ween the isolates lack Plasmodium falciparum homologs and are predicted to be involved in host-parasi

50 loss of CL triggering rapid turnover of MCU homologs and impaired calcium transport.

51 lobal unfolding canonically executed by ClpX homologs and provides insight into how substrate-chapero

52 ER-resident protein with no known structural homologs and unclear ER function.

53 P sequences are also identified in other CAX homologs and/or Ca(2+) transporters, including the mamma

54 different course from those of their rhodium homologs, and even allow performing otherwise inviable t

55 e chicken Chd7 gene and its human and murine homologs, and we show that let-7g overexpression in mice

56 Fhb7 GST homologs are absent in plants, and our evidence supports

57 MISTR homologs are also found in plants, yeasts, a fish virus,

58 ss different kingdoms shows that 29 plant TA homologs are clustered as a plant-specific TA clade in c

59 ering time pathways in many studies, and its homologs are found throughout the plant lineage.

60 If oocytes containing exchangeless homologs are selected against during meiosis, the incide

61 ic recombination, which is initiated between homologs at >200 sites originating from meiotic double-s

62 c and S. aureus strains encode multiple tsaI homologs at the tspA locus, suggestive of additional rol

63 B. burgdorferi has an FlhF homolog (BB0270).

64 The loss-of-function mutant of BIN2 and its homologs, bin2-3 bil1 bil2, displays abnormal chloroplas

65 RNA helicase bad response to refrigeration 2 homolog (BRR2) is required for the activation of the spl

66 residues that is conserved across arrestin-2 homologs, but absent in arrestin-3 that likely accounts

67 Release factor homolog C12orf65 (mtRF-R) and RNA binding protein C6orf2

68 ddition, B. burgdorferi encodes a second Lon homolog called Lon-1.

69 inding by plant high-light-inducible protein homologs, called ONE-HELIX PROTEINS (OHPs), is lacking.

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

71 reaks (DSBs) targeted by CRISPR-Cas9 to both homologs can stimulate IHR and associated copy-neutral l

72 molecular level and expanded to higher-order homolog carbenes such as butadiynylcyclopropenylidene an

73 The DsbD functional homolog CcdA is a six-TM-helix membrane protein that pro

74 izzy-related protein (Fzr) and its mammalian homolog Cdh1 function as key regulators of endoreplicati

75 Further, we identify the archaeal ESCRT-III homolog, CdvB, as a key target of the proteasome and sho

76 Drosophila, nephrocytes with reduced filamin homolog Cher displayed altered filtration capacity, but

77 gen Pseudomonas aeruginosa contains two ClpP homologs: ClpP1 and ClpP2.

78 An Arabidopsis thaliana HglS homolog coexpresses with known lysine catabolism enzymes

79 unlike other shuttling factors, Ddi1 and its homologs contain a conserved helical domain (helical dom

80 A Ran binding protein (RanBP) homolog, CpRbp1, from Cryphonectria parasitica, has been

81 her identified the RESPIRATORY BURST OXIDASE HOMOLOG D (RBOHD) protein as a key player in mediating r

82 on initiation factor 4GI (eIF4GI) and of its homolog, death-associated protein 5 (DAP5), are elevated

83 tify disinhibition of phosphatase and tensin homolog deleted on chromosome 10 (PTEN), a negative PI3K

84 est that Ca(2+)/CaM sensitivity in CaMKII is homolog dependent and includes substantial contributions

85 specificity of Escherichia coli AlkB and its homologs, difficulties in assaying their repair activiti

86 s at unprotected forks are degraded by MRE11 homolog double-strand break repair nuclease (MRE11).

87 ctor 1A Y-linked, together with its X-linked homolog EIF1AX Evolutionary loss of a Y-linked microRNA

88 ly, it has been suggested that the bacterial homolog ELIC (Erwinia chrysanthemi ligand-gated ion chan

89 edback loop that inhibits DSB formation when homologs engage one another.

90 , what chromosomal process is recognized as "homolog engagement" remains unclear.

91 Growth factors activate Ras homolog enriched in brain (Rheb), which in turn activate

92 Ras homolog enriched in brain, an mTOR activator, rescued th

93 esponds to nitrogen levels through RelA-SpoT homolog enzymes, detecting glutamine concentration using

94 Recent studies suggest that a dynamin-homolog, Eps15 homology domain protein 1, catalyzes fiss

95 It also requires enhancer of rudimentary homolog (ERH), which copurifies with Microprocessor and

96 (NS1) is a WUSCHEL-related homeobox3 (WOX3) homolog expressed at the margins of leaf primordia, and

97 and activated) and chemoattractant receptor homolog expressed on Th2 cells (CRTH2)-expressing CD4(+)

98 Mutations in eyes shut homolog (EYS), a secreted extracellular matrix protein c

99 expression in the presence of activated Ras homolog family member A (RhoA) induces precocious polari

100 with the GTPase-signaling small molecule ras homolog family member A (RhoA).

101 in the constitutive activation of RhoA (ras homolog family member A) and impaired flow-induced endot

102 species, but is always lower than the Omp85 homolog, FhaC.

103 ral and biochemical analysis of Oryza sativa homolog FLO7 reveals identical activity to HglS despite

104 teins were compared with their EBOV and MARV homologs for innate immune pathway modulation.

105 Unlike other bacterial GLUT homologs (for example, XylE), GlcP(Se) has a loose H(+)/

106 A BafA homolog from a related pathogen, Bartonella quintana, is

107 Here we show that SG7.AF, the albicin homolog from An. freeborni, has a similar potency to alb

108 a(2+) "mini-sensor" in YfkE, a bacterial CAX homolog from Bacillus subtilis.

109 restingly, bioinformatics analysis of PMEL17 homologs from other mammals uncovered that long and shor

110 ved already described interactions shared by homologs from other T4SSs as well as new and described i

111 tion, and Kirsten rat sarcoma viral oncogene homolog gene (KRAS) mutation.

112 ERK1/2 phosphorylation and activation of Ras homolog gene family member A.

113 abetes-increased semaphorin 6A (SEMA6A); Ras homolog gene family, member A (RhoA); phosphatase and te

114 However, NmU homologs have been elusive in Mollusca, the second large

115 ls because these cells express the cortactin homolog hematopoietic cell-specific lyn substrate-1.

116 receptor (EGFR) family (EGFR1-4 or the human homologs HER1-4).

117 lted in the identification of the fused toes homolog-Hook-FHIP (FHF) complex as a novel AP-4 accessor

118 The specific functions of these homologs, however, are largely elusive.

119 coeruleus, inferior and superior colliculus homologs, hypothalamus, preoptic area, septum, nucleus o

120 onserved in other herpesviral protein kinase homologs.IMPORTANCE Viral infection dramatically changes

121 e identification of a possible mushroom body homolog in Brachyura as problematic.

122 Plasmodium berghei Yop1 (PbYop1) is a REEP5 homolog in Plasmodium.

123 a Saccharomyces cerevisiae Cdc28/Pho85-like homolog in Symbiodiniaceae.

124 Although there is no GNP1 homolog in the tea plant, we assessed the theanine trans

125 the LH language network but also in their RH homologs in all of the youngest children (ages 4 through

126 oration of LRO function and carboxylesterase homologs in C. elegans and other animals may reveal addi

127 A proliferation of H-NS homologs in Erwiniaceae includes the first observation o

128 accharomyces cerevisiae protein Ddi1 and its homologs in higher eukaryotes have been proposed to serv

129 Finally, we identify AcrIIA1(NTD) homologs in other Firmicutes and demonstrate that they h

130 the retention of CENP-T and additional CCAN homologs in other independently derived CenH3-deficient

131 ropose that redox regulation evolved in FN3K homologs in response to changing cellular redox conditio

132 This study identified three BiP homologs in the Solanum tuberosum (potato) genome using

133 In Drosophila, the Gsx homolog, Ind, similarly represses or stimulates transcri

134 fferences, with a preponderance of MLH1-less homologs involving chromosomes 21 or 22.

135 eiotic pairing between parental chromosomes (homologs) is required for formation of haploid gametes.

136 mor suppressor, PTEN (phosphatase and tensin homolog), is well studied in endometrial cancer, recent

137 served in staphyloccocal OatA and most other homologs, is not present in the previously characterized

138 structure and mechanism of the closest KWL1 homolog, KWL1-b (ZEAMA_GRMZM2G305329).

139 that R-spondin-2, the ligand of Lgr5 and its homologs Lgr4/6 and stem-cell-expressed E3 ligases Rnf43

140 r, in vertebrates, little is known about its homolog Llgl1.

141 We find that human JPX and its mouse homolog, lncRNA Jpx, have deep divergence in their nucle

142 Phosphatase and tensin homolog located on chromosome 10 (PTEN) is a tumor suppr

143 suggest that the mammalian TSP-12 and TSP-14 homologs may also function in regulating transmembrane p

144 t tumors had increased synthesis of the MCT1 homolog MCT4/SLC16A, a known resistance factor to MCT1 i

145 study provides the first evidence of ARF6/8 homolog-mediated petal development outside the core eudi

146 MLH1), MutS homolog 2 (MSH2), MSH6, and PMS1 homolog, mismatch repair system component 2 (PMS2) was p

147 mono-methyltransferase Trr and its mammalian homologs, MLL3/4, cause only minor changes in gene expre

148 MRAP2 and its homolog MRAP1 have an unusual membrane topology and are

149 ular motors to transport the bacterial actin homolog MreB and the Rod PG synthesis complexes away fro

150 nterpart of the cell shape-determining actin homolog MreB in cell elongation.

151 y sigma(I)-dependent upregulation of an MreB homolog, MreBH, which localizes the LytE autolysin to th

152 In Arabidopsis thaliana, the METTL3 homolog, mRNA adenosine methylase (MTA) introduces N (6)

153 ing molecules, which can be detected by MutS homolog (MSH) mismatch repair protein heterodimers.

154 More recently, we have studied the mouse homolog, mWAKE/ANKFN1, and our data suggest that its bas

155 domains between UNC-89 and its two mammalian homologs, obscurin and SPEG: kinase, a non-domain region

156 erentiating the kinetic parameters in pMHCII homologs, observing that peptide interactions throughout

157 e self-assembling monomer, a bridge-expanded homolog of [2.2]paracyclophane-4,7,12,15-tetracarboxamid

158 As in mice, an X-linked homolog of a bull Y-amplified gene has become testis-spe

159 Its activity is further enhanced by CpeZ (a homolog of a chaperone-like protein first characterized

160 Mutants lacking KIN-29, the C. elegans homolog of a mammalian Salt-Inducible Kinase (SIK) that

161 e contains a gene coding for a DNA-modifying homolog of a tRNA-deazapurine modification enzyme, toget

162 ls that TALP-3 coordinates with ANKR-26, the homolog of ANKRD26, to orchestrate proper cilia gating.

163 interacts with the citrus protein CsACD2, a homolog of Arabidopsis (Arabidopsis thaliana) ACCELERATE

164 ting the T(RM)-defining transcription factor homolog of Blimp-1 in T cells (Hobit) to fate map the T(

165 crease in language activation only in the RH homolog of Broca's area.

166 a novel role for the enzymatically inactive homolog of CASP8, the long isoform of cellular FLICE-lik

167 Loss of Cdk8, the fly homolog of CDK19, causes larval lethality, which is supp

168 e human FXR) with upregulation of ech-1.1 (a homolog of enoyl-CoA hydratase involved in fatty acid be

169 that the V. cholerae gene VC2714, encoding a homolog of Escherichia coli OmpR, was a virulence repres

170 Molluscum contagiosum virus contains a homolog of F13L termed MC021L.

171 ologs of EV-specific proteins, including the homolog of F13L, MC021L.

172 omplex with key gating component DYF-19, the homolog of FBF1.

173 Using rodent hepacivirus (RHV), a homolog of HCV that shares many characteristics of HCV i

174 la, we found that decapentaplegic (dpp), the homolog of human bone morphogenetic proteins BMP2 and BM

175 KSHV viral interleukin-6 (vIL-6) is a viral homolog of human IL-6 (hIL-6) that is expressed in KSHV-

176 or histocompatibility complex (MHC), a mouse homolog of human leukocyte antigen-E (HLA-E), inhibits a

177 ed by ectromelia virus and that is the mouse homolog of human smallpox.

178 UNC-104 is the Caenorhabditis elegans homolog of kinesin-3 KIF1A known for its fast shuffling

179 Cell adhesion molecule close homolog of L1 (CHL1) and the dopamine receptor D2 (DRD2)

180 SYD-2 is the homolog of liprin-alpha in C. elegans known to activate

181 ting that Drosophila Adar, despite being the homolog of mammalian ADAR2, also has functions similar t

182 r from Pyrococcus horikoshii, is an archaeal homolog of mammalian membrane transport proteins-known a

183 (Myo), an Activin family member, and a close homolog of mammalian Myostatin (Mstn), is a muscle-deriv

184 us RNA interference (RNAi) factor ERI-6/7, a homolog of MOV10 helicase, a retrotransposon and retrovi

185 4-dependent RdDM represses the expression of HOMOLOG OF RPW8 4 (HR4) and alters its response to subme

186 Signaling is attenuated by a homolog of the AAA+ ATPase Pch2/TRIP13, which binds and

187 o sequence comparison, however, a functional homolog of the coreceptor Get2/CAML remained elusive.

188 We recently identified the Hrq1 helicase, a homolog of the disease-linked enzyme RecQ-like helicase

189 This process genetically requires FLD, a homolog of the H3K4 demethylase LSD1.

190 Here, we show that Drosophila mutants in the homolog of the human CYFIP1, a gene linked to autism and

191 fects were dependent on daf-12 (a functional homolog of the human FXR) with upregulation of ech-1.1 (

192 ransporter highly specific for glucose and a homolog of the human glucose transporters (GLUT, SLC2 fa

193 A potential homolog of the human receptor for 12-S-HETE, gpr31, is e

194 rhabditis elegans, we uncover that TALP-3, a homolog of the Joubert syndrome protein TALPID3, is a TF

195 odimeric ABC transporter TmrAB, a functional homolog of the transporter associated with antigen proce

196 BsYetJ is a bacterial homolog of transmembrane BAX inhibitor-1 motif-containin

197 the bacterial cell division protein FtsZ (a homolog of tubulin); 5) is competitive with paclitaxel f

198 The only barley homolog of wheat awn inhibitor gene B1, HORVU2Hr1G077570

199 ctivation of the eIF2alpha kinase CPC-3 (the homolog of yeast and mammalian GCN2), and rhythmic activ

200 e's ATP:proton ratio as 3:10 and revealing a homolog of yeast subunit f in the membrane region, which

201 s sufficient to explain the lack of detected homologs of a large number of lineage-specific genes in

202 ated by cell-autonomous function of the worm homologs of a NMDAR subunit and CaMKII.

203 C. elegans MALT-1 forms a complex with homologs of Act1 and IRAK and appears to function both a

204 on multiple alignments across vertebrates of homologs of AD-associated-genes.

205 of this regulatory scheme and carry hijacked homologs of AmrZ that repress CRISPR-Cas expression and

206 for its role in the lipidation of the human homologs of ATG8 (i.e., LC3 and homologs) on double memb

207 Several viruses encode homologs of cellular Bcl-2-proteins (vBcl-2) to inhibit

208 cation of a small molecule that targets both homologs of cGAS has been challenging.

209 e POU-homeodomain factors Pou2f1/Pou2f2, the homologs of Drosophila temporal identity factors nub/pdm

210 s predicted to encode several vaccinia virus homologs of EV-specific proteins, including the homolog

211 HLH121 also interacts with the three closest homologs of ILR3 (i.e., basic-helix-loop-helix 34 [bHLH3

212 es as well as proliferative cells expressing homologs of known mammalian stem cell markers.

213 of developmental control genes that include homologs of mammalian Zinc finger of the cerebellum and

214 am in C. elegans IMPORTANCE C. elegans lacks homologs of most mammalian pattern recognition receptors

215 However, homologs of NF-kappaB and many upstream signaling compon

216 Homologs of penicillin N effector genes cefD1 and cefD2

217 CGEP homologs of photosynthetic and nonphotosynthetic bacteri

218 The closest homologs of poxin exist in the genomes of insect viruses

219 Here, we focus on a pair of closely related homologs of the AUXIN RESPONSE FACTOR family, AqARF6 and

220 iana) and Oryza sativa revealed that several homologs of the candidates are differentially expressed

221 sects, have lost CenH3 while having retained homologs of the CCAN.

222 FA biosynthesis and suggest the existence of homologs of the enzymes identified here that could funct

223 s We find that M. smegmatis, which possesses homologs of the Escherichia coli uvrA, uvrB, and uvrC ge

224 We show that homologs of the identified protein-coding genes as well

225 roles for the kinases Cla4 and Ste20, yeast homologs of the mammalian PAK2 family, and the Ste11 MAP

226 MiR-371-373 are the human homologs of the mouse miR-290 family, which are the most

227 ble gene repertoire for predicted structural homologs of the neutralizing Ab MR78 that is specific to

228 Bacterial chaperones ClpB and DnaK, homologs of the respective eukaryotic heat shock protein

229 The insect homologs of vertebrate NmU are categorized as PRXamide f

230 in the gene encoding phosphatase and tensin homolog on chromosome ten (PTEN) are diagnosed with PTEN

231 of the human homologs of ATG8 (i.e., LC3 and homologs) on double membranes during autophagy as well a

232 asing the function of the C. elegans torsinA homolog, OOC-5, rescues the sterility and premature agin

233 encode tumor necrosis factor receptor (TNFR) homologs or viral TNFR (vTNFR).

234 Additionally, the rice NbP3IP homolog (OsP3IP) also mediated p3 degradation and intera

235 othesis: that lineage-specific genes do have homologs outside of the lineage that, even while evolvin

236 s DSB formation and biases repair of DSBs to homologs over sister chromatids.

237 psis thaliana) mitochondria contain four OXA homologs: OXA1a, OXA1b, OXA2a, and OXA2b.

238 selectively inhibited DNA binding by p53 and homologs p63/p73, but did not affect E2F1, TCF1, and c-M

239 coordination between DSB strand exchange and homolog pairing as a critical determinant for recombinat

240 Homolog pairing depends on recombination initiation via

241 netochores take on new functions that impact homolog pairing, recombination, and the orientation of k

242 Programmed death-1 homolog (PD-1H), a CD28/B7 family molecule, coinhibits T

243 falciparum reticulocyte binding-like protein homolog (PfRh) family of proteins play a pivotal role in

244 h good selectivity over the human functional homolog PIG-A.

245 hat Arabidopsis PLDgamma1, but not its close homologs PLDgamma2 and PLDgamma3, is specifically involv

246 antagonise apoptosis triggered by the dsRNA-homolog poly(I:C), however the exact mechanism by which

247 raphy mass spectrometry to search for the JH homologs present in the hemolymph of fourth instar nymph

248 n p53 (Tp53/p53)- and phosphatase and tensin homolog (PTEN) deficiencies, and combined p53- and PTEN-

249 GS12 associated with phosphatase and tension homolog (PTEN) via the PDZ domain to upregulate the phos

250 Expression of the phosphatase and tensin homolog (PTEN), which is one of the direct targets of mi

251 ily, member A (RhoA); phosphatase and tensin homolog (PTEN); and nuclear factor-kappaB (NF-kappaB).

252 The mammalian homolog, PUF60, also displays anti-inflammatory properti

253 in, we characterize Saccharomyces cerevisiae homologs Put6 and Put7 of MCUR1 as regulators of mitocho

254 syndrome group B (CSB) protein or its yeast homolog Rad26.

255 e, 1-aminocyclopropane-1-carboxylate oxidase homologs, receptor-like protein kinases were expressed a

256 an z scores did not improve in contralateral homolog regions for verb generation (from -2.7 +/- 0.54

257 netic analysis suggested that VvAHGD and its homologs represent a new aldehyde dehydrogenase (ALDH) f

258 6 trans-regulators (mammalian RPP25 and YBX2 homologs, respectively) as direct substrates in vitro.

259 of NCLDV metabolic genes and their cellular homologs reveals distinct clustering of viral sequences

260 However, how RqcH and its eukaryotic homologs (Rqc2 and NEMF), despite their relatively simpl

261 er stressful conditions, bacterial RelA-SpoT Homolog (RSH) enzymes synthesize the alarmone (p)ppGpp,

262 fluidic channels and compare it to the yeast homolog Sae2.

263 GCNA homologs Spartan (DVC-1) and Wss1 resolve DNA-protein cr

264 eases (HPs) and noncatalytic serine protease homologs (SPHs) and inhibited by serpins.

265 differentiation can be replaced by its mouse homolog steroidogenic factor 1 (mSF-1).

266 motions were absent or diminished in alpha7 homologs, suggesting a unique role in alpha7 activation.

267 es RNAP forms a clade distinct from cellular homologs, suggesting an ancient acquisition of this enzy

268 orted duplex are poorly conserved among McrB homologs, suggesting that other mechanisms may exist for

269 gra pars compacta and ventral tegmental area homologs, superficial mamillary area, laterodorsal tegme

270 TbArl13 catalyzes two TbArl3 homologs, TbArl3A and TbArl3C, suggesting the presence o

271 ve pathogen Candida albicans encodes an Rme1 homolog that is part of a transcriptional circuitry cont

272 es a vacuolar membrane casein kinase I (CKI) homolog that nonredundantly functions in fusion regulati

273 r, a comparative analysis of alpha7 with its homologs that cannot trigger channel opening has not bee

274 as correlated with downregulation of STYLISH homologs that have previously been shown to control nect

275 od based only upon DMS datasets and sequence homologs that predicts the impact of missense mutations

276 ic genetic variation among eukaryotic Hsp104 homologs that specifically antagonized TDP-43 condensati

277 t LJM17 produced IgG1 antibodies (human IgG4 homolog) that strongly cross-reacted with recombinant DS

278 , as previously reported for the prokaryotic homolog, the Erwinia chrysanthemi ligand-gated ion chann

279 ssing in rodents and activation of its human homolog, the ventromedial prefrontal cortex, has been im

280 y that human CXCR5IFN-gammaCD8 T cells are a homolog to murine CXCR5IFN-gammaCD8 T cells (termed anti

281 carnitine shuttle complex, in particular the homolog to the brain-specific isoform of CPT1C which fun

282 Only a single homolog to the cargo carrier protein Unc119 has been ide

283 Chlamydia encodes homologs to proteins in the Rsb phosphoregulatory partne

284 d the existence of a new family of proteins, homologs to the CTD, the C-terminal domain-like caroteno

285 tive search for three-dimensional structural homologs to the proteins of 20 key phylogenetically dist

286 ule inhibitor of MDM2 (mouse double minute 2 homolog) to upregulate and increase activation of p53.

287 r results support the view that the types of homologs used for function transfer are largely irreleva

288 eplacing the mouse C3 gene with the human C3 homolog using VelociGene technology.

289 nical force applied to alphaE-catenin or its homolog vinculin favors the strongly bound state, and th

290 adhesion protein alphaE-catenin but not its homolog vinculin.

291 he Wiskott-Aldrich syndrome protein and SCAR homolog (WASH) complex that activates actin nucleation a

292 mapping, we reveal that POC16 and its human homolog WDR90 are components of the microtubule wall alo

293 Using archaea homologs, we construct asymmetric forms of proteasomes.

294 r, we identified a pair of fungal desaturase homologs which contained either an Ile or a Gly at this

295 ed to identify any outer-membrane translocon homologs, which raised the question of the origin of E.

296 ic study revealed that EcLsi1 and EcLsi6 are homologs while EcLsi2 and EcLsi3 form another pair of ho

297 he brightest green fluorescent protein (GFP) homolog yet characterized and a reversibly photochromic

298 rminal helical domain present in Class 2 OLD homologs yet preserves the spatial organization of the n

299 we report that the Saccharomyces cerevisiae homolog Yta7(ATAD2) is a deposition factor for the centr

300 reduced miR-203, higher levels of the murine homolog Zfp217, and increased Akt activity and mammary e