ライフサイエンスコーパス: homologous

1 against high lethal dose challenges against homologous A/PR/8/34 and A/Aichi/2/68 viruses and protec

2 first intron of Dmp1 and Dspp genes that are homologous across species lines.

3 such as sleep and circadian rhythm, that are homologous across species will facilitate the implementa

4 Integrins alphaMbeta2 and alphaXbeta2 are homologous adhesive receptors that are expressed on many

5 ted (Philippines) and 60% protection against homologous (Aichi) H3N2 viruses.

6 n explain the strong selectivity compared to homologous aminopeptidases ERAP1 and ERAP2.

7 Homologous and heterologous cross-linked polymers of whe

8 errets, inducing antibodies that neutralized homologous and heterologous H5 viruses with different de

9 f arabinose, SLT16 (pCZ1) expressed both the homologous and heterologous O-antigens, whereas in the a

10 hese data suggest durable protection against homologous and heterologous Pf parasites can be achieved

11 activity, and earlier virus clearance after homologous and heterosubtypic [A/Philippines/2/82 (H3N2)

12 ic, and fibril amyloid-beta (Abeta) by three homologous antibodies (solanezumab, crenezumab, and thei

13 r regions of the CC, where fibers connecting homologous areas of the parietal cortex course.

14 were protected against rechallenge with the homologous as well as a distinct isolate with only minut

15 Here, we show that oligomerization of a homologous bacterial Roco protein depends on the nucleot

16 Here, we provide a counterexample where homologous behaviors are produced by neurons with differ

17 Using homologous binding and whole-cell recording assays, we f

18 D researchers are increasingly incorporating homologous biological measures to assess markers of risk

19 Five homologous bis-alpha,omega-azidoethylammonium alkanes we

20 and a co-crystal structure of L-45 with the homologous Brd PfGCN5 from Plasmodium falciparum rationa

21 using a set of domains that are structurally homologous but evolved with widely varying sequence iden

22 ory GTPases, but is atypical in having a non-homologous, C-terminal domain of approximately 20 kDa an

23 (Cav1 and Cav2) and sodium channels possess homologous CaM-binding motifs, known as IQ motifs in the

24 imulated sterilizing immunity against lethal homologous challenge and complete protection against het

25 owed immunogenicity and protection against a homologous challenge that was better than that conferred

26 nized mice does not impair protection from a homologous challenge; however, it does significantly imp

27 ent, we quantified the mobility of a pair of homologous chromosomal loci in the interphase nuclei of

28 In meiotic prophase I, homologous chromosome pairing is promoted through chromo

29 f large single-stranded DNA fragments of the homologous chromosome pairs allows for the independent s

30 Genes on the remaining homologous chromosome, however, are not recurrently muta

31 Schizosaccharomyces pombe meiotic prophase, homologous chromosomes are co-aligned by linear elements

32 In budding yeast meiosis, homologous chromosomes become linked by chiasmata and th

33 l complex (SC), which forms between pairs of homologous chromosomes during meiosis from yeast to huma

34 absent in oocytes during meiotic resumption, homologous chromosomes failed to segregate accurately du

35 EPSPS gene to pericentromeric regions of two homologous chromosomes in glyphosate sensitive A tubercu

36 ucing organisms, crossover formation between homologous chromosomes is necessary for proper chromosom

37 For this program, crossovers between homologous chromosomes play an essential mechanical role

38 conserved proteinaceous structure that holds homologous chromosomes together and is required for the

39 During meiosis, homologous chromosomes undergo crossover recombination,

40 on the pericentromeric region on one pair of homologous chromosomes was detected.

41 -protein ring complex (RC) localized between homologous chromosomes, promotes chromosome congression

42 luster positions are indeed conserved within homologous coding sequences across diverse eukaryotic, b

43 conserved at specific positions in a set of homologous coding sequences, for example to tune transla

44 These findings show that significant homologous contacts can occur between long ssRNA and dsD

45 It contains two homologous copies of a six-transmembrane-helix (6-TM) do

46 that does not resemble the one proposed for homologous CorA channels.

47 We found molecular evidence to propose homologous derivatives from the CoP (olivary pretectal,

48 Gain-of-function CXCR4 mutations that affect homologous desensitization of the receptor have been rep

49 correlated with increased expression of the homologous DNA recombination enzyme RAD51 and tumors ove

50 , knockdown of FEN1 significantly attenuated homologous DNA repair efficiency and enhanced cytotoxic

51 recombinase functions to mediate repair via homologous DNA strand invasion to form D-loops.

52 aced by the heterocyclization (Cy) domain, a homologous domain that performs two consecutive reaction

53 We also show that the PCL extended homologous domains are required for efficient recruitmen

54 long single-stranded (ss) RNAs with cognate homologous double-stranded (ds) DNA in vitro Using magne

55 x, is responsible for pairing the ssDNA with homologous double-stranded DNA (dsDNA), which serves as

56 We thus now propose that, in somatic cells, homologous dsDNA-dsDNA interactions between a small numb

57 Canonical non-homologous end joining (c-NHEJ) repairs DNA double-stran

58 motes the two major DSB repair pathways, non-homologous end joining (NHEJ) and homologous recombinati

59 Homology-directed repair and non-homologous end joining (NHEJ) are the two major DSB repa

60 to arise from a moderate attenuation of non-homologous end joining (NHEJ) repair, the role of DEK in

61 omology-directed recombination (HDR) and non-homologous end joining (NHEJ).

62 DNA-PKcs, which is integral to the non-homologous end joining pathway, thus negatively regulate

63 to enhanced phosphorylation of DNA-PK, a non-homologous end joining repair protein, in Hec-108 cells.

64 critical role in ICL repair was seen for non-homologous end-joining (cku-80) or base excision repair

65 II (TOP2) are rejoined by TDP2-dependent non-homologous end-joining (NHEJ) but whether this promotes

66 that combined inactivation of the XRCC4 non-homologous end-joining (NHEJ) DNA repair gene and p53 ef

67 lele-specific gene disruption induced by non-homologous end-joining (NHEJ) DNA repair offers a potent

68 Non-homologous end-joining (NHEJ) is the most prominent DNA

69 logy directed repair (HDR) and decreased non-homologous end-joining (NHEJ) repair, suggesting that Ww

70 amage being channelled through repair by non-homologous end-joining (NHEJ).

71 d break (DSB) repair pathways, including non-homologous end-joining (NHEJ).

72 nstrate the importance of TDP2-dependent non-homologous end-joining in protecting both gene transcrip

73 As a member of the non-homologous end-joining pathway, it is also involved in r

74 the proximity of the break were due to a non-homologous end-joining pathway, while larger deletions w

75 mycoredoxin cluster, we also characterized a homologous enzyme of Corynebacterium glutamicum (NCgl233

76 Finally, we identify tandem homologous exons regulated by U2AF and show that their p

77 e 11p13, is an intergenic region between Ets homologous factor (EHF) and Apaf-1 interacting protein (

78 titative O-Man glycoproteomics to identify a homologous family of four putative protein O-mannosyltra

79 r all four FMDV serotypes tested following a homologous FMDV vaccination regime.

80 and-binding sites from various analogous and homologous function templates.

81 Pan-genome analysis identified 10,110 homologous gene clusters present only in a subset of str

82 A total of 331 homologous gene clusters were essential for fitness duri

83 validated by qRT-PCR, and compared with the homologous genes from S. japonica, a species in the same

84 KEY MESSAGE: The homologous genes OsbHLH068 and AtbHLH112 have partially

85 to those obtained following coinfection with homologous, genetically tagged, pH1N1 viruses as a contr

86 2, and neutralization was largely toward the homologous genotype.

87 Homologous glycosyltransferases assemble a similar core

88 erologous A/H3N2, for example, was 84.0% for homologous H3N2 seroconverters versus 11.4% for nonseroc

89 rcing a conformation more similar to that of homologous (i.e., non-seam) contacts by which it regular

90 n be explained by a combination of a lack of homologous immunity, frequent reinfections, weak competi

91 any pathogens is driven by type-specific or "homologous" immunity, which promotes the spread of varia

92 ally biosynthesized, therefore, they are not homologous in the aetiology of metabolic disease.

93 immunity against a lethal challenge dose of homologous influenza virus.

94 tural studies reveal that Hi1a comprises two homologous inhibitor cystine knot domains separated by a

95 nemically with long dsDNA via periodic short homologous interactions, e.g. mediated by RNA/DNA triple

96 that can distinguish between the two highly homologous isozymes.

97 memory, but rodent studies on the putatively homologous lateral entorhinal cortex suggest that it als

98 , but nearly all were constructed by merging homologous loci into single "consensus" sequences, gener

99 ed as the ability of one locus to affect its homologous locus in trans Although it was first discover

100 ete multiple voltage plateaus observed for a homologous macrocyclic dimer and an acyclic derivative o

101 rily with the E. coli P4 were submitted to a homologous mastitis challenge.

102 ism by which these specialized cells utilize homologous members of a core cardiac transcription facto

103 ammation (targeting chemoattractant receptor-homologous molecules expressed on TH2 lymphocytes, PDE4,

104 We next recorded from and controlled homologous neuromodulatory cells in mice; alertness-rela

105 ted subjects after in vitro stimulation with homologous (NF54) or heterologous (7G8) PfSPZ were highl

106 homologous TEMPO oxoammonium salts and three homologous nitroxide radicals have been prepared and cha

107 ers that are encoded by different numbers of homologous operons in Actinobacteria.

108 Being homologous organelles, the primary cilium and the OS sha

109 volve once recombination is halted between a homologous pair of chromosomes.

110 roles in other meiotic processes, including homologous pairing, recombination, and chromosome segreg

111 uld be efficiently rejected even though most homologous pairings form irreversible products.

112 netic and physiological studies suggest that homologous peroxidases are already present in mycetozoan

113 After CHMI with homologous Pf parasites 19 wk after final immunization,

114 signaling proteins (Sts-1 and Sts-2) are two homologous phosphatases that negatively regulate signali

115 olymers was significantly lower than that in homologous polymers, suggesting that each protein compon

116 effectively in heterologous polymers than in homologous polymers.

117 dent cytolysins (CDCs) represent a family of homologous pore-forming proteins secreted by many Gram-p

118 corresponds to the natural amino acid at the homologous position in STAT6, does not change the specif

119 covalent binding states, and for two highly homologous proteases, calpain-1 and calpain-2.

120 asurements of CCAAT/enhancer-binding protein homologous protein (chop) and immunoglobulin heavy chain

121 changes correlated with an increase in C/EBP homologous protein (CHOP) expression and the activation

122 the absence of ARC increased levels of C/EBP homologous protein (CHOP) in wild type isolated islets s

123 Ablation of CCAAT-enhancer-binding protein homologous protein (CHOP), the major ER stress-associate

124 complex, including Reticulocyte binding-like Homologous protein 5 (PfRH5) and the RH5-interacting pro

125 G9a-like protein (GLP) and G9a are highly homologous protein lysine methyltransferases (PKMTs) sha

126 Comparison of homologous protein models identified highly conserved re

127 activating transcription factor 4 and C/EBP homologous protein up-regulation, associated with caspas

128 nd is essential for embryonic development, a homologous protein, Ctr2, has been proposed to function

129 nstructions of TCPM mutants in which the non-homologous proteins are individually deleted, we propose

130 35 of Ebola virus and to known structures of homologous proteins in the measles, mumps, and Nipah vir

131 telomere-associated proteins and reveals how homologous proteins undergo functional evolution.

132 the type of amino acid, its conservation in homologous proteins, and its tendency of being exposed t

133 umb domain and 8-KD domain) conserved in the homologous proteins.

134 movements observed for the active states of homologous proteins.

135 analysis of genotype patterns revealed that homologous reassortment was random while heterologous re

136 ved unresolvable by X-ray crystallography in homologous receptors.

137 Moreover, functional assays showed impaired homologous recombination (HR) and nonhomologous end-join

138 We found that the functions of BRCA1 in homologous recombination (HR) and replication fork prote

139 1 variants or mutants in two HDR mechanisms, homologous recombination (HR) and single strand annealin

140 ling and stability.BRCA2 is involved in both homologous recombination (HR) and the protection of stal

141 herapies in the clinic.Germline mutations in homologous recombination (HR) DNA repair genes are linke

142 ve that bi-allelic pathogenic alterations in homologous recombination (HR) DNA repair-related genes a

143 e maintenance and cancer suppression require homologous recombination (HR) DNA repair.

144 lso demonstrate gene-targeted integration by homologous recombination (HR) in all three of the homoeo

145 equent recruitment of RIF1, which suppresses homologous recombination (HR) in G1 cells.

146 We describe a method to multiplex homologous recombination (HR) in human hematopoietic ste

147 Homologous recombination (HR) is a DNA double-strand bre

148 Homologous recombination (HR) is a major mechanism to re

149 ense BRCA1 or BRCA2 variants known to impair homologous recombination (HR) on the basis of this signa

150 breaks (DSBs) are mainly repaired either by homologous recombination (HR) or by nonhomologous end-jo

151 Current models of bacterial homologous recombination (HR) posit that extensive resec

152 RAD52 is a homologous recombination (HR) protein that is conserved

153 Induction of homologous recombination (HR) repair genes was reduced w

154 strate that Sirt1 interacts and deacetylates homologous recombination (HR) repair machinery proteins,

155 s in Drosophila cells revealed that faithful homologous recombination (HR) repair of heterochromatic

156 roficiency for DNA repair via the error-free homologous recombination (HR) repair pathway.

157 peutics especially for tumors with deficient homologous recombination (HR) repair.

158 that DNA double-strand break (DSB) repair by homologous recombination (HR) was compromised.

159 tants are defective for DNA damage repair by homologous recombination (HR), and have altered HR prote

160 RAD51D is a key player in DNA repair by homologous recombination (HR), and RAD51D truncating var

161 ajor pathways known to mend DNA DSBs, namely homologous recombination (HR), nonhomologous end-joining

162 repair of DNA double-strand breaks (DSBs) by homologous recombination (HR), the molecular mechanism u

163 ication forks are most commonly repaired via homologous recombination (HR), which begins with 5' end

164 eins BRCA1 and BRCA2 play essential roles in homologous recombination (HR)-mediated DNA repair, which

165 ethyltransferase PRMT5 as a key regulator of homologous recombination (HR)-mediated double-strand bre

166 PA exchanges during the multistep process of homologous recombination (HR).

167 rs (PARPi) is toxic to cells with defects in homologous recombination (HR).

168 hways, non-homologous end joining (NHEJ) and homologous recombination (HR).

169 histone variant that promotes DNA repair by homologous recombination (HR).

170 key regulator of cell-cycle checkpoints and homologous recombination (HR).

171 stress by stimulating DNA end resection and homologous recombination (HR).

172 onse (DDR) and is required for DSB repair by homologous recombination (HR).

173 tated FLT3 and JAK2 confers interchromosomal homologous recombination (iHR), a precedent for CN-LOH.

174 redispose chromosomes to meiotic non-allelic homologous recombination (NAHR) events and thus lead to

175 e mechanism is independent of Rad51-directed homologous recombination and avoids the creation of doub

176 paired by 2 major mechanisms: BRCA-dependent homologous recombination and DNA-dependent protein kinas

177 enerated insertions in this gene by directed homologous recombination and found that the cah1 mutant

178 s is associated with repeats and non-allelic homologous recombination and furthermore that young repe

179 Trp53 (-/-);Brca2 (-/-) cells have defective homologous recombination and increased sensitivity to bo

180 ignificance: Dual targeting of MYC-regulated homologous recombination and PARP-mediated DNA repair yi

181 Homologous recombination and repair factors are known to

182 SWIB5 in influencing mtDNA architecture and homologous recombination at specific intermediate-sized

183 1 arrest axis as an unanticipated outcome of homologous recombination deficiency, which triggers cell

184 of heterozygosity (LOH) might also represent homologous recombination deficiency.

185 As a result, depletion of USP21 decreases homologous recombination efficiency, causes an increase

186 g approach we show that increasing levels of homologous recombination enhance the efficiency with whi

187 ction can be used to recover relatively rare homologous recombination events.

188 versal and illuminate a complex interplay of homologous recombination factors in fork remodeling and

189 pon additional deletion of TOP1, implicating homologous recombination for the repair of Top1-induced

190 We used homologous recombination in C57BL/6 NJ (B6N) and 129S1/S

191 xon deletion or complete gene correction via homologous recombination in myogenic cells.

192 the stabilization of transcripts involved in homologous recombination in response to DNA damage.

193 nd annealing (SDSA) is the preferred mode of homologous recombination in somatic cells leading to an

194 markably, these defects impair DNA repair by homologous recombination indicating that SPB integrity i

195 Homologous recombination involving sister chromatids is

196 A critical step in the homologous recombination is a search for a corresponding

197 Homologous recombination is inhibited during the G1 phas

198 Finally, we demonstrate that homologous recombination is required for repairing lesio

199 f PIMMS2 function through gene disruption by homologous recombination leads to normal development of

200 While recruitment of the homologous recombination machinery is well characterized

201 lts provide a mechanism for how MRN promotes homologous recombination on nucleosome-coated DNA.

202 th alternative nonhomologous end-joining and homologous recombination pathways.

203 uble-stand break repair via facilitating DNA homologous recombination processes and highlighted the g

204 aic gene editing in founder animals, and low homologous recombination rates.

205 ermore, reduced OFD1 impaired DSB repair via homologous recombination repair (HRR).

206 on synthesis (TLS), Fanconi anemia (FA), and homologous recombination repair pathways.

207 plays a central role in DNA replication and homologous recombination repair, and is known to be invo

208 Homologous recombination repairs DNA double-strand break

209 ocesses ranging from repairing DNA damage by homologous recombination to generation of genetic divers

210 We used homologous recombination to precisely delete foraging, g

211 sults identify a late role of BRCA1-BARD1 in homologous recombination, an attribute of the tumour sup

212 he repair of mitotic double-strand breaks by homologous recombination, but its relationship to 5' end

213 When DSBs are repaired by homologous recombination, DNA ends can undergo extensive

214 This mechanism, combined with frequent homologous recombination, is likely responsible for the

215 -way junctions are structures present during homologous recombination, repair of double stranded DNA

216 ch other and with other proteins involved in homologous recombination, such as DprA, thus placing the

217 Besides its role in homologous recombination, the tumor suppressor BRCA2 pro

218 nscriptional silencing and repair of DSBs by homologous recombination.

219 ll as DNA double-strand break repair through homologous recombination.

220 predominantly of CNVs mediated by nonallelic homologous recombination.

221 differs from the process in G2 that leads to homologous recombination.

222 ntire gene cluster in mouse germline through homologous recombination.

223 epaired through nonhomologous end joining or homologous recombination.

224 sses repair by nonhomologous end-joining and homologous recombination.

225 nd invasion reaction that takes place during homologous recombination.

226 hen introns spread to empty target sites via homologous recombination.

227 y generating intronic insertions via in vivo homologous recombination.

228 ions, a mutational signature associated with homologous-recombination-repair deficiency.

229 Incorporation of these triplets in the homologous region of ZEB1 does not affect protein transl

230 ecombination is a search for a corresponding homologous region on DNA, which is called a homology sea

231 ngineering (CREATE), links each guide RNA to homologous repair cassettes that both edit loci and func

232 olymerase inhibition and that restoration of homologous repair function may be a mechanism of disease

233 A library of 29 homologous Ru-based olefin metathesis catalysts has been

234 conversion, non-reciprocal transfer from one homologous sequence to another, is a major force in evol

235 uperfamily of phosphotransferases that share homologous sequences and structural motifs and have many

236 roves structure prediction accuracy of other homologous sequences beyond the accuracy obtained by seq

237 Detecting homologous sequences in organisms is an essential step i

238 In some cases, we also downloaded published, homologous sequences of the ITS region of fungi inspecte

239 oteins that do not have sufficient number of homologous sequences to derive reliable co-evolution pro

240 ng data in secondary structure prediction to homologous sequences.

241 We present the new homologous series (C(NH2)3)(CH3NH3)nPbnI3n+1 (n = 1, 2,

242 anism Caenorhabditis elegans produce various homologous series of l-ascarylose-derived glycolipids ca

243 -DPPH assay was developed for separating the homologous series of oligomeric proanthocyanidins and th

244 232 azaarene congeners distributed in eight homologous series, including alkylated derivatives and t

245 a novel role for RIPK1 and RIPK3, a pair of homologous serine/threonine kinases previously implicate

246 Human APOBEC3H and homologous single-stranded DNA cytosine deaminases are u

247 eading in water are reported for a series of homologous squaraine dyes with different substituents (s

248 sequencing of each of the complementary and homologous strands.

249 However in cases where no homologous structural templates can be detected, fold re

250 A family of six homologous subunits, Mcm2, -3, -4, -5, -6, and -7, each

251 million protein domains classified into 2737 homologous superfamilies, doubling the number of predict

252 By identifying homologous SV-containing reads from different technologi

253 Melibe leonina and Dendronotus iris exhibit homologous swimming behaviors, consisting of alternating

254 e viscosity profiles of ferropericlase using homologous temperature scaling and find that viscosity i

255 e phase problem for proteins that lack close homologous templates.

256 Three new homologous TEMPO oxoammonium salts and three homologous

257 ever, since they are plentiful and extremely homologous, these PE/PPEs are very challenging to study,

258 SNPs were found within 39 transcripts highly homologous to 49 publically-searched rubber biosynthesis

259 span of genomic DNA in C. porcellus that is homologous to a portion of mammalian CD59 and show that

260 orting model-based behavior are structurally homologous to and overlapping with those thought to carr

261 EDE1 (Endosperm DEfective 1) is homologous to AUG8 [3].

262 f T-cell reactivity to Mtb epitopes that are homologous to bacteria in the microbiome in persons with

263 oraenol synthase is an oxidosqualene cyclase homologous to bacterial lanosterol synthases and distinc

264 calized at chromosome 2p23.1-p21 and is most homologous to CAPN13 (36% sequence identity), which is l

265 atalyzes cortisol biosynthesis and is highly homologous to CYP11B2, is unclear.

266 e (RING)-type E3s, thereby restricting it to homologous to E6AP C-terminus (HECT) and RING-in-between

267 entified MoGlo3 as an ArfGAP protein that is homologous to Glo3p of the budding yeast Saccharomyces c

268 ion of mutated mouse CRMP4 (S540Y), which is homologous to human CRMP4 (S541Y), in cultured hippocamp

269 92a suppresses expression of sirt2, which is homologous to human sir2 and sirt3.

270 gh light-inducible proteins (Hlips) that are homologous to light-harvesting antenna of plants and alg

271 e report that HRPU-2, an RNA-binding protein homologous to mammalian heterogeneous nuclear ribonucleo

272 G0 or G1 transgene in nephrocytes, fly cells homologous to mammalian podocytes, induced increased end

273 Imd is a receptor-proximal adaptor protein homologous to mammalian RIP1 that is regulated by proteo

274 hort form of membrane IgE (mIgES ), which is homologous to mouse mIgE, and the up-regulation of the l

275 ative from the H6PGA4 R. rickettsia protein, homologous to OmpA.

276 In this study, two genes homologous to OsMYBS1, MYBS1 and MYBS2, were investigate

277 xploiting allosterism in plasmin, a protease homologous to other allosteric serine proteases.

278 mammalian replisome component C20orf43/RTF2 (homologous to S. pombe Rtf2) must be removed for fork re

279 ous system (CNS) from a neural plate that is homologous to that of vertebrates, allowing direct topol

280 stome ancestor possessed a molecular toolkit homologous to that which drives canonical MYD88-dependen

281 T-oligo, a guanine-rich oligonucleotide homologous to the 3'-telomeric overhang of telomeres, el

282 B is a mitochondrion-associated protein with homologous to the E6-AP Cterminus (HECT) E3 ubiquitin li

283 76C, S1176L, and G1178S), three of which are homologous to the gating mutations of cystic fibrosis tr

284 we show that an HD-Zip transcription factor homologous to the LATE MERISTEM IDENTITY1 (LMI1) gene of

285 in the Bengalese finch brain-a premotor area homologous to the mammalian premotor cortex-alters the s

286 ion of Teb2 and Teb3, which are structurally homologous to the RPA middle and small subunits, respect

287 ition reveals that corazonin, a neuropeptide homologous to the vertebrate gonadotropin-releasing horm

288 These cells are homologous to the Vgamma9Vdelta2 T cell population ident

289 ural and genomic features of collagen IV are homologous to those of non-bilaterian animal phyla and B

290 EGFP-HSV1-tk construct flanked by sequences homologous to those surrounding the breakpoint.

291 They are highly homologous transcription factors that regulate the expre

292 d the frequency with which segments carrying homologous versus heterologous packaging signals were in

293 the H7 WIV completely protected mice against homologous viral challenge, and antibodies directed agai

294 tects both mice and ferrets from lethal H5N1 homologous virus challenge.

295 tralising antibody seroresponses against the homologous Wa-strain were seen in 40 (85%, 72-94) of 47

296 tope by changing 3 amino acids so that it is homologous with a known H3 immunogenic epitope sequence

297 in the brain: agrp1, considered functionally homologous with the mammalian AgRP, and agrp2.

298 ex responsible for type IV pilus assembly is homologous with the type II protein secretion complex.

299 CpsY is homologous with transcriptional regulators of Streptococ

300 X chromosomes separate during meiosis I, and homologous X chromatids segregate to the functional sper