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1 able databases) and 49% are gene duplicates (paralogues).
2  protein gene RPL22A, but not its unenriched paralogue.
3 ponds with a key, conserved eukaryotic Rad51 paralogue.
4 nBank and the large number of highly similar paralogues.
5 s, but in S. maritima is encoded by over 100 paralogues.
6           Most teleost fish possess two MSTN paralogues.
7 tic conservation with respect to their human paralogues.
8 n function between the closely related SEC23 paralogues.
9 ects in OXS2 and three of the four OXS2-like paralogues.
10 ncluding RAD51-related proteins termed Rad51 paralogues.
11 on of these non-redundant, tandemly arranged paralogues.
12 rk of vertebrate calpains, including teleost paralogues.
13 PA1 gene but Arabidopsis possesses five RPA1 paralogues.
14 RIM5alpha orthologues and in closely related paralogues.
15 gene duplication and creation of families of paralogues.
16 tional diversity among the 3 Arabidopsis CRT paralogues.
17 ing members of the miR-17-92 cluster and its paralogues.
18 al divergence relative to their SLO1 channel paralogues.
19 B. napus with the participation of ABI1-like paralogues.
20 nce and functional divergence of the BnaABI1 paralogues.
21                 The four pathways share MtrA paralogues, a periplasmic electron carrier cytochrome, a
22                           Multiple myosin II paralogues accumulate at mammalian epithelial cell-cell
23             Here we show that all four RAD51 paralogues act in DNA repair, recombination and RAD51 su
24                                    The RAD51 paralogues act in the homologous recombination (HR) path
25 S domain-containing protein ENL, but not its paralogue AF9, is required for disease maintenance in ac
26 rst reported comprehensive analysis of Hsp90 paralogue affinity and selectivity in the clinical Hsp90
27 degree of similarity between the S. gordonii paralogues, analysis of SecA-SecA2 chimeras indicates th
28 s that specifically antagonize each receptor paralogue and yet cross-react with the human and mouse s
29 d the zebrafish genome to identify potential paralogues and confirmed their homology, bringing the to
30 n IPTL, as shown by the accumulation of LC3B paralogues and diminishment of lysosome associated membr
31 , has revealed that these proteins are Rad51 paralogues and mediate DNA binding of this complex.
32 s, which are the most diverged region of the paralogues and probably evolved independently after a ge
33 monstrate correlation between Notch and Mef2 paralogues and support the notion that Notch-MEF2 synerg
34  suggesting functional coupling between Cas6 paralogues and their downstream effector complexes.
35 SM/type III-A and CMR/type III-B), five Cas6 paralogues and two different CRISPR-repeat families (AB
36 a suggest the involvement of two other mak-1 paralogues and two orthologues of p38 MAP kinase.
37                    B. subtilis has four ltaS paralogues and we show how their roles are partially dif
38 residues in evolutionarily related proteins (paralogues) and, where appropriate, transfers annotation
39 agonists that selectively target each Jagged paralogue, and determine a crystal structure that explai
40                                Rec2, a Rad51 paralogue, and Rad52 are additional components of the ho
41 ed sequence heterogeneity in mammalian Notch paralogues, and should allow the development of paralogu
42 lt of the expression of multiple Kir2 family paralogues, and the inwardly rectifying conductance cont
43                   The functionally conserved paralogues appear to target to compartments associated w
44 r because of the observation that various PC paralogues are activated at different organellar pH valu
45                 In human and primates, ATAD3 paralogues are encoded by three genes (ATAD3A, 3B and 3C
46 at is found in budding yeast where the RAD51 paralogues are fully dependent on the SRS2 anti-recombin
47 n supernumerary chromosomes and whether EBR1 paralogues are functional is currently unknown.
48        Because the functionally diversifying paralogues are still closely related to and derived from
49               ARID3B has two closely related paralogues, ARID3A and ARID3C.
50  establishes a role for this tissue-specific paralogue as a ribosomal component.
51 an contains approximately the same number of paralogues as found in the two soybean homeologues combi
52                   These Acinetobacter baylyi paralogues belong to the largest family of prokaryotic t
53 itration calorimetry studies show that these paralogues bind the product of the methylation reaction,
54  only the major binding modes that relay pan-paralogue binding or, conversely, paralogue selectivity,
55 cking the endogenous bak1 and its functional paralogue, bkk1, produced plants that were viable but ex
56 ession pattern of two evolutionarily distant paralogues, BnaA01.ABI1.a and BnaC07.ABI1.b in B. napus
57  were not compensated by the closely related paralogue Bright-derived protein (Bdp)/Arid3b, suffered
58 ling tight co-expression between the IGF-IRa paralogues, but expression divergence comparing IGF-IRa
59 ared the physical binding properties of each paralogue by surface plasmon resonance and determined th
60                                The caspase-8 paralogue c-FLIP is a good candidate for a molecular rhe
61             The conformations of C4b and its paralogue C3b are shown to be remarkably conserved, sugg
62                                       A TsdA paralogue (C8j_0040), lacking the unusual His-Cys haem l
63 ome duplication, which suggests that ancient paralogues can remain in the same regulatory networks fo
64 uely, C. neoformans has two functional Cdc42 paralogues, Cdc42 and Cdc420.
65 is a key effector in abscission, whereas its paralogue, CHMP4C, is a component in the abscission chec
66 that in zebrafish two subfunctionalized cmas paralogues co-exist, we introduce a novel and unique mod
67  that HELQ interacts directly with the RAD51 paralogue complex BCDX2 and functions in parallel to the
68 us proteins, evolved from a more ancient two-paralogue complex because of a gene duplication that was
69 pression of the endogenous MAF2 gene and its paralogues, confounding functional assessment.
70           The transcripts of these clustered paralogues contribute to a large majority of the mRNA po
71 activation are the histone acetyltransferase paralogues CREB-binding protein (CBP) and p300.
72         Finally, we show that Dchs1, and its paralogue Dchs2, function in a partially redundant fashi
73 and HrpS functionalities suggest how partial paralogue degeneration has potentially led to a novel co
74              Relative expression of the EBR1 paralogues depends on growth conditions and on the prese
75     Here we show in mice that different NAIP paralogues determine the specificity of the NLRC4 inflam
76       Spiking experiments with purified SUMO paralogues determined that we could detect as little as
77  aeruginosa genome encodes a closely related paralogue DksA2 that lacks the Zn-finger motif.
78 acking Dcx and/or its structurally conserved paralogue, doublecortin-like kinase 1 (Dclk1), show impa
79 ABI1 gene orthologue and Brassica napus gene paralogues encoding protein phosphatase 2C (PP2C, group
80                        Conversely, the ESX-1 paralogue EspG(1) interacted with a PE/PPE couple secret
81 blished with what degree of specificity CheR paralogues exert their activity.
82                                        These paralogues exhibit sequence and copy number variation am
83      To determine how tissue-specific septin paralogue expression may shape core heteromer repertoire
84 plasmic domain 6 amino acids longer than its paralogue, Fcgr3.
85 indicated that expression of two fibronectin paralogues, fn1 and fn1b, are induced by injury in epica
86                    In zebrafish, there are 2 paralogues for adtrp (i.e., adtrp1 and adtrp2).
87                          GOLPH3L is a GOLPH3 paralogue found in all vertebrate genomes, although prev
88 l locus shared with the dual TOR1A and TOR1B paralogues found in tertrapods.
89 heniformis and Bacillus pumilus as well as a paralogue from B. subtilis called YweA.
90 ally completely conserved in orthologues and paralogues from invertebrates to humans, and clinical fo
91 the kinetic properties of two different Cas6 paralogues from S. solfataricus.
92  establish that salmonids retain two IGF-IRa paralogues from ssWGD and a single IGF-IRb copy.
93    Individual AdoMetDC-SpdSyn fusion protein paralogues from Tetrahymena exhibit undetectable AdoMetD
94  proteins in Paramecium cells, we found that paralogues from the two most recent whole-genome duplica
95 pressed ubiquitously, suggesting distinctive paralogue functions.
96  and I304N mutant FMRP isoforms and the FMRP paralogues FXR1P and FXR2P (also known as FXR1 and FXR2)
97 et al. investigate the role of Gata6 and its paralogue Gata4 in mouse embryonic pancreas and show tha
98 uivalently, while mutation of only one RAD51 paralogue gene significantly impedes VSG switching.
99 ry microRNAs and temporal divergence of gene paralogues generated in the teleost genome duplication.
100            In T. brucei, four putative RAD51 paralogue genes have been identified by sequence homolog
101 an Golgi reassembly stacking protein (GRASP) paralogues, GRASP55 (GORASP2) and Rab8a.
102     We conclude that it is unlikely that the paralogues have a function in primary myogenesis.
103                                          Two paralogues have a redundant role in LTA synthesis during
104           Our data demonstrate that Survivin paralogues have different characteristics of phosphospec
105                                      The two paralogues have distinct inductive properties: Tbx6 indu
106 ic clones showed that the effects that these paralogues have on proliferation serve to promote cell c
107 ound that it includes a cohesive outgroup of paralogues (herein coined LoaP), which are often positio
108  Using zebrafish, we found that the HNF1beta paralogues hnf1ba and hnf1bb, which encode homeodomain t
109  expression assays reveal that Hoxb4 and its paralogue Hoxd4 are necessary and sufficient for cell se
110 l extension (CTE) by contrasting HP1a to its paralogue, HP1b.
111 uctures of tau55-HPD and its closely related paralogue Huf and used in silico docking methods to iden
112       We performed the same experiment for a paralogue human melanocortin receptor (hMC1R) and a mous
113                            Different IL-4/13 paralogues (IL-4/13 A and IL-4/13B) exist in teleost fis
114  function of gp96 (HSP90b1, grp94), an HSP90 paralogue in the endoplasmic reticulum (ER), is believed
115 er, the specific cells expressing this Notch paralogue in the mammary gland remain unknown.
116  switching from the clag 3.2 to the clag 3.1 paralogue in vitro.
117 ssed the in vivo activities of SCCRO and its paralogues in cullin neddylation.
118 or understanding the role of the human RAD51 paralogues in Fanconi anaemia and cancer predisposition.
119   The exclusive presence of highly conserved paralogues in higher organisms led us to assess whether
120                There are 13 confirmed septin paralogues in mammals, which may be ubiquitous or tissue
121 ous to heteromeric complex formation by BRE1 paralogues in other organisms, yBre1 forms a homo-multim
122 .graminearum and other fungi but as multiple paralogues in pathogenic F.oxysporum strains.
123 nt a comprehensive analysis of MtrA and MtrC paralogues in S. oneidensis to define the roles of these
124  demonstrate an unexpected role of the Rad51 paralogues in stabilizing the Rad51 filament against a b
125 ay in dicots may have functionally redundant paralogues in switchgrass and therefore require further
126 trand invasion, however, the function of the paralogues in the process of homologous recombination is
127  that the differential use of duplicated MRF paralogues in this novel two-component myogenic system f
128 tentially broad role for RNase G, an RNase E paralogue, in the trimming of 5'-monophosphorylated ends
129            The conserved budding yeast Rad51 paralogues, including Rad55, Rad57, Csm2 and Psy3 are in
130        We also show that the T. brucei RAD51 paralogues interact, and that the complexes they form ma
131  that requires Arg67, a residue conserved in paralogues, IRAK-1 and 3(M).
132 dies suggest that silencing of either clag 3 paralogue is associated with the enrichment of specific
133 sociated ClpX must recruit ClpP, for which a paralogue is not duplicated within any of the nitrogen f
134            A distinguishing feature of these paralogues is an H-to-R change in an amino acid that int
135 esults show that the presence of these three paralogues is associated with different activities, both
136                      Having two FtsK/SpoIIIE paralogues is not conserved among endospore-forming bact
137        The Shu complex, which contains RAD51 paralogues, is involved in the decision between homologo
138    Here we characterise Tbx6r, a unique Tbx6 paralogue isolated from the amphibian Xenopus.
139 vated protein kinase Slt2p, its pseudokinase paralogue, Kdx1p, and an associating transcription facto
140 lso report that a high dose of either of two paralogue kinases, Kin1 and Kin2, overcomes the defectiv
141 esults in an increased reliance on the FabHb paralogue leading to a greater proportion of straight ch
142 ucing a single historical mutation from each paralogue lineage into the resurrected ancestral protein
143                        Mammals express three paralogues: lipins 1, 2, and 3.
144 eine-rich transcriptional regulator, and its paralogues (LMO2, LMO3 and LMO4) have each been previous
145        Gain/amplification of MIR17HG and its paralogue loci was observed in 50% of adult-mBL.
146 d the possibility that additional JAM family paralogues may also function in muscle development.
147 e amygdala (high Utx), implying that the two paralogues may be differentially regulated.
148          Furthermore, possession of two MoeA paralogues may explain the formation of both molybdopter
149 circle accumulation, suggesting that the two paralogues mediate overlapping and nonredundant function
150 on assays show that CheR2, but not the other paralogues, methylates the McpS and McpT chemotaxis rece
151 ysine-4 (H3K4)-methyltransferase MLL3 or its paralogue MLL4.
152 nnotation errors, nomenclature variation and paralogues; moreover, GenBank's structure and tools are
153                     In contrast, TRIM family paralogues most closely related to TRIM5 did not.
154                              Vertebrate SoxE paralogues, most notably Sox9/10, are essential for NC i
155 transcription factor FOUR LIPS (FLP) and its paralogue MYB88 regulate terminal divisions during stoma
156                                      A third paralogue, Mycl1, is dispensable for normal embryonic de
157                        RNAi against the NDE1 paralogue NDEL1 has no such effects.
158                   Here we show that the NPR1 paralogues NPR3 and NPR4 are SA receptors that bind SA w
159                            The transaldolase paralogue NQM1 and the transcription factor VHR1 interac
160  previously reported role of Nup157, and its paralogue Nup170, in chromatin organization.
161 TBC1D1), a Rab GTPase-activating protein and paralogue of Akt substrate of 160 kDa (AS160), has been
162                                          The paralogue of Alx1, Alx4, was not functionally interchang
163 Gene expression studies identified MtLAX2, a paralogue of Arabidopsis (Arabidopsis thaliana) AUX1, as
164                   We also show that iBraf, a paralogue of Braf35, forms heterodimers with Braf35.
165  protease 50 (TSP50) and the testis-specific paralogue of CCCTC-binding factor, BORIS (brother of the
166 to suggest that a nitrogen fixation-specific paralogue of ClpX is used to control the accumulation of
167                                   L3MBTL1, a paralogue of Drosophila tumor suppressor lethal(3)malign
168 efect, is to modulate utrophin, a functional paralogue of dystrophin, able to compensate for the prim
169 nants of PC activation, we analyzed PC1/3, a paralogue of furin that is activated at a pH of approxim
170      However, POLRMT also interacts with the paralogue of h-mtTFB2, h-mtTFB1, which is a 12S ribosoma
171 ein, which suggests that NS1 is a structural paralogue of hRSV matrix (M) protein.
172 L) is a nucleolar protein and the vertebrate paralogue of nucleostemin (NS).
173            ORP4 (OSBP2) is a closely related paralogue of OSBP, but its function is unknown.
174  mature ribosomes, whereas Mrt4 is a nuclear paralogue of P0.
175  and also inhibit the activity of RNase G, a paralogue of RNase E.
176 nt evidence indicating that SlrA, which is a paralogue of SinI, is like SinI, an antirepressor that b
177 protein (TBP)-associated factor 7l (Taf7l; a paralogue of Taf7) and TBP-related factor 2 (Trf2) are c
178                 Here we report that TAF7L, a paralogue of TFIID subunit TAF7, is enriched in adipocyt
179 ong the regulated genes was Rv0190/MT0200, a paralogue of the copper metalloregulatory repressor CsoR
180                 As the endoplasmic reticulum paralogue of the cytosolic HSP90, gp96 (GRP94, HSP90b1)
181                                Blo t 21 is a paralogue of the group 5 allergen, Blo t 5, a major alle
182                                    StpA is a paralogue of the nucleoid-associated protein H-NS that i
183                                  SYCP2L is a paralogue of the synaptonemal complex protein SYCP2 and
184   The SAS6-like (SAS6L) protein, a truncated paralogue of the ubiquitous basal body/centriole protein
185 hiamin pyrimidine synthase (thiC) revealed a paralogue of thiC (bzaF) clustered with anaerobic vitami
186                      The recently identified paralogue of XRCC4 and XLF (PAXX) factor has homology to
187 4(yeast)/Pelota(mammals) and Hbs1, which are paralogues of eRF1 and eRF3, are implicated in these pro
188 iRNA precursors, and previously unrecognized paralogues of functionally important miRNA families (e.g
189        Signatures of subfunctionalisation of paralogues of Hox genes are revealed in the appendages o
190  share 4 unique microRNA families, 15 unique paralogues of more primitive microRNA families, and 22 u
191                                        Three paralogues of NudC are known in vertebrates: NudC, NudC-
192 ere a comparative analysis of the three CheR paralogues of Pseudomonas putida.
193 oteins of streptococci and staphylococci are paralogues of SecA and are presumed to have an analogous
194 l other adaptin complex subunits, as well as paralogues of the syntaxins and Rabs specific for the ot
195 aricus and related crenarchaea contain three paralogues of the tfb gene.
196  the Tmem16a transcript in addition to other paralogues of the Tmem16a family.
197                                  Assays with paralogues on chromosomes 18 and 20 (18|20 PRT) and chro
198  coactivator CREB binding protein (CBP), its paralogue p300, and the retinoblastoma protein (pRb; als
199                The histone acetyltransferase paralogues p300 and CREB-binding protein (CBP) are key t
200 roteins interact directly with ATML1 and its paralogue PDF2 and that silencing of both HD-ZIP transcr
201 lino oligonucleotides we show that both Tbx6 paralogues perform essential functions in the developmen
202 B forms homodimers and heterodimers with its paralogue PHOX2A in vitro, we tested the hypothesis that
203                                          The paralogues play differential roles in actin and septin o
204 istoyl sequence in SCCRO3, one of four SCCRO paralogues present in humans that localizes to the membr
205 r the evolution of complexity in other multi-paralogue protein complexes.
206 ation about the role of QUA2 and its closest paralogues, QUASIMODO2 LIKE1 (QUL1) and QUL2.
207 product of RAD51B interacts with that of its paralogue RAD51, which is associated with congenital mir
208                       In yeast the two Rad51 paralogues, Rad55 and Rad57, have been shown to be invol
209                                          The paralogue ratio test (PRT) is a simple, cost-effective m
210 e methods of copy number typing based on the paralogue ratio test (PRT) to assess beta-defensin copy
211           DEFB copy number was determined by paralogue ratio test.
212 urpose of this study was to evaluate whether paralogue ratio tests (PRT) using real-time PCR can accu
213                                     Combined paralogue ratio tests (PRTs) were used to distinguish th
214                         In this work, we use paralogue ratio tests, microsatellite analysis, read dep
215 he function of OTT3 and compared it with its paralogues RBM15 and SHARP.
216 RNA-binding motif protein 15 (RBM15) and its paralogue RBM15B, which bind the m(6)A-methylation compl
217                                         Five paralogues (RecQ1, Bloom, Werner, RecQ4, and RecQ5) are
218 ge of protists, demonstrating that the Rad51 paralogue repertoire in T. brucei is unusually large amo
219 g mutants in both ecotypes lacking the DELLA paralogues REPRESSOR OF ga1-3 (RGA) and GA INSENSITIVE (
220 d us to assess whether compensation by SCCRO paralogues rescues lethality in SCCRO(-/-) mice.
221                  Variant expression of these paralogues results in the use of alternative invasion pa
222 erized the interaction between NUPR1 and the paralogue RING1B in vitro, in silico, and in cellulo.
223  degrades highly structured RNA, whereas its paralogue, RNase II, is unable to do so.
224 hough the function of RNF114 is unknown, its paralogue RNF125 has been shown to regulate the RIG-I/MD
225 ffects are specific to rhomboid, because its paralogue roughoid is neither required nor sufficient fo
226 thin the genome in a strain lacking the Rpl8 paralogue RPL8A, demonstrating that the gene targeted fo
227        Missense mutations in the human COPII paralogues SEC23A and SEC23B result in craniolenticulosu
228 es and set the ground for the development of paralogue selective inhibitors.
229  analysis that allows for rationalization of paralogue selectivity and defines not only the major bin
230  relay pan-paralogue binding or, conversely, paralogue selectivity, but also identifies molecular cha
231                            Apparently, these paralogues share few partners and create new sets of int
232 tion patterns, and that less closely related paralogues showed evidence of both conservation and dive
233     Identical experiments with purified SUMO paralogues showed that SUMO-1 was well digested by our p
234 lear positioning in guard cells, whereas its paralogue SINE2 contributes to innate immunity against a
235             Trypanosoma brucei encodes three paralogue single-protein OSTs called TbSTT3A, TbSTT3B, a
236                                Humans have a paralogue, SMN2, whose exon 7 is predominantly skipped,
237 udied the poorly characterized SNX20 and its paralogue SNX21, which contain an N-terminal PX domain a
238           Our studies emphasize the value of paralogue-specific antagonists in dissecting the contrib
239 3% identical in amino acid sequence but have paralogue-specific effects on cell proliferation, metast
240 alogues, and should allow the development of paralogue-specific ligand-blocking antibodies.
241 ar determinants of the bound orientation and paralogue specificity of a SIM are unclear.
242 and the L. monocytogenes genome contains two paralogues, spxA1 and spxA2 Here, we demonstrate that sp
243 xidative stress requires the activity of two paralogues, SpxA1 and SpxA2.
244 The nucleoid-associated protein H-NS and its paralogue StpA are global regulators of gene expression
245 erminal region (RQC) found in the other RecQ paralogues; such a region consists of a zinc domain and
246                     Deletion of IscA and its paralogue SufA results in an E. coli mutant that fails t
247  other protists possess highly divergent XPB paralogues suggesting that XPBs specialized in transcrip
248  together with studies on Fur homologues and paralogues, suggests that in fact the Zn2 site is the re
249    Structure-guided mutagenesis of the close paralogue SWEET1 from Arabidopsis identified key residue
250 om other chromatin remodellers including its paralogue SWR1.
251 ed structure is similar to that found in the paralogue Talin head domain.
252 -43, we knocked out zebrafish Tardbp and its paralogue Tardbp (TAR DNA binding protein-like), which l
253 ls in the presence of low levels of the TatA paralogue TatE.
254 f the xenophagy cargo receptor Ndp52 and its paralogue Tax1bp1, which we demonstrate here to be a bon
255 e show that downregulation of TCF7L1 and its paralogue TCF7L2 reduces tumor growth in a xenograft mod
256 CUL3(KBTBD8) monoubiquitylates NOLC1 and its paralogue TCOF1, the mutation of which underlies the neu
257 ed by heterodimer formation with an inactive paralogue termed prozyme.
258  that a knockout of the gene for the smaller paralogue, termed XPB-R (R for repair) resulted in viabl
259                  T-STAR is a tissue-specific paralogue that regulates the alternative splicing of neu
260               Finally, we document the Rad51 paralogues that are encoded by a wide range of protists,
261 in vivo, which preferred endogenous SUMO-2/3 paralogues that form poly-chains.
262 2 and RING 1A, which are partially redundant paralogues that together account for the E3 ubiquitin li
263 istent with the Shu complex containing Rad51 paralogues, the methyl methanesulphonate sensitivity of
264 mited use for environmental barcoding due to paralogues, the potential for unidentifiable chimaeras a
265 that Csm2 interacts with Rad51 and the Rad51 paralogues, the Rad55-Rad57 heterodimer and that the Shu
266 show that the Saccharomyces cerevisiae Rad51 paralogues, the Rad55-Rad57 heterodimer, counteract the
267 cellular roles for these P. aeruginosa SPase paralogues; the role of PA1303 is integrated with the qu
268 ate cell-specific expression of the teashirt paralogue tiptop, which is not normally expressed in lar
269 intercalating between principal cells, and a paralogue, tiptop, is expressed in forming tubules.
270 Here we investigate the contribution of each paralogue to resistance to host stress.
271 olic enzyme non-quiescent mutant 1 (NQM1), a paralogue to the pentose phosphate pathway enzyme transa
272       For some genes S. maritima has evolved paralogues to generate coding sequence diversity, where
273 ignaling pathways recruit distinct myosin II paralogues to generate the contractile apparatus at apic
274 rsing out the contribution of the four Hsp90 paralogues to the perceived biological activity with the
275 l element that is recognized by TUT7 and its paralogues, TUT4 (ZCCHC11) and TUT2 (GLD2/PAPD4).
276 a showed differences in the induction of the paralogues under dehydration stress.
277      The regional expression of the Y-linked paralogue Uty (ubiquitously transcribed tetratricopeptid
278   We identified wake-up-call (wuc), a lin-52 paralogue, via a physical interaction with the tMAC lin-
279 ma-carboxylation in osteoblasts, whereas its paralogue, VKORC1L1, is dispensable for this function an
280                                 Two of these paralogues, VPS26A and VPS26B, are expressed in humans.
281 -2/simian immunodeficiency virus (SIV) SIVsm paralogue Vpx, hijack the CRL4(DCAF1) E3 ubiquitin ligas
282            Arabidopsis thaliana VTC2 and its paralogue VTC5 function as GDP-L-galactose phosphorylase
283                In C. elegans, MEC-17 and its paralogue W06B11.1 are redundantly required for acetylat
284    The functional divergence between kindlin paralogues was assessed using the sequence swap (chimera
285 s transcriptional divergence between the two paralogues was associated with high levels of histone H3
286 hat led to the functional diversification of paralogues, we tracked duplicate retention patterns, exp
287 new inhibitors targeting MraY as well as its paralogues, WecA and TarO.
288 omains are extremely similar, WelLFY and its paralogue WelNDLY exhibit distinct DNA-binding specifici
289  the miR-17 approximately 92 cluster and its paralogues were also highly expressed in ALK(+) ALCL and
290                                         cmas paralogues were maintained in fishes of the Otocephala c
291                        In mammals, 13 septin paralogues were recently shown to assemble into core het
292 inding to histone tails of the human class A paralogue, which has a histidine at this position, is se
293 or the potential function of the human RAD51 paralogues, which are known to be involved in cancer pre
294 t nonmammalian vertebrates have two Survivin paralogues, which we name class A and B.
295   Several ribosomal protein families contain paralogues whose roles may be equivalent or specialized
296                Eukaryotes also possess Rad51 paralogues, whose exact role in recombination remains to
297 s, however, possess two highly divergent XPB paralogues with only the larger being identified as a TF
298                       This suggests that EB1 paralogues within one species may interact with overlapp
299               We also show that Mdm1 and its paralogue Ydr179w-a (named Nvj3 in this study) localize
300 ector domain of Ptr1, the M. jannaschii Ptr2 paralogue, yields only very weak activation.

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