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1 ry, non-catalytic, rubredoxin-like iron site is conserved in 3-hydroxyanthranilate 3,4-dioxygenase (H
2 served across the tree of life and appear to be conserved in a hierarchical fashion, possibly linked
3 ism in the cell cycle, we first show that it is conserved in a distinct cyclin subtype (Ccn1).
4 deficiency and enhanced herbivory resistance is conserved in a diversity of plants, including crops.
5 he syncytial feto-maternal interface; and it is conserved in a functional state in a series of Monode
6    Further, the antitumoral effect of miR-28 is conserved in a primary murine in vivo model of BL.
7                Melanoma antigen (MAGE) genes are conserved in all eukaryotes and encode for proteins
8    Mitogen-activated protein kinase cascades are conserved in all eukaryotes.
9             Alpha-, beta-, and gamma-tubulin are conserved in all eukaryotes.
10 S (Regulator of G-protein Signaling) protein are conserved in all eukaryotes.
11                      These cysteine residues are conserved in all four desmoglein family members.
12 nt proteins from herpes simplex virus 1 that are conserved in all herpesviruses: pUL7 and pUL51.
13  Ser(286) and Ser(297) phosphorylation sites are conserved in all plant branching enzymes and are loc
14 e BDNF gene organization and coding sequence are conserved in all vertebrates.
15                  The four structural changes are conserved in all x-ray structures of the RXR ligand-
16 factor-independent symbiosis and, hence, may be conserved in all vascular plant endosymbioses describ
17                                   The finger is conserved in all algal septin sequences, suggesting a
18                Stearoyl-CoA desaturase (SCD) is conserved in all eukaryotes and introduces the first
19 tein family with a modular architecture that is conserved in all eukaryotes.
20 due, which determines the disease phenotype, is conserved in all eukaryotic members of the Cys-loop r
21 4-amino-acid (aa) palmitoylated protein that is conserved in all herpesviruses.
22 ied recombinant flavin-dependent enzyme that is conserved in all known pathways for epoxyketone biosy
23  hybridization and immunohistochemistry, and is conserved in all Mabuya species tested, spanning over
24             This process, meiotic silencing, is conserved in all mammals studied to date, but its pur
25                          This family of USPs is conserved in all mycobacteria, and we suggest that th
26  mutates a cytoplasmic arginine residue that is conserved in all neuroligins.
27                    The SR7-SR9 region, which is conserved in all other plakin domains, forms a rigid
28                               The I2 protein is conserved in all poxviruses that infect vertebrates,
29 well-defined phosphodegron, a sequence which is conserved in all primates.
30 ewly identified store-sensing gate structure is conserved in all RyR and inositol 1,4,5-trisphosphate
31 -spectrum phospholipid transfer protein that is conserved in all sequenced Plasmodium species and is
32              Though the core dimer structure is conserved in all the forms, structural heterogeneity
33 m(1)G37 methyltransferase enzyme TrmD, which is conserved in all three domains of life as a tight 3',
34            Archease is a 16-kDa protein that is conserved in all three domains of life.
35 erves as the primary site of phosphorylation is conserved in all translational GTPases from bacteria
36 olidated in a single organ, the liver, which is conserved in all vertebrates.
37 n, fibrinogen, into a polymeric fibrin clot, is conserved in all vertebrates.
38 hereas the majority of human T cell epitopes were conserved in all sublineages, the proportion of var
39 igate whether inhibition by divalent cations is conserved in an invertebrate SLO2 channel we cloned t
40 ypoxia-inducible factor (HIF) sensing system is conserved in animals, but not in other organisms.
41                                       As APH is conserved in Apicomplexa, these findings highlight a
42 ent named conoid protein hub 1 (CPH1), which is conserved in apicomplexan parasites.
43 porting that the essential function of CBL10 is conserved in Arabidopsis and tomato.
44                                         PINA is conserved in archaea and vital for S. islandicus viab
45                               This mechanism is conserved in at least two rodents and humans, making
46  p53 in cell death and cell cycle regulation are conserved in both DNA damage and differentiation.
47 s that interact with the active site mannose are conserved in both GH130 mannoside phosphorylases and
48                         Despite this epitope being conserved in both genotypes, the corresponding CD8
49 uitos implying that the requirement for ERI3 is conserved in both DENV hosts.
50        Thus, CaMKIV-mTOR-dependent autophagy is conserved in both immune and nonimmune/parenchymal ce
51 us Nedd8 binding sequence, L(X7)R(X5)F(X)ALQ is conserved in both Smurfs.
52 that BMP signaling-based germ cell induction is conserved in both the mouse Mus musculus and the cric
53          We found that only 14% of their BSs were conserved in both species and that these contained
54 dies suggested that the roles of VRN1 and FT are conserved in Brachypodium distachyon yet identified
55                                         MET1 is conserved in C3 and C4 plants and green algae but is
56                      Although these residues are conserved in CCK2R, mutating them had a distinct imp
57 at the KIAA0753/OFIP protein, whose sequence is conserved in ciliated species, associates with centro
58 hydrophobic surface on the Hrr25 N-lobe that is conserved in CK1delta-family kinases, suggesting a ro
59 Finally, we show that the CTCF-binding motif is conserved in CMV because a similar DNA sequence was f
60  SID spectrum, with the differences observed being conserved, in comparison to unactivated complex, a
61 estigate whether this influence of serotonin is conserved in crabs and whether these behaviours are s
62 catalytic functions in the template proteins were conserved in CslB, and their point mutation abolish
63 also show that AXL expression in radial glia is conserved in developing mouse and ferret cortex and i
64      This TCP/HD-ZIP genetic module seems to be conserved in dicot and monocotyledonous species to pr
65  found that the properties of the excitation were conserved in different brain areas.
66 architectures but also cleavage location can be conserved in distant architecturally related proteins
67 ily members that do not antagonize SAMD9 but are conserved in distantly related C7 family members fro
68 st identified in Arabidopsis, but appears to be conserved in diverse higher plant species.
69                                         Ngs1 is conserved in diverse fungi that have GlcNAc catabolic
70 ost-transcriptional control of miR171 levels is conserved in diverse rice species.
71                                       TDP-43 is conserved in Drosophila, where it has been the topic
72 idues affected by MEGF10 mutations in humans are conserved in drpr.
73                  Moreover, this relationship was conserved in each clinical subgroup, despite the het
74 eir differentiation into specialized subsets is conserved in early vertebrates.
75 r mechanism that localizes KaiC to the poles is conserved in Escherichia coli, another Gram-negative
76                                         FMOs are conserved in eukaryotes and induced by multiple life
77                               Vps13 proteins are conserved in eukaryotes, but their molecular functio
78                                Dnmt2 enzymes are conserved in eukaryotes, where they methylate C38 of
79                           The U4/U6 di-snRNA is conserved in eukaryotes and is part of the U4/U6.U5 t
80  DNA double-strand break repair pathway that is conserved in eukaryotes.
81 that these RNA pol III type 2-like promoters are conserved in eukaryotic genomes.
82 y receptors, yet none of the known receptors are conserved in evolution.
83  vivo, suggesting that our in vitro findings are conserved in evolution.
84 ndrome is the GEF for Arl3, and its function is conserved in evolution.
85 of viral RNA, and show that this interaction is conserved in evolutionarily distant influenza viruses
86                  We show that this mechanism is conserved in evolutionary very distant species.
87          Here we quantify how that diversity is conserved in ex situ collections across the world's b
88  constraining octane for omega-hydroxylation are conserved in family 4 P450s.
89 e of long-chain alpha2,6-linked sialic acids is conserved in ferret, pig and human soft palate.
90                                    This gene is conserved in fishes as well as tetrapods.
91        Although similar structures appear to be conserved in fission yeast, computational modeling an
92 er to AtPIN1, Sister-of-PIN1 (SoPIN1), which is conserved in flowering plants.
93 Rvb2-Tah1-Pih1 (R2TP) protein complex, which is conserved in fungi and animals.
94                          The fact that MXREs are conserved in genes outside of the methanol utilizati
95  an ancient mechanism of control as the uORF is conserved in GGP genes from mosses to angiosperms.
96 static interactions with polar residues that are conserved in GH7 cellobiohydrolases, but not in GH7
97                      The P234 site in AtBZR1 is conserved in GmBZL2 (P216) and mutation of GmBZL2(P21
98     Serine-rich repeat glycoproteins (SRRPs) are conserved in Gram-positive bacteria.
99 he ArsC (arsenate reductase) protein family, is conserved in Gram-positive bacteria, and interacts wi
100 d a core set of genes, named GreenCut2, that are conserved in green algae and plants.
101 ably, the pomalidomide-induced reprogramming was conserved in hematopoietic progenitors from individu
102  to a previously uncharacterized family that is conserved in heterokont algae.
103 rect axon guidance, a role for P4Hs that may be conserved in higher organisms.
104                                    The strap is conserved in higher eukaryotes but absent from yeast
105                                  The protein is conserved in higher plants and bryophytes but absent
106 H DEFECT FACTOR 1 (CDF1) in Arabidopsis that is conserved in higher plants and Synechocystis.
107                   This essential role of E93 is conserved in holometabolous insects as TcE93 RNAi in
108       Among the four residues, 271A and 684S are conserved in human and pH1N1 viruses but not in avia
109                      Brg1-regulated pathways are conserved in human Shh-type medulloblastoma, and Brg
110 promoting effects of EDA receptor activation are conserved in human skin repair.
111                     These metabolic pathways are conserved in human TIE2(+) HSCs.
112 he biochemical functions identified for Sld3 are conserved in human Treslin, suggesting that Treslin
113 ociated pairs detected in the mouse brain, 9 are conserved in human.
114 otif in Drosophila APC2, and that this motif is conserved in human APC2, but not human APC1.
115          The function of the C-terminal tail is conserved in human Atlastin.
116 delling complex, an interaction that we show is conserved in human cancer cells.
117 hat defines an organelle-exclusion zone that is conserved in human cells.
118 turity and neurotransmitter uptake function, is conserved in human development, and is disrupted by n
119 narily young LINE-1 elements, a pattern that is conserved in human ESCs.
120  The extent to which local protein synthesis is conserved in human neurons is unknown.
121 ke receptors on T cells, and this regulation is conserved in human T cells.
122               We show that lamin dysfunction is conserved in human tauopathy, as super-resolution mic
123 mplate recognition element found in ciliates is conserved in human telomerase RNA.
124 -secretion decoupling genes to modulate GSIS was conserved in human beta cells.
125  Interestingly, the effect on ubiquitination was conserved in human cells, suggesting a novel mechani
126         Our observations in the mouse models were conserved in human cells.
127 T3 inhibition on cell fate and proliferation were conserved in human myoblasts.
128 cers and showed that most epigenetic changes are conserved in humans and mice.
129                                Most circRNAs are conserved in humans and specific ones are deregulate
130  visceral fat that-given that these pathways are conserved in humans-might serve as potential therape
131 urface of its TPR domain using residues that are conserved in humans.
132       We show the prevalence of complex LSVs is conserved in humans and identify hundreds of LSVs tha
133                                 This pathway is conserved in humans, suggesting that it may be a viab
134  by Aurora A, suggesting that this mechanism is conserved in humans.
135 ase expression, indicating that this pathway is conserved in humans.
136              This ChREBP/G6PC signaling axis is conserved in humans.
137  a distinct protein isoform, a response that was conserved in humans with genetic or acquired cardiom
138 mitoleate, 45% of which define pathways that were conserved in humans.
139                  The upward growth direction is conserved in indica and japonica rice varieties, sugg
140                             sfRNA production is conserved in insect-specific, mosquito-borne, and tic
141 formation that may precede dimer closure and is conserved in intact TRAP1 in solution.
142 nts revealed impaired autophagic flux, which was conserved in kidney epithelial cells derived from bo
143 ificities of the glycosyltransferase domains are conserved in KpsC homologs from other bacterial spec
144 es in linker regions of LDLR class A repeats are conserved in LDLR from man to Xenopus and found in o
145 y related to the semantic content of stimuli was conserved in light non-rapid eye movement (NREM) sle
146  one another into a secondary structure that is conserved in lincRNA-p21 among primates.
147 the FPs of 3 different lineages of beta-CoVs are conserved in location within the S glycoproteins and
148 to damage repair and regeneration in mammals are conserved in lower organisms, indicating that it is
149                  TDP-43-mediated impairments are conserved in mammalian cells, and, importantly, the
150      Moreover, Bub1 NHEJ function appears to be conserved in mammalian cells.
151 ex and provide evidence that this regulation is conserved in mammalian cells.
152                                This activity is conserved in mammalian homologs; additionally, mtClpX
153 cts on enhancing HSPC homing and engraftment are conserved in mammals.
154 her this represents an uptake mechanism that is conserved in mammals and how these cells affect funct
155                              Peroxisomal LDH is conserved in mammals and likely contributes to redox
156 ted in nematodes, but whether this mechanism is conserved in mammals has been disputed.
157                         Whether this pathway is conserved in mammals remains unknown.
158                  Although genomic imprinting is conserved in mammals, ICRs are genetically divergent
159 sion of two genes, HIST2H2AA3 and HIST1H2BC, is conserved in mammals.
160  parallel topology, is thermally stable, and is conserved in mammals.
161 te that the control of synaptic genes by p53 is conserved in mammals.
162 NA damage-induced nuclear Dicer accumulation is conserved in mammals.
163  whether the regulation and function of ALPI were conserved in mammals.
164                                These kinases are conserved in many eukaryotes including humans, sugge
165 nments show that the lipid-interaction sites are conserved in many family members but less so in thos
166 duced by other metabolism, and AcuI and PrpE are conserved in many organisms across all domains of li
167      In contrast, delta- and epsilon-tubulin are conserved in many, but not all, eukaryotes and are a
168                           We found that CrsR is conserved in many aquatic proteobacteria, and most of
169 d methionine, producing the 25 kDa form that is conserved in many bacteria and protozoans.
170 togenes CdaA diadenylate cyclase domain that is conserved in many human pathogens.
171     The gene pair encoding PsXEG1 and PsXLP1 is conserved in many Phytophthora species, and the P. pa
172 ition and formation of this membrane network is conserved in maturing primitive and definitive erythr
173  of size-dependent lymph node drug targeting are conserved in melanomas, suggesting their applicabili
174 eria shows that the (p)ppGpp-GMK interaction is conserved in members of Firmicutes, Actinobacteria, a
175 ases (GT4) and contains an E-X7-E motif that is conserved in members of GT4 and two other GT families
176 hese data confirm that health benefits of CR are conserved in monkeys and suggest that CR mechanisms
177 As and their target genes revealed that many are conserved in monocots.
178 nneling pathway of bifunctional PutA enzymes is conserved in monofunctional PRODH-P5CDH enzyme pairs.
179  phylogeny, these interactions are likely to be conserved in more-complex species.
180  Intriguingly, PA-241Y, which 36285 encodes, is conserved in more than 90% of human seasonal H1N1 vir
181 ls cellular survival, surface BCR expression is conserved in most mature B-cell lymphomas.
182 ons of present day higher plant's Rca, which is conserved in most species seem to have evolved in cha
183 ristic of C11-family cysteine proteases that are conserved in multiple pathogenic Bacteroides spp. an
184 rtantly, the CR-independent membrane binding was conserved in murine and canine muscles.
185       We show that the AtZAR1 immune pathway is conserved in N. benthamiana and identify AtZAR1 domai
186            The ability to counteract SERINC5 was conserved in Nef encoded by diverse primate immunode
187 nimal model and show that these interactions are conserved in neurons and in transgenic mice.
188 y to drive TFH cell differentiation in vitro was conserved in non-human primates but not in mice.
189                  We identified 524 DHSs that are conserved in nonhuman primates but accelerated in th
190 oducts without function, ~9% of the peptides are conserved in ORFs in mouse transcripts, as are 74% o
191 ions affect TBC1D24 amino acid residues that are conserved in orthologs ranging from fruit fly to hum
192 en codon usage and protein disorder tendency are conserved in other eukaryotes.
193           Notably, residues at the interface are conserved in other members of the CDC family, sugges
194 for stem cell-mediated regeneration that may be conserved in other adult stem cell niches.
195 ed at beta-strands 3, 5, and 6, is likely to be conserved in other B. cellulosolvens type I cohesins.
196                             This model could be conserved in other bacteria, including the pathogenic
197  epidermal cell-cell fusion--a role that may be conserved in other epithelia.
198  is consistent between mice and rats and may be conserved in other species.
199 ostasis in anticipation of fertilization may be conserved in other species.
200                               The E-loop may be conserved in other systems in order to play similar r
201        NsdD's role in repressing conidiation is conserved in other aspergilli, as deleting nsdD cause
202 iors in Drosophila This phosphorylation site is conserved in other insects, including mosquitoes, ind
203 ations in Kir1.1 suggest that this mechanism is conserved in other Kir channels.
204               We show that myomaker function is conserved in other mammalian orthologs; however, rela
205 t the regulatory function of MYB31 and MYB42 is conserved in other monocots, specifically in sorghum
206                         This Sox2-Hippo axis is conserved in other Sox2-dependent cancers such as gli
207                          Moreover, this rank is conserved in other zebrafish embryonic assays and Dro
208                  We show that these residues are conserved in p21 and p57, suggesting that a similar
209 whether the Rab1-dependent secretory pathway is conserved in parasites, we have analyzed the role of
210  involved in (R)-16 binding to SARS-3CL(pro) are conserved in PEDV-3CL(pro); however, the sequence va
211 governing circadian activator stability that are conserved in perhaps all eukaryotes, and suggest tha
212    Since the transcriptional mechanisms that are conserved in phage and mitochondrial RNAPs have been
213 tic analyses show that all of these features are conserved in PHPT homologues from Gram-negative and
214            The presence of these rate motifs is conserved in phylogenetically distant members of the
215 he elicitin domain, a molecular pattern that is conserved in Phytophthora species.
216 is revealed that a majority of these modules are conserved in Picea abies The high spatial resolution
217                       Although its orthologs are conserved in plant pathogenic fungi, their functions
218 /Rhodospirillaceae-like phosphatases (RLPHs) are conserved in plants and several other eukaryotes, bu
219 ction in the maturation of FeS proteins that is conserved in plants, and is closely allied to the fun
220 of Pol epsilon in replicative stress sensing is conserved in plants, and provide, to our knowledge, t
221                   Although nuclear migration is conserved in plants, its importance for plant develop
222                                  Kis and Kid are conserved in plasmids encoding multiple antibiotic r
223 a indicate that the benefits of CR on ageing are conserved in primates.
224 evidence that the enzymatic function of BCO2 is conserved in primates and link regulation of BCO2 gen
225 tereotyped distribution of cellular polygons is conserved in proliferating tissues among metazoans.
226 mals remains unknown, although TRH receptors are conserved in proto- and deuterostomians.
227               PstSCR1 homologs were found to be conserved in Pst, and in its closest relatives, Pucci
228            By contrast, HOXD digit enhancers are conserved in pythons, and HOXD gene expression in th
229                             Five differences were conserved in quadriceps muscles from dystrophic mic
230 evelopmentally timed floral organ abscission is conserved in regulating drought-triggered leaf abscis
231       Although a subset of alternative sites are conserved in related species, implying functional po
232  Hooft anomaly matching condition: anomalies are conserved in renormalization group flow.
233 ong them, the Lsr (LuxS-regulated) QS system is conserved in scores of bacteria, and its signal molec
234                 These pathological responses are conserved in seminiferous tubules from Gravin(-/-) m
235  target sites fall within two domains, which are conserved in sequence/structure indicating their imp
236 cific to the targeted gene's sequence, which is conserved in several bacterial genera, and the oligom
237                     The biosynthetic pathway is conserved in several other bacterial genomes, and our
238 ptor binding region of the HN protein, which is conserved in several paramyxoviruses.IMPORTANCE Oncol
239  EPCR-binding surfaces of CIDRalpha1 domains are conserved in shape and bonding potential, despite dr
240 gonize bone marrow stromal antigen 2 (BST-2) is conserved in some HIV-2 isolates, where it is control
241 w that the RNA interference (RNAi) machinery is conserved in Stentor.
242  higher eukaryotes, since the key components are conserved in structure and function throughout evolu
243 e gene signature of SZ hiPSC-derived neurons is conserved in SZ hiPSC neural progenitor cells (NPCs).
244 e also show that native protein conformation is conserved in TENG-ESI, and that patterned ion deposit
245     Moreover, the HIV-1 and SIV Vif proteins are conserved in terms of their interactions with HIV-1
246 evealed that, while the active-site residues are conserved in TgALD1, key catalytic residues are abse
247                   Nevertheless, this pathway is conserved, in that SSA events have been found in seve
248 and olfactory receptor (Or) genes of MP-OSNs are conserved in the agricultural pest D. suzukii.
249 P and the paired uORFs allowing ATF4 control are conserved in the entire metazoa except nematoda.
250 ne whether renal primary ciliogenic programs are conserved in the eye, and to characterize the functi
251                 Importantly, these functions are conserved in the human homolog, ZMPSTE24, although d
252 re functional epitope contacts residues that are conserved in the human USP family, and thus it is li
253  summary, we show that ciliogenesis programs are conserved in the kidneys and eyes of zebrafish and m
254 wo clades and found 151 candidate genes that are conserved in the Listeria sensu stricto species.
255 eractions between Myosin VIIa and Myosin IIa are conserved in the mammalian cochlea and in human reti
256               Although six MCU gene homologs are conserved in the model plant Arabidopsis (Arabidopsi
257 een Ascaris and Parascaris, whereas only 10% are conserved in the more divergent T. canis.
258 ced conformational changes of the PHR domain are conserved in the mutant despite the lack of proton t
259               The majority of these proteins are conserved in the nonpathogenic species Leptospira bi
260 ults show that major trunk lymphatic vessels are conserved in the zebrafish, and provide a thorough a
261 a-CaMKII), and here we ask whether this role is conserved in the adult brain.
262                                           It is conserved in the alphabaculoviruses and expressed at
263 f a novel PCNA interacting protein NreA that is conserved in the archaea and that has a PIP motif at
264             The site of methylation on PP2Ac is conserved in the catalytic subunits of PP4 and PP6, a
265                                    This role is conserved in the fungus Sordaria However, functional
266  protein in Chlamydomonas reinhardtii, which is conserved in the green lineage and induced by high li
267             The fusogenic activity of Minion is conserved in the human orthologue, and co-expression
268 ind that this mechanism of self-organization is conserved in the human prostate.
269 se miR-431 seed sequence in the Smad4 3' UTR is conserved in the human SMAD4 3' UTR, inhibition of mi
270 ratase (GMD) and GDP-L-fucose synthase (FS), is conserved in the parasite genome, but the importance
271 SAL1 for activation of chloroplast signaling is conserved in the plant kingdom, and the plant protein
272     Moreover, the autorepressed conformation is conserved in the repressor class of orphan nuclear re
273 /ZP-C linker that is not observed in ZP2 but is conserved in the sequence of deafness/Crohn's disease
274         Here, we show that this relationship is conserved in the simple eukaryote Dictyostelium and e
275      However, disruption of this site, which is conserved in the Streptomyces venezuelae GlgE enzyme,
276                               This landscape was conserved in the decreased DNA methylation1 mutant.
277              Phenazine conidiation signaling was conserved in the genetic model A. nidulans and media
278                  Nevertheless, many antigens were conserved in the core genome, and strains' antigeni
279       The pro-haematopoietic effects of EETs were conserved in the developing zebrafish embryo, where
280 donor, a hallmark of rhodopsin proton pumps, are conserved in these cryptophyte proteins.
281  whether the antifungal mechanisms of MtDef4 are conserved in these fungi.
282   Although the low spherule phenotype of M41 was conserved in TOCs, each of the other tested IBV stra
283                Few of the loci were found to be conserved in two other legume species (chickpea [Cice
284 evealed by SUMO E1 structures are thought to be conserved in Ub E1, there is currently a lack of stru
285 ns of the TL and Gre factors in RNA cleavage are conserved in various species, with important variati
286 suggesting a role for this amino acid, which is conserved in vertebrate orthologs.
287  this function in wound healing is likely to be conserved in vertebrates.
288                                       Fz-PCP is conserved in vertebrates, but an understanding in ver
289  this 'stochastic' mode of PGC specification is conserved in vertebrates, including non-rodent mammal
290         Furthermore, this mode of regulation is conserved in vertebrates.
291                                         InlP is conserved in virulent L. monocytogenes strains but ab
292 nts, indicating this differentiation circuit is conserved in vivo.
293               This Metformin-mediated effect was conserved in vivo; Metformin-treatment significantly
294 mains: the acidic region, the WUS-box, which is conserved in WUS-related HOMEOBOX family members, and
295 iscoelastic behavior of the kinetochore that is conserved in yeast and mammalian cells.
296           The AP2 complex of the CME pathway is conserved in yeast, animals, and plants, and has been
297 zed WRDPLVDID domain (residues 637-645) that is conserved in yeast, mice, and humans.
298 f CTD Ser2 residues at 5' ends of genes that is conserved in yeast.
299            Although circadian rhythms of Vo2 were conserved in young lean CT-1(-/-) mice (2 mo), CT-1
300                                 These motifs are conserved in zebrafish V2 (zfV2) that also rescued V

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