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