1 hat a single, characteristic computation may
be common to all.
2 s revealed that 2,820 (52.4%) of these genes
were common to all 11 E. coli strains, yet only 173 UPEC
3 ntified a 48-kDa outer membrane protein that
is common to all 12 capsular serotypes of A. pleuropneum
4 single enzymes and 10 enzyme pairs proved to
be common to all 13 S. aureus strains, including many th
5 Many of these genes
are common to all 4 viruses and their roles in the predi
6 the resulting potential for oxidative stress
is common to all aerobically growing organisms.
7 tide polymorphism (SNP) loci on chromosome 2
was common to all affected sheep and it was the basis fo
8 i forms a body-centered cubic lattice, which
is common to all alkali metals.
9 Locomotion
is common to all animals and is essential for survival.
10 A 1.6-kb DNA amplicon that
was common to all AP-PCR profiles was extracted from aga
11 dal extent of the hippocampal formation that
was common to all behavioral conditions examined.
12 Attachment of the central bilin, which
is common to all biliprotein subunits, may facilitate al
13 reviously been described, which is likely to
be common to all box H/ACA snoRNP-substrate complexes.
14 which in the case of the latter two signals
are common to all cell types tested.
15 trol functional classes of REST targets that
are common to all cell types, whilst atypical motifs par
16 ental components of many signalling pathways
are common to all cells.
17 is stimulated by minute amounts of IFN-1 and
is common to all cells, is termed robust.
18 nce alignment, this structural feature might
be common to all cellulosomal clostridial CBM4 modules.
19 By performing a search for proteins that
are common to all CGIs, here we show high enrichment for
20 n the first 2 h host transcriptional changes
are common to all challenges indicating that Type III ef
21 ing and protection of exoskeletal chitin may
be common to all chitinous invertebrates.
22 tion-18 clones, only a single point mutation
was common to all clones: a cytosine-to-uracil transitio
23 hesize that similar superexchange mechanisms
are common to all cross-conjugated D-B-A triads.
24 uction of IL-1beta and systemic inflammation
are common to all cryopyrinopathy disorders, skeletal ab
25 Among them, only twelve compounds
were common to all cultivars in both peel and flesh.
26 pendently, other major domestication alleles
are common to all cultivated O. sativa varieties.
27 d aspects in the mechanism of oxidation that
is common to all cytochrome P450s.
28 exclusion and dielectric polarization, that
are common to all dense polar liquids.
29 feature, known as the boson peak (BP), which
is common to all disordered materials.
30 One of these factors
was common to all disorders, and another was exclusive t
31 e (NTase) domain and an OB domain (these two
are common to all DNA ligases) as well as a distinctive
32 Both of these properties
are common to all DNA strand exchange proteins examined
33 The spatial organization of metabolism
is common to all domains of life.
34 UPEC strains, whereas the role of genes that
are common to all E. coli has received much less attenti
35 otein oligomer formation elucidated here may
be common to all ETS proteins that autoinhibit.
36 lity group (HMG) chromosomal proteins, which
are common to all eukaryotes, bind DNA in a non-sequence
37 e core kinetochore consists of proteins that
are common to all eukaryotes.
38 n TBP consists of a 180 amino acid core that
is common to all eukaryotes, fused to a vertebrate-speci
39 role of neutrophils to producing lung injury
is common to all existing models of TRALI.
40 ovement, which remains to be elucidated, may
be common to all families of motor proteins.
41 e to each farm but did not vary over time or
were common to all farms at a given site but varied by s
42 hey may form a proton transport pathway that
is common to all [
FeFe]-hydrogenases.
43 toprotective mechanism that has been altered
is common to all flowering plants and crops, the finding
44 1 (EBNA1) and EBV-encoded small RNAs (EBERs)
are common to all forms of EBV latency, caspase-1 cleava
45 ges among orbitofrontal-striatal regions may
be common to all forms of OCD.
46 This pathology
is common to all forms of human pulmonary hypertension.
47 es specific for the DNA-binding domain, that
is common to all forms, identify multiple proteins.
48 In contrast, 18 ORFs
are common to all four isolates and may represent the mi
49 first part of the C-factor signaling pathway
is common to all four C-factor-dependent responses.
50 itional pattern of ectopic expression, which
was common to all four promoters.
51 Only 14 genes
were common to all four conditions.
52 (100% of reads) showed 50-53% of these data
were common to all four methods, and revealed trace bact
53 /MS) identified 1693 proteins, some of which
were common to all fractions and others of which were un
54 dependent of the carboxyl terminus, they may
be common to all functional alpha(1a)AR isoforms.
55 nthesis via inhibition of transglycosylation
is common to all glycopeptides (vancomycin) and lipoglyc
56 hat there is a protein shell that appears to
be common to all groups of double-stranded RNA viruses.
57 ique to each group and a criterion task that
was common to all groups.
58 ely applicable since the production of CoASH
is common to all HAT enzymes, regardless of protein subs
59 depletion of CD4-negative gammadelta T cells
is common to all HIV+ individuals.
60 Genetic alterations that
are common to all HNSCC types are likely to be important
61 Although this reproductive strategy
is common to all Hymenoptera, sex-determination is not s
62 anomaly among those so far investigated that
is common to all iAMP21 patients, and therefore the init
63 ine whether joint use of NF-kappaB and C/EBP
is common to all IL-17 target genes, we performed a comp
64 In particular, no strain
was common to all infants who developed necrotizing ente
65 Indeed, several glycans
were common to all isoform fractions that were analyzed.
66 te 1980s, yet no single virulence factor has
been common to all isolates from infected patients.
67 About 200 of these domain families
are common to all kingdoms of life and account for nearl
68 ein families found within a genome appear to
be common to all kingdoms of life.
69 een the nucleotidyltransferase domain, which
is common to all ligases, and the N-terminal domain Ia,
70 pparent during the chronic disease stage and
was common to all M. tuberculosis strains tested.
71 Replant disease of apple
is common to all major apple growing regions of the worl
72 in cortex reflect the fact that this feature
is common to all mammals.
73 n the intron of the homeotic gene DEFICIENS,
is common to all mantled clones and is associated with a
74 a switch-related target-locked P3b component
was common to all mapping conditions.
75 asite with a developmental cycle believed to
be common to all members of the genus Chlamydia.
76 This targeting of a receptor subunit that
is common to all members of an otherwise diverse family
77 rs by the phosphoryl transfer chemistry that
is common to all members of the PLD superfamily.
78 CueR, and ZntR indicates that this hinge may
be common to all MerR family members.
79 is driven by thermodynamic constraints that
are common to all metabolic pathways and pathway-specifi
80 is driven by thermodynamic constraints that
are common to all metabolic pathways and pathway-specifi
81 Although a core group of molecules
was common to all methods, each platform contributed a u
82 ind within the 120-bp conserved region which
is common to all minicircle classes; the remaining appro
83 between protein sequence and enzyme function
is common to all modular PKSs and makes these enzymes an
84 onal form of the asymptotic sampling formula
is common to all mutation models.
85 ggesting that activity toward this substrate
is common to all myotubularin family enzymes.
86 LC phase of the saturated phospholipids that
are common to all natural and clinical lung surfactants.
87 hether regulation of myelination by activity
is common to all neuronal subtypes or only some.
88 n may lie within the C-terminal portion that
is common to all NfeD homologues.
89 defects in the assembly and transport of NFs
are common to all NFL mutants studied thus far, but the
90 ctivator binding site, features that seem to
be common to all NGFI-B subfamily members.
91 omplex since the glycine-binding NR1 subunit
is common to all NMDARs investigated.
92 -terminal domain and a central G domain that
are common to all Obg proteins.
93 a5 isoform specific, whereas the other exons
are common to all of the RARbeta isoforms.
94 The fundamental mechanism appears to
be common to all of the photoactivatable and reversibly
95 perties because the HA-binding motif on CD44
is common to all of the isoforms.
96 , Bi and Sb due to the resonant bonding that
is common to all of them.
97 pparent, a portion of this signaling pathway
is common to all of these genes.
98 Platelet activation
is common to all of these pathways.
99 ox. 1.3kb and approx. 1.9kb transcripts that
are common to all organs, including the adult and prepub
100 he forebrain without the thalamic relay that
is common to all other sensory pathways.
101 t patients include a behavioral therapy that
is common to all participants.
102 regulating cell phenotype in the cortex that
are common to all parts of the neuraxis.
103 sses a conserved epitope known as H.8, which
is common to all pathogenic Neisseria species.
104 acycline exposure and subsequent progression
were common to all patients, and 38 of 40 were paclitaxe
105 acycline exposure and subsequent progression
were common to all patients.
106 ackbone hydrogen bonding interactions, which
are common to all peptides and proteins, is a simple ref
107 the part of the 3'-untranslated region that
is common to all previously characterized cathepsin B mR
108 tion in these structures on overexposure may
be common to all primates, including humans.
109 s abundance patterns, and a solar origin may
be common to all primordial mantle noble gases.
110 Interdomain contacts
are common to all prokaryotic Family GH15 proteins.
111 inetics of amyloid formation--a feature that
is common to all proteins implicated in neurodegenerativ
112 4 years of schooling (ages 7-11 years) that
were common to all pupils.
113 sites within the conserved alpha5 helix that
is common to all Rab family members.
114 mino acids in the C-X(3)-C-X(2)-C motif that
is common to all radical SAM enzymes, while the other is
115 The presence of either GluR2 or GluR3
was common to all receptor clusters.
116 If these three characteristics
were common to all resistant insects, specific crop-vari
117 -terminal C2B domain is the only module that
is common to all RIMs but is only distantly related to w
118 nputs from the SC to temporal visual cortex,
is common to all rodents and possibly most mammals.
119 The spv operon
is common to all Salmonella virulence plasmids.
120 evealed two dominant bacterial families that
were common to all sample types: Ruminococcaceae and Lac
121 nd between data and models, an approach that
is common to all science disciplines.
122 The two domains form the core subunit that
is common to all seven members of the NOX family.
123 Veillonellaceae and Lachnospiraceae families
were common to all sites, but the distributions of their
124 This observation
was common to all six promiscuous B7 epitopes identified
125 GF1 single-nucleotide polymorphism haplotype
is common to all small breeds and nearly absent from gia
126 Because these abnormalities
are common to all somatic cells, it is unlikely that dys
127 everal classification systems available that
are common to all species and link a protein sequence to
128 it is unknown whether RE-induced forgetting
is common to all species.
129 sus, GG/tNNANNNT, of which the ANNNT portion
is common to all sporulation-associated sigma factors, a
130 rray analyses revealed that this requirement
is common to all STAT5 target genes.
131 PFP/A(1)
was common to all strains from the outbreak and 11 hospi
132 Nearly 90% of the ORFs
were common to all strains examined, but, given the vari
133 The end point of graft survival
was common to all studies.
134 In addition to the problems that
are common to all such studies in critical illness, tria
135 zyme I (EI), a highly conserved protein that
is common to all sugar branches of the PTS.
136 bsent in cartilaginous and bony fish, and it
is common to all tetrapods.
137 or its unique RNA processing mechanisms that
are common to all the kinetoplastidea including Leishman
138 ng up-regulated expression of KCNA genes may
be common to all the gene family and play a functional r
139 of a low-energy ligand conformer family that
is common to all the ligands.
140 culated using a 456-base region of cox1 that
was common to all the data sets (median h=0.70130, media
141 ion or loss of a vulnerable group of neurons
is common to all these disorders and may allow the devel
142 Many of these molecules
are common to all three cell lines, whereas some are dif
143 onal inclusions, and neurodegeneration, that
are common to all three diseases.
144 n Apetala 2 (AP2)-type transcription factor,
are common to all three pathways.
145 ined (nonredundant) set of proteins actually
are common to all three strains.
146 of superfamilies are bacteria-specific, most
are common to all three superkingdoms of life and togeth
147 y sites of euchromatic underreplication that
are common to all three tissues and others that are tiss
148 ults show that the high-voltage potentiation
is common to all three channel types.
149 at at least a portion of the conduction path
is common to all three conducting states.
150 One synonymous variant
was common to all three families and was shown to induce
151 creased proximal joint IgG and C3 deposition
was common to all three genotypes in comparison with wil
152 r of origins and chromosome content per cell
was common to all three known suppressor mutations.
153 Indeed, 90% of SRF sites also bound by ELK4
were common to all three cell types.
154 tokine, apoptosis, and lymphocyte genes that
were common to all three infection groups.
155 aptor protein, important for MAPK signaling,
were common to all three IP-MS experiments.
156 Even though some clusters
were common to all three libraries, most putative genes
157 ee hundred and fifty-six (40%) polymorphisms
were common to all three populations and 366 (41%) were
158 genes (PIK3R3, ATP2A1, PI3, ADAM8, and HCN4)
were common to all top 20 significant genes that were id
159 ntaining 11 exons of which eight (exons 2-9)
are common to all transcripts and contain the entire cod
160 onsisting of GTPase and beta-barrel domains,
is common to all translational GTPases.
161 common to both TNT and RDX treatments, and 3
were common to all treatments.
162 ork for endoderm development that appears to
be common to all triploblastic metazoans.
163 Thus, this structure appears to
be common to all trypanosomatid protozoa and defines a n
164 MIDAS) on one edge of the beta-sandwich that
is common to all TSPs and may serve as a binding site fo
165 Eight amino acid coding changes
were common to all vaccine viruses; an additional two we
166 Certain aspects of care
are common to all vascular surgery procedures, including
167 e reduced to relatively simple elements that
are common to all vertebrates.
168 is a mechanism of epigenetic regulation that
is common to all vertebrates.
169 Because they
are common to all virulent Shigella spp., they are ideal
170 ion necessary for object and spatial scaling
is common to all visual cortical areas.
171 body heat and exhaled carbon dioxide (CO2),
are common to all warm-blooded hosts.
172 that belongs to the genus Gluconobacter and
is common to all wild-caught flies in this study, but ab