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1 ects of A1492G or A1493G (or both) mutations were compensated by 2'fluorine substitutions in the mRNA
2 of dispensable genes, whereas 15-28% of them are compensated by a duplicate, and only 4-17% are buffe
3 oup box and import-dependent phosphorylation are compensated by a microsatellite-associated transcrip
4 prachiasmatic nucleus (SCN) neurons, and may be compensated by a change in Rbfox2 expression.
5 ing rarefaction inside the plasma center can be compensated by a gas stream application.
6 ts flanking regions and such mutations could be compensated by a hydrophobic substitution elsewhere w
7    In many cases, their reduced capacity can be compensated by a more intensive educational intervent
8 orm with the lower intrinsic birth rate must be compensated by a more than proportionately lower comp
9 at a growth-inhibiting mutation in Ufe1p can be compensated by a mutation in Sec20p.
10 wo proteins if a mutation in one protein can be compensated by a mutation in the second.
11 d by thymidine kinase 2 (TK2) deficiency can be compensated by a nucleoside kinase from Drosophila me
12         Higher energy expenditure appears to be compensated by a parallel increase in food intake.
13 ation, and this loss is expected at times to be compensated by a selected event of a particular type:
14         A significant reduction of GLS could be compensated by a small increase of GCS or wall thickn
15  of the Y305F-PP(i) hydrogen bond appears to be compensated by a very slight shift in the position of
16           However, the unsaturation seems to be compensated by a weak M-C(arene) bonding interaction
17 n which the confinement of each lattice beam is compensated by a blue-detuned laser beam.
18 gma donation from the MeAN ligand to Cu that is compensated by a decrease in the extent of peroxo to
19 tion enthalpy (deltaH=+7.5 kcalmol(-1)) that is compensated by a favorable association entropy (Tdelt
20 haracterized by an unfavorable enthalpy that is compensated by a favorable entropy, making the intera
21 ) loses one water of hydration, but the loss is compensated by a hydrogen bond, first with the backbo
22 nteractions in the noncovalent Mo(8) cluster is compensated by a more extended hydrogen-bond network
23 eviates from structure-based prediction, and is compensated by a net entropy increase providing at le
24              This architectural interruption is compensated by a new topological feature of quadruple
25 ce with an ISM, the negative potential drift is compensated by a positive potential drift related to
26 naptic downscaling during stimulation, which is compensated by a reduced drive after stimulation.
27 substitution of Tyr to Phe in the YMDD motif is compensated by a second substitution of Met to Val in
28                            We find that this is compensated by a shear-dependent increase in the numb
29                     X-chromosome gene dosage is compensated by a specialized protein complex that inc
30                   A large enthalpic decrease was compensated by a large loss of conformational entrop
31  smaller ovaries and fruit as expected, this was compensated by a larger number of fruit-due mainly t
32 tuitive, negative activation enthalpy, which was compensated by a significant decrease in the activat
33  the impairments to hepatocyte proliferation were compensated by a response of oval cells in Nemo(Del
34 that, on average, a deleterious mutation can be compensated by about nine different intragenic compen
35  compensation behavior, i.e., most of donors are compensated by acceptors or vice versa, is self-regu
36 vers, in (JAX)CAV1-/- livers CAV1 deficiency is compensated by activation of anabolic metabolism (pen
37                 Mechanistically, loss of p21 was compensated by activation of Sestrin2, which impaire
38  one region of the cortical motor system may be compensated by activity in areas that retain corticof
39 n predictable and incremental steps that can be compensated by adaptive methylation/demethylation.
40 The destabilizing effects of these mutations are compensated by additional somatic mutations located
41  the transgenic TCRbeta chain, and that this was compensated by additional contacts formed by endogen
42  region a lower number of neurons firing can be compensated by adjustments in firing rate or place fi
43         Expression of human PLN in the mouse is compensated by alterations in Ca2+-handling proteins
44 e and after mixing, and variations in T(2)'s are compensated by an S(0) reference (no mixing).
45  the diminution of flow at high pressure can be compensated by an increase in voltage.
46 rved when parental genotypes are missing can be compensated by an increase of offspring number.
47 n, a decrease in the rate of the elimination is compensated by an increase in affinity for OAS, leadi
48                              Loss of RIIbeta is compensated by an increase in the RIalpha isoform, ge
49  a decline in presynaptic release properties is compensated by an increased excitatory response.
50 ric field existing near the cell center line is compensated by an opposing inward-directed radial ele
51  presenilin-mediated ER Ca(2+) leak function was compensated by an increase in expression and functio
52 ateral striatum revealed a 20% decrease that was compensated by an increase in ipsilateral ventricula
53  hematopoietic activity in the marrow, which was compensated by an increase in mobilization and recru
54                  Reduced insulin sensitivity was compensated by an increased insulin response to gluc
55 s GILZ during the resolution of inflammation is compensated by AnxA1 overexpression.
56 tal for photosynthesis and growth and cannot be compensated by any other AEF or anoxic metabolic resp
57 gnetic coupling between the Dy(III) ions can be compensated by application of a small (700 Oe) dc fie
58 ith aging than the virus infection and could be compensated by applying a 5x higher dose of DEET.
59               Fibre cooling after the T-jump was compensated by applying a warming (40 kHz AC, 200 ms
60 eadily contorted when their internal strains are compensated by attraction with the inner surfaces an
61 o any bends in the first half of the segment are compensated by bends in the opposite direction in th
62 ent 6-6 ring system to a 6-5 ring system can be compensated by bridge homologation to restore the ove
63 the role of CaBP-D28k in calcium homeostasis is compensated by CaBP-D9k, we generated VDR/CaBP-D28k d
64 ateau" phase in which cell loss by apoptosis was compensated by cell proliferation, followed by a lat
65  way that changes in cis-regulatory elements are compensated by changes in trans-regulatory elements.
66         We show that the loss of binding can be compensated by changes at the P10 position.
67 mperature-induced changes in neural networks are compensated by changing their neuromodulatory state:
68 rbenium-like transition state is approached, is compensated by closing the anionic loop, L6, onto the
69 se in the edge energy of scalloped membranes is compensated by concomitant decrease in the deformatio
70 large energetic loss due to dehydration must be compensated by coordination with protein atoms.
71 s on the polymer backbone in these materials are compensated by covalently bonded counter-ions.
72 ial accessory role, or perhaps that its loss is compensated by cross talk or redundancy with other pe
73 ulated by influences that compensate for, or are compensated by, decreased IGF-I synthesis.
74  an expansion of the active site that cannot be compensated by donor-acceptor distance sampling.
75 uses a drastic defect in mRNA synthesis that is compensated by down-regulation of mRNA degradation, r
76  those gene deletions that have no phenotype are compensated by duplicate genes.
77 l diversity and the lack of somatic mutation are compensated by early onset of TdT activity and other
78                  Inactivation of NHEJ or SSA is compensated by elevated HR.
79  beta-cell lipid blindness), but this defect was compensated by elevated plasma levels of FFAs and ke
80 ) function in mice with Serca2 knockout (KO) is compensated by enhanced plasmalemmal Ca(2+) fluxes.
81  autoimmunity, and suggest that its loss can be compensated by ERK2.
82 ifferentiation noted in CD4(Stat3)(-/-) mice is compensated by exaggerated increases in Foxp3-, IL-10
83 ns in an additive way (e.g., little time can be compensated by extra attention or extra stimulus inte
84 k of intracellular TLR9-associated HMGB1 can be compensated by extracellular HMGB1.
85 haracterized by an unfavorable enthalpy that is compensated by favorable entropic contributions.
86 ppropriate anchor residue at P2 in AMQMLKETI is compensated by favorable interactions of the glutamin
87  that the absence of deleted genome segments was compensated by gene expression from wild-type copies
88    This imbalance between fission and fusion is compensated by growth of mitochondrial organelles.
89 ux through NADPH oxidase is electrogenic and is compensated by H(+) efflux through proton channels th
90  that the structural orders with low entropy are compensated by high formation energies due to the pr
91            A subset of these differences can be compensated by higher levels of A315T expression, ind
92 iring rate in the network by deafferentation was compensated by homeostatic synaptic scaling of recur
93 tage, provided that defects in DC activation were compensated by IL-12 treatment early after infectio
94 ower rates of rbcL transcription in the dark are compensated by increased mRNA stability.
95 ta, which suggest that reduced cell size can be compensated by increased cell proliferation to allow
96 associated with sleep deprivation (SD) could be compensated by increased daytime energy consumption.
97 meric boundaries, and this effect appears to be compensated by increased recombination activity in ch
98              Thus, Crescent loss-of-function is compensated by increased expression of its ventral co
99  expression in UCP1-KO mice, and loss of SLN is compensated by increased expression of UCP1 and brown
100    The inefficiency of the anaerobic pathway is compensated by increased glucose flux, a phenomenon f
101 e, such that reduced input from some factors is compensated by increased input from different regulat
102 OD mice is inefficient; however, this defect is compensated by increased proliferation of natural Tre
103 howed that loss of sulfation at one position is compensated by increased sulfation at other positions
104 xidoreductase activity of the complex, which was compensated by increased biogenesis of respiratory c
105                        Increased sterol loss was compensated by increased cholesterol synthesis in Ce
106                     The functional isolation was compensated by increased feedback excitation within
107 ains with terminus-proximal dusB-fis operons was compensated by increased fis expression such that th
108 m untreated Parp-2-/- mice, but this deficit was compensated by increased rates of self-renewal, asso
109 ly of primary and mixed consumers most often are compensated by increases in high-level consumers, wi
110         Loss of these polar interactions can be compensated by increasing the apolar character of eit
111 ults indicate that this filtering appears to be compensated by increasing the synaptic conductance at
112                 The reduction in force could be compensated, by increasing the duration of the Ca2+ t
113 otracer activity (100%, 50%, 25%, and 12.5%) was compensated by increasing acquisition time (2, 4, 8,
114 his failure of HAS1 to synthesize hyaluronan was compensated by increasing the cellular content of UD
115 e absence of myo-inositol synthesis in roots is compensated by inositol/ononitol transport in the phl
116 isruption of universal tertiary interactions is compensated by interactions with an enzyme that makes
117                               The BP cluster was compensated by interactions involving unpaired cytos
118  Therefore, the lower level of PDEalpha mRNA is compensated by its more efficient translation to achi
119          Yet the inefficiency of the ON cell is compensated by its presynaptic arrays providing a hig
120 ta indicate that laminin-111 function cannot be compensated by laminin-511.
121 n net radiative fluxes at the surface; these are compensated by larger changes in the sum of latent a
122 showing no evidence that an indel event must be compensated by local amino acid replacement.
123  thinning of the underlying crust appears to be compensated by mantle rocks of anomalously low densit
124  less severe chronic disability, which might be compensated by modifying the built environment and pr
125 ion or disease progression and that they may be compensated by more robust cellular responses.
126 sites, particularly in position -3, that may be compensated by more stringent requirements for positi
127  to a sub-optimal form (GUG or UUG) tends to be compensated by mutations in the Shine-Dalgarno sequen
128 re disruptive in the native complex, but can be compensated by mutations on the interacting partner.
129 vo, deleterious mutations at the H chain may be compensated by mutations on the L chain.
130  The unique roles of endothelial VEGF cannot be compensated by neuronal VEGF and underscores the high
131 ative stabilizing contacts during activation is compensated by non-native transient atomic interactio
132                           Weak binding sites are compensated by optimal syntax, whereas enhancers con
133  propose that defects in proteasome function are compensated by other proteases and that the combinat
134 nt role during mouse development that cannot be compensated by other Cdk inhibitors.
135 ion, morphological effects are subtle or may be compensated by other mechanisms.
136 ylated proteins and/or that its function may be compensated by other mechanisms.
137 er, a single O-glucose mutation in EGF12 can be compensated by other O-glucose residues in neighborin
138 cate that the lack of ERP/MKP-1 activity can be compensated by other phosphatases in vivo.
139 CD8(+) T-cell behavior but in some cases can be compensated by other signals.
140 ng cell proliferation and stress that cannot be compensated by other Ub genes.
141 indings indicate that increased VGCC density is compensated by other cellular Ca2+ regulatory mechani
142 s of exercise-trained miniature Yucatan pigs is compensated by other cellular Ca2+ regulatory mechani
143  bond network, such that loss of one contact is compensated by other new contacts.
144  the assembly of the [Fe-S] clusters of NifB was compensated by other non-nif machinery for the assem
145 ssion due to IRS-2 small interfering RNA can be compensated by overexpression of dominant-active muta
146 letion reduced Mnk1 activation, which cannot be compensated by p38beta.
147 s of Pax-6 binding to the -273/ -246 element is compensated by Pax-6 binding to the -306/-274 element
148 e affinity of the silanized surfaces for DNA was compensated by precoating the slide with single-stra
149 model into which loss of DAergic cells could be compensated by recruiting newly formed neurons.
150    This suggested that decreased degradation was compensated by reduced transcription, which was conf
151 auses charge in-neutrality in the GONR which is compensated by releasing *OH functional groups.
152        The lack of alpha3 and beta2m domains is compensated by replacing two hydrophobic patches at t
153 tion can cause dNTP imbalances, which cannot be compensated by RNR or other enzymatic activities.
154 is often associated with fitness loss, which is compensated by secondary mutations.
155 gesting that the reduction in sigma-donation is compensated by significant attenuation of pi-back-bon
156                     In addition, this effect was compensated by SIRT1 overexpression and accompanied
157 damping suppresses these excitations, it can be compensated by spin-transfer torques when an electric
158 to the 2'-amine substitution is rare and can be compensated by stabilizing folding conditions.
159 ]P lesion-induced distortion/destabilization is compensated by stabilizing aromatic ring system-base
160 d strengthening of the strongest storms will be compensated by storm tracks moving offshore at the la
161 ned by TCR affinity, except in one case that was compensated by substantial CD8 involvement.
162 asparagine variant of L11-C76 residue 69 has been compensated by substitution of a 1062/1076 base pai
163            The relative scale of impact must be compensated by systematic improvements whether by dep
164  residue 30's interaction with the substrate are compensated by the coevolving L449F and S451N cleava
165 ivity upon mutation of a TATA-box or DPE can be compensated by the addition of an MTE.
166 e fact that the Rep' protein function(s) can be compensated by the bacterial replication machinery to
167  that the weakened H-bonding in U-A pair may be compensated by the base stacking, and that the stacki
168 that the extinction of one species can often be compensated by the concurrent removal or population s
169 volve an increase in free energy, which must be compensated by the free energy released by the increm
170  was calculated and found to be too large to be compensated by the negative entropy of reduction of t
171 hat is, the loss of function in one copy can be compensated by the other copy or copies.
172  an intraperitoneal glucose tolerance curve, being compensated by the increased beta-oxidation and re
173 ack of this domain in the short RGS9 isoform is compensated by the action of a G protein effector sub
174  The weaker contribution of the variant CREs is compensated by the activity of two upstream elements
175 hat the loss of the hydrogen bond to alpha43 is compensated by the addition of a new hydrogen bond to
176                                    This loss is compensated by the AP2V mutation, which reorients the
177             Absence of CAV1 in mouse tissues is compensated by the development of a carbohydrate-depe
178                     This monogenic situation is compensated by the differential expression of two alt
179 othesize that the loss of these interactions is compensated by the entropic driving force for fluorin
180                      This low endothermicity is compensated by the entropy gain upon splitting the O-
181 ides unfold, a loss of intramolecular energy is compensated by the formation of additional water-pept
182 t to which the desolvation of buried charges is compensated by the formation of hydrogen bonds and io
183    The lower intrinsic affinity of CH donors is compensated by the high degree of preorganization exh
184 ial negative charge of the GDP leaving group is compensated by the Mg2+, and by the closing of loop L
185  population in which the loss of a stem cell is compensated by the multiplication of a neighbor, lead
186 PN, and its loss of pro-chemotactic activity is compensated by the release of OPN-CTF, which assumes
187 lts indicate that the decreasing temperature was compensated by the accelerated drying trends of soil
188  max2-1, the reduction in response to low Pi was compensated by the application of a synthetic strigo
189  demonstrated that the loss of SWA during SR was compensated by the end of the second recovery day.
190 n in oxidative PPP-mediated ribose synthesis was compensated by the HIF-1alpha-dependent activation o
191  in which the loss of self-splicing activity was compensated by the recruitment of host-encoded prote
192                       The loss of E-cadherin was compensated by the transcriptional upregulation of t
193 %, 24%, and 14% of the anterior corneal coma were compensated by the posterior cornea in the advanced
194        However, this lower absolute affinity is compensated by their lower molecular weight and more
195 lity of these species is on the decline this is compensated by their proficiency to reproduce asexual
196 ion of lipid headgroups of opposing bilayers is compensated by thermodynamically favorable interactio
197                           However, this loss was compensated by TNF-alpha preconditioning as the expr
198          We propose that the loss of UCP may be compensated by UCP2, a newly discovered homologue of
199                           Specific functions were compensated by upregulation of genes at low tempera
200                                Head movement was compensated by using coregistration between frames (
201                                       Images were compensated by using a compensation ratio and a run
202 me increase for atoms on the protein surface is compensated by volume decreases in water molecules ne
203    In Dictyostelium discoideum, loss of SCAR is compensated by WASP moving to the leading edge to gen

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