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1  show that stomatal CO(2) signaling requires basal ABA and SnRK2 signaling, but not SnRK2 activation.
2 duction, and the physiological importance of basal ABA signaling in stomatal regulation by CO(2) and,
3  the S4-S5 loop induced a larger increase in basal activity and agonist sensitivity at room temperatu
4 ha with alanine or methionine also increased basal activity.
5 lysosomal V-ATPase activity without altering basal activity.
6 loss of function, and residues that modulate basal activity.
7               Fmr1-KO rats exhibited reduced basal alpha power and enhanced gamma power, and these ra
8  increase in NOD1 abundance to 1.5-fold over basal amounts bypassed this low ligand concentration req
9                       Cancer cells with high basal AMPK activation are resistant to ferroptosis and A
10 ed population of VTA neurons projects to the basal amygdala (BA).
11 amine neurons in the VTA that project to the basal amygdala contribute to such a teaching signal for
12 e data also suggest a reciprocal shift, with basal and actin-activated ATPase activity of IFI-3a show
13 ysis on canine electrocardiograms containing basal and ANS-blockade segments.
14 ision, particularly to resolve errors at the basal and apical slices.
15 mouse B cell subpopulations showed different basal and BCR stimulation-induced phosphorylation levels
16    The cavity water column data exhibit both basal and benthic boundary layers, along with evidence o
17 airs native repressor activity and increases basal and DMRT2-mediated enhancer activity.
18 d risk of postprandial hypoglycaemic events, basal and dynamic betatrophin levels during the OGTT wer
19 e identified a potential role for hnRNP H in basal and dynamic mitochondrial function that informs me
20 ammatory stimulus in vivo and found that sub-basal and epithelial nerve densities in the cornea were
21 nNOS-expressing neurons drove changes in the basal and evoked arterial diameter without corresponding
22 large number of transition cells between the basal and spinous layer.
23 tacks had sub-optimal coverage (i.e. missing basal and/or apical slices), however most of them were l
24 hydraulic efficiency-safety trade-off in the basal angiosperms.
25                            We found that the basal arbor grew substantially between postnatal day 7 (
26 ale dataset of 849 3D reconstructions of the basal arbor of pyramidal neurons collected across early
27 a demographic forest model, we show that the basal area and compositional changes during forest succe
28 h increasing treatment intensity (decreasing basal area).
29              Clinical and neurophysiological basal assessment showed a moderate involvement of the me
30                                          The basal ATPase activity of Q2O2 Rca is repressed but stron
31                                YecSC had low basal ATPase activity that was moderately stimulated by
32                                              Basal autophagy in kidney cells is essential for the mai
33 lagella by initiating the production of hook basal bodies (HBBs), protein structures that anchor the
34 n of central MT pairs, proper orientation of basal bodies, and synchronized beating of motile cilia.
35 rotubule network and mitotic spindle and, as basal bodies, nucleate cilia and flagella.
36 ong BBP164 and the other three regulators of basal body assembly revealed that BBP164 and BBP65 are i
37 4 and found that it has an essential role in basal body biogenesis in T. brucei Further investigation
38 6 and TbBLD10 for their stabilization in the basal body.
39 vel inhibitors of ciliogenesis in normal and basal breast cancer cells.
40  with metastatic recurrence, particularly in basal breast cancer.
41 ug L(-1), respectively in the modified flask basal broth (MFBB) under shaking condition.
42 survival and S6 phosphorylation and enhanced basal calcium levels in human CLL cells.
43 view the effects of glucocorticoids on fetal basal cardiovascular function and on the fetal cardiovas
44 integrin Myospheroid, which is necessary for basal cell adhesion, is mislocalized in Sac1(ts) retinas
45 ks cyclophosphamide-induced intermediate and basal cell apoptosis, likely by phosphorylated AKT, and
46 tate and lung adenocarcinoma to melanoma and basal cell carcinoma.
47      Fgfr2KO mice had evidence of pathologic basal cell endoreplication associated with absent phosph
48 eed to better understand the contribution of basal cell hyperplasia and associated mucosecretory dysf
49 be replicated using LAE and SAE immortalized basal cell lines derived from healthy nonsmokers.Conclus
50                                Modulation of basal cell plasticity may represent a relevant target fo
51        The roles of Scrib and Lgl1 in apical-basal cell polarity have been studied extensively, but l
52  morula stage, outer cells acquire an apical-basal cell polarity, with expression of atypical protein
53 toward the expansion of the secretory primed basal cell subset in IPF.
54 d differentiation of human iPSCs into airway basal cells ("iBCs"), a population resembling the stem c
55 irmed that NOTCH2 maintains undifferentiated basal cells and restricts basal-to-ciliated differentiat
56 train secretory differentiation.Conclusions: Basal cells are dynamically regulated in disease and are
57 cible developmental trajectory: initiated in basal cells exhibiting an epithelial-to-mesenchymal tran
58 ike engulfment and entrainment of underlying basal cells, constituting a tumor-suppressive effect.
59 cell types, as well as six subpopulations of basal cells.
60 alveolar epithelial type II (AT2) or KRT5(+) basal cells.
61 ts a potential function of SMO in regulating basal ciliary trafficking of GLI2 when the pathway is of
62 illary light reflex, CT findings (compressed basal cistern and midline shift >=5 mm), presence of hyp
63 tation, terminal segment stenosis and absent basal collaterals.
64 en observed in dividing cells that lack more basal components [3].
65 e, associated with increased adiposity under basal conditions, and glucose intolerance and insulin re
66 nnel activity is dynamically modulated under basal conditions, during beta-adrenergic stimulation, an
67  interact to regulate channel activity under basal conditions, during beta-adrenergic stimulation, an
68  activity of cardiac Ca(V)1.2 channels under basal conditions, during sympathetic activation, and in
69                                        Under basal conditions, endocytosed AMPA receptors are rapidly
70 LTD and behavior that were not present under basal conditions.
71 " chains, where each promoter remains in the basal conformation.
72 l surface, facilitating infection of AT2 and basal cultures with SARS-CoV-2 and identifying club cell
73                              In our model, a basal-dendrites/somatic compartment included fast-inacti
74  better (77% vs. 23%; P < 0.001), mean tumor basal diameter (5.4 mm vs. 6.2 mm; P = 0.03), mean tumor
75 ar Melanoma Study (COMS) size, tumor largest basal diameter (LBD), and tumor thickness on prognostica
76                                  The mean MH basal diameter was 899.4 mum and the mean inner diameter
77 A shift of the fissures of both lungs in the basal direction was apparent for the older subjects, con
78 s in loss of F-actin and expansion of apical-basal domains, which comes at the expense of lateral mem
79 ention-free approach to mathematically model basal ECM turnover during embryogenesis by exploiting ou
80 iated by PuHox52 governs AR formation at the basal ends of stem cuttings from poplar trees.
81 h was induced rapidly (within 15 min) at the basal ends of stems upon cutting and played a key regula
82                    Free hydrogen (H(2)) is a basal energy source underlying chemosynthetic activity w
83 and 16 thereof were significantly altered in basal EV upon IL-13 treatment.
84                IFN-alpha/-beta have very low basal expression levels but are strongly induced upon ac
85 was accompanied by a significant increase in basal expression of IRF8 that was further induced by int
86         Furthermore, macrophages have low/no basal expression of ST2.
87 th periphery and brain, as well as increased basal extracellular dopamine in prefrontal cortex and 5-
88 proteases in the haltere, which prevents the basal extracellular matrix remodelling necessary for win
89 ented in MCSFA-HFD, accompanied by increased basal fatty acid oxidation, maintained glucose metabolic
90  aiding future investigations on the role of basal foot across different cilia systems.
91 -resolution imaging, we identify CEP112 as a basal foot protein and other candidate components of thi
92                                          The basal forebrain (BF) receives inputs from many nuclei of
93 stant symptoms are associated with losses of basal forebrain and striatal cholinergic neurons, sugges
94  that cholinergic input originating from the basal forebrain might similarly regulate inflammatory im
95 MENT When attention is required, cholinergic basal forebrain neurons may trigger increased release of
96 y, and freezing behavior, while thalamic and basal forebrain projections generate freezing behavior a
97                         Longitudinal loss of basal forebrain volume was larger in the preclinical com
98  to the hypothalamus, but not to the cortex, basal forebrain, or amygdala.
99             These data suggest that elevated basal FOXM1 activity predisposes HPV+ HNSCC to WEE1i-ind
100  and propanoate, which are considered as the basal function of Nrf2, while Keap1 KO-changed proteins
101                 We show that the main apical/basal functional differences can be accounted for by the
102      Reinforcement learning models treat the basal ganglia (BG) as an actor-critic network.
103 nds to treatments that decrease pathological basal ganglia (BG) beta oscillations (10-17 Hz in primat
104 culated in the neocortex and cortical lobes, basal ganglia (BG), hippocampi, and thalami.
105 ere located in the following areas: level of basal ganglia (caudate nucleus, putamen, corpus callosum
106     Subtype 2 showed increased volume in the basal ganglia and internal capsule, and otherwise normal
107 normal and stable anatomy, except for larger basal ganglia and internal capsule, not explained by ant
108  gene expression patterns and found that the basal ganglia and medium spiny neurons were most enriche
109 mal and patients demonstrate the role of the basal ganglia and other interconnected structures, such
110 racterize the functional interaction between basal ganglia and thalamus, we demonstrated that patient
111                                          The basal ganglia are important for movement and reinforceme
112 milar manner as the hyperdirect and indirect basal ganglia circuitry.
113 ctivity in HVC and occurred independently of basal ganglia circuitry.
114 y among cognitive, motor, and limbic cortico-basal ganglia circuits.
115 telencephalic signaling center important for basal ganglia development known in other vertebrates (i.
116 d to PD and Dystonia are likely amplified by basal ganglia downstream structures.
117 tory of tissue iron concentration across the basal ganglia during adolescence and provide evidence th
118 related directed medial prefrontal cortex to basal ganglia effective connectivity is abnormally incre
119 nals in the striatum play a critical role in basal ganglia function, such as reinforcement and motor
120 ation of potential volumetric changes of the basal ganglia in patients with PD who underwent staged S
121 e of Pontocerebellar Hypoplasia with typical basal ganglia involvement on neuroimaging.
122 r, the normative developmental trajectory of basal ganglia iron concentration during adolescence and
123 r, our results suggest a prolonged period of basal ganglia iron enrichment that extends into the mid-
124 utility of actions can be implemented in the basal ganglia network.
125 ry of beta bursting, both locally and across basal ganglia networks, impacts on motor performance in
126 logical methods to detail the progression of basal ganglia neuron type-specific pathology and the def
127 ursts of beta frequency band activity in the basal ganglia of patients with Parkinson's disease (PD)
128  sampled single-unit activity from connected basal ganglia output and thalamic nuclei (globus pallidu
129 centration using R2* relaxometry within four basal ganglia regions, including the caudate, putamen, n
130 ntum across patients, but not in cortical or basal ganglia regions.
131 ity between the medial prefrontal cortex and basal ganglia related to depression.
132 ntal cortex with reward prediction errors in basal ganglia support exploration of latent task represe
133                                     Atypical basal ganglia tissue iron levels have been linked to imp
134                            In contrast, some basal ganglia, cerebellar, and limited cortical areas sh
135                                          The basal ganglia, especially the caudate nucleus 'head' (CD
136  synchronization in the insular, cerebellum, basal ganglia, thalamus, operculum, frontoparietal corti
137                                   Within the basal ganglia, the globus pallidus pars externa (GPe) ha
138  A key role in this process is played by the basal ganglia, where neural activity and plasticity are
139  striatum is the main input structure of the basal ganglia.
140 the cerebral cortex, the cerebellum, and the basal ganglia.
141 d attention-related visual processing in the basal ganglia.
142 ease conditions associated with the mPFC and basal ganglia.
143 nificant hippocampal inhibition of amygdala, basal-ganglia, thalamus, orbital frontal cortex, inferio
144 cortico-thalamic connectivity within cortico-basal-ganglia-thalamic circuits.
145                 Further, we demonstrate that basal gene expression patterns are predictive of changes
146 tic analysis places these bat viruses as the basal group within the KoRV-related retroviruses.
147      In both cell types, promoters with high basal H3K4me2/3 activate in spite of some residual H3K27
148            The maturation of high-frequency (basal) hair cells was also affected in Ca(V) 1.3(-/-) mi
149 ysmal atrial fibrillation, basal QTc values, basal heart rate and dual antiviral therapy, age(OR 1.06
150 y, age(OR 1.06, 95% C.I. 1.00-1.13, p<0.05), basal heart rate(OR 1.07, 95% C.I. 1.02-1.13, p<0.01) an
151 c levels and leukocyte count and directly to basal heart rates(p<0.01).At multivariate stepwise analy
152 ll proliferation, without a reduction of the basal Iba1-positive population in the substantia nigra.
153                       The betaCA3 pathway of basal immunity is independent on stomatal- and salicylic
154 all metabolism/integrity in betaCA3-mediated basal immunity under both CO(2) conditions.
155 persensitive to SA could enhance SA-mediated basal immunity without compromising effector-triggered i
156                  Tipe0(-/-) enterocytes show basal induction of the Clu(+) regenerative program and a
157 est predictor of increased troponin was high basal inferolateral wall T2 (odds ratio, 18.2 [95% CI, 3
158                               An upregulated basal inflammatory profile accounted for reduced Escheri
159 E pigments, and retraction of microvilli and basal infoldings.
160 ates microtubule turnover, causing increased basal insulin secretion, depleting insulin vesicles from
161                         Daily injections for basal insulin therapy are far from ideal resulting in hy
162 redox stress confirmed that KEAP1 sheds many basal interactions and becomes associated with known lys
163 initiated by disconnections on the Prismatic Basal interfaces which establish the lattice corresponde
164 the SAE; 2) in the SAE, ACE2 is expressed in basal, intermediate, club, mucus, and ciliated cells; 3)
165                           Adult muscles show basal JAK-STAT signalling activity in the absence of any
166  acanthothoracids, the most phylogenetically basal jawed vertebrates with teeth, belonging to the gen
167 nt from those of WT vessels, suggesting that basal K(ATP) channel activity in LSM is not an essential
168 use many target cells are present, including basal keratinocytes, fibroblasts, dendritic cells, and l
169  edge protrusions but remain attached to the basal lamina, depressing more central neighbours to "tel
170 ed progenitor type lacking attachment to the basal lamina.
171 quence data available today, particularly on basal land plants and Charophyta, more attention should
172 Here we discuss recent investigations of how basal land plants make and sense hormones.
173 s showed a weak positive correlation between basal leaf angle and pathogenicity level in Johnsongrass
174                                         When basal leaf angle distribution data were correlated with
175 omyelocytic leukemia (PML) protein increased basal level of cccDNA transcription activity and partial
176  process in H. volcanii that operates at low basal levels and is induced by DNA breaks.
177 or, dipeptidyl peptidase 4 (DPP4) and higher basal levels of interferon in these cells.
178 ding that strains with both higher and lower basal levels tend to enrich their proteomes with antioxi
179  cells rise in frequency, only to decline to basal levels thereafter.
180        p53 is a short-lived protein with low basal levels under normal homeostasis conditions.
181 n the obese or normal-weight pregnant women (basal levels: 13.66 +/- 5.88 vs. 19.03 +/- 4.15 vs. 15.6
182                                          The basal lighting, consisting of blue 455 nm, red 627 and 6
183 nked gene, TTK, was most highly expressed in basal-like BC across multiple data sets.
184  radiosensitizing strategy for patients with basal-like BC, and efforts toward this end are currently
185 show that Aurora B expression is elevated in basal-like breast cancer (BLBC) compared with other brea
186 es has driven therapeutic advances; however, basal-like breast cancer (BLBC) remains clinically intra
187 indicated a higher double-positive signal in basal-like breast cancer than in luminal A or luminal B
188 h were specifically open and unmethylated in basal-like breast cancer.
189 source of airway stem/progenitors other than basal-like cells remains uncertain.
190 ulate expression of hundreds of genes in the basal-like gene expression signature, which were associa
191                                          The basal-like phenotype is consistent with the known sensit
192  tumor cells or forced expression of ZEB1 in basal-like tumor cells, two triple-negative breast cance
193 inuous variable), subtype (HER2-enriched and basal-like vs rest), and 13 genes composed the final mod
194 BP4-activated macrophages markedly increased basal lipolysis and impaired insulin-mediated lipolysis
195 h divalent lead [Pb(II)] at the surface of a basal litharge (PbO) layer.
196 m of D2R knockout mice, this mutant restored basal locomotor activity and cocaine-induced locomotor a
197 rtificial intelligence algorithm to classify basal lung opacities according to underlying pathologies
198 volvement of the lateral and postero-lateral basal LV and is associated mostly with variants in desmo
199 rrent suppression while maintaining a normal basal M-current activity in neurons.
200 ers that differed between normal luminal and basal mammary cells.
201 ates (i.e., the anterior entopeduncular area-basal medial ganglionic eminence of mammals).
202 e inflowing warm water layer and the rate of basal melting.
203 ly UP2 is seen in Saprolegnia spp. which are basal members of the oomycetes.
204 on channel-expressing pacemaker cells in the basal metazoan Hydra by using a combination of single-ce
205             Ctenophora is an early-branching basal metazoan lineage, which may have evolved neurons a
206 -0.001 +/- 0.021, and 0.004 +/- 0.035 in the basal, mid-, and apical slices, respectively (mean +/- s
207 I alpha2 mice did not show any difference in basal motor coordination, locomotor activity, or conditi
208  reducing pulmonary arterial pressure lowers basal MSNA in healthy humans.
209                 RIPK1 loss results in a high basal mTORC1 activity that drives defective lysosomes in
210 s glutamine-fueled anaplerosis that reverses basal Muller cell metabolism from production to consumpt
211 y arterial pressure is positively related to basal muscle sympathetic nerve activity (MSNA) under con
212                                          The basal muscle temperature (T(m) ) was lower in PAD rats t
213 te the profound diversity among ctenophores, basal neuroanatomical data are limited to representative
214 turnover rates in cultured brain cells under basal neuronal activity and found that protein turnover
215        Herein, we review what is known about basal NF-kappaBs and how that knowledge informs on the e
216 c frequency (CF) place and within one octave basal of the CF.
217  STFP memory without significantly affecting basal olfaction.
218 nced barrier integrity, so that directional (basal or apical) 5HT secretion was measurable.
219  the single NF-kappaB proteins found in some basal organisms have dual roles in development and immun
220 DM2 protein levels but resulted in increased basal p53 levels and growth defects in vitro and in vivo
221 ocated more basally, forming a robust apical-basal pattern.
222  55.9% were lymph node negative, 73.9% had a basal phenotype, and 67.5% received previous anthracycli
223 erone receptor expression (ER+/PR+), to more basal phenotypes characterized by active proliferation,
224 hronic iAs drives the transition toward more basal phenotypes characterized by impaired hormone recep
225 ned hydrophobic and hydrophilic regions: the basal plane and edges, respectively, the interplay of wh
226 mensional molecular network with defect-free basal plane of single-layer graphene.
227 zation densities are in general lower at the basal plasma membrane due to partial limited accessibili
228 s AP-1B-coated structures at or close to the basal plasma membrane in cell protrusions.
229  Hedgehog (Hh) is expressed in some anterior basal plate domains and by notochord and floorplate cell
230 y, and confocal biomicroscopy of corneal sub-basal plexus (SBP).
231  cells disperse from clusters lacking apical-basal polarity, a hallmark of advanced epithelial cancer
232 th and/or cell proliferation, loss of apical-basal polarity, and appearance of epithelial-to-mesenchy
233        Phylogenetic analysis places SFV in a basal position among a new subgroup of recently recogniz
234 and energy to support growth(1-3) or to meet basal power requirements(4) during periods of resource s
235 ased contractility also impaired movement of basal progenitors during hair placode morphogenesis and
236 ctivation of cMET, a master regulator of the basal program, and simultaneously promoted expression an
237 male gender, paroxysmal atrial fibrillation, basal QTc values, basal heart rate and dual antiviral th
238 ultaneous up-regulation of vimentin and high basal Rac1-GTP levels when measured biochemically.
239 ry and data are also shown to agree that the basal rates of both R(d) and V(cmax) assessed at 25 degr
240                          Following 3 days of basal recordings, reserpine was administered on three co
241 ponsible for anthocyanin pigmentation of the basal region ('cup') in the petal of C. gracilis ssp. so
242 genetic data confirm that RNLs contribute to basal resistance, are fully required for TNL signaling,
243 lies act in an unequally redundant manner in basal resistance, effector-triggered immunity (ETI) and
244 ired for Avr2 recognition but contributes to basal resistance.
245 bacteria, fungi, algae, and protozoans and a basal resource for the aquatic food web, showed high PFA
246       In doing so, we measure the effects of basal resource richness on food chain length, niche brea
247                                Flows of most basal resources were negatively related to resource C:P,
248 plenic T cells from the HFS mice, glycolysis/basal respiration ratio was significantly reduced and re
249         We use metabolic modeling to predict basal ROS production levels (ROStype) for 695 of these s
250 hiskers, by fitting a 3D Bezier curve to the basal section of each target whisker.
251                                Moreover, the basal SG lack the competence to respond to FGFR signalin
252 ted in mislocalization of cone nuclei to the basal side of ONL in mouse retina.
253 l typically extending from the apical to the basal side of the developing cortex.
254 h along which their nuclei can return to the basal side.
255     NHBE cells secrete EVs to the apical and basal side.
256 ind that, in addition to sensing osmolarity, basal skin cells in zebrafish larvae are also sensitive
257 ifying tsunami backwash deposits, namely the basal soft sediment micro-deformations.
258        In cells expressing the C674S mutant, basal SR calcium content was decreased by 31% and the H(
259                                           At basal steady state Zip14 KO mice exhibited a phenotype t
260 , intestinal-specific AhR knockout increases basal stem cell and crypt injury-induced cell proliferat
261 nto fully polarized, functional units with a basal stem cell niche and luminal differentiated cell zo
262                                              Basal stem cells fuel development, homeostasis, and rege
263 f multiple specialized cell types, including basal stem cells, mucus-secreting goblet cells, motile c
264  to discern disease-dependent changes within basal stem cells.Methods: Single-cell RNA sequencing was
265 illion years old), the phylogenetically most basal stem osteichthyan, visualized by synchrotron micro
266                                 We show that basal stem/progenitor cell maintenance is regulated by a
267                                  Human adult basal stem/progenitor cells (BSCs) obtained from chronic
268 iquid interface cultures from primary airway basal stem/progenitor cells; this can be replicated usin
269  recovers aralar-KO neurons from deficits in basal-stimulated and glutamate-stimulated respiration, e
270 R and CD63 and contained significantly lower basal stores of histamine.
271 thout substantial remodeling of pre-existing basal structures.
272 es than unexposed ER+ tumors, in particular, basal subtypes that tend to develop therapy resistance a
273 land and the peduncle, optic, dorso-lateral, basal, subvertical, frontal, magnocellular, and buccal l
274 d epithelium, nuclei synthesize DNA near the basal surface and move apically to divide.
275 ochastic nuclear movement between apical and basal surfaces of neuroepithelia during interkinetic nuc
276 u suppression could even unravel a defect in basal synaptic transmission in a mouse model of amyloid
277 ophagy and mitochondrial fusion and promotes basal tearing.
278 sterior shh pallidal domain representing the basal telencephalic signaling center important for basal
279 soma in cave Astyanax in the olfactory bulb, basal telencephalon, preoptic nuclei, ventral thalamus,
280  for HSF1 - between Antarctic fishes and the basal temperate notothenioid Eleginops maclovinus.
281 er Doppler on the fingertip for 3 minutes at basal temperature (SBFBT) and at 37 degrees C (SBF37) (t
282 ing the following formula: (SBF37-SBFBT)/(37-basal temperature).
283 B12 as a candidate enzyme capable of driving basal testosterone production in the testis.
284 roduction by the testis but does not control basal testosterone production.
285  that SGs are equally distributed apical and basal to the CG membrane, so that the apical SGs are not
286 n speed was as large as 1 mm/s in the region basal to the peak responding location.
287 s undifferentiated basal cells and restricts basal-to-ciliated differentiation, and we present eviden
288 of hydromineral balance is an evolutionarily basal trait among vertebrates.
289  polymerase II subunits and their associated basal transcription factors, with the coordinated gain a
290 ion at dawn and dusk, which are enriched for basal transcription regulation, mRNA processing and expo
291 lcitonin gene-related peptide expression and basal trigeminal nociception.
292 quencing to generate a cellular landscape of basal TSPO gene expression in the hippocampus of adult (
293 xperimentally difficult to determine whether basal turnover is also important.
294 ongest inverse association was observed with basal-type tumors (MVHRQ5vsQ1: 0.67; 95% CI: 0.45, 1.01;
295  the pathophysiology of U-HAE increasing the basal vascular permeability.
296  oxide scavenging potency of CFH, increasing basal vascular tone and impairing tissue perfusion.
297 mice, with BMP signaling being restricted to basal VSNs and at the marginal zones of the VNO: the sit
298 he functional maturation and connectivity of basal VSNs.
299 thesise that under thinner ice, increases in basal water pressure offset a larger proportion of the i
300     ANO1 was expressed within the esophageal basal zone, and expression correlated positively with di

 
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