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1 e presence of resting levels of free [Mg(2+)]cyto (1 mM).
2                                     At [Ca2+]cyto = 100 nM, [Ca2+]mito remained near the lower limit
3 etermined [Ca2+]cyto under both basal ([Ca2+]cyto = 130 +/- 35 nM) and exocytosis-stimulated conditio
4 the specific juxtamembrane region within the CYTO (A375-P394) mediates homodimerization, and is domin
5                              To determine if cyto- and chemoarchitectonic characteristics are consist
6 d parvalbumin to identify the distinguishing cyto- and chemoarchitectonic features of the core, later
7         The observed regional differences in cyto- and chemoarchitectural features may reflect functi
8  the base of a combined analysis of multiple cyto- and chemoarchitectural stains and dense sequential
9 ng 117 white matter tracts and several novel cyto- and chemoarchitecturally defined structures, and t
10 the rat parietal cortical domain in terms of cyto- and chemoarchitecture as well as thalamic connecti
11 ns to determine the neuronal connections and cyto- and chemoarchitecture of the PVH in the commonly u
12 ular communication is the release of soluble cyto- and chemokines.
13 t three-dimensional (3D) concordance maps of cyto- and fiber architecture of the human brain, combini
14 gi-Cox and Nissl methods we investigated the cyto- and fiberarchitecture as well as the morphology of
15 tes revealed that Wnt5a is not essential for cyto- and functional differentiation, a role in luminal
16 s on lipid, protein oxidations and potential cyto- and genotoxic effects on intestinal epithelial cel
17 and haloacetamides that are found to be more cyto- and genotoxic than regulated DBPs.
18 nochloramine that have been shown to be more cyto- and genotoxic than regulated DBPs.
19  act in synergy to confer resistance to both cyto- and genotoxicities of NQO, whereas protection affo
20 e efflux result in low-level protection from cyto- and genotoxicities, this protection is greatly enh
21 metric probes that are used to measure their cyto- and genotoxicity may lead to inaccurate readings.
22                                The predicted cyto- and genotoxicity of DBPs was calculated using publ
23      Mismatch repair (MMR) strongly enhances cyto- and genotoxicity of several chemotherapeutic agent
24  (30 nm in diameter) which exhibit excellent cyto- and hemocompatibility and undergo MMP-induced asse
25  to the cervical spinal cord and distinctive cyto- and immunoarchitecture.
26 1 ex vivo hemispheres and processed them for cyto- and myelo-architectonic analysis.
27 phy combined with a detailed analysis of the cyto- and myelo-architecture.
28 O are columnar entities that correspond with cyto- and myeloarchitectonic inhomogeneities within the
29         We examined this issue using classic cyto- and myeloarchitectonic stains, immunolabeling for
30  fusion in eastern gorillas by examining the cyto- and myeloarchitecture within this region and obser
31  to be an effective alternative to potential cyto- and neurotoxic anti-VEGF agents in the treatment o
32             The mechanism of suramin-induced cyto- and neurotoxicity remains unclear.
33 hemotherapeutic drugs distribute through the cyto- and nucleoplasm of drug-sensitive cells but are ex
34 ynamics of several different proteins in the cyto- and nucleoplasm of living cells.
35 etaphase and resulting in complete mixing of cyto- and nucleoplasm.
36                        Based on quantitative cyto- and receptor architectonic analyses, we identified
37 macaque s32 and p32 supports equivalences in cyto- and receptor architecture.
38  for OB-BP1 confirmed high expression in the cyto- and syncytiotrophoblasts of the placenta.
39 Here we describe the topography, the chemo-, cyto-, and myeloarchitectonics, and the ultrastructure o
40 -GSA (array) cohort; (3) AD in a Han Chinese-Cyto (array) cohort; and (4) two AD Thai cohorts.
41 eukocytes and down regulated tumor-promoting cyto-/chemokine profile in bronchoalveolar lavage fluid,
42 s associated with immune cell activation and cyto-/chemokines in C9orf72 HRE mutant microglia versus
43  enhances the expression of pro-inflammatory cyto-/chemokines, such as IL8 and TNF, and promotes cell
44 raction was greatly impaired in PSGL-1 Delta cyto- expressing cells.
45 differentiation and excluding pathognomonic (cyto-)genetic alterations.
46                                    Employing cyto-, myelo-, and chemoarchitectural staining technique
47                  We performed a quantitative cyto-/myelo- and receptor architectonical analysis to pr
48                         Thus, differences in cyto-/myelo- and receptor architecture segregate the cor
49 ns however did not cause any increase in the cyto- or genotoxic (DNA strand breaks) effects in intest
50  of almond milk did not cause any changes in cyto- or genotoxic effects and antigenotoxic capability
51 ng in vivo tonotopic mapping with postmortem cyto- or myeloarchitectonics from the same individual.
52     Liquid cellular compartments form in the cyto- or nucleoplasm and can regulate aberrant protein a
53 smic and transmembrane domains of FtsN (FtsN(Cyto - TM)) facilitated localization of FtsN independent