ライフサイエンスコーパス: cyto-

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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 gi-Cox and Nissl methods we investigated the cyto- and fiberarchitecture as well as the morphology of

14 tes revealed that Wnt5a is not essential for cyto- and functional differentiation, a role in luminal

15 s on lipid, protein oxidations and potential cyto- and genotoxic effects on intestinal epithelial cel

16 and haloacetamides that are found to be more cyto- and genotoxic than regulated DBPs.

17 act in synergy to confer resistance to both cyto- and genotoxicities of NQO, whereas protection affo

18 e efflux result in low-level protection from cyto- and genotoxicities, this protection is greatly enh

19 metric probes that are used to measure their cyto- and genotoxicity may lead to inaccurate readings.

20 The predicted cyto- and genotoxicity of DBPs was calculated using publ

21 Mismatch repair (MMR) strongly enhances cyto- and genotoxicity of several chemotherapeutic agent

22 to the cervical spinal cord and distinctive cyto- and immunoarchitecture.

23 1 ex vivo hemispheres and processed them for cyto- and myelo-architectonic analysis.

24 phy combined with a detailed analysis of the cyto- and myelo-architecture.

25 O are columnar entities that correspond with cyto- and myeloarchitectonic inhomogeneities within the

26 We examined this issue using classic cyto- and myeloarchitectonic stains, immunolabeling for

27 fusion in eastern gorillas by examining the cyto- and myeloarchitecture within this region and obser

28 to be an effective alternative to potential cyto- and neurotoxic anti-VEGF agents in the treatment o

29 The mechanism of suramin-induced cyto- and neurotoxicity remains unclear.

30 hemotherapeutic drugs distribute through the cyto- and nucleoplasm of drug-sensitive cells but are ex

31 ynamics of several different proteins in the cyto- and nucleoplasm of living cells.

32 etaphase and resulting in complete mixing of cyto- and nucleoplasm.

33 macaque s32 and p32 supports equivalences in cyto- and receptor architecture.

34 for OB-BP1 confirmed high expression in the cyto- and syncytiotrophoblasts of the placenta.

35 Here we describe the topography, the chemo-, cyto-, and myeloarchitectonics, and the ultrastructure o

36 eukocytes and down regulated tumor-promoting cyto-/chemokine profile in bronchoalveolar lavage fluid,

37 enhances the expression of pro-inflammatory cyto-/chemokines, such as IL8 and TNF, and promotes cell

38 raction was greatly impaired in PSGL-1 Delta cyto- expressing cells.

39 differentiation and excluding pathognomonic (cyto-)genetic alterations.

40 ns however did not cause any increase in the cyto- or genotoxic (DNA strand breaks) effects in intest

41 of almond milk did not cause any changes in cyto- or genotoxic effects and antigenotoxic capability

42 ng in vivo tonotopic mapping with postmortem cyto- or myeloarchitectonics from the same individual.

43 smic and transmembrane domains of FtsN (FtsN(Cyto - TM)) facilitated localization of FtsN independent

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