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1 y large population of precursor ions remains undissociated after the UV photoactivation period in ord
2 nt mechanisms, which indicated that both the undissociated and monodissociated anions of MH2Q were ki
3 (2+) complex is much higher than that of the undissociated ATP(4-).
4 r, different studies on Pt(111) suggested an undissociated bilayer structure in which the outer half
5 preferentially partitioned into molecules of undissociated boric acid and are then volatised during r
6 lations) studies, which find only the H down undissociated case.
7                   These layers or the intact undissociated CB were loaded with the fluorescent Ca2+ i
8  relevant ligand-receptor signaling from the undissociated cell fractions in massively parallel singl
9 at hair cell properties can be determined in undissociated cells and are likely to provide a good est
10 as therefore concluded that C152 is the only undissociated cysteine on the enzyme at pH 6.0, the pH o
11                                              Undissociated dihydroxy bile acids, alone or with 1-palm
12 lepipeds, and arrest at planar slip bands of undissociated dislocations.
13  probe the locations of radical sites in the undissociated electron transfer products as well as dist
14        The hydrosulphide ion (HS(-)) and its undissociated form, hydrogen sulphide (H(2)S), which are
15 II) from IRB can alleviate the inhibition of undissociated H2S on microorganisms through iron sulfide
16 CS-GrB complexes were very stable, remaining undissociated in salt concentrations upwards to 500 mM (
17 quid extraction to prevent inhibition due to undissociated MCCAs at a pH of 5.5 and circumvented the
18 idual MCMs either surviving until detection (undissociated) or dissociating into lower order multimer
19 fied gaussians to represent the peaks due to undissociated oxyHb, D (approximately 200 kDa), T+L (app
20 e first evidence for local Ca2+ signaling in undissociated pancreatic tissue.
21  UVPD mass spectra via resonance ejection of undissociated precursor ions after photoactivation.
22 ugh the exclusion of the large population of undissociated precursor ions with an MS(3) strategy, the
23 uld be due to the transmembrane transport of undissociated Sc hydroxo-complexes.
24                             We find that the undissociated structure leads to a vertical displacement
25 and-receptor interaction measurements within undissociated tissue sections.
26 ere recorded from outer hair cells (OHCs) in undissociated tissues from the organ of Corti.
27  to directly analyze the chemosensitivity of undissociated tumor tissue.
28 lts show that although aromatic acids in the undissociated (uncharged) form can diffuse across bacter
29                                              Undissociated volatile acid eluites (e.g., H2S, HCN, H2C
30 d inhibition due to higher concentrations of undissociated volatile fatty acids, help to explain the
31 yer observed on Ru(0001) cannot be formed of undissociated water molecules.