ライフサイエンスコーパス: inner shell

1 n that involves all interactions outside the inner shell.

2 ne)bisacrylamide (DHEA) cross-linked pNIPMAm inner shell.

3 the outer shell and amine groups in the core/inner shell.

4 hrough the membrane bilayer to attach to the inner shell.

5 cent work reveals that pressure may make the inner shell 5p electrons of Cs reactive, causing Cs to e

6 stalline iron as the core, iron oxide as the inner shell and amorphous Si-S-O compound as the outer s

7 Our theory captures both the inner shell and outer shell coordination of divalent cat

8 eraction between hydroxyl groups in the PIOH inner shell and P2VP chains in the PS-b-P2VP diblock cop

9 hannel, from the outside of the virus to the inner shell, and erects a large dome domain directly abo

10 nd illustrate the impact of this hydrophobic inner shell approach.

11 rate unusually low sensitivity of a 1.14 mum inner-shell clock transition in neutral Tm atoms to BBR.

12 A quantum-mechanical treatment of the inner-shell complex with both a dielectric continuum and

13 entifies H(3)O(+) and H(2)O(5)(+) as natural inner-shell complexes, corresponding to the cases of n =

14 ium cation by a DNA base, with unprecedented inner-shell (direct) coordination of penta-hydrated sodi

15 rial states with high densities and multiple inner-shell electron excitations even for higher Z eleme

16 o displace a valence electron and often also inner shell electrons from LC eluents and atmospheric ga

17 f the elements and the non-reactivity of the inner-shell electrons are two related principles of chem

18 ility of the CsF(n) compounds shows that the inner-shell electrons can become the main components of

19 Rapid photoejection of inner-shell electrons produces 'hollow' atoms and an int

20 is observed through the energy shift of the inner-shell electrons.

21 The inner-shell extraction process changes the electrical ch

22 The scaffolding protein, which forms inner shells in the procapsid and B capsid, is exception

23 nfirmed that this protein forms thick-walled inner shells in the procapsid and the B capsid.

24 scattering indicating that the zinc ion has inner-shell interactions with one or more RNA ligands.

25 he heavy atom, providing further targets for inner-shell ionization and resulting in the emission of

26 and bromocyclo-pentane upon Br(3d) and C(1s) inner-shell ionization using coincidence ion momentum im

27 cture of the repeating hexameric unit of the inner shell is different from all other known capsid pro

28 In bacteriophage Phi6, this inner shell is first assembled as an icosahedral procaps

29 An example is XFEL-driven inner-shell Kalpha(1) (2p(3/2) -> 1s(1/2)) X-ray lasing

30 photoelectron is pulled out from a localized inner-shell molecular orbital by an X-ray photon.

31 l a view of the catalytic center in which an inner shell of conserved nucleotides is pivotal for pept

32 sity map of these capsids reveals a distinct inner shell of density-the RNA.

33 This 'arginine pocket' is lined with an inner shell of hydrophobic interactions that are ringed

34 aeroides, Glu L212 and Asp L213 represent an inner shell of residues of particular importance in prot

35 The Sec23p-Sec24p complex, which forms the inner shell of the COPII coat, sorts cargo into ER-deriv

36 zation of more highly charged cations to the inner shell of the ion atmosphere.

37 216 fold as a beta-sandwich which forms the inner shell of the T=3 capsid and residues 217 to 308 fo

38 ng protruding (P) domains are lifted off the inner shell of the virus.

39 of Co-N-doped graphitic carbon (Co-NGC) and inner shells of N-doped microporous carbon (NC) by templ

40 e arrangement suggesting the presence of an "inner shell" of lipids around membrane proteins that is

41 ergy is partitioned into three parts: 1) the inner-shell or chemical contribution that includes direc

42 B-capsids retain a relatively well preserved inner shell (or "small core") of scaffolding-assembly pr

43 measuring ion kinetics, our work shows that inner-shell photoelectron energies can also be sensitive

44 Inner-shell photoionization creates positive charge, whi

45 fragmentation process induced by bromine 3d inner-shell photoionization is used to identify the cis

46 te possible future X-ray control of physical inner-shell processes.

47 f a double-walled carbon nanotube, while the inner shell provides an unstrained reference pattern.

48 The coat inner shell recruits the Sec13p-Sec31p complex, leading

49 ning the photon energy of exciting X-rays to inner-shell resonances of the ions.

50 of the solubility difference, the unreacted inner shell section can be selectively dissolved by 2-pr

51 spatial resolution and the ability to access inner-shell states of heavy atoms.

52 anostructure with Li2O outer-shell and Li2O2 inner-shell surfaces.

53 addition creates a well-defined hydrophobic "inner shell" that suppresses water from disrupting the o

54 lis are encased by two concentric shells: an inner shell (the 'cortex'), made of peptidoglycan; and a

55 Such transparency, due to the presence of inner-shell vacancies, can be induced in all atomic, mol

56 of electronic states associated with double inner-shell vacancies.

57 Erosion of the inner shell via periodate-mediated cleavage of the 1,2-d

58 tes that in the predominant structure, eight inner-shell water molecules solvate the metal ion and do

59 e simplest model of IC 4997 suggests a thick inner shell with a density of about 107 atoms/cm3 and an