ライフサイエンスコーパス: terminal group

1 g of the spine, performed 6 hours after IRE (terminal group).

2 g systematic sampling from the corresponding terminal group.

3 ach the reduction potential of the diazonium terminal groups.

4 ntaining 5'-phosphomonoester and 3'-hydroxyl terminal groups.

5 aining 25% surface density of reactive azide terminal groups.

6 icular the separation of the two alkyl-amino terminal groups.

7 ent force fields and three different peptide terminal groups.

8 ration by adjusting the interactions between terminal groups.

9 solvation-like interaction with the -OCH(3) terminal groups.

10 methyl (CH(3)) or hydrophilic hydroxyl (OH) terminal groups.

11 al secondary amine group with respect to the terminal groups.

12 osited onto two SAMs differing only by their terminal groups, 4-benzenedithiol (BDT) and 4-methylbenz

13 The synthesis of the first terminal Group 9 hydrazido(2-) complex, Cp*IrN(TMP) (6)

14 the detection of ions characteristic of the terminal groups (alcohol, amine, carboxylic acid).

15 Three different terminal groups, an amino, a hydroxyl, and a carboxyl, w

16 This report describes N-terminal group analysis of six new proteins isolated fro

17 ed with minimal alpha-epimerization in the C-terminal group and allow for the coupling of N-terminal

18 lecular weight, increased amount of hydroxyl terminal groups and ferric reducing activities.

19 e the effect of the electron-richness of the terminal groups and of the bridging (hetero)arene on del

20 tively.Structure and data variability within terminal groups are displayed using small trees that hav

21 the same nucleic base sequence and different terminal groups are investigated at the interface betwee

22 cause partitioning free energies of N- and C-terminal groups are missing.

23 s using trialkoxysilane inks with functional terminal groups are presented, where the same ink-covere

24 gher than in DPPC for all carbons except the terminal groups at 30 mol % but were not significantly d

25 r124, a member of the large family of long N-terminal group B G protein-coupled receptors, few member

26 ent a unique function attributed to a long N-terminal group B-type G protein-coupled receptor in a ma

27 h a length of 11 carbon atoms and a carboxyl terminal group can efficiently block the charge transfer

28 The aggregated tree containing terminal groups can be annotated using aggregation of st

29 h enzyme binding pockets, while variation of terminal groups conferred the physicochemical and pharma

30 trifluoromethyl ketones containing neutral N-terminal groups displayed good oral activity, while thos

31 sidering a previous observation that a CH(3) terminal group favors penetration as the dominant initia

32 geting agents via either carboxylic or amine terminal groups for a number of biomedical applications,

33 oups in canthaxanthin) and of hole-accepting terminal groups for oxidations (as in beta-carotene).

34 avored by the presence of electron-accepting terminal groups for reductions (as the two carbonyl grou

35 whereas monomers with pyridine and thiophene terminal groups gave significantly higher rates of polym

36 ased polyoxometalate clusters with different terminal groups have been patterned successfully onto se

37 Hence, enlarging the conjugated area of the terminal-group in these A-D-A-type SMAs is a promising a

38 top electrode and a variety of heterocyclic terminal groups indicate that the metal-free bipyridyl g

39 , and methionine phosphinate bind with the N-terminal group interacting with Co2 and with the respect

40 regulated by small differences in the Al-SAM terminal group interaction energies.

41 ns of hepta-1,2,4,6-tetraenes with different terminal groups is investigated utilizing the unified re

42 adsorption of the PNA molecule with neutral terminal groups is the hydrophobic interaction of the no

43 electrostatic interactions with the anionic terminal groups, leading to contraction and a marked dec

44 tron photo-recycling process that modify the terminal group of a self-assembled monolayer on plasmoni

45 mutant revealed an interaction between the C-terminal group of the peptide and Glu(229) of the recept

46 Thus, by modifying the N-terminal group of tripeptidyl TFMKs, inhibitors can be d

47 he electrode surfaces changed with different terminal groups of the thiol molecules.

48 X-ray crystallography; the locations of the terminal groups of these ligands were not defined in the

49 lectrochemically reducing two axialdiazonium terminal groups on a molecule, thereby producing direct

50 The effect of the two N-terminal groups on the size distribution and quantity of

51 Monomers with spacer -O- or -C(CF(3))(2) and terminal group R = Ph exhibited similar kinetic behavior

52 BODA monomers with different spacer (X) and terminal groups (R) were compared.

53 eveal that one lysine probably has an -NH(2)-terminal group (rather than NH(3)(+)).

54 id that had carboxylic acid groups and amine terminal groups, respectively, and was confirmed by FTIR

55 to fit into the available screen space, with terminal groups selected based on sequence similarity.

56 of peptidyl TFMKs possessing a variety of N-terminal groups, several compounds were identified which

57 In compression, terminal groups sterically interact to stiffen the netwo

58 an be synthesized, we demonstrate how ligand terminal groups such as methyl, carboxyl and amine can b

59 tivities of different alkenes with different terminal groups that correlate with the electron affinit

60 ying the overall size and shape of the amino-terminal group; that modifications at both the amino and

61 the case where the PNA molecule has charged terminal groups, the main driving force of adsorption is

62 hylene glycol) (PEG) coupled with functional terminal groups to promote water-solubility and biocompa

63 havior, analogous to systems involving -COOH terminal groups to which cytochrome c can be attached el

64 lent interfacial bonds, fragmentation around terminal groups was found.

65 rimers of different generations with various terminal groups were analyzed, for the first time, using

66 ed the core structure of HPP but added bulky terminal groups were turned over to give products analog

67 ticles results in surface coating with amine-terminal groups, which act as a platform for a variety o

68 ormed SAM templates incorporated with alkyne terminal groups, which could further anchor the azido su

69 poration of polarizable chalcogen atoms into terminal groups, while controlling the molecular length

70 ymes appeared to act directly on the charged terminal group, with the highest clearance rates for ter

71 The f/Im and f/Py terminal groups yielded no advantage for their respectiv