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 ates associated with both N-defects and C-OH terminal groups.

4 ach the reduction potential of the diazonium terminal groups.

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

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

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

8 ent force fields and three different peptide terminal groups.

9 ration by adjusting the interactions between terminal groups.

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

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

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

13 with analogous zwitterions with only anionic terminal groups.

14 tional silanes on silanols, silica surfaces' terminal groups.

15 ons by employing either a hydrophobic -CH(3) terminal group (1-hexanethiol), a hydrophilic -OH termin

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

17 nal group (1-hexanethiol), a hydrophilic -OH terminal group (6-mercaptohexanol), or an equimolar mixt

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

19 ymethine chain and various electron-acceptor terminal groups A(1).

20 A dendrimer bearing 81 triazolylferrocenyl terminal groups adopts a more compact shell-like structu

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

22 These terminal groups allow for the formation of stable molecu

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

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

25 filtration (IMF-CMF), as assessed by free N-terminal group analysis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

41 glycol (PEG) functionalized with a maleimide terminal group for protein conjugation.

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

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

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

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

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

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

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

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

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

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

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

53 Changes in the terminal group lead to alterations in collision-induced

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

55 Among the three rhodanine-derived terminal groups, N-alkylthiazolonethione revealed the st

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

57 ue to hydrogen bonding between the -B(OH)(2) terminal group of the crosslinker and the I of the [PbI(

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

59 The effects of the terminal group of the SAM were probed by measuring quant

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

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

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

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

64 By tailoring the terminal groups on the perovskite surface and modifying

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

66 composition of the interface related to the terminal group orientation.

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

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

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

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

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

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

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

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

75 using different halide, or trimethylstannyl, terminal groups, suggestive of an electronically transpa

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

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

78 Due to less hindering terminal groups, the diammonio analogue forms more stabl

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

80 s correlated with the ability of different N-terminal groups to induce either an M or a P helix in so

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

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

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

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

85 um)-xylylene derivatives bearing carboxylate terminal groups were investigated as guests for the cucu

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

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

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

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

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

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