ライフサイエンスコーパス: tachyplesin

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1 in potency of 2-10-fold compared to that of tachyplesin.

2 nt for the membrane-disruptive activities of tachyplesins.

3 was examined in two peptide series based on tachyplesin, a known beta-stranded antimicrobial peptide

4 4 dendrimer are comparable to protegrins and tachyplesins, a family of potent antimicrobials containi

5 Finally, the combination of tachyplesin and human serum markedly inhibited the proli

6 y to identify a protein that interacted with tachyplesin and isolated a sequence corresponding to the

7 Treatment of cells with tachyplesin and serum increased in membrane permeability

8 en together, these observations suggest that tachyplesin binds to both hyaluronan on the cell surface

9 ed the charge and hydrophobic amino acids of tachyplesin, but contained zero to four covalent constra

10 e charges resembling those in protegrins and tachyplesins, but were less cytotoxic.

11 nt constraints, included a cyclic tricystine tachyplesin (ccTP 1).

12 In this study, a synthetic tachyplesin conjugated to the integrin homing domain RGD

13 Cyclic tachyplesins consisting of 14 and 18 amino acids are con

14 ting showed that treatment of cells with RGD-tachyplesin could activate caspase 9, caspase 8, and cas

15 O-PRO-1, and FITC-dextran indicated that RGD-tachyplesin could induce apoptosis in both tumor and end

16 The in vivo studies indicated that the RGD-tachyplesin could inhibit the growth of tumors on the ch

17 e disulfide-stabilized antimicrobial peptide tachyplesin I (TP) in lipid bilayers are determined by s

18 role of amphipathicity using an analogue of tachyplesin I (TP-I), CDT (KWFRVYRGIYRRR-NH(2)), in whic

19 an NMR structural investigation of wild-type tachyplesin I and three linear derivatives (denoted TPY4

20 also determined the structures of wild-type tachyplesin I and TPY4 in the presence of dodecylphospho

21 elle and aqueous solution for both wild-type tachyplesin I and TPY4 reveals two requirements for high

22 cribe the chemical synthesis of a variant of tachyplesin I in which its two disulfide bonds are in a

23 Tachyplesin I is a 17-residue peptide isolated from the

24 Tachyplesin I is a cyclic beta-sheet antimicrobial pepti

25 The four cysteine residues in tachyplesin I play a structural role in imparting amphip

26 Our substrate is based on tachyplesin I, a 17-mer peptide that folds into a beta h

27 For a beta-sheet peptide tachyplesin I, which may be quite ordered at the solid/l

28 rization of the disulfide bonds in nonnative tachyplesin I.

29 Tachyplesin-I (TP-I) is a 17-residue beta-hairpin antimi

30 When TSU tumor cells were treated with tachyplesin in the presence of serum, activated C4b and

31 The in vitro results showed that RGD-tachyplesin inhibited the proliferation of both cultured

32 Tachyplesin is a small, cationic peptide that possesses

33 Tachyplesin is an antimicrobial peptide present in leuko

34 Tachyplesin seemed to activate the classic complement ca

35 eric cystine-stabilized beta-strand (CSbeta) tachyplesin (TP) in a panel of 10 test organisms.

36 rophobic amino acid) found in protegrins and tachyplesins whereas the octapeptide R8 (RLYRKVYG) consi

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