ライフサイエンスコーパス: D form

1 the biologically active 1,25(OH)(2) vitamin D form.

2 ng increases in each of the mRFC-b, -c, and -d forms.

3 ecificity to the ss RSS heptamer than to the ds form.

4 hat most biological DNA targets are found in ds form.

5 ranose (alnumycin C) and pyranose (alnumycin D) forms.

6 her single-stranded (SS) or double-stranded (DS) form.

7 to transcriptionally active double-stranded (ds) forms.

8 , herpes simplex virus envelope glycoprotein D formed a cis-complex with HVEM, yet surprisingly, prom

9 Its incorporation with chemotherapy and P/D forms a new lung-sparing treatment paradigm for patien

10 prebent" site on the DNA, K(d) = 1.4 nM, HMG-D forms a non-sequence-specific complex with the DNA as

11 On the other hand, D forms a stable radical with no known role in oxygen ev

12 rose whether the two components, gD-B and gD-D, form a heterodimer mediated by an unpaired cysteine l

13 region of the micelles (the asterisks denote D-form amino acid).

14 he ferrous CO-saturated abc trimer and chain d form an (abcd)4 complex of 285 kDa at neutral pH.

15 ing signal of the major pilin, BcpA, sortase D forms an amide bond between the C-terminal threonine a

16 The procapsid contains 240 copies of protein D, forming an external scaffold, and 60 copies each of t

17 s the highest association constant among the D-form analogues.

18 trite structurally modifies complex I in its D-form and impedes its return to the active state.

19 This was due to the accumulation of the D-form and its slow, substrate-dependent reconversion to

20 The D-form and the L-form were equally effective.

21 DNA when the target is in a double stranded (ds) form and compare the response to single stranded (ss

22 by antioxidant N-acetylcysteine (both L and D-forms) and by a variety of PKC-specific inhibitors.

23 , most likely converts to a double-stranded (ds) form, and integrates into the host genome.

24 was prone to conversion into its previtamin D form by thermal equilibration, the corresponding 19-no

25 a putative CD95 binding surface within FADD DD formed by alpha helices 2 and 3.

26 Deep eutectic solvent (DES) formed by mixing of choline chloride and phenol was

27 Activation by factor D (forming C3bBb) increased the complex half-life; howev

28 ent to support the import of both L-form and D-form conjugates in permeabilized cells.

29 By contrast, the DD form did not inhibit uptake.

30 ) = Ph, R(2) = Me; R(1) = Me, R(2) = Et) (1a-d) formed difluoro derivatives (2a-d) in the presence of

31 The CO-saturated chain d forms dimers, (d)2, and tetramers, (d)4.

32 antigenic forms, D and C, of which only the D form elicits a robust neutralizing response.

33 ng activity that is stereospecific for their d-form enantiomers and can be stimulated dramatically by

34 by Mn(2+) are highly stereospecific for the d-form enantiomers of tyrosine and Dopa.

35 Ft and Ds form heterodimeric bridges that convey polarity infor

36 Actinomycin D formed high-affinity, kinetically stable complexes tha

37 two-hybrid interaction assay shows that Bic-D forms homodimers.

38 The DMSOR(mod)D form, identified by its characteristic Raman spectrum,

39 versity of multiple Ixodes ricinus cathepsin D forms (IrCDs).

40 LB forms a duplex and stem loops SL-C and SL-D form kissing complexes, as expected from previous stud

41 The p75(NTR) DD forms non-covalent, low-affinity symmetric dimers in

42 monstrate that IscS binds preferentially the D form of apo-IscU.

43 The surprising efficacy of the d form of GsMTx4 peptide has important therapeutic impli

44 Administration of the nonnaturally occurring D form of the DWEYS pentapeptide prevents these antibodi

45 new quasiracemate crystals that contain the d form of the magainin 2 derivative along with an l-pept

46 R325-infected HEp-2 cells lacked the D' form of ICP4, and roscovitine blocked the appearance

47 Here we show that these mutant or 'd' forms of MEC-4 and MEC-10 produce a constitutively ac

48 We now demonstrate accumulation of the D-form of complex I in human epithelial kidney cells aft

49 he hypoxic transition from the A-form to the D-form of complex I may be protective, because it would

50 aptamer was developed that binds the natural D-form of the HIV-1 trans-activation responsive (TAR) RN

51 -L-valine residues were replaced with L- and D-forms of N-methylvalines, N-methylthreonines, N-methyl

52 The L- and D-forms of poly(sodium N-undecanoyl valinate) provide ba

53 es (e.g., acetobromoglucose) with the L- and D-forms of serine and threonine are distinctly different

54 Although the free D-forms of the NLS were proteolytically resistant in cyt

55 ligands for SP-D, and biologically relevant d-forms of the pentoses are better competitors than the

56 ic acid, chosen because there are endogenous D-forms of these amino acids in animals.

57 dimeric (AB), and scrambled homodimeric (CC, DD) forms of these peptides were synthesized and examine

58 rmation data, the catalytic activity of the [DD] forms of deltaA-Raf:ER and deltaRaf-1:ER was about t

59 In general the [DD] forms of the deltaRaf-1:ER and deltaA-Raf:ER protein

60 t stable BMP9 dimers could form either with (D-form) or without (M-form) an intermolecular disulfide

61 ng the V(1) and V(0) domains whereas subunit D forms part of a central stalk.

62 e polyanionic ON backbone and stabilizes the ds-form relative to the ss-form.

63 of a single L-amino acid in a peptide to its D-form results in altered bioactivity, with some DAACPs

64 1, which are present on the beta-sheet C and D, form salt bridges with the head group of PI(4,5)P2.

65 is in an ss form, not in a double-stranded (ds) form, ss AAV genomes with BrdU can be readily tracke

66 Because BcPh DEs form substantial amounts of deoxyadenosine adducts a

67 e nucleoside diphosphate kinase Nm23-H4/NDPK-D forms symmetrical hexameric complexes in the mitochond

68 Residues at positions a and d form the interhelical interface and are usually hydrop

69 microsomes, along with FeSO4, the amount of D formed was greater than control values, indicating tha