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 hat most biological DNA targets are found in ds form.

4 ecificity to the ss RSS heptamer than to the 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 related to the macroscopic properties of the DES formed.

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

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

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

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

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

14 e the activities of two recombinant human SP-D forms against representative LPAIV strains, including

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

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

17 ropose that Osa and its target genes opa and D form an incoherent feedforward loop (FFL) and a new me

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

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

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

21 peptides were prepared in their mirror-image d-form and assessed for binding against native l-CCL22.

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

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

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

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

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

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

28 Amino acids (AAs) in the d-form are involved in multiple pivotal neurological pro

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

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

31 Unfortunately, DEs formed by conventional emulsion generation approache

32 emical characterization of a new hydrophobic DES formed by octanoic acid and l-proline (C8:Pro) was p

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

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

35 Herein, we designed D-pai-A-pai-D form chromophores (TAZD1-TAZD5) via end-capped redistr

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

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

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

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

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

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

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

43 iron(III) chloride as oxidising agents in a DES formed from the mixture of choline chloride and ethy

44 Ft and Ds form heterodimeric bridges that convey polarity infor

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

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

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

48 through release of asymmetry present in the D-form inter-protomer interactions.

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

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

51 Gasdermin D forms large, ~21 nm diameter pores in the plasma membr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 work presents a novel deep eutectic solvent (DES) formed of octylamine and oxalic acid (Oct-Oxa) that

72 sion B-DNA, the most stable double-stranded (ds) form of DNA, undergoes cooperative elongation into a

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

74 After capturing the 3-D form over an 8-yr production cycle, a ray-tracing meth

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

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

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

78 1, which are present on the beta-sheet C and D, form salt bridges with the head group of PI(4,5)P2.

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

80 Because BcPh DEs form substantial amounts of deoxyadenosine adducts a

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

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

83 gence of a dominant viral variant (from the "D-form" to the "G-form") that carried an amino acid subs

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