ライフサイエンスコーパス: hydroxylapatite

1 Chromatography over hydroxylapatite allowed separation of two enzymically ac

2 diates bacterial attachment to saliva-coated hydroxylapatite, an in vitro tooth model.

3 CL synthase was further purified by hydroxylapatite and cytidine diphosphate diacylglycerol

4 ms of NM23-H1 protein during purification by hydroxylapatite and gel filtration column high performan

5 aration, gel filtration, and ionic exchange, hydroxylapatite, and affinity chromatographies.

6 After chromatography on DEAE-Sephacel, hydroxylapatite, and Mono Q and precipitation at pH 5.8,

7 by chromatography with DE53, Affi-Gel Blue, hydroxylapatite, and Mono Q.

8 omatographic method (DEAE-cellulose, calcium hydroxylapatite, and Sephadex G-150) that yields enzymat

9 urified from bovine brain by anion exchange, hydroxylapatite, and size exclusion chromatography.

10 el AcA 34, DEAE-Sephacel, heparin-Sepharose, hydroxylapatite, and Ultrogel AcA 44.

11 fect on S. mutans adherence to saliva-coated hydroxylapatite beads, but in conjunction with glucans s

12 oscopies, that the nanoscale crystallites of hydroxylapatite (Ca(5)(PO(4))(3)(OH)), which are the fun

13 y occlusion (RAO) following glabella calcium hydroxylapatite (CaHA) injection, and to explore appropr

14 ing hydrophobic, anion-exchange, sizing, and hydroxylapatite chromatographies.

15 nnectors readily formed ordered arrays after hydroxylapatite chromatography but not before.

16 ity partially purified by anion-exchange and hydroxylapatite chromatography is an efficient catalyst

17 peaks of monomers and stable connectors upon hydroxylapatite chromatography perhaps because of dissoc

18 identical to that of the latter study, that hydroxylapatite chromatography removes AP50 from impure

19 from conditioned media by immunoaffinity and hydroxylapatite chromatography.

20 hed by either preparative electrophoresis or hydroxylapatite chromatography.

21 purified by using amylose-resin affinity and hydroxylapatite chromatography.

22 le connectors that formed arrays even before hydroxylapatite chromatography.

23 Mono Q, Sephacryl S300HR, and hydroxylapatite column chromatography in the presence of

24 rmed long chains and sparse microcolonies on hydroxylapatite disks but failed to accumulate and form

25 The luxS mutant formed less biofilm on hydroxylapatite disks, especially when grown in biofilm

26 in biofilm formation on microtiter plates or hydroxylapatite disks.

27 However, the same mineral type (carbonated hydroxylapatite) does not yield the same material proper

28 healthy 24-year-old women received a Calcium Hydroxylapatite filler injection to her nose bridge for

29 f ophthalmic artery emboli following Calcium Hydroxylapatite filler injection to the nose bridge.

30 (montmorillonite for nucleotides, illite and hydroxylapatite for amino acids) induces the formation o

31 ated the action of DMP1 in the regulation of hydroxylapatite (HA) formation and crystal growth.

32 in hydrogels, either alone or complexed with hydroxylapatite (HA) nanoparticles.

33 edict the concentrations of minority ions in hydroxylapatite (Mg(2+) and CO(3)(2-)/Na(+)) that plausi

34 ressure liquid chromatography separations on hydroxylapatite, Mono Q, and Superdex 75 gel filtration

35 hierarchical material composed primarily of hydroxylapatite nanowires, is susceptible to degradation

36 n exchange, hydrophobic interaction, Mono Q, hydroxylapatite, phenyl-Sepharose, and chromatofocusing

37 was isolated by sequential chromatography on hydroxylapatite, protein A-G, Mono Q, and Superose 12.

38 reported that oligonucleotides adsorbed onto hydroxylapatite provide suitable templates for the oligo

39 ibody 1.1 (MAb 1.1) binds both saliva-coated hydroxylapatite (sHA) and platelets.

40 Streptococcus sanguis binds to saliva-coated hydroxylapatite (sHA), an in vitro model of the enamel p

41 rtant in mediating adhesion to saliva-coated hydroxylapatite (SHA), an in vitro tooth adhesion model.

42 in vitro tooth surface model, saliva-coated hydroxylapatite (SHA), or in its ability to express the

43 chous fimbriae and adhesion to saliva-coated hydroxylapatite (SHA).

44 ich salivary proteins, preventing binding to hydroxylapatite surfaces.

45 Cosmetic injection of calcium hydroxylapatite to the nose bridge can result in arteria

46 cycles can be carried out on the surface of hydroxylapatite, whereas in the liquid phase the cycle c