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1 region of horse onto the surface of magnetic microcarriers.
2 d to generate monodisperse VEGF encapsulated microcarriers.
3  allows creating large libraries of nanotags/microcarriers.
4  cells cultured on porous fibronectin-coated microcarriers.
5 endothelial cells cultured and superfused on microcarriers.
6  on abundant, large neutral lipid-containing microcarriers, also found in other SP-expressing Drosoph
7 RNA heterohybrids on the surface of magnetic microcarriers, and their recognition with an antibody se
8 together, the data suggest that CultiSpher-G microcarriers are a useful in vitro system to examine th
9 hylindocarbocyanine perchlorate (DiI)-coated microcarriers are shot at high speed onto the surfaces o
10                                        These microcarriers are transferred to females during mating w
11                      Remarkably, SP is a key microcarrier assembly and disassembly factor.
12  that, despite the critical role SP plays in microcarrier assembly in D. melanogaster, appears to be
13 report a multienzyme-functionalized magnetic microcarriers-assisted isothermal strand-displacement po
14 olabeled with 35S-Cys-Met and harvested from microcarrier bead cultures, which significantly improves
15                   In vitro, PAEC cultured on microcarrier beads and incubated with non-anticoagulated
16          IECs (HT-29.cl19a) were cultured on microcarrier beads in simulated microgravity using a rot
17 ned previously using macrophages attached to microcarrier beads suspended in a stirred vessel.
18  labeling with ectopic implantation of FGF-4 microcarrier beads we have found that FGF-4 acts as a po
19 t bovine aortic endothelial cells (BAECs) on microcarrier beads were incubated in the presence or abs
20                            Cells attached to microcarrier beads were perfused with 26 mm [1,6-(13)C2]
21                  Model 2: PAEC were grown on microcarrier beads, coated with CHC, and incubated with
22 lls, seeded and polarized on collagen-coated microcarrier beads, using a three-dimensional culture sy
23 nce of a Pt-porphyrin complex immobilized on microcarrier beads, which are used as the cell culture s
24  assay system utilizing HUVEC immobilized on microcarrier beads, which eliminates the detection of th
25                        Cells are attached to microcarrier beads, which serve as the disposable and re
26 vidual cells, cell spheroids and cell-seeded microcarrier beads.
27 D aggregates, which remained attached to the microcarrier beads.
28 VEC or to HEK293 cell monolayers anchored to microcarrier beads.
29 ing to HUVEC and HEK293 cells immobilized on microcarrier beads.
30 se Hamster Ovary M1 cells grown on Cytodex-3 microcarrier beads.
31  pilocarpine) delivered to cells attached to microcarrier beads.
32 sks containing HEL299 feeder cells seated on microcarrier beads.
33 rability, and efficacy of transplantation of microcarrier-bound human RPE cells versus a sham surgery
34  investigated the use of macroporous gelatin microcarriers, CultiSpher-G, as a convenient laboratory
35 ot change in parallel cell columns made from microcarriers cultured in 25 mM glucose (0.97+/-0.2 of b
36  were tested by addition of 25 mM glucose to microcarrier cultures.
37                 Herein, we develop a cryogel microcarrier delivery system which takes advantage of th
38 as assayed by presenting matrix deposited on microcarriers directly to migrating pronephric ducts in
39      Eventually, the capability of developed microcarriers for bone tissue formation was examined in
40 dy highlights the potential of using cryogel microcarriers for long-term delivery of neurotrophic gro
41 ed for the efficient production of nano- and microcarriers for various applications.
42                                              Microcarriers generated with the on-chip technique showe
43 refinement methods, such as preconditioning, microcarriers, genetic safety switches and universal (im
44 wne replicates in MRC-5 fibroblasts grown on microcarriers, (ii) DB particles recovered from 2-bromo-
45          Transplantation of hepatocytes with microcarriers in the peritoneal cavity efficiently rescu
46 icrocarriers with DNA, (ii) transferring the microcarriers into a cartridge to make a 'bullet', and (
47 with one or more dyes; (ii) transferring the microcarriers into a cartridge to make a bullet; (iii) p
48  cells or intact tissue; and (iv) firing the microcarriers into cells or tissue.
49  a 'bullet', and (iii) firing the DNA-coated microcarriers into cells using a pulse of helium gas.
50 y and calcium content analysis of MSCs-laden microcarriers loaded into injectable hydrogels revealed
51  This biosensor involves the use of magnetic microcarriers (MBs) modified with covalently immobilized
52 onsists of cell monolayers grown on ~150 mum microcarriers (MCs).
53 n, we use microalga Spirulina platensis as a microcarrier of Amifostine to construct an oral delivery
54   The presented approach to design bioactive microcarriers offer sustained sequential delivery of bon
55 s of the intracellular constituents of yeast microcarriers on the thermal and oxidative stability of
56  to determine optimum time of infection in a microcarrier process.
57                         Dynamic culturing of microcarriers showcased their great potential to boost M
58  sperm in females also do not produce normal microcarriers, suggesting that this male-specific defect
59 s revealed that transplantation of MSC-laden microcarriers supports ectopic bone formation in the rat
60 lamine) (PDA) was then functionalized to the microcarriers surface for BMP-2 conjugation.
61                 The PDA functionalization of microcarriers surface not only provided immobilization o
62  both media supported scalable culture in 3D microcarrier systems using CellBIND microcarriers, with
63 on in the presence and morphology of seminal microcarriers that, despite the critical role SP plays i
64         Based on a readily available natural microcarrier, this work presents a convenient oral deliv
65 vantage of the benefits provided by magnetic microcarriers to implement a competitive immunoassay inv
66 d-anti-dsDNA (b-dsDNA) as efficient magnetic microcarriers to selectively capture anti-dsDNA autoanti
67 ture studies demonstrated that these cryogel microcarriers were cytocompatible with neuronal and micr
68                                 Finally, the microcarriers were incorporated into an injectable algin
69                                          The microcarriers were seeded with mesenchymal stem cells (M
70     There are three major steps: (i) coating microcarriers with DNA, (ii) transferring the microcarri
71 There are four major steps: (i) coating gold microcarriers with one or more dyes; (ii) transferring t
72 form generated monodisperse VEGF-loaded PLGA microcarriers with size-dependent release patterns.
73  aims to design multifunctional cell therapy microcarriers with the capability of sequential delivery
74 re in 3D microcarrier systems using CellBIND microcarriers, with significantly better performance obs