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1 eins to outflow facility in anterior segment perfusion culture.
2  facility were assessed in human and porcine perfusion culture.
3 on was disrupted after versican silencing in perfusion culture.
4 ncrease outflow facility in anterior segment perfusion culture.
5 n of disaccharide units, in anterior segment perfusion culture.
6 nterior segments of human eyes maintained in perfusion culture.
7 creted factor profile during several days of perfusion culture.
8 nt during a high-cell-concentration CHO cell perfusion culture.
9 they are being differentiated or expanded in perfusion cultures.
10                                    Lab-scale perfusion cultures (350 mL) were used to demonstrate the
11 n biosynthesis increased outflow facility in perfusion culture and induced atypical ECM molecule inte
12 how scalable strategies for the fabrication, perfusion culture and volumetric analysis of large tissu
13 n of the DEX-inducible gene MYOC only in the perfusion-cultured anterior segments with DEX-induced OH
14                 OHT can be induced by DEX in perfusion-cultured bovine anterior segments.
15 on provided by fluid shear forces in 3D flow perfusion culture can indeed enhance the expression of t
16 STAT3 by secreted factors under microfluidic perfusion culture demonstrated that STAT3 activation and
17 iosciences developed an automated continuous perfusion culture device for expansion of hematopoietic
18 us to human and porcine anterior segments in perfusion culture did not significantly affect outflow r
19 portant for the optimization of fed-batch or perfusion culture for directing cell growth and improvin
20 implement a control policy for fed-batch and perfusion cultures has prompted increased efforts in pro
21 ates proliferation of endogenous TM cells in perfusion cultured human eyes from aged donors.
22                                              Perfusion-cultured human anterior segments were used to
23 inant Gremlin added to the medium of ex vivo perfusion-cultured human eye anterior segments caused th
24    Addition of recombinant sFRP-1 to ex vivo perfusion-cultured human eyes decreased outflow facility
25  induction of the myocilin proteins in three perfusion-cultured human eyes, in which DEX-induced elev
26 aqueous humor and in the perfusate medium of perfusion-cultured human eyes.
27 atment at two dose levels (100 or 500 nM) in perfusion cultured Indian cadaveric eyes to investigate
28                                          Our perfusion culture method extends tumor slice viability,
29 sing an intact porcine common carotid artery perfusion culture model, that nicotine and cotinine, the
30  a high concentration (>20 million cells/mL) perfusion culture of an IgG1-producing Chinese hamster o
31 tention device based on inertial sorting for perfusion culture of suspended mammalian cells.
32                                         Flow perfusion culture permits the generation and study of a
33 becular meshwork (TM) of human eyes in organ-perfusion culture, resulting in high-level expression of
34 entiate, and function in a three-dimensional perfusion culture system while maintaining a progenitor
35                 The tissues were viable in a perfusion culture system, with endothelialization and an
36 logy of the bovine trabecular meshwork after perfusion culture was similar to that of freshly dissect
37                         Anterior segments in perfusion culture were treated with recombinant ADAMTSs