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1 ncrease outflow facility in anterior segment perfusion culture.
2 n of disaccharide units, in anterior segment perfusion culture.
3 eins to outflow facility in anterior segment perfusion culture.
4 facility were assessed in human and porcine perfusion culture.
5 on was disrupted after versican silencing in perfusion culture.
6 they are being differentiated or expanded in perfusion cultures.
8 n biosynthesis increased outflow facility in perfusion culture and induced atypical ECM molecule inte
9 n of the DEX-inducible gene MYOC only in the perfusion-cultured anterior segments with DEX-induced OH
11 on provided by fluid shear forces in 3D flow perfusion culture can indeed enhance the expression of t
12 STAT3 by secreted factors under microfluidic perfusion culture demonstrated that STAT3 activation and
13 iosciences developed an automated continuous perfusion culture device for expansion of hematopoietic
14 us to human and porcine anterior segments in perfusion culture did not significantly affect outflow r
15 implement a control policy for fed-batch and perfusion cultures has prompted increased efforts in pro
17 inant Gremlin added to the medium of ex vivo perfusion-cultured human eye anterior segments caused th
18 Addition of recombinant sFRP-1 to ex vivo perfusion-cultured human eyes decreased outflow facility
19 induction of the myocilin proteins in three perfusion-cultured human eyes, in which DEX-induced elev
21 sing an intact porcine common carotid artery perfusion culture model, that nicotine and cotinine, the
22 a high concentration (>20 million cells/mL) perfusion culture of an IgG1-producing Chinese hamster o
25 becular meshwork (TM) of human eyes in organ-perfusion culture, resulting in high-level expression of
26 entiate, and function in a three-dimensional perfusion culture system while maintaining a progenitor
27 logy of the bovine trabecular meshwork after perfusion culture was similar to that of freshly dissect
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