2011
DOI: 10.1016/j.biomaterials.2011.01.049
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The performance of laminin-containing cryogel scaffolds in neural tissue regeneration

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Cited by 143 publications
(106 citation statements)
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“…However, the direct calculations of the PSD with quantitative analysis of SEM images were not carried out in this paper [80]. Additionally, Jurga et al [112] prepared bioactive scaffolds using cryogelation of dextran or gelatine linked to laminin. The textural characteristics of native cryogels were analysed using CLSM.…”
mentioning
confidence: 98%
“…However, the direct calculations of the PSD with quantitative analysis of SEM images were not carried out in this paper [80]. Additionally, Jurga et al [112] prepared bioactive scaffolds using cryogelation of dextran or gelatine linked to laminin. The textural characteristics of native cryogels were analysed using CLSM.…”
mentioning
confidence: 98%
“…Such pores are ideal for cell aggregates to adhere and develop a micro-niche. The pore size between 80-100 µm of dextran or gelatin cryogels was previously shown to be optimal for stem cells derived from human cord blood adhesion and neural differentiation [12]. Subsequently it was shown that gelatin-based cryogels scaffolds with the pore size ranging from 20 to 120 allow encapsulation of bigger in size mesenchymal stem cells (hUCMSCs) and when supplemented with neuromorphogenes promote their neural differentiation in vitro [32].…”
Section: Discussionmentioning
confidence: 99%
“…Jurga et al 51 created cryogels containing LM (0.01% w/v) and fish skin gelatin (4.4% w/v) that were crosslinked with glutaraldehyde for mechanical stability. In hippocampal organotypic cultures, the gelatin-LM cryogels showed intensive migration of NF200 + neuroblasts throughout the entire volume of the scaffold.…”
Section: Central Nervous System Regenerationmentioning
confidence: 99%