scholarly journals Simple Synthetic Molecular Hydrogels from Self-Assembling Alkylgalactonamides as Scaffold for 3D Neuronal Cell Growth

2018 ◽  
Vol 10 (20) ◽  
pp. 17004-17017 ◽  
Author(s):  
Anaïs Chalard ◽  
Laurence Vaysse ◽  
Pierre Joseph ◽  
Laurent Malaquin ◽  
Sandrine Souleille ◽  
...  
2011 ◽  
Vol 257 (20) ◽  
pp. 8535-8541 ◽  
Author(s):  
Ok Ja Yoon ◽  
Hyun Jung Lee ◽  
Yeong Mi Jang ◽  
Hyun Woo Kim ◽  
Won Bok Lee ◽  
...  

2012 ◽  
Author(s):  
Annika Enejder ◽  
Helen Fink ◽  
Hans-Georg Kuhn

2012 ◽  
Vol 100B (4) ◽  
pp. 940-947 ◽  
Author(s):  
Uta Reich ◽  
Elena Fadeeva ◽  
Athanasia Warnecke ◽  
Gerrit Paasche ◽  
Peter Müller ◽  
...  

Small ◽  
2015 ◽  
Vol 11 (38) ◽  
pp. 5047-5053 ◽  
Author(s):  
Ben Newland ◽  
Petra B. Welzel ◽  
Heike Newland ◽  
Claudia Renneberg ◽  
Petr Kolar ◽  
...  

2016 ◽  
Vol 27 (17) ◽  
pp. 175303 ◽  
Author(s):  
Eunhee Kim ◽  
Seung-Jun Yoo ◽  
Eunjung Kim ◽  
Tae-Hwan Kwon ◽  
Li Zhang ◽  
...  

2006 ◽  
Vol 394 (2) ◽  
Author(s):  
Ginger S. Withers

The ability to control the placement of cells and the assembly of networks in vitro has tremendous potential for understanding the regulation of development as well as for generating artificial tissues. To date, most engineering tools that can place materials with precision are not compatible with the requirements of living cells, and so approaches to tissue engineering have focused on patterning substrates as a way of controlling cell growth rather than patterning cells directly. In this issue of Biochemical Journal, however, Eagles et al. adapt electrohydrodynamic printing technology to ‘print’ living cells from a neuronal cell line on to a substrate. The importance of this approach is that it has the potential for unprecedented control over the position of cells in culture by directly placing them, thus allowing for the systematic assembly of cell networks.


2015 ◽  
Vol 21 (1) ◽  
pp. 65-76 ◽  
Author(s):  
Dennis Jgamadze ◽  
Li Liu ◽  
Steffen Vogler ◽  
Liang-Yin Chu ◽  
Sophie Pautot

2019 ◽  
Vol 20 (5) ◽  
pp. 1170 ◽  
Author(s):  
Caroline Nunes-Xavier ◽  
Laura Zaldumbide ◽  
Olaia Aurtenetxe ◽  
Ricardo López-Almaraz ◽  
José López ◽  
...  

Dual-specificity phosphatases (DUSPs) are important regulators of neuronal cell growth and differentiation by targeting proteins essential to neuronal survival in signaling pathways, among which the MAP kinases (MAPKs) stand out. DUSPs include the MAPK phosphatases (MKPs), a family of enzymes that directly dephosphorylate MAPKs, as well as the small-size atypical DUSPs, a group of low molecular-weight enzymes which display more heterogeneous substrate specificity. Neuroblastoma (NB) is a malignancy intimately associated with the course of neuronal and neuroendocrine cell differentiation, and constitutes the source of more common extracranial solid pediatric tumors. Here, we review the current knowledge on the involvement of MKPs and small-size atypical DUSPs in NB cell growth and differentiation, and discuss the potential of DUSPs as predictive biomarkers and therapeutic targets in human NB.


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