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Characterization of HA/βTCP 3-D printed scaffolds for custom bone repair applications
Chapter by: Witek, L.; Murriky, A.; Clark, E.; Smay, J.; Pines, M.; Silva, N.; Ricci, J. L.
in: Proceedings of the 2010 IEEE 36th Annual Northeast Bioengineering Conference, NEBEC 2010 by
[S.l.] : Elsevier Inc., 2010
pp. ?-?
ISBN: 9781424468799
CID: 2866502
Is lacunocanalicular flow the transducer of mechanical tension stress to osteogenesis in distraction? [Meeting Abstract]
Davidson, Edward H; Sultan, Steven M; Butala, Parag; Knobel, Denis; Tutela, John Paul; Canizares, Orlando; Wagner, IJanelle; Witek, Lukasz; Hu, Bin; Warren, Stephen M
ISI:000281708600185
ISSN: 1072-7515
CID: 2162652
Comparison of gene expression of mitogenic kinin path in adherent and non-adherent CD 34-stem cells using oligonucleotide microarrays
Stojko, Rafał; Witek, Andrzej; Głogowska, Joanna; Mazurek, Urszula; Chromy, Grzegorz; Wilk, Krzysztof; Witek, Lukasz; Bojdys-Szyndlar, Monika; Machaj, Krzysztof; Pojda, Zygmunt
One of the more interesting cells present in the umbilical cord blood - as far as their potential clinical use is concerned - are stem cells not presenting the CD34 antigen. These are the pluripotential cells with their biological properties similar to mesenchymal stem cells, with the ability to differentiate into such tissue types as bone, cartilage, nervous (to some extent), glia and muscle. The authors compared the activity of genes coding the proteins in mitogenic signal paths activated by kinin receptors using oligonucleotide microarrays in adherent and non-adherent CD 34- cells derived from umbilical cord blood. In the linear regression model with a 95% prognosis area for differentiating genes outside this area, the following genes were selected: c-jun (present in 3 isoforms) and c-fos. The fos and jun genes create the AP-1 transcriptive factor which regulates the expression of genes taking part in numerous cellular processes, including the cell cycle and mitosis. The obtained results shed some light on the molecular processes behind the MSC proliferation and are a starting point for further studies on the mesenchymal stem cell biology.
PMID: 18296262
ISSN: 1897-5631
CID: 2983132