Faissner A - Search Results

1

Brain tumor-initiating cells export tenascin-C associated with exosomes to suppress T cell activity.

Mirzaei R, Sarkar S, Dzikowski L, Rawji KS, Khan L, Faissner A, Bose P, Yong VW. Mirzaei R, et al. Among authors: faissner a. Oncoimmunology. 2018 Aug 6;7(10):e1478647. doi: 10.1080/2162402X.2018.1478647. eCollection 2018. Oncoimmunology. 2018. PMID: 30288344 Free PMC article.

2

Tenascin-C is expressed by human glioma in vivo and shows a strong association with tumor blood vessels.

Brösicke N, van Landeghem FK, Scheffler B, Faissner A. Brösicke N, et al. Among authors: faissner a. Cell Tissue Res. 2013 Nov;354(2):409-30. doi: 10.1007/s00441-013-1704-9. Epub 2013 Aug 21. Cell Tissue Res. 2013. PMID: 23963648

3

Influence of the extracellular matrix on endogenous and transplanted stem cells after brain damage.

Roll L, Faissner A. Roll L, et al. Among authors: faissner a. Front Cell Neurosci. 2014 Aug 19;8:219. doi: 10.3389/fncel.2014.00219. eCollection 2014. Front Cell Neurosci. 2014. PMID: 25191223 Free PMC article. Review.

4

Tenascin-C preserves microglia surveillance and restricts leukocyte and, more specifically, T cell infiltration of the ischemic brain.

Manrique-Castano D, Dzyubenko E, Borbor M, Vasileiadou P, Kleinschnitz C, Roll L, Faissner A, Hermann DM. Manrique-Castano D, et al. Among authors: faissner a. Brain Behav Immun. 2021 Jan;91:639-648. doi: 10.1016/j.bbi.2020.10.016. Epub 2020 Oct 22. Brain Behav Immun. 2021. PMID: 33122023 Free article.

5

Tenascin-C restricts reactive astrogliosis in the ischemic brain.

Dzyubenko E, Manrique-Castano D, Pillath-Eilers M, Vasileiadou P, Reinhard J, Faissner A, Hermann DM. Dzyubenko E, et al. Among authors: faissner a. Matrix Biol. 2022 Jun;110:1-15. doi: 10.1016/j.matbio.2022.04.003. Epub 2022 Apr 14. Matrix Biol. 2022. PMID: 35430380 Free article.

6

The guanine nucleotide exchange factor Vav3 intervenes in the migration pathway of oligodendrocyte precursor cells on tenascin-C.

Schäfer I, Bauch J, Wegrzyn D, Roll L, van Leeuwen S, Jarocki A, Faissner A. Schäfer I, et al. Among authors: faissner a. Front Cell Dev Biol. 2022 Nov 30;10:1042403. doi: 10.3389/fcell.2022.1042403. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 36531963 Free PMC article.

7

Neural stem/progenitor cells express 20 tenascin C isoforms that are differentially regulated by Pax6.

von Holst A, Egbers U, Prochiantz A, Faissner A. von Holst A, et al. Among authors: faissner a. J Biol Chem. 2007 Mar 23;282(12):9172-81. doi: 10.1074/jbc.M608067200. Epub 2007 Jan 30. J Biol Chem. 2007. PMID: 17264084 Free article.

8

An induction gene trap screen in neural stem cells reveals an instructive function of the niche and identifies the splicing regulator sam68 as a tenascin-C-regulated target gene.

Moritz S, Lehmann S, Faissner A, von Holst A. Moritz S, et al. Among authors: faissner a. Stem Cells. 2008 Sep;26(9):2321-31. doi: 10.1634/stemcells.2007-1095. Epub 2008 Jul 10. Stem Cells. 2008. PMID: 18617690

9

Tenascin C and tenascin R similarly prevent the formation of myelin membranes in a RhoA-dependent manner, but antagonistically regulate the expression of myelin basic protein via a separate pathway.

Czopka T, Von Holst A, Schmidt G, Ffrench-Constant C, Faissner A. Czopka T, et al. Among authors: faissner a. Glia. 2009 Dec;57(16):1790-801. doi: 10.1002/glia.20891. Glia. 2009. PMID: 19459213

10

Analysis of combinatorial variability reveals selective accumulation of the fibronectin type III domains B and D of tenascin-C in injured brain.

Dobbertin A, Czvitkovich S, Theocharidis U, Garwood J, Andrews MR, Properzi F, Lin R, Fawcett JW, Faissner A. Dobbertin A, et al. Among authors: faissner a. Exp Neurol. 2010 Sep;225(1):60-73. doi: 10.1016/j.expneurol.2010.04.019. Epub 2010 May 5. Exp Neurol. 2010. PMID: 20451518

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