Felbor U - Search Results

1

Loss of CCM3 impairs DLL4-Notch signalling: implication in endothelial angiogenesis and in inherited cerebral cavernous malformations.

You C, Sandalcioglu IE, Dammann P, Felbor U, Sure U, Zhu Y. You C, et al. Among authors: felbor u. J Cell Mol Med. 2013 Mar;17(3):407-18. doi: 10.1111/jcmm.12022. Epub 2013 Feb 7. J Cell Mol Med. 2013. PMID: 23388056 Free PMC article.

2

A two-hit mechanism causes cerebral cavernous malformations: complete inactivation of CCM1, CCM2 or CCM3 in affected endothelial cells.

Pagenstecher A, Stahl S, Sure U, Felbor U. Pagenstecher A, et al. Among authors: felbor u. Hum Mol Genet. 2009 Mar 1;18(5):911-8. doi: 10.1093/hmg/ddn420. Epub 2008 Dec 16. Hum Mol Genet. 2009. PMID: 19088124 Free PMC article.

3

Correlation of the venous angioarchitecture of multiple cerebral cavernous malformations with familial or sporadic disease: a susceptibility-weighted imaging study with 7-Tesla MRI.

Dammann P, Wrede K, Zhu Y, Matsushige T, Maderwald S, Umutlu L, Quick HH, Hehr U, Rath M, Ladd ME, Felbor U, Sure U. Dammann P, et al. Among authors: felbor u. J Neurosurg. 2017 Feb;126(2):570-577. doi: 10.3171/2016.2.JNS152322. Epub 2016 May 6. J Neurosurg. 2017. PMID: 27153162

4

Highly variable intrafamilial manifestations of a CCM3 mutation ranging from acute childhood cerebral haemorrhage to late-onset meningiomas.

Fauth C, Rostasy K, Rath M, Gizewski E, Lederer AG, Sure U, Zschocke J, Felbor U. Fauth C, et al. Among authors: felbor u. Clin Neurol Neurosurg. 2015 Jan;128:41-3. doi: 10.1016/j.clineuro.2014.10.023. Epub 2014 Nov 6. Clin Neurol Neurosurg. 2015. PMID: 25462093 No abstract available.

5

Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex.

Stahl S, Gaetzner S, Voss K, Brackertz B, Schleider E, Sürücü O, Kunze E, Netzer C, Korenke C, Finckh U, Habek M, Poljakovic Z, Elbracht M, Rudnik-Schöneborn S, Bertalanffy H, Sure U, Felbor U. Stahl S, et al. Among authors: felbor u. Hum Mutat. 2008 May;29(5):709-17. doi: 10.1002/humu.20712. Hum Mutat. 2008. PMID: 18300272

6

Cerebral cavernous malformation protein CCM1 inhibits sprouting angiogenesis by activating DELTA-NOTCH signaling.

Wüstehube J, Bartol A, Liebler SS, Brütsch R, Zhu Y, Felbor U, Sure U, Augustin HG, Fischer A. Wüstehube J, et al. Among authors: felbor u. Proc Natl Acad Sci U S A. 2010 Jul 13;107(28):12640-5. doi: 10.1073/pnas.1000132107. Epub 2010 Jun 24. Proc Natl Acad Sci U S A. 2010. PMID: 20616044 Free PMC article.

7

Regulation of β1 integrin-Klf2-mediated angiogenesis by CCM proteins.

Renz M, Otten C, Faurobert E, Rudolph F, Zhu Y, Boulday G, Duchene J, Mickoleit M, Dietrich AC, Ramspacher C, Steed E, Manet-Dupé S, Benz A, Hassel D, Vermot J, Huisken J, Tournier-Lasserve E, Felbor U, Sure U, Albiges-Rizo C, Abdelilah-Seyfried S. Renz M, et al. Among authors: felbor u. Dev Cell. 2015 Jan 26;32(2):181-90. doi: 10.1016/j.devcel.2014.12.016. Dev Cell. 2015. PMID: 25625207 Free article.

8

Constitutional de novo and postzygotic mutations in isolated cases of cerebral cavernous malformations.

Rath M, Spiegler S, Nath N, Schwefel K, Di Donato N, Gerber J, Korenke GC, Hellenbroich Y, Hehr U, Gross S, Sure U, Zoll B, Gilberg E, Kaderali L, Felbor U. Rath M, et al. Among authors: felbor u. Mol Genet Genomic Med. 2016 Dec 20;5(1):21-27. doi: 10.1002/mgg3.256. eCollection 2017 Jan. Mol Genet Genomic Med. 2016. PMID: 28116327 Free PMC article.

9

First large genomic inversion in familial cerebral cavernous malformation identified by whole genome sequencing.

Spiegler S, Rath M, Hoffjan S, Dammann P, Sure U, Pagenstecher A, Strom T, Felbor U. Spiegler S, et al. Among authors: felbor u. Neurogenetics. 2018 Jan;19(1):55-59. doi: 10.1007/s10048-017-0531-7. Epub 2017 Dec 2. Neurogenetics. 2018. PMID: 29197946

10

Genetics of cerebral cavernous angioma.

Felbor U, Sure U, Grimm T, Bertalanffy H. Felbor U, et al. Zentralbl Neurochir. 2006 Aug;67(3):110-6. doi: 10.1055/s-2006-933537. Zentralbl Neurochir. 2006. PMID: 16958007 Review.

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