Ivandic B - Search Results

1

A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.

Meder B, Rühle F, Weis T, Homuth G, Keller A, Franke J, Peil B, Lorenzo Bermejo J, Frese K, Huge A, Witten A, Vogel B, Haas J, Völker U, Ernst F, Teumer A, Ehlermann P, Zugck C, Friedrichs F, Kroemer H, Dörr M, Hoffmann W, Maisch B, Pankuweit S, Ruppert V, Scheffold T, Kühl U, Schultheiss HP, Kreutz R, Ertl G, Angermann C, Charron P, Villard E, Gary F, Isnard R, Komajda M, Lutz M, Meitinger T, Sinner MF, Wichmann HE, Krawczak M, Ivandic B, Weichenhan D, Gelbrich G, El-Mokhtari NE, Schreiber S, Felix SB, Hasenfuß G, Pfeufer A, Hübner N, Kääb S, Arbustini E, Rottbauer W, Frey N, Stoll M, Katus HA. Meder B, et al. Among authors: ivandic b. Eur Heart J. 2014 Apr;35(16):1069-77. doi: 10.1093/eurheartj/eht251. Epub 2013 Jul 12. Eur Heart J. 2014. PMID: 23853074

2

HBEGF, SRA1, and IK: Three cosegregating genes as determinants of cardiomyopathy.

Friedrichs F, Zugck C, Rauch GJ, Ivandic B, Weichenhan D, Müller-Bardorff M, Meder B, El Mokhtari NE, Regitz-Zagrosek V, Hetzer R, Schäfer A, Schreiber S, Chen J, Neuhaus I, Ji R, Siemers NO, Frey N, Rottbauer W, Katus HA, Stoll M. Friedrichs F, et al. Among authors: ivandic b. Genome Res. 2009 Mar;19(3):395-403. doi: 10.1101/gr.076653.108. Epub 2008 Dec 8. Genome Res. 2009. PMID: 19064678 Free PMC article.

3

Large-scale mutation screening in patients with dilated or hypertrophic cardiomyopathy: a pilot study using DGGE.

Zeller R, Ivandic BT, Ehlermann P, Mücke O, Zugck C, Remppis A, Giannitsis E, Katus HA, Weichenhan D. Zeller R, et al. J Mol Med (Berl). 2006 Aug;84(8):682-91. doi: 10.1007/s00109-006-0056-2. Epub 2006 May 20. J Mol Med (Berl). 2006. PMID: 16715312

4

Incomplete nonsense-mediated decay of mutant lamin A/C mRNA provokes dilated cardiomyopathy and ventricular tachycardia.

Geiger SK, Bär H, Ehlermann P, Wälde S, Rutschow D, Zeller R, Ivandic BT, Zentgraf H, Katus HA, Herrmann H, Weichenhan D. Geiger SK, et al. J Mol Med (Berl). 2008 Mar;86(3):281-9. doi: 10.1007/s00109-007-0275-1. Epub 2007 Nov 7. J Mol Med (Berl). 2008. PMID: 17987279

5

Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene.

Ehlermann P, Weichenhan D, Zehelein J, Steen H, Pribe R, Zeller R, Lehrke S, Zugck C, Ivandic BT, Katus HA. Ehlermann P, et al. BMC Med Genet. 2008 Oct 28;9:95. doi: 10.1186/1471-2350-9-95. BMC Med Genet. 2008. PMID: 18957093 Free PMC article.

6

Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation.

Luedde M, Ehlermann P, Weichenhan D, Will R, Zeller R, Rupp S, Müller A, Steen H, Ivandic BT, Ulmer HE, Kern M, Katus HA, Frey N. Luedde M, et al. Cardiovasc Res. 2010 Jun 1;86(3):452-60. doi: 10.1093/cvr/cvq009. Epub 2010 Jan 18. Cardiovasc Res. 2010. PMID: 20083571

7

Whole-genome analysis of gene expression associates the ubiquitin-proteasome system with the cardiomyopathy phenotype in disease-sensitized congenic mouse strains.

Ivandic BT, Mastitsky SE, Schönsiegel F, Bekeredjian R, Eils R, Frey N, Katus HA, Brors B. Ivandic BT, et al. Cardiovasc Res. 2012 Apr 1;94(1):87-95. doi: 10.1093/cvr/cvs080. Epub 2012 Feb 2. Cardiovasc Res. 2012. PMID: 22308238

8

Fine mapping of Dyscalc1, the major genetic determinant of dystrophic cardiac calcification in mice.

Korff S, Schoensiegel F, Riechert N, Weichenhan D, Katus HA, Ivandic BT. Korff S, et al. Physiol Genomics. 2006 May 16;25(3):387-92. doi: 10.1152/physiolgenomics.00010.2006. Physiol Genomics. 2006. PMID: 16705021

9

Calcification of myocardial necrosis is common in mice.

Korff S, Riechert N, Schoensiegel F, Weichenhan D, Autschbach F, Katus HA, Ivandic BT. Korff S, et al. Virchows Arch. 2006 May;448(5):630-8. doi: 10.1007/s00428-005-0071-7. Epub 2005 Oct 7. Virchows Arch. 2006. PMID: 16211391

10

Atrial natriuretic peptide and osteopontin are useful markers of cardiac disorders in mice.

Schoensiegel F, Bekeredjian R, Schrewe A, Weichenhan D, Frey N, Katus HA, Ivandic BT. Schoensiegel F, et al. Comp Med. 2007 Dec;57(6):546-53. Comp Med. 2007. PMID: 18246866

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