Weichenhan D - 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: weichenhan d. 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

A locus on chromosome 7 determines dramatic up-regulation of osteopontin in dystrophic cardiac calcification in mice.

Aherrahrou Z, Axtner SB, Kaczmarek PM, Jurat A, Korff S, Doehring LC, Weichenhan D, Katus HA, Ivandic BT. Aherrahrou Z, et al. Among authors: weichenhan d. Am J Pathol. 2004 Apr;164(4):1379-87. doi: 10.1016/S0002-9440(10)63224-5. Am J Pathol. 2004. PMID: 15039225 Free PMC article.

3

S100A1 gene transfer: a strategy to strengthen engineered cardiac grafts.

Remppis A, Pleger ST, Most P, Lindenkamp J, Ehlermann P, Schweda C, Löffler E, Weichenhan D, Zimmermann W, Eschenhagen T, Koch WJ, Katus HA. Remppis A, et al. Among authors: weichenhan d. J Gene Med. 2004 Apr;6(4):387-94. doi: 10.1002/jgm.513. J Gene Med. 2004. PMID: 15079813

4

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. Among authors: weichenhan d. Virchows Arch. 2006 May;448(5):630-8. doi: 10.1007/s00428-005-0071-7. Epub 2005 Oct 7. Virchows Arch. 2006. PMID: 16211391

5

Increased proinflammatory endothelial response to S100A8/A9 after preactivation through advanced glycation end products.

Ehlermann P, Eggers K, Bierhaus A, Most P, Weichenhan D, Greten J, Nawroth PP, Katus HA, Remppis A. Ehlermann P, et al. Among authors: weichenhan d. Cardiovasc Diabetol. 2006 Mar 30;5:6. doi: 10.1186/1475-2840-5-6. Cardiovasc Diabetol. 2006. PMID: 16573830 Free PMC article.

6

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. Among authors: weichenhan d. Physiol Genomics. 2006 May 16;25(3):387-92. doi: 10.1152/physiolgenomics.00010.2006. Physiol Genomics. 2006. PMID: 16705021

7

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. Among authors: weichenhan d. 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

8

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. Among authors: weichenhan d. 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

9

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. Among authors: weichenhan d. Comp Med. 2007 Dec;57(6):546-53. Comp Med. 2007. PMID: 18246866

10

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. Among authors: weichenhan d. BMC Med Genet. 2008 Oct 28;9:95. doi: 10.1186/1471-2350-9-95. BMC Med Genet. 2008. PMID: 18957093 Free PMC article.

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