21 results for author:"Weichenhan D." in Literature citations
Results Customize
› Repeat search in UniProtKB (34)
| Genome-wide methylation screen in low-grade breast cancer identifies novel epigenetically altered genes as potential biomarkers for tumor diagnosis. Faryna M., Konermann C., Aulmann S., Bermejo J.L., Brugger M., Diederichs S., Rom J., Weichenhan D., Claus R., Rehli M. et al. FASEB J. 26:4937-4950(2012) · Mapped (19) |
| Epigenetic deregulation of TCF21 inhibits metastasis suppressor KISS1 in metastatic melanoma. Arab K., Smith L.T., Gast A., Weichenhan D., Huang J.P., Claus R., Hielscher T., Espinosa A.V., Ringel M.D., Morrison C.D. et al. Carcinogenesis 32:1467-1473(2011) · Mapped (1) |
| 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., Muller A., Steen H., Ivandic B.T., Ulmer H.E. et al. Cardiovasc. Res. 86:452-460(2010) · Mapped (5) |
| Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy. Hassel D., Dahme T., Erdmann J., Meder B., Huge A., Stoll M., Just S., Hess A., Ehlermann P., Weichenhan D. et al. |
| HBEGF, SRA1, and IK: Three cosegregating genes as determinants of cardiomyopathy. Friedrichs F., Zugck C., Rauch G.J., Ivandic B., Weichenhan D., Muller-Bardorff M., Meder B., El Mokhtari N.E., Regitz-Zagrosek V., Hetzer R. et al. Genome Res. 19:395-403(2009) · Mapped (23) |
| 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 B.T., Katus H.A. BMC Med. Genet. 9:95-95(2008) · Mapped (8) |
| A mouse translocation associated with Caspr5-2 disruption and perinatal lethality. Weichenhan D., Traut W., Gongrich C., Himmelbauer H., Busch L., Monyer H., Winking H. Mamm. Genome 19:675-686(2008) · Mapped (7) |
| Atrial natriuretic peptide and osteopontin are useful markers of cardiac disorders in mice. Schoensiegel F., Bekeredjian R., Schrewe A., Weichenhan D., Frey N., Katus H.A., Ivandic B.T. Comp. Med. 57:546-553(2007) · Mapped (14) |
| Incomplete nonsense-mediated decay of mutant lamin A/C mRNA provokes dilated cardiomyopathy and ventricular tachycardia. Geiger S.K., Bar H., Ehlermann P., Walde S., Rutschow D., Zeller R., Ivandic B.T., Zentgraf H., Katus H.A., Herrmann H. et al. J. Mol. Med. 86:281-289(2008) · Mapped (8) |
| New members of the neurexin superfamily: multiple rodent homologues of the human CASPR5 gene. Traut W., Weichenhan D., Himmelbauer H., Winking H. |
| Fine mapping of Dyscalc1, the major genetic determinant of dystrophic cardiac calcification in mice. Korff S., Schoensiegel F., Riechert N., Weichenhan D., Katus H.A., Ivandic B.T. Physiol. Genomics 25:387-392(2006) · Mapped (13) |
| 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 P.P., Katus H.A., Remppis A. Cardiovasc Diabetol 5:6-6(2006) · Mapped (3) |
| Cardiac adenoviral S100A1 gene delivery rescues failing myocardium. Most P., Pleger S.T., Volkers M., Heidt B., Boerries M., Weichenhan D., Loffler E., Janssen P.M., Eckhart A.D., Martini J. et al. J. Clin. Invest. 114:1550-1563(2004) · Mapped (2) |
| A locus on chromosome 7 determines dramatic up-regulation of osteopontin in dystrophic cardiac calcification in mice. Aherrahrou Z., Axtner S.B., Kaczmarek P.M., Jurat A., Korff S., Doehring L.C., Weichenhan D., Katus H.A., Ivandic B.T. Am. J. Pathol. 164:1379-1387(2004) · Mapped (3) |
| Source and component genes of a 6-200 Mb gene cluster in the house mouse. Weichenhan D., Kunze B., Winking H., Van Geel M., Osoegawa K., De Jong P.J., Traut W. |
| Restoration of the Mendelian transmission ratio by a deletion in the mouse chromosome 1 HSR. Weichenhan D., Kunze B., Traut W., Winking H. Genet. Res. 71:119-125(1998) · Mapped (35) |
| Evolution by fusion and amplification: the murine Sp100-rs gene cluster. Weichenhan D., Kunze B., Traut W., Winking H. Cytogenet. Cell Genet. 80:226-231(1998) · UniProtKB (2) · Mapped (14) |
| Structure and expression of the murine Sp100 nuclear dot gene. Weichenhan D., Kunze B., Zacker S., Traut W., Winking H. |
| Absence of correlation between Sry polymorphisms and XY sex reversal caused by the M. m. domesticus Y chromosome. Carlisle C., Winking H., Weichenhan D., Nagamine C.M. |
| A member of the mouse LRR transcript family with homology to the human Sp100 gene. Plass C., Weichenhan D., Kunze B., Hellwig T., Schneider C., Bautz F.A., Grzeschik K.H., Traut W., Winking H. |
| A transcript family from a long-range repeat cluster of the house mouse. Weichenhan D., Kunze B., Plass C., Hellwig T., Winking H., Traut W. Genome 38:239-245(1995) · Mapped (4) |