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Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study.
Kofler B, Mueller EE, Eder W, Stanger O, Maier R, Weger M, Haas A, Winker R, Schmut O, Paulweber B, Iglseder B, Renner W, Wiesbauer M, Aigner I, Santic D, Zimmermann FA, Mayr JA, Sperl W. Kofler B, et al. Among authors: sperl w. BMC Med Genet. 2009 Apr 21;10:35. doi: 10.1186/1471-2350-10-35. BMC Med Genet. 2009. PMID: 19383124 Free PMC article.
The mitochondrial T16189C polymorphism is associated with coronary artery disease in Middle European populations.
Mueller EE, Eder W, Ebner S, Schwaiger E, Santic D, Kreindl T, Stanger O, Paulweber B, Iglseder B, Oberkofler H, Maier R, Mayr JA, Krempler F, Weitgasser R, Patsch W, Sperl W, Kofler B. Mueller EE, et al. Among authors: sperl w. PLoS One. 2011 Jan 26;6(1):e16455. doi: 10.1371/journal.pone.0016455. PLoS One. 2011. PMID: 21298061 Free PMC article.
Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma.
Mayr JA, Meierhofer D, Zimmermann F, Feichtinger R, Kögler C, Ratschek M, Schmeller N, Sperl W, Kofler B. Mayr JA, et al. Among authors: sperl w. Clin Cancer Res. 2008 Apr 15;14(8):2270-5. doi: 10.1158/1078-0432.CCR-07-4131. Clin Cancer Res. 2008. PMID: 18413815
244 results