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Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathies.
Clemen CS, Fischer D, Roth U, Simon S, Vicart P, Kato K, Kaminska AM, Vorgerd M, Goldfarb LG, Eymard B, Romero NB, Goudeau B, Eggermann T, Zerres K, Noegel AA, Schröder R. Clemen CS, et al. Among authors: eggermann t. FEBS Lett. 2005 Jul 4;579(17):3777-82. doi: 10.1016/j.febslet.2005.05.051. FEBS Lett. 2005. PMID: 15978589 Free article.
On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria.
Schröder R, Goudeau B, Simon MC, Fischer D, Eggermann T, Clemen CS, Li Z, Reimann J, Xue Z, Rudnik-Schöneborn S, Zerres K, van der Ven PF, Fürst DO, Kunz WS, Vicart P. Schröder R, et al. Among authors: eggermann t. Hum Mol Genet. 2003 Mar 15;12(6):657-69. doi: 10.1093/hmg/ddg060. Hum Mol Genet. 2003. PMID: 12620971
Corrigendum to "Effect of CACNA1C rs1006737 on neural correlates of verbal fluency in healthy individuals" [NeuroImage volume 49 (2010) 1831-1836].
Krug A, Nieratschker V, Markov V, Krach S, Jansen A, Zerres K, Eggermann T, Stöcker T, Jon Shah N, Treutlein J, Mühleisen TW, Kircher T. Krug A, et al. Among authors: eggermann t. Neuroimage. 2024 Aug 15;297:120741. doi: 10.1016/j.neuroimage.2024.120741. Epub 2024 Jul 23. Neuroimage. 2024. PMID: 39048493 Free article. No abstract available.
DNA diagnosis in hereditary nephropathies.
Zerres K, Eggermann T, Rudnik-Schöneborn S. Zerres K, et al. Among authors: eggermann t. Clin Nephrol. 2001 Sep;56(3):181-92. Clin Nephrol. 2001. PMID: 11597032
Autosomal recessive polycystic kidney disease (ARPKD).
Zerres K, Rudnik-Schöneborn S, Senderek J, Eggermann T, Bergmann C. Zerres K, et al. Among authors: eggermann t. J Nephrol. 2003 May-Jun;16(3):453-8. J Nephrol. 2003. PMID: 12832752
357 results