Visual Universitätsmedizin Mainz

Ausgewählte Publikationen

Fend-Guella DL, von Kopylow K, Spiess AN, Schulze W, Salzbrunn A, Diederich S, El Hajj N, Haaf T, Zechner U, Linke M. (2019). “The DNA methylation profile of human spermatogonia at single-cell- and single-allele-resolution refutes its role in spermatogonial stem cell function and germ cell differentiation” Mol Hum Reprod. 2019 Jun 6;25(6):283-294

Xu, X, Smorag L, Nakamura T, Kimura T, Dressel R, Fitzner A, Tan X, Linke M, Zechner U, Engel W, Pantakani DV K. (2015). “Dppa3 expression is critical for generation of fully reprogrammed iPS cells and maintenance of Dlk1-Dio3 imprinting“ Nature Communications 6:6008

Siuda D, Wu Z, Chen  Y, Guo L, Linke M, Zechner U, Xia N, Reifenberg G, Kleinert H, Förstermann U, Li H. (2014). “Social isolation-induced epigenetic changes in midbrain of adult mice“ Journal of physiology and pharmacology 65(2): 247-255

Fatima A, Kaifeng S, Dittmann S,  Xu G,  Gupta MK, Linke M, Zechner U, Nguemo F, Milting H,  Farr M,  Hescheler J, Sarić T. (2013). “The Disease-Specific Phenotype in Cardiomyocytes Derived from Induced Pluripotent Stem Cells of Two Long QT Syndrome Type 3 Patients“.PLoS ONE 8(12): e83005

Rieusset A, Schaller F, Unmehopa U, Matarazzo V, Watrin F, Linke M, Georges B, Bischof J, Dijkstra F, Bloemsma M, Corby S, Michel FJ, Wevrick R, Zechner U, Swaab D, Dudley K, Bezin L, Muscatelli F. (2013). “Stochastic Loss of Silencing of the Imprinted Ndn/NDN Allele, in a Mouse Model and Humans with Prader-Willi Syndrome, Has Functional Consequences“ PLoS Genetics 9(9): e1003752

Marquardt JU, Fischer K, Baus K, Kashyap A, Ma S, Krupp M, Linke M, Teufel A, Zechner U, Strand D, Thorgeirsson SS, Galle PR, Strand S. (2013). “SIRT6 dependent genetic and epigenetic alterations are associated with poor clinical outcome in HCC patients.” Hepatology. 58(3): 1054–1064.