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  2. Arnold GJ, Frohlich T. Dynamic proteome signatures in gametes, embryos and their maternal environment. Reprod Fertil Dev (accepted) 2.4

  3. Bashamboo A, Ledig S, Wieacker P, Achermann JC, McElreavy K: New technologies for the identification of novel genetic markers of sex development (DSD). Sex Dev 4:213-224, Epub (2010). 3.0

  4. Bauersachs S, Blum H, Krebs S, Frohlich T, Arnold GJ, Wolf E. Creating new knowledge for ruminant reproduction from rapidly expanding and evolving scientific databases. In: Reproduction in Domestic Ruminants VII (eds. MC Lucy, JL Pate, MC Smith, TE Spencer), Nottingham University Press, ISBN 978-1-907284-14-4 (in press)

  5. Berendt FJ, Fröhlich T, Bolbrinker P, Boelhauve M, Güngör T, Habermann FA, Wolf E, Arnold GJ. Highly sensitive saturation labeling reveals changes in abundance of cell cycle-associated proteins and redox enzyme variants during oocyte maturation in vitro. Proteomics 2009 Feb;9(3):550-64. PubMed PMID: 19137544. 4.4

  6. Bogdanova N, Siebers U, Kelsch R, Markoff A, Röpke A,, Exeler R, Tsokas J, Wieacker P: Blood chimerism in a girl with Down syndrome and possible freemartin effect leading to aplasia of the Müllerian derivatives. Hum Reprod 25: 1339-1343, Epub (2010). 3.9

  7. Bohring, A., Stamm, T., Spaich, C., Haase, C., Spree, K., Hehr, U., Hoffmann, M., Ledig, S., Sel, S., Wieacker, P., Röpke, A. (2009) WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes. American Journal of Human Genetics, 85, 97-105. 2.5

  8. Dihazi, H., Dihazi, G.H., Nolte, J., Meyer, S., Jahn, O., Müller, G.A., Engel, W. (2009) Multipotent adult germline stem cells and embryonic stem cells: comparative proteomic approach. J Proteome Res. 8(12):5497-5510. 5.1

  9. Eichenlaub-Ritter U, Trapphoff T. Chromosomal and cytoplasmic context determines predisposition to maternal age-related aneuploidy: brief overview and update on MCAK in mammalian oocytes. Bioch. Soc. Transactions, (2010) doi 10-1044BST038 3.4

  10. Eichenlaub-Ritter U, Wieczorek M, Lüke S, Seidel T. Age Related Changes in Mitochondrial Function and New Approaches to Study Redox Regulation in Mammalian Oocytes in Response to Age or Maturation Conditions. Mitochondrion (2010) doi:10.1016/j.mito.2010.08.011 4.1

  11. Georg I, Bagheri-Fam S, Knower KC, Wieacker P, Scherer G, Harley VR: Mutations of the SRY-responsive enhancer of SOX9 are uncommon in XY gonadal dysgenesis. Sex Dev, Epub (2010). 3.0

  12. Hansmann, T., Heinzmann J., Wrenzycki, C., Zechner U., Niemann H. and Haaf T. (2010) Characterization of differentially methylated regions in three bovine imprinted genes: a model for studying human germ-cell and embryo development. Cytogenetic and Genome Research, accepted for publication (letter of acceptance included in attachment A). 1.7

  13. Hillier SGSmitz JEichenlaub-Ritter U Folliculogenesis and oogenesis: from basic science to the clinic. Mol Hum Reprod 16:617-20 (Editorial). 3.0

  14. Jakubiczka S, Schröder C, Ullmann R, Volleth M, Ledig S, Gilberg E, Kroisel P, Wieacker P: Translocation and deletion around SOX9 in a patient with acampomelic campomelic dysplasia and sex reversal. Sex Dev 4:143-149, Epub (2010). 3.0

  15. Khromov, T., Pantakani D.V., K., Nolte, J., Wolf, M., Dressel, W., Engel, W., Zechner, U. (2010) Global and gene-specific histone modification profiles of mouse multipotent adult germline stem cells. Mol. Hum. Reprod. (in press). (Manuscript and decision letter attached). 3.0

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  17. Ko K, Hübner K, Müller-Keuker J, Schöler HR. In vitro derivation of germ cells from embryonic stem cells. Frontiers in Bioscience 15:46, 2010 3.7

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  19. Ledig S, Hiort O, Scherer G, Hoffmann M, Wolf G, Morlot S, Kuechler A, Wieacker P: Array-CGH analysis in patients with syndromic and non-syndromic XY gonadal dysgenesis: evaluation of array-CGH as diagnostic tool and search for new candidate loci. Hum Reprod 25:2637-2646, Epub (2010b). 3.9

  20. Ledig S, Röpke A, Haeusler G, Hinney B, Wieacker P: BMP15 mutations in XX gonadal dysgenesis and premature ovarian failure. Am J Obstet Gynecol 198:84.e1-5 (2008). 3.3

  21. Ledig S, Schippert C, Strick R, Beckmann MW, Oppelt PG, Wieacker P: Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome. Fertil Steril, Epub (2010c). 4.0

  22. Ledig, S., Röpke, A. and Wieacker, P. (2010a) Copy number variants in premature ovarian failure and ovarian dysgenesis. Sexual Development, 4, 225-232. 3.0

  23. Leidenfrost S, Boelhauve M, Reichenbach M, Güngör T, Reichenbach HD, Sinowatz F, Wolf E, Habermann FA. Cell arrest and cell death in mammalian preimplantation development: lessons from the bovine model. PLoS One. 2011; 6(7):e22121. doi: 10.1371/journal.pone.0022121. Epub 2011 Jul 21. PubMed PMID: 21811561

  24. May, A., Kirchner, R., Müller, H., Hartmann, P., El Hajj, N., Tresch, A., Zechner, U., Mann, W., Haaf, T. (2009) Multiplex RT-PCR expression analysis of developmentally important genes in individual mouse preimplantation embryos and blastomeres. Biol. Reprod. 80: 194-202. 3.3

  25. Meyer, S., Nolte, J., Opitz, L., Salinas-Riester, G., Engel, W. (2010) Pluripotent embryonic stem cells and multipotent adult germline stem cells reveal similar transcriptomes including pluripotency-related genes. Mol Hum Reprod. doi: 10.1093/molehr/gaq060 3.0

  26. Niemann, H., Carnwath, JW., Herrmann D., Wieczorek, G., Lemme E., Lucas-Hahn, A., Olek, S. (2010) DNA Methylation patterns reflect epigenetic reprogramming in bovine embryos. Cellular Reprogramming 12 (1): 33-42

  27. Nolte, J., Michelmann, H.W., Wolf, M., Wulf, G., Nayernia, K., Meinhardt, A., Zechner, U., Engel, W. (2010) PSCDGs of mouse multipotent adult germline stem cells can enter and progress through meiosis to form haploid male germ cells in vitro. Differentiation. doi:10.1016/j.diff.2010.08.001. 3.3

  28. Pliushch G, Schneider E, Weise D, El Hajj N, Tresch A, Seidmann L, Coerdt W, Müller AM, Zechner U, Haaf T. Extreme methylation values of imprinted genes in human abortions and stillbirths. Am J Pathol 2010; 176:1084-1090 5.7

  29. Poplinski A, Wieacker P, Kliesch S, Gromoll J: Severe XIST hypomethylation clearly distinguishes (SRY+) 46,XX-maleness from Klinefelter syndrome. Eur J Endocrinol 162:169-175 (2010). 3.5

  30. Reichenbach M, Lim T, Reichenbach HD, Guengoer T, Habermann FA, Matthiesen M, Hofmann A, Weber F, Zerbe H, Grupp T, Sinowatz F, Pfeifer A, Wolf E. Germ-line transmission of lentiviral PGK-EGFP integrants in transgenic cattle: new perspectives for experimental embryology. Transgenic Res 2010 Aug;19(4):549-56. Epub 2009 Oct 28. PubMed PMID: 19862638. 2.5

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  33. Schneider E, Pliushch G, El Hajj N, Galetzka D, Puhl A, Schorsch M, Frauenknecht K, Riepert T, Tresch A, Müller AM, Coerdt W, Zechner U. Haaf T. Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns. Nucleic Acids Res 2010; 38:3880-3890 7.5

  34. Sriraman V, Eichenlaub-Ritter U, Bartsch JW, Rittger A, Mulders SM, Richards JS. (2008) Regulated expression of ADAM8 (a disintegrin and metalloprotease domain 8) in the mouse ovary: evidence for a regulatory role of luteinizing hormone, progesterone receptor, and epidermal growth factor-like growth factors. Biol Reprod. 78:1038-48. 3.3

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  36. Trapphoff T, El Hajj N, Zechner U, Haaf T, Eichenlaub-Ritter, U. DNA integrity, growth pattern, spindle formation, chromosomal constitution and imprinting patterns of oocytes from vitrified preantral follicles. Hum. Reprod., in press (letter of acceptance included in attachment C) 3.9

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  39. Vogt E, Sanhaji M, Klein W, Seidel T, Wordeman L, Eichenlaub-Ritter U. (2010) MCAK is present at centromeres, midspindle and chiasmata and involved in silencing of the spindle assembly checkpoint in mammalian oocytes. Mol Hum Reprod. 16:665-84.

  40. Vogt E, Kipp A, Eichenlaub-Ritter U. Aurora kinase B, epigenetic state of centromeric heterochromatin and chiasma resolution in oocytes. Reprod Biomed Online. 200919:352-68.

  41. Vogt E, Kirsch-Volders M, Parry J, Eichenlaub-Ritter U. Spindle formation, chromosome segregation and the spindle checkpoint in oocytes and susceptibility to meiotic error. Mutat Res. 2008; 651:14-29. 3.6

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  46. Zechner U, Pliushch G, Schneider E, El Hajj N, Tresch A, Shufaro Y, Seidmann L, Coerdt W, Müller AM, Haaf T. Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conception. Mol Hum Reprod. 2010;16:704-713. 3.0

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  49. Zovoilis, A., Pantazi, A., Smorag, L., Opitz, L., Salinas-Riester, G., Wolf, M., Zechner, U., Holubowska, A., Stewart, C.L., Engel, W. (2010) Embryonic stem cell related miRNAs are involved in differentiation of pluripotent cells originating from the germ line. Mol. Hum. Reprod. doi: 10.1093/molehr/gaq053 3.0