PuRe Publications

The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Journal Article (139)

Journal Article

Geffers, L.; Herrmann, B. G.; Eichele, G.: Web-based digital gene expression atlases for the mouse. Mammalian Genome 23, pp. 525 - 538 (2012)

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Kämpjärvi, K.; Mäkinen, N.; Kilpivaara, O.; Arola, J.; Heinonen, H.-R.; Böhm, J.; Abdel-Wahab, O.; Lehtonen, H. J.; Pelttari, L. M.; Mehine, M. et al.; Schrewe, H.; Nevanlinna, H.; Levine, R. L.; Hokland, P.; Böhling, T.; Mecklin, J.-P.; Bützow, R.; Aaltonen, L. A.; Vahteristo, P.: Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer. British Journal of Cancer 107, pp. 1761 - 1765 (2012)

MPG.PuRe

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Wittler, L.; Hilger, A.; Proske, J.; Pennimpede, T.; Draaken, M.; Ebert, A.-K.; Rösch, W.; Stein, R.; Nöthen, M. M.; Reutter, H. et al.; Ludwig, M.: Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias. Gene 506 (2), pp. 392 - 395 (2012)

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Krautzberger, M. K.; Kosiol, B.; Scholze, M.; Schrewe, H.: Expression of vasorin (Vasn) during embryonic development of the mouse. Gene Expression Patterns 12 (5-6), pp. 167 - 171 (2012)

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Kammerer, R.; Rüttiger, L.; Riesenberg, R.; Schäuble, C.; Krupar, R.; Kamp, A.; Sunami, K.; Eisenried, A.; Hennenberg, M.; Grunert, F. et al.; Breß, A.; Battaglia, S.; Schrewe, H.; Knipper, M.; Schneider, M. R.: Loss of the mammal-specific tectorial membrane component CEA cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies. Journal of Biological Chemistry 287, pp. 21584 - 21598 (2012)

MPG.PuRe

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Bauer, H.; Schindler, S.; Charon, Y.; Willert, J.; Kusecek, B.; Herrmann, B. G.: The nucleoside diphosphate kinase gene Nme3 acts as quantitative trait locus promoting non-Mendelian inheritance. PLoS Genetics 8 (3), Article e1002567 (2012)

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Schwaerzer, G. K.; Hiepen, C.; Schrewe, H.; Nickel, J.; Ploeger, F.; Sebald, W.; Mueller, T.; Knaus, P.: New insights into the molecular mechanism of multiple synostoses syndrome (SYNS): mutation within the GDF5 knuckle epitope causes noggin-resistance. Journal of Bone and Mineral Research 27 (2), pp. 429 - 442 (2012)

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Diaz-Lacava, A.; Walier, M.; Penacino, G.; Wienker, T. F.; Baur, M. P.: Spatial assessment of Argentinean genetic admixture with geographical information systems. Forensic Sci Int Genet 5 (4), pp. 297 - 302 (2011)

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Diaz-Lacava, A.; Walier, M.; Willuweit, S.; Wienker, T. F.; Fimmers, R.; Baur, M. P.; Roewer, L.: Geostatistical inference of main Y-STR-haplotype groups in Europe. Forensic Sci Int Genet 5 (2), pp. 91 - 4 (2011)

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El-Maarri, O.; Walier, M.; Behne, F.; van Uum, J.; Singer, H.; Diaz-Lacava, A.; Nusgen, N.; Niemann, B.; Watzka, M.; Reinsberg, J. et al.; van der Ven, H.; Wienker, T.; Stoffel-Wagner, B.; Schwaab, R.; Oldenburg, J.: Methylation at global LINE-1 repeats in human blood are affected by gender but not by age or natural hormone cycles. PLoS ONE 6 (1), p. e16252 - e16252 (2011)

MPG.PuRe

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