Publications

Max Planck Institute for Molecular Genetics

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 (168)

Journal Article

Hucho, T. B.; Dina, O. A.; Kuhn, J.; Levine, J. D.: Estrogen controls PKCe-dependent mechanical hyperalgesia through direct action on nociceptive neurons. European Journal of Neuroscience: European Neuroscience Association 24 (2), pp. 527 - 534 (2006)

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Wendeler, M. W.; Jung, R.; Himmelbauer, H.; Geßner, R.: Unique gene structure and paralogy define the 7D-cadherin family. Cellular and Molecular Life Sciences 63 (13), pp. 1564 - 1573 (2006)

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Bartsch, O.; Rasi, S.; Delicado, A.; Dyack, S.; Neumann, L. M.; Seemanová, E.; Volleth, M.; Haaf, T.; Kalscheuer, V. M.: Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein–Taybi syndrome. Human Genetics 120 (3), pp. 179 - 186 (2006)

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Budny, B.; Chen, W.; Omran, H.; Fliegauf, M.; Tzschach, A.; Wisniewska, M.; Jensen, L. R.; Raynaud, M.; Shoichet, S. A.; Badura, M. et al.; Lenzner, S.; Latos-Bielenska, A.; Ropers, H.-H.: A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome. Human Genetics 120 (2), pp. 171 - 178 (2006)

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Hu, Y.-H.; Warnatz, H.-J.; Vanhecke, D.; Wagner, F.; Fiebitz, A.; Thamm, S.; Kahlem, P.; Lehrach, H.; Yaspo, M.-L.; Janitz, M.: Cell array-based intracellular localization screening reveals novel functional features of human chromosome 21 proteins. BMC Genomics 7, p. 155 - 155 (2006)

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Iskakova, M. B.; Szaflarski, W.; Dreyfus, M.; Remme, J.; Nierhaus, K.: Troubleshooting coupled in in vitro transcription–translation system derived from Escherichia coli cells: synthesis of high-yield fully active proteins. Nucleic Acids Research 34 (19), p. e135 - e135 (2006)

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Hummel, M.; Bentink, S.; Berger, H.; Klapper, W.; Wessendorf, S.; Barth, T. F.E.; Bernd, H.-W.; Cogliatti, S. B.; Dierlamm, J.; Feller, A. C. et al.; Hansmann, M.-L.; Haralambieva, E.; Harder, L.; Hasenclever, D.; Kühn, M.; Lenze, D.; Lichter, P.; Martin-Subero, J. I.; Möller, P.; Müller-Hermelink, H.-K.; Ott, G.; Parwaresch, R. M.; Pott, C.; Rosenwald, A.; Rosolowski, M.; Schwaenen, C.; Stürzenhofecker, B.; Szczepanowski, M.; Trautmann, H.; Wacker, H.-H.; Spang, R.; Loeffler, M.; Trümper, L.; Stein, H.; Siebert, R.: A Biologic Definition of Burkitt's Lymphoma from Transcriptional and Genomic Profiling. The New England Journal of Medicine: NEJM / Publ. by the Massachusetts Medical Society 354 (23), pp. 2419 - 2430 (2006)

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Ropers, H.-H.: X-linked mental retardation: many genes for a complex disorder. Opinion in Genetics & Development 16 (3), pp. 260 - 269 (2006)

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Tagariello, A.; Heller, R.; Greven, A.; Kalscheuer, V. M.; Molter, T.; Rauch, A.; Kress, W.; Winterpacht, A.: Balanced translocation in a patient with craniosynostosis disrupts the SOX6 gene and an evolutionary conserved non-transcribed region. Journal of Medical Genetics 43, pp. 534 - 540 (2006)

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Piovani, G.; Borsani, G.; Bertini, V.; Kalscheuer, V. M.; Viertel, P.; Bellotti, D.; Valseriati, D.; Barlati, S.: Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype. European Journal of Medical Genetics 49 (3), pp. 215 - 223 (2006)

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Groene, J.; Mansmann, U.; Meister, R.; Staub, E.; Roepcke, S.; Heinze, M.; Klaman, I.; Brümmendorf, T.; Hermann, K.; Loddenkemper, C. et al.; Pilarsky, C.; Mann, B.; Adams, H.-P.; Buhr, H. J.; Rosenthal, A.: Transcriptional census of 36 microdissected colorectal cancers yields a gene signature to distinguish UICC II and III. International Journal of Cancer 119 (8), pp. 1829 - 1836 (2006)

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Dadgar, S.; Hagens, O.; Dadgar, S. R.; Haghighi, E. N.; Schimpf, S.; Wissinger, B.; Garshasbi, M.: Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy. Experimental Eye Research 83 (3), pp. 702 - 706 (2006)

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Halic, M.; Gartmann, M.; Schlenker, O.; Mielke, T.; Pool, M. R.; Sinning, I.; Beckmann, R.: Signal recognition particle receptor exposes the ribosomal translocon binding site. Science 312 (5774), pp. 745 - 747 (2006)

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Gamerdinger, U.; Bosse, K.; Eggermann, T.; Kalscheuer, V. M.; Schwanitz, G.; Engels, H.: First report of a partial trisomy 3q12-q23 de novo—FISH breakpoint determination and phenotypic characterization. European Journal of Medical Genetics 49 (3), pp. 225 - 234 (2006)

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Türkmen, S.; Demirhan, O.; Hoffmann, K.; Diers, A.; Zimmer, C.; Sperling, K.; Mundlos, S.: Cerebellar hypoplasia and quadrupedal locomotion in humans as a recessive trait mapping to chromosome 17p. Journal of Medical Genetics 43 (5), pp. 461 - 464 (2006)

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Weigel, C.; Seitz, H.: Bacteriophage replication modules. FEMS Microbiology Reviews 30 (3), pp. 321 - 381 (2006)

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Muzny, D. M.; Scherer, S. E.; Kaul, R.; Wang, J.; Yu, J.; Sudbrak, R.; Buhay, C. J.; Chen, R.; Cree, A.; Ding, Y. et al.; Dugan-Rocha, S.; Gill, R.; Gunaratne, P.; Harris, R. A.; Hawes, A. C.; Hernandez, J.; Hodgson, A. V.; Hume, J.; Jackson, A.; Khan, Z. M.; Kovar-Smith, C.; Lewis, L. R.; Lozado, R. J.; Metzker, M. L.; Milosavljevic, A.; Miner, G. R.; Morgan, M. B.; Nazareth, L. V.; Scott, G.; Sodergren, E.; Song, X.-Z.; Steffen, D.; Wei, S.; Wheeler, D. A.; Wright, M. W.; Worley, K. C.; Yuan, Y.; Zhang, Z.; Adams, C. Q.; Ansari-Lari, A.; Ayele, M.; Brown, M. J.; Chen, G.; Chen, Z.; Clendenning, J.; Clerc-Blankenburg, K. P.; Chen, R.; Chen, Z.; Davis, C.; Delgado, O.; Dinh, H. H.; Dong, W.; Draper, H.; Ernst, S.; Fu, G.; Gonzalez-Garay, M. L.; Garcia, D. K.; Gillett, W.; Gu, J.; Hao, B.; Haugen, E.; Havlak, P.; He, X.; Hennig, S.; Hu, S.; Huang, W.; ackson, L. R. J.; Jacob, L. S.; Kelly, S. H.; Kube, M.; Levy, R.; Li, Z.; Liu, B.; Liu, J.; Liu, W.; Maheshwari, M.; Nguyen, B.-V.; Okwuonu, G. O.; Palmeiri, A.; Pasternak, S.; Perez, L. M.; Phelps, K. A.; Plopper, F. J. H.; Qiang, B.; Raymond, C.; Rodriguez, R.; Saenphimmachak, C.; Santibanez, J.; Shen, H.; Shen, Y.; Subramanian, S.; Tabor, P. E.; Verduzco, D.; Waldron, L.; Wang, J.; Wang, J.; Wang, Q.; Williams, G. A.; Wong, G. K.-S.; Yao, Z.; Zhang, J.; Zhang, X.; Zhao, G.; Zhou, J.; Zhou, Y.; Nelson, D.; Lehrach, H.; Reinhardt, R.; Naylor, S. L.; Yang, H.; Olson, M.; Weinstock, G.; Gibbs, R. A.: The DNA sequence, annotation and analysis of human chromosome 3. Nature 440 (7088), pp. 1194 - 1198 (2006)

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Muzny, D. M.; Scherer, S. E.; Kaul, R.; Wang, J.; Yu, J.; Sudbrak, R.; Buhay, C. J.; Chen, R.; Cree, A.; Ding, Y. et al.; Dugan-Rocha, S.; Gill, R.; Gunaratne, P.; Harris, R. A.; Hawes, A. C.; Hernandez, J.; Hodgson, A. V.; Hume, J.; Jackson, A.; Khan, Z. M.; Kovar-Smith, C.; Lewis, L. R.; Lozado, R. J.; Metzker, M. L.; Milosavljevic, A.; Miner, G. R.; Morgan, M. B.; Nazareth, L. V.; Scott, G.; Sodergren, E.; Song, X.-Z.; Steffen, D.; Wei, S.; Wheeler, D. A.; Wright, M. W.; Worley, K. C.; Yuan, Y.; Zhang, Z.; Adams, C. Q.; Ansari-Lari, A.; Ayele, M.; Brown, M. J.; Chen, G.; Chen, Z.; Clendenning, J.; Clerc-Blankenburg, K. P.; Chen, R.; Chen, Z.; Davis, C.; Delgado, O.; Dinh, H. H.; Dong, W.; Draper, H.; Ernst, S.; Fu, G.; Gonzalez-Garay, M. L.; Garcia, D. K.; Gillett, W.; Gu, J.; Hao, B.; Haugen, E.; Havlak, P.; He, X.; Hennig, S.; Hu, S.; Huang, W.; ackson, L. R. J.; Jacob, L. S.; Kelly, S. H.; Kube, M.; Levy, R.; Li, Z.; Liu, B.; Liu, J.; Liu, W.; Maheshwari, M.; Nguyen, B.-V.; Okwuonu, G. O.; Palmeiri, A.; Pasternak, S.; Perez, L. M.; Phelps, K. A.; Plopper, F. J. H.; Qiang, B.; Raymond, C.; Rodriguez, R.; Saenphimmachak, C.; Santibanez, J.; Shen, H.; Shen, Y.; Subramanian, S.; Tabor, P. E.; Verduzco, D.; Waldron, L.; Wang, J.; Wang, J.; Wang, Q.; Williams, G. A.; Wong, G. K.-S.; Yao, Z.; Zhang, J.; Zhang, X.; Zhao, G.; Zhou, J.; Zhou, Y.; Nelson, D.; Lehrach, H.; Reinhardt, R.; Naylor, S. L.; Yang, H.; Olson, M.; Weinstock, G.; Gibbs, R. A.: The DNA sequence, annotation and analysis of human chromosome 3. Nature 440 (7088), pp. 1194 - 1198 (2006)

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Muzny, D. M.; Scherer, S. E.; Kaul, R.; Wang, J.; Yu, J.; Sudbrak, R.; Buhay, C. J.; Chen, R.; Cree, A.; Ding, Y. et al.; Dugan-Rocha, S.; Gill, R.; Gunaratne, P.; Harris, R. A.; Hawes, A. C.; Hernandez, J.; Hodgson, A. V.; Hume, J.; Jackson, A.; Khan, Z. M.; Kovar-Smith, C.; Lewis, L. R.; Lozado, R. J.; Metzker, M. L.; Milosavljevic, A.; Miner, G. R.; Morgan, M. B.; Nazareth, L. V.; Scott, G.; Sodergren, E.; Song, X.-Z.; Steffen, D.; Wei, S.; Wheeler, D. A.; Wright, M. W.; Worley, K. C.; Yuan, Y.; Zhang, Z.; Adams, C. Q.; Ansari-Lari, A.; Ayele, M.; Brown, M. J.; Chen, G.; Chen, Z.; Clendenning, J.; Clerc-Blankenburg, K. P.; Chen, R.; Chen, Z.; Davis, C.; Delgado, O.; Dinh, H. H.; Dong, W.; Draper, H.; Ernst, S.; Fu, G.; Gonzalez-Garay, M. L.; Garcia, D. K.; Gillett, W.; Gu, J.; Hao, B.; Haugen, E.; Havlak, P.; He, X.; Hennig, S.; Hu, S.; Huang, W.; ackson, L. R. J.; Jacob, L. S.; Kelly, S. H.; Kube, M.; Levy, R.; Li, Z.; Liu, B.; Liu, J.; Liu, W.; Maheshwari, M.; Nguyen, B.-V.; Okwuonu, G. O.; Palmeiri, A.; Pasternak, S.; Perez, L. M.; Phelps, K. A.; Plopper, F. J. H.; Qiang, B.; Raymond, C.; Rodriguez, R.; Saenphimmachak, C.; Santibanez, J.; Shen, H.; Shen, Y.; Subramanian, S.; Tabor, P. E.; Verduzco, D.; Waldron, L.; Wang, J.; Wang, J.; Wang, Q.; Williams, G. A.; Wong, G. K.-S.; Yao, Z.; Zhang, J.; Zhang, X.; Zhao, G.; Zhou, J.; Zhou, Y.; Nelson, D.; Lehrach, H.; Reinhardt, R.; Naylor, S. L.; Yang, H.; Olson, M.; Weinstock, G.; Gibbs, R. A.: The DNA sequence, annotation and analysis of human chromosome 3. Nature 440 (7088), pp. 1194 - 1198 (2006)

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Tzschach, A.; Krause-Plonka, I.; Menzel, C.; Knoblauch, A.; Toennies, H.; Hoeltzenbein, M.; Radke, M.; Ropers, H.-H.; Kalscheuer, V. M.: Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion. American Journal of Medical Genetics Part A 140 (10), pp. 1108 - 1110 (2006)

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