Publications of M. Moser

Moser, M.; Matthiesen, S.; Kirfel, J.; Schorle, H.; Bergmann, C.; Senderek, J.; Rudnik-Schoneborn, S.; Zerres, K.; Buettner, R.: A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD). Hepatology 41 (5), pp. 1113 - 1121 (2005)

Muhlig-Versen, M.; da Cruz, A. B.; Tschape, J. A.; Moser, M.; Buttner, R.; Athenstaedt, K.; Glynn, P.; Kretzschmar, D.: Loss of Swiss cheese/neuropathy target esterase activity causes disruption of phosphatidylcholine homeostasis and neuronal and glial death in adult Drosophila. Journal of Neuroscience 25 (11), pp. 2865 - 2873 (2005)

Oess, S.; Gemhard, S.; Moser, M.; Graf, S.; Schilling, K.; Fässler, R.; Muller-Ester, W.: No synthase interacting protein is indispensable for embryonic development. Naunyn-Schmiedebergs Archives of Pharmacology 371 (Suppl. Suppl. 1), p. R38 - R38 (2005)

Rothhammer, T.; Poser, I.; Soncin, F.; Bataille, F.; Moser, M.; Bosserhoff, A. K.: Bone morphogenic proteins are overexpressed in malignant melanoma and promote cell invasion and migration. Cancer Research 65 (2), pp. 448 - 456 (2005)

Huttl, S.; Michalakis, S.; Seeliger, M.; Luo, D. G.; Acar, N.; Geiger, H.; Hudl, K.; Mader, R.; Haverkamp, S.; Moser, M. et al.; Pfeifer, A.; Gerstner, A.; Yau, K. W.; Biel, M.: Impaired channel targeting and retinal degeneration in mice lacking the cyclic nucleotide-gated channel subunit CNGB1. Journal of Neuroscience 25 (1), pp. 130 - 138 (2005)

Wang, H. V.; Vaupel, K.; Buettner, R.; Bosserhoff, A. K.; Moser, M.: Identification and embryonic expression of a new AP-2 transcription factor, AP-2 epsilon. Developmental Dynamics 231 (1), pp. 128 - 135 (2004)

Moser, M.; Li, Y.; Vaupel, K.; Kretzschmar, D.; Kluge, R.; Glynn, P.; Buettner, R.: Placental failure and impaired vasculogenesis result in embryonic lethality for neuropathy target esterase-deficient mice. Molecular and Cellular Biology 24 (4), pp. 1667 - 1679 (2004)

Bergmann, C.; Senderek, J.; Küpper, F.; Schneider, F.; Dornia, C.; Windelen, E.; Eggermann, T.; Rudnik-Schöneborn, S.; Kirfel, J.; Furu, L. et al.; Onuchic, L. E.; Rossetti, S.; Harris, P. C.; Somlo, S.; Guay-Woodford, L.; Germino, G. G.; Moser, M.; Büttner, R.; Zerres, K.: PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD). Human Mutation 23 (5), pp. 453 - 463 (2004)

Bergmann, C.; Senderek, J.; Schneider, F.; Dornia, C.; Kupper, F.; Eggermann, T.; Rudnik-Schöneborn, S.; Kirfel, J.; Moser, M.; Büttner, R. et al.; Zerres, K.: PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD). Human Mutation 23 (5), pp. 487 - 495 (2004)

Bosserhoff, A. K.; Moser, M.; Buettner, R.: Characterization and expression pattern of the novel MIA homolog TANGO. Gene Expression Patterns 4, pp. 473 - 479 (2004)

Rudlowski, C.; Moser, M.; Becker, A. J.; Rath, W.; Buttner, R.; Schröder, W.; Schurmann, A.: GLUT1 mRNA and protein expression in ovarian borderline tumors and cancer. Oncology 66 (5), pp. 404 - 410 (2004)

Zerres, K.; Senderek, J.; Rudnik-Schoneborn, S.; Eggermann, T.; Kunze, J.; Mononen, T.; Kaariainen, H.; Kirfel, J.; Moser, M.; Buettner, R. et al.; Bergmann, C.: New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene. Clinical Genetics 66, pp. 53 - 57 (2004)

Rudlowski, C.; Becker, A. J.; Schroder, W.; Rath, W.; Büttner, R.; Moser, M.: GLUT1 messenger RNA and protein induction relates to the malignant transformation of cervical cancer. American Journal of Clinical Pathology 120 (5), pp. 691 - 698 (2003)

Bosserhoff, A. K.; Moser, M.; Schölmerich, J.; Buettner, R.; Hellerbrand, C.: Specific expression and regulation of the new melanoma inhibitory activity-related gene MIA2 in hepatocytes. Journal of Biological Chemistry 278 (17), pp. 15225 - 15231 (2003)

Weiskirchen, R.; Moser, M.; Günther, K.; Weiskirchen, S.; Gressner, A. M.: The murine latent transforming growth factor-β binding protein (Ltbp-1) is alternatively spliced, and maps to a region syntenic to human chromosome 2p21-22. Gene 308, pp. 43 - 52 (2003)

Braun, A.; Bordoy, R.; Stanchi, F.; Moser, M.; Kostka, G.; Ehler, E.; Brandau, O.; Fässler, R.: PINCH2 is a new five LIM domain protein, homologous to PINCH and localized to focal adhesions. Experimental Cell Research 284 (2), pp. 239 - 248 (2003)

Moser, M.; Dahmen, S.; Kluge, R.; Gröne, H.; Dahmen, J.; Kunz, D.; Schorle, H.; Buettner, R.: Terminal renal failure in mice lacking transcription factor AP-2 beta. Laboratory Investigation 83 (4), pp. 571 - 578 (2003)

Bergmann, C.; Senderek, J.; Sedlacek, B.; Pegiazoglou, I.; Puglia, P.; Eggermann, T.; Rudnik-Schoneborn, S.; Furu, L.; Onuchic, L. F.; De Baca, M. et al.; Germino, G. G.; Guay-Woodford, L.; Somlo, S.; Moser, M.; Buttner, R.; Zerres, K.: Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). Journal of the American Society of Nephrology 14 (1), pp. 76 - 89 (2003)

Nagasawa, Y.; Matthiesen, S.; Onuchic, L. F.; Hou, X. Y.; Bergmann, C.; Esquivel, E.; Senderek, J.; Ren, Z. Y.; Zeltner, R.; Furu, L. et al.; Avner, E.; Moser, M.; Somlo, S.; Guay-Woodford, L.; Buttner, R.; Zerres, K.; Germino, G. G.: Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene. Journal of the American Society of Nephrology 13 (9), pp. 2246 - 2258 (2002)

Moser, M.; Bosserhoff, A.-K.; Hunziker, E. B.; Sandell, L.; Fässler, R.; Buettner, R.: Ultrastructural cartilage abnormalities in MIA/CD-RAP-deficient mice. Molecular and Cellular Biology 22, pp. 1438 - 1445 (2002)