Publications of M. Moser

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)

Mueller, A. G.; Moser, M.; Kluge, R.; Leder, S.; Blum, M.; Büttner, R.; Joost, H. G.; Schürmann, A.: Embryonic Lethality Caused by Apoptosis during Gastrulation in Mice Lacking the Gene of the ADP-Ribosylation Factor-Related Protein 1. Molecular and Cellular Biology 22 (5), pp. 1488 - 1494 (2002)

Immler, R.; Nadolni, W.; Morikis, V.; Rohwedder, I.; Tilgner, J.; Grommes, J.; Bertsch, A.; Yevtushenko, A.; Kurz, A. R. M.; Soehnlein, O. et al.; Moser, M.; Gudermann, T.; Dietzel, S.; Barnea, E.; Simon, S. I.; Zierler, S.; Pruenster, M.; Sperandio, M.: KV1.3 in neutrophil function -An embryonic-derived peptide reveals a crucial role of KV1.3 during neutrophil recruitment-. In ACTA PHYSIOLOGICA, 227 (Suppl. 719), S 17-03. WILEY, 111 RIVER ST, HOBOKEN 07030-5774, NJ USA (2019)

Hubeau, C.; Gerard, C.; Carnet, O.; Moser, M.; Noel, A.; Cataldo, D.; Rocks, N.: ADAM28 deletion in mice impacts lung metastasis formation. In European Respiratory Journal, 52 (Suppl. 62), OA5377. 28th International Congress of the European-Respiratory-Society (ERS), Paris, FRANCE, September 15, 2018 - September 19, 2018. (2018)

Spadaro, M.; Winklmeier, S.; Beltran, E.; Macrini, C.; Hoeftberger, R.; Schuh, E.; Thaler, F.; Gerdes, L. A.; Laurent, S.; Gerhards, R. et al.; Braendle, S.; Dornmair, K.; Moser, M.; Krishnamoorthy, G.; Kamp, F.; Jenne, D.; Hohlfeld, R.; Kmpfel, T.; Lassmann, H.; Kawakami, N.; Meinl, E.: Pathogenic mechanisms of human autoantibodies against myelin oligodendrocyte glycoprotein. In Multiple Sclerosis Journal, 23 3_suppl Ed., p. 976 - 976. 7th Joint European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS)-Americas-Committee-for-Treatment-and-Research-in-Multiple-Scle rosis (ACTRIMS), Paris, FRANCE, October 25, 2017 - October 28, 2017. SAGE, London (2017)

Pokidysheva, E.; Boudko, S.; Vranka, J.; Keene, D.; Tufa, S.; Zentek, K.; Moser, M.; Fässler, R.; Ware, J.; Baechinger, H. P.: Prolyl 3-hydroxylation of type IV collagen is obligatory to avoid early embryoniclethality in mice. In GLYCOBIOLOGY, 22 (11), p. 1524 - 1524. Joint Meeting of the Society-for-Glycobiology and American-Society-for-Matrix-Biology, San Diego, CA, November 11, 2012 - November 14, 2012. OXFORD UNIV PRESS INC, JOURNALS DEPT, 2001 EVANS RD, CARY, NC 27513 USA (2012)