Publikationen von M. Moser

Christoffersen, C.; Jauhiainen, M.; Moser, M.; Porse, B.; Ehnholm, C.; Fässler, R.; Dahlback, B.; Nielsen, L. B.: Effect of apolipoprotein M on modulation of HDL in APOM transgenic and APOM deficient mice. Atherosclerosis Supplements 8 (1), S. 211 - 212 (2007)

Arndt, S.; Poser, I.; Moser, M.; Bosserhoff, A. K.: Fussel-15, a novel Ski/Sno homolog protein, antagonizes BMP signaling. Molecular and Cellular Neuroscience 34 (4), S. 603 - 611 (2007)

Hommel, A.; Zahn, C.; Schmidt, S.; Kluge, R.; Augustin, R.; Jaschke, A.; Moser, M.; Joost, H. G.; Schurmann, A.: Lack of white adipose tissue in fat-specific Atfrp1 null-mutants. Naunyn-Schmiedebergs Archives of Pharmacology 375 (Suppl. Suppl. 1), S. 36 - 36 (2007)

Pfeifer, A.; Eigenbrod, S.; Al-Khadra, S.; Hofmann, A.; Mitteregger, G.; Moser, M.; Bertsch, U.; Kretzschmar, H.: Lentivector-mediated RNAi efficiently suppresses prion protein and prolongs survival of scrapie-infected mice. Journal of Clinical Investigation 116 (12), S. 3204 - 3210 (2006)

Kirfel, J.; Senderek, J.; Moser, M.; Roper, A.; Stendel, C.; Bergmann, C.; Zerres, K.; Buettner, R.: Cloning, expression and characterization of the murine orthologue of SBF2, the gene mutated in Charcot-Marie-Tooth disease type 4B2. Gene Expression Patterns 6 (8), S. 978 - 984 (2006)

Ussar, S.; Wang, H. V.; Linder, S.; Fässler, R.; Moser, M.: The Kindlins: Subcellular localization and expression during murine development. Experimental Cell Research 312 (16), S. 3142 - 3151 (2006)

Wenke, A. K.; Rothhammer, T.; Moser, M.; Bosserhoff, A. K.: Regulation of integrin α10 expression in chondrocytes by the transcription factors AP-2 epsilon and Ets-1. Biochemical and Biophysical Research Communications 345 (1), S. 495 - 501 (2006)

Bergmann, C.; Frank, V.; Kupper, F.; Kamitz, D.; Hanten, J.; Berges, P.; Mager, S.; Moser, M.; Kirfel, J.; Buttner, R. et al.; Senderek, J.; Zerres, K.: Diagnosis, pathogenesis, and treatment prospects in cystic kidney disease. Molecular Diagnosis & Therapy 10 (3), S. 163 - 174 (2006)

Stanchi, F.; Bordoy, R.; Kudlacek, O.; Braun, A.; Pfeifer, A.; Moser, M.; Fässler, R.: Consequences of loss of PINCH2 expression in mice. Journal of Cell Science 118 (24), S. 5899 - 5910 (2005)

Senderek, J.; Krieger, M.; Stendel, C.; Bergmann, C.; Moser, M.; Breitbach-Faller, N.; Rudnik-Schoneborn, S.; Blaschek, A.; Wolf, N. I.; Harting, I. et al.; North, K.; Smith, J.; Muntoni, F.; Brockington, M.; Quijano-Roy, S.; Renault, F.; Herrmann, R.; Hendershot, L. M.; Schroder, J. M.; Lochmuller, H.; Topaloglu, H.; Voit, T.; Weis, J.; Ebinger, F.; Zerres, K.: Mutations in SIL1 cause Marinesco-Sjogren syndrome, a cerebellar ataxia with cataract and myopathy. Nature Genetics 37 (12), S. 1312 - 1314 (2005)

Arndt, S.; Poser, I.; Schubert, T.; Moser, M.; Bosserhoff, A. K.: Cloning and functional characterization of a new Ski homolog, Fussel-18, specifically expressed in neuronal tissues. Laboratory Investigation 85 (11), S. 1330 - 1341 (2005)

Drews, F.; Sawitza, I.; Moser, M.; Gressner, A. M.; Weiskirchen, R.: Latent transforming growth factor-A binding protein-1 (LTBP) knockout - A tool for better understanding of liver fibrosis progression? Hepatology 42 (4 Suppl. Suppl. 1), S. 735A - 736A (2005)

Li, S. H.; Bordoy, R.; Stanchi, F.; Moser, M.; Braun, A.; Kudlacek, O.; Wewer, U. M.; Yurchenco, P. D.; Fässler, R.: PINCH1 regulates cell-matrix and cell-cell adhesions, cell polarity and cell survival during the peri-implantation stage. Journal of Cell Science 118 (13), S. 2913 - 2921 (2005)

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), S. 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), S. 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), S. 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), S. 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), S. 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), S. 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), S. 1667 - 1679 (2004)