Publications of M. Moser

Drews, F.; Knöbel, S.; Moser, M.; Muhlack, K. G.; Mohren, S.; Stoll, C.; Bosio, A.; Gressner, A. M.; Weiskirchen, R.: Disruption of the latent transforming growth factor-β binding protein-1 gene causes alteration in facial structure and influences TGF-β bioavailability. Biochimica et Biophysica Acta 1783, pp. 34 - 48 (2008)

Gawlik, V.; Schmidt, S.; Scheepers, A.; Wennemuth, G.; Augustin, R.; Aumuller, G.; Moser, M.; Al-Hasani, H.; Kluge, R.; Joost, H. G. et al.; Schurmann, A.: Targeted disruption of Slc2a8 (GLUT8) reduces motility and mitochondrial potential of spermatozoa. MOLECULAR MEMBRANE BIOLOGY 25 (3), pp. 224 - 235 (2008)

Ussar, S.; Moser, M.; Widmaier, M.; Rognoni, E.; Harrer, C.; Genzel-Boroviczeny, O.; Fässler, R.: Loss of Kindlin-1 Causes Skin Atrophy and Lethal Neonatal Intestinal Epithelial Dysfunction. PLoS Genetics 4 (12), e1000289, pp. [1] - [12] (2008)

Nieswandt, B.; Moser, M.; Pleines, I.; Varga-Szabo, D.; Monkley, S.; Critchley, D.; Fässler, R.: Loss of talin1 in platelets abrogates integrin activation, platelet aggregation, and thrombus formation in vitro and in vivo. Journal of Experimental Medicine 204 (13), pp. 3113 - 3118 (2007)

Drews, F.; Knöbel, S.; Moser, M.; Muhlack, K.G.; Mohren, S.; Stoll, C.; Bosio, A.; Gressner, A.M.; Weiskirchen, R.: Disruption of the latent transforming growth factor-β binding protein-1 gene causes alteration in facial structure and influences TGF-β bioavailability. Biochimica et Biophysica Acta 1783 [2008] (1), pp. 34 - 48 (2007)

Takahashi, S.; Leiss, M.; Moser, M.; Ohashi, T.; Kitao, T.; Heckmann, D.; Pfeifer, A.; Kessler, H.; Takagi, J.; Erickson, H. P. et al.; Fässler, R.: The RGD motif in fibronectin is essential for development but dispensable for fibril assembly. Journal of Cell Biology 178 (1), pp. 167 - 178 (2007)

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), pp. 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), pp. 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), p. 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), pp. 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), pp. 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), pp. 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), pp. 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), pp. 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), pp. 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), pp. 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), pp. 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), pp. 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), pp. 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), pp. 1113 - 1121 (2005)