Publikationen von M. Moser
Alle Typen
Zeitschriftenartikel (138)
101.
Zeitschriftenartikel
4 (12), e1000289, S. [1] - [12] (2008)
Loss of Kindlin-1 Causes Skin Atrophy and Lethal Neonatal Intestinal Epithelial Dysfunction. PLoS Genetics 102.
Zeitschriftenartikel
204 (13), S. 3113 - 3118 (2007)
Loss of talin1 in platelets abrogates integrin activation, platelet aggregation, and thrombus formation in vitro and in vivo. Journal of Experimental Medicine 103.
Zeitschriftenartikel
1783 [2008] (1), S. 34 - 48 (2007)
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 104.
Zeitschriftenartikel
178 (1), S. 167 - 178 (2007)
The RGD motif in fibronectin is essential for development but dispensable for fibril assembly. Journal of Cell Biology 105.
Zeitschriftenartikel
8 (1), S. 211 - 212 (2007)
Effect of apolipoprotein M on modulation of HDL in APOM transgenic and APOM deficient mice. Atherosclerosis Supplements 106.
Zeitschriftenartikel
34 (4), S. 603 - 611 (2007)
Fussel-15, a novel Ski/Sno homolog protein, antagonizes BMP signaling. Molecular and Cellular Neuroscience 107.
Zeitschriftenartikel
375 (Suppl. Suppl. 1), S. 36 - 36 (2007)
Lack of white adipose tissue in fat-specific Atfrp1 null-mutants. Naunyn-Schmiedebergs Archives of Pharmacology 108.
Zeitschriftenartikel
116 (12), S. 3204 - 3210 (2006)
Lentivector-mediated RNAi efficiently suppresses prion protein and prolongs survival of scrapie-infected mice. Journal of Clinical Investigation 109.
Zeitschriftenartikel
6 (8), S. 978 - 984 (2006)
Cloning, expression and characterization of the murine orthologue of SBF2, the gene mutated in Charcot-Marie-Tooth disease type 4B2. Gene Expression Patterns 110.
Zeitschriftenartikel
312 (16), S. 3142 - 3151 (2006)
The Kindlins: Subcellular localization and expression during murine development. Experimental Cell Research 111.
Zeitschriftenartikel
345 (1), S. 495 - 501 (2006)
Regulation of integrin α10 expression in chondrocytes by the transcription factors AP-2 epsilon and Ets-1. Biochemical and Biophysical Research Communications 112.
Zeitschriftenartikel
10 (3), S. 163 - 174 (2006)
Diagnosis, pathogenesis, and treatment prospects in cystic kidney disease. Molecular Diagnosis & Therapy 113.
Zeitschriftenartikel
118 (24), S. 5899 - 5910 (2005)
Consequences of loss of PINCH2 expression in mice. Journal of Cell Science 114.
Zeitschriftenartikel
37 (12), S. 1312 - 1314 (2005)
Mutations in SIL1 cause Marinesco-Sjogren syndrome, a cerebellar ataxia with cataract and myopathy. Nature Genetics 115.
Zeitschriftenartikel
85 (11), S. 1330 - 1341 (2005)
Cloning and functional characterization of a new Ski homolog, Fussel-18, specifically expressed in neuronal tissues. Laboratory Investigation 116.
Zeitschriftenartikel
42 (4 Suppl. Suppl. 1), S. 735A - 736A (2005)
Latent transforming growth factor-A binding protein-1 (LTBP) knockout - A tool for better understanding of liver fibrosis progression? Hepatology 117.
Zeitschriftenartikel
118 (13), S. 2913 - 2921 (2005)
PINCH1 regulates cell-matrix and cell-cell adhesions, cell polarity and cell survival during the peri-implantation stage. Journal of Cell Science 118.
Zeitschriftenartikel
41 (5), S. 1113 - 1121 (2005)
A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD). Hepatology 119.
Zeitschriftenartikel
25 (11), S. 2865 - 2873 (2005)
Loss of Swiss cheese/neuropathy target esterase activity causes disruption of phosphatidylcholine homeostasis and neuronal and glial death in adult Drosophila. Journal of Neuroscience 120.
Zeitschriftenartikel
371 (Suppl. Suppl. 1), S. R38 - R38 (2005)
No synthase interacting protein is indispensable for embryonic development. Naunyn-Schmiedebergs Archives of Pharmacology