Publications of M. Moser
All genres
Journal Article (141)
121.
Journal Article
41 (5), pp. 1113 - 1121 (2005)
A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD). Hepatology 122.
Journal Article
25 (11), pp. 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 123.
Journal Article
371 (Suppl. Suppl. 1), p. R38 - R38 (2005)
No synthase interacting protein is indispensable for embryonic development. Naunyn-Schmiedebergs Archives of Pharmacology 124.
Journal Article
65 (2), pp. 448 - 456 (2005)
Bone morphogenic proteins are overexpressed in malignant melanoma and promote cell invasion and migration. Cancer Research 125.
Journal Article
25 (1), pp. 130 - 138 (2005)
Impaired channel targeting and retinal degeneration in mice lacking the cyclic nucleotide-gated channel subunit CNGB1. Journal of Neuroscience 126.
Journal Article
231 (1), pp. 128 - 135 (2004)
Identification and embryonic expression of a new AP-2 transcription factor, AP-2 epsilon. Developmental Dynamics 127.
Journal Article
24 (4), pp. 1667 - 1679 (2004)
Placental failure and impaired vasculogenesis result in embryonic lethality for neuropathy target esterase-deficient mice. Molecular and Cellular Biology 128.
Journal Article
23 (5), pp. 453 - 463 (2004)
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD). Human Mutation 129.
Journal Article
23 (5), pp. 487 - 495 (2004)
PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD). Human Mutation 130.
Journal Article
4, pp. 473 - 479 (2004)
Characterization and expression pattern of the novel MIA homolog TANGO. Gene Expression Patterns 131.
Journal Article
66 (5), pp. 404 - 410 (2004)
GLUT1 mRNA and protein expression in ovarian borderline tumors and cancer. Oncology 132.
Journal Article
66, pp. 53 - 57 (2004)
New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene. Clinical Genetics 133.
Journal Article
120 (5), pp. 691 - 698 (2003)
GLUT1 messenger RNA and protein induction relates to the malignant transformation of cervical cancer. American Journal of Clinical Pathology 134.
Journal Article
278 (17), pp. 15225 - 15231 (2003)
Specific expression and regulation of the new melanoma inhibitory activity-related gene MIA2 in hepatocytes. Journal of Biological Chemistry 135.
Journal Article
308, pp. 43 - 52 (2003)
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 136.
Journal Article
284 (2), pp. 239 - 248 (2003)
PINCH2 is a new five LIM domain protein, homologous to PINCH and localized to focal adhesions. Experimental Cell Research 137.
Journal Article
83 (4), pp. 571 - 578 (2003)
Terminal renal failure in mice lacking transcription factor AP-2 beta. Laboratory Investigation 138.
Journal Article
14 (1), pp. 76 - 89 (2003)
Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). Journal of the American Society of Nephrology 139.
Journal Article
13 (9), pp. 2246 - 2258 (2002)
Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene. Journal of the American Society of Nephrology 140.
Journal Article
22, pp. 1438 - 1445 (2002)
Ultrastructural cartilage abnormalities in MIA/CD-RAP-deficient mice. Molecular and Cellular Biology