Publications of M. Moser
All genres
Journal Article (136)
121.
Journal Article
231 (1), pp. 128 - 135 (2004)
Identification and embryonic expression of a new AP-2 transcription factor, AP-2 epsilon. Developmental Dynamics 122.
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 123.
Journal Article
23 (5), pp. 453 - 463 (2004)
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD). Human Mutation 124.
Journal Article
23 (5), pp. 487 - 495 (2004)
PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD). Human Mutation 125.
Journal Article
4, pp. 473 - 479 (2004)
Characterization and expression pattern of the novel MIA homolog TANGO. Gene Expression Patterns 126.
Journal Article
66 (5), pp. 404 - 410 (2004)
GLUT1 mRNA and protein expression in ovarian borderline tumors and cancer. Oncology 127.
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 128.
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 129.
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 130.
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 131.
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 132.
Journal Article
83 (4), pp. 571 - 578 (2003)
Terminal renal failure in mice lacking transcription factor AP-2 beta. Laboratory Investigation 133.
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 134.
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 135.
Journal Article
22, pp. 1438 - 1445 (2002)
Ultrastructural cartilage abnormalities in MIA/CD-RAP-deficient mice. Molecular and Cellular Biology 136.
Journal Article
22 (5), pp. 1488 - 1494 (2002)
Embryonic Lethality Caused by Apoptosis during Gastrulation in Mice Lacking the Gene of the ADP-Ribosylation Factor-Related Protein 1. Molecular and Cellular Biology Meeting Abstract (7)
137.
Meeting Abstract
227 (Suppl. 719), S 17-03. WILEY, 111 RIVER ST, HOBOKEN 07030-5774, NJ USA (2019)
KV1.3 in neutrophil function -An embryonic-derived peptide reveals a crucial role of KV1.3 during neutrophil recruitment-. In ACTA PHYSIOLOGICA, 138.
Meeting Abstract
52 (Suppl. 62), OA5377. 28th International Congress of the European-Respiratory-Society (ERS), Paris, FRANCE, September 15, 2018 - September 19, 2018. (2018)
ADAM28 deletion in mice impacts lung metastasis formation. In European Respiratory Journal, 139.
Meeting Abstract
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)
Pathogenic mechanisms of human autoantibodies against myelin oligodendrocyte glycoprotein. In Multiple Sclerosis Journal, 140.
Meeting Abstract
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)
Prolyl 3-hydroxylation of type IV collagen is obligatory to avoid early embryoniclethality in mice. In GLYCOBIOLOGY,