Moser M - Search Results

1

Targeted disruption of the mouse Csrp2 gene encoding the cysteine- and glycine-rich LIM domain protein CRP2 result in subtle alteration of cardiac ultrastructure.

Sagave JF, Moser M, Ehler E, Weiskirchen S, Stoll D, Günther K, Büttner R, Weiskirchen R. Sagave JF, et al. Among authors: moser m. BMC Dev Biol. 2008 Aug 19;8:80. doi: 10.1186/1471-213X-8-80. BMC Dev Biol. 2008. PMID: 18713466 Free PMC article.

2

The murine latent transforming growth factor-beta binding protein (Ltbp-1) is alternatively spliced, and maps to a region syntenic to human chromosome 2p21-22.

Weiskirchen R, Moser M, Günther K, Weiskirchen S, Gressner AM. Weiskirchen R, et al. Among authors: moser m. Gene. 2003 Apr 10;308:43-52. doi: 10.1016/s0378-1119(03)00464-5. Gene. 2003. PMID: 12711389

3

LIM-domain protein cysteine- and glycine-rich protein 2 (CRP2) is a novel marker of hepatic stellate cells and binding partner of the protein inhibitor of activated STAT1.

Weiskirchen R, Moser M, Weiskirchen S, Erdel M, Dahmen S, Buettner R, Gressner AM. Weiskirchen R, et al. Among authors: moser m. Biochem J. 2001 Nov 1;359(Pt 3):485-96. doi: 10.1042/0264-6021:3590485. Biochem J. 2001. PMID: 11672422 Free PMC article.

4

Disruption of the latent transforming growth factor-beta binding protein-1 gene causes alteration in facial structure and influences TGF-beta bioavailability.

Drews F, Knöbel S, Moser M, Muhlack KG, Mohren S, Stoll C, Bosio A, Gressner AM, Weiskirchen R. Drews F, et al. Among authors: moser m. Biochim Biophys Acta. 2008 Jan;1783(1):34-48. doi: 10.1016/j.bbamcr.2007.08.004. Epub 2007 Aug 29. Biochim Biophys Acta. 2008. PMID: 17950478 Free article.

5

PINCH2 is a new five LIM domain protein, homologous to PINCHand localized to focal adhesions.

Braun A, Bordoy R, Stanchi F, Moser M, Kostka G G, Ehler E, Brandau O, Fässler R. Braun A, et al. Among authors: moser m. Exp Cell Res. 2003 Apr 1;284(2):239-50. doi: 10.1016/s0014-4827(02)00039-3. Exp Cell Res. 2003. PMID: 12651156

6

Embryonic lethality caused by apoptosis during gastrulation in mice lacking the gene of the ADP-ribosylation factor-related protein 1.

Mueller AG, Moser M, Kluge R, Leder S, Blum M, Büttner R, Joost HG, Schürmann A. Mueller AG, et al. Among authors: moser m. Mol Cell Biol. 2002 Mar;22(5):1488-94. doi: 10.1128/MCB.22.5.1488-1494.2002. Mol Cell Biol. 2002. PMID: 11839814 Free PMC article.

7

Diagnosis, pathogenesis, and treatment prospects in cystic kidney disease.

Bergmann C, Frank V, Küpper F, Kamitz D, Hanten J, Berges P, Mager S, Moser M, Kirfel J, Büttner R, Senderek J, Zerres K. Bergmann C, et al. Among authors: moser m. Mol Diagn Ther. 2006;10(3):163-74. doi: 10.1007/BF03256455. Mol Diagn Ther. 2006. PMID: 16771602 Review.

8

PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD).

Bergmann C, Senderek J, Schneider F, Dornia C, Küpper F, Eggermann T, Rudnik-Schöneborn S, Kirfel J, Moser M, Büttner R, Zerres K. Bergmann C, et al. Among authors: moser m. Hum Mutat. 2004 May;23(5):487-95. doi: 10.1002/humu.20019. Hum Mutat. 2004. PMID: 15108281

9

Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1).

Bergmann C, Senderek J, Sedlacek B, Pegiazoglou I, Puglia P, Eggermann T, Rudnik-Schöneborn S, Furu L, Onuchic LF, De Baca M, Germino GG, Guay-Woodford L, Somlo S, Moser M, Büttner R, Zerres K. Bergmann C, et al. Among authors: moser m. J Am Soc Nephrol. 2003 Jan;14(1):76-89. doi: 10.1097/01.asn.0000039578.55705.6e. J Am Soc Nephrol. 2003. PMID: 12506140

10

PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD).

Bergmann C, Senderek J, Küpper F, Schneider F, Dornia C, Windelen E, Eggermann T, Rudnik-Schöneborn S, Kirfel J, Furu L, Onuchic LF, Rossetti S, Harris PC, Somlo S, Guay-Woodford L, Germino GG, Moser M, Büttner R, Zerres K. Bergmann C, et al. Among authors: moser m. Hum Mutat. 2004 May;23(5):453-63. doi: 10.1002/humu.20029. Hum Mutat. 2004. PMID: 15108277 Review.

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