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Korthaus Dirk,

** = Publications listed in SCI/SSCI/Pubmed

2010

Published (citable) presentations at scientific conferences (A2)

Zach, D; Korthaus, D; Tsujita, M; Plank, N; Walter, I; Reme, C; Rülicke, T (2010): Characterization of a Mouse Model for Primary Congenital Glaucoma. 38-38.-Scand Felasa - New Paradigms in Laboratory Animal Science; June 14-17, 2010; Helsinki, Finland.

2008

Anderl, S; Müller, S; Korthaus, D; Schmidt, V; Müller, M; Rülicke, T (2008): A New Kit Allel, Causing a Mild Phenotype in the Mouse. 272-273.-XX. International Congress of Genetics; JUL 12-17, 2008; Berlin, Deutschland.

2007

Korthaus, D; Andersen, L; Lassnig, C; Müller, S; Rülicke, T (2007): Refinement of tissue biopsy for PCR based genotyping of GM mice by using hair samples. -6th Transgenic Technology Meeting (TT2007); 12.-14.02.2007; Australien.

2006

Journal Article

** Grosse, J; Tarnow, P; Römpler, H; Schneider, B; Sedlmeier, R; Huffstadt, U; Korthaus, D; Nehls, M; Wattler, S; Schöneberg, T; Biebermann, H; Augustin, M (2006): N-ethyl-N-nitrosourea-based generation of mouse models for mutant G protein-coupled receptors. Physiol Genomics. 2006; 26(3):209-217
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Published (citable) presentations at scientific conferences (A2)

Korthaus, D; Andersen, L; Lassnig, C; Müller, S; Rülicke, T (2006): Refinement of tissue biopsy for PCR based genotyping of GM mice by using hair samples. GV Solas/ESLAV/IGTp Scientific Meeting , Freiburg, Germany, Germany, 10.-12.09.2006. GV Solas/ESLAV/IGTp Scientific Meeting , Freiburg, Germany, 10.-12.09.2006.

2005

Journal Article

** Augustin, M; Sedlmeier, R; Peters, T; Huffstadt, U; Kochmann, E; Simon, D; Schöniger, M; Garke-Mayerthaler, S; Laufs, J; Mayhaus, M; Franke, S; Klose, M; Graupner, A; Kurzmann, M; Zinser, C [and 10 others] (2005): Efficient and fast targeted production of murine models based on ENU mutagenesis. Mamm Genome. 2005; 16(6):405-413

2004

** Meyer, CW; Korthaus, D; Jagla, W; Cornali, E; Grosse, J; Fuchs, H; Klingenspor, M; Roemheld, S; Tschöp, M; Heldmaier, G; De Angelis, MH; Nehls, M (2004): A novel missense mutation in the mouse growth hormone gene causes semidominant dwarfism, hyperghrelinemia, and obesity. Endocrinology. 2004; 145(5):2531-2541
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** Runkel, F; Marquardt, A; Stoeger, C; Kochmann, E; Simon, D; Kohnke, B; Korthaus, D; Wattler, F; Fuchs, H; Hrabé de Angelis, M; Stumm, G; Nehls, M; Wattler, S; Franz, T; Augustin, M (2004): The dominant alopecia phenotypes Bareskin, Rex-denuded, and Reduced Coat 2 are caused by mutations in gasdermin 3. Genomics. 2004; 84(5):824-835

2003

** Peters, T; Sedlmeier, R; Büssow, H; Runkel, F; Lüers, GH; Korthaus, D; Fuchs, H; Hrabé de Angelis, M; Stumm, G; Russ, AP; Porter, RM; Augustin, M; Franz, T (2003): Alopecia in a novel mouse model RCO3 is caused by mK6irs1 deficiency. J Invest Dermatol. 2003; 121(4):674-680
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1998

** Resch, K; Korthaus, D; Wedemeyer, N; Lengeling, A; Ronsiek, M; Thiel, C; Baer, K; Jockusch, H; Schmitt-John, T (1998): Homology between human chromosome 2p13.3 and the wobbler critical region on mouse chromosome 11: comparative high-resolution mapping of STS and EST loci on YAC/BAC contigs. Mamm Genome. 1998; 9(11):893-898

1997

** Korthaus, D; Wedemeyer, N; Lengeling, A; Ronsiek, M; Jockusch, H; Schmitt-John, T (1997): Integrated radiation hybrid map of human chromosome 2p13: possible involvement of dynactin in neuromuscular diseases. Genomics. 1997; 43(2):242-244

1996

** Korthaus, D; Wedemeyer, N; Wiegand, C; Jockusch, H (1996): The gene for cytoplasmatic malate dehydrogenase, Mor2, is closely linked to the wobbler spinal muscular atrophy gene (wr). Mamm Genome. 1996; 7(3):250-250

** Wedemeyer, N; Lengeling, A; Ronsiek, M; Korthaus, D; Baer, K; Wuttke, M; Jockusch, H (1996): YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p. Genomics. 1996; 32(3):447-454

1995

Schmitt-John, T; Schmidt, VC; Augustin, M; Korthaus, D; Jockusch, H (1995): Neue genetische Strategien für die Positionsklonierung von "Krankheitsgenen" der Maus. Bioforum (22) 86-90.

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