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N-ethyl-N-nitrosourea-based generation of mouse models for mutant G protein-coupled receptors.
Grosse J, Tarnow P, Römpler H, Schneider B, Sedlmeier R, Huffstadt U, Korthaus D, Nehls M, Wattler S, Schöneberg T, Biebermann H, Augustin M. Grosse J, et al. Among authors: korthaus d. Physiol Genomics. 2006 Aug 16;26(3):209-17. doi: 10.1152/physiolgenomics.00289.2005. Epub 2006 May 23. Physiol Genomics. 2006. PMID: 16720677 Free article.
Alopecia in a novel mouse model RCO3 is caused by mK6irs1 deficiency.
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. Peters T, et al. Among authors: korthaus d. J Invest Dermatol. 2003 Oct;121(4):674-80. doi: 10.1046/j.1523-1747.2003.12491.x. J Invest Dermatol. 2003. PMID: 14632181 Free article.
Efficient and fast targeted production of murine models based on ENU mutagenesis.
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, Wolf A, Voelkel M, Kellner M, Kilian M, Seelig S, Koppius A, Teubner A, Korthaus D, Nehls M, Wattler S. Augustin M, et al. Among authors: korthaus d. Mamm Genome. 2005 Jun;16(6):405-13. doi: 10.1007/s00335-004-3028-2. Mamm Genome. 2005. PMID: 16075367
Mutations in dynein link motor neuron degeneration to defects in retrograde transport.
Hafezparast M, Klocke R, Ruhrberg C, Marquardt A, Ahmad-Annuar A, Bowen S, Lalli G, Witherden AS, Hummerich H, Nicholson S, Morgan PJ, Oozageer R, Priestley JV, Averill S, King VR, Ball S, Peters J, Toda T, Yamamoto A, Hiraoka Y, Augustin M, Korthaus D, Wattler S, Wabnitz P, Dickneite C, Lampel S, Boehme F, Peraus G, Popp A, Rudelius M, Schlegel J, Fuchs H, Hrabe de Angelis M, Schiavo G, Shima DT, Russ AP, Stumm G, Martin JE, Fisher EM. Hafezparast M, et al. Among authors: korthaus d. Science. 2003 May 2;300(5620):808-12. doi: 10.1126/science.1083129. Science. 2003. PMID: 12730604
11 results