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Mutation of the Na(+)-K(+)-2Cl(-) cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.
Kemter E, Rathkolb B, Bankir L, Schrewe A, Hans W, Landbrecht C, Klaften M, Ivandic B, Fuchs H, Gailus-Durner V, Hrabé de Angelis M, Wolf E, Wanke R, Aigner B. Kemter E, et al. Among authors: fuchs h. Am J Physiol Renal Physiol. 2010 Jun;298(6):F1405-15. doi: 10.1152/ajprenal.00522.2009. Epub 2010 Mar 10. Am J Physiol Renal Physiol. 2010. PMID: 20219826 Free article.
Genome-wide, large-scale production of mutant mice by ENU mutagenesis.
Hrabé de Angelis MH, Flaswinkel H, Fuchs H, Rathkolb B, Soewarto D, Marschall S, Heffner S, Pargent W, Wuensch K, Jung M, Reis A, Richter T, Alessandrini F, Jakob T, Fuchs E, Kolb H, Kremmer E, Schaeble K, Rollinski B, Roscher A, Peters C, Meitinger T, Strom T, Steckler T, Holsboer F, Klopstock T, Gekeler F, Schindewolf C, Jung T, Avraham K, Behrendt H, Ring J, Zimmer A, Schughart K, Pfeffer K, Wolf E, Balling R. Hrabé de Angelis MH, et al. Among authors: fuchs h, fuchs e. Nat Genet. 2000 Aug;25(4):444-7. doi: 10.1038/78146. Nat Genet. 2000. PMID: 10932192
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.
Vreugde S, Erven A, Kros CJ, Marcotti W, Fuchs H, Kurima K, Wilcox ER, Friedman TB, Griffith AJ, Balling R, Hrabé De Angelis M, Avraham KB, Steel KP. Vreugde S, et al. Among authors: fuchs h. Nat Genet. 2002 Mar;30(3):257-8. doi: 10.1038/ng848. Epub 2002 Feb 19. Nat Genet. 2002. PMID: 11850623
Genetics of dark skin in mice.
Fitch KR, McGowan KA, van Raamsdonk CD, Fuchs H, Lee D, Puech A, Hérault Y, Threadgill DW, Hrabé de Angelis M, Barsh GS. Fitch KR, et al. Among authors: fuchs h. Genes Dev. 2003 Jan 15;17(2):214-28. doi: 10.1101/gad.1023703. Genes Dev. 2003. PMID: 12533510 Free PMC article.
1,505 results