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Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Riedhammer KM, Nguyen TT, Koşukcu C, Calzada-Wack J, Li Y, Saygılı S, Wimmers V, Kim GJ, Chrysanthou M, Bakey Z, Kraiger M, Sanz-Moreno A, Amarie OV, Rathkolb B, Klein-Rodewald T, Garrett L, Hölter SM, Seisenberger C, Haug S, Marschall S, Wurst W, Fuchs H, Gailus-Durner V, Wuttke M, de Angelis MH, Ćomić J, Doğan ÖA, Özlük Y, Taşdemir M, Ağbaş A, Canpolat N, Ćalışkan S, Weber R, Bergmann C, Jeanpierre C, Saunier S, Lim TY, Hildebrandt F, Alhaddad B, Wu K, Antony D, Matschkal J, Schaaf C, Renders L, Schmaderer C, Meitinger T, Heemann U, Köttgen A, Arnold S, Ozaltin F, Schmidts M, Hoefele J. Riedhammer KM, et al. Among authors: fuchs h. medRxiv [Preprint]. 2023 Mar 22:2023.03.21.23287206. doi: 10.1101/2023.03.21.23287206. medRxiv. 2023. PMID: 36993625 Free PMC article. Updated. Preprint.
Electroretinography as a screening method for mutations causing retinal dysfunction in mice.
Dalke C, Löster J, Fuchs H, Gailus-Durner V, Soewarto D, Favor J, Neuhäuser-Klaus A, Pretsch W, Gekeler F, Shinoda K, Zrenner E, Meitinger T, Hrabé de Angelis M, Graw J. Dalke C, et al. Among authors: fuchs h. Invest Ophthalmol Vis Sci. 2004 Feb;45(2):601-9. doi: 10.1167/iovs.03-0561. Invest Ophthalmol Vis Sci. 2004. PMID: 14744904
Effects of G-protein mutations on skin color.
Van Raamsdonk CD, Fitch KR, Fuchs H, de Angelis MH, Barsh GS. Van Raamsdonk CD, et al. Among authors: fuchs h. Nat Genet. 2004 Sep;36(9):961-8. doi: 10.1038/ng1412. Epub 2004 Aug 22. Nat Genet. 2004. PMID: 15322542 Free PMC article.
Systematic, standardized and comprehensive neurological phenotyping of inbred mice strains in the German Mouse Clinic.
Schneider I, Tirsch WS, Faus-Kessler T, Becker L, Kling E, Busse RL, Bender A, Feddersen B, Tritschler J, Fuchs H, Gailus-Durner V, Englmeier KH, de Angelis MH, Klopstock T. Schneider I, et al. Among authors: fuchs h. J Neurosci Methods. 2006 Oct 15;157(1):82-90. doi: 10.1016/j.jneumeth.2006.04.002. Epub 2006 May 23. J Neurosci Methods. 2006. PMID: 16720049
A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse.
Rubio-Aliaga I, Soewarto D, Wagner S, Klaften M, Fuchs H, Kalaydjiev S, Busch DH, Klempt M, Rathkolb B, Wolf E, Abe K, Zeiser S, Przemeck GK, Beckers J, de Angelis MH. Rubio-Aliaga I, et al. Among authors: fuchs h. Genetics. 2007 Mar;175(3):1451-63. doi: 10.1534/genetics.106.067298. Epub 2006 Dec 18. Genetics. 2007. PMID: 17179084 Free PMC article.
Creatine improves health and survival of mice.
Bender A, Beckers J, Schneider I, Hölter SM, Haack T, Ruthsatz T, Vogt-Weisenhorn DM, Becker L, Genius J, Rujescu D, Irmler M, Mijalski T, Mader M, Quintanilla-Martinez L, Fuchs H, Gailus-Durner V, de Angelis MH, Wurst W, Schmidt J, Klopstock T. Bender A, et al. Among authors: fuchs h. Neurobiol Aging. 2008 Sep;29(9):1404-11. doi: 10.1016/j.neurobiolaging.2007.03.001. Epub 2007 Apr 9. Neurobiol Aging. 2008. PMID: 17416441
1,466 results