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Cognitive impairment and autistic-like behaviour in SAPAP4-deficient mice.
Schob C, Morellini F, Ohana O, Bakota L, Hrynchak MV, Brandt R, Brockmann MD, Cichon N, Hartung H, Hanganu-Opatz IL, Kraus V, Scharf S, Herrmans-Borgmeyer I, Schweizer M, Kuhl D, Wöhr M, Vörckel KJ, Calzada-Wack J, Fuchs H, Gailus-Durner V, Hrabě de Angelis M, Garner CC, Kreienkamp HJ, Kindler S. Schob C, et al. Among authors: fuchs h. Transl Psychiatry. 2019 Jan 16;9(1):7. doi: 10.1038/s41398-018-0327-z. Transl Psychiatry. 2019. PMID: 30664629 Free PMC article.
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
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
Power matters in closing the phenotyping gap.
Meyer CW, Elvert R, Scherag A, Ehrhardt N, Gailus-Durner V, Fuchs H, Schäfer H, Hrabé de Angelis M, Heldmaier G, Klingenspor M. Meyer CW, et al. Among authors: fuchs h. Naturwissenschaften. 2007 May;94(5):401-6. doi: 10.1007/s00114-006-0203-1. Epub 2007 Jan 10. Naturwissenschaften. 2007. PMID: 17216184
ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta.
Lisse TS, Thiele F, Fuchs H, Hans W, Przemeck GK, Abe K, Rathkolb B, Quintanilla-Martinez L, Hoelzlwimmer G, Helfrich M, Wolf E, Ralston SH, Hrabé de Angelis M. Lisse TS, et al. Among authors: fuchs h. PLoS Genet. 2008 Feb;4(2):e7. doi: 10.1371/journal.pgen.0040007. PLoS Genet. 2008. PMID: 18248096 Free PMC article.
1,449 results