Fuchs H - Search Results

1

Mesenchymal TNFR2 promotes the development of polyarthritis and comorbid heart valve stenosis.

Sakkou M, Chouvardas P, Ntari L, Prados A, Moreth K, Fuchs H, Gailus-Durner V, Hrabe de Angelis M, Denis MC, Karagianni N, Kollias G. Sakkou M, et al. Among authors: fuchs h. JCI Insight. 2018 Apr 5;3(7):e98864. doi: 10.1172/jci.insight.98864. eCollection 2018 Apr 5. JCI Insight. 2018. PMID: 29618659 Free PMC article.

2

Screening for dysmorphological abnormalities--a powerful tool to isolate new mouse mutants.

Fuchs H, Schughart K, Wolf E, Balling R, Hrabé de Angelis M. Fuchs H, et al. Mamm Genome. 2000 Jul;11(7):528-30. doi: 10.1007/s003350010101. Mamm Genome. 2000. PMID: 10886017 No abstract available.

3

MouseNet database: digital management of a large-scale mutagenesis project.

Pargent W, Heffner S, Schäble KF, Soewarto D, Fuchs H, Hrabé de Angelis M. Pargent W, et al. Among authors: fuchs h. Mamm Genome. 2000 Jul;11(7):590-3. doi: 10.1007/s003350010112. Mamm Genome. 2000. PMID: 10886028

4

V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in mice.

Graw J, Löster J, Soewarto D, Fuchs H, Reis A, Wolf E, Balling R, Hrabé de Angelis M. Graw J, et al. Among authors: fuchs h. Mamm Genome. 2002 Aug;13(8):452-5. doi: 10.1007/s00335-002-3021-6. Mamm Genome. 2002. PMID: 12226711

5

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

6

Sex-dependent susceptibility to Listeria monocytogenes infection is mediated by differential interleukin-10 production.

Pasche B, Kalaydjiev S, Franz TJ, Kremmer E, Gailus-Durner V, Fuchs H, Hrabé de Angelis M, Lengeling A, Busch DH. Pasche B, et al. Among authors: fuchs h. Infect Immun. 2005 Sep;73(9):5952-60. doi: 10.1128/IAI.73.9.5952-5960.2005. Infect Immun. 2005. PMID: 16113316 Free PMC article.

7

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

8

Identification of a Keratin 4 mutation in a chemically induced mouse mutant that models white sponge nevus.

McGowan KA, Fuchs H, Hrabé de Angelis M, Barsh GS. McGowan KA, et al. Among authors: fuchs h. J Invest Dermatol. 2007 Jan;127(1):60-4. doi: 10.1038/sj.jid.5700498. Epub 2006 Jul 20. J Invest Dermatol. 2007. PMID: 16858417 Free article.

9

New ENU-induced semidominant mutation, Ali18, causes inflammatory arthritis, dermatitis, and osteoporosis in the mouse.

Abe K, Fuchs H, Lisse T, Hans W, Hrabé de Angelis M. Abe K, et al. Among authors: fuchs h. Mamm Genome. 2006 Sep;17(9):915-26. doi: 10.1007/s00335-006-0014-x. Epub 2006 Sep 8. Mamm Genome. 2006. PMID: 16964445

10

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

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