Fuchs H - Search Results

1

Epigallocatechin gallate (EGCG) reduces the intensity of pancreatic amyloid fibrils in human islet amyloid polypeptide (hIAPP) transgenic mice.

Franko A, Rodriguez Camargo DC, Böddrich A, Garg D, Rodriguez Camargo A, Rathkolb B, Janik D, Aichler M, Feuchtinger A, Neff F, Fuchs H, Wanker EE, Reif B, Häring HU, Peter A, Hrabě de Angelis M. Franko A, et al. Among authors: fuchs h. Sci Rep. 2018 Jan 18;8(1):1116. doi: 10.1038/s41598-017-18807-8. Sci Rep. 2018. PMID: 29348618 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

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.

6

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

7

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.

8

MausDB: an open source application for phenotype data and mouse colony management in large-scale mouse phenotyping projects.

Maier H, Lengger C, Simic B, Fuchs H, Gailus-Durner V, Hrabé de Angelis M. Maier H, et al. Among authors: fuchs h. BMC Bioinformatics. 2008 Mar 26;9:169. doi: 10.1186/1471-2105-9-169. BMC Bioinformatics. 2008. PMID: 18366799 Free PMC article.

9

Phenotypic characterization of mouse models for bone-related diseases in the German Mouse Clinic.

Fuchs H, Lisse T, Hans W, Abe K, Thiele F, Gailus-Durner V, Hrabe de Angelis M. Fuchs H, et al. J Musculoskelet Neuronal Interact. 2008 Jan-Mar;8(1):13-4. J Musculoskelet Neuronal Interact. 2008. PMID: 18398253 Free article. Review. No abstract available.

10

A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?

Puk O, Esposito I, Söker T, Löster J, Budde B, Nürnberg P, Michel-Soewarto D, Fuchs H, Wolf E, Hrabé de Angelis M, Graw J. Puk O, et al. Among authors: fuchs h. Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4311-8. doi: 10.1167/iovs.09-3451. Epub 2009 Apr 30. Invest Ophthalmol Vis Sci. 2009. PMID: 19407009

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