Hrabě de Angelis M - Search Results

1

New mutation in the mouse Xpd/Ercc2 gene leads to recessive cataracts.

Kunze S, Dalke C, Fuchs H, Klaften M, Rössler U, Hornhardt S, Gomolka M, Puk O, Sabrautzki S, Kulka U, Hrabě de Angelis M, Graw J. Kunze S, et al. Among authors: hrabe de angelis m. PLoS One. 2015 May 7;10(5):e0125304. doi: 10.1371/journal.pone.0125304. eCollection 2015. PLoS One. 2015. PMID: 25951169 Free PMC article.

2

Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse.

Graw J, Jung M, Löster J, Klopp N, Soewarto D, Fella C, Fuchs H, Reis A, Wolf E, Balling R, Hrabé de Angelis M. Graw J, et al. Among authors: hrabe de angelis m. Genomics. 1999 Nov 15;62(1):67-73. doi: 10.1006/geno.1999.5974. Genomics. 1999. PMID: 10585769

3

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. Among authors: hrabe de angelis m. Mamm Genome. 2000 Jul;11(7):528-30. doi: 10.1007/s003350010101. Mamm Genome. 2000. PMID: 10886017 No abstract available.

4

Comet assay as a tool to screen for mouse models with inherited radiation sensitivity.

Schindewolf C, Lobenwein K, Trinczek K, Gomolka M, Soewarto D, Fella C, Pargent W, Singh N, Jung T, Hrabé de Angelis M. Schindewolf C, et al. Among authors: hrabe de angelis m. Mamm Genome. 2000 Jul;11(7):552-4. doi: 10.1007/s003350010106. Mamm Genome. 2000. PMID: 10886022

5

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: hrabe de angelis m. Mamm Genome. 2000 Jul;11(7):590-3. doi: 10.1007/s003350010112. Mamm Genome. 2000. PMID: 10886028

6

Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse.

Graw J, Löster J, Soewarto D, Fuchs H, Reis A, Wolf E, Balling R, Hrabé de Angelis M. Graw J, et al. Among authors: hrabe de angelis m. Invest Ophthalmol Vis Sci. 2001 Jun;42(7):1574-80. Invest Ophthalmol Vis Sci. 2001. PMID: 11381063

7

Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene.

Graw J, Löster J, Soewarto D, Fuchs H, Meyer B, Reis A, Wolf E, Balling R, Hrabé de Angelis M. Graw J, et al. Among authors: hrabe de angelis m. Invest Ophthalmol Vis Sci. 2001 Nov;42(12):2909-15. Invest Ophthalmol Vis Sci. 2001. PMID: 11687536

8

Characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract.

Graw J, Löster J, Soewarto D, Fuchs H, Meyer B, Reis A, Wolf E, Balling R, Hrabé de Angelis M. Graw J, et al. Among authors: hrabe de angelis m. Exp Eye Res. 2001 Dec;73(6):867-76. doi: 10.1006/exer.2001.1096. Exp Eye Res. 2001. PMID: 11846517

9

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: hrabe de angelis m. Nat Genet. 2002 Mar;30(3):257-8. doi: 10.1038/ng848. Epub 2002 Feb 19. Nat Genet. 2002. PMID: 11850623

10

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: hrabe de angelis m. Mamm Genome. 2002 Aug;13(8):452-5. doi: 10.1007/s00335-002-3021-6. Mamm Genome. 2002. PMID: 12226711

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