Fuchs H - Search Results

1

Crybb2 Mutations Consistently Affect Schizophrenia Endophenotypes in Mice.

Heermann T, Garrett L, Wurst W, Fuchs H, Gailus-Durner V, Hrabě de Angelis M, Graw J, Hölter SM. Heermann T, et al. Among authors: fuchs h. Mol Neurobiol. 2019 Jun;56(6):4215-4230. doi: 10.1007/s12035-018-1365-5. Epub 2018 Oct 6. Mol Neurobiol. 2019. PMID: 30291584

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: fuchs h. 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. Mamm Genome. 2000 Jul;11(7):528-30. doi: 10.1007/s003350010101. Mamm Genome. 2000. PMID: 10886017 No abstract available.

4

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

5

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

Hrabé de Angelis MH, Flaswinkel H, Fuchs H, Rathkolb B, Soewarto D, Marschall S, Heffner S, Pargent W, Wuensch K, Jung M, Reis A, Richter T, Alessandrini F, Jakob T, Fuchs E, Kolb H, Kremmer E, Schaeble K, Rollinski B, Roscher A, Peters C, Meitinger T, Strom T, Steckler T, Holsboer F, Klopstock T, Gekeler F, Schindewolf C, Jung T, Avraham K, Behrendt H, Ring J, Zimmer A, Schughart K, Pfeffer K, Wolf E, Balling R. Hrabé de Angelis MH, et al. Among authors: fuchs h, fuchs e. Nat Genet. 2000 Aug;25(4):444-7. doi: 10.1038/78146. Nat Genet. 2000. PMID: 10932192

6

Ethylnitrosourea-induced mutation in mice leads to the expression of a novel protein in the eye and to dominant cataracts.

Graw J, Klopp N, Löster J, Soewarto D, Fuchs H, Becker-Follmann J, Reis A, Wolf E, Balling R, Habré de Angelis M. Graw J, et al. Among authors: fuchs h. Genetics. 2001 Mar;157(3):1313-20. doi: 10.1093/genetics/157.3.1313. Genetics. 2001. PMID: 11238416 Free PMC article.

7

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: fuchs h. Invest Ophthalmol Vis Sci. 2001 Jun;42(7):1574-80. Invest Ophthalmol Vis Sci. 2001. PMID: 11381063

8

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: fuchs h. Invest Ophthalmol Vis Sci. 2001 Nov;42(12):2909-15. Invest Ophthalmol Vis Sci. 2001. PMID: 11687536

9

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: fuchs h. Exp Eye Res. 2001 Dec;73(6):867-76. doi: 10.1006/exer.2001.1096. Exp Eye Res. 2001. PMID: 11846517

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: fuchs h. Mamm Genome. 2002 Aug;13(8):452-5. doi: 10.1007/s00335-002-3021-6. Mamm Genome. 2002. PMID: 12226711

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