Fuchs H - Search Results

1

Fitch KR, McGowan KA, van Raamsdonk CD, Fuchs H, Lee D, Puech A, Hérault Y, Threadgill DW, Hrabé de Angelis M, Barsh GS. Fitch KR, et al. Among authors: fuchs h. Genes Dev. 2003 Jan 15;17(2):214-28. doi: 10.1101/gad.1023703. Genes Dev. 2003. PMID: 12533510 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

Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.

Kiernan AE, Zalzman M, Fuchs H, Hrabe de Angelis M, Balling R, Steel KP, Avraham KB. Kiernan AE, et al. Among authors: fuchs h. J Neurocytol. 1999 Oct-Nov;28(10-11):969-85. doi: 10.1023/a:1007090626294. J Neurocytol. 1999. PMID: 10900098

4

The Notch ligand Jagged1 is required for inner ear sensory development.

Kiernan AE, Ahituv N, Fuchs H, Balling R, Avraham KB, Steel KP, Hrabé de Angelis M. Kiernan AE, et al. Among authors: fuchs h. Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):3873-8. doi: 10.1073/pnas.071496998. Epub 2001 Mar 20. Proc Natl Acad Sci U S A. 2001. PMID: 11259677 Free PMC article.

5

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

6

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

7

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

8

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: fuchs h. Nat Genet. 2002 Mar;30(3):257-8. doi: 10.1038/ng848. Epub 2002 Feb 19. Nat Genet. 2002. PMID: 11850623

9

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

10

Alopecia in a novel mouse model RCO3 is caused by mK6irs1 deficiency.

Peters T, Sedlmeier R, Büssow H, Runkel F, Lüers GH, Korthaus D, Fuchs H, Hrabé de Angelis M, Stumm G, Russ AP, Porter RM, Augustin M, Franz T. Peters T, et al. Among authors: fuchs h. J Invest Dermatol. 2003 Oct;121(4):674-80. doi: 10.1046/j.1523-1747.2003.12491.x. J Invest Dermatol. 2003. PMID: 14632181 Free article.

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