Fuchs H - Search Results

1

The BEACH protein LRBA is required for hair bundle maintenance in cochlear hair cells and for hearing.

Vogl C, Butola T, Haag N, Hausrat TJ, Leitner MG, Moutschen M, Lefèbvre PP, Speckmann C, Garrett L, Becker L, Fuchs H, Hrabe de Angelis M, Nietzsche S, Kessels MM, Oliver D, Kneussel M, Kilimann MW, Strenzke N. Vogl C, et al. Among authors: fuchs h. EMBO Rep. 2017 Nov;18(11):2015-2029. doi: 10.15252/embr.201643689. Epub 2017 Sep 11. EMBO Rep. 2017. PMID: 28893864 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

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

5

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

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

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.

8

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

9

A mutation in the enamelin gene in a mouse model.

Seedorf H, Klaften M, Eke F, Fuchs H, Seedorf U, Hrabe de Angelis M. Seedorf H, et al. Among authors: fuchs h. J Dent Res. 2007 Aug;86(8):764-8. doi: 10.1177/154405910708600815. J Dent Res. 2007. PMID: 17652207

10

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.

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