Fuchs H - Search Results

1

The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice?

Clemen CS, Winter L, Strucksberg KH, Berwanger C, Türk M, Kornblum C, Florin A, Aguilar-Pimentel JA, Amarie OV, Becker L, Garrett L, Hans W, Moreth K, Neff F, Pingen L, Rathkolb B, Rácz I, Rozman J, Treise I, Fuchs H, Gailus-Durner V, de Angelis MH, Vorgerd M, Eichinger L, Schröder R. Clemen CS, et al. Among authors: fuchs h. Biochem Biophys Res Commun. 2018 Sep 18;503(4):2770-2777. doi: 10.1016/j.bbrc.2018.08.038. Epub 2018 Aug 9. Biochem Biophys Res Commun. 2018. PMID: 30100055 Free article.

2

The novel mouse microphthalmia mutations Mitfmi-enu5 and Mitfmi-bcc2 produce dominant negative Mitf proteins.

Hansdottir AG, Pálsdóttir K, Favor J, Neuhäuser-Klaus A, Fuchs H, de Angelis MH, Steingrímsson E. Hansdottir AG, et al. Among authors: fuchs h. Genomics. 2004 May;83(5):932-5. doi: 10.1016/j.ygeno.2003.10.013. Genomics. 2004. PMID: 15081122

3

An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice.

Ahituv N, Erven A, Fuchs H, Guy K, Ashery-Padan R, Williams T, de Angelis MH, Avraham KB, Steel KP. Ahituv N, et al. Among authors: fuchs h. Mamm Genome. 2004 Jun;15(6):424-32. doi: 10.1007/s00335-004-2334-z. Mamm Genome. 2004. PMID: 15181535

4

Effects of G-protein mutations on skin color.

Van Raamsdonk CD, Fitch KR, Fuchs H, de Angelis MH, Barsh GS. Van Raamsdonk CD, et al. Among authors: fuchs h. Nat Genet. 2004 Sep;36(9):961-8. doi: 10.1038/ng1412. Epub 2004 Aug 22. Nat Genet. 2004. PMID: 15322542 Free PMC article.

5

Characterization of a new mouse mutant, flouncer, with a balance defect and inner ear malformation.

Pau H, Hawker K, Fuchs H, De Angelis MH, Steel KP. Pau H, et al. Among authors: fuchs h. Otol Neurotol. 2004 Sep;25(5):707-13. doi: 10.1097/00129492-200409000-00010. Otol Neurotol. 2004. PMID: 15353999

6

A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.

Rhodes CR, Hertzano R, Fuchs H, Bell RE, de Angelis MH, Steel KP, Avraham KB. Rhodes CR, et al. Among authors: fuchs h. Mamm Genome. 2004 Sep;15(9):686-97. doi: 10.1007/s00335-004-2344-x. Mamm Genome. 2004. PMID: 15389316

7

Hush puppy: a new mouse mutant with pinna, ossicle, and inner ear defects.

Pau H, Fuchs H, de Angelis MH, Steel KP. Pau H, et al. Among authors: fuchs h. Laryngoscope. 2005 Jan;115(1):116-24. doi: 10.1097/01.mlg.0000150693.31130.a0. Laryngoscope. 2005. PMID: 15630379

8

Genomewide linkage analysis identifies novel genetic Loci for lung function in mice.

Reinhard C, Meyer B, Fuchs H, Stoeger T, Eder G, Rüschendorf F, Heyder J, Nürnberg P, de Angelis MH, Schulz H. Reinhard C, et al. Among authors: fuchs h. Am J Respir Crit Care Med. 2005 Apr 15;171(8):880-8. doi: 10.1164/rccm.200409-1204OC. Epub 2005 Jan 7. Am J Respir Crit Care Med. 2005. PMID: 15640362

9

A mouse keratin 1 mutation causes dark skin and epidermolytic hyperkeratosis.

McGowan KA, Aradhya S, Fuchs H, de Angelis MH, Barsh GS. McGowan KA, et al. Among authors: fuchs h. J Invest Dermatol. 2006 May;126(5):1013-6. doi: 10.1038/sj.jid.5700241. J Invest Dermatol. 2006. PMID: 16528356 Free article.

10

Systematic, standardized and comprehensive neurological phenotyping of inbred mice strains in the German Mouse Clinic.

Schneider I, Tirsch WS, Faus-Kessler T, Becker L, Kling E, Busse RL, Bender A, Feddersen B, Tritschler J, Fuchs H, Gailus-Durner V, Englmeier KH, de Angelis MH, Klopstock T. Schneider I, et al. Among authors: fuchs h. J Neurosci Methods. 2006 Oct 15;157(1):82-90. doi: 10.1016/j.jneumeth.2006.04.002. Epub 2006 May 23. J Neurosci Methods. 2006. PMID: 16720049

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