Fuchs H - Search Results

1

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.

2

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

3

Genetics of dark skin in mice.

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.

4

A novel missense mutation in the mouse growth hormone gene causes semidominant dwarfism, hyperghrelinemia, and obesity.

Meyer CW, Korthaus D, Jagla W, Cornali E, Grosse J, Fuchs H, Klingenspor M, Roemheld S, Tschöp M, Heldmaier G, De Angelis MH, Nehls M. Meyer CW, et al. Among authors: fuchs h. Endocrinology. 2004 May;145(5):2531-41. doi: 10.1210/en.2003-1125. Epub 2004 Jan 15. Endocrinology. 2004. PMID: 14726450

5

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

6

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

7

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

8

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

9

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

10

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

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