Fuchs H - Search Results

1

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

2

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.

3

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

4

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

5

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.

6

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

7

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

8

The dominant alopecia phenotypes Bareskin, Rex-denuded, and Reduced Coat 2 are caused by mutations in gasdermin 3.

Runkel F, Marquardt A, Stoeger C, Kochmann E, Simon D, Kohnke B, Korthaus D, Wattler F, Fuchs H, Hrabé de Angelis M, Stumm G, Nehls M, Wattler S, Franz T, Augustin M. Runkel F, et al. Among authors: fuchs h. Genomics. 2004 Nov;84(5):824-35. doi: 10.1016/j.ygeno.2004.07.003. Genomics. 2004. PMID: 15475261

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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