Drögemüller C - Search Results

1

A nonsense mutation in the optic atrophy 3 gene (OPA3) causes dilated cardiomyopathy in Red Holstein cattle.

Owczarek-Lipska M, Plattet P, Zipperle L, Drögemüller C, Posthaus H, Dolf G, Braunschweig MH. Owczarek-Lipska M, et al. Among authors: drogemuller c. Genomics. 2011 Jan;97(1):51-7. doi: 10.1016/j.ygeno.2010.09.005. Epub 2010 Oct 12. Genomics. 2011. PMID: 20923700 Free article.

2

[A database of available DNA tests in the dog].

Drögemüller C, Dolf G, Leeb T. Drögemüller C, et al. Schweiz Arch Tierheilkd. 2006 Aug;148(8):409-11. doi: 10.1024/0036-7281.148.8.409. Schweiz Arch Tierheilkd. 2006. PMID: 16933705 Free article. German.

3

PRNP promoter polymorphisms are associated with BSE susceptibility in Swiss and German cattle.

Haase B, Doherr MG, Seuberlich T, Drögemüller C, Dolf G, Nicken P, Schiebel K, Ziegler U, Groschup MH, Zurbriggen A, Leeb T. Haase B, et al. Among authors: drogemuller c. BMC Genet. 2007 Apr 16;8:15. doi: 10.1186/1471-2156-8-15. BMC Genet. 2007. PMID: 17437640 Free PMC article.

4

Evaluation of the CTSL2 gene as a candidate gene for alopecia X in Pomeranians and Keeshonden.

Mausberg EM, Drögemüller C, Leeb T, Dolf G, Rüfenacht S, Welle M. Mausberg EM, et al. Among authors: drogemuller c. Anim Biotechnol. 2007;18(4):291-6. doi: 10.1080/10495390701547461. Anim Biotechnol. 2007. PMID: 17934903

5

Exclusion of patched homolog 2 (PTCH2) as a candidate gene for alopecia X in Pomeranians and Keeshonden.

Mausberg EM, Drögemüller C, Dolf G, Rüfenacht S, Welle M, Leeb T. Mausberg EM, et al. Among authors: drogemuller c. Vet Rec. 2008 Jul 26;163(4):121-3. doi: 10.1136/vr.163.4.121. Vet Rec. 2008. PMID: 18660523 No abstract available.

6

Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease.

Drögemüller C, Drögemüller M, Leeb T, Mascarello F, Testoni S, Rossi M, Gentile A, Damiani E, Sacchetto R. Drögemüller C, et al. Among authors: drogemuller m. Genomics. 2008 Dec;92(6):474-7. doi: 10.1016/j.ygeno.2008.07.014. Epub 2008 Sep 25. Genomics. 2008. PMID: 18786632 Free article.

7

A mutation in hairless dogs implicates FOXI3 in ectodermal development.

Drögemüller C, Karlsson EK, Hytönen MK, Perloski M, Dolf G, Sainio K, Lohi H, Lindblad-Toh K, Leeb T. Drögemüller C, et al. Science. 2008 Sep 12;321(5895):1462. doi: 10.1126/science.1162525. Science. 2008. PMID: 18787161

8

Identification of the bovine Arachnomelia mutation by massively parallel sequencing implicates sulfite oxidase (SUOX) in bone development.

Drögemüller C, Tetens J, Sigurdsson S, Gentile A, Testoni S, Lindblad-Toh K, Leeb T. Drögemüller C, et al. PLoS Genet. 2010 Aug 26;6(8):e1001079. doi: 10.1371/journal.pgen.1001079. PLoS Genet. 2010. PMID: 20865119 Free PMC article.

9

A locus on chromosome 5 is associated with dilated cardiomyopathy in Doberman Pinschers.

Mausberg TB, Wess G, Simak J, Keller L, Drögemüller M, Drögemüller C, Webster MT, Stephenson H, Dukes-McEwan J, Leeb T. Mausberg TB, et al. Among authors: drogemuller c, drogemuller m. PLoS One. 2011;6(5):e20042. doi: 10.1371/journal.pone.0020042. Epub 2011 May 20. PLoS One. 2011. PMID: 21625443 Free PMC article.

10

A missense mutation in the skeletal muscle chloride channel 1 (CLCN1) as candidate causal mutation for congenital myotonia in a New Forest pony.

Wijnberg ID, Owczarek-Lipska M, Sacchetto R, Mascarello F, Pascoli F, Grünberg W, van der Kolk JH, Drögemüller C. Wijnberg ID, et al. Among authors: drogemuller c. Neuromuscul Disord. 2012 Apr;22(4):361-7. doi: 10.1016/j.nmd.2011.10.001. Epub 2011 Dec 23. Neuromuscul Disord. 2012. PMID: 22197188 Free article.

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