Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

30 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation.
Jagannathan V, Bannoehr J, Plattet P, Hauswirth R, Drögemüller C, Drögemüller M, Wiener DJ, Doherr M, Owczarek-Lipska M, Galichet A, Welle MM, Tengvall K, Bergvall K, Lohi H, Rüfenacht S, Linek M, Paradis M, Müller EJ, Roosje P, Leeb T. Jagannathan V, et al. PLoS Genet. 2013;9(10):e1003848. doi: 10.1371/journal.pgen.1003848. Epub 2013 Oct 3. PLoS Genet. 2013. PMID: 24098150 Free PMC article.
Two loci on chromosome 5 are associated with serum IgE levels in Labrador retrievers.
Owczarek-Lipska M, Lauber B, Molitor V, Meury S, Kierczak M, Tengvall K, Webster MT, Jagannathan V, Schlotter Y, Willemse T, Hendricks A, Bergvall K, Hedhammar A, Andersson G, Lindblad-Toh K, Favrot C, Roosje P, Marti E, Leeb T. Owczarek-Lipska M, et al. PLoS One. 2012;7(6):e39176. doi: 10.1371/journal.pone.0039176. Epub 2012 Jun 15. PLoS One. 2012. PMID: 22720065 Free PMC article.
A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism.
Frischknecht M, Niehof-Oellers H, Jagannathan V, Owczarek-Lipska M, Drögemüller C, Dietschi E, Dolf G, Tellhelm B, Lang J, Tiira K, Lohi H, Leeb T. Frischknecht M, et al. PLoS One. 2013;8(3):e60149. doi: 10.1371/journal.pone.0060149. Epub 2013 Mar 20. PLoS One. 2013. PMID: 23527306 Free PMC article.
Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.
Hytönen MK, Arumilli M, Lappalainen AK, Owczarek-Lipska M, Jagannathan V, Hundi S, Salmela E, Venta P, Sarkiala E, Jokinen T, Gorgas D, Kere J, Nieminen P, Drögemüller C, Lohi H. Hytönen MK, et al. PLoS Genet. 2016 May 17;12(5):e1006037. doi: 10.1371/journal.pgen.1006037. eCollection 2016 May. PLoS Genet. 2016. PMID: 27187611 Free PMC article.
[Frequency of gene defects in selected European retriever populations].
Owczarek-Lipska M, Thomas A, André C, Hölzer S, Leeb T. Owczarek-Lipska M, et al. Schweiz Arch Tierheilkd. 2011 Sep;153(9):418-20. doi: 10.1024/0036-7281/a000236. Schweiz Arch Tierheilkd. 2011. PMID: 21866517 Free article. German. No abstract available.
30 results