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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.

PLoS Genet. 2013;9(10):e1003848. doi: 10.1371/journal.pgen.1003848. Epub 2013 Oct 3.


Maine Coon renal screening: ultrasonographical characterisation and preliminary genetic analysis for common genes in cats with renal cysts.

Gendron K, Owczarek-Lipska M, Lang J, Leeb T.

J Feline Med Surg. 2013 Dec;15(12):1079-85. doi: 10.1177/1098612X13492164. Epub 2013 Jun 4.


A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption).

Owczarek-Lipska M, Jagannathan V, Drögemüller C, Lutz S, Glanemann B, Leeb T, Kook PH.

PLoS One. 2013 Apr 16;8(4):e61144. doi: 10.1371/journal.pone.0061144. Print 2013.


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.

PLoS One. 2013;8(3):e60149. doi: 10.1371/journal.pone.0060149. Epub 2013 Mar 20.


A 16-bp deletion in the canine PDK4 gene is not associated with dilated cardiomyopathy in a European cohort of Doberman Pinschers.

Owczarek-Lipska M, Mausberg TB, Stephenson H, Dukes-McEwan J, Wess G, Leeb T.

Anim Genet. 2013 Apr;44(2):239. doi: 10.1111/j.1365-2052.2012.02396.x. Epub 2012 Jul 27. No abstract available.


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.

PLoS One. 2012;7(6):e39176. doi: 10.1371/journal.pone.0039176. Epub 2012 Jun 15.


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.

Neuromuscul Disord. 2012 Apr;22(4):361-7. doi: 10.1016/j.nmd.2011.10.001. Epub 2011 Dec 23.


[Frequency of gene defects in selected European retriever populations].

Owczarek-Lipska M, Thomas A, André C, Hölzer S, Leeb T.

Schweiz Arch Tierheilkd. 2011 Sep;153(9):418-20. doi: 10.1024/0036-7281/a000236. German. No abstract available.


Relationship of porcine IGF2 imprinting status to DNA methylation at the H19 DMD and the IGF2 DMRs 1 and 2.

Braunschweig MH, Owczarek-Lipska M, Stahlberger-Saitbekova N.

BMC Genet. 2011 May 17;12:47. doi: 10.1186/1471-2156-12-47.


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.

Genomics. 2011 Jan;97(1):51-7. doi: 10.1016/j.ygeno.2010.09.005. Epub 2010 Oct 12.


The bovine dilated cardiomyopathy locus maps to a 1.0-Mb interval on chromosome 18.

Owczarek-Lipska M, Denis C, Eggen A, Leeb T, Posthaus H, Dolf G, Braunschweig MH.

Mamm Genome. 2009 Mar;20(3):187-92. doi: 10.1007/s00335-009-9171-z. Epub 2009 Feb 14.


The locus for bovine dilated cardiomyopathy maps to chromosome 18.

Guziewicz KE, Owczarek-Lipska M, Küffer J, Schelling C, Tontis A, Denis C, Eggen A, Leeb T, Dolf G, Braunschweig MH.

Anim Genet. 2007 Jun;38(3):265-9. Epub 2007 Apr 13.

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