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Items: 1 to 20 of 45

1.

An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome.

Marchant TW, Dietschi E, Rytz U, Schawalder P, Jagannathan V, Hadji Rasouliha S, Gurtner C, Waldvogel AS, Harrington RS, Drögemüller M, Kidd J, Ostrander EA, Warr A, Watson M, Argyle D, Ter Haar G, Clements DN, Leeb T, Schoenebeck JJ.

PLoS Genet. 2019 May 16;15(5):e1008102. doi: 10.1371/journal.pgen.1008102. eCollection 2019 May.

2.

Two MC1R loss-of-function alleles in cream-coloured Australian Cattle Dogs and white Huskies.

Dürig N, Letko A, Lepori V, Hadji Rasouliha S, Loechel R, Kehl A, Hytönen MK, Lohi H, Mauri N, Dietrich J, Wiedmer M, Drögemüller M, Jagannathan V, Schmutz SM, Leeb T.

Anim Genet. 2018 Aug;49(4):284-290. doi: 10.1111/age.12660. Epub 2018 Jun 22.

PMID:
29932470
3.

Inflammatory pattern of the infrapatellar fat pad in dogs with canine cruciate ligament disease.

Schmidli MR, Fuhrer B, Kurt N, Senn D, Drögemüller M, Rytz U, Spreng DE, Forterre S.

BMC Vet Res. 2018 May 16;14(1):161. doi: 10.1186/s12917-018-1488-y.

4.

Canine NAPEPLD-associated models of human myelin disorders.

Minor KM, Letko A, Becker D, Drögemüller M, Mandigers PJJ, Bellekom SR, Leegwater PAJ, Stassen QEM, Putschbach K, Fischer A, Flegel T, Matiasek K, Ekenstedt KJ, Furrow E, Patterson EE, Platt SR, Kelly PA, Cassidy JP, Shelton GD, Lucot K, Bannasch DL, Martineau H, Muir CF, Priestnall SL, Henke D, Oevermann A, Jagannathan V, Mickelson JR, Drögemüller C.

Sci Rep. 2018 Apr 11;8(1):5818. doi: 10.1038/s41598-018-23938-7.

5.

Genomic comparison of bovine papillomavirus 1 isolates from bovine, equine and asinine lesional tissue samples.

Koch C, Ramsauer AS, Drögemüller M, Ackermann M, Gerber V, Tobler K.

Virus Res. 2018 Jan 15;244:6-12. doi: 10.1016/j.virusres.2017.11.005. Epub 2017 Nov 4.

PMID:
29113823
6.

Canine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2.

Marchant TW, Johnson EJ, McTeir L, Johnson CI, Gow A, Liuti T, Kuehn D, Svenson K, Bermingham ML, Drögemüller M, Nussbaumer M, Davey MG, Argyle DJ, Powell RM, Guilherme S, Lang J, Ter Haar G, Leeb T, Schwarz T, Mellanby RJ, Clements DN, Schoenebeck JJ.

Curr Biol. 2017 Jun 5;27(11):1573-1584.e6. doi: 10.1016/j.cub.2017.04.057. Epub 2017 May 25.

7.

Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog.

Hirz M, Drögemüller M, Schänzer A, Jagannathan V, Dietschi E, Goebel HH, Hecht W, Laubner S, Schmidt MJ, Steffen F, Hilbe M, Köhler K, Drögemüller C, Herden C.

Mol Genet Metab. 2017 Mar;120(3):269-277. doi: 10.1016/j.ymgme.2016.12.007. Epub 2016 Dec 19.

PMID:
28024876
8.

Neuronal ceroid lipofuscinosis in an adult American Staffordshire Terrier.

Nolte A, Bello A, Drögemüller M, Leeb T, Brockhaus E, Baumgärtner W, Wohlsein P.

Tierarztl Prax Ausg K Kleintiere Heimtiere. 2016 Dec 5;44(6):431-437. Epub 2016 Oct 25. English, German.

PMID:
27778018
9.

An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat Texture.

Murgiano L, Waluk DP, Towers R, Wiedemar N, Dietrich J, Jagannathan V, Drögemüller M, Balmer P, Druet T, Galichet A, Penedo MC, Müller EJ, Roosje P, Welle MM, Leeb T.

G3 (Bethesda). 2016 Sep 8;6(9):2963-70. doi: 10.1534/g3.116.032433.

10.

A RAB3GAP1 SINE Insertion in Alaskan Huskies with Polyneuropathy, Ocular Abnormalities, and Neuronal Vacuolation (POANV) Resembling Human Warburg Micro Syndrome 1 (WARBM1).

Wiedmer M, Oevermann A, Borer-Germann SE, Gorgas D, Shelton GD, Drögemüller M, Jagannathan V, Henke D, Leeb T.

G3 (Bethesda). 2015 Nov 23;6(2):255-62. doi: 10.1534/g3.115.022707.

11.

A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy.

Steffen F, Bilzer T, Brands J, Golini L, Jagannathan V, Wiedmer M, Drögemüller M, Drögemüller C, Leeb T.

G3 (Bethesda). 2015 Oct 4;5(12):2611-7. doi: 10.1534/g3.115.021923.

12.

Impaired Cell Cycle Regulation in a Natural Equine Model of Asthma.

Pacholewska A, Jagannathan V, Drögemüller M, Klukowska-Rötzler J, Lanz S, Hamza E, Dermitzakis ET, Marti E, Leeb T, Gerber V.

PLoS One. 2015 Aug 20;10(8):e0136103. doi: 10.1371/journal.pone.0136103. eCollection 2015.

13.

A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease.

Kyöstilä K, Syrjä P, Jagannathan V, Chandrasekar G, Jokinen TS, Seppälä EH, Becker D, Drögemüller M, Dietschi E, Drögemüller C, Lang J, Steffen F, Rohdin C, Jäderlund KH, Lappalainen AK, Hahn K, Wohlsein P, Baumgärtner W, Henke D, Oevermann A, Kere J, Lohi H, Leeb T.

PLoS Genet. 2015 Apr 15;11(4):e1005169. doi: 10.1371/journal.pgen.1005169. eCollection 2015 Apr.

14.

The transcriptome of equine peripheral blood mononuclear cells.

Pacholewska A, Drögemüller M, Klukowska-Rötzler J, Lanz S, Hamza E, Dermitzakis ET, Marti E, Gerber V, Leeb T, Jagannathan V.

PLoS One. 2015 Mar 19;10(3):e0122011. doi: 10.1371/journal.pone.0122011. eCollection 2015. Erratum in: PLoS One. 2015;10(4):e0127372.

15.

A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM).

Gerber M, Fischer A, Jagannathan V, Drögemüller M, Drögemüller C, Schmidt MJ, Bernardino F, Manz E, Matiasek K, Rentmeister K, Leeb T.

PLoS One. 2015 Feb 10;10(2):e0108917. doi: 10.1371/journal.pone.0108917. eCollection 2015.

16.

A single codon insertion in the PICALM gene is not associated with subvalvular aortic stenosis in Newfoundland dogs.

Drögemüller M, Jagannathan V, Dolf G, Butenhoff K, Kottmann-Berger S, Wess G, Leeb T.

Hum Genet. 2015 Jan;134(1):127-9. doi: 10.1007/s00439-014-1506-5. Epub 2014 Nov 13. No abstract available.

PMID:
25391634
17.

Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) gene.

Drögemüller M, Jagannathan V, Welle MM, Graubner C, Straub R, Gerber V, Burger D, Signer-Hasler H, Poncet PA, Klopfenstein S, von Niederhäusern R, Tetens J, Thaller G, Rieder S, Drögemüller C, Leeb T.

PLoS One. 2014 Oct 8;9(10):e110125. doi: 10.1371/journal.pone.0110125. eCollection 2014.

18.

Hepatic fungal infection in a young beagle with unrecognised hereditary cobalamin deficiency (Imerslund-Gräsbeck syndrome).

Kook PH, Drögemüller M, Leeb T, Hinden S, Ruetten M, Howard J.

J Small Anim Pract. 2015 Feb;56(2):138-41. doi: 10.1111/jsap.12251. Epub 2014 Aug 8.

PMID:
25131805
19.

A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH).

Drögemüller M, Jagannathan V, Becker D, Drögemüller C, Schelling C, Plassais J, Kaerle C, Dufaure de Citres C, Thomas A, Müller EJ, Welle MM, Roosje P, Leeb T.

PLoS Genet. 2014 May 15;10(5):e1004370. doi: 10.1371/journal.pgen.1004370. eCollection 2014.

20.

Degenerative liver disease in young Beagles with hereditary cobalamin malabsorption because of a mutation in the cubilin gene.

Kook PH, Drögemüller M, Leeb T, Howard J, Ruetten M.

J Vet Intern Med. 2014 Mar-Apr;28(2):666-71. doi: 10.1111/jvim.12295. Epub 2014 Jan 27. No abstract available.

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