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Items: 1 to 20 of 152

1.

A canine DNM1 mutation is highly associated with the syndrome of exercise-induced collapse.

Patterson EE, Minor KM, Tchernatynskaia AV, Taylor SM, Shelton GD, Ekenstedt KJ, Mickelson JR.

Nat Genet. 2008 Oct;40(10):1235-9. doi: 10.1038/ng.224. Epub 2008 Sep 21.

PMID:
18806795
2.

Genotyping of exercise-induced collapse in Labrador retrievers using an allele-specific PCR.

Takanosu M, Mori H, Suzuki H, Suzuki K.

Vet J. 2012 Jul;193(1):293-5. doi: 10.1016/j.tvjl.2011.10.018. Epub 2011 Nov 21.

PMID:
22104507
3.

Presence and impact of the exercise-induced collapse associated DNM1 mutation in Labrador retrievers and other breeds.

Minor KM, Patterson EE, Keating MK, Gross SD, Ekenstedt KJ, Taylor SM, Mickelson JR.

Vet J. 2011 Aug;189(2):214-9. doi: 10.1016/j.tvjl.2011.06.022. Epub 2011 Jul 22.

PMID:
21782486
4.

Relationship between dynamin 1 mutation status and characteristics of recurrent episodes of exercise-induced collapse in Labrador Retrievers.

Furrow E, Minor KM, Taylor SM, Mickelson JR, Patterson EE.

J Am Vet Med Assoc. 2013 Mar 15;242(6):786-91. doi: 10.2460/javma.242.6.786.

PMID:
23445289
5.

Haplotype-defined linkage region for gPRA in Schapendoes dogs.

Lippmann T, Jonkisz A, Dobosz T, Petrasch-Parwez E, Epplen JT, Dekomien G.

Mol Vis. 2007 Feb 7;13:174-80.

6.

Characterization of the canine desmin (DES) gene and evaluation as a candidate gene for dilated cardiomyopathy in the Dobermann.

Stabej P, Imholz S, Versteeg SA, Zijlstra C, Stokhof AA, Domanjko-Petric A, Leegwater PA, van Oost BA.

Gene. 2004 Oct 13;340(2):241-9.

PMID:
15475165
7.

A mutation in the canine BHD gene is associated with hereditary multifocal renal cystadenocarcinoma and nodular dermatofibrosis in the German Shepherd dog.

Lingaas F, Comstock KE, Kirkness EF, Sørensen A, Aarskaug T, Hitte C, Nickerson ML, Moe L, Schmidt LS, Thomas R, Breen M, Galibert F, Zbar B, Ostrander EA.

Hum Mol Genet. 2003 Dec 1;12(23):3043-53. Epub 2003 Oct 7.

PMID:
14532326
8.

Linkage mapping of canine rod cone dysplasia type 2 (rcd2) to CFA7, the canine orthologue of human 1q32.

Kukekova AV, Nelson J, Kuchtey RW, Lowe JK, Johnson JL, Ostrander EA, Aguirre GD, Acland GM.

Invest Ophthalmol Vis Sci. 2006 Mar;47(3):1210-5.

PMID:
16505060
9.

Linkage analysis and comparative mapping of canine progressive rod-cone degeneration (prcd) establishes potential locus homology with retinitis pigmentosa (RP17) in humans.

Acland GM, Ray K, Mellersh CS, Gu W, Langston AA, Rine J, Ostrander EA, Aguirre GD.

Proc Natl Acad Sci U S A. 1998 Mar 17;95(6):3048-53.

11.

Fine mapping of canine XLPRA establishes homology of the human and canine RP3 intervals.

Zhang Q, Acland GM, Zangerl B, Johnson JL, Mao Z, Zeiss CJ, Ostrander EA, Aguirre GD.

Invest Ophthalmol Vis Sci. 2001 Oct;42(11):2466-71.

PMID:
11581184
12.

A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis.

Abitbol M, Thibaud JL, Olby NJ, Hitte C, Puech JP, Maurer M, Pilot-Storck F, Hédan B, Dréano S, Brahimi S, Delattre D, André C, Gray F, Delisle F, Caillaud C, Bernex F, Panthier JJ, Aubin-Houzelstein G, Blot S, Tiret L.

Proc Natl Acad Sci U S A. 2010 Aug 17;107(33):14775-80. doi: 10.1073/pnas.0914206107. Epub 2010 Aug 2.

13.

A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis.

Katz ML, Khan S, Awano T, Shahid SA, Siakotos AN, Johnson GS.

Biochem Biophys Res Commun. 2005 Feb 11;327(2):541-7.

PMID:
15629147
14.

Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3.

Sidjanin DJ, Lowe JK, McElwee JL, Milne BS, Phippen TM, Sargan DR, Aguirre GD, Acland GM, Ostrander EA.

Hum Mol Genet. 2002 Aug 1;11(16):1823-33.

PMID:
12140185
15.
16.

Efficient mapping of mendelian traits in dogs through genome-wide association.

Karlsson EK, Baranowska I, Wade CM, Salmon Hillbertz NH, Zody MC, Anderson N, Biagi TM, Patterson N, Pielberg GR, Kulbokas EJ 3rd, Comstock KE, Keller ET, Mesirov JP, von Euler H, Kämpe O, Hedhammar A, Lander ES, Andersson G, Andersson L, Lindblad-Toh K.

Nat Genet. 2007 Nov;39(11):1321-8. Epub 2007 Sep 30.

PMID:
17906626
17.

The EPHA2 gene is associated with cataracts linked to chromosome 1p.

Shiels A, Bennett TM, Knopf HL, Maraini G, Li A, Jiao X, Hejtmancik JF.

Mol Vis. 2008;14:2042-55. Epub 2008 Nov 12.

18.

A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.

Hmani-Aifa M, Ben Salem S, Benzina Z, Bouassida W, Messaoud R, Turki K, Khairallah M, Rebaï A, Fakhfekh F, Söderkvist P, Ayadi H.

Hum Genet. 2009 Oct;126(4):575-87. doi: 10.1007/s00439-009-0688-8. Epub 2009 Jun 14.

PMID:
19526372
19.

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.

Science. 2008 Sep 12;321(5895):1462. doi: 10.1126/science.1162525.

20.

Polymorphic microsatellite markers for genetic analysis of collagen genes in suspected collagenopathies in dogs.

Temwichitr J, Hazewinkel HA, van Hagen MA, Leegwater PA.

J Vet Med A Physiol Pathol Clin Med. 2007 Nov;54(9):522-6.

PMID:
17931229

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