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Items: 1 to 20 of 82

1.

Glomerulopathy and mutations in NPHS1 and KIRREL2 in soft-coated Wheaten Terrier dogs.

Littman MP, Wiley CA, Raducha MG, Henthorn PS.

Mamm Genome. 2013 Apr;24(3-4):119-26. doi: 10.1007/s00335-012-9445-8. Epub 2013 Jan 17.

PMID:
23325127
2.

Familial renal disease in soft-coated wheaten terriers.

Vaden SL, Littman MP, Cianciolo RE.

J Vet Emerg Crit Care (San Antonio). 2013 Mar-Apr;23(2):174-83. doi: 10.1111/vec.12027. Epub 2013 Mar 5. Review.

PMID:
23461660
3.

Evaluation of perinuclear anti-neutrophilic cytoplasmic autoantibodies as an early marker of protein-losing enteropathy and protein-losing nephropathy in Soft Coated Wheaten Terriers.

Allenspach K, Lomas B, Wieland B, Harris T, Pressler B, Mancho C, Lees GE, Vaden SL.

Am J Vet Res. 2008 Oct;69(10):1301-4. doi: 10.2460/ajvr.69.10.1301.

PMID:
18828686
4.
5.

Familial nephropathy in soft-coated wheaten terriers.

Nash AS, Creswick JA.

Vet Rec. 1988 Dec 17;123(25):654-5. No abstract available.

PMID:
3218054
6.

Two Independent Mutations in ADAMTS17 Are Associated with Primary Open Angle Glaucoma in the Basset Hound and Basset Fauve de Bretagne Breeds of Dog.

Oliver JA, Forman OP, Pettitt L, Mellersh CS.

PLoS One. 2015 Oct 16;10(10):e0140436. doi: 10.1371/journal.pone.0140436. eCollection 2015. Erratum in: PLoS One. 2016;11(5):e0156192.

7.

Evaluation of intestinal permeability and gluten sensitivity in Soft-Coated Wheaten Terriers with familial protein-losing enteropathy, protein-losing nephropathy, or both.

Vaden SL, Sellon RK, Melgarejo LT, Williams DA, Trogdon MM, VanCamp SD, Argenzio RA.

Am J Vet Res. 2000 May;61(5):518-24.

PMID:
10803646
8.

Multiple autoimmune diseases syndrome in Italian Greyhounds: preliminary studies of genome-wide diversity and possible associations within the dog leukocyte antigen (DLA) complex.

Pedersen NC, Liu H, Greenfield DL, Echols LG.

Vet Immunol Immunopathol. 2012 Jan 15;145(1-2):264-76. doi: 10.1016/j.vetimm.2011.11.015. Epub 2011 Nov 29.

PMID:
22178273
9.

Characterization of canine photoreceptor phosducin cDNA and identification of a sequence variant in dogs with photoreceptor dysplasia.

Zhang Q, Acland GM, Parshall CJ, Haskell J, Ray K, Aguirre GD.

Gene. 1998 Jul 30;215(2):231-9.

PMID:
9714819
11.

Mutations in the RSPO1 coding region are not the main cause of canine SRY-negative XX sex reversal in several breeds.

De Lorenzi L, Groppetti D, Arrighi S, Pujar S, Nicoloso L, Molteni L, Pecile A, Cremonesi F, Parma P, Meyers-Wallen V.

Sex Dev. 2008;2(2):84-95. doi: 10.1159/000129693. Epub 2008 Jun 20.

PMID:
18577875
12.

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.

13.

X chromosome inactivation patterns in normal and X-linked hereditary nephropathy carrier dogs.

Bell RJ, Lees GE, Murphy KE.

Cytogenet Genome Res. 2008;122(1):37-40. doi: 10.1159/000151314. Epub 2008 Oct 14.

PMID:
18931484
14.

Prevalence of perinuclear antineutrophilic cytoplasmic autoantibodies in serum of healthy Soft Coated Wheaten Terriers in the United Kingdom.

Wieland B, Summers JF, Häsler B, Mancho-Alonso C, Craig A, Allenspach K.

Am J Vet Res. 2012 Mar;73(3):404-8. doi: 10.2460/ajvr.73.3.404.

PMID:
22369533
16.

Clinical features of hypoadrenocorticism in soft-coated wheaten terrier dogs: 82 cases (1979-2013).

Haviland RL, Toaff-Rosenstein RL, Reeves MP, Littman MP.

Can Vet J. 2016 Apr;57(4):387-94.

17.

Genome-wide survey indicates involvement of loci on canine chromosomes 7 and 31 in patellar luxation in Flat-Coated Retrievers.

Lavrijsen IC, Leegwater PA, Wangdee C, van Steenbeek FG, Schwencke M, Breur GJ, Meutstege FJ, Nijman IJ, Cuppen E, Heuven HC, Hazewinkel HA.

BMC Genet. 2014 May 28;15:64. doi: 10.1186/1471-2156-15-64.

18.

A novel GUSB mutation in Brazilian terriers with severe skeletal abnormalities defines the disease as mucopolysaccharidosis VII.

Hytönen MK, Arumilli M, Lappalainen AK, Kallio H, Snellman M, Sainio K, Lohi H.

PLoS One. 2012;7(7):e40281. doi: 10.1371/journal.pone.0040281. Epub 2012 Jul 5.

19.

Genetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studies.

Miyadera K, Acland GM, Aguirre GD.

Mamm Genome. 2012 Feb;23(1-2):40-61. doi: 10.1007/s00335-011-9361-3. Epub 2011 Nov 8. Review.

20.

Expression of filtrin in human glomerular diseases.

Ihalmo P, Schmid H, Rastaldi MP, Mattinzoli D, Langham RG, Luimula P, Kilpikari R, Lassila M, Gilbert RE, Kerjaschki D, Kretzler M, Holthöfer H.

Nephrol Dial Transplant. 2007 Jul;22(7):1903-9. Epub 2007 Apr 18.

PMID:
17442742

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