Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 47

1.

Investigating inherited diseases in dogs.

Forman OP, Mellersh CS.

Vet Rec. 2014 May 17;174(20):512. doi: 10.1136/vr.g3295. No abstract available.

PMID:
24832891
[PubMed - indexed for MEDLINE]
2.

An Intronic SINE insertion in FAM161A that causes exon-skipping is associated with progressive retinal atrophy in Tibetan Spaniels and Tibetan Terriers.

Downs LM, Mellersh CS.

PLoS One. 2014 Apr 4;9(4):e93990. doi: 10.1371/journal.pone.0093990. eCollection 2014.

PMID:
24705771
[PubMed - in process]
Free PMC Article
3.

Genetic screening for PRA-associated mutations in multiple dog breeds shows that PRA is heterogeneous within and between breeds.

Downs LM, Hitti R, Pregnolato S, Mellersh CS.

Vet Ophthalmol. 2014 Mar;17(2):126-30. doi: 10.1111/vop.12122. Epub 2013 Nov 21.

PMID:
24255994
[PubMed - indexed for MEDLINE]
4.

Genome-wide association study identifies a novel canine glaucoma locus.

Ahonen SJ, Pietilä E, Mellersh CS, Tiira K, Hansen L, Johnson GS, Lohi H.

PLoS One. 2013 Aug 7;8(8):e70903. doi: 10.1371/journal.pone.0070903. eCollection 2013.

PMID:
23951034
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Missense mutation in CAPN1 is associated with spinocerebellar ataxia in the Parson Russell Terrier dog breed.

Forman OP, De Risio L, Mellersh CS.

PLoS One. 2013 May 31;8(5):e64627. doi: 10.1371/journal.pone.0064627. Print 2013.

PMID:
23741357
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

MHC class II association study in eight breeds of dog with hypoadrenocorticism.

Massey J, Boag A, Short AD, Scholey RA, Henthorn PS, Littman MP, Husebye E, Catchpole B, Pedersen N, Mellersh CS, Ollier WE, Kennedy LJ.

Immunogenetics. 2013 Apr;65(4):291-7. doi: 10.1007/s00251-013-0680-2. Epub 2013 Jan 29.

PMID:
23358933
[PubMed - indexed for MEDLINE]
7.

Multiple mechanisms contribute to leakiness of a frameshift mutation in canine cone-rod dystrophy.

Miyadera K, Brierley I, Aguirre-Hernández J, Mellersh CS, Sargan DR.

PLoS One. 2012;7(12):e51598. doi: 10.1371/journal.pone.0051598. Epub 2012 Dec 12.

PMID:
23251588
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation.

Forman OP, De Risio L, Stewart J, Mellersh CS, Beltran E.

BMC Genet. 2012 Jul 10;13:55. doi: 10.1186/1471-2156-13-55.

PMID:
22781464
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Late-onset progressive retinal atrophy in the Gordon and Irish Setter breeds is associated with a frameshift mutation in C2orf71.

Downs LM, Bell JS, Freeman J, Hartley C, Hayward LJ, Mellersh CS.

Anim Genet. 2013 Apr;44(2):169-77. doi: 10.1111/j.1365-2052.2012.02379.x. Epub 2012 Jun 12.

PMID:
22686255
[PubMed - indexed for MEDLINE]
10.

Congenital keratoconjunctivitis sicca and ichthyosiform dermatosis in Cavalier King Charles spaniel dogs. Part II: candidate gene study.

Hartley C, Barnett KC, Pettitt L, Forman OP, Blott S, Mellersh CS.

Vet Ophthalmol. 2012 Sep;15(5):327-32. doi: 10.1111/j.1463-5224.2012.00987.x. Epub 2012 Feb 16.

PMID:
22339941
[PubMed - indexed for MEDLINE]
11.

Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed.

Forman OP, Penderis J, Hartley C, Hayward LJ, Ricketts SL, Mellersh CS.

PLoS Genet. 2012 Jan;8(1):e1002462. doi: 10.1371/journal.pgen.1002462. Epub 2012 Jan 12.

PMID:
22253609
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Genome-wide association study in RPGRIP1(-/-) dogs identifies a modifier locus that determines the onset of retinal degeneration.

Miyadera K, Kato K, Boursnell M, Mellersh CS, Sargan DR.

Mamm Genome. 2012 Feb;23(1-2):212-23. doi: 10.1007/s00335-011-9384-9. Epub 2011 Dec 23.

PMID:
22193413
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Primary lens instability in ten related cats: clinical and genetic considerations.

Payen G, Hänninen RL, Mazzucchelli S, Forman OP, Mellersh CS, Savoldelli M, Chahory S.

J Small Anim Pract. 2011 Aug;52(8):402-10. doi: 10.1111/j.1748-5827.2011.01081.x.

PMID:
21797871
[PubMed - indexed for MEDLINE]
14.

A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations.

Downs LM, Wallin-Håkansson B, Boursnell M, Marklund S, Hedhammar Å, Truvé K, Hübinette L, Lindblad-Toh K, Bergström T, Mellersh CS.

PLoS One. 2011;6(6):e21452. doi: 10.1371/journal.pone.0021452. Epub 2011 Jun 27.

PMID:
21738669
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Ophthalmic and cone derived electrodiagnostic findings in outbred Miniature Long-haired Dachshunds homozygous for a RPGRIP1 mutation.

Busse C, Barnett KC, Mellersh CS, Adams VJ.

Vet Ophthalmol. 2011 May;14(3):146-52. doi: 10.1111/j.1463-5224.2010.00848.x.

PMID:
21521437
[PubMed - indexed for MEDLINE]
16.

Estimated frequency of the canine hyperuricosuria mutation in different dog breeds.

Karmi N, Brown EA, Hughes SS, McLaughlin B, Mellersh CS, Biourge V, Bannasch DL.

J Vet Intern Med. 2010 Nov-Dec;24(6):1337-42. doi: 10.1111/j.1939-1676.2010.0631.x.

PMID:
21054540
[PubMed - indexed for MEDLINE]
17.

Exonic mutations in the L2HGDH gene in Staffordshire bull terriers.

Short AD, Mellersh CS, Platt H, Carter SD, Timofte D, Lohi H, Ollier WE.

Vet Rec. 2010 Sep 18;167(12):455-7. doi: 10.1136/vr.c4476. No abstract available.

PMID:
20852250
[PubMed - indexed for MEDLINE]
18.

Phenotypic variation and genotype-phenotype discordance in canine cone-rod dystrophy with an RPGRIP1 mutation.

Miyadera K, Kato K, Aguirre-Hernández J, Tokuriki T, Morimoto K, Busse C, Barnett K, Holmes N, Ogawa H, Sasaki N, Mellersh CS, Sargan DR.

Mol Vis. 2009 Nov 11;15:2287-305.

PMID:
19936303
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Mutation in HSF4 is associated with hereditary cataract in the Australian Shepherd.

Mellersh CS, McLaughlin B, Ahonen S, Pettitt L, Lohi H, Barnett KC.

Vet Ophthalmol. 2009 Nov-Dec;12(6):372-8. doi: 10.1111/j.1463-5224.2009.00735.x.

PMID:
19883468
[PubMed - indexed for MEDLINE]
20.

Mutation in HSF4 associated with early but not late-onset hereditary cataract in the Boston Terrier.

Mellersh CS, Graves KT, McLaughlin B, Ennis RB, Pettitt L, Vaudin M, Barnett KC.

J Hered. 2007;98(5):531-3. Epub 2007 Jul 4.

PMID:
17611257
[PubMed - indexed for MEDLINE]
Free Article
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk