BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 12653325)

  • 1. Familial non-rcd1 generalised retinal degeneration in Irish setters.
    Djajadiningrat-Laanen SC; Boevé MH; Stades FC; van Oost BA
    J Small Anim Pract; 2003 Mar; 44(3):113-6. PubMed ID: 12653325
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cosegregation of codon 807 mutation of the canine rod cGMP phosphodiesterase beta gene and rcd1.
    Ray K; Baldwin VJ; Acland GM; Blanton SH; Aguirre GD
    Invest Ophthalmol Vis Sci; 1994 Dec; 35(13):4291-9. PubMed ID: 8002249
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Incidence of the gene mutation causal for rod-cone dysplasia type 1 in Irish setters in the UK.
    Petersen-Jones SM; Clements PJ; Barnett KC; Sargan DR
    J Small Anim Pract; 1995 Jul; 36(7):310-4. PubMed ID: 7474961
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Frequency of the codon 807 mutation in the cGMP phosphodiesterase beta-subunit gene in Irish setters and other dog breeds with hereditary retinal degeneration.
    Aguirre GD; Baldwin V; Weeks KM; Acland GM; Ray K
    J Hered; 1999; 90(1):143-7. PubMed ID: 9987922
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular diagnostic tests for ascertainment of genotype at the rod cone dysplasia 1 (rcd1) locus in Irish setters.
    Ray K; Baldwin VJ; Acland GM; Aguirre GD
    Curr Eye Res; 1995 Mar; 14(3):243-7. PubMed ID: 7796608
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene.
    Suber ML; Pittler SJ; Qin N; Wright GC; Holcombe V; Lee RH; Craft CM; Lolley RN; Baehr W; Hurwitz RL
    Proc Natl Acad Sci U S A; 1993 May; 90(9):3968-72. PubMed ID: 8387203
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Confirmation of the rod cGMP phosphodiesterase beta subunit (PDE beta) nonsense mutation in affected rcd-1 Irish setters in the UK and development of a diagnostic test.
    Clements PJ; Gregory CY; Peterson-Jones SM; Sargan DR; Bhattacharya SS
    Curr Eye Res; 1993 Sep; 12(9):861-6. PubMed ID: 8261797
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evaluation of cGMP-phosphodiesterase (PDE) subunits for causal association with rod-cone dysplasia 2 (rcd2), a canine model of abnormal retinal cGMP metabolism.
    Wang W; Acland GM; Ray K; Aguirre GD
    Exp Eye Res; 1999 Oct; 69(4):445-53. PubMed ID: 10504278
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An improved diagnostic test for rod cone dysplasia 1 (rcd1) using allele-specific polymerase chain reaction.
    Ray K; Tejero MD; Baldwin VJ; Aguirre GD
    Curr Eye Res; 1996 May; 15(5):583-7. PubMed ID: 8670760
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Non-allelism of three genes (rcd1, rcd2 and erd) for early-onset hereditary retinal degeneration.
    Acland GM; Fletcher RT; Gentleman S; Chader GJ; Aguirre GD
    Exp Eye Res; 1989 Dec; 49(6):983-98. PubMed ID: 2558906
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rod-cone dysplasia in Irish setters: a defect in cyclic GMP metabolism in visual cells.
    Aquirre G; Farber D; Lolley R; Fletcher RT; Chader GJ
    Science; 1978 Sep; 201(4361):1133-4. PubMed ID: 210508
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic testing for progressive retinal atrophy in Irish Setters, an update.
    Augusteyn RC
    Aust Vet J; 2002 Aug; 80(8):503. PubMed ID: 12224622
    [No Abstract]   [Full Text] [Related]  

  • 13. cGMP phosphodiesterase-alpha mutation causes progressive retinal atrophy in the Cardigan Welsh corgi dog.
    Petersen-Jones SM; Entz DD; Sargan DR
    Invest Ophthalmol Vis Sci; 1999 Jul; 40(8):1637-44. PubMed ID: 10393029
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Recent advances in understanding the spectrum of canine generalised progressive retinal atrophy.
    Clements PJ; Sargan DR; Gould DJ; Petersen-Jones SM
    J Small Anim Pract; 1996 Apr; 37(4):155-62. PubMed ID: 8731401
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An improved DNA-based test for detection of the codon 616 mutation in the alpha cyclic GMP phosphodiesterase gene that causes progressive retinal atrophy in the Cardigan Welsh Corgi.
    Petersen-Jones SM; Entz DD
    Vet Ophthalmol; 2002 Jun; 5(2):103-6. PubMed ID: 12071867
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Canine leukocyte adhesion deficiency: presence of the Cys36Ser beta-2 integrin mutation in an affected US Irish Setter cross-breed dog and in US Irish Red and White Setters.
    Foureman P; Whiteley M; Giger U
    J Vet Intern Med; 2002; 16(5):518-23. PubMed ID: 12322699
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa.
    McLaughlin ME; Sandberg MA; Berson EL; Dryja TP
    Nat Genet; 1993 Jun; 4(2):130-4. PubMed ID: 8394174
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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. PubMed ID: 22686255
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic screening for progressive retinal atrophy in the Australian population of Irish Setters.
    Maroudas P; Jobling AI; Augusteyn RC
    Aust Vet J; 2000 Nov; 78(11):773-4. PubMed ID: 11194724
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Generalized progressive retinal atrophy of Sloughi dogs is due to an 8-bp insertion in exon 21 of the PDE6B gene.
    Dekomien G; Runte M; Gödde R; Epplen JT
    Cytogenet Cell Genet; 2000; 90(3-4):261-7. PubMed ID: 11124530
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.