461 related articles for article (PubMed ID: 11133845)
1. Genomic organization and mutation analysis of the gene encoding lecithin retinol acyltransferase in human retinal pigment epithelium.
Ruiz A; Kuehn MH; Andorf JL; Stone E; Hageman GS; Bok D
Invest Ophthalmol Vis Sci; 2001 Jan; 42(1):31-7. PubMed ID: 11133845
[TBL] [Abstract][Full Text] [Related]
2. Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy.
Thompson DA; Li Y; McHenry CL; Carlson TJ; Ding X; Sieving PA; Apfelstedt-Sylla E; Gal A
Nat Genet; 2001 Jun; 28(2):123-4. PubMed ID: 11381255
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Cloning and characterization of the canine photoreceptor specific cone-rod homeobox (CRX) gene and evaluation as a candidate for early onset photoreceptor diseases in the dog.
Akhmedov NB; Baldwin VJ; Zangerl B; Kijas JW; Hunter L; Minoofar KD; Mellersh C; Ostrander EA; Acland GM; Farber DB; Aguirre GD
Mol Vis; 2002 Mar; 8():79-84. PubMed ID: 11951083
[TBL] [Abstract][Full Text] [Related]
5. The canine Recoverin (RCV1) gene: a candidate gene for generalized progressive retinal atrophy.
Dekomien G; Epplen JT
Mol Vis; 2002 Nov; 8():436-41. PubMed ID: 12447165
[TBL] [Abstract][Full Text] [Related]
6. Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases.
Sharon D; Yamamoto H; McGee TL; Rabe V; Szerencsei RT; Winkfein RJ; Prinsen CF; Barnes CS; Andreasson S; Fishman GA; Schnetkamp PP; Berson EL; Dryja TP
Invest Ophthalmol Vis Sci; 2002 Jun; 43(6):1971-9. PubMed ID: 12037007
[TBL] [Abstract][Full Text] [Related]
7. Genomic structure and assessment of the retinally expressed RFamide-related peptide gene in dominant cystoid macular dystrophy.
Schulz HL; Stoehr H; White K; van Driel MA; Hoyng CB; Cremers F; Weber BH
Mol Vis; 2002 Mar; 8():67-71. PubMed ID: 11951088
[TBL] [Abstract][Full Text] [Related]
8. Organization of the human IMPG2 gene and its evaluation as a candidate gene in age-related macular degeneration and other retinal degenerative disorders.
Kuehn MH; Stone EM; Hageman GS
Invest Ophthalmol Vis Sci; 2001 Dec; 42(13):3123-9. PubMed ID: 11726612
[TBL] [Abstract][Full Text] [Related]
9. A novel gene for autosomal dominant Stargardt-like macular dystrophy with homology to the SUR4 protein family.
Edwards AO; Donoso LA; Ritter R
Invest Ophthalmol Vis Sci; 2001 Oct; 42(11):2652-63. PubMed ID: 11581213
[TBL] [Abstract][Full Text] [Related]
10. Mammalian orthologs of C. elegans unc-119 highly expressed in photoreceptors.
Swanson DA; Chang JT; Campochiaro PA; Zack DJ; Valle D
Invest Ophthalmol Vis Sci; 1998 Oct; 39(11):2085-94. PubMed ID: 9761287
[TBL] [Abstract][Full Text] [Related]
11. Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene.
Acar C; Mears AJ; Yashar BM; Maheshwary AS; Andreasson S; Baldi A; Sieving PA; Iannaccone A; Musarella MA; Jacobson SG; Swaroop A
Mol Vis; 2003 Jan; 9():14-7. PubMed ID: 12552256
[TBL] [Abstract][Full Text] [Related]
12. Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis.
Rivolta C; Ayyagari R; Sieving PA; Berson EL; Dryja TP
Mol Vis; 2003 Feb; 9():49-51. PubMed ID: 12592226
[TBL] [Abstract][Full Text] [Related]
13. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
14. Cloning of a portion of the chromosomal gene and cDNA for human beta-fodrin, the nonerythroid form of beta-spectrin.
Chang JG; Scarpa A; Eddy RL; Byers MG; Harris AS; Morrow JS; Watkins P; Shows TB; Forget BG
Genomics; 1993 Aug; 17(2):287-93. PubMed ID: 8406479
[TBL] [Abstract][Full Text] [Related]
15. Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genes.
Tubb BE; Bardien-Kruger S; Kashork CD; Shaffer LG; Ramagli LS; Xu J; Siciliano MJ; Bryan J
Genomics; 2000 Apr; 65(2):146-56. PubMed ID: 10783262
[TBL] [Abstract][Full Text] [Related]
16. Evaluation of the gene encoding the gamma subunit of rod phosphodiesterase in retinitis pigmentosa.
Hahn LB; Berson EL; Dryja TP
Invest Ophthalmol Vis Sci; 1994 Mar; 35(3):1077-82. PubMed ID: 8125719
[TBL] [Abstract][Full Text] [Related]
17. Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerations.
Gao YQ; Danciger M; Longmuir R; Piriev NI; Zhao DY; Heckenlively JR; Fishman GA; Weleber RG; Jacobson SG; Stone EM; Farber DB
Invest Ophthalmol Vis Sci; 1999 Jul; 40(8):1818-22. PubMed ID: 10393054
[TBL] [Abstract][Full Text] [Related]
18. Evaluation of the canine RPE65 gene in affected dogs with generalized progressive retinal atrophy.
Dekomien G; Epplen JT
Mol Vis; 2003 Nov; 9():601-5. PubMed ID: 14627956
[TBL] [Abstract][Full Text] [Related]
19. Isolation and mapping of human T-cell protein tyrosine phosphatase sequences: localization of genes and pseudogenes discriminated using fluorescence hybridization with genomic versus cDNA probes.
Johnson CV; Cool DE; Glaccum MB; Green N; Fischer EH; Bruskin A; Hill DE; Lawrence JB
Genomics; 1993 Jun; 16(3):619-29. PubMed ID: 8325634
[TBL] [Abstract][Full Text] [Related]
20. Screening genes of the retinoid metabolism: novel LRAT mutation in leber congenital amaurosis.
Sénéchal A; Humbert G; Surget MO; Bazalgette C; Bazalgette C; Arnaud B; Arndt C; Laurent E; Brabet P; Hamel CP
Am J Ophthalmol; 2006 Oct; 142(4):702-4. PubMed ID: 17011878
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
