These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

338 related articles for article (PubMed ID: 9390563)

  • 1. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.
    Freund CL; Gregory-Evans CY; Furukawa T; Papaioannou M; Looser J; Ploder L; Bellingham J; Ng D; Herbrick JA; Duncan A; Scherer SW; Tsui LC; Loutradis-Anagnostou A; Jacobson SG; Cepko CL; Bhattacharya SS; McInnes RR
    Cell; 1997 Nov; 91(4):543-53. PubMed ID: 9390563
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene.
    Jacobson SG; Cideciyan AV; Huang Y; Hanna DB; Freund CL; Affatigato LM; Carr RE; Zack DJ; Stone EM; McInnes RR
    Invest Ophthalmol Vis Sci; 1998 Nov; 39(12):2417-26. PubMed ID: 9804150
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration.
    Swain PK; Chen S; Wang QL; Affatigato LM; Coats CL; Brady KD; Fishman GA; Jacobson SG; Swaroop A; Stone E; Sieving PA; Zack DJ
    Neuron; 1997 Dec; 19(6):1329-36. PubMed ID: 9427255
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.
    Lines MA; Hébert M; McTaggart KE; Flynn SJ; Tennant MT; MacDonald IM
    Ophthalmology; 2002 Oct; 109(10):1862-70. PubMed ID: 12359607
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.
    Sohocki MM; Sullivan LS; Mintz-Hittner HA; Birch D; Heckenlively JR; Freund CL; McInnes RR; Daiger SP
    Am J Hum Genet; 1998 Nov; 63(5):1307-15. PubMed ID: 9792858
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation.
    Furukawa T; Morrow EM; Cepko CL
    Cell; 1997 Nov; 91(4):531-41. PubMed ID: 9390562
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Crx-L253X Mutation Produces Dominant Photoreceptor Defects in TVRM65 Mice.
    Ruzycki PA; Linne CD; Hennig AK; Chen S
    Invest Ophthalmol Vis Sci; 2017 Sep; 58(11):4644-4653. PubMed ID: 28903150
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Functional analysis of cone-rod homeobox (CRX) mutations associated with retinal dystrophy.
    Chen S; Wang QL; Xu S; Liu I; Li LY; Wang Y; Zack DJ
    Hum Mol Genet; 2002 Apr; 11(8):873-84. PubMed ID: 11971869
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nuclear trafficking of photoreceptor protein crx: the targeting sequence and pathologic implications.
    Fei Y; Hughes TE
    Invest Ophthalmol Vis Sci; 2000 Sep; 41(10):2849-56. PubMed ID: 10967037
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function.
    Swaroop A; Wang QL; Wu W; Cook J; Coats C; Xu S; Chen S; Zack DJ; Sieving PA
    Hum Mol Genet; 1999 Feb; 8(2):299-305. PubMed ID: 9931337
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes.
    Chen S; Wang QL; Nie Z; Sun H; Lennon G; Copeland NG; Gilbert DJ; Jenkins NA; Zack DJ
    Neuron; 1997 Nov; 19(5):1017-30. PubMed ID: 9390516
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cone and cone-rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation.
    Kitiratschky VB; Nagy D; Zabel T; Zrenner E; Wissinger B; Kohl S; Jägle H
    Br J Ophthalmol; 2008 Aug; 92(8):1086-91. PubMed ID: 18653602
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene.
    Tzekov RT; Liu Y; Sohocki MM; Zack DJ; Daiger SP; Heckenlively JR; Birch DG
    Invest Ophthalmol Vis Sci; 2001 May; 42(6):1319-27. PubMed ID: 11328746
    [TBL] [Abstract][Full Text] [Related]  

  • 15. From CRX to CRD.
    Abitbol M; DuFier JL
    Nat Med; 1998 Jan; 4(1):18-9. PubMed ID: 9427598
    [No Abstract]   [Full Text] [Related]  

  • 16. Ocular findings in a Japanese family with an Arg41Trp mutation of the CRX gene.
    Itabashi T; Wada Y; Sato H; Kunikata H; Kawamura M; Tamai M
    Graefes Arch Clin Exp Ophthalmol; 2003 Jul; 241(7):535-540. PubMed ID: 12819982
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mechanistically distinct mouse models for CRX-associated retinopathy.
    Tran NM; Zhang A; Zhang X; Huecker JB; Hennig AK; Chen S
    PLoS Genet; 2014 Feb; 10(2):e1004111. PubMed ID: 24516401
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Incomplete penetrance of
    Chapi M; Sabbaghi H; Suri F; Alehabib E; Rahimi-Aliabadi S; Jamali F; Jamshidi J; Emamalizadeh B; Darvish H; Mirrahimi M; Ahmadieh H; Daftarian N
    Ophthalmic Genet; 2019 Jun; 40(3):259-266. PubMed ID: 31215831
    [No Abstract]   [Full Text] [Related]  

  • 19. Novel 615delC mutation in the CRX gene in a Japanese family with cone-rod dystrophy.
    Itabashi T; Wada Y; Sato H; Kawamura M; Shiono T; Tamai M
    Am J Ophthalmol; 2004 Nov; 138(5):876-7. PubMed ID: 15531334
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CrxRdy Cat: A Large Animal Model for CRX-Associated Leber Congenital Amaurosis.
    Occelli LM; Tran NM; Narfström K; Chen S; Petersen-Jones SM
    Invest Ophthalmol Vis Sci; 2016 Jul; 57(8):3780-92. PubMed ID: 27427859
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.