BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 3929383)

  • 1. Abnormal visual pathways in normally pigmented cats that are heterozygous for albinism.
    Leventhal AG; Vitek DJ; Creel DJ
    Science; 1985 Sep; 229(4720):1395-7. PubMed ID: 3929383
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Albinism, or the NOACH syndrome (the book of Enoch c.v. 1-20).
    van Dorp DB
    Clin Genet; 1987 Apr; 31(4):228-42. PubMed ID: 3109790
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic mechanisms determining the central visual pathways of mice.
    Guillery RW; Scott GL; Cattanach BM; Deol MS
    Science; 1973 Mar; 179(4077):1014-6. PubMed ID: 4687586
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Somatic mosaicism and allele complexity induced by CRISPR/Cas9 RNA injections in mouse zygotes.
    Yen ST; Zhang M; Deng JM; Usman SJ; Smith CN; Parker-Thornburg J; Swinton PG; Martin JF; Behringer RR
    Dev Biol; 2014 Sep; 393(1):3-9. PubMed ID: 24984260
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sensitivity deficits consistent with aberrant crossed visual pathways in human albinos.
    St John R; Timney B
    Invest Ophthalmol Vis Sci; 1981 Dec; 21(6):873-7. PubMed ID: 7309439
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Albinism. Recent advances.
    Jay B; Carroll W
    Trans Ophthalmol Soc U K (1962); 1980; 100(4):467-71. PubMed ID: 6797109
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Abnormal pigmentation and unusual morphogenesis of the optic stalk may be correlated with retinal axon misguidance in embryonic Siamese cats.
    Webster MJ; Shatz CJ; Kliot M; Silver J
    J Comp Neurol; 1988 Mar; 269(4):592-611. PubMed ID: 3372729
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Abnormal ipsilateral visual field representation in areas 17 and 18 of hypopigmented cats.
    Ault SJ; Leventhal AG; Vitek DJ; Creel DJ
    J Comp Neurol; 1995 Apr; 354(2):181-92. PubMed ID: 7782497
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Abnormalities of the central visual pathways in Prader-Willi syndrome associated with hypopigmentation.
    Creel DJ; Bendel CM; Wiesner GL; Wirtschafter JD; Arthur DC; King RA
    N Engl J Med; 1986 Jun; 314(25):1606-9. PubMed ID: 3713758
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Extrinsic modulation of retinal ganglion cell projections: analysis of the albino mutation in pigmentation mosaic mice.
    Rice DS; Goldowitz D; Williams RW; Hamre K; Johnson PT; Tan SS; Reese BE
    Dev Biol; 1999 Dec; 216(1):41-56. PubMed ID: 10588862
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Visual evoked potentials in Negro carriers of the gene for tyrosinase positive oculocutaneous albinism.
    Castle D; Kromberg J; Kowalsky R; Moosa R; Gillman N; Zwane E; Fritz V
    J Med Genet; 1988 Dec; 25(12):835-7. PubMed ID: 3148727
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Albinism and visual pathways.
    Dräger UC
    N Engl J Med; 1986 Jun; 314(25):1636-8. PubMed ID: 3713761
    [No Abstract]   [Full Text] [Related]  

  • 13. The recognition and management of albinism.
    Abadi R; Pascal E
    Ophthalmic Physiol Opt; 1989 Jan; 9(1):3-15. PubMed ID: 2512527
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Electrophysiologic evidence for normal optic nerve fiber projections in normally pigmented squinters.
    McCormack GL
    Invest Ophthalmol; 1975 Dec; 14(12):931-5. PubMed ID: 1104518
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Differentiation of heterozygotes in recessive albinism.
    Roberts DF; Kromberg JG; Jenkins T
    J Med Genet; 1986 Aug; 23(4):323-7. PubMed ID: 3091836
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Albinism in the domestic cat (Felis catus) is associated with a tyrosinase (TYR) mutation.
    Imes DL; Geary LA; Grahn RA; Lyons LA
    Anim Genet; 2006 Apr; 37(2):175-8. PubMed ID: 16573534
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Anatomical differences in optic nerve, chiasma and tractus opticus in human albinism as demonstrated by standardised clinical and MRI evaluation].
    Käsmann-Kellner B; Schäfer T; Krick CM; Ruprecht KW; Reith W; Schmitz BL
    Klin Monbl Augenheilkd; 2003 May; 220(5):334-44. PubMed ID: 12766823
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Correction of abnormal retinal pathways found with albinism by introduction of a functional tyrosinase gene in transgenic mice.
    Jeffery G; Schütz G; Montoliu L
    Dev Biol; 1994 Dec; 166(2):460-4. PubMed ID: 7813769
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Electroretinographic findings in human oculocutaneous albinism.
    Wack MA; Peachey NS; Fishman GA
    Ophthalmology; 1989 Dec; 96(12):1778-85. PubMed ID: 2516301
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autosomal recessive ocular albinism associated with a functionally significant tyrosinase gene polymorphism.
    Fukai K; Holmes SA; Lucchese NJ; Siu VM; Weleber RG; Schnur RE; Spritz RA
    Nat Genet; 1995 Jan; 9(1):92-5. PubMed ID: 7704033
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.