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 *

199 related articles for article (PubMed ID: 9020843)

  • 1. Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness.
    Yamamoto S; Sippel KC; Berson EL; Dryja TP
    Nat Genet; 1997 Feb; 15(2):175-8. PubMed ID: 9020843
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese.
    Fuchs S; Nakazawa M; Maw M; Tamai M; Oguchi Y; Gal A
    Nat Genet; 1995 Jul; 10(3):360-2. PubMed ID: 7670478
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses.
    Hayashi T; Gekka T; Takeuchi T; Goto-Omoto S; Kitahara K
    Ophthalmology; 2007 Jan; 114(1):134-41. PubMed ID: 17070587
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindness.
    Sippel KC; DeStefano JD; Berson EL; Dryja TP
    Invest Ophthalmol Vis Sci; 1998 Mar; 39(3):665-70. PubMed ID: 9501883
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Molecular genetic study of congenital stationary night blindness].
    Nakamura M; Miyake Y
    Nippon Ganka Gakkai Zasshi; 2004 Nov; 108(11):665-73. PubMed ID: 15584351
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Control of rhodopsin activity in vision.
    Baylor DA; Burns ME
    Eye (Lond); 1998; 12 ( Pt 3b)():521-5. PubMed ID: 9775212
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Biochemical evidence for pathogenicity of rhodopsin kinase mutations correlated with the oguchi form of congenital stationary night blindness.
    Khani SC; Nielsen L; Vogt TM
    Proc Natl Acad Sci U S A; 1998 Mar; 95(6):2824-7. PubMed ID: 9501174
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Increased susceptibility to light damage in an arrestin knockout mouse model of Oguchi disease (stationary night blindness).
    Chen J; Simon MI; Matthes MT; Yasumura D; LaVail MM
    Invest Ophthalmol Vis Sci; 1999 Nov; 40(12):2978-82. PubMed ID: 10549660
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture.
    Dryja TP
    Am J Ophthalmol; 2000 Nov; 130(5):547-63. PubMed ID: 11078833
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Wide-field true-colour imaging and clinical characterization of a novel GRK1 mutation in Oguchi disease.
    Ballios BG; Weisbrod D; Kohly R; Muni RH; Wright T; Yan P
    Doc Ophthalmol; 2020 Oct; 141(2):181-185. PubMed ID: 32146548
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.
    Zhang Q; Zulfiqar F; Riazuddin SA; Xiao X; Yasmeen A; Rogan PK; Caruso R; Sieving PA; Riazuddin S; Hejtmancik JF
    Mol Vis; 2005 Nov; 11():977-85. PubMed ID: 16319817
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel mutations in the arrestin gene and associated clinical features in Japanese patients with Oguchi's disease.
    Nakamura M; Yamamoto S; Okada M; Ito S; Tano Y; Miyake Y
    Ophthalmology; 2004 Jul; 111(7):1410-4. PubMed ID: 15234147
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The first case of Oguchi disease, type 2 in a Polish patient with confirmed GRK1 gene mutation.
    Skorczyk-Werner A; Kocięcki J; Wawrocka A; Wicher K; Krawczyńiski MR
    Klin Oczna; 2015; 117(1):27-30. PubMed ID: 26349155
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gene analysis and evaluation of the single founder effect in Japanese patients with Oguchi disease.
    Saga M; Mashima Y; Kudoh J; Oguchi Y; Shimizu N
    Jpn J Ophthalmol; 2004; 48(4):350-2. PubMed ID: 15295660
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 11-cis retinol dehydrogenase mutations as a major cause of the congenital night-blindness disorder known as fundus albipunctatus.
    Gonzalez-Fernandez F; Kurz D; Bao Y; Newman S; Conway BP; Young JE; Han DP; Khani SC
    Mol Vis; 1999 Dec; 5():41. PubMed ID: 10617778
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the SAG Gene.
    Hayashi T; Tsuzuranuki S; Kozaki K; Urashima M; Tsuneoka H
    Ophthalmic Res; 2011 Oct; 46(4):175-80. PubMed ID: 21447990
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Chinese family with Oguchi's disease due to compound heterozygosity including a novel deletion in the arrestin gene.
    Huang L; Li W; Tang W; Zhu X; Ou-Yang P; Lu G
    Mol Vis; 2012; 18():528-36. PubMed ID: 22419846
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man.
    Cideciyan AV; Zhao X; Nielsen L; Khani SC; Jacobson SG; Palczewski K
    Proc Natl Acad Sci U S A; 1998 Jan; 95(1):328-33. PubMed ID: 9419375
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
    Bech-Hansen NT; Naylor MJ; Maybaum TA; Sparkes RL; Koop B; Birch DG; Bergen AA; Prinsen CF; Polomeno RC; Gal A; Drack AV; Musarella MA; Jacobson SG; Young RS; Weleber RG
    Nat Genet; 2000 Nov; 26(3):319-23. PubMed ID: 11062471
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic analysis and clinical features of three Chinese patients with Oguchi disease.
    Wei X; Li H; Wu S; Zhu T; Sui R
    Doc Ophthalmol; 2023 Feb; 146(1):17-32. PubMed ID: 36417138
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.