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 *

182 related articles for article (PubMed ID: 8835523)

  • 1. Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp).
    Battinelli EM; Boyd Y; Craig IW; Breakefield XO; Chen ZY
    Mamm Genome; 1996 Feb; 7(2):93-7. PubMed ID: 8835523
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3.
    Sims KB; Lebo RV; Benson G; Shalish C; Schuback D; Chen ZY; Bruns G; Craig IW; Golbus MS; Breakefield XO
    Hum Mol Genet; 1992 May; 1(2):83-9. PubMed ID: 1301161
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene.
    Wu WC; Drenser K; Trese M; Capone A; Dailey W
    Arch Ophthalmol; 2007 Feb; 125(2):225-30. PubMed ID: 17296899
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity.
    Dickinson JL; Sale MM; Passmore A; FitzGerald LM; Wheatley CM; Burdon KP; Craig JE; Tengtrisorn S; Carden SM; Maclean H; Mackey DA
    Clin Exp Ophthalmol; 2006; 34(7):682-8. PubMed ID: 16970763
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Global gene expression analysis in a mouse model for Norrie disease: late involvement of photoreceptor cells.
    Lenzner S; Prietz S; Feil S; Nuber UA; Ropers HH; Berger W
    Invest Ophthalmol Vis Sci; 2002 Sep; 43(9):2825-33. PubMed ID: 12202498
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genotype-phenotype variations in five Spanish families with Norrie disease or X-linked FEVR.
    Riveiro-Alvarez R; Trujillo-Tiebas MJ; Gimenez-Pardo A; Garcia-Hoyos M; Cantalapiedra D; Lorda-Sanchez I; Rodriguez de Alba M; Ramos C; Ayuso C
    Mol Vis; 2005 Sep; 11():705-12. PubMed ID: 16163268
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy.
    Kondo H; Qin M; Kusaka S; Tahira T; Hasebe H; Hayashi H; Uchio E; Hayashi K
    Invest Ophthalmol Vis Sci; 2007 Mar; 48(3):1276-82. PubMed ID: 17325173
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Norrie disease gene: characterization of deletions and possible function.
    Chen ZY; Battinelli EM; Hendriks RW; Powell JF; Middleton-Price H; Sims KB; Breakefield XO; Craig IW
    Genomics; 1993 May; 16(2):533-5. PubMed ID: 8314592
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial cases of Norrie disease detected by copy number analysis.
    Arai E; Fujimaki T; Yanagawa A; Fujiki K; Yokoyama T; Okumura A; Shimizu T; Murakami A
    Jpn J Ophthalmol; 2014 Sep; 58(5):448-54. PubMed ID: 25023092
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sequence analysis and transcript identification within 1.5 MB of DNA deleted together with the NDP and MAO genes in atypical Norrie disease patients presenting with a profound phenotype.
    Suárez-Merino B; Bye J; McDowall J; Ross M; Craig IW
    Hum Mutat; 2001 Jun; 17(6):523. PubMed ID: 11385715
    [TBL] [Abstract][Full Text] [Related]  

  • 11. NDP gene mutations in 14 French families with Norrie disease.
    Royer G; Hanein S; Raclin V; Gigarel N; Rozet JM; Munnich A; Steffann J; Dufier JL; Kaplan J; Bonnefont JP
    Hum Mutat; 2003 Dec; 22(6):499. PubMed ID: 14635119
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Analysis of the NDP gene in a Chinese family with X-linked recessive Norrie disease].
    Mei L; Huang Y; Pan Q; Liang D; Wu L
    Zhonghua Yan Ke Za Zhi; 2015 May; 51(5):360-3. PubMed ID: 26311697
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and genetic analysis of Indian patients with NDP-related retinopathies.
    Sudha D; Ganapathy A; Mohan P; Mannan AU; Krishna S; Neriyanuri S; Swaminathan M; Rishi P; Chidambaram S; Arunachalam JP
    Int Ophthalmol; 2018 Jun; 38(3):1251-1260. PubMed ID: 28602015
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel nonsense mutation in the NDP gene in a Chinese family with Norrie disease.
    Liu D; Hu Z; Peng Y; Yu C; Liu Y; Mo X; Li X; Lu L; Xu X; Su W; Pan Q; Xia K
    Mol Vis; 2010 Dec; 16():2653-8. PubMed ID: 21179243
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sequence and chromosomal localization of the mouse brevican gene.
    Rauch U; Meyer H; Brakebusch C; Seidenbecher C; Gundelfinger ED; Beier DR; Fässler R
    Genomics; 1997 Aug; 44(1):15-21. PubMed ID: 9286696
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasms.
    Lev D; Weigl Y; Hasan M; Gak E; Davidovich M; Vinkler C; Leshinsky-Silver E; Lerman-Sagie T; Watemberg N
    Am J Med Genet A; 2007 May; 143A(9):921-4. PubMed ID: 17334993
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Comparative genomics on Norrie disease gene.
    Katoh M; Katoh M
    Int J Mol Med; 2005 May; 15(5):885-9. PubMed ID: 15806314
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease.
    Andarva M; Jamshidi J; Ghaedi H; Daftarian N; Emamalizadeh B; Alehabib E; Taghavi S; Pouriran R; Darvish H
    Clin Exp Optom; 2018 Mar; 101(2):255-259. PubMed ID: 28922694
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
    Zhang DL; Ji L; Li YD
    Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic organization, 5'-flanking region, and chromosomal localization of the human RGS3 gene.
    Chatterjee TK; Eapen A; Kanis AB; Fisher RA
    Genomics; 1997 Oct; 45(2):429-33. PubMed ID: 9344672
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.