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 *

195 related articles for article (PubMed ID: 28575130)

  • 21. 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]  

  • 22. Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis.
    Black GC; Perveen R; Bonshek R; Cahill M; Clayton-Smith J; Lloyd IC; McLeod D
    Hum Mol Genet; 1999 Oct; 8(11):2031-5. PubMed ID: 10484772
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel frameshift c.22_25dupGCAT mutation of the NDP gene in a Chinese infant with Norrie disease: A case report.
    Wang H; Liu Z; Zhou Y; Ma Y; Tao D
    Medicine (Baltimore); 2022 Jan; 101(1):e28523. PubMed ID: 35029917
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Norrie disease: extraocular clinical manifestations in 56 patients.
    Smith SE; Mullen TE; Graham D; Sims KB; Rehm HL
    Am J Med Genet A; 2012 Aug; 158A(8):1909-17. PubMed ID: 22786811
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis of familial exudative vitreoretinopathy and Norrie disease.
    Liu J; Zhu J; Yang J; Zhang X; Zhang Q; Zhao P
    Mol Genet Genomic Med; 2019 Jan; 7(1):e00503. PubMed ID: 30474316
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Epilepsy phenotypes in siblings with Norrie disease.
    Okumura A; Arai E; Kitamura Y; Abe S; Ikeno M; Fujimaki T; Yamamoto T; Shimizu T
    Brain Dev; 2015 Nov; 37(10):978-82. PubMed ID: 25944760
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Peripheral retinopathy in offspring of carriers of Norrie disease gene mutations. Possible transplacental effect of abnormal Norrin.
    Mintz-Hittner HA; Ferrell RE; Sims KB; Fernandez KM; Gemmell BS; Satriano DR; Caster J; Kretzer FL
    Ophthalmology; 1996 Dec; 103(12):2128-34. PubMed ID: 9003348
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Norrin stimulates cell proliferation in the superficial retinal vascular plexus and is pivotal for the recruitment of mural cells.
    Zuercher J; Fritzsche M; Feil S; Mohn L; Berger W
    Hum Mol Genet; 2012 Jun; 21(12):2619-30. PubMed ID: 22394677
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Planned preterm delivery and treatment of retinal neovascularization in Norrie disease.
    Sisk RA; Hufnagel RB; Bandi S; Polzin WJ; Ahmed ZM
    Ophthalmology; 2014 Jun; 121(6):1312-3. PubMed ID: 24529712
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. [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]  

  • 32. Report on Norrie's cytology.
    Todorova MG; Bubendorf L; Prünte C; Flammer J; Meyer P
    Acta Ophthalmol; 2012 Feb; 90(1):e81-2. PubMed ID: 21159148
    [No Abstract]   [Full Text] [Related]  

  • 33. The different functions of Norrin.
    Braunger BM; Tamm ER
    Adv Exp Med Biol; 2012; 723():679-83. PubMed ID: 22183393
    [No Abstract]   [Full Text] [Related]  

  • 34. [Norrie disease caused by a c.361C>T missense variant of the NDP gene in a pedigree].
    Yang F; Xiang J; Li H; Zhang Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jan; 37(1):25-27. PubMed ID: 31922590
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Screening for NDP mutations in 44 unrelated patients with familial exudative vitreoretinopathy or Norrie disease.
    Yang H; Li S; Xiao X; Guo X; Zhang Q
    Curr Eye Res; 2012 Aug; 37(8):726-9. PubMed ID: 22563645
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal diagnosis of Norrie disease after whole exome sequencing of an affected proband during an ongoing pregnancy: a case report.
    Marakhonov AV; Mishina IA; Kadyshev VV; Repina SA; Shurygina MF; Shchagina OA; Vasserman NN; Vasilyeva TA; Kutsev SI; Zinchenko RA
    BMC Med Genet; 2020 Oct; 21(Suppl 1):156. PubMed ID: 33092543
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Norrie disease: first mutation report and prenatal diagnosis in an Indian family.
    Ghosh M; Sharma S; Shastri S; Arora S; Shukla R; Gupta N; Deka D; Kabra M
    Indian J Pediatr; 2012 Nov; 79(11):1529-31. PubMed ID: 22674248
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The role of the hypoxia response in shaping retinal vascular development in the absence of Norrin/Frizzled4 signaling.
    Rattner A; Wang Y; Zhou Y; Williams J; Nathans J
    Invest Ophthalmol Vis Sci; 2014 Nov; 55(12):8614-25. PubMed ID: 25414188
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Fetal loss in homozygous mutant Norrie disease mice: a new role of Norrin in reproduction.
    Luhmann UF; Meunier D; Shi W; Lüttges A; Pfarrer C; Fundele R; Berger W
    Genesis; 2005 Aug; 42(4):253-62. PubMed ID: 16035034
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.