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 *

230 related articles for article (PubMed ID: 25489231)

  • 1. Screening for BEST1 gene mutations in Chinese patients with bestrophinopathy.
    Tian R; Yang G; Wang J; Chen Y
    Mol Vis; 2014; 20():1594-604. PubMed ID: 25489231
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation.
    Kubota D; Gocho K; Akeo K; Kikuchi S; Sugahara M; Matsumoto CS; Shinoda K; Mizota A; Yamaki K; Takahashi H; Kameya S
    Doc Ophthalmol; 2016 Jun; 132(3):233-43. PubMed ID: 27071392
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening of BEST1 Gene in a Chinese Cohort With Best Vitelliform Macular Dystrophy or Autosomal Recessive Bestrophinopathy.
    Tian L; Sun T; Xu K; Zhang X; Peng X; Li Y
    Invest Ophthalmol Vis Sci; 2017 Jul; 58(9):3366-3375. PubMed ID: 28687848
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biallelic Mutations in the BEST1 Gene: Additional Families with Autosomal Recessive Bestrophinopathy.
    Wivestad Jansson R; Berland S; Bredrup C; Austeng D; Andréasson S; Wittström E
    Ophthalmic Genet; 2016 Jun; 37(2):183-93. PubMed ID: 26333019
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.
    Sodi A; Menchini F; Manitto MP; Passerini I; Murro V; Torricelli F; Menchini U
    Mol Vis; 2011; 17():3078-87. PubMed ID: 22162627
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of Clinical and Genetic Heterogeneity With BEST1 Sequence Variations.
    Shah M; Broadgate S; Shanks M; Clouston P; Yu J; MacLaren RE; Németh AH; Halford S; Downes SM
    JAMA Ophthalmol; 2020 May; 138(5):544-551. PubMed ID: 32239196
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.
    Boon CJ; van den Born LI; Visser L; Keunen JE; Bergen AA; Booij JC; Riemslag FC; Florijn RJ; van Schooneveld MJ
    Ophthalmology; 2013 Apr; 120(4):809-20. PubMed ID: 23290749
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ocular phenotype analysis of a family with biallelic mutations in the BEST1 gene.
    Sharon D; Al-Hamdani S; Engelsberg K; Mizrahi-Meissonnier L; Obolensky A; Banin E; Sander B; Jensen H; Larsen M; Schatz P
    Am J Ophthalmol; 2014 Mar; 157(3):697-709.e1-2. PubMed ID: 24345323
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and Mutation Analysis of Patients with Best Vitelliform Macular Dystrophy or Autosomal Recessive Bestrophinopathy in Chinese Population.
    Gao T; Tian C; Hu Q; Liu Z; Zou J; Huang L; Zhao M
    Biomed Res Int; 2018; 2018():4582816. PubMed ID: 30498755
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Next generation sequencing identifies novel disease-associated BEST1 mutations in Bestrophinopathy patients.
    Nguyen TT; Poornachandra B; Verma A; Mehta RA; Phalke S; Battu R; Ramprasad VL; Peterson AS; Ghosh A; Seshagiri S
    Sci Rep; 2018 Jul; 8(1):10176. PubMed ID: 29976937
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel Missense Mutations in
    Jaffal L; Joumaa WH; Assi A; Helou C; Condroyer C; El Dor M; Cherfan G; Zeitz C; Audo I; Zibara K; El Shamieh S
    Genes (Basel); 2019 Feb; 10(2):. PubMed ID: 30781664
    [TBL] [Abstract][Full Text] [Related]  

  • 12. BESTROPHINOPATHY: A Spectrum of Ocular Abnormalities Caused by the c.614T>C Mutation in the BEST1 Gene.
    Toto L; Boon CJ; Di Antonio L; Battaglia Parodi M; Mastropasqua R; Antonucci I; Stuppia L; Mastropasqua L
    Retina; 2016 Aug; 36(8):1586-95. PubMed ID: 26716959
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel BEST1 gene mutations associated with two different forms of macular dystrophy in Tunisian families.
    Chibani Z; Abid IZ; Molbaek A; Söderkvist P; Feki J; Hmani-Aifa M
    Clin Exp Ophthalmol; 2019 Nov; 47(8):1063-1073. PubMed ID: 31254423
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical evaluation of two consanguineous families with homozygous mutations in BEST1.
    Piñeiro-Gallego T; Álvarez M; Pereiro I; Campos S; Sharon D; Schatz P; Valverde D
    Mol Vis; 2011; 17():1607-17. PubMed ID: 21738390
    [TBL] [Abstract][Full Text] [Related]  

  • 15. New best1 mutations in autosomal recessive bestrophinopathy.
    Fung AT; Yzer S; Goldberg N; Wang H; Nissen M; Giovannini A; Merriam JE; Bukanova EN; Cai C; Yannuzzi LA; Tsang SH; Allikmets R
    Retina; 2015 Apr; 35(4):773-82. PubMed ID: 25545482
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Typical best vitelliform dystrophy secondary to biallelic variants in BEST1.
    Dhoble P; Robson AG; Webster AR; Michaelides M
    Ophthalmic Genet; 2024 Feb; 45(1):38-43. PubMed ID: 36908234
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Novel BEST1 Mutation in Autosomal Recessive Bestrophinopathy.
    Lee CS; Jun I; Choi SI; Lee JH; Lee MG; Lee SC; Kim EK
    Invest Ophthalmol Vis Sci; 2015 Dec; 56(13):8141-50. PubMed ID: 26720466
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotype and genotype of patients with autosomal recessive bestrophinopathy.
    MacDonald IM; Gudiseva HV; Villanueva A; Greve M; Caruso R; Ayyagari R
    Ophthalmic Genet; 2012 Sep; 33(3):123-9. PubMed ID: 21809908
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic study.
    Low S; Davidson AE; Holder GE; Hogg CR; Bhattacharya SS; Black GC; Foster PJ; Webster AR
    Mol Vis; 2011; 17():2272-82. PubMed ID: 21921978
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Phenotypic and Genetic Spectrum of Autosomal Recessive Bestrophinopathy and Best Vitelliform Macular Dystrophy.
    Pfister TA; Zein WM; Cukras CA; Sen HN; Maldonado RS; Huryn LA; Hufnagel RB
    Invest Ophthalmol Vis Sci; 2021 May; 62(6):22. PubMed ID: 34015078
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.