186 related articles for article (PubMed ID: 24328569)
21. [Mutation-Dependent Mechanisms and Their Impact on Targeted Therapeutic Strategies with Reference to Bestrophin 1 and the Bestrophinopathies].
Milenkovic A; Brandl C; Nachtigal AL; Kellner U; Weber BHF
Klin Monbl Augenheilkd; 2020 Mar; 237(3):259-266. PubMed ID: 32120431
[TBL] [Abstract][Full Text] [Related]
22. BESTROPHIN1 mutations cause defective chloride conductance in patient stem cell-derived RPE.
Moshfegh Y; Velez G; Li Y; Bassuk AG; Mahajan VB; Tsang SH
Hum Mol Genet; 2016 Jul; 25(13):2672-2680. PubMed ID: 27193166
[TBL] [Abstract][Full Text] [Related]
23. Functional characterization of bestrophin-1 missense mutations associated with autosomal recessive bestrophinopathy.
Davidson AE; Millar ID; Burgess-Mullan R; Maher GJ; Urquhart JE; Brown PD; Black GC; Manson FD
Invest Ophthalmol Vis Sci; 2011 Jun; 52(6):3730-6. PubMed ID: 21330666
[TBL] [Abstract][Full Text] [Related]
24. The light peak of the electroretinogram is dependent on voltage-gated calcium channels and antagonized by bestrophin (best-1).
Marmorstein LY; Wu J; McLaughlin P; Yocom J; Karl MO; Neussert R; Wimmers S; Stanton JB; Gregg RG; Strauss O; Peachey NS; Marmorstein AD
J Gen Physiol; 2006 May; 127(5):577-89. PubMed ID: 16636205
[TBL] [Abstract][Full Text] [Related]
25. The role of bestrophin-1 in intracellular Ca(2+) signaling.
Strauß O; Müller C; Reichhart N; Tamm ER; Gomez NM
Adv Exp Med Biol; 2014; 801():113-9. PubMed ID: 24664688
[TBL] [Abstract][Full Text] [Related]
26. BEST1 expression in the retinal pigment epithelium is modulated by OTX family members.
Esumi N; Kachi S; Hackler L; Masuda T; Yang Z; Campochiaro PA; Zack DJ
Hum Mol Genet; 2009 Jan; 18(1):128-41. PubMed ID: 18849347
[TBL] [Abstract][Full Text] [Related]
27. Bestrophin1: A Gene that Causes Many Diseases.
Smith JJ; Nommiste B; Carr AF
Adv Exp Med Biol; 2019; 1185():419-423. PubMed ID: 31884648
[TBL] [Abstract][Full Text] [Related]
28. Differential effects of Best disease causing missense mutations on bestrophin-1 trafficking.
Johnson AA; Lee YS; Stanton JB; Yu K; Hartzell CH; Marmorstein LY; Marmorstein AD
Hum Mol Genet; 2013 Dec; 22(23):4688-97. PubMed ID: 23825107
[TBL] [Abstract][Full Text] [Related]
29. Volume sensitivity of the bestrophin family of chloride channels.
Fischmeister R; Hartzell HC
J Physiol; 2005 Jan; 562(Pt 2):477-91. PubMed ID: 15564283
[TBL] [Abstract][Full Text] [Related]
30. Mechanisms of cellular synchronization in the vascular wall. Mechanisms of vasomotion.
Matchkov VV
Dan Med Bull; 2010 Oct; 57(10):B4191. PubMed ID: 21040688
[TBL] [Abstract][Full Text] [Related]
31. CaV1.3 L-type channels, maxiK Ca(2+)-dependent K(+) channels and bestrophin-1 regulate rhythmic photoreceptor outer segment phagocytosis by retinal pigment epithelial cells.
Müller C; Más Gómez N; Ruth P; Strauss O
Cell Signal; 2014 May; 26(5):968-78. PubMed ID: 24407175
[TBL] [Abstract][Full Text] [Related]
32. Inhibition of Ca
Cordes M; Bucichowski P; Alfaar AS; Tsang SH; Almedawar S; Reichhart N; Strauß O
FASEB J; 2020 Mar; 34(3):4055-4071. PubMed ID: 31930599
[TBL] [Abstract][Full Text] [Related]
33. Evaluating BEST1 mutations in pluripotent stem cell-derived retinal pigment epithelial cells.
Kittredge A; Zhang Y; Yang T
Methods Enzymol; 2021; 654():365-382. PubMed ID: 34120722
[TBL] [Abstract][Full Text] [Related]
34. The spectrum of subclinical Best vitelliform macular dystrophy in subjects with mutations in BEST1 gene.
Querques G; Zerbib J; Santacroce R; Margaglione M; Delphin N; Querques L; Rozet JM; Kaplan J; Souied EH
Invest Ophthalmol Vis Sci; 2011 Jun; 52(7):4678-84. PubMed ID: 21436265
[TBL] [Abstract][Full Text] [Related]
35. Late development of vitelliform lesions and flecks in a patient with best disease: clinicopathologic correlation.
Mullins RF; Oh KT; Heffron E; Hageman GS; Stone EM
Arch Ophthalmol; 2005 Nov; 123(11):1588-94. PubMed ID: 16286623
[TBL] [Abstract][Full Text] [Related]
36. Bestrophin detected in the basal membrane of the retinal epithelium and drusen of monkeys with drusenoid maculopathy.
Gouras P; Braun K; Ivert L; Neuringer M; Mattison JA
Graefes Arch Clin Exp Ophthalmol; 2009 Aug; 247(8):1051-6. PubMed ID: 19421767
[TBL] [Abstract][Full Text] [Related]
37. Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosa.
Davidson AE; Millar ID; Urquhart JE; Burgess-Mullan R; Shweikh Y; Parry N; O'Sullivan J; Maher GJ; McKibbin M; Downes SM; Lotery AJ; Jacobson SG; Brown PD; Black GC; Manson FD
Am J Hum Genet; 2009 Nov; 85(5):581-92. PubMed ID: 19853238
[TBL] [Abstract][Full Text] [Related]
38. Induced Pluripotent Stem Cell Modeling of Best Disease and Autosomal Recessive Bestrophinopathy.
Lee JH; Oh JO; Lee CS
Yonsei Med J; 2020 Sep; 61(9):816-825. PubMed ID: 32882766
[TBL] [Abstract][Full Text] [Related]
39. Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies.
Allikmets R; Seddon JM; Bernstein PS; Hutchinson A; Atkinson A; Sharma S; Gerrard B; Li W; Metzker ML; Wadelius C; Caskey CT; Dean M; Petrukhin K
Hum Genet; 1999 Jun; 104(6):449-53. PubMed ID: 10453731
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
