251 related articles for article (PubMed ID: 24419318)
1. Zebrafish Cacna1fa is required for cone photoreceptor function and synaptic ribbon formation.
Jia S; Muto A; Orisme W; Henson HE; Parupalli C; Ju B; Baier H; Taylor MR
Hum Mol Genet; 2014 Jun; 23(11):2981-94. PubMed ID: 24419318
[TBL] [Abstract][Full Text] [Related]
2. Dysregulation of Ca(v)1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2.
Liu X; Kerov V; Haeseleer F; Majumder A; Artemyev N; Baker SA; Lee A
Channels (Austin); 2013; 7(6):514-23. PubMed ID: 24064553
[TBL] [Abstract][Full Text] [Related]
3. Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2.
Regus-Leidig H; Atorf J; Feigenspan A; Kremers J; Maw MA; Brandstätter JH
PLoS One; 2014; 9(1):e86769. PubMed ID: 24466230
[TBL] [Abstract][Full Text] [Related]
4. Keeping the balance.
Tom Dieck S
Channels (Austin); 2013; 7(6):418-9. PubMed ID: 24722264
[TBL] [Abstract][Full Text] [Related]
5. Cav1.4 IT mouse as model for vision impairment in human congenital stationary night blindness type 2.
Knoflach D; Kerov V; Sartori SB; Obermair GJ; Schmuckermair C; Liu X; Sothilingam V; Garcia Garrido M; Baker SA; Glösmann M; Schicker K; Seeliger M; Lee A; Koschak A
Channels (Austin); 2013; 7(6):503-13. PubMed ID: 24051672
[TBL] [Abstract][Full Text] [Related]
6. Cav1.4 dysfunction and congenital stationary night blindness type 2.
Koschak A; Fernandez-Quintero ML; Heigl T; Ruzza M; Seitter H; Zanetti L
Pflugers Arch; 2021 Sep; 473(9):1437-1454. PubMed ID: 34212239
[TBL] [Abstract][Full Text] [Related]
7. A Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night Blindness.
Kondo M; Das G; Imai R; Santana E; Nakashita T; Imawaka M; Ueda K; Ohtsuka H; Sakai K; Aihara T; Kato K; Sugimoto M; Ueno S; Nishizawa Y; Aguirre GD; Miyadera K
PLoS One; 2015; 10(9):e0137072. PubMed ID: 26368928
[TBL] [Abstract][Full Text] [Related]
8. Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A).
Waldner DM; Giraldo Sierra NC; Bonfield S; Nguyen L; Dimopoulos IS; Sauvé Y; Stell WK; Bech-Hansen NT
Channels (Austin); 2018 Jan; 12(1):17-33. PubMed ID: 29179637
[TBL] [Abstract][Full Text] [Related]
9. Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2.
Michalakis S; Shaltiel L; Sothilingam V; Koch S; Schludi V; Krause S; Zeitz C; Audo I; Lancelot ME; Hamel C; Meunier I; Preising MN; Friedburg C; Lorenz B; Zabouri N; Haverkamp S; Garcia Garrido M; Tanimoto N; Seeliger MW; Biel M; Wahl-Schott CA
Hum Mol Genet; 2014 Mar; 23(6):1538-50. PubMed ID: 24163243
[TBL] [Abstract][Full Text] [Related]
10. LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells.
Neuillé M; Cao Y; Caplette R; Guerrero-Given D; Thomas C; Kamasawa N; Sahel JA; Hamel CP; Audo I; Picaud S; Martemyanov KA; Zeitz C
Invest Ophthalmol Vis Sci; 2017 Mar; 58(3):1768-1778. PubMed ID: 28334377
[TBL] [Abstract][Full Text] [Related]
11. High-resolution optical imaging of zebrafish larval ribbon synapse protein RIBEYE, RIM2, and CaV 1.4 by stimulation emission depletion microscopy.
Lv C; Gould TJ; Bewersdorf J; Zenisek D
Microsc Microanal; 2012 Aug; 18(4):745-52. PubMed ID: 22832038
[TBL] [Abstract][Full Text] [Related]
12. Congenital stationary night blindness in mice - a tale of two Cacna1f mutants.
Lodha N; Bonfield S; Orton NC; Doering CJ; McRory JE; Mema SC; Rehak R; Sauvé Y; Tobias R; Stell WK; Bech-Hansen NT
Adv Exp Med Biol; 2010; 664():549-58. PubMed ID: 20238058
[TBL] [Abstract][Full Text] [Related]
13. Spectrum of Cav1.4 dysfunction in congenital stationary night blindness type 2.
Burtscher V; Schicker K; Novikova E; Pöhn B; Stockner T; Kugler C; Singh A; Zeitz C; Lancelot ME; Audo I; Leroy BP; Freissmuth M; Herzig S; Matthes J; Koschak A
Biochim Biophys Acta; 2014 Aug; 1838(8):2053-65. PubMed ID: 24796500
[TBL] [Abstract][Full Text] [Related]
14. A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family.
Vincent A; Wright T; Day MA; Westall CA; Héon E
Mol Vis; 2011; 17():3262-70. PubMed ID: 22194652
[TBL] [Abstract][Full Text] [Related]
15. Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics.
Dinet V; Ciccotosto GD; Delaunay K; Borras C; Ranchon-Cole I; Kostic C; Savoldelli M; El Sanharawi M; Jonet L; Pirou C; An N; Abitbol M; Arsenijevic Y; Behar-Cohen F; Cappai R; Mascarelli F
Mol Brain; 2016 Jun; 9(1):64. PubMed ID: 27267879
[TBL] [Abstract][Full Text] [Related]
16. The role of voltage-gated ion channels in visual function and disease in mammalian photoreceptors.
Rashwan R; Hunt DM; Carvalho LS
Pflugers Arch; 2021 Sep; 473(9):1455-1468. PubMed ID: 34255151
[TBL] [Abstract][Full Text] [Related]
17. Gain-of-function nature of Cav1.4 L-type calcium channels alters firing properties of mouse retinal ganglion cells.
Knoflach D; Schicker K; Glösmann M; Koschak A
Channels (Austin); 2015; 9(5):298-306. PubMed ID: 26274509
[TBL] [Abstract][Full Text] [Related]
18. Visual signal pathway reorganization in the Cacna1f mutant rat model.
Tao Y; Chen T; Liu B; Xue JH; Zhang L; Xia F; Pang JJ; Zhang ZM
Invest Ophthalmol Vis Sci; 2013 Mar; 54(3):1988-97. PubMed ID: 23425697
[TBL] [Abstract][Full Text] [Related]
19. Cacna1f gene decreased contractility of skeletal muscle in rat model with congenital stationary night blindness.
An J; Zhang L; Jiao B; Lu F; Xia F; Yu Z; Zhang Z
Gene; 2015 May; 562(2):210-9. PubMed ID: 25748727
[TBL] [Abstract][Full Text] [Related]
20. Differential role for synaptojanin 1 in rod and cone photoreceptors.
Holzhausen LC; Lewis AA; Cheong KK; Brockerhoff SE
J Comp Neurol; 2009 Dec; 517(5):633-44. PubMed ID: 19827152
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
