448 related articles for article (PubMed ID: 26368928)
1. 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]
2. 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]
3. Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.
Marmor MF; Zeitz C
Doc Ophthalmol; 2018 Aug; 137(1):57-62. PubMed ID: 30051303
[TBL] [Abstract][Full Text] [Related]
4. Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness.
Vincent A; Audo I; Tavares E; Maynes JT; Tumber A; Wright T; Li S; Michiels C; ; Condroyer C; MacDonald H; Verdet R; Sahel JA; Hamel CP; Zeitz C; Héon E
Am J Hum Genet; 2016 May; 98(5):1011-1019. PubMed ID: 27063057
[TBL] [Abstract][Full Text] [Related]
5. Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy.
Hayashi T; Hosono K; Kurata K; Katagiri S; Mizobuchi K; Ueno S; Kondo M; Nakano T; Hotta Y
Doc Ophthalmol; 2020 Apr; 140(2):147-157. PubMed ID: 31583501
[TBL] [Abstract][Full Text] [Related]
6. Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness.
Neuillé M; Malaichamy S; Vadalà M; Michiels C; Condroyer C; Sachidanandam R; Srilekha S; Arokiasamy T; Letexier M; Démontant V; Sahel JA; Sen P; Audo I; Soumittra N; Zeitz C
Clin Genet; 2016 Jun; 89(6):690-9. PubMed ID: 26822852
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. In vivo electroretinographic differentiation of rod, short-wavelength and long/medium-wavelength cone responses in dogs using silent substitution stimuli.
Mowat FM; Wise E; Oh A; Foster ML; Kremers J
Exp Eye Res; 2019 Aug; 185():107673. PubMed ID: 31128103
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Behavioral phenotypic properties of a natural occurring rat model of congenital stationary night blindness with Cacna1f mutation.
An J; Wang L; Guo Q; Li L; Xia F; Zhang Z
J Neurogenet; 2012 Sep; 26(3-4):363-73. PubMed ID: 22800190
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.
Bijveld MM; Florijn RJ; Bergen AA; van den Born LI; Kamermans M; Prick L; Riemslag FC; van Schooneveld MJ; Kappers AM; van Genderen MM
Ophthalmology; 2013 Oct; 120(10):2072-81. PubMed ID: 23714322
[TBL] [Abstract][Full Text] [Related]
14. A missense mutation in
Peachey NS; Hasan N; FitzMaurice B; Burrill S; Pangeni G; Karst SY; Reinholdt L; Berry ML; Strobel M; Gregg RG; McCall MA; Chang B
J Neurophysiol; 2017 Aug; 118(2):845-854. PubMed ID: 28490646
[No Abstract] [Full Text] [Related]
15. Keeping the balance.
Tom Dieck S
Channels (Austin); 2013; 7(6):418-9. PubMed ID: 24722264
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Clinical characterisation of the CABP4-related retinal phenotype.
Khan AO; Alrashed M; Alkuraya FS
Br J Ophthalmol; 2013 Mar; 97(3):262-5. PubMed ID: 23099293
[TBL] [Abstract][Full Text] [Related]
19. Phenotypic characterization of complete CSNB in the inbred research beagle: how common is CSNB in research and companion dogs?
Oh A; Loew ER; Foster ML; Davidson MG; English RV; Gervais KJ; Herring IP; Mowat FM
Doc Ophthalmol; 2018 Oct; 137(2):87-101. PubMed ID: 30051304
[TBL] [Abstract][Full Text] [Related]
20. Complete congenital stationary night blindness associated with a novel
Hayashi T; Murakami Y; Mizobuchi K; Koyanagi Y; Sonoda KH; Nakano T
Ophthalmic Genet; 2021 Aug; 42(4):412-419. PubMed ID: 33769208
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]