153 related articles for article (PubMed ID: 35538629)
1. Envisioning the development of a CRISPR-Cas mediated base editing strategy for a patient with a novel pathogenic
Bellingrath JS; McClements ME; Shanks M; Clouston P; Fischer MD; MacLaren RE
Ophthalmic Genet; 2022 Oct; 43(5):661-670. PubMed ID: 35538629
[TBL] [Abstract][Full Text] [Related]
2. In Silico CRISPR-Cas-Mediated Base Editing Strategies for Early-Onset, Severe Cone-Rod Retinal Degeneration in Three
Shamsnajafabadi H; Kaukonen M; Bellingrath JS; MacLaren RE; Cehajic-Kapetanovic J
Genes (Basel); 2024 May; 15(5):. PubMed ID: 38790254
[TBL] [Abstract][Full Text] [Related]
3. In Silico Analysis of Pathogenic
Bellingrath JS; McClements ME; Kaukonen M; Fischer MD; MacLaren RE
Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946856
[TBL] [Abstract][Full Text] [Related]
4. Analysis of CRB1 Pathogenic Variants Correctable with CRISPR Base and Prime Editing.
da Costa BL; Jenny LA; Maumenee IH; Tsang SH; Quinn PMJ
Adv Exp Med Biol; 2023; 1415():103-107. PubMed ID: 37440021
[TBL] [Abstract][Full Text] [Related]
5. Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populations.
Beryozkin A; Zelinger L; Bandah-Rozenfeld D; Harel A; Strom TA; Merin S; Chowers I; Banin E; Sharon D
Invest Ophthalmol Vis Sci; 2013 Mar; 54(3):2068-75. PubMed ID: 23449718
[TBL] [Abstract][Full Text] [Related]
6. Generation of CRB1 RP Patient-Derived iPSCs and a CRISPR/Cas9-Mediated Homology-Directed Repair Strategy for the CRB1 c.2480G>T Mutation.
da Costa BL; Li Y; Levi SR; Tsang SH; Quinn PMJ
Adv Exp Med Biol; 2023; 1415():571-576. PubMed ID: 37440088
[TBL] [Abstract][Full Text] [Related]
7. Analysis of Pathogenic Variants Correctable With CRISPR Base Editing Among Patients With Recessive Inherited Retinal Degeneration.
Fry LE; McClements ME; MacLaren RE
JAMA Ophthalmol; 2021 Mar; 139(3):319-328. PubMed ID: 33507217
[TBL] [Abstract][Full Text] [Related]
8. Rapid Variant Pathogenicity Analysis by CRISPR Activation of
Moon SY; Zhang D; Chen SC; Lamey TM; Thompson JA; McLaren TL; Chen FK; McLenachan S
CRISPR J; 2024 Apr; 7(2):100-110. PubMed ID: 38579141
[TBL] [Abstract][Full Text] [Related]
9. A novel pathogenic CRB1 variant presenting as Leber Congenital Amaurosis 8 and evaluation of gene editing feasibility.
Sylla MM; Kolesinkova M; da Costa BL; Maumenee IH; Tsang SH; Quinn PMJ
Doc Ophthalmol; 2023 Dec; 147(3):217-224. PubMed ID: 37804373
[TBL] [Abstract][Full Text] [Related]
10. The correlation between CRB1 variants and the clinical severity of Brazilian patients with different inherited retinal dystrophy phenotypes.
Motta FL; Salles MV; Costa KA; Filippelli-Silva R; Martin RP; Sallum JMF
Sci Rep; 2017 Aug; 7(1):8654. PubMed ID: 28819299
[TBL] [Abstract][Full Text] [Related]
11. CRB1 mutation spectrum in inherited retinal dystrophies.
den Hollander AI; Davis J; van der Velde-Visser SD; Zonneveld MN; Pierrottet CO; Koenekoop RK; Kellner U; van den Born LI; Heckenlively JR; Hoyng CB; Handford PA; Roepman R; Cremers FP
Hum Mutat; 2004 Nov; 24(5):355-69. PubMed ID: 15459956
[TBL] [Abstract][Full Text] [Related]
12.
Mairot K; Smirnov V; Bocquet B; Labesse G; Arndt C; Defoort-Dhellemmes S; Zanlonghi X; Hamroun D; Denis D; Picot MC; David T; Grunewald O; Pégart M; Huguet H; Roux AF; Kalatzis V; Dhaenens CM; Meunier I
Int J Mol Sci; 2021 Nov; 22(23):. PubMed ID: 34884448
[TBL] [Abstract][Full Text] [Related]
13. Detection of CRB1 mutations in families with retinal dystrophy through phenotype-oriented mutational screening.
Li S; Shen T; Xiao X; Guo X; Zhang Q
Int J Mol Med; 2014 Apr; 33(4):913-8. PubMed ID: 24535598
[TBL] [Abstract][Full Text] [Related]
14. A novel homozygous R764H mutation in crumbs homolog 1 causes autosomal recessive retinitis pigmentosa.
Tiab L; Largueche L; Chouchane I; Derouiche K; Munier FL; El Matri L; Schorderet DF
Mol Vis; 2013; 19():829-34. PubMed ID: 23592920
[TBL] [Abstract][Full Text] [Related]
15. Clinical and Therapeutic Evaluation of the Ten Most Prevalent
Lopes da Costa B; Kolesnikova M; Levi SR; Cabral T; Tsang SH; Maumenee IH; Quinn PMJ
Biomedicines; 2023 Jan; 11(2):. PubMed ID: 36830922
[TBL] [Abstract][Full Text] [Related]
16. Case report: autofluorescence imaging and phenotypic variance in a sibling pair with early-onset retinal dystrophy due to defective CRB1 function.
Tosi J; Tsui I; Lima LH; Wang NK; Tsang SH
Curr Eye Res; 2009 May; 34(5):395-400. PubMed ID: 19401883
[TBL] [Abstract][Full Text] [Related]
17. Characterization of CRB1 splicing in retinal organoids derived from a patient with adult-onset rod-cone dystrophy caused by the c.1892A>G and c.2548G>A variants.
Zhang X; Thompson JA; Zhang D; Charng J; Arunachalam S; McLaren TL; Lamey TM; De Roach JN; Jennings L; McLenachan S; Chen FK
Mol Genet Genomic Med; 2020 Nov; 8(11):e1489. PubMed ID: 32931148
[TBL] [Abstract][Full Text] [Related]
18. [Analysis of a patient with early-onset retinitis pigmentosa due to novel variants of CRB1 gene].
Yi M; Tao D; Yang Y; Liu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Sep; 40(9):1160-1164. PubMed ID: 37643966
[TBL] [Abstract][Full Text] [Related]
19. A single amino acid substitution (Cys249Trp) in Crb1 causes retinal degeneration and deregulates expression of pituitary tumor transforming gene Pttg1.
van de Pavert SA; Meuleman J; Malysheva A; Aartsen WM; Versteeg I; Tonagel F; Kamphuis W; McCabe CJ; Seeliger MW; Wijnholds J
J Neurosci; 2007 Jan; 27(3):564-73. PubMed ID: 17234588
[TBL] [Abstract][Full Text] [Related]
20. Identification of a novel CRB1 variant in a compound heterozygous state in a patient with CRB1-associated maculopathy and foveal retinoschisis.
Cheng Z; Hagan R; Yeo DCM
Ophthalmic Genet; 2022 Apr; 43(2):253-257. PubMed ID: 34783605
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
