146 related articles for article (PubMed ID: 32244200)
1. Establishment of induced pluripotent stem cell line CSUASOi003- A from an autosomal recessive retinitis pigmentosa patient carrying compound heterozygous mutations in CRB1 gene.
Zhou Y; Ding C; Xia S; Jing Y; Mao S; Liu J; Chen J; Chan HF; Tang S; Chen J
Stem Cell Res; 2020 Apr; 44():101742. PubMed ID: 32244200
[TBL] [Abstract][Full Text] [Related]
2. Generation of a human iPS cell line from a patient with retinitis pigmentosa due to EYS mutation.
Calado SM; Garcia-Delgado AB; De la Cerda B; Ponte-Zuñiga B; Bhattacharya SS; Díaz-Corrales FJ
Stem Cell Res; 2018 Dec; 33():251-254. PubMed ID: 30471616
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Using inducible lentiviral vectors to generate induced pluripotent stem cell line ZOCi001-A from peripheral blood cells of a patient with CRB1
Tang X; Liu X; Chen Z; Luo L; Liu X; Deng J; Li DW; Liu Y
Stem Cell Res; 2020 May; 45():101817. PubMed ID: 32387899
[TBL] [Abstract][Full Text] [Related]
5. Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa.
Guo X; Li J; Wang Q; Shu Y; Wang J; Chen L; Zhang H; Shi Y; Yang J; Lu F; Jiang L; Qu C; Gong B
Mol Med Rep; 2019 Sep; 20(3):2922-2928. PubMed ID: 31322236
[TBL] [Abstract][Full Text] [Related]
6. Establishment of an induced pluripotent stem cell line from a retinitis pigmentosa patient with compound heterozygous CRB1 mutation.
Zhang X; Zhang D; Chen SC; Lamey T; Thompson JA; McLaren T; De Roach JN; Chen FK; McLenachan S
Stem Cell Res; 2018 Aug; 31():147-151. PubMed ID: 30092450
[TBL] [Abstract][Full Text] [Related]
7. Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1.
Moon SY; Zhang D; Chen SC; Lamey TM; Thompson JA; McLaren TL; De Roach JN; Chen FK; McLenachan S
Stem Cell Res; 2021 Jul; 54():102403. PubMed ID: 34034222
[TBL] [Abstract][Full Text] [Related]
8. Homozygosity mapping identifies the Crumbs homologue 1 (Crb1) gene as responsible for a recessive syndrome of retinitis pigmentosa and nanophthalmos.
Zenteno JC; Buentello-Volante B; Ayala-Ramirez R; Villanueva-Mendoza C
Am J Med Genet A; 2011 May; 155A(5):1001-6. PubMed ID: 21484995
[TBL] [Abstract][Full Text] [Related]
9. Establishment of induced pluripotent stem cell line CSUASOi004-A by reprogramming peripheral blood mononuclear cells of a PRPF6-related dominant retinitis pigmentosa patient.
Zhou Y; Jing Y; Mao S; Liu J; Cui Z; Wang Y; Chen J; Chan HF; Tang S; Chen J
Stem Cell Res; 2020 May; 45():101793. PubMed ID: 32335390
[TBL] [Abstract][Full Text] [Related]
10. A case of CRB1-negative Coats-like retinitis pigmentosa.
Sarao V; Veritti D; Prosperi R; Pignatto S; Lanzetta P
J AAPOS; 2013 Aug; 17(4):414-6. PubMed ID: 23871396
[TBL] [Abstract][Full Text] [Related]
11. Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa.
Booij JC; Florijn RJ; ten Brink JB; Loves W; Meire F; van Schooneveld MJ; de Jong PT; Bergen AA
J Med Genet; 2005 Nov; 42(11):e67. PubMed ID: 16272259
[TBL] [Abstract][Full Text] [Related]
12. Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).
den Hollander AI; ten Brink JB; de Kok YJ; van Soest S; van den Born LI; van Driel MA; van de Pol DJ; Payne AM; Bhattacharya SS; Kellner U; Hoyng CB; Westerveld A; Brunner HG; Bleeker-Wagemakers EM; Deutman AF; Heckenlively JR; Cremers FP; Bergen AA
Nat Genet; 1999 Oct; 23(2):217-21. PubMed ID: 10508521
[TBL] [Abstract][Full Text] [Related]
13. LONG-TERM FOLLOW-UP OF PATIENTS WITH RETINITIS PIGMENTOSA TYPE 12 CAUSED BY CRB1 MUTATIONS: A Severe Phenotype With Considerable Interindividual Variability.
Mathijssen IB; Florijn RJ; van den Born LI; Zekveld-Vroon RC; Ten Brink JB; Plomp AS; Baas F; Meijers-Heijboer H; Bergen AA; van Schooneveld MJ
Retina; 2017 Jan; 37(1):161-172. PubMed ID: 27380427
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Generation of an induced pluripotent stem cell line (SJTUGHi001-A) from a patient with Retinitis Pigmentosa carrying c.77C > T mutation in RAX2 gene.
Bai X; Chen J; Zhao X; Zhu X; Ding X; Zhang T; Jiang M; Sun X
Stem Cell Res; 2024 Jun; 77():103390. PubMed ID: 38507880
[TBL] [Abstract][Full Text] [Related]
16. Generation and characterization of the human iPSC line CABi001-A from a patient with retinitis pigmentosa caused by a novel mutation in PRPF31 gene.
de la Cerda B; Díez-Lloret A; Ponte B; Vallés-Saiz L; Calado SM; Rodríguez-Bocanegra E; Garcia-Delgado AB; Moya-Molina M; Bhattacharya SS; Díaz-Corrales FJ
Stem Cell Res; 2019 Apr; 36():101426. PubMed ID: 30921587
[TBL] [Abstract][Full Text] [Related]
17. Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype.
Quinn PM; Mulder AA; Henrique Alves C; Desrosiers M; de Vries SI; Klooster J; Dalkara D; Koster AJ; Jost CR; Wijnholds J
Hum Mol Genet; 2019 Jan; 28(1):105-123. PubMed ID: 30239717
[TBL] [Abstract][Full Text] [Related]
18. CRB1 is required for recycling by RAB11A+ vesicles in human retinal organoids.
Buck TM; Quinn PMJ; Pellissier LP; Mulder AA; Jongejan A; Lu X; Boon N; Koot D; Almushattat H; Arendzen CH; Vos RM; Bradley EJ; Freund C; Mikkers HMM; Boon CJF; Moerland PD; Baas F; Koster AJ; Neefjes J; Berlin I; Jost CR; Wijnholds J
Stem Cell Reports; 2023 Sep; 18(9):1793-1810. PubMed ID: 37541258
[TBL] [Abstract][Full Text] [Related]
19. Microglial Cell Dysfunction in CRB1-Associated Retinopathies.
Alves CH; Wijnholds J
Adv Exp Med Biol; 2019; 1185():159-163. PubMed ID: 31884605
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
