These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

190 related articles for article (PubMed ID: 37561581)

  • 1. Nonviral base editing of KCNJ13 mutation preserves vision in a model of inherited retinal channelopathy.
    Kabra M; Shahi PK; Wang Y; Sinha D; Spillane A; Newby GA; Saxena S; Tong Y; Chang Y; Abdeen AA; Edwards KL; Theisen CO; Liu DR; Gamm DM; Gong S; Saha K; Pattnaik BR
    J Clin Invest; 2023 Oct; 133(19):. PubMed ID: 37561581
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Gene Augmentation and Readthrough Rescue Channelopathy in an iPSC-RPE Model of Congenital Blindness.
    Shahi PK; Hermans D; Sinha D; Brar S; Moulton H; Stulo S; Borys KD; Capowski E; Pillers DM; Gamm DM; Pattnaik BR
    Am J Hum Genet; 2019 Feb; 104(2):310-318. PubMed ID: 30686507
    [TBL] [Abstract][Full Text] [Related]  

  • 3. KCNJ13 Gene Deletion Impairs Cell Alignment and Phagocytosis in Retinal Pigment Epithelium Derived from Human-Induced Pluripotent Stem Cells.
    Kanzaki Y; Fujita H; Sato K; Hosokawa M; Matsumae H; Shiraga F; Morizane Y; Ohuchi H
    Invest Ophthalmol Vis Sci; 2020 May; 61(5):38. PubMed ID: 32437550
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Novel KCNJ13 Nonsense Mutation and Loss of Kir7.1 Channel Function Causes Leber Congenital Amaurosis (LCA16).
    Pattnaik BR; Shahi PK; Marino MJ; Liu X; York N; Brar S; Chiang J; Pillers DA; Traboulsi EI
    Hum Mutat; 2015 Jul; 36(7):720-7. PubMed ID: 25921210
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Human iPSC Modeling Reveals Mutation-Specific Responses to Gene Therapy in a Genotypically Diverse Dominant Maculopathy.
    Sinha D; Steyer B; Shahi PK; Mueller KP; Valiauga R; Edwards KL; Bacig C; Steltzer SS; Srinivasan S; Abdeen A; Cory E; Periyasamy V; Siahpirani AF; Stone EM; Tucker BA; Roy S; Pattnaik BR; Saha K; Gamm DM
    Am J Hum Genet; 2020 Aug; 107(2):278-292. PubMed ID: 32707085
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Conditional loss of Kcnj13 in the retinal pigment epithelium causes photoreceptor degeneration.
    Roman D; Zhong H; Yaklichkin S; Chen R; Mardon G
    Exp Eye Res; 2018 Nov; 176():219-226. PubMed ID: 30009826
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Focus on Kir7.1: physiology and channelopathy.
    Kumar M; Pattnaik BR
    Channels (Austin); 2014; 8(6):488-95. PubMed ID: 25558901
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Abnormal Electroretinogram after Kir7.1 Channel Suppression Suggests Role in Retinal Electrophysiology.
    Shahi PK; Liu X; Aul B; Moyer A; Pattnaik A; Denton J; Pillers DM; Pattnaik BR
    Sci Rep; 2017 Sep; 7(1):10651. PubMed ID: 28878288
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CRISPR-engineered mosaicism rapidly reveals that loss of Kcnj13 function in mice mimics human disease phenotypes.
    Zhong H; Chen Y; Li Y; Chen R; Mardon G
    Sci Rep; 2015 Feb; 5():8366. PubMed ID: 25666713
    [TBL] [Abstract][Full Text] [Related]  

  • 10. LEBER CONGENITAL AMAUROSIS WITH LARGE RETINAL PIGMENT CLUMPS CAUSED BY COMPOUND HETEROZYGOUS MUTATIONS IN KCNJ13.
    Perez-Roustit S; Marquette V; Bocquet B; Kaplan J; Perrault I; Meunier I; Hamel CP
    Retin Cases Brief Rep; 2017 Summer; 11(3):221-226. PubMed ID: 27203561
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gene Correction Recovers Phagocytosis in Retinal Pigment Epithelium Derived from Retinitis Pigmentosa-Human-Induced Pluripotent Stem Cells.
    Artero-Castro A; Long K; Bassett A; Ávila-Fernandez A; Cortón M; Vidal-Puig A; Jendelova P; Rodriguez-Jimenez FJ; Clemente E; Ayuso C; Erceg S
    Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33672445
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Functional Assessment of Patient-Derived Retinal Pigment Epithelial Cells Edited by CRISPR/Cas9.
    Foltz LP; Howden SE; Thomson JA; Clegg DO
    Int J Mol Sci; 2018 Dec; 19(12):. PubMed ID: 30572641
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new compact adenine base editor generated through deletion of HNH and REC2 domain of SpCas9.
    Qian Y; Wang D; Niu W; Zhao D; Li J; Liu Z; Gao X; Han Y; Lai L; Li Z
    BMC Biol; 2023 Jul; 21(1):155. PubMed ID: 37434184
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gene editing prospects for treating inherited retinal diseases.
    Benati D; Patrizi C; Recchia A
    J Med Genet; 2020 Jul; 57(7):437-444. PubMed ID: 31857428
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration.
    Burnight ER; Gupta M; Wiley LA; Anfinson KR; Tran A; Triboulet R; Hoffmann JM; Klaahsen DL; Andorf JL; Jiao C; Sohn EH; Adur MK; Ross JW; Mullins RF; Daley GQ; Schlaeger TM; Stone EM; Tucker BA
    Mol Ther; 2017 Sep; 25(9):1999-2013. PubMed ID: 28619647
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Altered phosphatidylinositol regulation of mutant inwardly rectifying K
    Vera E; Cornejo I; Niemeyer MI; Sepúlveda FV; Cid LP
    J Physiol; 2021 Jan; 599(2):593-608. PubMed ID: 33219695
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recessive mutations in KCNJ13, encoding an inwardly rectifying potassium channel subunit, cause leber congenital amaurosis.
    Sergouniotis PI; Davidson AE; Mackay DS; Li Z; Yang X; Plagnol V; Moore AT; Webster AR
    Am J Hum Genet; 2011 Jul; 89(1):183-90. PubMed ID: 21763485
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Precise in vivo functional analysis of DNA variants with base editing using ACEofBASEs target prediction.
    Cornean A; Gierten J; Welz B; Mateo JL; Thumberger T; Wittbrodt J
    Elife; 2022 Apr; 11():. PubMed ID: 35373735
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Biallelic CLCN2 mutations cause retinal degeneration by impairing retinal pigment epithelium phagocytosis and chloride channel function.
    Xu P; Chen Z; Ma J; Shan Y; Wang Y; Xie B; Zheng D; Guo F; Song X; Gao G; Ye K; Liu Y; Pan G; Jiang B; Peng F; Zhong X
    Hum Genet; 2023 Apr; 142(4):577-593. PubMed ID: 36964785
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comparison of retinal degeneration treatment with four types of different mesenchymal stem cells, human induced pluripotent stem cells and RPE cells in a rat retinal degeneration model.
    Liu Q; Liu J; Guo M; Sung TC; Wang T; Yu T; Tian Z; Fan G; Wu W; Higuchi A
    J Transl Med; 2023 Dec; 21(1):910. PubMed ID: 38098048
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.