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.
190 related articles for article (PubMed ID: 37759541)
1. Modeling of Lim SW; Na D; Lee H; Fang X; Cui S; Shin YJ; Lee KI; Lee JY; Yang CW; Chung BH Cells; 2023 Sep; 12(18):. PubMed ID: 37759541 [TBL] [Abstract][Full Text] [Related]
3. Generation of a human induced pluripotent stem cell line (CMCi001-A) from a patient with karyomegalic interstitial nephritis with homozygous frameshift deletion mutation c.1985_1994del10 of the FANCD2/FANCI-Associated Nuclease 1 gene. Na DH; Lim SW; Kim BM; Kim KW; Shin YJ; Chae H; Ko EJ; Yang CW; Kim M; Chung BH Stem Cell Res; 2020 Jul; 46():101876. PubMed ID: 32563974 [TBL] [Abstract][Full Text] [Related]
5. New familial cases of karyomegalic interstitial nephritis with mutations in the FAN1 gene. Rejeb I; Jerbi M; Jilani H; Gaied H; Elaribi Y; Hizem S; Aoudia R; Hedri H; Zaied C; Abid S; Bacha H; BenAbdallah T; BenJemaa L; Goucha R BMC Med Genomics; 2021 Jun; 14(1):160. PubMed ID: 34126972 [TBL] [Abstract][Full Text] [Related]
6. Persistent DNA damage underlies tubular cell polyploidization and progression to chronic kidney disease in kidneys deficient in the DNA repair protein FAN1. Airik M; Phua YL; Huynh AB; McCourt BT; Rush BM; Tan RJ; Vockley J; Murray SL; Dorman A; Conlon PJ; Airik R Kidney Int; 2022 Nov; 102(5):1042-1056. PubMed ID: 35931300 [TBL] [Abstract][Full Text] [Related]
7. Fan1 deficiency results in DNA interstrand cross-link repair defects, enhanced tissue karyomegaly, and organ dysfunction. Thongthip S; Bellani M; Gregg SQ; Sridhar S; Conti BA; Chen Y; Seidman MM; Smogorzewska A Genes Dev; 2016 Mar; 30(6):645-59. PubMed ID: 26980189 [TBL] [Abstract][Full Text] [Related]
8. A FANCD2/FANCI-Associated Nuclease 1-Knockout Model Develops Karyomegalic Interstitial Nephritis. Airik R; Schueler M; Airik M; Cho J; Porath JD; Mukherjee E; Sims-Lucas S; Hildebrandt F J Am Soc Nephrol; 2016 Dec; 27(12):3552-3559. PubMed ID: 27026368 [TBL] [Abstract][Full Text] [Related]
9. Karyomegalic interstitial nephritis with a novel FAN1 gene mutation and concurrent ALECT2 amyloidosis. Law S; Gillmore J; Gilbertson JA; Bass P; Salama AD BMC Nephrol; 2020 Feb; 21(1):74. PubMed ID: 32111193 [TBL] [Abstract][Full Text] [Related]
10. Modeling of Fabry disease nephropathy using patient derived human induced pluripotent stem cells and kidney organoid system. Cui S; Fang X; Lee H; Shin YJ; Koh ES; Chung S; Park HS; Lim SW; Lee KI; Lee JY; Yang CW; Chung BH J Transl Med; 2023 Feb; 21(1):138. PubMed ID: 36814269 [TBL] [Abstract][Full Text] [Related]
11. CRISPR/Cas9-mediated A4GALT suppression rescues Fabry disease phenotypes in a kidney organoid model. Cui S; Shin YJ; Fang X; Lee H; Eum SH; Ko EJ; Lim SW; Shin E; Lee KI; Lee JY; Lee CB; Bae SK; Yang CW; Chung BH Transl Res; 2023 Aug; 258():35-46. PubMed ID: 36805562 [TBL] [Abstract][Full Text] [Related]
12. KIAA1018/FAN1 nuclease protects cells against genomic instability induced by interstrand cross-linking agents. Yoshikiyo K; Kratz K; Hirota K; Nishihara K; Takata M; Kurumizaka H; Horimoto S; Takeda S; Jiricny J Proc Natl Acad Sci U S A; 2010 Dec; 107(50):21553-7. PubMed ID: 21115814 [TBL] [Abstract][Full Text] [Related]
13. Phenotypic and Genotypic Features of the Császár I; Kalmár T; Maróti Z; Ávéd J; Szederkényi E; Zombori J; Pankotai-Bodó G; Turkevi-Nagy S; Iványi B Int J Mol Sci; 2024 May; 25(11):. PubMed ID: 38892095 [TBL] [Abstract][Full Text] [Related]
14. FAN1, a DNA Repair Nuclease, as a Modifier of Repeat Expansion Disorders. Deshmukh AL; Porro A; Mohiuddin M; Lanni S; Panigrahi GB; Caron MC; Masson JY; Sartori AA; Pearson CE J Huntingtons Dis; 2021; 10(1):95-122. PubMed ID: 33579867 [TBL] [Abstract][Full Text] [Related]
15. CRISPR-Cas9-Mediated Correction of Lim SW; Fang X; Cui S; Lee H; Shin YJ; Ko EJ; Lee KI; Lee JY; Chung BH; Yang CW Int J Mol Sci; 2023 Feb; 24(3):. PubMed ID: 36769335 [TBL] [Abstract][Full Text] [Related]
16. A rare multisystemic disorder with chronic kidney disease: Karyomegalic interstitial nephritis due to homozygous FAN1 c.2260C>T variant. Guzel Dirim M; Dirim AB; Kaya B; Senkal N; Kalayci T; Aslanger A; Berker N; Kose M; Kilicaslan I; Yazici H Nephrology (Carlton); 2024 Dec; 29(12):968-972. PubMed ID: 39294548 [TBL] [Abstract][Full Text] [Related]
18. MLH1-mediated recruitment of FAN1 to chromatin for the induction of apoptosis triggered by O Rikitake M; Fujikane R; Obayashi Y; Oka K; Ozaki M; Hidaka M Genes Cells; 2020 Mar; 25(3):175-186. PubMed ID: 31955481 [TBL] [Abstract][Full Text] [Related]
19. IgA Nephropathy Concomitant With Karyomegalic Interstitial Nephritis. Wang Z; Ni X; Zhu S; Yue S Am J Med Sci; 2020 Sep; 360(3):287-292. PubMed ID: 32387117 [TBL] [Abstract][Full Text] [Related]
20. Case report: a 58 -year -old man with small kidneys and elevated liver enzymes. Dash J; Saudan P; Paoloni-Giacobino A; Moll S; de Seigneux S BMC Nephrol; 2020 Mar; 21(1):107. PubMed ID: 32220227 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]