119 related articles for article (PubMed ID: 37914484)
1. Three cases of karyomegalic interstitial nephritis with novel FAN1 mutations from a Chinese family.
Zhu H; Liu Y; Ding X; Liu X; Xu L; Zhao B; Yang X; Wang R
Nefrologia (Engl Ed); 2023; 43(4):491-493. PubMed ID: 37914484
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. Karyomegalic interstitial nephritis and DNA damage-induced polyploidy in Fan1 nuclease-defective knock-in mice.
Lachaud C; Slean M; Marchesi F; Lock C; Odell E; Castor D; Toth R; Rouse J
Genes Dev; 2016 Mar; 30(6):639-44. PubMed ID: 26980188
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair.
Zhou W; Otto EA; Cluckey A; Airik R; Hurd TW; Chaki M; Diaz K; Lach FP; Bennett GR; Gee HY; Ghosh AK; Natarajan S; Thongthip S; Veturi U; Allen SJ; Janssen S; Ramaswami G; Dixon J; Burkhalter F; Spoendlin M; Moch H; Mihatsch MJ; Verine J; Reade R; Soliman H; Godin M; Kiss D; Monga G; Mazzucco G; Amann K; Artunc F; Newland RC; Wiech T; Zschiedrich S; Huber TB; Friedl A; Slaats GG; Joles JA; Goldschmeding R; Washburn J; Giles RH; Levy S; Smogorzewska A; Hildebrandt F
Nat Genet; 2012 Jul; 44(8):910-5. PubMed ID: 22772369
[TBL] [Abstract][Full Text] [Related]
7. Karyomegalic Interstitial Nephritis: A Case Report and Review of the Literature.
Isnard P; Rabant M; Labaye J; Antignac C; Knebelmann B; Zaidan M
Medicine (Baltimore); 2016 May; 95(20):e3349. PubMed ID: 27196444
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. Common variants in FAN1, located in 15q13.3, confer risk for schizophrenia and bipolar disorder in Han Chinese.
Jian X; Chen J; Li Z; Fahira A; Shao W; Zhou J; Wang K; Wen Y; Zhang J; Yang Q; Pan D; Wang Z; Shi Y
Prog Neuropsychopharmacol Biol Psychiatry; 2020 Dec; 103():109973. PubMed ID: 32450113
[TBL] [Abstract][Full Text] [Related]
13. Genome stability, progressive kidney failure and aging.
Lans H; Hoeijmakers JH
Nat Genet; 2012 Jul; 44(8):836-8. PubMed ID: 22836089
[No Abstract] [Full Text] [Related]
14. FAN1 nuclease helps to delay Huntington disease.
Wood H
Nat Rev Neurol; 2022 Jun; 18(6):317. PubMed ID: 35534552
[No Abstract] [Full Text] [Related]
15. 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]
16. Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects.
Kim KH; Hong EP; Shin JW; Chao MJ; Loupe J; Gillis T; Mysore JS; Holmans P; Jones L; Orth M; Monckton DG; Long JD; Kwak S; Lee R; Gusella JF; MacDonald ME; Lee JM
Am J Hum Genet; 2020 Jul; 107(1):96-110. PubMed ID: 32589923
[TBL] [Abstract][Full Text] [Related]
17. Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington's disease knock-in mice is blocked by Mlh1 knock-out.
Loupe JM; Pinto RM; Kim KH; Gillis T; Mysore JS; Andrew MA; Kovalenko M; Murtha R; Seong I; Gusella JF; Kwak S; Howland D; Lee R; Lee JM; Wheeler VC; MacDonald ME
Hum Mol Genet; 2020 Nov; 29(18):3044-3053. PubMed ID: 32876667
[TBL] [Abstract][Full Text] [Related]
18. FAN1 exo- not endo-nuclease pausing on disease-associated slipped-DNA repeats: A mechanism of repeat instability.
Deshmukh AL; Caron MC; Mohiuddin M; Lanni S; Panigrahi GB; Khan M; Engchuan W; Shum N; Faruqui A; Wang P; Yuen RKC; Nakamori M; Nakatani K; Masson JY; Pearson CE
Cell Rep; 2021 Dec; 37(10):110078. PubMed ID: 34879276
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. FAN1-MLH1 interaction affects repair of DNA interstrand cross-links and slipped-CAG/CTG repeats.
Porro A; Mohiuddin M; Zurfluh C; Spegg V; Dai J; Iehl F; Ropars V; Collotta G; Fishwick KM; Mozaffari NL; Guérois R; Jiricny J; Altmeyer M; Charbonnier JB; Pearson CE; Sartori AA
Sci Adv; 2021 Jul; 7(31):. PubMed ID: 34330701
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
