Airik R - Search Results

1

Mitochondrial ROS Triggers KIN Pathogenesis in FAN1-Deficient Kidneys.

Airik M, Arbore H, Childs E, Huynh AB, Phua YL, Chen CW, Aird K, Bharathi S, Zhang B, Conlon P, Kmoch S, Kidd K, Bleyer AJ, Vockley J, Goetzman E, Wipf P, Airik R. Airik M, et al. Among authors: airik r. Antioxidants (Basel). 2023 Apr 8;12(4):900. doi: 10.3390/antiox12040900. Antioxidants (Basel). 2023. PMID: 37107275 Free PMC article.

2

Disruption of Multiple Overlapping Functions Following Stepwise Inactivation of the Extended Myc Network.

Wang H, Stevens T, Lu J, Airik M, Airik R, Prochownik EV. Wang H, et al. Among authors: airik r. Cells. 2022 Dec 16;11(24):4087. doi: 10.3390/cells11244087. Cells. 2022. PMID: 36552851 Free PMC article.

3

Premature aging and reduced cancer incidence associated with near-complete body-wide Myc inactivation.

Wang H, Lu J, Stevens T, Roberts A, Mandel J, Avula R, Ma B, Wu Y, Wang J, Land CV, Finkel T, Vockley JE, Airik M, Airik R, Muzumdar R, Gong Z, Torbenson MS, Prochownik EV. Wang H, et al. Among authors: airik r. Cell Rep. 2023 Aug 29;42(8):112830. doi: 10.1016/j.celrep.2023.112830. Epub 2023 Jul 22. Cell Rep. 2023. PMID: 37481724 Free PMC article.

4

Endothelial cells drive organ fibrosis in mice by inducing expression of the transcription factor SOX9.

Trogisch FA, Abouissa A, Keles M, Birke A, Fuhrmann M, Dittrich GM, Weinzierl N, Wink E, Cordero J, Elsherbiny A, Martin-Garrido A, Grein S, Hemanna S, Hofmann E, Nicin L, Bibli SI, Airik R, Kispert A, Kist R, Quanchao S, Kürschner SW, Winkler M, Gretz N, Mogler C, Korff T, Koch PS, Dimmeler S, Dobreva G, Heineke J. Trogisch FA, et al. Among authors: airik r. Sci Transl Med. 2024 Feb 28;16(736):eabq4581. doi: 10.1126/scitranslmed.abq4581. Epub 2024 Feb 28. Sci Transl Med. 2024. PMID: 38416842

5

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. Airik M, et al. Among authors: airik r. Kidney Int. 2022 Nov;102(5):1042-1056. doi: 10.1016/j.kint.2022.07.003. Epub 2022 Aug 2. Kidney Int. 2022. PMID: 35931300 Free PMC article.

6

Mitigation of portal fibrosis and cholestatic liver disease in ANKS6-deficient livers by macrophage depletion.

Airik M, McCourt B, Ozturk TT, Huynh AB, Zhang X, Tometich JT, Topaloglu R, Ozen H, Orhan D, Nejak-Bowen K, Monga SP, Hand TW, Ozaltin F, Airik R. Airik M, et al. Among authors: airik r. FASEB J. 2022 Feb;36(2):e22157. doi: 10.1096/fj.202101387R. FASEB J. 2022. PMID: 35032404 Free PMC article.

7

Biallelic ANKS6 mutations cause late-onset ciliopathy with chronic kidney disease through YAP dysregulation.

Schwarz H, Popp B, Airik R, Torabi N, Knaup KX, Stoeckert J, Wiech T, Amann K, Reis A, Schiffer M, Wiesener MS, Schueler M. Schwarz H, et al. Among authors: airik r. Hum Mol Genet. 2022 May 4;31(9):1357-1369. doi: 10.1093/hmg/ddab322. Hum Mol Genet. 2022. PMID: 34740236

8

Primary coenzyme Q10 nephropathy, a potentially treatable form of steroid-resistant nephrotic syndrome.

Tan W, Airik R. Tan W, et al. Among authors: airik r. Pediatr Nephrol. 2021 Nov;36(11):3515-3527. doi: 10.1007/s00467-020-04914-8. Epub 2021 Jan 22. Pediatr Nephrol. 2021. PMID: 33479824 Free PMC article. Review.

9

Loss of Anks6 leads to YAP deficiency and liver abnormalities.

Airik M, Schüler M, McCourt B, Weiss AC, Herdman N, Lüdtke TH, Widmeier E, Stolz DB, Nejak-Bowen KN, Yimlamai D, Wu YL, Kispert A, Airik R, Hildebrandt F. Airik M, et al. Among authors: airik r. Hum Mol Genet. 2020 Nov 4;29(18):3064-3080. doi: 10.1093/hmg/ddaa197. Hum Mol Genet. 2020. PMID: 32886109 Free PMC article.

10

Roscovitine blocks collecting duct cyst growth in Cep164-deficient kidneys.

Airik R, Airik M, Schueler M, Bates CM, Hildebrandt F. Airik R, et al. Kidney Int. 2019 Aug;96(2):320-326. doi: 10.1016/j.kint.2019.04.014. Epub 2019 May 8. Kidney Int. 2019. PMID: 31248650 Free PMC article.

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