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Airik, Rannar
Journal title:American Men & Women of Science : A Biographical Directory of Today’s Leaders in Physical, Biological and Related Sciences: A-BAX, 2022, p.135-135
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Airik, Rannar
Journal title:American Men & Women of Science : A Biographical Directory of Today’s Leaders in Physical, Biological and Related Sciences: A-BDE, 2021, p.133-133
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ArticlesPeer ReviewedFull Text
Primary coenzyme Q10 nephropathy, a potentially treatable form of steroid-resistant nephrotic syndrome
Author / Creator:Tan, Weizhen ; Airik, Rannar
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2021-11, Vol.36 (11), p.3515-3527
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JP4-039 Mitigates Cisplatin-Induced Acute Kidney Injury by Inhibiting Oxidative Stress and Blocking Apoptosis and Ferroptosis in Mice
Author / Creator:Airik, Merlin ; Clayton, Kacian ; Wipf, Peter ; Airik, Rannar
Publisher:Switzerland: MDPI AG
Journal title:Antioxidants, 2024-12, Vol.13 (12), p.1534
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Osteoclast stimulation factor 1 (Ostf1) KNOCKOUT increases trabecular bone mass in mice
Author / Creator:Vermeren, Matthieu ; Lyraki, Rodanthi ; Wani, Sachin ; Airik, Rannar ; Albagha, Omar ; Mort, Richard ; Hildebrandt, Friedhelm ; Hurd, Toby
Publisher:New York: Springer US
Journal title:Mammalian genome, 2017-12, Vol.28 (11-12), p.498-514
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Disruption of Multiple Overlapping Functions Following Stepwise Inactivation of the Extended Myc Network
Author / Creator:Wang, Huabo ; Stevens, Taylor ; Lu, Jie ; Airik, Merlin ; Airik, Rannar ; Prochownik, Edward V.
Publisher:Switzerland: MDPI AG
Journal title:Cells (Basel, Switzerland), 2022-12, Vol.11 (24), p.4087
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SDCCAG8 Interacts with RAB Effector Proteins RABEP2 and ERC1 and Is Required for Hedgehog Signaling
Author / Creator:Airik, Rannar ; Schueler, Markus ; Airik, Merlin ; Cho, Jang ; Ulanowicz, Kelsey A. ; Porath, Jonathan D. ; Hurd, Toby W. ; Bekker-Jensen, Simon ; Schrøder, Jacob M. ; Andersen, Jens S. ; Hildebrandt, Friedhelm
Publisher:United States: Public Library of Science
Journal title:PloS one, 2016-05, Vol.11 (5), p.e0156081-e0156081
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Mitochondrial ROS Triggers KIN Pathogenesis in FAN1-Deficient Kidneys
Author / Creator:Airik, Merlin ; Arbore, Haley ; Childs, Elizabeth ; Huynh, Amy B. ; Phua, Yu Leng ; Chen, Chi Wei ; Aird, Katherine ; Bharathi, Sivakama ; Zhang, Bob ; Conlon, Peter ; Kmoch, Stanislav ; Kidd, Kendrah ; Bleyer, Anthony J. ; Vockley, Jerry ; Goetzman, Eric ; Wipf, Peter ; Airik, Rannar
Publisher:Switzerland: MDPI AG
Journal title:Antioxidants, 2023-04, Vol.12 (4), p.900
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TSHZ3 and SOX9 Regulate the Timing of Smooth Muscle Cell Differentiation in the Ureter by Reducing Myocardin Activity
Author / Creator:Martin, Elise ; Caubit, Xavier ; Airik, Rannar ; Vola, Christine ; Fatmi, Ahmed ; Kispert, Andreas ; Fasano, Laurent
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-05, Vol.8 (5), p.e63721-e63721
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ArticlesPeer ReviewedFull Text
Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium
Author / Creator:Rudat, Carsten ; Grieskamp, Thomas ; Röhr, Christian ; Airik, Rannar ; Wrede, Christoph ; Hegermann, Jan ; Herrmann, Bernhard G. ; Schuster-Gossler, Karin ; Kispert, Andreas
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-11, Vol.9 (11), p.e112112-e112112
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COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
Author / Creator:Heeringa, Saskia F. ; Chernin, Gil ; Chaki, Moumita ; Zhou, Weibin ; Sloan, Alexis J. ; Ji, Ziming ; Xie, Letian X. ; Salviati, Leonardo ; Hurd, Toby W. ; Vega-Warner, Virginia ; Killen, Paul D. ; Raphael, Yehoash ; Ashraf, Shazia ; Ovunc, Bugsu ; Schoeb, Dominik S. ; McLaughlin, Heather M. ; Airik, Rannar ; Vlangos, Christopher N. ; Gbadegesin, Rasheed ; Hinkes, Bernward ; Saisawat, Pawaree ; Trevisson, Eva ; Doimo, Mara ; Casarin, Alberto ; Pertegato, Vanessa ; Giorgi, Gianpietro ; Prokisch, Holger ; Rötig, Agnès ; Nürnberg, Gudrun ; Becker, Christian ; Wang, Su ; Ozaltin, Fatih ; Topaloglu, Rezan ; Bakkaloglu, Aysin ; Bakkaloglu, Sevcan A. ; Müller, Dominik ; Beissert, Antje ; Mir, Sevgi ; Berdeli, Afig ; ϖzen, Seza ; Zenker, Martin ; Matejas, Verena ; Santos-Ocaña, Carlos ; Navas, Placido ; Kusakabe, Takehiro ; Kispert, Andreas ; Akman, Sema ; Soliman, Neveen A. ; Krick, Stefanie ; Mundel, Peter ; Reiser, Jochen ; Nürnberg, Peter ; Clarke, Catherine F. ; Wiggins, Roger C. ; Faul, Christian ; Hildebrandt, Friedhelm
Publisher:United States: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2011-05, Vol.121 (5), p.2013-2024
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ArticlesPeer ReviewedFull Text
FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair
Author / Creator:Zhou, Weibin ; Otto, Edgar A ; Cluckey, Andrew ; Airik, Rannar ; Hurd, Toby W ; Chaki, Moumita ; Diaz, Katrina ; Lach, Francis P ; Bennett, Geoffrey R ; Gee, Heon Yung ; Ghosh, Amiya K ; Natarajan, Sivakumar ; Thongthip, Supawat ; Veturi, Uma ; Allen, Susan J ; Janssen, Sabine ; Ramaswami, Gokul ; Dixon, Joanne ; Burkhalter, Felix ; Spoendlin, Martin ; Moch, Holger ; Mihatsch, Michael J ; Verine, Jerome ; Reade, Richard ; Soliman, Hany ; Godin, Michel ; Kiss, Denes ; Monga, Guido ; Mazzucco, Gianna ; Amann, Kerstin ; Artunc, Ferruh ; Newland, Ronald C ; Wiech, Thorsten ; Zschiedrich, Stefan ; Huber, Tobias B ; Friedl, Andreas ; Slaats, Gisela G ; Joles, Jaap A ; Goldschmeding, Roel ; Washburn, Joseph ; Giles, Rachel H ; Levy, Shawn ; Smogorzewska, Agata ; Hildebrandt, Friedhelm
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2012-08, Vol.44 (8), p.910-915
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Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis
Author / Creator:Saisawat, Pawaree ; Tasic, Velibor ; Vega-Warner, Virginia ; Kehinde, Elijah O. ; Günther, Barbara ; Airik, Rannar ; Innis, Jeffrey W. ; Hoskins, Bethan E. ; Hoefele, Julia ; Otto, Edgar A. ; Hildebrandt, Friedhelm
Publisher:Basingstoke: Elsevier Inc
Journal title:Kidney international, 2012-01, Vol.81 (2), p.196-200
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Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
Author / Creator:Hinkes, Bernward ; Wiggins, Roger C ; Gbadegesin, Rasheed ; Vlangos, Christopher N ; Seelow, Dominik ; Nürnberg, Gudrun ; Garg, Puneet ; Verma, Rakesh ; Chaib, Hassan ; Hoskins, Bethan E ; Ashraf, Shazia ; Becker, Christian ; Hennies, Hans Christian ; Goyal, Meera ; Wharram, Bryan L ; Schachter, Asher D ; Mudumana, Sudha ; Drummond, Iain ; Kerjaschki, Dontscho ; Waldherr, Rüdiger ; Dietrich, Alexander ; Ozaltin, Fatih ; Bakkaloglu, Aysin ; Cleper, Roxana ; Basel-Vanagaite, Lina ; Pohl, Martin ; Griebel, Martin ; Tsygin, Alexey N ; Soylu, Alper ; Müller, Dominik ; Sorli, Caroline S ; Bunney, Tom D ; Katan, Matilda ; Liu, Jinhong ; Attanasio, Massimo ; O'Toole, John F ; Hasselbacher, Katrin ; Mucha, Bettina ; Otto, Edgar A ; Airik, Rannar ; Kispert, Andreas ; Kelley, Grant G ; Smrcka, Alan V ; Gudermann, Thomas ; Holzman, Lawrence B ; Nürnberg, Peter ; Hildebrandt, Friedhelm
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2006-12, Vol.38 (12), p.1397-1405
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Tbx18 regulates the development of the ureteral mesenchyme
Author / Creator:Airik, R.
Publisher:United States: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2006-03, Vol.116 (3), p.663-674
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Mutation analysis in Bardet-Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals
Author / Creator:Janssen, Sabine ; Ramaswami, Gokul ; Davis, Erica E ; Hurd, Toby ; Airik, Rannar ; Kasanuki, Jennifer M ; Van Der Kraak, Lauren ; Allen, Susan J ; Beales, Philip L ; Katsanis, Nicholas ; Otto, Edgar A ; Hildebrandt, Friedhelm
Publisher:Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag
Journal title:Human genetics, 2011-01, Vol.129 (1), p.79-90
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ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ sub( 10) biosynthesis disruption
Author / Creator:Ashraf, Shazia ; Gee, Heon Yung ; Woerner, Stephanie ; Xie, Letian X ; Vega-Warner, Virginia ; Lovric, Svjetlana ; Fang, Humphrey ; Song, Xuewen ; Cattran, Daniel C ; Avila-Casado, Carmen ; Paterson, Andrew D ; Nitschke, Patrick ; Bole-Feysot, Christine ; Cochat, Pierre ; Esteve-Rudd, Julian ; Haberberger, Birgit ; Allen, Susan J ; Zhou, Weibin ; Airik, Rannar ; Otto, Edgar A ; Barua, Moumita ; Al-Hamed, Mohamed H ; Kari, Jameela A ; Evans, Jonathan ; Bierzynska, Agnieszka ; Saleem, Moin A ; Bockenhauer, Detlef ; Kleta, Robert ; El Desoky, Sherif ; Hacihamdioglu, Duygu O ; Gok, Faysal ; Washburn, Joseph ; Wiggins, Roger C ; Choi, Murim ; Lifton, Richard P ; Levy, Shawn ; Han, Zhe ; Salviati, Leonardo ; Prokisch, Holger ; Williams, David S ; Pollak, Martin ; Clarke, Catherine F ; Pei, York ; Antignac, Corinne ; Hildebrandt, Friedhelm
Journal title:The Journal of clinical investigation, 2013-12, Vol.123 (12), p.5179-5179
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ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ^sub 10^ biosynthesis disruption
Author / Creator:Ashraf, Shazia ; Gee, Heon Yung ; Woerner, Stephanie ; Xie, Letian X ; Vega-Warner, Virginia ; Lovric, Svjetlana ; Fang, Humphrey ; Song, Xuewen ; Cattran, Daniel C ; Avila-Casado, Carmen ; Paterson, Andrew D ; Nitschké, Patrick ; Bole-Feysot, Christine ; Cochat, Pierre ; Esteve-Rudd, Julian ; Haberberger, Birgit ; Allen, Susan J ; Zhou, Weibin ; Airik, Rannar ; Otto, Edgar A ; Barua, Moumita ; Al-Hamed, Mohamed H ; Kari, Jameela A ; Evans, Jonathan ; Bierzynska, Agnieszka ; Saleem, Moin A ; Böckenhauer, Detlef ; Kleta, Robert ; El Desoky, Sherif ; Hacihamdioglu, Duygu O ; Gok, Faysal ; Washburn, Joseph ; Wiggins, Roger C ; Choi, Murim ; Lifton, Richard P ; Levy, Shawn ; Han, Zhe ; Salviati, Leonardo ; Prokisch, Holger ; Williams, David S ; Pollak, Martin ; Clarke, Catherine F ; Pei, York ; Antignac, Corinne ; Hildebrandt, Friedhelm
Publisher:Ann Arbor: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2013-12, Vol.123 (12), p.5179
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Airik, Rannar

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Airik, Rannar

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

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JP4-039 Mitigates Cisplatin-Induced Acute Kidney Injury by Inhibiting Oxidative Stress and Blocking Apoptosis and Ferroptosis in Mice

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Osteoclast stimulation factor 1 (Ostf1) KNOCKOUT increases trabecular bone mass in mice

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

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SDCCAG8 Interacts with RAB Effector Proteins RABEP2 and ERC1 and Is Required for Hedgehog Signaling

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Mitochondrial ROS Triggers KIN Pathogenesis in FAN1-Deficient Kidneys

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TSHZ3 and SOX9 Regulate the Timing of Smooth Muscle Cell Differentiation in the Ureter by Reducing Myocardin Activity

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Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium

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COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

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FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair

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Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis

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Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

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Tbx18 regulates the development of the ureteral mesenchyme

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Mutation analysis in Bardet-Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals

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ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ sub( 10) biosynthesis disruption

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ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ^sub 10^ biosynthesis disruption

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