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rannar.airik@childrens.harvard.edu

Teenistuskäik

Töökohad ja ametid
01.01.2013–...   
Bostoni Lastehaigla
01.01.2009–31.12.2013   
Michigani Ülikool
01.01.2008–31.12.2009   
Hannoveri Meditsiiniülikool
 
 
Haridustee
2004–2008   
Hannoveri Meditsiiniülikool, molekulaarbioloogia PhD
2002–2004   
Tartu Ülikool, arengubioloogia MSc
1998–2002   
Tartu Ülikool, zooloogia BSc

Publikatsioonid

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Publikatsioon
 
1.1.
2013
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2013
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2012
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2012
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2011
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2007
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6.7.
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19.06.2019

Otsi publikatsiooni

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PublikatsioonAutoridAastaVäljaande pealkiriKlassifikaatorFailAsutused
Tbx18 expression demarcates multipotent precursor populations in the developing urogenital system but is exclusively required within the ureteric mesenchymal lineage to suppress a renal stromal fateBohnenpoll, Tobias; Bettenhausen, Eva; Weiss, Anna-Carina; Foik, Anna B.; Trowe, Mark-Oliver; Blank, Patrick; Airik, Rannar; Kispert, Andreas2013Developmental Biology1.1.Medizinische Hochschule Hannover
TSHZ3 and SOX9 Regulate the Timing of Smooth Muscle Cell Differentiation in the Ureter by Reducing Myocardin ActivityMartin, Elise; Caubit, Xavier; Airik, Rannar; Vola, Christine; Fatmi, Ahmed; Kispert, Andreas; Fasano, Laurent2013PLoS ONE1.1.
Canonical Wnt signaling regulates smooth muscle precursor development in the mouse ureterTrowe, Mark-Oliver; Airik, Rannar; Weiss, Anna-Carina; Farin, Henner F.; Foik, Anna B.; Bettenhausen, Eva; Schuster-Gossler, Karin; Taketo, Makoto Mark; Kispert, Andreas2012Development1.1.
FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repairZhou, 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 ... Hildebrandt, Friedhelm2012Nature Genetics1.1.
Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesisSaisawat, Pawaree; Tasic, Velibor; Vega-Warner, Virginia; Kehinde, Elijah O; Gunther, Barbara; Airik, Rannar; Innis, Jeffrey W; Hoskins, Bethan E; Hoefele, Julia; Otto, Edgar A; Hildebrandt, Friedhelm2012Kidney International1.1.
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafnessHeeringa, 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 ... Hildebrandt, Friedhelm2011The Journal of Clinical Investigation1.1.
Mutation analysis in Bardet–Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals (Human Genetics)Janssen, Sabine; Ramaswami, Gokul; Davis, EricaE.; Hurd, Toby; Airik, Rannar; Kasanuki, JenniferM.; Kraak, Lauren; Allen, SusanJ.; Beales, PhilipL.; Katsanis, Nicholas; Otto, EdgarA.; Hildebrandt, Friedhelm2011Human Genetics1.1.Michigani Ülikool
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategyOtto, EA; Ramaswami, G; Janssen, S; Chaki, M; Allen, SJ; Zhou, W; Airik, R; Hurd, TW; Ghosh, AK; Wolf, MT; Hoppe, B; Neuhaus, TJ; Bockenhauer, D; Milford, DV; Soliman, NA; Antignac, C; Saunier, S; Johnson, CA; Hildebrandt, F. GPN Study Group: Bergmann, C; Zerres, K ... Bitzan, M.2011Journal of Medical Genetics1.1.Tartu Ülikool, Arstiteaduskond, Lastekliinik, Pediaatria õppetool;
SA Tartu Ülikooli Kliinikum
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategyOtto, Edgar A; Ramaswami, Gokul; Janssen, Sabine; Chaki, Moumita; Allen, Susan J; Zhou, Weibin; Airik, Rannar; Hurd, Toby W; Ghosh, Amiya K; Wolf, Matthias T; Hoppe, Bernd; Neuhaus, Thomas J; Bockenhauer, Detlef; Milford, David V; Soliman, Neveen A; Antignac, Corinne; Saunier, Sophie; Johnson, Colin A; Hildebrandt, Friedhelm; the, GPN Study Group2011Journal of Medical Genetics1.1.
Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathyOtto, Edgar A; Hurd, Toby W; Airik, Rannar; Chaki, Moumita; Zhou, Weibin; Stoetzel, Corinne; Patil, Suresh B; Levy, Shawn; Ghosh, Amiya K; Murga-Zamalloa, Carlos A; van Reeuwijk, Jeroen; Letteboer, Stef J F; Sang, Liyun; Giles, Rachel H; Liu, Qin; Coene, Karlien L M; Estrada-Cuzcano, Alejandro; Collin, Rob W J; McLaughlin, Heather M; Held, Susanne ... Hildebrandt, Friedhelm2010Nature Genetics1.1.
Hydroureternephrosis due to loss of Sox9-regulated smooth muscle cell differentiation of the ureteric mesenchymeAirik, Rannar; Trowe, Mark-Oliver; Foik, Anna; Farin, Henner F.; Petry, Marianne; Schuster-Gossler, Karin; Schweizer, Michaela; Scherer, Gerd; Kist, Ralf; Kispert, Andreas2010Human Molecular Genetics1.1.
Loss of Sox9 in the periotic mesenchyme affects mesenchymal expansion and differentiation, and epithelial morphogenesis during cochlea development in the mouseTrowe, Mark-Oliver; Shah, Sadrick; Petry, Marianne; Airik, Rannar; Schuster-Gossler, Karin; Kist, Ralf; Kispert, Andreas2010Developmental Biology1.1.
Formation of the Sinus Node Head and Differentiation of Sinus Node Myocardium Are Independently Regulated by Tbx18 and Tbx3Wiese, Cornelia; Grieskamp, Thomas; Airik, Rannar; Mommersteeg, Mathilda T.M.; Gardiwal, Ajmal; de Gier-de Vries, Corrie; Schuster-Gossler, Karin; Moorman, Antoon F.M.; Kispert, Andreas; Christoffels, Vincent M.2009Circulation Research1.1.
The Tbx2 Primary Myocardium of the Atrioventricular Canal Forms the Atrioventricular Node and the Base of the Left VentricleAanhaanen, Wim T.J.; Brons, Janynke F.; Domínguez, Jorge N.; Rana, M. Sameer; Norden, Julia; Airik, Rannar; Wakker, Vincent; de Gier-de Vries, Corrie; Brown, Nigel A.; Kispert, Andreas; Moorman, Antoon F.M.; Christoffels, Vincent M.2009Circulation Research1.1.
Down the tube of obstructive nephropathies: The importance of tissue interactions during ureter developmentAirik, R; Kispert, A2007Kidney International1.1.
The prepattern transcription factor Irx3 directs nephron segment identityReggiani, Luca; Raciti, Daniela; Airik, Rannar; Kispert, Andreas; Brandli, Andre W.2007Genes and Development1.1.
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversibleHinkes, Bernward; Wiggins, Roger C; Gbadegesin, Rasheed; Vlangos, Christopher N; Seelow, Dominik; Nurnberg, 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, Rudiger ... Hildebrandt, Friedhelm2006Nature Genetics1.1.
Tbx18 regulates the developmentAirik, Rannar; Bussen, Markus; Singh, Manvendra K.; Petry, Marianne; Kispert, Andreas2006The Journal of Clinical Investigation1.1.
Gene expression analysis of Gata3(-/-) mice by using cDNA microarray technologyAirik, R.; Karner, M.; Karis, A.; Karner, J.2005Life Sciences1.1.Tartu Ülikool;
Tartu Ülikool, Bioloogia-geograafiateaduskond, Zooloogia ja hüdrobioloogia instituut;
ELNET;
Tartu Ülikool, Loodus- ja tehnoloogiateaduskond, Tartu Ülikooli Molekulaar- ja Rakubioloogia Instituut, Arengubioloogia õppetool;
Eesti Maaülikool, Rektori vastutusala, rektoraat
Gene expression analysis of Gata3-/- mice by using cDNA microarray technology : m.sc. thesis : developmental biologyAirik, Rannar20046.7.Tartu Ülikool