Universitätsklinikum Tübingen

Centre for Ophthalmology

↳ University Eye Hospital

↳ Institute for Ophthalmic Research

Institute for Ophthalmic Research

Ophthalmology Universität Tübingen
Sitemap » Home  » Research Units  » Ueffing Lab  » Members  » Prof. Dr. rer. nat. Marius Ueffing

Prof. Dr. rer. nat. Marius Ueffing

Position

Director, Institute for Ophthalmic Research

Contacts details

Address

Centre for Ophthalmology
Institute for Ophthalmic Research
Roentgenweg 11
72076 Tuebingen

Phone, fax

Phone+49 7071 29-84021
Fax+49 7071 29-4560

WWW

Emailmarius.ueffing@uni-tuebingen.de
 
 

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Selected publications

Griciuc A, Aron L, Ueffing M.
"Looking into eyes: rhodopsin pathologies in Drosophila.",
Adv Exp Med Biol. 2012;723:415-23. PubMed PMID: 22183360. Lookup in PubMed Lookup in Google Scholar

Kortvely E, Ueffing M.
"Common mechanisms for separate maculopathies?",
Adv Exp Med Biol. 2012;723:61-6. PubMed PMID: 22183316. Lookup in PubMed Lookup in Google Scholar

Kiel C, Vogt A, Campagna A, Chatr-aryamontri A, Swiatek-de Lange M, Beer M, Bolz S, Mack AF, Kinkl N, Cesareni G, Serrano L, Ueffing M.
"Structural and functional protein network analyses predict novel signaling functions for rhodopsin.",
Mol Syst Biol. 2011 Nov 22;7:551. doi: 10.1038/msb.2011.83. PubMed PMID: 22108793. Lookup in PubMed Lookup in Google Scholar

Stanton CM, Yates JR, den Hollander AI, Seddon JM, Swaroop A, Stambolian D, Fauser S, Hoyng C, Yu Y, Atsuhiro K, Branham K, Othman M, Chen W, Kortvely E, Chalmers K, Hayward C, Moore AT, Dhillon B, Ueffing M, Wright AF.
"Complement factor D in age-related macular degeneration.",
Invest Ophthalmol Vis Sci. 2011 Nov 11;52(12):8828-34. Print 2011. PubMed PMID: 22003108; PubMed Central PMCID: PMC3230905. Lookup in PubMed Lookup in Google Scholar

Van Campenhout CA, Eitelhuber A, Gloeckner CJ, Giallonardo P, Gegg M, Oller H, Grant SG, Krappmann D, Ueffing M, Lickert H.
"Dlg3 trafficking and apical tight junction formation is regulated by nedd4 and nedd4-2 e3 ubiquitin ligases.",
Dev Cell. 2011 Sep 13;21(3):479-91. PubMed PMID: 21920314. Lookup in PubMed Lookup in Google Scholar

Coene KL, Mans DA, Boldt K, Gloeckner CJ, van Reeuwijk J, Bolat E, Roosing S, Letteboer SJ, Peters TA, Cremers FP, Ueffing M, Roepman R.
The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase.",
Hum Mol Genet. 2011 Sep 15;20(18):3592-605. Epub 2011 Jun 17. PubMed PMID: 21685204. Lookup in PubMed Lookup in Google Scholar

Griciuc A, Aron L, Ueffing M.
"ER stress in retinal degeneration: a target for rational therapy?",
Trends Mol Med. 2011 Aug;17(8):442-51. Epub 2011 May 27. Review. PubMed PMID: 21620769. Lookup in PubMed Lookup in Google Scholar

Boldt K, Mans DA, Won J, van Reeuwijk J, Vogt A, Kinkl N, Letteboer SJ, Hicks WL, Hurd RE, Naggert JK, Texier Y, den Hollander AI, Koenekoop RK, Bennett J, Cremers FP, Gloeckner CJ, Nishina PM, Roepman R, Ueffing M.
"Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice.",
J Clin Invest. 2011 Jun 1;121(6):2169-80. doi: 10.1172/JCI45627. Epub 2011 May 23. PubMed PMID: 21606596; PubMed Central PMCID: PMC3104757. Lookup in PubMed Lookup in Google Scholar

Webb KJ, Coolen M, Gloeckner CJ, Stigloher C, Bahn B, Topp S, Ueffing M, Bally-Cuif L.
"The Enhancer of split transcription factor Her8a is a novel dimerisation partner for Her3 that controls anterior hindbrain neurogenesis in zebrafish.",
BMC Dev Biol. 2011 May 17;11:27. PubMed PMID: 21586122; PubMed Central PMCID: PMC3125270. Lookup in PubMed Lookup in Google Scholar

Del Río P, Irmler M, Arango-González B, Favor J, Bobe C, Bartsch U, Vecino E, Beckers J, Hauck SM, Ueffing M.
"GDNF-induced osteopontin from Müller glial cells promotes photoreceptor survival in the Pde6brd1 mouse model of retinal degeneration.",
Glia. 2011 May;59(5):821-32. doi: 10.1002/glia.21155. Epub 2011 Feb 28. PubMed PMID: 21360756 Lookup in PubMed Lookup in Google Scholar

Griciuc A, Aron L, Roux MJ, Klein R, Giangrande A, Ueffing M. (2010)
"Inactivation of VCP/ter94 suppresses retinal pathology caused by misfolded rhodopsin in Drosophila.",
PLoS Genet. Aug 26;6(8). pii: e1001075. Lookup in PubMed Lookup in Google Scholar

Kinzel D, Boldt K, Davis EE, Burtscher I, Trümbach D, Diplas B, Attié-Bitach T, Wurst W, Katsanis N, Ueffing M, Lickert H. (2010).
"Pitchfork regulates primary cilia disassembly and left-right asymmetry.",
Dev Cell. 2010 Jul 20;19(1):66-77. Lookup in PubMed Lookup in Google Scholar

Hauck SM, Dietter J, Kramer RL, Hofmaier F, Zipplies JK, Amann B, Feuchtinger A, Deeg CA, Ueffing M. (2010).
"Deciphering membrane-associated molecular processes in target tissue of autoimmune uveitis by label-free quantitative mass spectrometry.",
Mol Cell Proteomics. 9:2292-305 Lookup in PubMed Lookup in Google Scholar

Hauck SM, Gloeckner CJ, Harley ME, Schoeffmann S, Boldt K, Ekstrom PA, Ueffing M.
"Identification of paracrine neuroprotective candidate proteins by a functional assay-driven proteomics approach.",
Mol Cell Proteomics. 2008 Jul;7(7):1349-61. Lookup in PubMed Lookup in Google Scholar

Deeg CA, Raith AJ, Amann B, Crabb JW, Thurau SR, Hauck SM, Ueffing M, Wildner G, Stangassinger M.
"CRALBP is a highly prevalent autoantigen for human autoimmune uveitis.",
Clin Dev Immunol. 2007;2007:39245. Lookup in PubMed Lookup in Google Scholar

Paquet-Durand F, Silva J, Talukdar T, Johnson LE, Azadi S, van Veen T, Ueffing M, Hauck SM, Ekström PA.
"Excessive activation of poly(ADP-ribose)polymerase contributes to inherited photoreceptor degeneration in the retinal degeneration 1 mouse.",
J Neurosci. 2007 Sep 19;27(38):10311-9. Lookup in PubMed Lookup in Google Scholar

den Hollander AI, Koenekoop RK, Mohamed MD, Arts HH, Boldt K, Towns KV,Sedmak T, Beer M, Nagel-Wolfrum K, McKibbin M, Dharmaraj S, Lopez I, Ivings L,Williams GA, Springell K, Woods CG, Jafri H, Rashid Y, Strom TM, van der Zwaag B,Gosens I, Kersten FF, van Wijk E, Veltman JA, Zonneveld MN, van Beersum SE, Maumenee IH, Wolfrum U, Cheetham ME, Ueffing M, Cremers FP, Inglehearn CF, Roepman R. (2007).
"Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.",
Nat Genet. Jul;39:889-95. Lookup in PubMed Lookup in Google Scholar

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