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  last updated
October 01, 2014
Former terms:
Extracurricular activities for Summer Term 2014
Journal Club (56 121)
Thursday, 10.04.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Sabrina Unkel, Doktorandin
Thursday, 17.04.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Benedikt Nagel, Doktorand
Texier et al.
Elution Profile Analysis of SDS-induced Subcomplexes by Quantitative Mass Spectrometry.
Mol Cell Proteomics. 2014 May;13(5):1382-1391.
Thursday, 24.04.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Julia Junghans, Wahlmodulstudentin
Topic to be announced
Thursday, 08.05.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Karoline Wissmann, Doktorandin
Chen et al.
PRPF4 mutations cause autosomal dominant retinitis pigmentosa.
Hum Mol Genet. 2014 Jun 1;23(11):2926-39. doi: 10.1093/hmg/ddu005.
Thursday, 15.05.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Felix Graßmann, Doktorand
Hinkel et al.
Inhibition of microRNA-92a protects against ischemia/reperfusion injury in a large-animal model.
Circulation. 2013 Sep 3;128(10):1066-75. doi: 10.1161/CIRCULATIONAHA.113.001904.
Thursday, 22.05.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Shyamtanu Datta, Doktorand
Thursday, 05.06.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Lisa Braun, Masterstudentin
Traka et al.
WDR81 is necessary for purkinje and photoreceptor cell survival.
J Neurosci. 2013 Apr 17;33(16):6834-44. doi: 10.1523/JNEUROSCI.2394-12.2013.
Thursday, 12.06.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Sibylle Rosendahl, Doktorandin
Thursday, 26.06.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Maria Baier, Bachelorstudentin Molekulare Medizin
Schmid et al.
Mutation- and tissue-specific alterations of RPGR transcripts.
Invest Ophthalmol Vis Sci. 2010 Mar;51(3):1628-35. doi: 10.1167/iovs.09-4031.
Thursday, 10.07.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Anja Wessely, Bachelorstudentin Molekulare Medizin
Weedon et al.
Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis.
Nat Genet. 2014 Jan;46(1):61-4. doi: 10.1038/ng.2826.
Thursday, 17.07.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Stefanie Joos, med. Doktorandin
Byrne et al.
Retinoschisin gene therapy in photoreceptors, Mller glia or all retinal cells in the Rs1h-/- mouse.
Gene Ther. 2014 Jun;21(6):585-92. doi: 10.1038/gt.2014.31.
Thursday, 24.07.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Anja Schulz-Kuhnt, Bachelorstudentin Molekulare Medizin
Flachsbart et al.
Investigation of complement component C4 copy number variation in human longevity.
PLoS One. 2014 Jan 22;9(1):e86188. doi: 10.1371/journal.pone.0086188. eCollection 2014.
Thursday, 31.07.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Laura Kuhn, Bachelorstudentin
Thurman et al.
Detection of complement activation using monoclonal antibodies against C3d.
J Clin Invest. 2013 May 1;123(5):2218-30. doi: 10.1172/JCI65861.
Thursday, 18.09.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Topic to be announced
Thursday, 25.09.2014 12:30am; Seminar Room Human Genetics, A2, 2. Floor, Room 3
Topic to be announced