[Link zur Startseite Institut für Humangenetik - Universität Regensburg] [Link zur Startseite der Universität Regensburg]
[Bauteil_D3_frontal_200x150.jpg]
[Humangenetik_mit_Logo_656x150.gif]
[Logo Zentrum für familiären Brust- und Eierstockkrebs Regensburg | Brustkrebs | Eierstockkrebs] ZFBEK : [Logo Deutsches Konsortium Familiärer Brust- und Eierstockkrebs : [Logo PRO RETINA-Stiftung] PRO RETINA-Stiftung : RIGeL : [FOR1075 Auge] FOR1075 [FOR1075 Logo] : [Logo Universität Regensburg] : [Logo Universitätsklinikum Regensburg] : Retina Datenbank : BEST1 Datenbank : english [english flag]


  Letzte Aktualisierung
07. Juli 2017
Veranstaltungen im Wintersemester 2006/2007
Literaturseminar (55 661)
Freitag, 20.10.2006 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dipl. Biol. Johanna Förster, Doktorandin
Tan et al.
Expression of cone-photoreceptor-specific antigens in a cell line derived from retinal tumors in transgenic mice.
Invest Ophthalmol Vis Sci. 2004 Mar;45(3):764-8.

Tan et al. Expression of cone-photoreceptor-specific antigens in a cell line derived from retinal tumors in transgenic mice. Invest Ophthalmol Vis Sci. 2004 Mar;45(3):764-8.

Tan et al. Expression of cone-photoreceptor-specific antigens in a cell line derived from retinal tumors in transgenic mice. Invest Ophthalmol Vis Sci. 2004 Mar;45(3):764-8.
Dipl. Biol. Marton Fogarasi, Doktorand
Wang et al. TIMP-3 inhibits the procollagen N-proteinase ADAMTS-2. Biochem J. 2006 Sep 15;398(3):515-9.
Freitag, 27.10.2006 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dr. rer. nat. Bernd Becker, Postdoc
Komatsu et al. Loss of autophagy in the central nervous system causes neurodegeneration in mice. Nature. 2006 Jun 15;441(7095):880-4.
Dipl. Biol. Lars Fritsche, Doktorand
Yang et al. A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration. Science. 2006 Nov 10;314(5801):992-3.
Freitag, 03.11.2006 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dr. rer. nat. Christian Morsczeck, AG-Leiter
Benzing et al. Neural conversion of human embryonic stem cell colonies in the presence of fibroblast growth factor-2. Neuroreport. 2006 Nov 6;17(16):1675-81.
Stefan Bieber, FH-Forschungs-Praktikant
Chada et al. The synergy site of fibronectin is required for strong interaction with the platelet integrin alphaIIbbeta3. Ann Biomed Eng. 2006 Oct;34(10):1542-52.
Freitag, 10.11.2006 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dipl. Biol. Andreas Janßen, Doktorand
Hageman et al. An integrated hypothesis that considers drusen as biomarkers of immune-mediated processes at the RPE-Bruch's membrane interface in aging and age-related macular degeneration. Prog Retin Eye Res. 2001 Nov;20(6):705-32.
Dr. med. Britta Fiebig, Ärztin
Wu et al. Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans. Am J Hum Genet. 2006 Sep;79(3):574-9.
Freitag, 17.11.2006 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
PD Dr. rer. nat. Thomas Langmann, AG-Leiter
Sasmono et al. A macrophage colony-stimulating factor receptor-green fluorescent protein transgene is expressed throughout the mononuclear phagocyte system of the mouse. Blood. 2003 Feb 1;101(3):1155-63.
Maike Steffan, medizinische Doktorandin
Kang et al. Evaluation of models to predict BRCA germline mutations. Br J Cancer. 2006 Oct 9;95(7):914-20.
Freitag, 24.11.2006 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dipl. Biol. Thomas Loenhardt, Doktorand
Steiner-Champliaud et al. Retinoschisin forms a multi-molecular complex with extracellular matrix and cytoplasmic proteins: interactions with β2 laminin and αB-crystallin. Mol Vis. 2006 Aug 10;12:892-901.
Nina Zerelles, medizinische Doktorandin
Jaakson et al. Genotyping microarray (gene chip) for the ABCR (ABCA4) gene. Hum Mutat. 2003 Nov;22(5):395-403.
Freitag, 01.12.2006 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dipl. Biol. Florian Rauscher, Doktorand
Brown et al. Ranibizumab versus verteporfin for neovascular age-related macular degeneration. N Engl J Med. 2006 Oct 5;355(14):1432-44.

Rosenfeld et al. Ranibizumab for neovascular age-related macular degeneration. N Engl J Med. 2006 Oct 5;355(14):1419-31.
Freitag, 08.12.2006 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dipl. Biol. Johanna Förster, Doktorandin
Reiners et al. Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2. Hum Mol Genet. 2005 Dec 15;14(24):3933-43.
Dipl. Biol. Marton Fogarasi, Doktorand
Langton et al. Sorsby's fundus dystrophy mutations impair turnover of TIMP-3 by retinal pigment epithelial cells. Hum Mol Genet. 2005 Dec 1;14(23):3579-86.
Freitag, 15.12.2006 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dipl. Biol. Lars Fritsche, Doktorand
Bierut et al. Novel Genes Identified in a High Density Genome Wide Association Study for Nicotine Dependence. Hum Mol Genet. 2007 Jan 1;16(1):24-35
Freitag, 12.01.2007 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dr. rer. nat. Christian Morsczeck, AG-Leiter
Sonoyama et al. Mesenchymal stem cell-mediated functional tooth regeneration in Swine. PLoS ONE. 2006 Dec 20;1:e79.
Stefan Bieber, FH-Forschungs-Praktikant
Humphries et al. Retinopathy induced in mice by targeted disruption of the rhodopsin gene. Nat Genet. 1997 Feb;15(2):216-9.

Biel et al. Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3. Proc Natl Acad Sci U S A. 1999 Jun 22;96(13):7553-7.

Claes et al. Morphological characterization of the retina of the CNGA3(-/-)Rho(-/-) mutant mouse lacking functional cones and rods. Invest Ophthalmol Vis Sci. 2004 Jun;45(6):2039-48.
Freitag, 19.01.2007 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dipl. Biol. Andreas Janßen, Doktorand
Lein et al. Genom-wide atlas of gene expression in the adult mouse brain. Nature. 2007 Jan 11;445(7124):168-76
Dr. med. Britta Fiebig, Ärztin
Seal et al. Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet. 2006 Nov;38(11):1239-41.
Freitag, 26.01.2007 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
PD Dr. rer. nat. Thomas Langmann, AG-Leiter
Gilchrist et al. Systems biology approaches identify ATF3 as a negative regulator of Toll-like receptor 4. Nature. 2006 May 11;441(7090):173-8.
Nina Zerelles, medizinische Doktorandin
Fingert et al. Case of Stargardt disease caused by uniparental isodisomy. Arch Ophthalmol. 2006 May;124(5):744-5.
Freitag, 02.02.2007 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dipl. Biol. Thomas Loenhardt, Doktorand
Kimchi-Sarfaty et al. A "silent" polymorphism in the MDR1 gene changes substrate specificity. Science. 2007 Jan 26;315(5811):525-8.
Karin Weigelt, Diplomandin
Haynes et al. The P2Y12 receptor regulates microglial activation by extracellular nucleotides. Nat Neurosci. 2006 Dec;9(12):1512-9.
Freitag, 09.02.2007 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dipl. Biol. Florian Rauscher, Doktorand
Heintzman et al. Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome. Nat Genet. 2007 Mar;39(3):311-8.
Freitag, 16.02.2007 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Christine Lai, Bachelor-Studentin
Oh et al. Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL. Proc Natl Acad Sci U S A. 2007 Jan 30;104(5):1679-84.
Dipl. Biol. Marton Fogarasi, Doktorand
Marmorstein et al. Aberrant accumulation of EFEMP1 underlies drusen formation in Malattia Leventinese and age-related macular degeneration. Proc Natl Acad Sci USA. 2002 Oct 1;99(20):13067-72.
Freitag, 23.02.2007 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dipl. Biol. Johanna Förster, Doktorandin
van de Pavert et al. A single amino acid substitution (Cys249Trp) in Crb1 causes retinal degeneration and deregulates expression of pituitary tumor transforming gene Pttg1. J Neurosci. 2007 Jan 17;27(3):564-73.
Dipl. Biol. Lars Fritsche, Doktorand
Redon et al. Global variation in copy number in the human genome. Nature. 2006 Nov 23;444(7118):444-54.
Freitag, 02.03.2007 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dr. rer. nat. Christian Morsczeck, AG-Leiter
Wang et al. Endothelial cells derived from human embryonic stem cells form durable blood vessels in vivo. Nat Biotechnol. 2007 Mar;25(3):317-8.
Maike Steffan, medizinische Doktorandin
Smith et al. Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening. J Med Genet. 2007 Jan;44(1):10-15.
Freitag, 23.03.2007 08.30 Uhr; Seminarraum der Humangenetik, A2, 2. OG, Raum 3
Dipl. Biol. Andreas Janßen, Doktorand
Chen et al. Synthesis of complement factor H by retinal pigment epithelial cells is down-regulated by oxidized photoreceptor outer segments. Exp Eye Res. 2007 Apr;84(4):635-45.
Dr. med. Britta Fiebig, Ärztin
Marchant et al. New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophy. J Med Genet. 2007 Mar;44(3):e70.