Comparison of hybrid clones derived from human breast epithelial cells and three different cancer cell lines regarding in vitro cancer stem/ initiating cell properties
Fahlbusch, Sera Selina, Keil, Silvia, Epplen, Jörg T, Zänker, Kurt S, Dittmar, Thomas
Published in BMC cancer (19.05.2020)
Published in BMC cancer (19.05.2020)
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Journal Article
Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetries
Ocklenburg, Sebastian, Schmitz, Judith, Moinfar, Zahra, Moser, Dirk, Klose, Rena, Lor, Stephanie, Kunz, Georg, Tegenthoff, Martin, Faustmann, Pedro, Francks, Clyde, Epplen, Jörg T, Kumsta, Robert, Güntürkün, Onur
Published in eLife (01.02.2017)
Published in eLife (01.02.2017)
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Journal Article
Activation of NPY-Y2 receptors ameliorates disease pathology in the R6/2 mouse and PC12 cell models of Huntington's disease
Fatoba, Oluwaseun, Kloster, Eugen, Reick, Christiane, Saft, Carsten, Gold, Ralf, Epplen, Jörg T., Arning, Larissa, Ellrichmann, Gisa
Published in Experimental neurology (01.04.2018)
Published in Experimental neurology (01.04.2018)
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Journal Article
PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness
Arning, Larissa, Ocklenburg, Sebastian, Schulz, Stefanie, Ness, Vanessa, Gerding, Wanda M, Hengstler, Jan G, Falkenstein, Michael, Epplen, Jörg T, Güntürkün, Onur, Beste, Christian
Published in PloS one (27.06.2013)
Published in PloS one (27.06.2013)
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Journal Article
Pathogenetic and Clinical Aspects of Anti-Neutrophil Cytoplasmic Autoantibody-Associated Vasculitides
Lamprecht, Peter, Kerstein, Anja, Klapa, Sebastian, Schinke, Susanne, Karsten, Christian M, Yu, Xinhua, Ehlers, Marc, Epplen, Jörg T, Holl-Ulrich, Konstanze, Wiech, Thorsten, Kalies, Kathrin, Lange, Tanja, Laudien, Martin, Laskay, Tamas, Gemoll, Timo, Schumacher, Udo, Ullrich, Sebastian, Busch, Hauke, Ibrahim, Saleh, Fischer, Nicole, Hasselbacher, Katrin, Pries, Ralph, Petersen, Frank, Weppner, Gesche, Manz, Rudolf, Humrich, Jens Y, Nieberding, Relana, Riemekasten, Gabriela, Müller, Antje
Published in Frontiers in immunology (09.04.2018)
Published in Frontiers in immunology (09.04.2018)
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Journal Article
Handedness and the X chromosome: The role of androgen receptor CAG-repeat length
Arning, Larissa, Ocklenburg, Sebastian, Schulz, Stefanie, Ness, Vanessa, Gerding, Wanda M., Hengstler, Jan G., Falkenstein, Michael, Epplen, Jörg T., Güntürkün, Onur, Beste, Christian
Published in Scientific reports (09.02.2015)
Published in Scientific reports (09.02.2015)
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Journal Article
On the relevance of the NPY2-receptor variation for modes of action cascading processes
Beste, Christian, Stock, Ann-Kathrin, Epplen, Jörg T., Arning, Larissa
Published in NeuroImage (Orlando, Fla.) (15.11.2014)
Published in NeuroImage (Orlando, Fla.) (15.11.2014)
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Journal Article
Endocannabinergic modulation of central serotonergic activity in healthy human volunteers
Emons, Barbara, Arning, Larissa, Makulla, Vera-Estelle, Suchy, Maria-Theresia, Tsikas, Dimitrios, Lücke, Thomas, Epplen, Jörg T, Juckel, Georg, Roser, Patrik
Published in Annals of general psychiatry (17.03.2023)
Published in Annals of general psychiatry (17.03.2023)
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Journal Article
Prospective Evaluation of Predictive DNA Testing for Huntington’s Disease in a Large German Center
Ibisler, Aysegül, Ocklenburg, Sebastian, Stemmler, Susanne, Arning, Larissa, Epplen, Jörg T., Saft, Carsten, Hoffjan, Sabine
Published in Journal of genetic counseling (01.10.2017)
Published in Journal of genetic counseling (01.10.2017)
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Journal Article
Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes
Aydin, Gülsah, Dekomien, Gabriele, Hoffjan, Sabine, Gerding, Wanda Maria, Epplen, Jörg T, Arning, Larissa
Published in BMC neurology (09.01.2018)
Published in BMC neurology (09.01.2018)
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Journal Article
Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults
Ocklenburg, Sebastian, Arning, Larissa, Gerding, Wanda M., Hengstler, Jan G., Epplen, Jörg T., Güntürkün, Onur, Beste, Christian, Akkad, Denis A.
Published in Molecular neurobiology (01.11.2016)
Published in Molecular neurobiology (01.11.2016)
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Journal Article
Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization
Ocklenburg, Sebastian, Arning, Larissa, Hahn, Constanze, Gerding, Wanda M., Epplen, Jörg T., Güntürkün, Onur, Beste, Christian
Published in Behavioural brain research (20.11.2011)
Published in Behavioural brain research (20.11.2011)
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Journal Article
rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants
Glas, Jürgen, Seiderer, Julia, Wetzke, Martin, Konrad, Astrid, Török, Helga-Paula, Schmechel, Silke, Tonenchi, Laurian, Grassl, Christine, Dambacher, Julia, Pfennig, Simone, Maier, Kerstin, Griga, Thomas, Klein, Wolfram, Epplen, Jörg T, Schiemann, Uwe, Folwaczny, Christian, Lohse, Peter, Göke, Burkhard, Ochsenkühn, Thomas, Müller-Myhsok, Bertram, Folwaczny, Matthias, Mussack, Thomas, Brand, Stephan
Published in PloS one (05.09.2007)
Published in PloS one (05.09.2007)
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Journal Article
PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease
Taherzadeh-Fard, Elahe, Saft, Carsten, Akkad, Denis A, Wieczorek, Stefan, Haghikia, Aiden, Chan, Andrew, Epplen, Jörg T, Arning, Larissa
Published in Molecular neurodegeneration (19.05.2011)
Published in Molecular neurodegeneration (19.05.2011)
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Journal Article
The genetics of atopic dermatitis : recent findings and future options
HOFFJAN, Sabine, EPPLEN, Jörg T
Published in Journal of molecular medicine (Berlin, Germany) (01.09.2005)
Published in Journal of molecular medicine (Berlin, Germany) (01.09.2005)
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Journal Article
Cholecystokinin A receptor (CCKAR) gene variation is associated with language lateralization
Ocklenburg, Sebastian, Arning, Larissa, Gerding, Wanda M, Epplen, Jörg T, Güntürkün, Onur, Beste, Christian
Published in PloS one (14.01.2013)
Published in PloS one (14.01.2013)
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Journal Article
Ccdc66 null mutation causes retinal degeneration and dysfunction
GERDING, Wanda M, SCHREIBER, Sabrina, RÜLICKE, Thomas, IBRAHIM, Saleh, EPPLEN, Jörg T, PETRASCH-PARWEZ, Elisabeth, SCHULTE-MIDDELMANN, Tobias, DE CASTRO MARQUES, Andreia, ATORF, Jenny, AKKAD, Denis A, DEKOMIEN, Gabriele, KREMERS, Jan, DERMIETZEL, Rolf, GAL, Andreas
Published in Human molecular genetics (15.09.2011)
Published in Human molecular genetics (15.09.2011)
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Journal Article
Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset
Glas, Jürgen, Seiderer, Julia, Nagy, Melinda, Fries, Christoph, Beigel, Florian, Weidinger, Maria, Pfennig, Simone, Klein, Wolfram, Epplen, Jörg T, Lohse, Peter, Folwaczny, Matthias, Göke, Burkhard, Ochsenkühn, Thomas, Diegelmann, Julia, Müller-Myhsok, Bertram, Roeske, Darina, Brand, Stephan
Published in PloS one (29.04.2010)
Published in PloS one (29.04.2010)
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Journal Article
Automictic Reproduction in Interspecific Hybrids of Poeciliid Fish
Lampert, Kathrin P., Lamatsch, Dunja K., Fischer, Petra, Epplen, Jörg T., Nanda, Indrajit, Schmid, Michael, Schartl, Manfred
Published in Current biology (20.11.2007)
Published in Current biology (20.11.2007)
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Journal Article
Combinations of susceptibility genes are associated with higher risk for multiple sclerosis and imply disease course specificity
Akkad, Denis A, Olischewsky, Alexandra, Reiner, Franziska, Hellwig, Kerstin, Esser, Sarika, Epplen, Jörg T, Curk, Tomaz, Gold, Ralf, Haghikia, Aiden
Published in PloS one (26.05.2015)
Published in PloS one (26.05.2015)
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