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137 results for Epplen,+Jörg

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ArticlesPeer ReviewedFull Text
PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness
Author / Creator:Arning, Larissa ; Ocklenburg, Sebastian ; Schulz, Stefanie ; Ness, Vanessa ; Gerding, Wanda M. ; Hengstler, Jan G. ; Falkenstein, Michael ; Epplen, Jörg T. ; Güntürkün, Onur ; Beste, Christian
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-06, Vol.8 (6), p.e67251-e67251
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Comparison of hybrid clones derived from human breast epithelial cells and three different cancer cell lines regarding in vitro cancer stem/ initiating cell properties
Author / Creator:Fahlbusch, Sera Selina ; Keil, Silvia ; Epplen, Jörg T. ; Zänker, Kurt S. ; Dittmar, Thomas
Publisher:England: BioMed Central Ltd
Journal title:BMC cancer, 2020-05, Vol.20 (1), p.446-446, Article 446
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Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetries
Author / Creator: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
Publisher:England: eLife Science Publications, Ltd
Journal title:eLife, 2017-02, Vol.6
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PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease
Author / Creator:Taherzadeh-Fard, Elahe ; Saft, Carsten ; Akkad, Denis A ; Wieczorek, Stefan ; Haghikia, Aiden ; Chan, Andrew ; Epplen, Jörg T ; Arning, Larissa
Publisher:England: BioMed Central Ltd
Journal title:Molecular neurodegeneration, 2011-05, Vol.6 (1), p.32-32, Article 32
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rs1004819 Is the Main Disease-Associated IL23R Variant in German Crohn's Disease Patients: Combined Analysis of IL23R, CARD15, and OCTN1/2 Variants
Author / Creator: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
Publisher:United States: Public Library of Science
Journal title:PloS one, 2007-09, Vol.2 (9), p.e819-e819
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On the relevance of the NPY2-receptor variation for modes of action cascading processes
Author / Creator:Beste, Christian ; Stock, Ann-Kathrin ; Epplen, Jörg T. ; Arning, Larissa
Publisher:Amsterdam: Elsevier Inc
Journal title:NeuroImage (Orlando, Fla.), 2014-11, Vol.102, p.558-564
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ArticlesPeer ReviewedFull Text
Handedness and the X chromosome: The role of androgen receptor CAG-repeat length
Author / Creator:Arning, Larissa ; Ocklenburg, Sebastian ; Schulz, Stefanie ; Ness, Vanessa ; Gerding, Wanda M. ; Hengstler, Jan G. ; Falkenstein, Michael ; Epplen, Jörg T. ; Güntürkün, Onur ; Beste, Christian
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2015-02, Vol.5 (1), p.8325-8325, Article 8325
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ArticlesPeer ReviewedFull Text
Cholecystokinin A Receptor (CCKAR) Gene Variation Is Associated with Language Lateralization
Author / Creator:Ocklenburg, Sebastian ; Arning, Larissa ; Gerding, Wanda M. ; Epplen, Jörg T. ; Güntürkün, Onur ; Beste, Christian
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-01, Vol.8 (1), p.e53643-e53643
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ArticlesPeer ReviewedFull Text
Prospective Evaluation of Predictive DNA Testing for Huntington’s Disease in a Large German Center
Author / Creator:Ibisler, Aysegül ; Ocklenburg, Sebastian ; Stemmler, Susanne ; Arning, Larissa ; Epplen, Jörg T. ; Saft, Carsten ; Hoffjan, Sabine
Publisher:New York: Springer US
Journal title:Journal of genetic counseling, 2017-10, Vol.26 (5), p.1029-1040
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ArticlesPeer ReviewedFull Text
Endocannabinergic modulation of central serotonergic activity in healthy human volunteers
Author / Creator:Emons, Barbara ; Arning, Larissa ; Makulla, Vera-Estelle ; Suchy, Maria-Theresia ; Tsikas, Dimitrios ; Lücke, Thomas ; Epplen, Jörg T. ; Juckel, Georg ; Roser, Patrik
Publisher:England: BioMed Central Ltd
Journal title:Annals of general psychiatry, 2023-03, Vol.22 (1), p.11-11, Article 11
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Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults
Author / Creator:Ocklenburg, Sebastian ; Arning, Larissa ; Gerding, Wanda M. ; Hengstler, Jan G. ; Epplen, Jörg T. ; Güntürkün, Onur ; Beste, Christian ; Akkad, Denis A.
Publisher:New York: Springer US
Journal title:Molecular neurobiology, 2016-11, Vol.53 (9), p.6355-6361
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ArticlesPeer ReviewedFull Text
Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes
Author / Creator:Aydin, Gülsah ; Dekomien, Gabriele ; Hoffjan, Sabine ; Gerding, Wanda Maria ; Epplen, Jörg T. ; Arning, Larissa
Publisher:England: BioMed Central Ltd
Journal title:BMC neurology, 2018-01, Vol.18 (1), p.3-8, Article 3
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ArticlesPeer ReviewedFull Text
Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification
Author / Creator:Rutsch, Frank ; Ruf, Nico ; Vaingankar, Sucheta ; Toliat, Mohammad R. ; Suk, Anita ; Höhne, Wolfgang ; Schauer, Galen ; Lehmann, Mandy ; Roscioli, Tony ; Schnabel, Dirk ; Epplen, Jörg T. ; Knisely, Alex ; Superti-Furga, Andrea ; McGill, James ; Filippone, Marco ; Sinaiko, Alan R. ; Vallance, Hillary ; Hinrichs, Bernd ; Smith, Wendy ; Ferre, Merry ; Terkeltaub, Robert ; Nürnberg, Peter
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2003-08, Vol.34 (4), p.379-381
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ArticlesPeer ReviewedFull Text
Evidence for STAT4 as a Common Autoimmune Gene: rs7574865 Is Associated with Colonic Crohn's Disease and Early Disease Onset
Author / Creator: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
Publisher:United States: Public Library of Science
Journal title:PloS one, 2010-04, Vol.5 (4), p.e10373-e10373
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ArticlesPeer ReviewedFull Text
Combinations of Susceptibility Genes Are Associated with Higher Risk for Multiple Sclerosis and Imply Disease Course Specificity
Author / Creator:Akkad, Denis A. ; Olischewsky, Alexandra ; Reiner, Franziska ; Hellwig, Kerstin ; Esser, Sarika ; Epplen, Jörg T. ; Curk, Tomaz ; Gold, Ralf ; Haghikia, Aiden
Publisher:United States: Public Library of Science
Journal title:PloS one, 2015-05, Vol.10 (5), p.e0127632-e0127632
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ArticlesPeer ReviewedFull Text
Structural Asymmetry in the Frontal and Temporal Lobes Is Associated with PCSK6 VNTR Polymorphism
Author / Creator:Berretz, Gesa ; Arning, Larissa ; Gerding, Wanda M. ; Friedrich, Patrick ; Fraenz, Christoph ; Schlüter, Caroline ; Epplen, Jörg T. ; Güntürkün, Onur ; Beste, Christian ; Genç, Erhan ; Ocklenburg, Sebastian
Publisher:New York: Springer US
Journal title:Molecular neurobiology, 2019-11, Vol.56 (11), p.7765-7773
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SOX9 Duplication Linked to Intersex in Deer
Author / Creator:Kropatsch, Regina ; Dekomien, Gabriele ; Akkad, Denis A. ; Gerding, Wanda M. ; Petrasch-Parwez, Elisabeth ; Young, Neil D. ; Altmüller, Janine ; Nürnberg, Peter ; Gasser, Robin B. ; Epplen, Jörg T.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-09, Vol.8 (9), p.e73734
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Myelin Water Fraction Imaging Reveals Hemispheric Asymmetries in Human White Matter That Are Associated with Genetic Variation in PLP1
Author / Creator:Ocklenburg, Sebastian ; Anderson, Catrona ; Gerding, Wanda M. ; Fraenz, Christoph ; Schlüter, Caroline ; Friedrich, Patrick ; Raane, Maximilian ; Mädler, Burkhard ; Schlaffke, Lara ; Arning, Larissa ; Epplen, Jörg T. ; Güntürkün, Onur ; Beste, Christian ; Genç, Erhan
Publisher:New York: Springer US
Journal title:Molecular neurobiology, 2019-06, Vol.56 (6), p.3999-4012
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The genetics of atopic dermatitis: recent findings and future options
Author / Creator:Hoffjan, Sabine ; Epplen, Jörg T.
Publisher:Berlin: Springer
Journal title:Journal of molecular medicine (Berlin, Germany), 2005-09, Vol.83 (9), p.682-692
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PLP1 and CNTN1 gene variation modulates the microstructure of human white matter in the corpus callosum
Author / Creator:Anderson, Catrona ; Gerding, Wanda M ; Fraenz, Christoph ; Schlüter, Caroline ; Friedrich, Patrick ; Raane, Maximilian ; Arning, Larissa ; Epplen, Jörg T ; Güntürkün, Onur ; Beste, Christian ; Genç, Erhan ; Ocklenburg, Sebastian
Publisher:Heidelberg: Springer Nature B.V
Journal title:Brain Structure and Function, 2018-11, Vol.223 (8), p.3875-3887
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Showing 1 to 20 of 137 results

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PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness

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Comparison of hybrid clones derived from human breast epithelial cells and three different cancer cell lines regarding in vitro cancer stem/ initiating cell properties

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Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetries

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PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease

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rs1004819 Is the Main Disease-Associated IL23R Variant in German Crohn's Disease Patients: Combined Analysis of IL23R, CARD15, and OCTN1/2 Variants

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On the relevance of the NPY2-receptor variation for modes of action cascading processes

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Handedness and the X chromosome: The role of androgen receptor CAG-repeat length

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Cholecystokinin A Receptor (CCKAR) Gene Variation Is Associated with Language Lateralization

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Prospective Evaluation of Predictive DNA Testing for Huntington’s Disease in a Large German Center

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Endocannabinergic modulation of central serotonergic activity in healthy human volunteers

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Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults

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Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes

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Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification

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Evidence for STAT4 as a Common Autoimmune Gene: rs7574865 Is Associated with Colonic Crohn's Disease and Early Disease Onset

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Combinations of Susceptibility Genes Are Associated with Higher Risk for Multiple Sclerosis and Imply Disease Course Specificity

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Structural Asymmetry in the Frontal and Temporal Lobes Is Associated with PCSK6 VNTR Polymorphism

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SOX9 Duplication Linked to Intersex in Deer

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Myelin Water Fraction Imaging Reveals Hemispheric Asymmetries in Human White Matter That Are Associated with Genetic Variation in PLP1

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The genetics of atopic dermatitis: recent findings and future options

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PLP1 and CNTN1 gene variation modulates the microstructure of human white matter in the corpus callosum

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