Screening of the arrestin gene in dogs afflicted with generalized progressive retinal atrophy

por Dekomien, Gabriele, Epplen, Jörg Thomas
Publicado 2002

Variation in genes encoding eosinophil granule proteins in atopic dermatitis patients from Germany

por Parwez, Qumar, Stemmler, Susanne, Epplen, Jörg T, Hoffjan, Sabine
Publicado 2008

Genetic Variability of RXRB, PPARA, and PPARG in Wegener's Granulomatosis

por Wieczorek, Stefan, Knaup, Silvia, Gross, Wolfgang L., Epplen, Jörg T.
Publicado 2009

Age at onset of Huntington disease is not modulated by the R72P variation in TP53 and the R196K variation in the gene coding for the human caspase activated DNase (hCAD)

por Arning, Larissa, Kraus, Peter H, Saft, Carsten, Andrich, Jürgen, Epplen, Jörg T
Publicado 2005

Genomic NGFB variation and multiple sclerosis in a case control study

por Akkad, Denis A, Kruse, Niels, Arning, Larissa, Gold, Ralf, Epplen, Jörg T
Publicado 2008

Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs

por Akkad, Denis A, Gerding, Wanda M, Gasser, Robin B, Epplen, Jörg T
Publicado 2015

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

por Fahlbusch, Sera Selina, Keil, Silvia, Epplen, Jörg T., Zänker, Kurt S., Dittmar, Thomas
Publicado 2020

Glutathione S-Transferase Ω 1 variation does not influence age at onset of Huntington's disease

por Arning, Larissa, Jagiello, Peter, Wieczorek, Stefan, Saft, Carsten, Andrich, Jürgen, Epplen, Jörg T
Publicado 2004

ApoE polymorphisms in narcolepsy

por Gencik, Martin, Dahmen, Norbert, Wieczorek, Stefan, Kasten, Meike, Gencikova, Alexandra, Epplen, Jorg T
Publicado 2001

Genome-wide profiling of S/MAR-based replicon contact sites

por Hagedorn, Claudia, Gogol-Döring, Andreas, Schreiber, Sabrina, Epplen, Jörg T., Lipps, Hans J.
Publicado 2017

PanelDesign: Integrating Epidemiological Information into the Design of Diagnostic NGS Gene Panels

por Schmidtke, Jörg, Philipp, Peter, Rommel, Kathrin, Glaubitz, Ralf, Epplen, Jörg T., Krawczak, Michael
Publicado 2022

Haplotype-defined linkage region for gPRA in Schapendoes dogs

por Lippmann, Tanja, Jonkisz, Anna, Dobosz, Tadeusz, Petrasch-Parwez, Elisabeth, Epplen, Jörg T., Dekomien, Gabriele
Publicado 2007

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

por Ocklenburg, Sebastian, Arning, Larissa, Gerding, Wanda M., Epplen, Jörg T., Güntürkün, Onur, Beste, Christian
Publicado 2013

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

por Aydin, Gülsah, Dekomien, Gabriele, Hoffjan, Sabine, Gerding, Wanda Maria, Epplen, Jörg T., Arning, Larissa
Publicado 2018

Failure to confirm influence of Methyltetrahydrofolate reductase (MTHFR) polymorphisms on age at onset of Huntington disease

por Hansen, Wiebke, Saft, Carsten, Andrich, Jürgen, Müller, Thomas, Wieczorek, Stefan, Epplen, Jörg T, Arning, Larissa
Publicado 2005

Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2)

por Engelfried, Kathrin, Vorgerd, Matthias, Hagedorn, Michaela, Haas, Gerhard, Gilles, Jürgen, Epplen, Jörg T, Meins, Moritz
Publicado 2006

Complex genetic predisposition in adult and juvenile rheumatoid arthritis

por Miterski, Bianca, Drynda, Susanne, Böschow, Gundula, Klein, Wolfram, Oppermann, Joachim, Kekow, Jörn, Epplen, Jörg Thomas
Publicado 2004

Neurodegeneration in the olfactory bulb and olfactory deficits in the Ccdc66 -/- mouse model for retinal degeneration

por Schreiber, Sabrina, Petrasch-Parwez, Elisabeth, Porrmann-Kelterbaum, Elke, Förster, Eckart, Epplen, Jörg T., Gerding, Wanda M.
Publicado 2018

An extended association screen in multiple sclerosis using 202 microsatellite markers targeting apoptosis-related genes does not reveal new predisposing factors

por Gödde, René, Brune, Stefanie, Jagiello, Peter, Sindern, Eckhart, Haupts, Michael, Schimrigk, Sebastian, Müller, Norbert, Epplen, Jörg T
Publicado 2005

On the genetic involvement of apoptosis-related genes in Crohn's disease as revealed by an extended association screen using 245 markers: no evidence for new predisposing factors

por Wagenleiter, Sonja EN, Jagiello, Peter, Akkad, Denis A, Arning, Larissa, Griga, Thomas, Klein, Wolfram, Epplen, Jörg T
Publicado 2005