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Journal of Molecular Medicine (Berlin, Germany)|May 20, 2005
The genetics of atopic dermatitis: recent findings and future optionsSabine Hoffjan, Jörg T EpplenCellular and Molecular Biology (Noisy-Le-Grand, France)|May 28, 2002
On the genetic contribution to selected multifactorial diseases with autoimmune characteristicsBianca Miterski, Jörg T Epplen, Martin GencikMelanoma Research|March 29, 2006
Genomic stability in malignant melanoma of XiphophorusKatrin Zunker, Jörg T Epplen, Manfred SchartlAutoimmunity Reviews|January 18, 2005
Complex genetics of Wegener granulomatosisPeter Jagiello, Wolfgang L Gross, Jörg T EpplenCurrent Opinion in Rheumatology|October 30, 2009
Recent progress in the genetics of Wegener's granulomatosis and Churg-Strauss syndromeStefan Wieczorek, Julia U Holle, Jörg T EpplenJournal of Neurology|September 15, 2006
No association between synapsin III gene promoter polymorphisms and multiple sclerosis in German patientsDenis A Akkad, René Gödde, Jörg T EpplenElectrophoresis|August 21, 2003
Extra-pair sires as identified by means of standardized across-gel comparisons of multilocus DNA fingerprintsTim Schmoll, Volker Janzon, Jörg T Epplen, et al.Journal of Human Genetics|February 24, 2006
Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European populationStefan Wieczorek, Larissa Arning, Ingrid Alheite, et al.Neuropharmacology|November 9, 2010
The functional BDNF Val66Met polymorphism affects functions of pre-attentive visual sensory memory processesChristian Beste, Daniel Schneider, Jörg T Epplen, et al.European Journal of Medical Genetics|June 11, 2013
CNR1 variation is associated with the age at onset in Huntington diseaseEugen Kloster, Carsten Saft, Jörg T Epplen, et al.Pageof 13