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Human Genetics|July 16, 2011
An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood groupGuntram Borck, Naseebullah Kakar, Jochen Hoch, et al.
Thrombosis and Haemostasis|April 2, 2003
Identification of a novel urokinase receptor splice variant and its prognostic relevance in breast cancerThomas Luther, Matthias Kotzsch, Axel Meye, et al.
Epilepsia|May 28, 2008
The head nodding syndrome--clinical classification and possible causesAndrea S Winkler, Katrin Friedrich, Rebekka König, et al.
Proteomics|February 1, 2014
Imaging mass spectrometry to discriminate breast from pancreatic cancer metastasis in formalin-fixed paraffin-embedded tissuesRita Casadonte, Mark Kriegsmann, Friederike Zweynert, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 6, 2013
DARPin-targeting of measles virus: unique bispecificity, effective oncolysis, and enhanced safetyKatrin Friedrich, Jan Rh Hanauer, Steffen Prüfer, et al.
Molecular Therapy Oncolytics|April 28, 2016
Enhanced lysis by bispecific oncolytic measles viruses simultaneously using HER2/neu or EpCAM as target receptorsJan Rh Hanauer, Lisa Gottschlich, Dennis Riehl, et al.
Human Genetics|May 6, 2010
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsKatrin Friedrich, Lin Lee, Dru F Leistritz, et al.
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