Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Julia K. Bickmann"'
Publikováno v:
Current opinion in hematology. 24(5)
Arterial and venous thromboembolic diseases are associated with significant morbidity and mortality and present a major medical burden. Currently used anticoagulants for the prevention or treatment of thromboembolic events including heparins, vitamin
Autor:
D Berard, Jürgen J. Wenzel, Friederike Häuser, Heidi Rossmann, C Deyle, C Glowacki, Karl J. Lackner, Julia K. Bickmann, Carolin Neukirch
Publikováno v:
Genes & Immunity. 13:321-327
Crohn's disease and ulcerative colitis, the two main types of inflammatory bowel disease (IBD), were reported to be associated with a variety of genetic polymorphisms. A subset of these polymorphisms was identified in both diseases and only three of
Autor:
Matthias Miederer, Julia K. Bickmann, Wolf J. Mann, Erik Springer, Christian Fottner, Heidi Rossmann, Arno Schad, Matthias M. Weber, Konstantinos Papaspyrou, Dimitrios Koutsimpelas, Stefanie Sollfrank, Thomas J. Musholt, Karl J. Lackner, Oliver Bartsch
Publikováno v:
The Journal of clinical endocrinology and metabolism. 99(3)
Mutations in the four subunits of succinate dehydrogenase (SDH) are the cause for the hereditary paraganglioma (PGL) syndrome types 1-4 and are associated with multiple and recurrent pheochromocytomas and PGLs. SDHC mutations most frequently result i
Autor:
R Hassoun, S Sollfranck, D Bartsch, B Schneider-Rätzke, K Papaspyrou, WJ Mann, Julia K. Bickmann, Karl J. Lackner, Carolin Neukirch, Matthias M. Weber, Christian Fottner, Heidi Rossmann
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 121
Autor:
Julia K. Bickmann, Jürgen J. Wenzel, Heidi Rossmann, Karl J. Lackner, Carolin Neukirch, Thomas J. Musholt, Christian Fottner, Peter Lohse, Matthias M. Weber, Timo Minnemann, Stefan Neuwirth, Brigitte Schneider-Rätzke
Publikováno v:
Clinical chemistry. 55(7)
Background: Reliable PCR amplification of DNA fragments is the prerequisite for most genetic assays. We investigated the impact of G-quadruplex– or i-motif–like sequences on the reliability of PCR-based genetic analyses. Methods: We found the seq
Autor:
Heidi Rossmann, Matthias Wiebel, Carolin Neukirch, Wolfgang Kamin, Jürgen J. Wenzel, Manfred Stuhrmann, Julia K. Bickmann, Friederike Häuser, Karl J. Lackner
Publikováno v:
Clinical chemistry. 55(6)
Background: Cystic fibrosis (CF) is a common autosomal recessive genetic disorder caused by a variety of sequence alterations in the CFTR gene [cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)]. Becaus