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Matthias Watzka
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Journal Articles

The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine–based ER retention motif

Katrin J. Czogalla, Arijit Biswas, Simone Rost, Matthias Watzka, Johannes Oldenburg
Journal: Blood
Blood (2014) 124 (8): 1354–1362.
https://doi.org/10.1182/blood-2013-12-545988
Published: 2014
Includes: Supplemental data
Journal Articles

Human VKORC1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces

Katrin J. Czogalla, Arijit Biswas, Ann-Christin Wendeln, Philipp Westhofen, Clemens R. Müller, Matthias Watzka, Johannes Oldenburg
Journal: Blood
Blood (2013) 122 (15): 2743–2750.
https://doi.org/10.1182/blood-2013-05-501692
Published: 2013
Includes: Supplemental data
Journal Articles

Pharmacogenetics of Oral Anticoagulation - VKORC1-Haplotypes Determine the Inter-Individual and Inter-Ethnical Variability.

Christof Geisen, MD, Matthias Watzka, PhD, Katja Sittinger, MD, Beate Luxembourg, MD, Michael Steffens, MD, Clemens R. Müller, PhD, Thomas F. Wienker, MD, PhD, Edelgard Lindhoff-Last, MD, PhD, Erhard Seifried, MD, PhD, Johannes Oldenburg, MD, PhD
Journal: Blood
Blood (2006) 108 (11): 719.
https://doi.org/10.1182/blood.V108.11.719.719
Published: 2006
Journal Articles

Lack of F8 mRNA: a novel mechanism leading to hemophilia A

Osman El-Maarri, Heike Singer, Claudia Klein, Matthias Watzka, Ursula Herbiniaux, Hans H. Brackmann, Jörg Schröder, Jochen Graw, Clemens R. Müller, Wolfgang Schramm, Rainer Schwaab, Thomas Haaf, Peter Hanfland, Johannes Oldenburg
Journal: Blood
Blood (2006) 107 (7): 2759–2765.
https://doi.org/10.1182/blood-2005-09-3702
Published: 2006
Includes: Supplemental data