Search research articles
Contact Us
Filters
Showing results (21-30 of 34) with videos related to
Page
of 4
Sort By:
The Journal of Biological Chemistry
|
March 4, 2011
Human vitamin K 2,3-epoxide reductase complex subunit 1-like 1 (VKORC1L1) mediates vitamin K-dependent intracellular antioxidant function
Philipp Westhofen, Matthias Watzka, Milka Marinova, et al.
Epilepsy Research
|
May 14, 2003
Allopregnanolone serum levels and expression of 5 alpha-reductase and 3 alpha-hydroxysteroid dehydrogenase isoforms in hippocampal and temporal cortex of patients with epilepsy
Birgit Stoffel-Wagner, Matthias Watzka, Stephan Steckelbroeck, et al.
European Journal of Clinical Pharmacology
|
August 7, 2012
VKORC1-dependent pharmacokinetics of intravenous and oral phylloquinone (vitamin K1) mixed micelles formulation
Milka Marinova, Dieter Lütjohann, Olof Breuer, et al.
European Journal of Clinical Pharmacology
|
November 27, 2010
Prediction of phenprocoumon maintenance dose and phenprocoumon plasma concentration by genetic and non-genetic parameters
Christof Geisen, Beate Luxembourg, Matthias Watzka, et al.
Haematologica
|
September 8, 2006
Detection of heterozygous large deletions in the antithrombin gene using multiplex polymerase chain reaction and denatured high performance liquid chromatography
Anna Pavlova, Osman El-Maarri, Beate Luxembourg, et al.
Journal of Neurochemistry
|
April 2, 2004
Steroid sulfatase (STS) expression in the human temporal lobe: enzyme activity, mRNA expression and immunohistochemistry study
Stephan Steckelbroeck, Alexander Nassen, Bernhard Ugele, et al.
Human Mutation
|
November 24, 2021
GGCX variants leading to biallelic deficiency to γ-carboxylate GRP cause skin laxity in VKCFD1 patients
Suvoshree Ghosh, Katrin Kraus, Arijit Biswas, et al.
Journal of Neurochemistry
|
October 23, 2002
Characterization of the dehydroepiandrosterone (DHEA) metabolism via oxysterol 7alpha-hydroxylase and 17-ketosteroid reductase activity in the human brain
Stephan Steckelbroeck, Matthias Watzka, Dieter Lütjohann, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
August 29, 2003
Characterisation of estrogenic 17beta-hydroxysteroid dehydrogenase (17beta-HSD) activity in the human brain
Stephan Steckelbroeck, Matthias Watzka, Annette Reissinger, et al.
Thrombosis Research
|
August 25, 2014
Bleeding and non-bleeding phenotypes in patients with GGCX gene mutations
Matthias Watzka, Christof Geisen, Monika Scheer, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
The Journal of Biological Chemistry
|
March 4, 2011
Human vitamin K 2,3-epoxide reductase complex subunit 1-like 1 (VKORC1L1) mediates vitamin K-dependent intracellular antioxidant function
Philipp Westhofen, Matthias Watzka, Milka Marinova, et al.
Epilepsy Research
|
May 14, 2003
Allopregnanolone serum levels and expression of 5 alpha-reductase and 3 alpha-hydroxysteroid dehydrogenase isoforms in hippocampal and temporal cortex of patients with epilepsy
Birgit Stoffel-Wagner, Matthias Watzka, Stephan Steckelbroeck, et al.
European Journal of Clinical Pharmacology
|
August 7, 2012
VKORC1-dependent pharmacokinetics of intravenous and oral phylloquinone (vitamin K1) mixed micelles formulation
Milka Marinova, Dieter Lütjohann, Olof Breuer, et al.
European Journal of Clinical Pharmacology
|
November 27, 2010
Prediction of phenprocoumon maintenance dose and phenprocoumon plasma concentration by genetic and non-genetic parameters
Christof Geisen, Beate Luxembourg, Matthias Watzka, et al.
Haematologica
|
September 8, 2006
Detection of heterozygous large deletions in the antithrombin gene using multiplex polymerase chain reaction and denatured high performance liquid chromatography
Anna Pavlova, Osman El-Maarri, Beate Luxembourg, et al.
Journal of Neurochemistry
|
April 2, 2004
Steroid sulfatase (STS) expression in the human temporal lobe: enzyme activity, mRNA expression and immunohistochemistry study
Stephan Steckelbroeck, Alexander Nassen, Bernhard Ugele, et al.
Human Mutation
|
November 24, 2021
GGCX variants leading to biallelic deficiency to γ-carboxylate GRP cause skin laxity in VKCFD1 patients
Suvoshree Ghosh, Katrin Kraus, Arijit Biswas, et al.
Journal of Neurochemistry
|
October 23, 2002
Characterization of the dehydroepiandrosterone (DHEA) metabolism via oxysterol 7alpha-hydroxylase and 17-ketosteroid reductase activity in the human brain
Stephan Steckelbroeck, Matthias Watzka, Dieter Lütjohann, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
August 29, 2003
Characterisation of estrogenic 17beta-hydroxysteroid dehydrogenase (17beta-HSD) activity in the human brain
Stephan Steckelbroeck, Matthias Watzka, Annette Reissinger, et al.
Thrombosis Research
|
August 25, 2014
Bleeding and non-bleeding phenotypes in patients with GGCX gene mutations
Matthias Watzka, Christof Geisen, Monika Scheer, et al.
Page
of 4