Oldenburg J - Search Results

1

Structural Modeling Insights into Human VKORC1 Phenotypes.

Czogalla KJ, Watzka M, Oldenburg J. Czogalla KJ, et al. Among authors: oldenburg j. Nutrients. 2015 Aug 14;7(8):6837-51. doi: 10.3390/nu7085313. Nutrients. 2015. PMID: 26287237 Free PMC article. Review.

2

Sequence of the rat factor VIII cDNA.

Watzka M, Geisen C, Seifried E, Oldenburg J. Watzka M, et al. Among authors: oldenburg j. Thromb Haemost. 2004 Jan;91(1):38-42. doi: 10.1160/TH03-06-0336. Thromb Haemost. 2004. PMID: 14691566

3

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

El-Maarri O, Singer H, Klein C, Watzka M, Herbiniaux U, Brackmann HH, Schröder J, Graw J, Müller CR, Schramm W, Schwaab R, Haaf T, Hanfland P, Oldenburg J. El-Maarri O, et al. Among authors: oldenburg j. Blood. 2006 Apr 1;107(7):2759-65. doi: 10.1182/blood-2005-09-3702. Epub 2005 Dec 8. Blood. 2006. PMID: 16339403 Free article.

4

Vitamin K epoxide reductase complex subunit 1 (VKORC1): the key protein of the vitamin K cycle.

Oldenburg J, Bevans CG, Müller CR, Watzka M. Oldenburg J, et al. Antioxid Redox Signal. 2006 Mar-Apr;8(3-4):347-53. doi: 10.1089/ars.2006.8.347. Antioxid Redox Signal. 2006. PMID: 16677080 Review.

5

Detection of heterozygous large deletions in the antithrombin gene using multiplex polymerase chain reaction and denatured high performance liquid chromatography.

Pavlova A, El-Maarri O, Luxembourg B, Lindhoff-Last E, Kochhan L, Bruhn HD, Delev D, Watzka M, Seifried E, Oldenburg J. Pavlova A, et al. Among authors: oldenburg j. Haematologica. 2006 Sep;91(9):1264-7. Haematologica. 2006. PMID: 16956830

6

Functional promoter polymorphism in the VKORC1 gene is no major genetic determinant for coronary heart disease in Northern Germans.

Watzka M, Nebel A, El Mokhtari NE, Ivandic B, Müller J, Schreiber S, Oldenburg J. Watzka M, et al. Among authors: oldenburg j. Thromb Haemost. 2007 Jun;97(6):998-1002. Thromb Haemost. 2007. PMID: 17549303

7

Current pharmacogenetic developments in oral anticoagulation therapy: the influence of variant VKORC1 and CYP2C9 alleles.

Oldenburg J, Bevans CG, Fregin A, Geisen C, Müller-Reible C, Watzka M. Oldenburg J, et al. Thromb Haemost. 2007 Sep;98(3):570-8. Thromb Haemost. 2007. PMID: 17849045 Review.

8

The vitamin K cycle.

Oldenburg J, Marinova M, Müller-Reible C, Watzka M. Oldenburg J, et al. Vitam Horm. 2008;78:35-62. doi: 10.1016/S0083-6729(07)00003-9. Vitam Horm. 2008. PMID: 18374189 Review.

9

The first case of combined coagulation factor V and coagulation factor VIII deficiency in Poland due to a novel p.Tyr135Asn missense mutation in the MCFD2 gene.

Ivaskevicius V, Windyga J, Baran B, Bykowska K, Daugela L, Watzka M, Seifried E, Oldenburg J. Ivaskevicius V, et al. Among authors: oldenburg j. Blood Coagul Fibrinolysis. 2008 Sep;19(6):531-534. doi: 10.1097/MBC.0b013e3283061103. Blood Coagul Fibrinolysis. 2008. PMID: 18685427

10

VKORC1 deficiency in mice causes early postnatal lethality due to severe bleeding.

Spohn G, Kleinridders A, Wunderlich FT, Watzka M, Zaucke F, Blumbach K, Geisen C, Seifried E, Müller C, Paulsson M, Brüning JC, Oldenburg J. Spohn G, et al. Among authors: oldenburg j. Thromb Haemost. 2009 Jun;101(6):1044-50. Thromb Haemost. 2009. PMID: 19492146

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