Oldenburg J - Search Results

1

SARS-CoV-2 Infection: Modulator of Pulmonary Embolism Paradigm.

Akhter MS, Hamali HA, Mobarki AA, Rashid H, Oldenburg J, Biswas A. Akhter MS, et al. Among authors: oldenburg j. J Clin Med. 2021 Mar 4;10(5):1064. doi: 10.3390/jcm10051064. J Clin Med. 2021. PMID: 33806540 Free PMC article. Review.

2

Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function.

Ivaskevicius V, Biswas A, Bevans C, Schroeder V, Kohler HP, Rott H, Halimeh S, Petrides PE, Lenk H, Krause M, Miterski B, Harbrecht U, Oldenburg J. Ivaskevicius V, et al. Among authors: oldenburg j. Haematologica. 2010 Jun;95(6):956-62. doi: 10.3324/haematol.2009.017210. Epub 2010 Feb 23. Haematologica. 2010. PMID: 20179087 Free PMC article.

3

An update of the mutation profile of Factor 13 A and B genes.

Biswas A, Ivaskevicius V, Seitz R, Thomas A, Oldenburg J. Biswas A, et al. Among authors: oldenburg j. Blood Rev. 2011 Sep;25(5):193-204. doi: 10.1016/j.blre.2011.03.001. Epub 2011 Jun 2. Blood Rev. 2011. PMID: 21640452 Review.

4

Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients.

Yadegari H, Driesen J, Pavlova A, Biswas A, Hertfelder HJ, Oldenburg J. Yadegari H, et al. Among authors: oldenburg j. Thromb Haemost. 2012 Oct;108(4):662-71. doi: 10.1160/TH12-02-0089. Epub 2012 Aug 7. Thromb Haemost. 2012. PMID: 22871923

5

A common F13A1 intron 1 variant IVS1+12(A) is associated with mild FXIII deficiency in Caucasian population.

Ivaskevicius V, Biswas A, Thomas A, Lyonga S, Rott H, Halimeh S, Kappert G, Klammroth R, Scholz U, Eberl W, Harbrecht U, Gnida C, Hertfelder HJ, Marquardt N, Oldenburg J. Ivaskevicius V, et al. Among authors: oldenburg j. Ann Hematol. 2013 Jul;92(7):975-9. doi: 10.1007/s00277-013-1724-2. Epub 2013 Mar 19. Ann Hematol. 2013. PMID: 23508224

6

Insights into pathological mechanisms of missense mutations in C-terminal domains of von Willebrand factor causing qualitative or quantitative von Willebrand disease.

Yadegari H, Driesen J, Pavlova A, Biswas A, Ivaskevicius V, Klamroth R, Oldenburg J. Yadegari H, et al. Among authors: oldenburg j. Haematologica. 2013 Aug;98(8):1315-23. doi: 10.3324/haematol.2013.084111. Epub 2013 Mar 28. Haematologica. 2013. PMID: 23539537 Free PMC article.

7

In vitro secretion deficits are common among human coagulation factor XIII subunit B missense mutants: correlations with patient phenotypes and molecular models.

Biswas A, Thomas A, Bevans CG, Ivaskevicius V, Oldenburg J. Biswas A, et al. Among authors: oldenburg j. Hum Mutat. 2013 Nov;34(11):1490-500. doi: 10.1002/humu.22391. Epub 2013 Sep 13. Hum Mutat. 2013. PMID: 23913518

8

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

Czogalla KJ, Biswas A, Wendeln AC, Westhofen P, Müller CR, Watzka M, Oldenburg J. Czogalla KJ, et al. Among authors: oldenburg j. Blood. 2013 Oct 10;122(15):2743-50. doi: 10.1182/blood-2013-05-501692. Epub 2013 Aug 27. Blood. 2013. PMID: 23982176 Free article.

9

Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function.

Biswas A, Ivaskevicius V, Thomas A, Varvenne M, Brand B, Rott H, Haussels I, Ruehl H, Scholz U, Klamroth R, Oldenburg J. Biswas A, et al. Among authors: oldenburg j. Ann Hematol. 2014 Oct;93(10):1665-76. doi: 10.1007/s00277-014-2102-4. Epub 2014 Jun 3. Ann Hematol. 2014. PMID: 24889649

10

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

Czogalla KJ, Biswas A, Rost S, Watzka M, Oldenburg J. Czogalla KJ, et al. Among authors: oldenburg j. Blood. 2014 Aug 21;124(8):1354-62. doi: 10.1182/blood-2013-12-545988. Epub 2014 Jun 24. Blood. 2014. PMID: 24963046 Free article.

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