12 Einträge gefunden

1. Upshaw-Schulman syndrome-associated ADAMTS13 variants possess proteolytic activity at the surface of endothelial cells and in simulated circulation

   1. Letzer, Anton
   2. Lehmann, Katja
   3. Mess, Christian
   4. König, Gesa
   5. Obser, Tobias
   6. Peine, Sven
   7. Schneppenheim, Sonja

   2020 - Forschungsinformationssystem des UKE
2. Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations

   1. König, Gesa
   2. Obser, Tobias
   3. Marggraf, Olivier
   4. Schneppenheim, Sonja
   5. Budde, Ulrich
   6. Schneppenheim, Reinhard
   7. Brehm, Maria A

   2019 - Forschungsinformationssystem des UKE
3. Characterization of VWF gene conversions causing von Willebrand disease

   1. Ahmad, Firdos
   2. Kannan, Meganathan
   3. Obser, Tobias
   4. Budde, Ulrich
   5. Schneppenheim, Sonja
   6. Saxena, Renu
   7. Schneppenheim, Reinhard

   2019 - Forschungsinformationssystem des UKE
4. Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw-Schulman Syndrome Investigated in Germany

   1. Hassenpflug, Wolf Achim
   2. Obser, Tobias
   3. Bode, Julia
   4. Oyen, Florian
   5. Budde, Ulrich
   6. Schneppenheim, Sonja
   7. Schneppenheim, Reinhard

   2018 - Forschungsinformationssystem des UKE
5. Mutation G1629E Increases von Willebrand Factor Cleavage via a Cooperative Destabilization Mechanism

   1. Aponte-Santamaría, Camilo
   2. Lippok, Svenja
   3. Mittag, Judith J
   4. Obser, Tobias
   5. Schneppenheim, Reinhard
   6. Baldauf, Carsten
   7. Gräter, Frauke

   2017 - Forschungsinformationssystem des UKE
6. Shear-Induced Unfolding and Enzymatic Cleavage of Full-Length VWF Multimers

   1. Lippok, Svenja
   2. Radtke, Matthias
   3. Obser, Tobias
   4. Kleemeier, Lars
   5. Schneppenheim, Reinhard
   6. Budde, Ulrich
   7. Netz, Roland R

   2016 - Forschungsinformationssystem des UKE
7. von Willebrand factor is dimerized by protein disulfide isomerase

   1. Lippok, Svenja
   2. Kolšek, Katra
   3. Löf, Achim
   4. Eggert, Dennis
   5. Vanderlinden, Willem
   6. Müller, Jochen P
   7. König, Gesa

   2016 - Forschungsinformationssystem des UKE
8. Performance evaluation and multicentre study of a von Willebrand factor activity assay based on GPIb binding in the absence of ristocetin

   1. Patzke, Juergen
   2. Budde, Ulrich
   3. Huber, Andreas
   4. Méndez, Adriana
   5. Muth, Heidrun
   6. Obser, Tobias
   7. Peerschke, Ellinor

   2014 - Forschungsinformationssystem des UKE
9. Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion

   1. Langer, Florian
   2. Obser, Tobias
   3. Oyen, Florian
   4. Spath, Brigitte
   5. Holstein, Katharina
   6. Greinacher, Andreas
   7. White, James G

   2014 - Forschungsinformationssystem des UKE
10. Exponential size distribution of von Willebrand factor

    1. Lippok, Svenja
    2. Obser, Tobias
    3. Müller, Jochen P
    4. Stierle, Valentin K
    5. Benoit, Martin
    6. Budde, Ulrich
    7. Schneppenheim, Reinhard

    2013 - Forschungsinformationssystem des UKE
11. Characterisation of mutations and molecular studies of type 2 von Willebrand disease.

    1. Ahmad, Firdos
    2. Jan, Rifat
    3. Kannan, Meganathan
    4. Obser, Tobias
    5. Hassan, Md Imtaiyaz
    6. Oyen, Florian
    7. Budde, Ulrich

    2013 - Forschungsinformationssystem des UKE
12. Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization.

    1. Schneppenheim, Reinhard
    2. Lenk, Harald
    3. Obser, Tobias
    4. Oldenburg, Johannes
    5. Oyen, Florian
    6. Schneppenheim, Sonja
    7. Schwaab, Rainer

    2004 - Forschungsinformationssystem des UKE