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Kirstin Sandrock

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Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|November 30, 2010
Current Strategies in Diagnosis of Inherited Storage Pool DefectsKirstin Sandrock, Barbara Zieger
Hamostaseologie|April 29, 2022
Acquired von Willebrand Syndrome in ChildrenKirstin Sandrock-Lang, Hannah Glonnegger, Barbara Zieger
Hamostaseologie|December 23, 2021
Pathogenic Aspects of Inherited Platelet DisordersDoris Boeckelmann, Hannah Glonnegger, Kirstin Sandrock-Lang, et al.
Hamostaseologie|February 25, 2015
Inherited platelet disordersKirstin Sandrock-Lang, Rüdiger Wentzell, Sentot Santoso, et al.
Traffic (Copenhagen, Denmark)|December 8, 2009
The nuclear import of the small GTPase Rac1 is mediated by the direct interaction with karyopherin alpha2Kirstin Sandrock, Heike Bielek, Kristina Schradi, et al.
Blood|December 25, 2010
Platelet secretion defect in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL-5)Kirstin Sandrock, Lea Nakamura, Thomas Vraetz, et al.
Biological Chemistry|July 20, 2011
Characterization of human septin interactionsKirstin Sandrock, Ingrid Bartsch, Susanne Bläser, et al.
Blood Cells, Molecules & Diseases|November 8, 2017
A novel nonsense mutation in a patient with Hermansky-Pudlak syndrome type 4Kirstin Sandrock-Lang, Doris Böckelmann, Wolfgang Eberl, et al.
Biological Chemistry|August 10, 2011
Lethal phenotype of mice carrying a Sept11 null mutationSabrina Röseler, Kirstin Sandrock, Ingrid Bartsch, et al.
Blood Cells, Molecules & Diseases|March 13, 2017
Novel mutation in two brothers with Hermansky Pudlak syndrome type 3Kirstin Sandrock-Lang, Ingrid Bartsch, Nina Buechele, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|November 30, 2010
Current Strategies in Diagnosis of Inherited Storage Pool DefectsKirstin Sandrock, Barbara Zieger
Hamostaseologie|April 29, 2022
Acquired von Willebrand Syndrome in ChildrenKirstin Sandrock-Lang, Hannah Glonnegger, Barbara Zieger
Hamostaseologie|December 23, 2021
Pathogenic Aspects of Inherited Platelet DisordersDoris Boeckelmann, Hannah Glonnegger, Kirstin Sandrock-Lang, et al.
Hamostaseologie|February 25, 2015
Inherited platelet disordersKirstin Sandrock-Lang, Rüdiger Wentzell, Sentot Santoso, et al.
Traffic (Copenhagen, Denmark)|December 8, 2009
The nuclear import of the small GTPase Rac1 is mediated by the direct interaction with karyopherin alpha2Kirstin Sandrock, Heike Bielek, Kristina Schradi, et al.
Blood|December 25, 2010
Platelet secretion defect in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL-5)Kirstin Sandrock, Lea Nakamura, Thomas Vraetz, et al.
Biological Chemistry|July 20, 2011
Characterization of human septin interactionsKirstin Sandrock, Ingrid Bartsch, Susanne Bläser, et al.
Blood Cells, Molecules & Diseases|November 8, 2017
A novel nonsense mutation in a patient with Hermansky-Pudlak syndrome type 4Kirstin Sandrock-Lang, Doris Böckelmann, Wolfgang Eberl, et al.
Biological Chemistry|August 10, 2011
Lethal phenotype of mice carrying a Sept11 null mutationSabrina Röseler, Kirstin Sandrock, Ingrid Bartsch, et al.
Blood Cells, Molecules & Diseases|March 13, 2017
Novel mutation in two brothers with Hermansky Pudlak syndrome type 3Kirstin Sandrock-Lang, Ingrid Bartsch, Nina Buechele, et al.
Pageof 2