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T Wiedmer

Showing results (41-50 of 55) with videos related to

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The Journal of Biological Chemistry|July 18, 1997
Molecular cloning of human plasma membrane phospholipid scramblase. A protein mediating transbilayer movement of plasma membrane phospholipidsQ Zhou, J Zhao, J G Stout, et al.
The Journal of Clinical Investigation|December 1, 1994
Production and characterization of transformed B-lymphocytes expressing the membrane defect of Scott syndromeH Kojima, D Newton-Nash, H J Weiss, et al.
The Journal of Clinical Investigation|May 1, 1997
Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipidsJ G Stout, F Bassé, R A Luhm, et al.
The Journal of Cell Biology|July 13, 2000
Sphingomyelin hydrolysis to ceramide during the execution phase of apoptosis results from phospholipid scrambling and alters cell-surface morphologyA D Tepper, P Ruurs, T Wiedmer, et al.
The Journal of Biological Chemistry|September 15, 1991
Platelet-derived microparticles express high affinity receptors for factor VIIIG E Gilbert, P J Sims, T Wiedmer, et al.
Blood|February 7, 2001
Transcriptional control of the human plasma membrane phospholipid scramblase 1 gene is mediated by interferon-alphaQ Zhou, J Zhao, F Al-Zoghaibi, et al.
Blood|August 15, 1993
Complement-induced vesiculation and exposure of membrane prothrombinase sites in platelets of paroxysmal nocturnal hemoglobinuriaT Wiedmer, S E Hall, T L Ortel, et al.
Blood|January 15, 1992
Defective Ca(2+)-induced microvesiculation and deficient expression of procoagulant activity in erythrocytes from a patient with a bleeding disorder: a study of the red blood cells of Scott syndromeE M Bevers, T Wiedmer, P Comfurius, et al.
Endocrine-Related Cancer|January 25, 2017
Hypo-methylation mediates chromosomal instability in pancreatic NETI Marinoni, A Wiederkeher, T Wiedmer, et al.
Blood|January 1, 1991
Identification of a platelet dense granule membrane protein that is deficient in a patient with the Hermansky-Pudlak syndromeJ M Gerrard, D Lint, P J Sims, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
The Journal of Biological Chemistry|July 18, 1997
Molecular cloning of human plasma membrane phospholipid scramblase. A protein mediating transbilayer movement of plasma membrane phospholipidsQ Zhou, J Zhao, J G Stout, et al.
The Journal of Clinical Investigation|December 1, 1994
Production and characterization of transformed B-lymphocytes expressing the membrane defect of Scott syndromeH Kojima, D Newton-Nash, H J Weiss, et al.
The Journal of Clinical Investigation|May 1, 1997
Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipidsJ G Stout, F Bassé, R A Luhm, et al.
The Journal of Cell Biology|July 13, 2000
Sphingomyelin hydrolysis to ceramide during the execution phase of apoptosis results from phospholipid scrambling and alters cell-surface morphologyA D Tepper, P Ruurs, T Wiedmer, et al.
The Journal of Biological Chemistry|September 15, 1991
Platelet-derived microparticles express high affinity receptors for factor VIIIG E Gilbert, P J Sims, T Wiedmer, et al.
Blood|February 7, 2001
Transcriptional control of the human plasma membrane phospholipid scramblase 1 gene is mediated by interferon-alphaQ Zhou, J Zhao, F Al-Zoghaibi, et al.
Blood|August 15, 1993
Complement-induced vesiculation and exposure of membrane prothrombinase sites in platelets of paroxysmal nocturnal hemoglobinuriaT Wiedmer, S E Hall, T L Ortel, et al.
Blood|January 15, 1992
Defective Ca(2+)-induced microvesiculation and deficient expression of procoagulant activity in erythrocytes from a patient with a bleeding disorder: a study of the red blood cells of Scott syndromeE M Bevers, T Wiedmer, P Comfurius, et al.
Endocrine-Related Cancer|January 25, 2017
Hypo-methylation mediates chromosomal instability in pancreatic NETI Marinoni, A Wiederkeher, T Wiedmer, et al.
Blood|January 1, 1991
Identification of a platelet dense granule membrane protein that is deficient in a patient with the Hermansky-Pudlak syndromeJ M Gerrard, D Lint, P J Sims, et al.
Pageof 6