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Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie
|
July 24, 2014
Physiology of iron metabolism
Sophie Waldvogel-Abramowski, Gérard Waeber, Christoph Gassner, et al.
Blood Reviews
|
October 24, 2013
Iron and transfusion medicine
Sophie Waldvogel-Abramovski, Gérard Waeber, Christoph Gassner, et al.
Transfusion
|
April 5, 2013
Novel RHD alleles with weak hemagglutination and genetic Exon 9 diversity: weak D Types 45.1, 75, and 76
Christoph Gassner, Irene Utz, Harald Schennach, et al.
Pediatric Blood & Cancer
|
February 23, 2018
Molecular characterization and multidisciplinary management of Gerbich hemolytic disease of the newborn
Rebecca N Levitt, Elise Gourri, Christoph Gassner, et al.
Transfusion
|
May 22, 2014
High-throughput Kell, Kidd, and Duffy matrix-assisted laser desorption/ionization, time-of-flight mass spectrometry-based blood group genotyping of 4000 donors shows close to full concordance with serotyping and detects new alleles
Stefan Meyer, Caren Vollmert, Nadine Trost, et al.
Biochemical and Biophysical Research Communications
|
August 26, 2014
Mesenchymal stem cells from osteoporotic patients reveal reduced migration and invasion upon stimulation with BMP-2 or BMP-7
Florian Haasters, Denitsa Docheva, Christoph Gassner, et al.
Frontiers in Immunology
|
December 27, 2024
A structure-based <i>in silico</i> analysis of the Kell blood group system
Gabriele Mayr, Maike Bublitz, Tim A Steiert, et al.
Transfusion
|
November 22, 2014
RHD variants in Flanders, Belgium
Vicky S T Van Sandt, Christoph Gassner, Marie-Paule Emonds, et al.
Forensic Science International. Genetics
|
July 2, 2013
Multiple recurrent mutations at four human Y-chromosomal single nucleotide polymorphism sites in a 37 bp sequence tract on the ARSDP1 pseudogene
Harald Niederstätter, Burkhard Berger, Daniel Erhart, et al.
British Journal of Haematology
|
March 9, 2017
Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles
Elise Gourri, Gregory A Denomme, Yvonne Merki, et al.
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of 8
Search research articles
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Showing results (31-40 of 80) with videos related to
Sort By:
Page
of 8
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie
|
July 24, 2014
Physiology of iron metabolism
Sophie Waldvogel-Abramowski, Gérard Waeber, Christoph Gassner, et al.
Blood Reviews
|
October 24, 2013
Iron and transfusion medicine
Sophie Waldvogel-Abramovski, Gérard Waeber, Christoph Gassner, et al.
Transfusion
|
April 5, 2013
Novel RHD alleles with weak hemagglutination and genetic Exon 9 diversity: weak D Types 45.1, 75, and 76
Christoph Gassner, Irene Utz, Harald Schennach, et al.
Pediatric Blood & Cancer
|
February 23, 2018
Molecular characterization and multidisciplinary management of Gerbich hemolytic disease of the newborn
Rebecca N Levitt, Elise Gourri, Christoph Gassner, et al.
Transfusion
|
May 22, 2014
High-throughput Kell, Kidd, and Duffy matrix-assisted laser desorption/ionization, time-of-flight mass spectrometry-based blood group genotyping of 4000 donors shows close to full concordance with serotyping and detects new alleles
Stefan Meyer, Caren Vollmert, Nadine Trost, et al.
Biochemical and Biophysical Research Communications
|
August 26, 2014
Mesenchymal stem cells from osteoporotic patients reveal reduced migration and invasion upon stimulation with BMP-2 or BMP-7
Florian Haasters, Denitsa Docheva, Christoph Gassner, et al.
Frontiers in Immunology
|
December 27, 2024
A structure-based <i>in silico</i> analysis of the Kell blood group system
Gabriele Mayr, Maike Bublitz, Tim A Steiert, et al.
Transfusion
|
November 22, 2014
RHD variants in Flanders, Belgium
Vicky S T Van Sandt, Christoph Gassner, Marie-Paule Emonds, et al.
Forensic Science International. Genetics
|
July 2, 2013
Multiple recurrent mutations at four human Y-chromosomal single nucleotide polymorphism sites in a 37 bp sequence tract on the ARSDP1 pseudogene
Harald Niederstätter, Burkhard Berger, Daniel Erhart, et al.
British Journal of Haematology
|
March 9, 2017
Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles
Elise Gourri, Gregory A Denomme, Yvonne Merki, et al.
Page
of 8