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P Gane

Showing results (81-90 of 91) with videos related to

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Molecular Membrane Biology|July 1, 1997
Phosphatidylserine exposure and aminophospholipid translocase activity in Rh-deficient erythrocytesD Geldwerth, B Cherif-Zahar, D Helley, et al.
The Journal of Biological Chemistry|June 27, 1998
The Lutheran blood group glycoproteins, the erythroid receptors for laminin, are adhesion moleculesW El Nemer, P Gane, Y Colin, et al.
Blood|September 10, 1998
Arg89Cys substitution results in very low membrane expression of the Duffy antigen/receptor for chemokines in Fy(x) individualsC Tournamille, C Le Van Kim, P Gane, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 1, 1996
Molecular analysis of selected Rh variantsF Noizat-Pirenne, I Mouro, P Gane, et al.
Vox Sanguinis|January 1, 1987
Heterogeneity of anti-A and anti-B monoclonal reagents. Agglutination of some weak ABH erythrocyte variants and recognition of synthetic oligosaccharide and tissue antigensP Gane, J Vellayoudom, R Mollicone, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|April 4, 2006
Functional interaction between Rh proteins and the spectrin-based skeleton in erythroid and epithelial cellsV Nicolas, I Mouro-Chanteloup, C Lopez, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|April 4, 2006
Ammonium transport properties of HEK293 cells expressing RhCG mutants: preliminary analysis of structure/function by site-directed mutagenesisN Zidi-Yahiaoui, P Ripoche, C Le Van Kim, et al.
British Journal of Haematology|September 30, 1998
Shift from Rh-positive to Rh-negative phenotype caused by a somatic mutation within the RHD gene in a patient with chronic myelocytic leukaemiaB Chérif-Zahar, V Bony, R Steffensen, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|June 3, 2008
Role of Lu/BCAM in abnormal adhesion of sickle red blood cells to vascular endotheliumW El Nemer, E Gauthier, M-P Wautier, et al.
Blood|December 3, 1998
High adenosine deaminase level among healthy probands of Diamond Blackfan anemia (DBA) cosegregates with the DBA gene region on chromosome 19q13. The DBA Working Group of Société d'Immunologie Pédiatrique (SHIP)T N Willig, J L Pérignon, P Gustavsson, et al.
Pageof 10

Showing results (81-90 of 91) with videos related to

Sort By:
Pageof 10
Molecular Membrane Biology|July 1, 1997
Phosphatidylserine exposure and aminophospholipid translocase activity in Rh-deficient erythrocytesD Geldwerth, B Cherif-Zahar, D Helley, et al.
The Journal of Biological Chemistry|June 27, 1998
The Lutheran blood group glycoproteins, the erythroid receptors for laminin, are adhesion moleculesW El Nemer, P Gane, Y Colin, et al.
Blood|September 10, 1998
Arg89Cys substitution results in very low membrane expression of the Duffy antigen/receptor for chemokines in Fy(x) individualsC Tournamille, C Le Van Kim, P Gane, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 1, 1996
Molecular analysis of selected Rh variantsF Noizat-Pirenne, I Mouro, P Gane, et al.
Vox Sanguinis|January 1, 1987
Heterogeneity of anti-A and anti-B monoclonal reagents. Agglutination of some weak ABH erythrocyte variants and recognition of synthetic oligosaccharide and tissue antigensP Gane, J Vellayoudom, R Mollicone, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|April 4, 2006
Functional interaction between Rh proteins and the spectrin-based skeleton in erythroid and epithelial cellsV Nicolas, I Mouro-Chanteloup, C Lopez, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|April 4, 2006
Ammonium transport properties of HEK293 cells expressing RhCG mutants: preliminary analysis of structure/function by site-directed mutagenesisN Zidi-Yahiaoui, P Ripoche, C Le Van Kim, et al.
British Journal of Haematology|September 30, 1998
Shift from Rh-positive to Rh-negative phenotype caused by a somatic mutation within the RHD gene in a patient with chronic myelocytic leukaemiaB Chérif-Zahar, V Bony, R Steffensen, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|June 3, 2008
Role of Lu/BCAM in abnormal adhesion of sickle red blood cells to vascular endotheliumW El Nemer, E Gauthier, M-P Wautier, et al.
Blood|December 3, 1998
High adenosine deaminase level among healthy probands of Diamond Blackfan anemia (DBA) cosegregates with the DBA gene region on chromosome 19q13. The DBA Working Group of Société d'Immunologie Pédiatrique (SHIP)T N Willig, J L Pérignon, P Gustavsson, et al.
Pageof 10