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Nicole Lucien

Showing results (1-10 of 8) with videos related to

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Blood|January 25, 2002
Partial deletion in the JK locus causing a Jk(null) phenotypeNicole Lucien, Jacques Chiaroni, Jean-Pierre Cartron, et al.
Blood|July 20, 2002
Short deletion within the blood group Dombrock locus causing a Do(null) phenotypeNicole Lucien, Jean-Louis Celton, Pierre-Yves Le Pennec, et al.
The Journal of Biological Chemistry|December 26, 2001
Erythroid expression and oligomeric state of the AQP3 proteinNathalie Roudier, Pascal Bailly, Pierre Gane, et al.
Transfusion|December 2, 2008
Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndromeLionel Arnaud, François Salachas, Nicole Lucien, et al.
The Journal of Biological Chemistry|July 3, 2002
Antigenic and functional properties of the human red blood cell urea transporter hUT-B1Nicole Lucien, Frédéric Sidoux-Walter, Nathalie Roudier, et al.
EMBO Molecular Medicine|March 19, 2013
Disruption of SMIM1 causes the Vel- blood typeBryan A Ballif, Virginie Helias, Thierry Peyrard, et al.
Transfusion|May 25, 2010
A functional AQP1 allele producing a Co(a-b-) phenotype revises and extends the Colton blood group systemLionel Arnaud, Virginie Helias, Cécile Menanteau, et al.
American Journal of Human Genetics|November 9, 2010
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemiaLionel Arnaud, Carole Saison, Virginie Helias, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Blood|January 25, 2002
Partial deletion in the JK locus causing a Jk(null) phenotypeNicole Lucien, Jacques Chiaroni, Jean-Pierre Cartron, et al.
Blood|July 20, 2002
Short deletion within the blood group Dombrock locus causing a Do(null) phenotypeNicole Lucien, Jean-Louis Celton, Pierre-Yves Le Pennec, et al.
The Journal of Biological Chemistry|December 26, 2001
Erythroid expression and oligomeric state of the AQP3 proteinNathalie Roudier, Pascal Bailly, Pierre Gane, et al.
Transfusion|December 2, 2008
Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndromeLionel Arnaud, François Salachas, Nicole Lucien, et al.
The Journal of Biological Chemistry|July 3, 2002
Antigenic and functional properties of the human red blood cell urea transporter hUT-B1Nicole Lucien, Frédéric Sidoux-Walter, Nathalie Roudier, et al.
EMBO Molecular Medicine|March 19, 2013
Disruption of SMIM1 causes the Vel- blood typeBryan A Ballif, Virginie Helias, Thierry Peyrard, et al.
Transfusion|May 25, 2010
A functional AQP1 allele producing a Co(a-b-) phenotype revises and extends the Colton blood group systemLionel Arnaud, Virginie Helias, Cécile Menanteau, et al.
American Journal of Human Genetics|November 9, 2010
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemiaLionel Arnaud, Carole Saison, Virginie Helias, et al.
Pageof 1