N. Lucien

发表

Partial deletion in the JK locus causing a Jk(null) phenotype.

J. Chiaroni, J. Cartron, P. Bailly, 2002, Blood.

Antigenic and Functional Properties of the Human Red Blood Cell Urea Transporter hUT-B1*

J. Cartron, P. Ripoche, P. Bailly, 2002, The Journal of Biological Chemistry.

Molecular heterogeneity of the Jk(null) phenotype: expression analysis of the Jk(S291P) mutation found in Finns.

P. Sistonen, P. Bailly, N. Lucien, 2000, Blood.

the Jk ( S 291 P ) mutation found in Finns phenotype : expression analysis ofnullMolecular heterogeneity of the Jk

Joann, P. Sistonen, J. Cartron, 2000 .

Characterization of the Gene Encoding the Human Kidd Blood Group/Urea Transporter Protein

J. Cartron, P. Bailly, P. Le Pennec, 1998, The Journal of Biological Chemistry.

UT-B1 urea transporter is expressed along the urinary and gastrointestinal tracts of the mouse.

P. Bruneval, P. Bailly, C. Mandet, 2005, American journal of physiology. Regulatory, integrative and comparative physiology.

A CCACC motif mediates negative transcriptional regulation of the human erythropoietin receptor.

J. Cartron, N. Lucien, S. Chrétien, 1995, European journal of biochemistry.

At Physiological Expression Levels the Kidd Blood Group/Urea Transporter Protein Is Not a Water Channel*

P. Deen, J. Cartron, P. Ripoche, 1999, The Journal of Biological Chemistry.

A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia.

A. D. de Brevern, L. D. Da Costa, H. Tamary, 2010, American journal of human genetics.

Erythroid Expression and Oligomeric State of the AQP3 Protein*

P. Gane, J. Cartron, P. Ripoche, 2002, The Journal of Biological Chemistry.

Short deletion within the blood group Dombrock locus causing a Do(null) phenotype.

J. Cartron, P. Bailly, P. Le Pennec, 2002, Blood.

Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndrome

F. Salachas, T. Maisonobe, J. Cartron, 2009, Transfusion.

phenotype Short deletion within the blood group Dombrock locus causing a Donull

P. Pennec, J. Cartron, P. Bailly, 2013 .

Characterization of the gene encoding the human Kidd blood group/urea transporter protein. Evidence for splice site mutations in Jknull individuals.

P. Bailly, P. Le Pennec, N. Lucien, 1998, The Journal of biological chemistry.

Disruption of SMIM1 causes the Vel− blood type

M. le Gall, C. Menanteau, J. Cartron, 2013, EMBO molecular medicine.

Disruption of SMIM 1 causes the Vel S blood type

M. Gall, C. Menanteau, J. Cartron, 2013 .

the Jk(S291P) mutation found in Finns Molecular heterogeneity of the Jknull phenotype: expression analysis of

P. Sistonen, J. Cartron, P. Bailly, 2013 .

A functional AQP1 allele producing a Co(a–b–) phenotype revises and extends the Colton blood group system

C. Menanteau, J. Cartron, P. Ripoche, 2010, Transfusion.