A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia

Lionel Arnaud, Carole Saison, Virginie Helias, +20

The American Journal of Human Genetics

Transcriptional RegulationDevelopmental BiologyGenetic DisorderGeneticsInherited Metabolic Disease +8

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

Nicole Lucien, Frédéric Sidoux-Walter, Bernadette Olivès, +4

Journal of Biological Chemistry

GeneticsMolecular BiologyMolecular GeneticsGene EncodingProtein Genetics +14

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

Nicole Lucien, Freádeáric Sidoux-Walter, Nathalie Roudier, +5

Journal of Biological Chemistry

HistocompatibilityImmunohematologyFunctional PropertiesGeneticsImmunology +24

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

Frédéric Sidoux-Walter, Nicole Lucien, Bernadette Olivès, +7

Journal of Biological Chemistry

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

Frédéric Sidoux-Walter, Nicole Lucien, Riikka Nissinen, +5

Blood

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

Nicole Lucien, Patrick Bruneval, Chantal Mandet, +1

American Journal of Physiology-Regulatory, Integrative and Comparative Physiology

Digestive TractCellular PhysiologyGastrointestinal TractsCell SignalingUrological Research +17

Disruption of <i>SMIM1</i> causes the Vel− blood type

Bryan A. Ballif, Virginie Helias, Thierry Peyrard, +7

EMBO Molecular Medicine

Autoimmune DiseaseVel− Blood TypeDisease MechanismMedicineHematology +6

Partial deletion in the JK locus causing a Jknull phenotype

Nicole Lucien, Jacques Chiaroni, Jean‐Pierre Cartron, +1

Blood

Erythroid Expression and Oligomeric State of the AQP3 Protein

Nathalie Roudier, Pascal Bailly, Pierre Gane, +4

Journal of Biological Chemistry

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

Nicole Lucien, Jean-Louis Celton, Pierre‐Yves Le Pennec, +2

Blood