Publications by authors named "Jean Pierre Cartron"

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Lack of the human choline transporter-like protein SLC44A2 causes hearing impairment and a rare red blood phenotype.
Bérengère Koehl, Cédric Vrignaud, Mahmoud Mikdar, Thankam S Nair, Lucy Yang, Jean Pierre Cartron

EMBO Mol Med· March 2023

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Renal allograft DARCness in subclinical acute and chronic active ABMR.
Johannes Kläger, Farsad Eskandary, Georg A Böhmig, Nicolas Kozakowski, Alexander Kainz, Jean-Pierre Cartron

Transpl Int· August 2021

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Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders.
Romain Duval, Gaël Nicolas, Alexandra Willemetz, Yoshiko Murakami, Mahmoud Mikdar, Jean-Pierre Cartron

Blood· July 2021

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A new efficient tool for non-invasive diagnosis of fetomaternal platelet antigen incompatibility.
Yasmine Ouzegdouh Mammasse, Christophe Chenet, Damien Drubay, Corinne Martageix, Jean-Pierre Cartron

Br J Haematol· September 2020

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Lack of the multidrug transporter MRP4/ABCC4 defines the PEL-negative blood group and impairs platelet aggregation.
Slim Azouzi, Mahmoud Mikdar, Patricia Hermand, Emilie-Fleur Gautier, Virginie Salnot, Jean-Pierre Cartron

Blood· February 2020

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Maximal Oxygen Consumption Is Reduced in Aquaporin-1 Knockout Mice.
Samer Al-Samir, Dominique Goossens, Jean-Pierre Cartron, Søren Nielsen, Frank Scherbarth

Front Physiol· August 2016

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17 International Haemovigilance Seminar: Paris (France), 9-11 March 2016.
Erica Wood, Paula Bolton-Maggs, Jean-Claude Faber, Kevin Land Martin Schipperus, Peter Tomasulo, Jean-Pierre Cartron

Blood Transfus· March 2016

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Deletion of Exons 3 through 5 of ABCG2 causes the Jr(a-) phenotype in a West African woman.
Carole Saison, Jean-Pierre Cartron, Lionel Arnaud

Transfusion· November 2015

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SMIM1 is a type II transmembrane phosphoprotein and displays the Vel blood group antigen at its carboxyl-terminus.
Lionel Arnaud, Liam P Kelley, Virginie Helias, Jean-Pierre Cartron, Bryan A Ballif

FEBS Lett· November 2015

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Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization.
Geoff Daniels, Bryan A Ballif, Virginie Helias, Carole Saison, Shane Grimsley, Jean-Pierre Cartron

Blood· June 2015

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Mice expressing RHAG and RHD human blood group genes.
Dominique Goossens, Nelly da Silva, Sylvain Metral, Ulrich Cortes, Isabelle Callebaut, Jean-Pierre Cartron

PLoS One· August 2014

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Lethal autoimmune hemagglutination due to an immunoglobulin A autoagglutinin with Band 3 specificity.
Abdulgabar Salama, Daniel Janvier, Beate Mayer, Carole Saison, Henriette Moscatelli, Jean-Pierre Cartron

Transfusion· August 2014

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Activity and distribution of intracellular carbonic anhydrase II and their effects on the transport activity of anion exchanger AE1/SLC4A1.
Samer Al-Samir, Symeon Papadopoulos, Renate J Scheibe, Joachim D Meißner, Jean-Pierre Cartron

J Physiol· October 2013

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In vitro generated Rh(null) red cells recapitulate the in vivo deficiency: a model for rare blood group phenotypes and erythroid membrane disorders.
Marie Cambot, Christelle Mazurier, Florence Canoui-Poitrine, Nicolas Hebert, Julien Picot, Jean-Pierre Cartron

Am J Hematol· May 2013

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Disruption of SMIM1 causes the Vel- blood type.
Bryan A Ballif, Virginie Helias, Thierry Peyrard, Cécile Menanteau, Carole Saison, Jean-Pierre Cartron

EMBO Mol Med· May 2013

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Molecular analysis of the rare in(Lu) blood type: toward decoding the phenotypic outcome of haploinsufficiency for the transcription factor KLF1.
Virginie Helias, Carole Saison, Thierry Peyrard, Eliane Vera, Claude Prehu, Jean-Pierre Cartron

Hum Mutat· January 2013

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Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior.
Carole Saison, Virginie Helias, Bryan A Ballif, Thierry Peyrard, Hervé Puy, Jean-Pierre Cartron

Nat Genet· January 2012

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ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis.
Virginie Helias, Carole Saison, Bryan A Ballif, Thierry Peyrard, Junko Takahashi, Jean-Pierre Cartron

Nat Genet· January 2012

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Blood group genotyping by high-throughput DNA analysis applied to 356 reagent red blood cell samples.
Sandrine Kappler-Gratias, Thierry Peyrard, Marylise Beolet, Denise Amiranoff, Cécile Menanteau, Jean-Pierre Cartron

Transfusion· January 2011

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A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia.
Lionel Arnaud, Carole Saison, Virginie Helias, Nicole Lucien, Dominique Steschenko, Jean-Pierre Cartron

Am J Hum Genet· November 2010

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A functional AQP1 allele producing a Co(a-b-) phenotype revises and extends the Colton blood group system.
Lionel Arnaud, Virginie Helias, Cécile Menanteau, Thierry Peyrard, Nicole Lucien, Jean-Pierre Cartron

Transfusion· October 2010

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Intercellular adhesion molecule-4 and CD36 are implicated in the abnormal adhesiveness of sickle cell SAD mouse erythrocytes to endothelium.
Marie-Marcelle Trinh-Trang-Tan, Camilo Vilela-Lamego, Julien Picot, Marie-Paule Wautier, Jean-Pierre Cartron

Haematologica· May 2010

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Generation and characterisation of Rhd and Rhag null mice.
Dominique Goossens, Marie-Marcelle Trinh-Trang-Tan, Martine Debbia, Pierre Ripoche, Camilo Vilela-Lamego, Jean-Pierre Cartron

Br J Haematol· January 2010

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Functional analysis of human RhCG: comparison with E. coli ammonium transporter reveals similarities in the pore and differences in the vestibule.
Nedjma Zidi-Yahiaoui, Isabelle Callebaut, Sandrine Genetet, Caroline Le Van Kim, Jean-Pierre Cartron

Am J Physiol Cell Physiol· September 2009

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In Memoriam: Charles Salmon (1925-2009).
Jean-Pierre Cartron, Philippe Rouger

Transfusion· June 2009

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