Jean-pierre Cartron

Paris, France

Last Updated: 09/26/2026

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Found 14 publications

Renal allograft DARCness in subclinical acute and chronic active ABMR.

Renal allograft DARCness in subclinical acute and chronic active ABMR.

Journal: Transplant international : official journal of the European Society for Organ Transplantation
Published: January 10, 2021

Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders.

Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders.

Journal: Blood
Published: November 03, 2020

A new efficient tool for non-invasive diagnosis of fetomaternal platelet antigen incompatibility.

A new efficient tool for non-invasive diagnosis of fetomaternal platelet antigen incompatibility.

Journal: British journal of haematology
Published: December 20, 2019

Lack of the multidrug transporter MRP4/ABCC4 defines the PEL-negative blood group and impairs platelet aggregation.

Lack of the multidrug transporter MRP4/ABCC4 defines the PEL-negative blood group and impairs platelet aggregation.

Journal: Blood
Published: July 03, 2019

Maximal Oxygen Consumption Is Reduced in Aquaporin-1 Knockout Mice.

Maximal Oxygen Consumption Is Reduced in Aquaporin-1 Knockout Mice.

Journal: Frontiers in physiology
Published: May 09, 2016

SMIM1 is a type II transmembrane phosphoprotein and displays the Vel blood group antigen at its carboxyl-terminus.

SMIM1 is a type II transmembrane phosphoprotein and displays the Vel blood group antigen at its carboxyl-terminus.

Journal: FEBS letters
Published: July 12, 2015

Deletion of Exons 3 through 5 of ABCG2 causes the Jr(a-) phenotype in a West African woman.

Deletion of Exons 3 through 5 of ABCG2 causes the Jr(a-) phenotype in a West African woman.

Journal: Transfusion
Published: April 20, 2015

Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization.

Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization.

Journal: Blood
Published: February 27, 2015

Mice expressing RHAG and RHD human blood group genes.

Mice expressing RHAG and RHD human blood group genes.

Journal: PloS one
Published: July 26, 2013

Activity and distribution of intracellular carbonic anhydrase II and their effects on the transport activity of anion exchanger AE1/SLC4A1.

Activity and distribution of intracellular carbonic anhydrase II and their effects on the transport activity of anion exchanger AE1/SLC4A1.

Journal: The Journal of physiology
Published: July 24, 2013

Lethal autoimmune hemagglutination due to an immunoglobulin A autoagglutinin with Band 3 specificity.

Lethal autoimmune hemagglutination due to an immunoglobulin A autoagglutinin with Band 3 specificity.

Journal: Transfusion
Published: July 13, 2013

In vitro generated Rh(null) red cells recapitulate the in vivo deficiency: a model for rare blood group phenotypes and erythroid membrane disorders.

In vitro generated Rh(null) red cells recapitulate the in vivo deficiency: a model for rare blood group phenotypes and erythroid membrane disorders.

Journal: American journal of hematology
Published: February 05, 2013
Showing 1-12 of 14

Last Updated: 09/26/2026