J. Cartron

发表

Cloning and functional expression of a urea transporter from human bone marrow cells.

P. Ripoche, P. Bailly, B. Olivès, 1994, The Journal of biological chemistry.

Kidd Blood Group and Urea Transport Function of Human Erythrocytes Are Carried by the Same Protein (*)

M. Mattei, J. Cartron, P. Bailly, 1995, The Journal of Biological Chemistry.

A unique gene encodes spliceoforms of the B-cell adhesion molecule cell surface glycoprotein of epithelial cancer and of the Lutheran blood group glycoprotein

M. Mattei, Y. Colin, J. Cartron, 1996 .

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.

Lack of the human choline transporter-like protein CTL2 causes hearing impairment and a rare red blood cell phenotype

N. Mohandas, Y. Colin, T. Peyrard, 2022, medRxiv.

Characterization of the gene encoding the human LW blood group protein in LW+ and LW- phenotypes.

P. Rouger, P. Bailly, P. Le Pennec, 1996, Blood.

Erythropoietin‐induced erythroid differentiation of the human erythroleukemia cell line TF‐1 correlates with impaired STAT5 activation.

F. Verdier, P. Mayeux, S. Chrétien, 1996, The EMBO journal.

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.

UT-B1 proteins in rat: tissue distribution and regulation by antidiuretic hormone in kidney.

P. Gane, P. Ripoche, P. Bailly, 2002, American journal of physiology. Renal physiology.

MOLECULAR GENETIC BASIS OF RH AND LW BLOOD GROUPS

Y. Colin, P. Bailly, J. Cartron, 1994, Vox sanguinis.

Endothelial cells of the kidney vasa recta express the urea transporter HUT11.

J. Cartron, P. Ripoche, P. Bailly, 1997, Kidney international.

Evidence for distinct vascular and tubular urea transporters in the rat kidney.

L. Bankir, P. Ripoche, P. Bailly, 1996, Journal of the American Society of Nephrology : JASN.

Use of two chemically synthesised H acceptors as substrates for A and B blood group gene‐specified glycosyltransferases

J. Cartron, J. Badet, C. Mulet, 1976, FEBS letters.

The Heterogeneity of Erythrocyte Antigen Distribution in Human Normal Phenotypes: an Immunoelectron Microscopy Study

F. Reyes, J. Cartron, B. Dreyfus, 1976, British journal of haematology.

ATYPICAL TRANSMISSION OF ABO BLOOD GROUPS IN A FRENCH FAMILY

J. Cartron, A. Noel, J. Badet, 1982, Journal of immunogenetics.

DETECTION OF A1A2 AND A2AAm1 HETEROZYGOTES AMONG HUMAN A BLOOD GROUP PHENOTYPES

J. Cartron, J. Cartron, C. Salmon, 1976, Journal of immunogenetics.

High frequency antigens of human erythrocyte membrane sialoglycoproteins, V. Characterization of the Gerbich blood group antigens: Ge2 and Ge3.

D. Blanchard, J. Cartron, W. Dahr, 1987, Biological chemistry Hoppe-Seyler.

Terminology for Red Cell Surface Antigens

P. Sistonen, D. Anstee, C. Levene, 1999, Vox Sanguinis.

The LW blood group glycoprotein is homologous to intercellular adhesion molecules.

I. Callebaut, J. Mornon, P. Bailly, 1994, Proceedings of the National Academy of Sciences of the United States of America.

The molecular basis of the Kidd blood group polymorphism and its lack of association with type 1 diabetes susceptibility.

J. Todd, T. Merriman, J. Cartron, 1997, Human molecular genetics.

Characterization of the recombination hot spot involved in the genomic rearrangement leading to the hybrid D-CE-D gene in the D(VI) phenotype.

G. Matassi, I. Mouro, B. Chérif-Zahar, 1997, American journal of human genetics.

Lack of RHCE-encoded proteins in the D--phenotype may result from homologous recombination between the two RH genes.

B. Chérif-Zahar, V. Raynal, J. Cartron, 1996, Blood.

Prenatal determination of fetal RhD type by DNA amplification

Y. Colin, B. Chérif-Zahar, R. Warwick, 1994, The New England journal of medicine.

Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C.

A. Chishti, K. Andrabi, J. Delaunay, 1993, Blood.

Two-dimensional iodopeptide mapping demonstrates that erythrocyte Rh D, c, and E polypeptides are structurally homologous but nonidentical.

P. Agre, D. Blanchard, C. Bloy, 1988, Blood.

carried by distinct polypeptide chains polypeptide and demonstration that the Rh(D), (c), and (E) antigens are Determination of the N-terminal sequence of human red cell Rh(D)

K. Beyreuther, D. Blanchard, C. Bloy, 2011 .

Determination of the N-terminal sequence of human red cell Rh(D) polypeptide and demonstration that the Rh(D), (c), and (E) antigens are carried by distinct polypeptide chains.

K. Beyreuther, J. Cartron, D. Blanchard, 1988, Blood.

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.

Structural characterization of the epitope recognized by the new anti‐Fy6 monoclonal antibody NaM185‐2C3

C. Tournamille, Y. Colin, K. Waśniowska, 2002, Transfusion medicine.

Molecular analysis of the structure and expression of the RH locus in individuals with D--, Dc-, and DCw- gene complexes.

J. Cartron, Y. Colin, B. Chérif-Zahar, 1994, Blood.

individuals with D--, Dc-, and DCw- gene complexes Molecular analysis of the structure and expression of the RH locus in

Y. Colin, B. Chérif-Zahar, V. Raynal, 2011 .

Structural analysis of the RH-like blood group gene products in nonhuman primates

P. Calvas, A. Blancher, Y. Colin, 1995, Immunogenetics.

Organization of the human RH50A gene (RHAG) and evolution of base composition of the RH gene family.

G. Matassi, P. Rouger, B. Chérif-Zahar, 1998, Genomics.

A human monoclonal anti‐D antibody which detects a nonconformation‐dependent epitope on the RhD protein by immunoblot

A. Blancher, I. Mouro, Y. Colin, 1997, British journal of haematology.

DNA polymorphism analysis of HLA class II genes in unrelated children and in first-degree relatives with type I diabetes.

E. Tozzo, I. Deschamps, J. Cartron, 1991, Diabetes research.

Functional differentiation of the human red blood cell and kidney urea transporters.

L. Abrami, P. Ripoche, P. Bailly, 1996, The American journal of physiology.

Hereditary stomatocytosis and Rh-deficient patients exhibit distinct molecular defects.

P. Bailly, J. Cartron, D. Wang, 1992, Blood.

Surface orientation and antigen properties of Rh and LW polypeptides of the human erythrocyte membrane.

B. Chérif-Zahar, D. Blanchard, C. Bloy, 1990, The Journal of biological chemistry.

Molecular basis of the altered antigenic expression of RhD in weak D(Du) and RhC/e in RN phenotypes.

P. Gane, Y. Colin, P. Le Pennec, 1996, Blood.

Assay of α‐N‐Acetylgalactosaminyltransferases in Human Sera: Further Evidence for Several Types of Am Individuals

J. Cartron, J. Cartron, J. Badet, 1975, Vox sanguinis.

STUDY OF THE α‐N‐ACETYLGALACTOSAMINYLTRANSFERASE IN SERA AND RED CELL MEMBRANES OF HUMAN A SUBGROUPS

J. Cartron, J. Cartron, J. Badet, 1978, Journal of immunogenetics.

Blood Group Terminology 1995: ISBT Working Party on Terminology for Red Cell Surface Antigens

P. Sistonen, C. Levene, M. Overbeeke, 1995, Vox sanguinis.

Distinction of the Glycophorin C Locus from the Diego, Dombrock and Yt Blood Group Loci

J. Cartron, T. Zelinski, G. Coghlan, 1991, Vox sanguinis.

Erythroid‐specific activity of the glycophorin B promoter requires GATA‐1 mediated displacement of a repressor.

P. Romeo, J. Cartron, C. Rahuel, 1992, The EMBO journal.

The repressor which binds the -75 GATA motif of the GPB promoter contains Ku70 as the DNA binding subunit.

D. Thomas, R. Barbey, O. Bertrand, 1999, Nucleic acids research.

Susceptibility to invasion by Plasmodium falciparum of some human erythrocytes carrying rare blood group antigens

J. Cartron, J. Soulier, J. Cartron, 1983, British journal of haematology.

The presence of at least two different H-blood-group-related beta-D-gal alpha-2-L-fucosyltransferases in human serum and the genetics of blood group H substances.

J. Le Pendu, R. Oriol, J. Cartron, 1985, American journal of human genetics.

A genetic polymorphism of a human urinary mucin

D. Swallow, J. Cartron, G. Corney, 1983, Annals of human genetics.