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J.-P. Cartron

Researcher at French Institute of Health and Medical Research

Publications -  155
Citations -  5329

J.-P. Cartron is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Gene & Antigen. The author has an hindex of 38, co-authored 154 publications receiving 5227 citations. Previous affiliations of J.-P. Cartron include Collège de France & Paris Diderot University.

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Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy–negative individuals

TL;DR: It is shown that the Duffy antigen/chemokine receptor gene (DARC) is composed of a single exon and that most Duffy–negative blacks carry a silent FY*B allele with a single T to C substitution at nucleotide −46.
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Molecular genetic basis of the human Rhesus blood group system.

TL;DR: With the recent cloning of the RhD gene, these findings provide the molecular genetic basis that determine D, C, c, E and e specificities.
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Cloning and functional expression of a urea transporter from human bone marrow cells.

TL;DR: expression studies in Xenopus oocytes demonstrated that HUT11 mediates a facilitated urea transport that was inhibited, as described in mammalian erythrocytes, by very low concentrations of phloretin, p-chloromercuribenzene sulfonate, and urea analogues.
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Localization of the human Rh blood group gene structure to chromosome region 1p34.3–1p36.1 by in situ hybridization

TL;DR: A cDNA clone, RhIXb (1384 bp), encoding the entire protein sequence of a human blood group Rh polypeptide has been used to map the Rh locus, by in situ hybridization, to the region p34.3–p36.1 of chromosome 1.
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Insights into the structure and function of membrane polypeptides carrying blood group antigens

TL;DR: This review will focus on selected blood groups systems (RH, JK, FY, LU, LW, KEL and XK) which are representative of these classes of molecules, in order to illustrate how these studies may bring new information on common and variant phenotypes and for understanding both the mechanisms of tissue specific expression and the potential function of these antigens.