Cartron JP - Search Results

1

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

Duval R, Nicolas G, Willemetz A, Murakami Y, Mikdar M, Vrignaud C, Megahed H, Cartron JP, Masson C, Wehbi S, Koehl B, Hully M, Siquier K, Chemlay N, Rotig A, Lyonnet S, Colin Y, Barcia G, Cantagrel V, Le Van Kim C, Hermine O, Kinoshita T, Peyrard T, Azouzi S. Duval R, et al. Among authors: cartron jp. Blood. 2021 Jul 1;137(26):3660-3669. doi: 10.1182/blood.2020009810. Blood. 2021. PMID: 33763700 Free article.

2

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

Rouillac C, Gane P, Cartron J, Le Pennec PY, Cartron JP, Colin Y. Rouillac C, et al. Among authors: cartron jp, cartron j. Blood. 1996 Jun 1;87(11):4853-61. Blood. 1996. PMID: 8639859 Free article.

3

Partial deletion in the JK locus causing a Jk(null) phenotype.

Lucien N, Chiaroni J, Cartron JP, Bailly P. Lucien N, et al. Among authors: cartron jp. Blood. 2002 Feb 1;99(3):1079-81. doi: 10.1182/blood.v99.3.1079. Blood. 2002. PMID: 11807016 Free article.

4

Cell-surface expression of RhD blood group polypeptide is posttranscriptionally regulated by the RhAG glycoprotein.

Mouro-Chanteloup I, D'Ambrosio AM, Gane P, Le Van Kim C, Raynal V, Dhermy D, Cartron JP, Colin Y. Mouro-Chanteloup I, et al. Among authors: cartron jp. Blood. 2002 Aug 1;100(3):1038-47. Blood. 2002. PMID: 12130520 Free article.

5

Short deletion within the blood group Dombrock locus causing a Do(null) phenotype.

Lucien N, Celton JL, Le Pennec PY, Cartron JP, Bailly P. Lucien N, et al. Among authors: cartron jp. Blood. 2002 Aug 1;100(3):1063-4. doi: 10.1182/blood-2001-12-0298. Blood. 2002. PMID: 12130524 Free article.

6

Evidence that the red cell skeleton protein 4.2 interacts with the Rh membrane complex member CD47.

Mouro-Chanteloup I, Delaunay J, Gane P, Nicolas V, Johansen M, Brown EJ, Peters LL, Van Kim CL, Cartron JP, Colin Y. Mouro-Chanteloup I, et al. Among authors: cartron jp. Blood. 2003 Jan 1;101(1):338-44. doi: 10.1182/blood-2002-04-1285. Epub 2002 Sep 5. Blood. 2003. PMID: 12393467 Free article.

7

Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.

Noizat-Pirenne F, Lee K, Pennec PY, Simon P, Kazup P, Bachir D, Rouzaud AM, Roussel M, Juszczak G, Ménanteau C, Rouger P, Kotb R, Cartron JP, Ansart-Pirenne H. Noizat-Pirenne F, et al. Among authors: cartron jp. Blood. 2002 Dec 1;100(12):4223-31. doi: 10.1182/blood-2002-01-0229. Epub 2002 Aug 1. Blood. 2002. PMID: 12393640 Free article.

8

Rh-RhAG/ankyrin-R, a new interaction site between the membrane bilayer and the red cell skeleton, is impaired by Rh(null)-associated mutation.

Nicolas V, Le Van Kim C, Gane P, Birkenmeier C, Cartron JP, Colin Y, Mouro-Chanteloup I. Nicolas V, et al. Among authors: cartron jp. J Biol Chem. 2003 Jul 11;278(28):25526-33. doi: 10.1074/jbc.M302816200. Epub 2003 Apr 28. J Biol Chem. 2003. PMID: 12719424 Free article.

9

Structure-function analysis of the extracellular domains of the Duffy antigen/receptor for chemokines: characterization of antibody and chemokine binding sites.

Tournamille C, Filipe A, Wasniowska K, Gane P, Lisowska E, Cartron JP, Colin Y, Le Van Kim C. Tournamille C, et al. Among authors: cartron jp. Br J Haematol. 2003 Sep;122(6):1014-23. doi: 10.1046/j.1365-2141.2003.04533.x. Br J Haematol. 2003. PMID: 12956774 Free article.

10

Sequence, evolution and ligand binding properties of mammalian Duffy antigen/receptor for chemokines.

Tournamille C, Blancher A, Le Van Kim C, Gane P, Apoil PA, Nakamoto W, Cartron JP, Colin Y. Tournamille C, et al. Among authors: cartron jp. Immunogenetics. 2004 Jan;55(10):682-94. doi: 10.1007/s00251-003-0633-2. Epub 2004 Jan 8. Immunogenetics. 2004. PMID: 14712331

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