Jean‐pierre Cartron
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Biology
Jean‐pierre Cartron's Degrees
- PhD Molecular Biology Université Paris Cité
- Masters Genetics Université Paris Cité
- Bachelors Biology Université Paris Cité
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(Suggest an Edit or Addition)Jean‐pierre Cartron's Published Works
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Published Works
- Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy–negative individuals (1995) (709)
- The human Rhesus-associated RhAG protein and a kidney homologue promote ammonium transport in yeast (2000) (332)
- Molecular cloning and protein structure of a human blood group Rh polypeptide. (1990) (289)
- Molecular cloning and primary structure of the human blood group RhD polypeptide. (1992) (282)
- Molecular genetic basis of the human Rhesus blood group system (1993) (268)
- Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis (1991) (240)
- Expression of chemokines and chemokine receptors during human renal transplant rejection. (2001) (237)
- Defective urinary concentrating ability due to a complete deficiency of aquaporin-1. (2001) (204)
- Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis. (1991) (201)
- A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia. (2010) (187)
- Defining the Rh blood group antigens. Biochemistry and molecular genetics. (1994) (163)
- RhAG protein of the Rhesus complex is a CO2 channel in the human red cell membrane (2008) (155)
- Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety. (2002) (150)
- Human Rhesus-associated glycoprotein mediates facilitated transport of NH(3) into red blood cells. (2004) (150)
- The red cell LW blood group protein is an intercellular adhesion molecule which binds to CD11/CD18 leukocyte integrins (1995) (142)
- Characterization of the Gene Encoding the Human Kidd Blood Group/Urea Transporter Protein (1998) (141)
- ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis (2012) (140)
- RhBG and RhCG, the putative ammonia transporters, are expressed in the same cells in the distal nephron. (2003) (137)
- The Lutheran Blood Group Glycoproteins, the Erythroid Receptors for Laminin, Are Adhesion Molecules* (1998) (137)
- Molecular biology of the Rh antigens. (1991) (135)
- Epinephrine acts through erythroid signaling pathways to activate sickle cell adhesion to endothelium via LW-αvβ3 interactions (2004) (131)
- Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency (1996) (131)
- Comparison of the carbohydrate-binding specificities of seven N-acetyl-D-galactosamine-recognizing lectins. (1990) (128)
- Rh proteins: key structural and functional components of the red cell membrane. (2006) (126)
- Arg89Cys substitution results in very low membrane expression of the Duffy antigen/receptor for chemokines in Fy(x) individuals. (1998) (121)
- Expression of RhCG, a new putative NH(3)/NH(4)(+) transporter, along the rat nephron. (2002) (120)
- Increased adhesion to endothelial cells of erythrocytes from patients with polycythemia vera is mediated by laminin alpha5 chain and Lu/BCAM. (2007) (119)
- Insights into the Structure and Function of Membrane Polypeptides Carrying Blood Group Antigens (1998) (117)
- Evidence that the red cell skeleton protein 4.2 interacts with the Rh membrane complex member CD47. (2003) (116)
- Rearrangements of the blood group RhD gene associated with the DVI category phenotype. (1994) (116)
- Time‐course expression of polypeptides carrying blood group antigens during human erythroid differentiation (1999) (115)
- RH blood group system and molecular basis of Rh-deficiency. (1999) (115)
- Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior (2012) (114)
- Rh-RhAG/Ankyrin-R, a New Interaction Site between the Membrane Bilayer and the Red Cell Skeleton, Is Impaired by Rhnull-associated Mutation* (2003) (114)
- Molecular characterization of a new urea transporter in the human kidney (1996) (113)
- Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes. (1995) (113)
- Organization of the gene (RHCE) encoding the human blood group RhCcEe antigens and characterization of the promoter region. (1994) (111)
- Blood Group Terminology 1995: ISBT Working Party on Terminology for Red Cell Surface Antigens (1995) (110)
- Prenatal determination of fetal RhD type by DNA amplification. (1993) (104)
- Structural and functional diversity of blood group antigens. (2001) (99)
- AQP3 Deficiency in Humans and the Molecular Basis of a Novel Blood Group System, GIL* (2002) (96)
- Binding Sites of Leukocyte β2 Integrins (LFA-1, Mac-1) on the Human ICAM-4/LW Blood Group Protein* (2000) (96)
- The Duffy antigen receptor for chemokines is up-regulated during acute renal transplant rejection and crescentic glomerulonephritis. (2000) (93)
- Molecular basis for the dialysis disequilibrium syndrome: altered aquaporin and urea transporter expression in the brain. (2005) (93)
- Localization of the human Rh blood group gene structure to chromosome region 1p34.3–1p36.1 by in situ hybridization (1991) (93)
- Molecular basis and PCR-DNA typing of the Fya/fyb blood group polymorphism (1995) (90)
- 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. (1985) (88)
- Normal human serum contains natural antibodies reactive with autologous ABO blood group antigens. (1999) (88)
- Different Transport Mechanisms in Plant and Human AMT/Rh-type Ammonium Transporters (2006) (88)
- Biosynthesis of blood group I antigens. Identification of a UDP-GlcNAc:GlcNAc beta 1-3Gal(-R) beta 1-6(GlcNAc to Gal) N-acetylglucosaminyltransferase in hog gastric mucosa. (1984) (87)
- A study of the role of parvovirus B19 in rheumatoid arthritis. (1995) (86)
- Genetic ablation of Rhbg in the mouse does not impair renal ammonium excretion. (2005) (85)
- Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease (2008) (84)
- Human Rhesus B and Rhesus C glycoproteins: properties of facilitated ammonium transport in recombinant kidney cells. (2005) (83)
- Red Cell ICAM-4 Is a Novel Ligand for Platelet-activated αIIbβ3 Integrin* (2003) (82)
- Demonstration of T-transferase deficiency in Tn-polyagglutinable blood samples. (1978) (82)
- Demonstration of T-transferase deficiency in Tn-polyagglutinable blood samples. (1978) (82)
- Primary structure of the oligosaccharide determinant of blood group Cad specificity. (1983) (82)
- Isolation of cDNA clones and complete amino acid sequence of human erythrocyte glycophorin C. (1986) (79)
- Antigenic and Functional Properties of the Human Red Blood Cell Urea Transporter hUT-B1* (2002) (78)
- Large-Scale Pre-Diagnosis Study of Fetal RHD Genotyping by PCR on Plasma DNA from RhD-Negative Pregnant Women (2012) (78)
- Specificity and sensitivity of RHD genotyping methods by PCR‐based DNA amplification (1997) (78)
- Protein Kinase A-dependent Phosphorylation of Lutheran/Basal Cell Adhesion Molecule Glycoprotein Regulates Cell Adhesion to Laminin α5* (2005) (77)
- Purification and partial characterization of the erythrocyte Kx protein deficient in McLeod patients. (1995) (76)
- Blood Group Terminology 1990 (1990) (76)
- Multiple Rh messenger RNA isoforms are produced by alternative splicing. (1992) (74)
- Epinephrine acts through erythroid signaling pathways to activate sickle cell adhesion to endothelium via LW-alphavbeta3 interactions. (2004) (73)
- At Physiological Expression Levels the Kidd Blood Group/Urea Transporter Protein Is Not a Water Channel* (1999) (71)
- Human erythrocyte glycophorin C. Gene structure and rearrangement in genetic variants. (1989) (70)
- Close Association of the First and Fourth Extracellular Domains of the Duffy Antigen/Receptor for Chemokines by a Disulfide Bond Is Required for Ligand Binding* (1997) (69)
- Human monoclonal antibody against Rh(D) antigen: partial characterization of the Rh(D) polypeptide from human erythrocytes. (1987) (69)
- Hydrophobic cluster analysis and modeling of the human Rh protein three-dimensional structures. (2006) (66)
- Comparison of two methods of high-molecular-weight DNA isolation from human leucocytes. (1983) (66)
- Immunochemical characterization of rhesus proteins with antibodies raised against synthetic peptides. (1993) (65)
- Human erythrocyte glycophorins: protein and gene structure analyses. (1992) (65)
- UDP-GlcNAc:Gal beta 1-4Glc(NAc) beta 1-3N-acetylglucosaminyltransferase. Identification and characterization in human serum. (1983) (65)
- Rh blood group antigens: protein and gene structure. (1993) (65)
- Involvement of Rh blood group polypeptides in the maintenance of aminophospholipid asymmetry. (1990) (62)
- Biosynthesis of ABH and Lewis antigens in normal and transplanted kidneys. (1980) (62)
- Biosynthesis of ABH and Lewis antigens in normal and transplanted kidneys. (1980) (62)
- Erythroid adhesion molecules in sickle cell disease: effect of hydroxyurea. (2008) (62)
- Galactosyltransferase and membrane glycoprotein abnormality in human platelets from Tn-syndrome donors (1979) (61)
- PCR‐based determination of Rhc and RhE status of fetuses at risk of Rhc and RhE haemolytic disease (1994) (61)
- The Members of the RH Gene Family (RH50 and RH30) Followed Different Evolutionary Pathways (1999) (60)
- Organization of the Human LU Gene and Molecular Basis of the Lua/Lub Blood Group Polymorphism (1997) (58)
- Cloning of the gene encoding the human erythropoietin receptor. (1991) (58)
- 'Weak A' phenotypes. Relationship between red cell agglutinability and antigen site density. (1974) (57)
- Endothelial Lu/BCAM glycoproteins are novel ligands for red blood cell alpha4beta1 integrin: role in adhesion of sickle red blood cells to endothelial cells. (2007) (57)
- Red cell ICAM-4 is a novel ligand for platelet-activated alpha IIbbeta 3 integrin. (2003) (57)
- Anomalies of Blood Group Antigens and Erythrocyte Enzymes in Two Types of Chronic Refractory Anaemia (1969) (57)
- Glycophorins B and C from human erythrocyte membranes. Purification and sequence analysis. (1987) (54)
- Structure–function analysis of the extracellular domains of the Duffy antigen/receptor for chemokines: characterization of antibody and chemokine binding sites (2003) (54)
- Red cell membrane CO2 permeability in normal human blood and in blood deficient in various blood groups, and effect of DIDS. (2006) (53)
- Alloimmune neonatal neutropenia. (1991) (52)
- Role of RhAG and AQP1 in NH3 and CO2 gas transport in red cell ghosts: a stopped-flow analysis. (2006) (51)
- Disruption of SMIM1 causes the Vel− blood type (2013) (51)
- Characterization of ICAM-4 binding to the I domains of the CD11a/CD18 and CD11b/CD18 leukocyte integrins. (2003) (50)
- Molecular defects of the RHCE gene in Rh-deficient individuals of the amorph type. (1998) (50)
- A novel gene member of the human glycophorin A and B gene family. Molecular cloning and expression. (1990) (49)
- Cell-surface expression of RhD blood group polypeptide is posttranscriptionally regulated by the RhAG glycoprotein. (2002) (48)
- Noninvasive fetal RHD genotyping from maternal plasma. Use of a new developed Free DNA Fetal Kit RhD. (2007) (48)
- Gerbich blood group deficiency of the Ge:-1,-2,-3 and Ge:-1,-2,3 types. Immunochemical study and genomic analysis with cDNA probes. (1987) (48)
- Characterization of cDNA clones for human glycophorin A. Use for gene localization and for analysis of normal of glycophorin-A-deficient (Finnish type) genomic DNA. (1988) (47)
- Isoforms of the Lutheran/Basal Cell Adhesion Molecule Glycoprotein Are Differentially Delivered in Polarized Epithelial Cells (1999) (46)
- Two new alleles of the RHCE gene in Black individuals: the RHce allele ceMO and the RHcE allele cEMI (2001) (46)
- Gerbich reactivity in 4.1(—) hereditary elliptocytosis and protein 4.1 level in blood group Gerbich deficiency (1987) (46)
- Structure and expression of the RH locus in the Rh-deficiency syndrome. (1993) (45)
- Heterogeneous molecular background of the weak C, VS+, hrB–, HrB– phenotype in black persons (2009) (45)
- Lack of G blood group antigen in DIIIb erythrocytes is associated with segmental DNA exchange between RH genes (1995) (44)
- Putative oncogenic role of the erythropoietin receptor in murine and human erythroleukemia cells. (1994) (43)
- Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization. (2015) (43)
- Direct interaction between the Lu/B‐CAM adhesion glycoproteins and erythroid spectrin † (2004) (43)
- A unique gene encodes spliceoforms of the B-cell adhesion molecule cell surface glycoprotein of epithelial cancer and of the Lutheran blood group glycoprotein. (1996) (42)
- High adenosine deaminase level among healthy probands of Diamond Blackfan anemia (DBA) cosegregates with the DBA gene region on chromosome 19q13. The DBA Working Group of Société d'Immunologie Pédiatrique (SHIP). (1998) (42)
- Virus-induced autoimmune thrombocytopenia and neutropenia. (1992) (41)
- Characterization of the Laminin Binding Domains of the Lutheran Blood Group Glycoprotein* (2001) (41)
- Structural homology between glycophorins C and D of human erythrocytes. (1989) (41)
- When renal allografts turn darc1 (2003) (41)
- The nonexpression of CD36 on reticulocytes and mature red blood cells does not modify the clinical course of patients with sickle cell anemia. (2001) (41)
- Differential expression of the Kell blood group and CD10 antigens: two related membrane metallopeptidases during differentiation of K562 cells by phorbol ester and hemin (1998) (40)
- Molecular basis for elliptocytosis associated with glycophorin C and D deficiency in the Leach phenotype. (1991) (40)
- Immunochemical analysis of the Kx protein from human red cells of different Kell phenotypes using antibodies raised against synthetic peptides (1997) (40)
- Genetic inactivation of the laminin alpha5 chain receptor Lu/BCAM leads to kidney and intestinal abnormalities in the mouse. (2008) (40)
- Single-cell analysis of the RhD blood type for use in preimplantation diagnosis in the prevention of severe hemolytic disease of the newborn. (1995) (39)
- Clonal expression of the Tn antigen in erythroid and granulocyte colonies and its application to determination of the clonality of the human megakaryocyte colony assay. (1982) (39)
- Properties of the blood group LW glycoprotein and preliminary comparison with Rh proteins. (1989) (39)
- Enhanced Expression of Duffy Antigen in the Lungs During Suppurative Pneumonia (2003) (39)
- Activity and distribution of intracellular carbonic anhydrase II and their effects on the transport activity of anion exchanger AE1/SLC4A1 (2013) (39)
- Blood Group Terminology 1995 (1995) (39)
- Heterogeneity of blood group RhE variants revealed by serological analysis and molecular alteration of the RHCE gene and transcript (1998) (38)
- Terminology for Red Cell Surface Antigens (1996) (38)
- Molecular Analysis of the Rare In(Lu) Blood Type: Toward Decoding the Phenotypic Outcome of Haploinsufficiency for the Transcription Factor KLF1 (2013) (38)
- Hybrid glycophorins from human erythrocyte membranes. Isolation and complete structural analysis of the novel sialoglycoprotein from St(a+) red cells. (1987) (38)
- Identification of a α-NeuAc-(2→3)-β-d-galactopyranosyl N-acetyl-β-d-galactosaminyltransferase in human kidney (1986) (37)
- Integrin receptor specificity for human red cell ICAM-4 ligand. Critical residues for alphaIIbeta3 binding. (2004) (37)
- Isolation and characterization of an N-acetylgalactosamine specific lectin from Salvia sclarea seeds. (1986) (37)
- Pj variant, a new hybrid MNSs glycoprotein of the human red-cell membrane. (1982) (37)
- Molecular basis and expression of the LWa/LWb blood group polymorphism. (1995) (37)
- Functional interaction between Rh proteins and the spectrin-based skeleton in erythroid and epithelial cells. (2006) (37)
- A novel single missense mutation identified along the RH50 gene in a composite heterozygous Rhnull blood donor of the regulator type. (1998) (36)
- Erythroid Expression and Oligomeric State of the AQP3 Protein* (2002) (36)
- Partial deletion in the JK locus causing a Jk(null) phenotype. (2002) (35)
- Alteration of the genes for glycophorin A and B in glycophorin-A-deficient individuals. (1988) (35)
- The Ammonium Transporter RhBG (2005) (35)
- Identification of a novel ganglioside on erythrocytes with blood group Cad specificity. (1985) (35)
- Immunochemical characterization of the human blood cell membrane glycoprotein recognized by the monoclonal antibody 12E7. (1987) (34)
- Evidence that the c, D and E epitopes of the human Rh blood group system are on separate polypeptide molecules. (1988) (34)
- Flow cytometric analysis of the association between blood group‐related proteins and the detergent‐insoluble material of K562 cells and erythroid precursors (2001) (33)
- Tentative model for the mapping of D epitopes on the RhD polypeptide. (1996) (33)
- ABH and Lewis glycosyltransferases in human red cells, lymphocytes and platelets. (1980) (33)
- Glycophorin C and related glycoproteins: structure, function, and regulation. (1993) (32)
- Characterization of the blood group Kell (K1) antigen with a human monoclonal antibody. (1989) (32)
- International Society of Blood Transfusion working party on terminology for red cell surface antigens (2001) (32)
- Severe autoimmune hemolytic anemia caused by a warm IgA autoantibody directed against the third loop of band 3 (RBC anion‐exchange protein 1) (2002) (32)
- Molecular Basis of Human Blood Group Antigens (1995) (31)
- Molecular Basis of the RhCW (Rh8) and RhCX (Rh9) Blood Group Specificities (1995) (30)
- Transcriptional regulation of the KEL gene and Kell protein expression in erythroid and non-erythroid cells. (2001) (30)
- Heterogeneity of neutrophil antibodies in patients with primary Sjögren's syndrome. (1995) (30)
- Functional analysis of human RhCG: comparison with E. coli ammonium transporter reveals similarities in the pore and differences in the vestibule. (2009) (30)
- Molecular Genetics of Human Erythrocyte Sialoglycoproteins Glycophorins A, B, C, and D (1990) (30)
- ISBT Working Party on Terminology for Red Cell Surface Antigens: São Paulo Report (1993) (30)
- Molecular background of D(C)(e) haplotypes within the white population (2002) (30)
- Surface modifications in the platelets of a patient with alpha-N-acetyl-D-galactosamine residues, the Tn-syndrome. (1982) (30)
- Characterization of the gene encoding the human LW blood group protein in LW+ and LW- phenotypes (1996) (30)
- THE LEWIS SYSTEM: NEW HISTOCOMPATIBILITY ANTIGENS IN RENAL TRANSPLANTATION (1978) (29)
- Structure of the promoter region and tissue specificity of the human glycophorin C gene. (1989) (29)
- Rh-deficiency of the regulator type caused by splicing mutations in the human RH50 gene. (1998) (29)
- Association of human erythrocyte membrane glycoproteins with blood-group Cad specificity. (1982) (29)
- Organization of the human LU gene and molecular basis of the Lu(a)/Lu(b) blood group polymorphism. (1997) (29)
- Cloning, expression, and chromosomal mapping of a human ATPase II gene, member of the third subfamily of P-type ATPases and orthologous to the presumed bovine and murine aminophospholipid translocase. (1999) (29)
- Blood group genotyping by high‐throughput DNA analysis applied to 356 reagent red blood cell samples (2011) (28)
- Spleen focus-forming virus long terminal repeat insertional activation of the murine erythropoietin receptor gene in the T3Cl-2 friend leukemia cell line. (1991) (28)
- Murine monoclonal antibodies against a unique determinant of erythrocytes, related to Rh and U antigens: expression on normal and malignant erythrocyte precursors and Rhnull red cells (1990) (27)
- Different domains regulate the human erythropoietin receptor gene transcription. (1994) (27)
- Characterization of murine monoclonal antibodies directed against the Kell blood group glycoprotein (1991) (26)
- Glycophorins C and D are generated by the use of alternative translation initiation sites. (1996) (26)
- Characterization of the D, c, E and G antigens of the Rh blood group system with human monoclonal antibodies. (1988) (25)
- Shift from Rh‐positive to Rh‐negative phenotype caused by a somatic mutation within the RHD gene in a patient with chronic myelocytic leukaemia (1998) (25)
- Chromatographic separation of recombinant human erythropoietin isoforms. (1997) (25)
- Early expression of glycophorin C during normal and leukemic human erythroid differentiation. (1989) (25)
- α‐2‐L‐Fucosyltransferase Activity in Sera of Individuals with H‐Deficient Red Cells and Normal H Antigen in Secretions (1983) (24)
- The ABCB6 mutation p.Arg192Trp is a recessive mutation causing the Lan− blood type (2013) (24)
- Promoter sequence and chromosomal organization of the genes encoding glycophorins A, B and E. (1990) (24)
- Presence of the Tn antigen on hematopoietic progenitors from patients with the Tn syndrome. (1985) (24)
- A study of the coregulation and tissue specificity of XG and MIC2 gene expression in eukaryotic cells. (2000) (23)
- Role of Lu/BCAM in abnormal adhesion of sickle red blood cells to vascular endothelium. (2008) (23)
- Analysis of deletions in three McLeod patients: exclusion of the XS locus from the Xp21.1-Xp21.2 region. (2000) (23)
- Short deletion within the blood group Dombrock locus causing a Do(null) phenotype. (2002) (23)
- Structure determination of oligosaccharides isolated from Cad erythrocyte membranes by permethylation analysis and 500-MHz 1H-NMR spectroscopy. (1985) (23)
- High-frequency antigens of human erythrocyte membrane sialoglycoproteins. VI. Monoclonal antibodies reacting with the N-terminal domain of glycophorin C. (1989) (23)
- Fine mapping of the Duffy antigen binding site for the Plasmodium vivax Duffy-binding protein. (2005) (23)
- Comparative study of glycophorin A derived O-glycans from human Cad, Sd(a+) and Sd(a-) erythrocytes. (1985) (22)
- RH Blood Groups and Rh-Deficiency Syndrome (1995) (22)
- The molecular basis of the Rhesus antigen Ew (2004) (22)
- International Society of Blood Transfusion Committee on terminology for red cell surface antigens: Vancouver Report (2003) (22)
- Kell and Kx, two disulfide-linked proteins of the human erythrocyte membrane are phosphorylated in vivo. (1998) (21)
- Cytotoxicity of anti-PP1Pk antibodies and possible relationship with early abortions of p mothers. (1983) (21)
- Cytotoxicity of anti-PP1Pk antibodies and possible relationship with early abortions of p mothers. (1983) (21)
- Structural variability of the neutral carbohydrate moiety of cow colostrum kappa-casein as a function of time after parturition. Identification of a tetrasaccharide with blood group I specificity. (1988) (21)
- Relationship between chimpanzee Rh-like genes and the R-C-E-F blood group system. (1993) (21)
- Erythrocyte glycophorin B deficiency may occur by two distinct gene alterations (1991) (21)
- Anti-Fc gamma receptor III autoantibody is associated with soluble receptor in rheumatoid arthritis serum and synovial fluid. (1995) (20)
- Molecular basis of the RhCW (Rh8) and RhCX (Rh9) blood group specificities. (1995) (20)
- Intercellular adhesion molecule-4 and CD36 are implicated in the abnormal adhesiveness of sickle cell SAD mouse erythrocytes to endothelium (2010) (20)
- Groups of alpha-D-galactosyl transferase activity in sera of individuals with normal B phenotype. (1974) (19)
- Generation and characterisation of Rhd and Rhag null mice (2010) (18)
- Current genetic problems in the ABO blood group system. (1973) (18)
- The origin of human B and T cells from multipotent stem cells: a study of the Tn syndrome (1983) (18)
- Comparative analysis by two-dimensional iodopeptide mapping of the RhD protein and LW glycoprotein. (1990) (18)
- The Ammonium Transporter RhBG REQUIREMENT OF A TYROSINE-BASED SIGNAL AND ANKYRIN-G FOR BASOLATERAL TARGETING AND MEMBRANE ANCHORAGE IN POLARIZED KIDNEY EPITHELIAL CELLS* (2005) (17)
- Erythrocyte webb‐type glycophorin C variant lacks N‐glycosylation due to an asparagine to serine substitution (1991) (17)
- INTERNATIONAL SOCIETY OF BLOOD TRANSFUSION SOCIÉTÉ INTERNATIONALE DE TRANSFUSION SANGUINE: ISBT Working Party on Terminology for Red Cell Surface Antigens: Los Angeles Report (1991) (17)
- H-deficient blood groups of Reunion Island. III. alpha-2-L-fucosyltransferase activity in sera of homozygous and heterozygous individuals. (1983) (17)
- Protein blood group antigens of the human red cell : structure, function, and clinical significance (1992) (17)
- Structure of a ganglioside with Cad blood group antigen activity. (1986) (17)
- Structure of the 5' flanking region of the gene encoding human glycophorin A and analysis of its multiple transcripts. (1989) (16)
- Characterization of a UDP-Gal:Galβ1–3GalNAc α1,4-Galactosyltransferase Activity in a Mamestra brassicaeCell Line* (1998) (16)
- Repressed β-1,3-galactosyltransferase in the Tn syndrome (1998) (16)
- Isolation from human urines of a mucin with blood group SDa activity. (1982) (16)
- Level of the A, B and H blood group glycosyltransferases in red cell membranes from patients with malignant hemopathies. (1984) (16)
- Maximal Oxygen Consumption Is Reduced in Aquaporin-1 Knockout Mice (2016) (15)
- Interaction of Vicia graminea anti-N lectin with cell surface glycoproteins from erythrocytes with rare blood group antigens. (1984) (15)
- Antigen site distribution among weak A' red cell populations. A study of A3, Ax and Aend variants. (1977) (15)
- Expanded bed chromatography for one-step purification of mannose binding lectin from tulip bulbs using mannose immobilized on DEAE Streamline (1998) (15)
- SMIM1 is a type II transmembrane phosphoprotein and displays the Vel blood group antigen at its carboxyl‐terminus (2015) (15)
- Failure of granulocyte colony-stimulating factor in alloimmune neonatal neutropenia. (1995) (14)
- Biosynthesis of the blood group Pk and P1 antigens by human kidney microsomes. (1992) (14)
- FY*X real‐time polymerase chain reaction with melting curve analysis associated with a complete one‐step real‐time FY genotyping (2007) (14)
- Characterization of a mouse laminin receptor gene homologous to the human blood group Lutheran gene (1999) (14)
- Identification of udp-galactose : Lactose (lactosylceramide) α-4 and β-3 galactosyltransferases in human kidney (1986) (14)
- Lack of the multidrug transporter MRP4/ABCC4 defines the PEL-negative blood group and impairs platelet aggregation. (2019) (14)
- In vitro generated Rhnull red cells recapitulate the in vivo deficiency: A model for rare blood group phenotypes and erythroid membrane disorders (2013) (13)
- The E-box of the human glycophorin B promoter is involved in the erythroid-specific expression of the GPB gene. (1999) (13)
- Purification and biological activity of a recombinant human erythropoietin produced by lymphoblastoid cells. (1994) (13)
- MATCHING RENAL GRAFTS (1978) (13)
- Ubc9 interacts with Lu/BCAM adhesion glycoproteins and regulates their stability at the membrane of polarized MDCK cells. (2007) (13)
- Miltenberger Class I and II erythrocytes carry a variant of glycophorin A. (1983) (13)
- Induction of Tk polyagglutination by Bacteroides fragilis culture supernatants. Associated modifications of A B H and I i antigens. (1979) (13)
- Rh antibodies after kidney transplantation. (1981) (11)
- The 1.35-kb and 7.5-kb Duffy mRNA isoforms are differently regulated in various regions of brain, differ by the length of their 5' untranslated sequence, but encode the same polypeptide. (1997) (11)
- Mesures quantitatives des antigènes A, A1, B, H, I et i Application à la pathologie (1969) (11)
- Chromatography of human immunoglobulin G on immobilized drimarene rubine R/K-5BL. Study of mild, efficient elution procedures. (1994) (11)
- Molecular characterization of the rh-like locus and gene transcripts from the rhesus monkey (Macaca mulatta) (1994) (11)
- Increase of blood group A and loss of blood group Sda activity in the mucus from human neoplastic colon. (1980) (11)
- Characterization of a new erythroid/megakaryocyte-specific nuclear factor that binds the promoter of the housekeeping human glycophorin C gene. (1990) (11)
- Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndrome (2009) (11)
- Membrane receptors for Vicia graminea anti-N lectin and its binding to native and neuraminidase-treated human erythrocytes. (1983) (10)
- Quantitative analysis of XG blood group and CD99 antigens on human red cells (2000) (10)
- A functional AQP1 allele producing a Co(a–b–) phenotype revises and extends the Colton blood group system (2010) (10)
- Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders. (2021) (10)
- The nonexpression of CD 36 on reticulocytes and mature red blood cells does not modify the clinical course of patients with sickle cell anemia (2001) (10)
- Mice Expressing RHAG and RHD Human Blood Group Genes (2013) (10)
- Characterization and specific assay for a galactoside beta-3-galactosyltransferase of human kidney. (1988) (10)
- Structure and expression of the mouse homologue of the XK gene (1999) (10)
- Selective expression of blood group antigens on human teratocarcinoma cell lines. (1981) (10)
- Molecular basis of red cell protein antigen deficiencies. (2000) (9)
- Post-transcriptional regulation of the cell surface expression of glycophorins A, B, and E. (1994) (9)
- A Novel Single Missense Mutation Identified Along the RH 50 Gene in a Composite Heterozygous (1998) (9)
- Specificity of anti-Mg antibody--a study with synthetic peptides and glycopeptides. (1984) (9)
- Screening of a large number of dyes for the separation of human immunoglobulin G2 from the other immunoglobulin G subclasses immunoglobulin G2 enrichment on immobilized Procion Yellow HE-4R. (1997) (9)
- MULTIPLE RH MRNAS ISOFORMS ARE PRODUCED BY ALTERNATIVE SPLICING (1992) (9)
- A CCACC motif mediates negative transcriptional regulation of the human erythropoietin receptor. (1995) (9)
- Tk polyagglutination produced in vitro by an endo-beta-galactosidase. (1980) (9)
- Characterization of a murine monoclonal antibody specific for the human P1 blood group antigen. (1987) (9)
- The dantu erythrocyte phenotype of the NE variety (1987) (9)
- A monoclonal antibody directed against the homologous N-terminal domain of glycophorin A and B. (1984) (9)
- Phage‐derived monoclonal anti‐Lua (2006) (9)
- Non Hodgkin's lymphoma presenting as neutropenia related to an IgM monoclonal anti-i antibody. (1996) (9)
- Non Hodgkin's lymphoma presenting as neutropenia related to an IgM monoclonal anti-i antibody. (1996) (9)
- Repressed beta-1,3-galactosyltransferase in the Tn syndrome. (1998) (8)
- Elevated IgE levels in the serum of multitransfused patients. Possible role in transfusion reactions. (1974) (8)
- Quantitative analysis of XG blood group and CD99 antigens on human red cells (2000) (8)
- Elevated IgE levels in the serum of multitransfused patients. Possible role in transfusion reactions. (1974) (8)
- MNSs and major glycophorins of human erythrocytes. (1995) (8)
- Ammonium transport properties of HEK293 cells expressing RhCG mutants: preliminary analysis of structure/function by site-directed mutagenesis. (2006) (8)
- Preparation and biological properties of monoclonal antibodies against human erythropoietin. (1993) (8)
- Identification of a alpha-NeuAc-(2----3)-beta-D-galactopyranosyl N-acetyl-beta-D-galactosaminyltransferase in human kidney. (1986) (8)
- The Tn receptors of human red cells and platelets. (1980) (8)
- Spanish Rhnull family caused by a silent Rh gene: Hematological, serological, and biochemical studies (1992) (8)
- Assay of α-TV-Acetylgalactosaminyltransferases in Human Sera (1975) (8)
- Lethal autoimmune hemagglutination due to an immunoglobulin A autoagglutinin with Band 3 specificity (2014) (8)
- Phosphatidylserine exposure and aminophospholipid translocase activity in Rh-deficient erythrocytes. (1997) (8)
- The Mz variety of the St(a+) phenotype--a variant of glycophorin A exhibiting a deletion. (1990) (8)
- The extracellular domain of the human erythropoietin receptor: expression as a fusion protein in Escherichia coli, purification, and biological properties. (1999) (8)
- Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemia (1987) (8)
- Observations on the reactions between D-positive red cells and ( 125 I)IgM anti-D molecules and subunits. (1971) (8)
- Detection of Combined ABH and Lewis Glycosphingolipids in Sera of H‐Deficient Donors (1985) (7)
- Efficient production of biologically active human recombinant proteins in human lymphoblastoid cells from integrative and episomal expression vectors. (1994) (7)
- Rh-deficiency syndrome (2001) (7)
- New procedures for glycophorin A purification with high yield and high purity. (2001) (7)
- Urea transport and Kidd blood groups. (1995) (7)
- Wrb ANTIGEN NOT REQUIRED FOR INVASION OF HUMAN ERYTHROCYTES BY PLASMODIUM FALCIPARUM (1984) (6)
- Rh DNA--coordinator's report. (1996) (6)
- Recipient's HLA-DR phenotype and renal graft outcome. (1983) (6)
- Blood groups: genetics and physiology (2010) (6)
- H deficient phenotypes: A proposed practical classification Bombay Ah, Hz, Hm. (1980) (6)
- 1 Biochemistry and molecular genetics of Rh antigens (1991) (6)
- Serological and Biochemical Investigations on the N.E. Variety of the Dantu Red Cell Phenotype (1986) (6)
- An ubiquitous isoform of glycophorin C is produced by alternative splicing. (1990) (5)
- Kx, a quantitatively minor protein from human erythrocytes, is palmitoylated in vivo. (1998) (5)
- Recent advances in molecular and genetic analysis of Rh blood group structures. (1993) (5)
- Acquired B antigen: further studies using synthetic oligosaccharides. (1983) (5)
- [Not-for-profit: A report from the fourth annual symposium of ethics held by the National Institute for Blood Transfusion (France)]. (2017) (5)
- Generation of mice with inactivated Rh or Rhag genes. (2006) (5)
- GPIaIIa as a Candidate Target for Anti-platelet Autoantibody Occurrin during Valproate Therapy and Associated with Peroperative Bleeding (2000) (5)
- Disruption of SMIM 1 causes the Vel S blood type (2013) (5)
- A new efficient tool for non‐invasive diagnosis of fetomaternal platelet antigen incompatibility (2020) (5)
- [A molecular approach to the structure, polymorphism and function of blood groups]. (1996) (5)
- Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14–q21 (1986) (5)
- Red cell and endothelial Lu/BCAM beyond sickle cell disease. (2008) (5)
- Chromatography of bovine lactoserum on the immobilized metallized dye Drimarene Rubine R/K 5BL modulation of selectivity by metal exchange and application to purification of milk immunoglobulins (1996) (5)
- Molecular analysis of selected Rh variants. (1996) (4)
- A new AQP1 null allele identified in a Gypsy woman who developed an anti‐CO3 during her first pregnancy (2012) (4)
- Phage-derived monoclonal anti-Lu. (2006) (4)
- Neutropénie auto-immune et infection à parvovirus B19. (1992) (4)
- Rh haemolytic disease of the newborn and Rh genotyping by RFLP--and allele-specific--PCR. (1995) (4)
- GRANULOCYTE-ASSOCIATED IMMUNOGLOBULINS IN RENAL TRANSPLANT RECIPIENTS WITH CYTOMEGALOVIRUS INFECTION (1988) (4)
- DAL: a new partial RHD phenotype (2001) (4)
- Influence of the size of the polar head of non-ionic detergents on membrane proteins immunoaffinity purification. (1994) (4)
- [Neonatal neutropenia]. (2020) (4)
- Immunopurification of the blood group RhD protein from human erythrocyte membranes. (1999) (4)
- Different H deficient phenotypes present in one kindred. (1980) (3)
- Interaction of synthetic glycopeptides carrying clusters ofO-glycosidic disaccharide chains (β-d-Gal(1–3)-α-d-GalNAc) withβ-d-galactose-binding lectins (1984) (3)
- [Voluntariness and blood donation: Proceedings of an ethics seminar held at the National Institute for Blood Transfusion]. (2016) (3)
- [Acquired and constitutional neutropenia in children]. (1994) (3)
- Immunochemical characterisation of monoclonal antibodies directed to glycophorins A and/or B. (1997) (3)
- Quantitative studies of Gm allotypes. I. Reappraisal of the method using an autoanalyzer. (1976) (3)
- Structure of human erythrocyte glycophorin C deduced from cDNA analysis. (1986) (3)
- [Erythrocyte agglutination]. (1979) (3)
- RFLPs for the human erythrocyte membrane glycophorin C gene. (1987) (3)
- A Single Point Mutation at a Splice Site Generates a Silent RH50 Gene in a Composite Heterozygous Rhnull Blood Donor (1999) (3)
- Observatoire du pneumocoque de la région Centre, du 1er avril 1999 au 31 mars 20001The pneumococcus “observatoire” of the Centre region in France, data collected between April 1, 1999 and May 31, 2000 (2002) (3)
- Report on monoclonal Rh antibodies serological and biochemical investigations. (1988) (3)
- Red cell membrane diseases and blood group abnormalities. (1983) (3)
- DNA polymorphism of the RC8 sequence on the short arm of the X chromosome in a French population. (1984) (3)
- Biochemistry and molecular genetics of Rh antigens. (1991) (3)
- Evidence that the RHD(VI) deletion genotype does not exist. (1997) (3)
- Flow cytometric evaluation of non anti-RH1(D) monoclonal Rh antibodies. (1996) (3)
- [Quantitative and thermodynamic study of weak A erythrocyte phenotypes]. (1976) (2)
- The two-gene model of the RH blood-group locus. (1995) (2)
- Localization of blood-group A and I antigenic sites on inside-out and rightside-out human erythrocyte membrane vesicles. (1979) (2)
- [Allelic enhancement]. (1976) (2)
- Renal allograft DARCness in subclinical acute and chronic active ABMR (2021) (2)
- [Autoimmune neutropenia and parvovirus B19 infection]. (1992) (2)
- [The P system]. (1980) (2)
- Early erythroid markers as probes for normal and leukaemic erythroid differentiation. (1987) (2)
- [Studies of modifications of blood group antigens in 11 cases of "refractory anemia"]. (1969) (2)
- Ion-exchange chromatography of proteins: modulation of selectivity by addition of organic solvents to mobile phase: Application to single-step purification of a proteinase inhibitor from corn and study of the mechanism of selectivity modulation (1998) (2)
- Blood Group Genotyping by High-Throughput DNA-Analysis: Application to the Panel National de Référence du CNRGS (2011) (2)
- International Conference on Rh protein superfamily (2006) (2)
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- Evaluation of several affinity chromatographic supports for the purification of maltose-binding protein from Escherichia coli. (1993) (2)
- Epinephrine Acts Via Erythroid Signaling Pathways to Activate Sickle Cell Adhesion to Endothelium Via LWa v b 3 Interactions (2004) (2)
- [A monoclonal antibody, specific for Burkitt's lymphoma, is also a blood group Pk antibody]. (1984) (2)
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- Role of Rh (rhesus) complex in K‐Cl cotransport (KCC) regulation in red blood cells (RBCs) of Rh and Rh‐associated glycoprotein (RhAg) knockout (KO) mice (2009) (1)
- Antiplatelets antibodies in systemic lupus erythematosus (S.L.E.) (1986) (1)
- Deletion of Exons 3 through 5 of ABCG2 causes the Jr(a−) phenotype in a West African woman (2015) (1)
- Un nouvel exemple d'anti-Dob (1977) (1)
- [The erythrocyte membrane]. (1978) (1)
- A new murine monoclonal antibody against Kx protein (2003) (1)
- [Refractive anemia, preleukemic states and multiple enzymatic anomalies]. (1968) (1)
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- Immunochemical characterization of the human blood cell membrane glycoprotein recognized by the monoclonal antibody 12 E 7 France LATRON (2005) (1)
- [Erythrocyte phenotypes in Gabon. I. Hemotypologic data]. (1980) (1)
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- [Non-cardiogenic pulmonary edema after transfusion of plasma containing an anti-HLA-B21 antibody]. (1991) (1)
- Groups of alpha-D- galactosyltransferase activity in sera of individuals with normal B phenotype. II. Relationship between transferase activity and red cell agglutinability. (1976) (1)
- [Production and characterization of monoclonal antibodies with P1 specificity]. (1986) (1)
- EVALUATION OF RECEPTOR SITES FOR PLASMODIUM FALCIPARUM (MALARIA) ON HUMAN ERYTHROCYTES. CHEMICAL SYNTHESIS OF PEPTIDES RELEVANT TO GLYCOPHORIN A. (1987) (1)
- ALLOIMMUNISATION TO MONOCYTES AND GRANULOCYTES AFTER LEUCOCYTE-POOR PLATELET TRANSFUSIONS (1982) (1)
- Isoelectrofocusing pattern of 2-alpha-L, 3-alpha-L and 4-alpha-L fucosyltransferases from human milk and serum. (1981) (0)
- [Comparative study of various methods of identifying Du antigens]. (1974) (0)
- [The biochemical aspects of blood group antigens]. (1976) (0)
- Description de l’activité thermoagglutinante de deux types différents d’auto-anticorps anti-érythrocytes γM anti-I (1972) (0)
- Individuals x Duffy Antigen/Receptor for Chemokines in Fy Arg89Cys Substitution Results in Very Low Membrane Expression of the (2010) (0)
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- Molecular cloning andprotein structure ofahumanbloodgroup Rhpolypeptide (1990) (0)
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- [Double population of red blood cells for ABH antigens in 3 aged subjects]. (1970) (0)
- [Adhesion molecules in red cell-endothelium interactions: Impact on sickle cell disease and malaria (INTS-Institut Pasteur joint meeting, Paris July 3-4,2008)]. (2008) (0)
- [A family with an "Hm" phenotype transmitted over 3 generations]. (1978) (0)
- In vitro generation of human red blood cells: a research model (2007) (0)
- Characterization of a UDP-Gal:Galbeta1-3GalNAc alpha1, 4-galactosyltransferase activity in a Mamestra brassicae cell line. (1998) (0)
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- [A new case of anti-Do b]. (1977) (0)
- Molecular basis of RH blood groups and Rhnull deficiency syndrome (1997) (0)
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- erythroid differentiation of thehumanerythroleukemia cell line TF-1correlates withimpaired STAT5activation (1996) (0)
- [Elective phagocytosis of polynuclear neutrophils caused by medullary macrophages and autoimmune neutropenia in children]. (1997) (0)
- [Human Rhesus-associated glycoprotein and transmembrane transport of NH3]. (2005) (0)
- Molecular cloning and protein structure of a human blood group Rh polypeptide ( erythrocyte membrane / Rh antigen / cDNA / RNA blot-hybridization analysis ) (0)
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- About collection of blood and clinical use of blood components and ethical considerations--Thoughts from the Ethical Committee of the National Institute for Blood Transfusion, France (2018) (0)
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- Structural modifications of platelet membrane glycoprotein GPIb in the Tn syndrome. (1988) (0)
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- Papers to be published in forthcoming issues. Toward more effective antifungal therapy: the prospects of combination therapy (2004) (0)
- Comment on: Parvorivus B19 in rheumatoid arthritis. Authors' reply (1996) (0)
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- monoclonal antibody Characterization of the blood group Kell (K1) antigen with a human (2011) (0)
- phenotype Short deletion within the blood group Dombrock locus causing a Donull (2013) (0)
- Alloimmune neonatal neutropenias (2003) (0)
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- 17th International Haemovigilance Seminar: Paris (France), 9-11 March 2016. (2016) (0)
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- 7 The repressor which binds the –75 GATA motif of the GPB promoter contains Ku70 as the DNA binding (1999) (0)
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- Agarose precipitation pattern with dextran-sulfate in viral hepatitis. (1971) (0)
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- the Jk ( S 291 P ) mutation found in Finns phenotype : expression analysis ofnullMolecular heterogeneity of the Jk (2000) (0)
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