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Jacques Elion
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49
Denamur, Erick
30
Krishnamoorthy, Rajagopal
28
Bingen, Edouard
24
Ducrocq, Rolande
21
Labie, Dominique
14
Lapouméroulie, Claudine
13
Picard, Bertrand
12
Maier-Redelsperger, Micheline
11
Girot, Robert
11
Brahimi, Naima
10
Vilmer, Etienne
10
Zago, Marco
8
Cavé, Hélène
8
Benkerrou, Malika
7
de Montalembert, Mariane
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All Publications
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2009: Dossou-Yovo Omer Placide; Zaccaria Isabelle; Benkerrou Malika; Hauchecorne Michelle; Alberti Corinne; Rahimy Mohamed Chérif; Elion Jacques; Lapoumeroulie Claudine
Effects of RANTES and MBL2 gene polymorphisms in sickle cell disease clinical outcomes: association of the g.In1.1T>C RANTES variant with protection against infections.
American journal of hematology 2009;84(6):378-80.
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2008: Odièvre Marie-Hélène; Bony Viviane; Benkerrou Malika; Lapouméroulie Claudine; Alberti Corinne; Ducrocq Rolande; Jacqz-Aigrain Evelyne; Elion Jacques; Cartron Jean-Pierre
Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease.
Haematologica 2008;93(4):502-10.
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2008: Cartron J-P; Elion J
Erythroid adhesion molecules in sickle cell disease: effect of hydroxyurea.
Transfusion clinique et biologique : journal de la Société française de transfusion sanguine 2008;15(1-2):39-50.
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2008: Mesbah-Amroun Hamida; Rouabhi Fatiha; Ducrocq Rolande; Elion Jacques
Molecular basis of alpha-thalassemia in Algeria.
Hemoglobin 2008;32(3):273-8.
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2007: Dossou-Yovo Omer Placide; Lapoumeroulie Claudine; Hauchecorne Michelle; Zaccaria Isabelle; Ducrocq Rolande; Krishnamoorthy Rajagopal; Rahimy Mohamed Chérif; Elion Jacques
Variants of the mannose-binding lectin gene in the Benin population: heterozygosity for the p.G57E allele may confer a selective advantage.
Human biology; an international record of research 2007;79(6):687-97.
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2007: Sznajer Yves; Keren Boris; Baumann Clarisse; Pereira Sabrina; Alberti Corinne; Elion Jacques; Cavé Hélène; Verloes Alain
The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene.
Pediatrics 2007;119(6):e1325-31.
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2007: Odièvre Marie-Hélène; Brun Manuel; Krishnamoorthy Rajagopal; Lapouméroulie Claudine; Elion Jacques
Sodium phenyl butyrate downregulates endothelin-1 expression in cultured human endothelial cells: relevance to sickle-cell disease.
American journal of hematology 2007;82(5):357-62.
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2006: Chaar Vicky; Tarer Vanessa; Etienne-Julan Maryse; Diara Jean Pierre; Elion Jacques; Romana Marc
ET-1 and ecNOS gene polymorphisms andsusceptibility to acute chest syndrome and painful vaso-occlusive crises in children with sickle cell anemia.
Haematologica 2006;91(9):1277-8.
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2006: Chaar Vicky; Kéclard Lysiane; Etienne-Julan Maryse; Diara Jean Pierre; Elion Jacques; Krishnamoorthy Rajagopal; Romana Marc
UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia.
American journal of hematology 2006;81(5):377-9.
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2006: Tarer Vanessa; Etienne-Julan Maryse; Diara Jean-Pierre; Belloy Marie Sylvaine; Mukizi-Mukaza Martin; Elion Jacques; Romana Marc
Sickle cell anemia in Guadeloupean children: pattern and prevalence of acute clinical events.
European journal of haematology 2006;76(3):193-9.
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2006: Silva Wilson Araújo; Bortolini Maria Cátira; Schneider Maria Paula Cruz; Marrero Andrea; Elion Jacques; Krishnamoorthy Rajagopal; Zago Marco Antonio
MtDNA haplogroup analysis of black Brazilian and sub-Saharan populations: implications for the Atlantic slave trade.
Human biology; an international record of research 2006;78(1):29-41.
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2006: Tredano Mohammed; Cooper David N; Stuhrmann Manfred; Christodoulou John; Chuzhanova Nadia A; Roudot-Thoraval Françoise; Boëlle Pierre-Yves; Elion Jacques; Jeanpierre Marc; Feingold Josué; Couderc Rémy; Bahuau Michel
Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP-B) deficiency.
American journal of medical genetics. Part A 2006;140(1):62-9.
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2005: Messaoud T; Bel Haj Fredj S; Bibi A; Elion J; Férec C; Fattoum S
[Molecular epidemiology of cystic fibrosis in Tunisia]
Annales de biologie clinique 2005;63(6):627-30.
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2005: Lapouméroulie Claudine; Benkerrou Malika; Odièvre Marie Hélène; Ducrocq Rolande; Brun Manuel; Elion Jacques
Decreased plasma endothelin-1 levels in children with sickle cell disease treated with hydroxyurea.
Haematologica 2005;90(3):401-3.
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2005: Chaar Vicky; Kéclard Lysiane; Diara Jean Pierre; Leturdu Claudine; Elion Jacques; Krishnamoorthy Rajagopal; Clayton John; Romana Marc
Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia.
Haematologica 2005;90(2):188-99.
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2005: Acquaviva Cécile; Benoist Jean-François; Pereira Sabrina; Callebaut Isabelle; Koskas Thu; Porquet Dominique; Elion Jacques
Molecular basis of methylmalonyl-CoA mutase apoenzyme defect in 40 European patients affected by mut(o) and mut- forms of methylmalonic acidemia: identification of 29 novel mutations in the MUT gene.
Human mutation 2005;25(2):167-76.
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2004: Trampont Paul; Roudier Martine; Andrea Anne-Marie; Nomal Nelly; Mignot Therese-Marie; Leborgne-Samuel Yanick; Ravion Sylvie; Clayton John; Mary Didier; Elion Jacques; Decastel Monique
The placental-umbilical unit in sickle cell disease pregnancy: a model for studying in vivo functional adjustments to hypoxia in humans.
Human pathology 2004;35(11):1353-9.
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2004: Bortolini Maria Cátira; Da Silva Wilson A; Zago Marco Antônio; Elion Jacques; Krishnamoorthy Rajagopal; Goncalves Vanessa F; Pena Sergio D J
The phylogeography of mitochondrial DNA haplogroup L3g in Africa and the Atlantic slave trade.
American journal of human genetics 2004;75(3):522-4; author reply 524-6.
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2004: Romana Marc; Diara Jean-Pierre; Doumbo Lydia; Muralitharan Shanmugakonar; Ramasawmy Rajendranath; Keclard Lysiane; Tarer Vanessa; Chaar Vicky; Elion Jacques; Krishnamoorthy Rajagopal; Clayton John
Angiotensinogen gene associated polymorphisms and risk of stroke in sickle cell anemia: Additional data supporting an association.
American journal of hematology 2004;76(3):310-1.
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2004: Tredano Mohammed; Griese Matthias; Brasch Frank; Schumacher Silja; de Blic Jacques; Marque Stéphanie; Houdayer Claude; Elion Jacques; Couderc Rémy; Bahuau Michel
Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease.
American journal of medical genetics. Part A 2004;126A(1):18-26.
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2004: Kueviakoe Irénée; Gerard Nathalie; Krishnamoorthy Rajagopal; Pereira Sabrina; Elion Jacques; Ducrocq Rolande
A new high A2-beta-thalassemia due to a 468 bp deletion (-475 to -8) in the beta-globin gene promoter of the intact beta-globin structural gene.
Hemoglobin 2004;28(1):69-72.
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2004: Elion Jacques E; Brun Manuel; Odièvre Marie-Heléne; Lapouméroulie Claudine L; Krishnamoorthy Rajagopal
Vaso-occlusion in sickle cell anemia: role of interactions between blood cells and endothelium.
The hematology journal : the official journal of the European Haematology Association / EHA 2004;5 Suppl 3():S195-8.
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2003: Tredano Mohammed; Griese Matthias; de Blic Jacques; Lorant Tifenn; Houdayer Claude; Schumacher Silja; Cartault François; Capron Frédérique; Boccon-Gibod Liliane; Lacaze-Masmonteil Thierry; Renolleau Sylvain; Delaisi Bertrand; Elion Jacques; Couderc Rémy; Bahuau Michel
Analysis of 40 sporadic or familial neonatal and pediatric cases with severe unexplained respiratory distress: relationship to SFTPB.
American journal of medical genetics. Part A 2003;119A(3):324-39.
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2003: Cusin V; Clermont O; Gérard B; Chantereau D; Elion J
Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling.
Journal of medical genetics 2003;40(4):e39.
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2003: Loirat Chantal; André Jean Luc; Champigneulle Jacqueline; Acquaviva Cécile; Chantereau Dominique; Bourquard Rosine; Elion Jacques; Denamur Erick
WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms' tumour.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2003;18(4):823-5.
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2003: Brun M; Bourdoulous S; Couraud P O; Elion J; Krishnamoorthy R; Lapoumeroulie C
Hydroxyurea downregulates endothelin-1 gene expression and upregulates ICAM-1 gene expression in cultured human endothelial cells.
The pharmacogenomics journal 2003;3(4):215-26.
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2002: Bardakdjian-Michau Josiane; Guilloud-Batailie Monique; Maier-Redelsperger Micheline; Elion Jacques; Girot Robert; Feingold Josué; Galactéros Frédéric; de Montalembert Mariane
Decreased morbidity in homozygous sickle cell disease detected at birth.
Hemoglobin 2002;26(3):211-7.
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2002: Benkerrou Malika; Delarche Charlotte; Brahimi Lamia; Fay Michèle; Vilmer Etienne; Elion Jacques; Gougerot-Pocidalo Marie-Anne; Elbim Carole
Hydroxyurea corrects the dysregulated L-selectin expression and increased H(2)O(2) production of polymorphonuclear neutrophils from patients with sickle cell anemia.
Blood 2002;99(7):2297-303.
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2002: Tamouza Ryad; Neonato Maria Grazia; Busson Marc; Marzais François; Girot Robert; Labie Dominique; Elion Jacques; Charron Dominique
Infectious complications in sickle cell disease are influenced by HLA class II alleles.
Human immunology 2002;63(3):194-9.
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2001: Acquaviva C; Benoist J F; Callebaut I; Guffon N; Ogier de Baulny H; Touati G; Aydin A; Porquet D; Elion J
N219Y, a new frequent mutation among mut(degree) forms of methylmalonic acidemia in Caucasian patients.
European journal of human genetics : EJHG 2001;9(8):577-82.
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2001: Mercier J C; Bingen E; Schlegel N; Elion J; Casanova J L; Mira J P; Beaufils F
[Meningococcal purpura fulminans: untoward result of genetic polymorphism?]
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2001;8(8):843-52.
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2001: Zertal-Zidani S; Ducrocq R; Weil-Olivier C; Elion J; Krishnamoorthy R
A novel delta beta fusion gene expresses hemoglobin A (HbA) not Hb Lepore: Senegalese delta(0)beta(+) thalassemia.
Blood 2001;98(4):1261-3.
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2001: Duriez P; Clermont O; Bonacorsi S; Bingen E; Chaventré A; Elion J; Picard B; Denamur E
Commensal Escherichia coli isolates are phylogenetically distributed among geographically distinct human populations.
Microbiology (Reading, England) 2001;147(Pt 6):1671-6.
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2001: Ducrocq R; Benkerrou M; Brahimi L; Belloy M; Briard M L; Vilmer E; Elion J
[Neonatal screening for sickle cell anemia: evaluation of a five-year experience in an area of northern Paris]
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2001;8(5):474-80.
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2001: Tredano M; Blic J D; Griese M; Fournet J C; Elion J; Bahuau M
[Clinical, biological and genetic heterogeneity of the inborn errors of pulmonary surfactant metabolism: SP-B deficiency and alveolar proteinosis]
Annales de biologie clinique 2001;59(2):131-48.
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2001: Tredano M; De Blic J; Griese M; Fournet J C; Elion J; Bahuau M
Clinical biological and genetic heterogeneity of the inborn errors of pulmonary surfactant metabolism.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2001;39(2):90-108.
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2001: Zago M A; Silva W A; Gualandro S; Yokomizu I K; Araujo A G; Tavela M H; Gerard N; Krishnamoorthy R; Elion J
Rearrangements of the beta-globin gene cluster in apparently typical betaS haplotypes.
Haematologica 2001;86(2):142-5.
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2001: Benoist J F; Acquaviva C; Callebaut I; Guffon N; Ogier de Baulny H; Mornon J P; Porquet D; Elion J
Molecular and structural analysis of two novel mutations in a patient with mut(-) methylmalonyl-CoA deficiency.
Molecular genetics and metabolism 2001;72(2):181-4.
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2001: Ducrocq R; Pascaud O; Bévier A; Finet C; Benkerrou M; Elion J
Strategy linking several analytical methods of neonatal screening for sickle cell disease.
Journal of medical screening 2001;8(1):8-14.
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2000: Bardakjian J; Benkerrou M; Bernaudin F; Briard M L; Ducrocq R; Lambilliotte A; Léna-Russo D; de Montalembert M; Thuret I; Bégué P; Elion J; Galactéros F;
[Neonatal screening of sickle cell anemia in metropolitan France]
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2000;7(12):1261-3.
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2000: Denamur E; Lecointre G; Darlu P; Tenaillon O; Acquaviva C; Sayada C; Sunjevaric I; Rothstein R; Elion J; Taddei F; Radman M; Matic I
Evolutionary implications of the frequent horizontal transfer of mismatch repair genes.
Cell 2000;103(5):711-21.
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2000: Attié-Castro F A; Zago M A; Lavinha J; Elion J; Rodriguez-Delfin L; Guerreiro J F; Franco R F
Ethnic heterogeneity of the factor XIII Val34Leu polymorphism.
Thrombosis and haemostasis 2000;84(4):601-3.
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2000: Neonato M G; Guilloud-Bataille M; Beauvais P; Bégué P; Belloy M; Benkerrou M; Ducrocq R; Maier-Redelsperger M; de Montalembert M; Quinet B; Elion J; Feingold J; Girot R
Acute clinical events in 299 homozygous sickle cell patients living in France. French Study Group on Sickle Cell Disease.
European journal of haematology 2000;65(3):155-64.
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2000: Gérard B; Ginet N; Matthijs G; Evrard P; Baumann C; Da Silva F; Gérard-Blanluet M; Mayer M; Grandchamp B; Elion J
Genotype determination at the survival motor neuron locus in a normal population and SMA carriers using competitive PCR and primer extension.
Human mutation 2000;16(3):253-63.
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2000: Tredano M; Cneude F; Denamur E; Truffert P; Capron F; Manouvrier S; Feldmann D; Couderc R; Elion J; Lacaze-Masmonteil T
[Constitutional deficiency of pulmonary surfactant protein B: clinical presentation, histologic and molecular diagnosis]
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2000;7(6):641-4.
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2000: Denamur E; Bocquet N; Baudouin V; Da Silva F; Veitia R; Peuchmaur M; Elion J; Gubler M C; Fellous M; Niaudet P; Loirat C
WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis.
Kidney international 2000;57(5):1868-72.
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2000: Aguilar-Martinez P; Schved J F; Badens C; Thuret I; Michel G; Neonato M G; Peltier J Y; Girot R; Pissard S; Galacteros F; Bachir D; Rose C; Picot M C; Denamur E; Elion J
Iron overload in thalassaemias and genetic haemochromatosis.
European journal of haematology 2000;64(4):279-80.
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2000: Bonacorsi S P; Clermont O; Tinsley C; Le Gall I; Beaudoin J C; Elion J; Nassif X; Bingen E
Identification of regions of the Escherichia coli chromosome specific for neonatal meningitis-associated strains.
Infection and immunity 2000;68(4):2096-101.
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2000: Zago M A; Silva W A; Dalle B; Gualandro S; Hutz M H; Lapoumeroulie C; Tavella M H; Araujo A G; Krieger J E; Elion J; Krishnamoorthy R
Atypical beta(s) haplotypes are generated by diverse genetic mechanisms.
American journal of hematology 2000;63(2):79-84.
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2000: Gérard N; Elion J; Krishnamoorthy R
[Pharmacogenetics or "farm-ecogenetics"?]
Journal de la Société de biologie 2000;194(1):9-13.
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1999: Nagel R L; Krishnamoorthy R; Fattoum S; Elion J; Genard N; Romero J; Fabry M E
The erythrocyte effects of haemoglobin O(ARAB).
British journal of haematology 1999;107(3):516-21.
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1999: Badens C; Jassim N; Martini N; Mattei J F; Elion J; Lena-Russo D
Characterization of a new polymorphism, IVS-I-108 (T-->C), and a new beta-thalassemia mutation, -27 (A-->T), discovered in the course of a prenatal diagnosis.
Hemoglobin 1999;23(4):339-44.
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1999: Denamur E; Bocquet N; Mougenot B; Da Silva F; Martinat L; Loirat C; Elion J; Bensman A; Ronco P M
Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases.
Journal of the American Society of Nephrology : JASN 1999;10(10):2219-23.
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1999: Neonato M G; Lu C Y; Guilloud-Bataille M; Lapouméroulie C; Nabeel-Jassim H; Dabit D; Girot R; Krishnamoorthy R; Feingold J; Besmond C; Elion J
Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections.
European journal of human genetics : EJHG 1999;7(6):679-86.
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1999: Da Silva W A; Bortolini M C; Meyer D; Salzano F M; Elion J; Krishnamoorthy R; Schneider M P; De Guerra D C; Layrisse Z; Castellano H M; Weimer T D; Zago M A
Genetic diversity of two African and sixteen South American populations determined on the basis of six hypervariable loci.
American journal of physical anthropology 1999;109(4):425-37.
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1999: Maier-Redelsperger M; Labie D; Elion J
Long-term hydroxyurea treatment in young sickle cell patients.
Current opinion in hematology 1999;6(2):115-20.
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1999: Franco R F; Elion J; Tavella M H; Santos S E; Zago M A
The prevalence of factor V Arg306-->Thr (factor V Cambridge) and factor V Arg306-->Gly mutations in different human populations.
Thrombosis and haemostasis 1999;81(2):312-3.
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1999: Picard B; Garcia J S; Gouriou S; Duriez P; Brahimi N; Bingen E; Elion J; Denamur E
The link between phylogeny and virulence in Escherichia coli extraintestinal infection.
Infection and immunity 1999;67(2):546-53.
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1999: Labie D; Elion J
[Molecular and cellular pathophysiology of sickle cell anemia]
Pathologie-biologie 1999;47(1):7-12.
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1999: Tredano M; van Elburg R M; Kaspers A G; Zimmermann L J; Houdayer C; Aymard P; Hull W M; Whitsett J A; Elion J; Griese M; Bahuau M
Compound SFTPB 1549C-->GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency.
Human mutation 1999;14(6):502-9.
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1998: Franco R F; Elion J; Lavinha J; Krishnamoorthy R; Tavella M H; Zago M A
Heterogeneous ethnic distribution of the 844ins68 in the cystathionine beta-synthase gene.
Human heredity 1998;48(6):338-42.
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1998: Maier-Redelsperger M; Elion J; Girot R
F reticulocytes assay: a method to evaluate fetal hemoglobin production.
Hemoglobin 1998;22(5-6):419-25.
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1998: Dixméras I; Lapouméroulie C; Tallec L P; Bens M; Elion J; Vandewalle A; Denamur E
CFTR regions containing duodenum specific DNase I hypersensitive sites drive expression in intestinal crypt cells but not in fibroblasts.
Biochemical and biophysical research communications 1998;250(2):328-34.
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1998: Badens C; Merghoub T; Lena-Russo D; Labie D; Elion J; Mattei J F
A novel polymorphism 3' to the beta-globin gene.
Hemoglobin 1998;22(4):387-90.
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1998: Jassim N; Merghoub T; Pascaud O; al Mukharraq H; Ducrocq R; Labie D; Elion J; Krishnamoorthy R; Arrayed S A
Molecular basis of beta-thalassemia in Bahrain: an epicenter for a Middle East specific mutation.
Annals of the New York Academy of Sciences 1998;850():407-9.
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1998: Maier-Redelsperger M; de Montalembert M; Flahault A; Neonato M G; Ducrocq R; Masson M P; Girot R; Elion J
Fetal hemoglobin and F-cell responses to long-term hydroxyurea treatment in young sickle cell patients. The French Study Group on Sickle Cell Disease.
Blood 1998;91(12):4472-9.
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1998: Jeanpierre C; Denamur E; Henry I; Cabanis M O; Luce S; Cécille A; Elion J; Peuchmaur M; Loirat C; Niaudet P; Gubler M C; Junien C
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.
American journal of human genetics 1998;62(4):824-33.
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1998: Bingen E; Picard B; Brahimi N; Mathy S; Desjardins P; Elion J; Denamur E
Phylogenetic analysis of Escherichia coli strains causing neonatal meningitis suggests horizontal gene transfer from a predominant pool of highly virulent B2 group strains.
The Journal of infectious diseases 1998;177(3):642-50.
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1998: Verlingue C; Vuillaumier S; Mercier B; Le Gac M; Elion J; Férec C; Denamur E
Absence of mutations in the interspecies conserved regions of the CFTR promoter region in cystic fibrosis (CF) and CF related patients.
Journal of medical genetics 1998;35(2):137-40.
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1998: Franco R F; Araújo A G; Guerreiro J F; Elion J; Zago M A
Analysis of the 677 C-->T mutation of the methylenetetrahydrofolate reductase gene in different ethnic groups.
Thrombosis and haemostasis 1998;79(1):119-21.
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1998: Franco R F; Santos S E; Elion J; Tavella M H; Zago M A
Prevalence of the G20210A polymorphism in the 3'-untranslated region of the prothrombin gene in different human populations.
Acta haematologica 1998;100(1):9-12.
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1998: Ducrocq R; Bévier A; Leneveu A; Maier-Redelsperger M; Bardakdjian-Michau J; Badens C; Elion J
Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell disease.
Journal of medical screening 1998;5(1):27-30.
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1997: Merghoub T; Perichon B; Maier-Redelsperger M; Dibenedetto S P; Samperi P; Ducrocq R; Feingold N; Elion J; Schiliro G; Labie D; Krishnamoorthy R
Dissection of the association status of two polymorphisms in the beta-globin gene cluster with variations in F-cell number in non-anemic individuals.
American journal of hematology 1997;56(4):239-43.
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1997: Vuillaumier S; Dixmeras I; Messaï H; Lapouméroulie C; Lallemand D; Gekas J; Chehab F F; Perret C; Elion J; Denamur E
Cross-species characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene reveals multiple levels of regulation.
The Biochemical journal 1997;327 ( Pt 3)():651-62.
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1997: Merghoub T; Sanchez-Mazas A; Tamouza R; Lu C Y; Bouzid K; Ardjoun F Z; Labie D; Lapouméroulie C; Elion J
Haemoglobin D-Ouled Rabah among the Mozabites: a relevant variant to trace the origin of Berber-speaking populations.
European journal of human genetics : EJHG 1997;5(6):390-6.
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1997: Bingen E; Bonacorsi S; Brahimi N; Denamur E; Elion J
Virulence patterns of Escherichia coli K1 strains associated with neonatal meningitis.
Journal of clinical microbiology 1997;35(11):2981-2.
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1997: Matic I; Radman M; Taddei F; Picard B; Doit C; Bingen E; Denamur E; Elion J
Highly variable mutation rates in commensal and pathogenic Escherichia coli.
Science (New York, N.Y.) 1997;277(5333):1833-4.
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1997: Helley D; Besmond C; Ducrocq R; da Silva F; Guillin M C; Bezeaud A; Elion J
Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell disease.
Human genetics 1997;100(2):245-8.
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1997: de Montalembert M; Belloy M; Bernaudin F; Gouraud F; Capdeville R; Mardini R; Philippe N; Jais J P; Bardakdjian J; Ducrocq R; Maier-Redelsperger M; Elion J; Labie D; Girot R
Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. The French Study Group on Sickle Cell Disease.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 1997;19(4):313-8.
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1997: François B; Krishnamoorthy R; Elion J
Comparative study of Mycobacterium paratuberculosis strains isolated from Crohn's disease and Johne's disease using restriction fragment length polymorphism and arbitrarily primed polymerase chain reaction.
Epidemiology and infection 1997;118(3):227-33.
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1997: Chang Y P; Maier-Redelsperger M; Smith K D; Contu L; Ducroco R; de Montalembert M; Belloy M; Elion J; Dover G J; Girot R
The relative importance of the X-linked FCP locus and beta-globin haplotypes in determining haemoglobin F levels: a study of SS patients homozygous for beta S haplotypes.
British journal of haematology 1997;96(4):806-14.
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1997: Gérard B; Le Heuzey M F; Brunie G; Lewine P; Saiag M C; Cacheux V; Da Silva F; Dugas M; Mouren-Simeoni M C; Elion J; Grandchamp B
Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children.
Annales de génétique 1997;40(3):139-44.
-
1997: Gouya L; Pascaud O; Munck A; Elion J; Denamur E
Novel mutation (A141D) in exon 4 of the CFTR gene identified in an Algerian patient.
Human mutation 1997;10(1):86-7.
-
1996: Doit C; Denamur E; Picard B; Geslin P; Elion J; Bingen E
Mechanisms of the spread of penicillin resistance in Streptococcus pneumoniae strains causing meningitis in children in France.
The Journal of infectious diseases 1996;174(3):520-8.
-
1996: Cavé H; Guidal C; Elion J; Vilmer E; Grandchamp B
A low rate of loss of heterozygosity is found at many different loci in childhood B-lineage acute lymphocytic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(9):1486-91.
-
1996: Labie D; Elion J
Sequence polymorphisms of potential functional relevance in the beta-globin gene locus.
Hemoglobin 1996;20(2):85-101.
-
1996: Gérard B; Peponnet C; Brunie G; Cavé H; Denamur E; d'Auriol L; Monplaisir N; Simon F; Elion J; Grandchamp B
Fluorometric detection of HIV-1 genome through use of an internal control, inosine-substituted primers, and microtiter plate format.
Clinical chemistry 1996;42(5):696-703.
-
1996: Merghoub T; Maier-Redelsperger M; Labie D; Perichon B; Feingold N; Dibenedetto S P; Schiliro G; Samperi P; Ducrocq R; Elion J; Krishnamoorthy R
Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals.
Blood 1996;87(6):2607.
-
1996: Labie D; Elion J
[Sickle cell anemia: model of variability in expression of monogenic disease]
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 1996;3(2):101-3.
-
1996: Guidal-Giroux C; Gérard B; Cavé H; Duval M; Rohrlich P; Elion J; Vilmer E; Grandchamp B
Deletion mapping indicates that MTS1 is the target of frequent deletions at chromosome 9p21 in paediatric acute lymphoblastic leukaemias.
British journal of haematology 1996;92(2):410-9.
-
1996: Bingen E; Denamur E; Brahimi N; Elion J
Genotyping may provide rapid identification of Escherichia coli K1 organisms that cause neonatal meningitis.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 1996;22(1):152-6.
-
1996: Badens C; Thuret I; Michel G; Krawczak M; Mattei J F; Lena-Russo D; Labie D; Elion J
Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the beta-globin gene.
Human mutation 1996;8(1):89-92.
-
1996: Messaoud T; Verlingue C; Denamur E; Pascaud O; Quéré I; Fattoum S; Elion J; Férec C
Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutations.
European journal of human genetics : EJHG 1996;4(1):20-4.
-
1995: Cavé H; Gérard B; Martin E; Guidal C; Devaux I; Weissenbach J; Elion J; Vilmer E; Grandchamp B
Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1.
Blood 1995;86(10):3869-75.
-
1995: Desjardins P; Picard B; Kaltenböck B; Elion J; Denamur E
Sex in Escherichia coli does not disrupt the clonal structure of the population: evidence from random amplified polymorphic DNA and restriction-fragment-length polymorphism.
Journal of molecular evolution 1995;41(4):440-8.
-
1995: Sayada C; Vretou E; Orfila J; Elion J; Denamur E
Heterogeneity within the first constant segment of the major outer membrane protein gene in Chlamydia trachomatis serovar D/Da distinguishes 2 lineages.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1995;318(9):943-9.
-
1995: Bingen E; Doit C; Bouillie C; Blanchard B; Geslin P; Bourillon A; Elion J
Multiple recurrences and relapse of Streptococcus pneumoniae meningitis.
Lancet 1995;346(8970):311.
-
1995: Sayada C; Denamur E; Grandchamp B; Orfila J; Elion J
Denaturing gradient gel electrophoresis analysis for the detection of point mutations in the Chlamydia trachomatis major outer-membrane protein gene.
Journal of medical microbiology 1995;43(1):14-25.
-
1995: Sayada C; Andersen A A; Storey C; Milon A; Eb F; Hashimoto N; Hirai K; Elion J; Denamur E
Usefulness of omp1 restriction mapping for avian Chlamydia psittaci isolate differentiation.
Research in microbiology 1995;146(2):155-65.
-
1994: Labie D; Elion J; Beldjord C
On the diversity of beta-globin mutations, a reflection of recent historic events in Israel.
American journal of human genetics 1994;55(6):1284-5.
-
1994: Dufourcq R; Vuillaumier S; Pascaud O; Guidal C; Oury J F; Elion J; Denamur E
Compound heterozygosity for delta F508 and F508C: a cautionary note on the molecular diagnosis of cystic fibrosis.
Prenatal diagnosis 1994;14(12):1176-7.
-
1994: Fournier T; Mejdoubi N; Lapoumeroulie C; Hamelin J; Elion J; Durand G; Porquet D
Transcriptional regulation of rat alpha 1-acid glycoprotein gene by phenobarbital.
The Journal of biological chemistry 1994;269(44):27175-8.
-
1994: Triadou P; Maier-Redelsperger M; Krishnamoorty R; Deschamps A; Casadevall N; Dunda O; Ducrocq R; Elion J; Girot R; Labie D
Fetal haemoglobin variations following hydroxyurea treatment in patients with cyanotic congenital heart disease.
Nouvelle revue française d'hématologie 1994;36(5):367-72.
-
1994: Messaoud T; Abdennebi M; Elion J; Fattoum S
[Cystic fibrosis mutations in the Tunisian population]
La Tunisie médicale 1994;72(8-9):509-12.
-
1994: Bingen E H; Denamur E; Elion J
Use of ribotyping in epidemiological surveillance of nosocomial outbreaks.
Clinical microbiology reviews 1994;7(3):311-27.
-
1994: Sayada C; Picard B; Elion J; Krishnamoorthy R
A simple procedure to differentiate ailA and ailNA gene variants among human pathogenic Yersinia enterocolitica strains.
Molecular and cellular probes 1994;8(3):187-91.
-
1994: Bennani C; Bouhass R; Perrin-Pecontal P; Tamouza R; Malou M; Elion J; Trabuchet G; Beldjord C; Benabadji M; Labie D
Anthropological approach to the heterogeneity of beta-thalassemia mutations in northern Africa.
Human biology; an international record of research 1994;66(3):369-82.
-
1994: Cavé H; Mariani P; Grandchamp B; Elion J; Denamur E
Reliability of PCR directly from stool samples: usefulness of an internal standard.
BioTechniques 1994;16(5):809-10.
-
1994: Sayada C; Picard B; Elion J; Krishnamoorthy R
Genomic fingerprinting of Yersinia enterocolitica species by degenerate oligonucleotide-primed polymerase chain reaction.
Electrophoresis 1994;15(5):562-5.
-
1994: Picard B; Denamur E; Barakat A; Elion J; Goullet P
Genetic heterogeneity of Pseudomonas aeruginosa clinical isolates revealed by esterase electrophoretic polymorphism and restriction fragment length polymorphism of the ribosomal RNA gene region.
Journal of medical microbiology 1994;40(5):313-22.
-
1994: Guidal C; Lapouméroulie C; Krishnamoorthy R; Elion J
Sequence correction and reassignment of the TaqI polymorphic site in the human inter-gamma-globin gene region, an African-specific marker.
Human biology; an international record of research 1994;66(2):323-8.
-
1994: Mariani-Kurkdjian P; Denamur E; Milon A; Picard B; Cave H; Lambert-Zechovsky N; Loirat C; Goullet P; Sansonetti P J; Elion J
Identification of a clone of Escherichia coli O103:H2 as potential agent of hemolytic-uremic syndrome in France.
Journal of clinical microbiology 1994;32(3):860.
-
1994: Perichon B; Clemenceau S; Romand A; Elion J; Kaplan C; Krishnamoorthy R
An additional HpaII polymorphism in exon 2 of the human platelet membrane glycoprotein IIIa gene.
Human genetics 1994;93(3):353-4.
-
1994: Cavé H; Bingen E; Elion J; Denamur E
Differentiation of Escherichia coli strains using randomly amplified polymorphic DNA analysis.
Research in microbiology 1994;145(2):141-50.
-
1994: Sayada C; Andersen A; Rodriguez P; Eb F; Milon A; Elion J; Denamur E
Homogeneity of the major outer membrane protein gene of feline Chlamydia psittaci.
Research in veterinary science 1994;56(1):116-8.
-
1994: Clemenceau S; Perichon B; Elion J; Kaplan C; Krishnamoorthy R
An improved DNA-based identification of fetuses at risk for HPA-1a (PlA1) neonatal alloimmune thrombocytopenia.
British journal of haematology 1994;86(1):198-200.
-
1994: Pescatore P; Marteau P; Lemière E; Xerri B; Denamur E; Elion J; Matuchansky C; Rambaud J C
[Mucoviscidosis discovered after the age of 25 years. Review and follow-up of cases of the literature]
Gastroentérologie clinique et biologique 1994;18(3):195-9.
-
1994: Vilmer E; Quelvennec E; Plouvier E; Denamur E; Rohrlich P; Elion J; Sterkers G
HLA-mismatched cord blood transplantation: immunological studies.
Blood cells 1994;20(2-3):235-41.
-
1993: de Montalembert M; Maier-Redelsperger M; Girot R; Belloy M; Vilmer E; Ducrocq R; Guidal C; Elion J
Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children.
Blood 1993;82(8):2595-6.
-
1993: Bingen E H; Weber M; Derelle J; Brahimi N; Lambert-Zechovsky N Y; Vidailhet M; Navarro J; Elion J
Arbitrarily primed polymerase chain reaction as a rapid method to differentiate crossed from independent Pseudomonas cepacia infections in cystic fibrosis patients.
Journal of clinical microbiology 1993;31(10):2589-93.
-
1993: Ducrocq R; Tachdjian G; Oury J F; Brunie G; Fenneteau O; Schlegel N; Blot P; Elion J
Measurement of adult hemoglobin in fetal blood samples by high-performance liquid chromatography as purity control for the prenatal diagnosis of chromosomal abnormalities.
Fetal diagnosis and therapy 1993;8(5):317-24.
-
1993: Denamur E; Picard B; Decoux G; Denis J B; Elion J
The absence of correlation between allozyme and rrn RFLP analysis indicates a high gene flow rate within human clinical Pseudomonas aeruginosa isolates.
FEMS microbiology letters 1993;110(3):275-80.
-
1993: Périchon B; Ragusa A; Lapouméroulie C; Romand A; Moi P; Ikuta T; Labie D; Elion J; Krishnamoorthy R
Inter-ethnic polymorphism of the beta-globin gene locus control region (LCR) in sickle-cell anemia patients.
Human genetics 1993;91(5):464-8.
-
1993: Bennani C; Tamouza R; Rouabhi F; Benabadji M; Malou M; Elion J; Labie D; Beldjord C
The spectrum of beta-thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy.
British journal of haematology 1993;84(2):335-7.
-
1993: Kahane S; Gonen R; Sayada C; Elion J; Friedman M G
Description and partial characterization of a new Chlamydia-like microorganism.
FEMS microbiology letters 1993;109(2-3):329-33.
-
1993: Bingen E; Boissinot C; Desjardins P; Cave H; Brahimi N; Lambert-Zechovsky N; Denamur E; Blot P; Elion J
Arbitrarily primed polymerase chain reaction provides rapid differentiation of Proteus mirabilis isolates from a pediatric hospital.
Journal of clinical microbiology 1993;31(5):1055-9.
-
1993: Mariani-Kurkdjian P; Denamur E; Milon A; Picard B; Cave H; Lambert-Zechovsky N; Loirat C; Goullet P; Sansonetti P J; Elion J
Identification of a clone of Escherichia coli O103:H2 as a potential agent of hemolytic-uremic syndrome in France.
Journal of clinical microbiology 1993;31(2):296-301.
-
1993: Bingen E H; Desjardins P; Arlet G; Bourgeois F; Mariani-Kurkdjian P; Lambert-Zechovsky N Y; Denamur E; Philippon A; Elion J
Molecular epidemiology of plasmid spread among extended broad-spectrum beta-lactamase-producing Klebsiella pneumoniae isolates in a pediatric hospital.
Journal of clinical microbiology 1993;31(2):179-84.
-
1993: Bingen E; Cavé H; Aujard Y; Lambert-Zechovsky N; Desjardins P; Elion J; Denamur E
Molecular analysis of multiply recurrent meningitis due to Escherichia coli K1 in an infant.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 1993;16(1):82-5.
-
1993: Loirat C; Baudouin V; Sonsino E; Mariani-Kurdjian P; Elion J
Hemolytic-uremic syndrome in the child.
Advances in nephrology from the Necker Hospital 1993;22():141-68.
-
1992: Sayada C; Denamur E; Elion J
Complete sequence of the major outer membrane protein-encoding gene of Chlamydia trachomatis serovar Da.
Gene 1992;120(1):129-30.
-
1992: Bingen E; Denamur E; Lambert-Zechovsky N; Elion J
[Contribution of molecular typing in the surveillance of nosocomial infections. Experience in pediatric hospitals]
Presse médicale (Paris, France : 1983) 1992;21(32):1504-6.
-
1992: Tachdjian G; Benabdennebi M; Guidal C; Sayada C; Lapouméroulie C; Elion J
Analysis of the 5' flanking sequence of the G gamma globin gene by denaturing gradient gel electrophoresis confirms the heterogeneity of the Bantu beta S haplotype.
Human genetics 1992;90(1-2):23-6.
-
1992: Bingen E; Denamur E; Lambert-Zechovsky N; Braimi N; el Lakany M; Elion J
DNA restriction fragment length polymorphism differentiates recurrence from relapse in treatment failures of Streptococcus pyogenes pharyngitis.
Journal of medical microbiology 1992;37(3):162-4.
-
1992: Beldjord C; Ducrocq R; Nadifi S; Lapoumeroulie C; Elion J; Labie D
A haplotype-linked four base pair deletion upstream of the A gamma globin gene coincides with decreased gene expression.
Human genetics 1992;89(6):625-8.
-
1992: Bingen E H; Mariani-Kurkdjian P; Lambert-Zechovsky N Y; Desjardins P; Denamur E; Aujard Y; Vilmer E; Elion J
Ribotyping provides efficient differentiation of nosocomial Serratia marcescens isolates in a pediatric hospital.
Journal of clinical microbiology 1992;30(8):2088-91.
-
1992: Bingen E H; Denamur E; Picard B; Goullet P; Lambert-Zechovsky N Y; Brahimi N; Mercier J C; Beaufils F; Elion J
Molecular epidemiology unravels the complexity of neonatal Escherichia coli acquisition in twins.
Journal of clinical microbiology 1992;30(7):1896-8.
-
1992: Fajardy I; Levy-Marchal C; Gu X F; Krishnamoorthy R; Elion J; Czernichow P
[Respective weight of genotypes DQA1 and DQB1 associated with insulin-dependent diabetes in French children]
Diabète & métabolisme 1992;18(4):298-305.
-
1992: Ragusa A; Lombardo M; Beldjord C; Ruberto C; Lombardo T; Elion J; Nagel R L; Krishnamoorthy R
Genetic epidemiology of beta-thalassemia in Sicily: do sequences 5' to the G gamma gene and 5' to the beta gene interact to enhance HbF expression in beta-thalassemia?
American journal of hematology 1992;40(3):199-206.
-
1992: Lambert-Zechovsky N; Bingen E; Denamur E; Brahimi N; Brun P; Mathieu H; Elion J
Molecular analysis provides evidence for the endogenous origin of bacteremia and meningitis due to Enterobacter cloacae in an infant.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 1992;15(1):30-2.
-
1992: Guemira F; Abbes S; Ducrocq R; Elion J; Fattoum S
[HbD Iran-beta-thalassemia association in a Tunisian family]
Annales de pédiatrie 1992;39(6):369-74.
-
1992: Bingen E; Denamur E; Lambert-Zechovsky N; Brahimi N; el Lakany M; Elion J
Rapid genotyping shows the absence of cross-contamination in Enterobacter cloacae nosocomial infections.
The Journal of hospital infection 1992;21(2):95-101.
-
1992: Vilmer E; Sterkers G; Rahimy C; Denamur E; Elion J; Broyart A; Lescoeur B; Tiercy J M; Gerota J; Blot P
HLA-mismatched cord-blood transplantation in a patient with advanced leukemia.
Transplantation 1992;53(5):1155-7.
-
1992: Sayada C; Denamur E; Xerri B; Orfila J; Catalan F; Elion J
[Epidemiology of Chlamydia trachomatis using analysis of gene encoding of the major outer membrane protein]
Pathologie-biologie 1992;40(5):583-9.
-
1992: Lapouméroulie C; Dunda O; Ducrocq R; Trabuchet G; Mony-Lobé M; Bodo J M; Carnevale P; Labie D; Elion J; Krishnamoorthy R
A novel sickle cell mutation of yet another origin in Africa: the Cameroon type.
Human genetics 1992;89(3):333-7.
-
1992: Bingen E; Denamur E; Picard B; Goullet P; Lambert-Zechovsky N; Foucaud P; Navarro J; Elion J
Molecular epidemiological analysis of Pseudomonas aeruginosa strains causing failure of antibiotic therapy in cystic fibrosis patients.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology 1992;11(5):432-7.
-
1992: Lu C Y; Gérard N; Méreaux A G; Chaventré A; Joly J P; Elion J; Krishnamoorthy R
A rare FokI RFLP in the human dopamine D2 receptor gene (DRD2).
Human genetics 1992;89(3):360.
-
1992: Bingen E; Denamur E; Lambert-Zechovsky N; Aujard Y; Brahimi N; Geslin P; Elion J
Analysis of DNA restriction fragment length polymorphism extends the evidence for breast milk transmission in Streptococcus agalactiae late-onset neonatal infection.
The Journal of infectious diseases 1992;165(3):569-73.
-
1992: Zeliszewski D; Tiercy J M; Boitard C; Gu X F; Loche M; Krishnamoorthy R; Simonney N; Elion J; Bach J F; Mach B
Extensive study of DRB, DQA, and DQB gene polymorphism in 23 DR2-positive, insulin-dependent diabetes mellitus patients.
Human immunology 1992;33(2):140-7.
-
1992: Elion J; Berg P E; Lapouméroulie C; Trabuchet G; Mittelman M; Krishnamoorthy R; Schechter A N; Labie D
DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation.
Blood 1992;79(3):787-92.
-
1992: Bingen E; Denamur E; Lambert-Zechovsky N; Boissinot C; Brahimi N; Aujard Y; Blot P; Elion J
Mother-to-infant vertical transmission and cross-colonization of Streptococcus pyogenes confirmed by DNA restriction fragment length polymorphism analysis.
The Journal of infectious diseases 1992;165(1):147-50.
-
1991: Denamur E; Sayada C; Souriau A; Orfila J; Rodolakis A; Elion J
Restriction pattern of the major outer-membrane protein gene provides evidence for a homogeneous invasive group among ruminant isolates of Chlamydia psittaci.
Journal of general microbiology 1991;137(11):2525-30.
-
1991: Sayada C; Denamur E; Orfila J; Catalan F; Elion J
Rapid genotyping of the Chlamydia trachomatis major outer membrane protein by the polymerase chain reaction.
FEMS microbiology letters 1991;67(1):73-8.
-
1991: Bingen E H; Denamur E; Lambert-Zechovsky N Y; Elion J
Evidence for the genetic unrelatedness of nosocomial vancomycin-resistant Enterococcus faecium strains in a pediatric hospital.
Journal of clinical microbiology 1991;29(9):1888-92.
-
1991: Trabuchet G; Elion J; Dunda O; Lapouméroulie C; Ducrocq R; Nadifi S; Zohoun I; Chaventre A; Carnevale P; Nagel R L
Nucleotide sequence evidence of the unicentric origin of the beta C mutation in Africa.
Human genetics 1991;87(5):597-601.
-
1991: Gu X F; Larger E; Clauser E; Bessaoud K; Krishnamoorthy R; Elion J; Assan R
HLA-DQA1 and DQB1 alleles in French and Algerian type 1 diabetic subjects.
Diabetes research (Edinburgh, Scotland) 1991;17(4):189-97.
-
1991: Traore O; Carnevale P; Kaptue-Noche L; M'Bede J; Desfontaine M; Elion J; Labie D; Nagel R L
Preliminary report on the use of desferrioxamine in the treatment of Plasmodium falciparum malaria.
American journal of hematology 1991;37(3):206-8.
-
1991: Bingen E H; Denamur E; Lambert-Zechovsky N Y; Bourdois A; Mariani-Kurkdjian P; Cezard J P; Navarro J; Elion J
DNA restriction fragment length polymorphism differentiates crossed from independent infections in nosocomial Xanthomonas maltophilia bacteremia.
Journal of clinical microbiology 1991;29(7):1348-50.
-
1991: Trabuchet G; Elion J; Baudot G; Pagnier J; Bouhass R; Nigon V M; Labie D; Krishnamoorthy R
Origin and spread of beta-globin gene mutations in India, Africa, and Mediterranea: analysis of the 5' flanking and intragenic sequences of beta S and beta C genes.
Human biology; an international record of research 1991;63(3):241-52.
-
1991: Denamur E; Picard B; Goullet P; Bingen E; Lambert N; Elion J
Complexity of Pseudomonas aeruginosa infection in cystic fibrosis: combined results from esterase electrophoresis and rDNA restriction fragment length polymorphism analysis.
Epidemiology and infection 1991;106(3):531-9.
-
1991: Mura C; Broyart J P; Jacqz E; Elion J; Krishnamoorthy R
NcoI RFLP in the pseudogene (CYP2D8P) of the human debrisoquine 4-hydroxylase locus.
Nucleic acids research 1991;19(5):1162.
-
1991: Berg P E; Mittelman M; Elion J; Labie D; Schechter A N
Increased protein binding to a -530 mutation of the human beta-globin gene associated with decreased beta-globin synthesis.
American journal of hematology 1991;36(1):42-7.
-
1991: Labie D; Elion J; Girot R
[The X chromosome, fetal hemoglobin and sickle cell anemia]
Nouvelle revue française d'hématologie 1991;33(2):139-41.
-
1991: Vilmer E; Sterkers G; Rahimy C; Elion J; Broyart A; Lescoeur B; Gerota J; Loche M; Tiercy J M; Blot P
HLA-mismatched cord blood transplantation in a patient with advanced leukemia.
Bone marrow transplantation 1991;7 Suppl 2():125.
-
1990: Vallet-Colom I; Lévy-Marchal C; Zarrouk D; Tichet J; Krishnamoorthy R; Czernichow P; Elion J
HLA-DQB 1 codon 57 and genetic susceptibility to type 1 (insulin-dependent) diabetes mellitus in French children.
Diabetologia 1990;33(3):174-6.
-
1989: Labie D; Srinivas R; Dunda O; Dode C; Lapoumeroulie C; Devi V; Devi S; Ramasami K; Elion J; Ducrocq R
Haplotypes in tribal Indians bearing the sickle gene: evidence for the unicentric origin of the beta S mutation and the unicentric origin of the tribal populations of India.
Human biology; an international record of research 1989;61(4):479-91.
-
1989: Cao S X; Mishoe H; Elion J; Berg P E; Schechter A N
Activation of the human epsilon- and beta-globin promoters by SV40 T antigen.
The Biochemical journal 1989;258(3):769-76.
-
1989: Ragusa A; Lombardo M; Lombardo T; Beldjord C; Nagel R L; Elion J; Labie D; Krishnamoorthy R
Sequence variations in the 3' A gamma enhancer are silent polymorphisms.
Progress in clinical and biological research 1989;316B():409-17.
-
1988: Le Bonniec B; Sauloy J; Ducrocq R; Elion J
Analysis of ligand-binding data without knowledge of bound or free ligand molar concentration.
Analytical biochemistry 1988;174(1):280-90.
-
1988: Gu X F; Elion J; Ouagued M; Clauser E; Assan R; Krishnamoorthy R
A simple strategy to amplify specifically the HLA-DQ beta gene region with genomic DNA as template.
FEBS letters 1988;236(1):23-6.
-
1988: Bezeaud A; Elion J; Guillin M C
Functional characterization of thrombin Salakta: an abnormal thrombin derived from a human prothrombin variant.
Blood 1988;71(3):556-61.
-
1987: Ducrocq R; Le Bonniec B; Carlier O; Assan R; Elion J
Measurement of glycated albumin in diabetic patients by biospecific affinity chromatography.
Journal of chromatography 1987;419():75-83.
-
1987: Denninger M H; Jandrot-Perrus M; Elion J; Bertrand O; Homandberg G A; Mosesson M W; Guillin M C
ADP-induced platelet aggregation depends on the conformation or availability of the terminal gamma chain sequence of fibrinogen. Study of the reactivity of fibrinogen Paris 1.
Blood 1987;70(2):558-63.
-
1987: Guemira F; Hajji F; Sellami M; Abbes S; Ducrocq R; Elion J; Fattoum S
[A case of hemoglobin D Punjab in Tunisia. Characterization and structural study]
Archives de l'Institut Pasteur de Tunis 1987;64(3):341-9.
-
1986: Arapinis C; Elion J; Labie D; Krishnamoorthy R
Differences in DNase I sensitivity and methylation within the human beta-globin gene domain and correlation with expression.
European journal of biochemistry / FEBS 1986;156(1):123-9.
-
1986: Guillin M C; Bezeaud A; Rabiet M J; Elion J
Congenitally abnormal prothrombin and thrombin.
Annals of the New York Academy of Sciences 1986;485():56-65.
-
1986: Elion J; Boissel J P; Le Bonniec B; Bezeaud A; Jandrot-Perrus M; Rabiet M J; Guillin M C
Proteolytic derivatives of thrombin.
Annals of the New York Academy of Sciences 1986;485():16-26.
-
1985: Intrator S; Elion J; Thomasset M; Brehier A
Purification, immunological and biochemical characterization of rat 28 kDa cholecalcin (cholecalciferol-induced calcium-binding proteins). Identity between renal and cerebellar cholecalcins.
The Biochemical journal 1985;231(1):89-95.
-
1985: Angles-Cano E; Balaton A; Le Bonniec B; Genot E; Elion J; Sultan Y
Production of monoclonal antibodies to the high fibrin-affinity, tissue-type plasminogen activator of human plasma. Demonstration of its endothelial origin by immunolocalization.
Blood 1985;66(4):913-20.
-
1985: Ducrocq R; Bachour H; Belkhodja R; Berriche S; Elion J
Evidence for nonenzymic glycation of antithrombin III in diabetic patients.
Clinical chemistry 1985;31(2):338-9.
-
1985: Troungos C; Krishnamoorthy R; Elion J; Lombardo T; Sortino G; Cacciola E; Labie D
Multiple molecular bases for thalassemia intermedia in east Sicily.
Annals of the New York Academy of Sciences 1985;445():106-10.
-
1984: Eberentz-Lhomme C; Ducrocq R; Intrator S; Elion J; Nunez E; Assan R
Haemoglobinopathies: a pitfall in the assessment of glycosylated haemoglobin by ion-exchange chromatography.
Diabetologia 1984;27(6):596-8.
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1984: Eberentz-Lhomme C; Ducrocq R; Intrator S; Elion J; Nunez E; Assan R
Haemoglobinopathies, malaria, and other interferences with HBA1 assessment.
Diabète & métabolisme 1984;10(5):304-10.
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1984: Ducrocq R; Berriche S; Dalle M T; Elion J
Rapid quantification of Hb Hope in heterozygotes.
Clinical chemistry 1984;30(8):1425.
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1984: Boissel J P; Le Bonniec B; Rabiet M J; Labie D; Elion J
Covalent structures of beta and gamma autolytic derivatives of human alpha-thrombin.
The Journal of biological chemistry 1984;259(9):5691-7.
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1984: Rabiet M J; Jandrot-Perrus M; Boissel J P; Elion J; Josso F
Thrombin Metz: characterization of the dysfunctional thrombin derived from a variant of human prothrombin.
Blood 1984;63(4):927-34.
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1983: Kuhn J M; Rieu M; Rochette J; Krishnamoorthy R; Labie D; Elion J; Luton J P; Bricaire H
Influence of thyroid status on hemoglobin A2 expression.
The Journal of clinical endocrinology and metabolism 1983;57(2):344-8.
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1983: Krishnamoorthy R; Cahour A; Elion J; Hartmann L; Labie D
Monosaccharides bound to hemoglobins in normal and diabetic individuals. Evidence for glucose, mannose and galactose as sugars released by methanolysis of the different hemoglobin components.
European journal of biochemistry / FEBS 1983;132(2):345-50.
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1982: Pagnier J; Elion J; Lapouméroulie C; Vigneron C; Labie D
Homozygous deletional alpha + thalassaemia associated with unequal expression of the two remaining alpha 1 genes (alpha 1A and alpha 1Q).
British journal of haematology 1982;52(1):115-25.
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1982: Krishnamoorthy R; Elion J; Kuhn J M; Lagrange J L; Rochette J; Luton J P; Bricaire H; Labie D
Haemoglobin A2 is elevated in hyperthyroid patients.
Nouvelle revue française d'hématologie 1982;24(1):39-40.
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1981: Dode C; Thiesce A; Labie D; Elion J
Isolation and characterization of the vitamin K dependent domain of human prothrombin.
Biochemical and biophysical research communications 1981;103(2):461-8.
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1981: Labie D; Elion J
[Recent data concerning abnormal hemoglobins (author's transl)]
Annales de biologie clinique 1981;39(4):197-203.
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1981: Mann K G; Elion J; Butkowski R J; Downing M; Nesheim M E
Prothrombin.
Methods in enzymology 1981;80 Pt C():286-302.
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1980: Lecompte M F; Miller I R; Elion J; Benarous R
Interaction of prothrombin and its fragments with monolayers containing phosphatidylserine. 1. Binding of prothrombin and its fragment I to phosphatidylserine-containing monolayers.
Biochemistry 1980;19(15):3434-9.
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1980: Dode C; Rabiet M J; Bertrand O; Labie D; Elion J
Characterization of a proteolytically modified form of human prothorombin.
Biochemical and biophysical research communications 1980;94(2):660-6.
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1980: Wajcman H; Elion J; Boissel J P; Labie D; Jos J; Girot R
A silent hemoglobin variant: hemoglobin necker enfants-malades alpha 20 (B1) His leads to Tyr.
Hemoglobin 1980;4(2):177-84.
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1979: Rabiet M J; Elion J; Labie D; Josso F
Purification and partial characterization of a new variant of human prothrombin: prothrombin Metz.
FEBS letters 1979;108(1):287-91.
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1979: Rabiet M J; Elion J; Benarous R; Labie D; Josso F
Activation of prothrombin Barcelona. Evidence for active high molecular weight intermediates.
Biochimica et biophysica acta 1979;584(1):66-75.
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1979: Elion J; Wajcman H; Belkhodja-Dunda O; Lapoumeroulie C; Labie D; Messerschmitt J; Staal A M; Desablens B
[Hemoglobin J Amiens beta 17 (A 14) Lys replaced by Asn. Coincidence of a functionally silent new abnormal hemoglobin and a polycythemia vera (author's transl)]
Nouvelle revue française d'hématologie 1979;21(4):347-52.
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1977: Butkowski R J; Elion J; Downing M R; Mann K G
Primary structure of human prethrombin 2 and alpha-thrombin.
The Journal of biological chemistry 1977;252(14):4942-57.
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1977: Hatzfeld A; Elion J; Mennecier F; Schapira F
Purification of aldolase C from rat brain and hepatoma.
European journal of biochemistry / FEBS 1977;77(1):37-43.
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1977: Downing M R; Elion J; Butkowski R J; Mann K G
Thrombin: structural features related to specificity.
Bibliotheca haematologica 1977;44():39-53.
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1976: Elion J; Benarous R; Labie D
Isolation of preliminary characterization of a vitamin K dependent peptide from human prothrombin.
Thrombosis and haemostasis 1976;35(1):82-6.
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1976: Benarous R; Elion J; Labie D
Ca++ binding properties of human prothrombin.
Biochimie 1976;58(4):391-4.
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1975: Benarous R; Elion J
Proceedings: Binding of Ca++ to human prothrombin.
Thrombosis et diathesis haemorrhagica 1975;34(2):592.
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1974: Labie D; Belkhodja O; Coquelet M L; Elion J; Wajcman H
[A case of hemoglobin Korle Bu (beta 73(E17) Asp yields Asn) in the Ivory Coast. Arguments for the diffusion of the gene. New technical approach (author's transl)]
Nouvelle revue française d'hématologie 1974;14(5):601-6.
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1973: Elion J; Belkhodja O; Wajcman H; Labie D
Two variants of hemoglobin D in the algerian population: hemoglobin D Ouled Rabah 19 (BI) Asn leads to Lys and hemoglobin D Iran 22 (Br) Glu leads to Gln.
Biochimica et biophysica acta 1973;310(2):360-4.
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1973: Wajcman H; Elion J; Labie D
[Heat stability of hemoglobin: theoretical and practical value of a kinetic method of study]
Nouvelle revue française d'hématologie 1973;13(1):89-93.
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