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List of works by Jacques Elion

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)

scientific article published in September 1974

A low rate of loss of heterozygosity is found at many different loci in childhood B-lineage acute lymphocytic leukemia.

scientific article published in September 1996

A microfluidic approach to study the effect of mechanical stress on erythrocytes in sickle cell disease

scientific article published on 01 September 2018

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.

scientific article published in February 2004

A novel delta beta fusion gene expresses hemoglobin A (HbA) not Hb Lepore: Senegalese delta(0)beta(+) thalassemia

scientific article published on 01 August 2001

A novel polymorphism 3' to the beta-globin gene

scientific article published on 01 July 1998

A rare FokI RFLP in the human dopamine D2 receptor gene (DRD2)

scientific article published on May 1, 1992

A silent hemoglobin variant: hemoglobin necker enfants-malades alpha 20 (B1) His leads to Tyr

scientific article published on 01 January 1980

A simple procedure to differentiate ailA and ailNA gene variants among human pathogenic Yersinia enterocolitica strains.

scientific article published on June 1994

A simple strategy to amplify specifically the HLA-DQ beta gene region with genomic DNA as template

scientific article published on 01 August 1988

ACC policy statement. Recommended guidelines for training in adult clinical cardiac electrophysiology. Electrophysiology/ Electrocardiography Subcommittee, American College of Cardiology

scientific article published on 01 August 1991

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

scientific article published on 01 August 1987

Activation of prothrombin Barcelona evidence for active high molecular weight intermediates ⬇️

scientific article published on April 18, 1979

Activation state of alpha4beta1 integrin on sickle red blood cells is linked to the duffy antigen receptor for chemokines (DARC) expression.

scientific article

An additional HpaII polymorphism in exon 2 of the human platelet membrane glycoprotein IIIa gene

scientific article published on 01 March 1994

Analysis of 40 sporadic or familial neonatal and pediatric cases with severe unexplained respiratory distress: relationship to SFTPB

scientific article published on 01 June 2003

Analysis of DNA restriction fragment length polymorphism extends the evidence for breast milk transmission in Streptococcus agalactiae late-onset neonatal infection

scientific article published on March 1, 1992

Analysis of the 677 C-->T mutation of the methylenetetrahydrofolate reductase gene in different ethnic groups

scientific article published on 01 January 1998

Anthropological approach to the heterogeneity of beta-thalassemia mutations in northern Africa.

scientific article

Association between Duffy antigen receptor for chemokines expression and levels of inflammation markers in sickle cell anemia patients.

scientific article

Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia

scientific article published on 01 February 2005

Association of adenylyl cyclase 6 rs3730070 polymorphism and hemolytic level in patients with sickle cell anemia

scientific article

Atypical ?s haplotypes are generated by diverse genetic mechanisms

scientific article published in February 2000

Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children

scientific article published on 01 October 1993

CFTRRegions Containing Duodenum Specific DNase I Hypersensitive Sites Drive Expression in Intestinal Crypt Cells but Not in Fibroblasts ⬇️

scientific article published on September 18, 1998

Ca++ binding properties of human prothrombin

scientific article published on January 1, 1976

Cell-derived microparticles and sickle cell disease chronic vasculopathy in sub-Saharan Africa: A multinational study

scientific article published on 29 November 2020

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

scientific article published on 01 November 1999

Characterization of a proteolytically modified form of human prothorombin

scientific article published on 01 May 1980

Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3.

scientific article

Clinical and haematological risk factors for cerebral macrovasculopathy in a sickle cell disease newborn cohort: a prospective study.

scientific article published on 5 January 2016

Commensal Escherichia coli isolates are phylogenetically distributed among geographically distinct human populations

scientific article published on 01 June 2001

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

scientific article published on 01 June 1997

Complete sequence of the major outer membrane protein-encoding gene of Chlamydia trachomatis serovar Da

scientific article published on October 12, 1992

Compound heterozygosity Hb S/Hb Hope (β136Gly→Asp): a pitfall in the newborn screening for sickle cell disease ⬇️

scientific article published on January 1, 1998

Compound heterozygosity for delta F508 and F508C: a cautionary note on the molecular diagnosis of cystic fibrosis

scientific article published on 01 December 1994

Congenitally abnormal prothrombin and thrombin.

scientific article

Contrast echo washout curves from the left ventricle: application of basic principles of indicator-dilution theory and calculation of ejection fraction.

scientific article published on July 1987

Coronary arteriography in the intact rabbit: demonstration of coronary vasomotor and electrocardiographic effects of ergonovine and indomethacin in rabbits after abrupt cessation of prolonged nitroglycerin treatment.

scientific article published on August 1987

Correlation of continuous wave Doppler velocities with cardiac catheterization gradients: an experimental model of aortic stenosis

scientific article published on 01 December 1985

Covalent structures of beta and gamma autolytic derivatives of human alpha-thrombin

scientific article published on 01 May 1984

Cross-species characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene reveals multiple levels of regulation.

scientific article published on November 1997

Cystic fibrosis mutations in the Tunisian population ⬇️

scientific article

DICOM media interchange standards for cardiology: initial interoperability demonstration.

scientific article published on January 1995

DNA restriction fragment length polymorphism differentiates crossed from independent infections in nosocomial Xanthomonas maltophilia bacteremia ⬇️

scientific article published on July 1, 1991

DNA restriction fragment length polymorphism differentiates recurrence from relapse in treatment failures of Streptococcus pyogenes pharyngitis

scientific article published on 01 September 1992

Decreased morbidity in homozygous sickle cell disease detected at birth.

scientific article published in August 2002

Decreased plasma endothelin-1 levels in children with sickle cell disease treated with hydroxyurea.

scientific article

Degree of Anemia, Indirect Markers of Hemolysis, and Vascular Complications of Sickle Cell Disease in Africa.

scientific article published on 20 September 2017

Deletion mapping indicates that MTS1 is the target of frequent deletions at chromosome 9p21 in paediatric acute lymphoblastic leukaemias.

scientific article published in February 1996

Denaturing gradient gel electrophoresis analysis for the detection of point mutations in the Chlamydia trachomatis major outer-membrane protein gene ⬇️

scientific article published on July 1, 1995

Differences in DNase I sensitivity and methylation within the human beta-globin gene domain and correlation with expression

scientific article published on 01 April 1986

Differential modulation of adhesion molecule expression by hydroxycarbamide in human endothelial cells from the micro- and macrocirculation: potential implications in sickle cell disease vasoocclusive events

scientific article

Differentiation of Escherichia coli strains using randomly amplified polymorphic DNA analysis.

scientific article published in February 1994

Direct detection of verotoxin genes in stool samples by polymerase chain reaction in hemolytic uremic syndrome patients in France.

scientific article published in February 1997

Dissection of the association status of two polymorphisms in the beta-globin gene cluster with variations in F-cell number in non-anemic individuals

scientific article published on 01 December 1997

Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutations.

scientific article

Dominique Labie (1920-2016)

scientific article published on 25 May 2016

ET-1 and ecNOS gene polymorphisms andsusceptibility to acute chest syndrome and painful vaso-occlusive crises in children with sickle cell anemia

scientific article published on 01 September 2006

Echocardiographic Assessment of the Cardiac Anatomy in Patients With Multifocal Atrial Tachycardia: A Comparison With Atrial Fibrillation

scientific article published on 01 April 1994

Editorial for Special Issue "Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies"

scientific article published on 20 September 2019

Effect of hydroxyurea on adhesion proteins in sickle cell anemia

scientific article published on 23 January 2009

Effect of interleukin-8 and RANTES on the Gardos channel activity in sickle human red blood cells: role of the Duffy antigen receptor for chemokines.

scientific article published on 2 March 2010

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

scientific article published in June 2009

Epidemiology of Chlamydia trachomatis using analysis of gene encoding of the major outer membrane protein

scientific article published on May 1992

Ethnic heterogeneity of the factor XIII Val34Leu polymorphism

scientific article published on 01 October 2000

Evidence for nonenzymic glycation of antithrombin III in diabetic patients

scientific article published on 01 February 1985

Evidence for the genetic unrelatedness of nosocomial vancomycin-resistant Enterococcus faecium strains in a pediatric hospital.

scientific article published on September 1991

Evolutionary implications of the frequent horizontal transfer of mismatch repair genes

scientific article

Extensive study of DRB, DQA, and DQB gene polymorphism in 23 DR2-positive, insulin-dependent diabetes mellitus patients

scientific article published on February 1, 1992

F reticulocytes assay: a method to evaluate fetal hemoglobin production

scientific article published on 01 September 1998

Fetal haemoglobin variations following hydroxyurea treatment in patients with cyanotic congenital heart disease

scientific article published on 01 October 1994

Fetal hemoglobin and F-cell responses to long-term hydroxyurea treatment in young sickle cell patients. The French Study Group on Sickle Cell Disease.

scientific article published in June 1998

Fetal hemoglobin and hydroxycarbamide moduate both plasma concentration and cellular origin of circulating microparticles in sickle cell anemia children ⬇️

scientific article published on February 12, 2013

Fluorometric detection of HIV-1 genome through use of an internal control, inosine-substituted primers, and microtiter plate format.

scientific article published in May 1996

Functional characterization of thrombin Salakta: an abnormal thrombin derived from a human prothrombin variant.

scientific article published in March 1988

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?

scientific article published on 01 July 1992

Genetic heterogeneity of Pseudomonas aeruginosa clinical isolates revealed by esterase electrophoretic polymorphism and restriction fragment length polymorphism of the ribosomal RNA gene region.

scientific article published in May 1994

Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections.

scientific article

Genetic variation among major human geographic groups supports a peculiar evolutionary trend in PAX9.

scientific article

Genomic imbalances detected by array-CGH in patients with syndromal ocular developmental anomalies

scientific article published on 11 January 2012

Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease

scientific article published on 25 November 2009

Genotyping may provide rapid identification of Escherichia coli K1 organisms that cause neonatal meningitis.

scientific article published in January 1996

HLA-DQA1 and DQB1 alleles in French and Algerian type 1 diabetic subjects.

scientific article published on August 1991

HLA-DQB 1 codon 57 and genetic susceptibility to type 1 (insulin-dependent) diabetes mellitus in French children

scientific article published on 01 March 1990

HLA-mismatched cord blood transplantation in a patient with advanced leukemia

scientific article published on January 1, 1991

HLA-mismatched cord blood transplantation: immunological studies

scientific article published on 01 January 1994

HLA-mismatched cord-blood transplantation in a patient with advanced leukemia

scientific article published on 01 May 1992

Haemoglobin A2 is elevated in hyperthyroid patients

scientific article published on 01 January 1982

Haemoglobin D-Ouled Rabah among the Mozabites: a relevant variant to trace the origin of Berber-speaking populations.

scientific article

Haemoglobin F, A2, and S levels in subjects with or without sickle cell trait in south-eastern Gabon

scientific article published on 23 February 2017

Haemoglobinopathies: a pitfall in the assessment of glycosylated haemoglobin by ion-exchange chromatography.

scientific article published in December 1984

HbD Iran-beta-thalassemia association in a Tunisian family

scientific article published on June 1, 1992

Hemolytic-uremic syndrome in the child.

scientific article

Heterogeneity within the first constant segment of the major outer membrane protein gene in Chlamydia trachomatis serovar D/Da distinguishes 2 lineages

scientific article published on 01 September 1995

Heterogeneous ethnic distribution of the 844ins68 in the cystathionine beta-synthase gene

scientific article published on 01 November 1998

Heterozygous HbAC but not HbAS is associated with higher newborn birthweight among women with pregnancy-associated malaria.

scientific article

Highly Variable Mutation Rates in Commensal and Pathogenic Escherichia coli

scientific article published in Science

Homogeneity of the major outer membrane protein gene of feline Chlamydia psittaci.

scientific article published on January 1994

Homozygous deletional α+thalassaemia associated with unequal expression of the two remaining α1genes (α1Aand α1Q)

article

Hydroxycarbamide decreases sickle reticulocyte adhesion to resting endothelium by inhibiting endothelial lutheran/basal cell adhesion molecule (Lu/BCAM) through phosphodiesterase 4A activation

scientific article

Hydroxycarbamide modulates components involved in the regulation of adenosine levels in blood cells from sickle-cell anemia patients

scientific article published on 03 April 2014

Hydroxyurea downregulates endothelin-1 gene expression and upregulates ICAM-1 gene expression in cultured human endothelial cells.

scientific article published in January 2003

Identification of a clone of Escherichia coli O103:H2 as a potential agent of hemolytic-uremic syndrome in France

scientific article

Identification of a clone of Escherichia coli O103:H2 as potential agent of hemolytic-uremic syndrome in France.

scientific article published in March 1994

Impact of glucose-6-phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: a prospective study

scientific article published on 10 October 2013

Improvement of medical care in a cohort of newborns with sickle-cell disease in North Paris: impact of national guidelines

scientific article published on 7 April 2016

Increased protein binding to a -530 mutation of the human beta-globin gene associated with decreased beta-globin synthesis

scientific article published on 01 January 1991

Infectious complications in sickle cell disease are influenced by HLA class II alleles.

scientific article

Influence of aortic valve disease on systolic stiffness of the human left ventricular myocardium

scientific article published on 01 May 1987

Influence of thyroid status on hemoglobin A2 expression

scientific article published on 01 August 1983

Interaction of prothrombin and its fragments with monolayers containing phosphatidylserine. 1. Binding of prothrombin and its fragment I to phosphatidylserine-containing monolayers.

scientific article published in July 1980

Iron overload in thalassaemias and genetic haemochromatosis

scientific article published on 01 April 2000

Isolation and characterization of the vitamin K dependent domain of human prothrombin

scientific article published on 01 November 1981

Isolation of preliminary characterization of a vitamin K dependent peptide from human prothrombin

scientific article published on 01 February 1976

Left heart opacification with peripheral venous injection of a new saccharide echo contrast agent in dogs.

scientific article

Long-term hydroxyurea treatment in young sickle cell patients.

scientific article

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.

scientific article published in November 1995

Measurement of adult hemoglobin in fetal blood samples by high-performance liquid chromatography as purity control for the prenatal diagnosis of chromosomal abnormalities

scientific article published on 01 September 1993

Measurement of glycated albumin in diabetic patients by biospecific affinity chromatography

scientific article published on 01 August 1987

Mechanisms of the spread of penicillin resistance in Streptococcus pneumoniae strains causing meningitis in children in France

scientific article published on 01 September 1996

Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate Strength

scientific article

Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease

scientific article

Molecular Basis of β‐Thalassemia in Bahrain: An Epicenter for a Middle East Specific Mutationa ⬇️

scientific article published on June 30, 1998

Molecular analysis of multiply recurrent meningitis due to Escherichia coli K1 in an infant.

scientific article published in January 1993

Molecular analysis provides evidence for the endogenous origin of bacteremia and meningitis due to Enterobacter cloacae in an infant.

scientific article published in July 1992

Molecular basis of alpha-thalassemia in Algeria.

scientific article

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.

scientific article published in February 2005

Molecular epidemiological analysis of Pseudomonas aeruginosa strains causing failure of antibiotic therapy in cystic fibrosis patients

scientific article published on May 1, 1992

Molecular epidemiology of plasmid spread among extended broad-spectrum beta-lactamase-producing Klebsiella pneumoniae isolates in a pediatric hospital.

scientific article published on February 1993

Molecular epidemiology unravels the complexity of neonatal Escherichia coli acquisition in twins.

scientific article published on July 1992

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.

scientific article published on May 1983

Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases

scientific article published on 01 October 1999

Mother-to-infant vertical transmission and cross-colonization of Streptococcus pyogenes confirmed by DNA restriction fragment length polymorphism analysis

scientific article published on January 1, 1992

Multiple molecular bases for thalassemia intermedia in east Sicily

scientific article published on 01 January 1985

Multiple recurrences and relapse of Streptococcus pneumoniae meningitis

scientific article published on 01 July 1995

Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease

scientific article published on 01 April 2004

Neonatal screening for sickle cell anemia: evaluation of a five-year experience in an area of northern Paris

scientific article published in May 2001

Neonatal screening for sickle cell disease in France.

scientific article

New approach to accurate interpretation of sickle cell disease newborn screening by applying multiple of median cutoffs and ratios

scientific article published on 21 May 2018

New insights into red cell rheology and adhesion in patients with sickle cell anaemia during vaso-occlusive crises

scientific article published on 22 November 2018

Newborn Screening for Sickle Cell Disease in Europe

scientific article published on 12 February 2019

Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference

scientific article published on 18 October 2018

Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the beta-globin gene

scientific article published on 01 January 1996

On the diversity of beta-globin mutations, a reflection of recent historic events in Israel.

scientific article published on December 1994

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

scientific article published on 01 June 1991

Origin of the prevalentSFTPBindel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP-B) deficiency

scientific article published on 01 January 2006

Pathophysiological insights in sickle cell disease.

scientific article published on October 2011

Pathophysiology of sickle cell disease

scientific article published on December 2010

Phenotypic expression and origin of the rare beta-thalassemia splice site mutation HBB:c.315 + 1G>T

scientific article published on 01 June 2010

Phylogenetic analysis of Escherichia coli strains causing neonatal meningitis suggests horizontal gene transfer from a predominant pool of highly virulent B2 group strains

scientific article published on 01 March 1998

Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell disease ⬇️

scientific article published on August 1, 1997

Pre- and postnatal phenotype of 6p25 deletions involving theFOXC1gene

article

Preliminary report on the use of desferrioxamine in the treatment ofPlasmodium falciparum malaria ⬇️

scientific article published on July 1, 1991

Prevalence of the G20210A polymorphism in the 3'-untranslated region of the prothrombin gene in different human populations.

scientific article published in January 1998

Prior exposure of endothelial cells to hydroxycarbamide alters the flow dynamics and adhesion of sickle red blood cells

scientific article published on January 2014

Proceedings: Binding of Ca++ to human prothrombin

scientific article published on 01 November 1975

Production of monoclonal antibodies to the high fibrin-affinity, tissue-type plasminogen activator of human plasma. Demonstration of its endothelial origin by immunolocalization

scientific article published on 01 October 1985

Proteolytic derivatives of thrombin

scientific article published on 01 January 1986

Prothrombin

scientific article published on 01 January 1981

Purification and partial characterization of a new variant of human prothrombin: prothrombin Metz

scientific article published on 01 December 1979

Purification of Aldolase C from Rat Brain and Hepatoma ⬇️

scientific article published on July 1, 1977

Purpura fulminans méningococcique : rencontre malheureuse de polymorphismes génétiques ?

scientific article published on 01 August 2001

Rapid genotyping of the Chlamydia trachomatis major outer membrane protein by the polymerase chain reaction

scientific article published on September 15, 1991

Rapid genotyping shows the absence of cross-contamination in Enterobacter cloacae nosocomial infections.

scientific article published in June 1992

Rapid quantification of Hb Hope in heterozygotes.

scientific article

Recent data concerning abnormal hemoglobins (author's transl)

scientific article published on January 1, 1981

Reliability of PCR directly from stool samples: usefulness of an internal standard.

scientific article published in May 1994

Respective weight of genotypes DQA1 and DQB1 associated with insulin-dependent diabetes in French children

scientific article published on 01 July 1992

Restriction pattern of the major outer-membrane protein gene provides evidence for a homogeneous invasive group among ruminant isolates of Chlamydia psittaci

scientific article published on November 1, 1991

Ribotyping provides efficient differentiation of nosocomial Serratia marcescens isolates in a pediatric hospital ⬇️

scientific article published on August 1, 1992

Sequence correction and reassignment of the TaqI polymorphic site in the human inter-gamma-globin gene region, an African-specific marker.

scientific article published in April 1994

Sequence polymorphisms of potential functional relevance in the beta-globin gene locus.

scientific article published on May 1996

Sequence variations in the 3' A gamma enhancer are silent polymorphisms

scientific article published on 01 January 1989

Sex in Escherichia coli does not disrupt the clonal structure of the population: evidence from random amplified polymorphic DNA and restriction-fragment-length polymorphism

scientific article published on 01 October 1995

Sickle cell anemia in Guadeloupean children: pattern and prevalence of acute clinical events

scientific article published on 01 March 2006

Strategy linking several analytical methods of neonatal screening for sickle cell disease

scientific article published on 01 January 2001

Strong association between a new marker of hemolysis and glomerulopathy in sickle cell anemia.

scientific article published on 15 September 2010

Systematic correlation of continuous-wave Doppler and hemodynamic measurements in patients with aortic stenosis.

scientific article published in February 1986

Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children.

scientific article published in January 1997

The Phylogeography of Mitochondrial DNA Haplogroup L3g in Africa and the Atlantic Slave Trade

scientific article published in September 2004

The erythrocyte effects of haemoglobin O(ARAB)

scientific article published on 01 December 1999

The missing middle of sickle therapeutics: Multi-agent therapy, targeting risk, using biomarkers

scientific article published on 23 October 2018

The placental-umbilical unit in sickle cell disease pregnancy: a model for studying in vivo functional adjustments to hypoxia in humans

scientific article published on 01 November 2004

The prevalence of factor V Arg306-->Thr (factor V Cambridge) and factor V Arg306-->Gly mutations in different human populations.

scientific article

The problem of sickle cell disease in Africa

scientific article published on December 1, 2010

The spectrum of beta-thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy.

scientific article

Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. The French Study Group on Sickle Cell Disease.

scientific article published on July 1997

Thrombin Metz: characterization of the dysfunctional thrombin derived from a variant of human prothrombin

scientific article published on 01 April 1984

Thrombin: Structural Features Related to Specificity1 ⬇️

scientific article published on January 1, 1977

Thrombosis of mitral valve prosthesis presenting as abdominal pain

scientific article published on 01 March 1999

Transcriptional regulation of rat alpha 1-acid glycoprotein gene by phenobarbital.

scientific article

Two variants of hemoglobin D in the algerian population: Hemoglobin D ouled rabah β19 (B1) Asn → Lys and hemoglobin D Iran β22 (B4) Glu → Gln ⬇️

scientific article published on June 15, 1973

UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia

scientific article published on 01 May 2006

Unsuspected glucose-6-phosphate dehydrogenase deficiency presenting as symptomatic methemoglobinemia with severe hemolysis after fava bean ingestion in a 6-year-old boy.

scientific article

Use of ribotyping in epidemiological surveillance of nosocomial outbreaks

scientific article published on July 1994

Usefulness of omp1 restriction mapping for avian Chlamydia psittaci isolate differentiation ⬇️

scientific article published on February 1, 1995

Variants of the mannose-binding lectin gene in the Benin population: heterozygosity for the p.G57E allele may confer a selective advantage. 2007.

scientific article published in December 2009

Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals

scientific article published on 01 March 1996

Vaso-occlusion in sickle cell anemia: role of interactions between blood cells and endothelium.

scientific article published on January 2004

Virulence patterns of Escherichia coli K1 strains associated with neonatal meningitis.

scientific article published on November 1997

WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms' tumour

scientific article published on 01 April 2003

[Clinical, biological and genetic heterogeneity of the inborn errors of pulmonary surfactant metabolism: SP-B deficiency and alveolar proteinosis]

scientific article published on 01 March 2001

[Constitutional deficiency of pulmonary surfactant protein B: clinical presentation, histologic and molecular diagnosis]

scientific article published on 01 June 2000

[Contribution of molecular typing in the surveillance of nosocomial infections. Experience in pediatric hospitals]

scientific article published on 01 October 1992

[Flowcharts for the diagnosis and the molecular characterization of hemoglobinopathies]

scientific article published on 01 July 2010

[Molecular and cellular pathophysiology of sickle cell anemia]

scientific article published on 01 January 1999

[Molecular epidemiology of cystic fibrosis in Tunisia]

scientific article

[Mucoviscidosis discovered after the age of 25 years. Review and follow-up of cases of the literature]

scientific article published on 01 January 1994

[Neonatal screening of sickle cell anemia in metropolitan France]

scientific article published on 01 December 2000

[Pharmacogenetics or "farm-ecogenetics"?]

scientific article published on 01 January 2000

[Sickle cell anemia: model of variability in expression of monogenic disease]

scientific article published on 01 February 1996

[Sickle cell disease: pneumococcus escapes prevention and adapts to the disease. Consequences on vaccine design]

scientific article published on 10 November 2014

[The X chromosome, fetal hemoglobin and sickle cell anemia]

scientific article published on 01 January 1991

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