D. Labie

发表

D. Labie, Joe Felsenstein, 1991, Nature.

Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa.

D. Labie, R. Nagel, C. Beldjord, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.

D. Labie, R. Nagel, H. Wajcman, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type.

D. Labie, R. Nagel, H. Wajcman, 1985, The New England journal of medicine.

Structural analysis of the 5' flanking region of the beta-globin gene in African sickle cell anemia patients: further evidence for three origins of the sickle cell mutation in Africa.

D. Labie, Y. Chebloune, Claudine Faure, 1988, Proceedings of the National Academy of Sciences of the United States of America.

A novel sickle cell mutation of yet another origin in Africa: the Cameroon type

D. Labie, J. Elion, J. Bodo, 1992, Human Genetics.

Characterization of a proteolytically modified form of human prothorombin.

D. Labie, C. Dodé, O. Bertrand, 1980, Biochemical and biophysical research communications.

Structural bases of the inhibitory effects of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S.

D. Labie, R. Nagel, H. Wajcman, 1979, Proceedings of the National Academy of Sciences of the United States of America.

Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia trait.

D. Labie, C. Junien, J. Kaplan, 1982, Human heredity.

Presence of an African β‐globin gene cluster haplotype in normal chromosomes in sicily

D. Labie, R. Nagel, A. Ragusa, 1992, American journal of hematology.

Asymptomatic and mild β-thalassemia in homozygotes and compound heterozygotes for the IVS 2 + 1 G > A mutation : role of the β-globin gene haplotype

D. Labie, L. Bernini, M. Maier‐Redelsperger, 2003 .

Asymptomatic and mild beta-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G-->A mutation: role of the beta-globin gene haplotype.

D. Labie, L. Bernini, M. Maier‐Redelsperger, 2003, Haematologica.

A leftward deletional α+ thalassemia found in East Sicily in conjunction with heterozygous β-thalassemia

D. Labie, R. Krishnamoorthy, T. Lombardo, 2004, Human Genetics.

Immobilized pH gradients for isoelectric focusing: Interaction between histones and histone‐like proteins with the charged polyacrylamide matrix

D. Labie, P. Righetti, M. Delpech, 1983 .

Automated analysis of mature red blood cells and reticulocytes in SS and SC disease.

D. Labie, A. Flahault, M. Maier‐Redelsperger, 2004, Blood cells, molecules & diseases.

Sickle gene. Its origin and diffusion from West Africa.

D. Labie, R. Nagel, H. Lachman, 1981, The Journal of clinical investigation.

[Recurrent fever in malaria: a main advantage for Plasmodium falciparum?].

D. Labie, 2005, Medecine sciences : M/S.

[The Mycobacterium genome: biological study and evolutionary interpretation].

D. Labie, 2003, Medecine sciences : M/S.

Annotated Definition of BCL11A and HMIP-2 Haplotypes Through the Analysis of Sicilian β-Thalassemia Patients with High Levels of Fetal Hemoglobin

D. Labie, M. Buccheri, T. Lombardo, 2013, Hemoglobin.

Membrane expansion as a mechanism explaining the antisickling action of ticlopidine observed in vitro

D. Labie, H. Wajcman, J. Castaigne, 1985, American journal of hematology.

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

D. Labie, J. Elion, R. Krishnamoorthy, 1986, European journal of biochemistry.

Abnormal hemoglobins in mauritius Island

D. Labie, R. Nagel, R. Ducrocq, 1995, American journal of hematology.

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

D. Labie, J. Elion, F. Josso, 1979, FEBS letters.

Quantitation of hemoglobin A1c: a rapid, automated precision-chromatography technique.

D. Labie, B. Dastugue, H. Wajcman, 1979, Clinica chimica acta; international journal of clinical chemistry.

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.

D. Labie, J. Elion, A. Cahour, 1983, European journal of biochemistry.

Increased protein binding to a −530 mutation of the human β‐globin gene associated with decreased β‐globin synthesis

A. Schechter, D. Labie, J. Elion, 1991, American journal of hematology.

Novel and unusual deletion‐insertion thalassemic mutation in exon 1 of the β‐globin gene

D. Labie, J. Elion, M. Krawczak, 1996, Human mutation.

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

D. Labie, J. Elion, R. Tamouza, 1994, Human biology.

β‐Thalassemia in Algeria

D. Labie, C. Beldjord, C. Bennani, 1990 .

A novel beta thalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3' end of IVS 2.

D. Labie, C. Beldjord, R. Krishnamoorthy, 1988, Nucleic acids research.

Beta thalassemia due to a novel mutation in IVS 1 sequence donor site consensus sequence creating a restriction site.

D. Labie, R. Krishnamoorthy, C. Lapouméroulie, 1986, Biochemical and biophysical research communications.

Long-term hydroxyurea treatment in young sickle cell patients.

D. Labie, J. Elion, M. Maier‐Redelsperger, 1999, Current opinion in hematology.

The -158 site 5' to the G gamma gene and G gamma expression.

D. Labie, R. Nagel, A. Ragusa, 1985, Blood.

Analysis of crossover type in the α-3·7 haplotype among sickle cell anemia patients from various parts of Africa

D. Labie, C. Dodé, J. Rochette, 1988, Human Genetics.

The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF level.

D. Labie, R. Nagel, R. Krishnamoorthy, 1987, Blood.

Fetal Hemoglobin Expression

D. Labie, A. Ragusa, R. Krishnamoorthy, 2006 .

Nucleotide Variations inthe3'A'y Enhancer RegionAreLinked to IB-Gene Cluster Haplotypes andAreUnrelated to Fetal Hemoglobin Expression

D. Labie, C. Beldjord, A. Ragusa, 1989 .

GENETICS OF HEMOCHROMATOSIS *

D. Labie, J. Frézal, M. Lamy, 1958 .

Importation route of the sickle cell trait into Portugal: contribution of molecular epidemiology.

D. Labie, J. Lavinha, L. Romão, 1992, Human biology.

Atypical haplotypes linked to the βs gene in Africa are likely to be the product of recombination

D. Labie, R. Nagel, A. Georges, 1988 .

βS gene in sicily is in linkage disequilibrium with the benin haplotype: Implications for gene flow

D. Labie, R. Nagel, A. Ragusa, 1988, American journal of hematology.

The sickle gene polymorphism in North Africa.

D. Labie, R. Nagel, C. Beldjord, 1981, Blood.

La résistance au paludisme. Interaction de facteurs multiples.

D. Labie, 1997 .

Nucleotide sequence evidence of the unicentric origin of the βC mutation in Africa

D. Labie, R. Nagel, J. Elion, 1991, Human Genetics.

mutation globin gene correlates with the phenotypic expression of the beta s DNA sequence variation in a negative control region 5' to the beta-

A. Schechter, D. Labie, J. Elion, 2011 .

DNA Sequence Variation in a Negative Control Region 5 ’ to the p-Globin Gene Correlates With the Phenotypic Expression of the pS Mutation

A. Schechter, D. Labie, J. Elion, 2003 .

DNA sequence variation in a negative control region 5' to the beta- globin gene correlates with the phenotypic expression of the beta s mutation

A. Schechter, D. Labie, J. Elion, 1992 .

[Home and leisure accidents' mortality].

D. Labie, 2007, Medecine sciences : M/S.

Three-Year Follow-Up of Hydroxyurea Treatment in Severely Ill Children with Sickle Cell Disease

D. Labie, J. Jais, J. Elion, 1997 .

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

D. Labie, J. Jais, J. Elion, 1997, Journal of pediatric hematology/oncology.

[Diabetes care in sub-Saharan Africa].

D. Labie, 2007, Medecine sciences : M/S.

[Plasmodium's stratagems to be protected in the invaded organisms].

D. Labie, 2005, Medecine sciences : M/S.

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

D. Labie, J. Elion, 1996, Hemoglobin.

Alpha-thalassemia is related to prolonged survival in sickle cell anemia.

D. Labie, R. Nagel, H. Lachman, 1983, Blood.

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

D. Labie, J. Elion, R. Tamouza, 2002, Human immunology.

Diversity of sequence haplotypes associated with beta-thalassaemia mutations in Algeria: implications for their origin.

D. Labie, G. Trabuchet, V. Nigon, 1998, Gene.

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.

D. Labie, J. Elion, J. Pagnier, 1991, Human biology.

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.

D. Labie, J. Elion, C. Dodé, 1989, Human biology.

The consequences and implications of the multicentric origin of the Hb S gene.

D. Labie, R. Nagel, 1985, Progress in clinical and biological research.

A new unstable hemoglobin mutated in β 98 (FG 5) Val → Ala: Hb Djelfa

D. Labie, H. Wajcman, G. Gacon, 1975 .

A new case of haemoglobin Bucuresti in a Cuban family: further functional studies.

D. Labie, L. Bernini, B. Colombe, 1975, Journal of medical genetics.

Appearance of β globin synthesis in erythroid cells of Ferrara β°-thalassaemic patients following blood transfusion

D. Labie, C. Vullo, F. Conconi, 1975, Nature.

An attempt at demonstrating the existence of a nonsense mutation in -thalassemia.

D. Labie, F. Conconi, J. Dreyfus, 1972, European journal of biochemistry.

Unstable Haemoglobin with a Modified Affinity for Oxygen in a French Patient

D. Labie, Y. Beuzard, J. Rosa, 1970 .

Titration curves by combined isoelectric focusing--electrophoresis on a thin layer of agarose gel

D. Labie, J. Elion, R. Krishnamoorthy, 1982 .

Titration curves of polypeptide chains by combined isoelectric focusing-electrophoresis in 8 M urea.

D. Labie, P. Righetti, C. Lapouméroulie, 1979, Journal of chromatography.

Foetal Haemoglobin, Erythrocytes Containing Foetal Haemoglobin, and Hematological Features in Congolese Patients with Sickle Cell Anaemia

D. Labie, G. Avvisati, C. Gregorj, 2012, Anemia.

Immobilized pH gradients and reversed-phase high-performance liquid chromatography: a strategy for characterization of haemoglobin variants with electrophoretic mobility identical to that of Hb A. The case of Hb San Diego.

D. Labie, P. Righetti, H. Wajcman, 1984, Journal of chromatography.

Homozygous deletional α+ thalassaemia associated with unequal expression of the two remaining α1 genes (α1A and α1Q)

D. Labie, J. Elion, C. Lapouméroulie, 1982 .

Titration curves of liganded hemoglobins by combined isoelectric focusing—electrophoresis

D. Labie, P. Righetti, R. Krishnamoorthy, 1978, FEBS letters.

Protein titration curves by combined isoelectric focusing-electrophoresis with hemoglobin mutants as models

D. Labie, E. Gianazza, R. Krishnamoorthy, 1978 .

Hemoglobin variants in Europe.

D. Labie, 1980, Hemoglobin.

Hemoglobins of an Amphibia, the Neotenous Ambystoma mexicanum. Complete Amino‐Acid Sequence of the α Chain of the Major Component Using Automatic Solid‐Phase Edman Degradation

D. Labie, H. Wajcman, J. Boissel, 1980 .

Preliminary report on the use of desferrioxamine in the treatment of Plasmodium falciparum malaria

D. Labie, O. Traoré, R. Nagel, 1991, American journal of hematology.

Structural and functional studies of hemoglobin Barcelona (α2β2 94 Asp (FG1) → his): Consequences of altering an important intrachain salt bridge involved in the alkaline Bohr effect

D. Labie, H. Wajcman, C. Poyart, 1982 .

Structural and functional studies of hemoglobin Barcelona (alpha 2 beta 2 94 Asp (FG1) replaced by His). Consequences of altering an important intrachain salt bridge involved in the alkaline Bohr effect.

D. Labie, H. Wajcman, C. Poyart, 1982, Journal of molecular biology.

Hemoglobins of an amphibia, the neotenous Ambystoma mexicanum. Complete amino-acid sequence of the alpha chain of the major component using automatic solid-phase Edman degradation.

D. Labie, H. Wajcman, J. Boissel, 1980, European journal of biochemistry.

An unusual case of leukemia with high fetal hemoglobin: demonstration of abnormal hemoglobin synthesis localized in a red cell clone.

D. Labie, C. Mathiot, B. Varet, 1977, Blood.

Abnormal hemoglobin synthesis in some leukemic patients.

D. Labie, J. Pagnier, 1975, Biochimie.

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

D. Labie, J. Elion, T. Merghoub, 1997, American journal of hematology.

Origine multicentrique de la mutation S

D. Labie, 1987 .

Genetic heterogeneity of sickle mutations.

D. Labie, R. Nagel, 1987, Acta haematologica.

HAPLOTYPE-VI-ASSOCIATED MILD β+-THALASSAEMIA IN SICILY: MEDITERRANEAN TYPE?

D. Labie, R. Cacciola, T. Lombardo, 1983, The Lancet.

Genetic variations in human fetal globin gene microsatellites and their functional relevance

M. Fichera, D. Labie, A. Ragusa, 1999, Human Genetics.

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

D. Labie, J. Elion, T. Merghoub, 1996, Blood.

HLA-E*0101 allele in homozygous state favors severe bacterial infections in sickle cell anemia.

D. Labie, R. Tamouza, M. Busson, 2007, Human immunology.

Known and Potential Sources for Epistatic Effects in Sickle Cell Anemia

D. Labie, R. Nagel, M. Fabry, 1989, Annals of the New York Academy of Sciences.

Isolation and partial characterization of hemoglobin A1b

D. Labie, G. Gacon, R. Krishnamoorthy, 1977, FEBS letters.

Nucleic Acids Research

D. Labie, C. Beldjord, C. Lapouméroulie, 2008, Nucleic Acids Research.

[IL28 (interferon lambda3) gene polymorphisms and response to IFN-alpha treatment in patients infected with hepatitis virus C].

D. Labie, H. Gilgenkrantz, 2010, Medecine sciences : M/S.

Heterogeneity of haplotypes among patients with severe Cooley disease in Eastern Sicily

D. Labie, A. Ragusa, M. Lombardo, 1986, Human Genetics.

Multiple Molecular Bases for Thalassemia Intermedia in East Sicily a

D. Labie, J. Elion, R. Krishnamoorthy, 1985, Annals of the New York Academy of Sciences.

DNA haplotype distribution in Algerian β thalassaemia patients

D. Labie, S. Amselem, C. Beldjord, 1988, Human Genetics.

α-Globin loci in homozygous β-thalassemia intermedia

D. Labie, R. Girot, C. Lapouméroulie, 1983, Human Genetics.

High genetic polymorphism of hemoglobin disorders in Laos

D. Labie, C. Lapouméroulie, D. Sicard, 1979, Human Genetics.

Haemoglobin D-Ouled Rabah among the Mozabites: A Relevant Variant to Trace the Origin of Berber-Speaking Populations

D. Labie, A. Sanchez‐Mazas, J. Elion, 1997, European journal of human genetics : EJHG.

Hemoglobin Cocody [β21(B3)Asp→Asn] Hematologic Aspects of Heterozygosity and of Hb Cocody/β+-Thalassemia

D. Labie, J. Boissel, R. Cabannes, 1985 .

Application of high-performance liquid chromatography to abnormal hemoglobin studies: Characterization of hemoglobins D in ivory coast and description of a new variant Hb cocody (β 21 (B3) Asp → Asn)

D. Labie, H. Wajcman, J. Boissel, 1981 .

Consequences of heme loss in unstable hemoglobins: A study of hemoglobin köln

D. Labie, H. Wajcman, S. Haidas, 1971, FEBS Letters.

Hb J Lome β59 (E3) Lys → Asn Associated with Hpfh in a Togolese Family

D. Labie, H. Wajcman, J. Pagnier, 1979 .

Hemoglobin J Lome β 59 (E3) Lys → Asn A new fast moving variant found in a Togolese

D. Labie, H. Wajcman, K. Amegnizin, 1977 .

An unusual case of leukemia with high fetal hemoglobin: demonstration of abnormal hemoglobin synthesis localized in a red cell clone

D. Labie, C. Mathiot, B. Varet, 1977 .

Hb j mexico in algeria: Arguments for an heterogenous distribution of α genes

D. Labie, J. Pagnier, G. Trabuchet, 1976 .

The amino acid sequence of the δ-β chains of hemoglobin LeporeAugusta = LeporeWashington

D. Labie, T. Huisman, W. Schroeder, 1966 .

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

D. Labie, N. Casadevall, J. Elion, 1994, Nouvelle revue francaise d'hematologie.

MOLECULAR HETEROGENEITY OF b-THALASSEMIA IN ALGERIA : HOW TO FACE UP TO A MAJOR HEALTH

D. Labie, C. Beldjord, N. Carion, 2009 .

Hb Setif: G1 (94)α Asp → Tyr a new α chain hemoglobin variant with substitution of the residue involved in a hydrogen bond between unlike subunits

D. Labie, H. Wajcman, O. Belkhodja, 1972, FEBS letters.

Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem

D. Labie, C. Beldjord, N. Carion, 2009, Hemoglobin.

Molecular basis of α-thalassemia in Sicily

M. Fichera, D. Labie, R. Tamouza, 1997, Human Genetics.

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

D. Labie, J. Elion, T. Merghoub, 1998 .

Molecular basis of beta-thalassemia in Bahrain: an epicenter for a Middle East specific mutation.

D. Labie, J. Elion, T. Merghoub, 1998, Annals of the New York Academy of Sciences.

Beta-thalassemia in Algeria.

D. Labie, C. Beldjord, C. Bennani, 1990, Annals of the New York Academy of Sciences.

DNA haplotype distribution in Algerian beta thalassaemia patients. An extended evaluation by family studies and representative molecular characterization.

D. Labie, S. Amselem, C. Beldjord, 1988, Human genetics.

DNA haplotypes and the beta s globin gene.

D. Labie, R. Nagel, 1989, Progress in clinical and biological research.

Isoelectrofocusing: a method of multiple applications for hemoglobin studies.

D. Labie, H. Wajcman, R. Krishnamoorthy, 1976, Clinica chimica acta; international journal of clinical chemistry.

Impairment of the growth of Plasmodium falciparum in HbEE erythrocytes.

D. Labie, R. Nagel, H. Tanowitz, 1981, The Journal of clinical investigation.

A novel sickle gene of yet another origin in Africa: The Cameroon type

D. Labie, J. Elion, J. Bodo, 1992 .

Uniparental disomy: a novel mechanism for thalassemia major [letter]

D. Labie, C. Beldjord, D. Vanhaeke, 1992 .

Hemoglobins S and C in Upper Volta

D. Labie, R. Nagel, J. Pagnier, 2004, Human Genetics.

[Familial diphosphoglycerate mutase deficiency: hematological and biochemical study].

D. Labie, A. Najman, F. Demaugre, 1972, Nouvelle revue francaise d'hematologie.

HÆMOGLOBINOPATHIES AND G.-6-P.D. DEFICIENCY IN LAOS

D. Labie, J. Kaplan, D. Sicard, 1978, The Lancet.

Hozygous Cases for Hemoglobin J Mexico (α50 (E3)Gln→Glu) Evidence for a Duplicated α Gene with Unequal Expression

D. Labie, J. Pagnier, G. Trabuchet, 1976 .

Genetic and biosynthetic studies of families carrying hemoglobin J α Mexico: Association of α-thalassemia with Hb J

D. Labie, G. Trabuchet, M. Benabadji, 1978, Human Genetics.

Activation of prothrombin Barcelona. Evidence for active high molecular weight intermediates.

D. Labie, R. Benarous, M. Rabiet, 1979, Biochimica et biophysica acta.

Abnormal activation of a human prothrombin variant: Prothrombin barcelona

D. Labie, R. Benarous, M. Rabiet, 1978, FEBS letters.

Isolation and partial characterization of a human prothrombin variant: prothrombin Barcelona.

D. Labie, R. Benarous, J. Lavergne, 1974, Biochemical and biophysical research communications.

Hemoglobin Barcelona beta 94 (FG1) Asp leads to His : a new hemoglobin Variant with increased oxygen affinity.

D. Labie, H. Wajcman, C. Poyart, 1981, Nouvelle revue francaise d'hematologie.

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

D. Labie, B. L. Le Bonniec, M. Rabiet, 1984, The Journal of biological chemistry.

2,3-diphosphoglycerate content and oxygen affinity as a function of red cell age in normal individuals.

D. Labie, J. Kaplan, S. Haidas, 1971, Blood.

Haemoglobin I Toulouse: β66 (E 10) Lys → Glu: a New Abnormal Haemoglobin with a Mutation localized on the E 10 Porphyrin Surrounding Zone

D. Labie, H. Wajcman, R. Bierme, 1969, Nature.

Structure and function of Hb Saint-Jacques (α2β2 140 (H18) Ala → Thr): A new high-oxygen-affinity variant with altered bisphosphoglycerate binding

D. Labie, H. Wajcman, J. Rochette, 1984 .

Hemoglobin fort de France (α245(CD3) HisåArg β2) A new variant with increased oxygen affinity

D. Labie, H. Wajcman, G. Gacon, 1977 .

Change in A3 Hæmoglobin due to β-Chain

D. Labie, J. Rosa, 1962, Nature.

Evidence for a distinct fraction of hemoglobin, specifically associated with the young erythrocytes.

D. Labie, J. Dreyfus, G. Schapira, 1962, Biochemical and biophysical research communications.

Functional properties of hemoglobin Hammersmith.

D. Labie, H. Wajcman, A. Leroux, 1973, Biochimie.

A Second Case of Bemoglobxn Grady, Repetitive in the Middle of the α Chain

D. Labie, H. Wajcman, G. Gacon, 1976 .

Association of Hb e with β° Thalassemia

D. Labie, H. Wajcman, G. Gacon, 1978 .

Two new hemoglobin variants with deletion. Hemoglobin tours: Thr 8 7 (F 3 ) deleted and hemoglobin St Antoine: Gly-Leu 74-75 (E 18-19 deleted. Consequences for oxygen affinity and protein stability.

D. Labie, H. Wajcman, G. Schapira, 1973, Biochimica et biophysica acta.

A case of hemoglobin M Boston. New data about valency hybrids brought by isoelectrofocusing study.

D. Labie, H. Wajcman, R. Krishnamoorthy, 1976, Biomedicine / [publiee pour l'A.A.I.C.I.G.].

A new case of hemoglobin Genova α2 β228(B10) Leu → Pro further studies on the mechanism of instability and defective synthesis

D. Labie, M. Solal, 1973 .

Four new haplotypes observed in Algerian β-thalassemia patients

D. Labie, G. Lenoir, C. Beldjord, 2004, Human Genetics.

[A novel mechanism for genetic diseases: transcription of antisense RNA may silence a gene].

D. Labie, 2004, Medecine sciences : M/S.

The spectrum of β‐thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy

D. Labie, J. Elion, R. Tamouza, 1993, British journal of haematology.

Inter-ethnic polymorphism of the β-globin gene locus control region (LCR) in sickle-cell anemia patients

D. Labie, J. Elion, P. Moi, 1993, Human Genetics.

[BCL11A represses HbF expression and varies during ontogeny].

D. Labie, 2009, Medecine sciences : M/S.

Nucleotide variations in the 3' A gamma enhancer region are linked to beta-gene cluster haplotypes and are unrelated to fetal hemoglobin expression.

D. Labie, R. Nagel, E. Bouhassira, 1989, American Journal of Human Genetics.

DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation.

A. Schechter, D. Labie, J. Elion, 1992, Blood.

Uniparental disomy: a novel mechanism for thalassemia major.

D. Labie, C. Beldjord, D. Vanhaeke, 1992, Blood.

A gene conversion located 5' to the A gamma gene in linkage disequilibrium with the Bantu haplotype in sickle cell anemia.

D. Labie, R. Nagel, H. Lachman, 1989, The Journal of clinical investigation.

Inefficient erythropoiesis during severe sickle cell chemia

D. Labie, 2006 .

Interaction between cytochrome b5 and hemoglobin: involvement of beta 66 (E10) and beta 95 (FG2) lysyl residues of hemoglobin.

D. Labie, J. Kaplan, G. Gacon, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Interaction between cytochrome b 5 and hemoglobin : Involvement of f 66 ( El 0 ) and p 95 ( FG 2 ) lysyl residues of hemoglobin

D. Labie, J. Kaplan, G. Gacon, 2022 .

Evolution of the Specific Activity of the Free Glycine of the Tissues; SUR L'ABSENCE D'UN POOL METABOLIQUE UNIQUE DU GLYCOCOLLE LIBRE DES TISSUS

D. Labie, J. Kruh, J. Dreyfus, 1959 .

[Conflict and emerging infectious diseases].

D. Labie, 2008, Medecine sciences : M/S.

β-Chain contact sites in the haemoglobin S polymer

D. Labie, R. Nagel, H. Wajcman, 1980, Nature.

Purification of Chromosomal Hmg Proteins by HPLC Characterization of Two New Species: HMG O and HMG X

D. Labie, M. Delpech, J. Boissel, 1985 .

Isolation And Characterization Of The Vitamin K Dependent Domain Of Human Prothrombin

D. Labie, C. Dodé, J. Elion, 1981, Thrombosis and Haemostasis.

Genetics of Adaptation to High Altitude

D. Labie, J. Elion, 2012 .

[Children'rights: how they are respected?].

D. Labie, 2006, Medecine sciences : M/S.

Disturbed hemoglobin synthesis during erythroleukemia.

D. Labie, J. Pagnier, G. Schapira, 1974, Biochimie.

Familial diphosphoglyceratemutase deficiency. Influence on the oxygen affinity curves of hemoglobin

D. Labie, A. Najman, J. Leroux, 1970, FEBS letters.

Influence of thyroid status on hemoglobin A2 expression.

D. Labie, J. Elion, J. Luton, 1983, The Journal of clinical endocrinology and metabolism.

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

D. Labie, J. Elion, R. Girot, 1991, Nouvelle revue francaise d'hematologie.

Structural and functional study of Hb Nancy β 145 (HC 2) Tyr → Asp a high oxygen affinity hemoglobin

D. Labie, H. Wajcman, G. Gacon, 1975 .

Hemoglobin E: Its oxygen affinity in relation with the ionic environment

D. Labie, A. Najman, Henri Wajcman, 1974, FEBS letters.

Hemoglobin M Saskatoon: further data on biophysics and oxygen equilibrium.

D. Labie, H. Wajcman, F. Travers, 1971, Biochimica et biophysica acta.

Hemoglobin toulouse alpha 2 beta 2 66 (E 10) LysGlu. Structure and consequences in molecular pathology.

D. Labie, R. Bierme, J. Rosa, 1971, Biochimica et biophysica acta.

RAPID DETECTION OF A MEDITERRANEAN β° SPLICE JUNCTION MUTATION BY DNA AMPLIFICATION AND BsaB1 MAPPING

D. Labie, C. Beldjord, R. Krishnamoorthy, 1990 .

Unstable alpha‐chain hemoglobin variants with factitious beta‐thalassemia biosynthetic ratio: Hb questembert (α131[H14] Ser→Pro) and Hb Caen (α132[H15] Val→Gly)

D. Labie, O. Reman, H. Wajcman, 1993 .

Two novel CD1 E alleles identified in black African individuals.

D. Labie, A. Toubert, R. Tamouza, 2002, Tissue antigens.

A Silent Hemoglobin Variant: Hemoglobin Necker Enfants-Malades α 20 (Bl) His → Tyr

D. Labie, J. Elion, H. Wajcman, 1980 .

[Congenital non-spherocytic haemoloytic anaemia due to haemoglobin köln. clinical aspects and structural study (author's transl)].

D. Labie, H. Wajcman, C. Rozman, 1975, Sangre.

[BCL11A controls the expression of the human fetal hemoglobin].

D. Labie, 2012, Medecine sciences : M/S.

Cinetique de l'incorporation de la [14C]arginine dans differents peptides de l'hemoglobine de lapin

D. Labie, J. Kruh, G. Schapira, 1960 .

A Congenitally Abnormal Prothrombin: Prothrombin Barcelona

D. Labie, R. Benarous, J. Lavergne, 1975 .

New Variant of Haemoglobin G, Haemoglobin GParis

D. Labie, G. Schapira, 1966, Nature.

[Molecular and cellular pathophysiology of sickle cell anemia].

D. Labie, J. Elion, 1999, Pathologie-biologie.

A haplotype-linked four base pair deletion upstream of the Aγ globin gene coincides with decreased gene expression

D. Labie, J. Elion, S. Nadifi, 1992, Human Genetics.

Linkage between fetal A gamma globin chain polymorphism and DNA polymorphism of the human beta gene cluster in beta thalassaemia.

D. Labie, P. Rouyer‐Fessard, Y. Beuzard, 1984, Molecular biology & medicine.

A new unstable hemoglobin mutated in beta 98 (FG 5) Val leads to Ala: hb Djelfa.

D. Labie, H. Wajcman, G. Gacon, 1975, FEBS Letters.

Interspecific Hybridization of Hæmoglobin

D. Labie, J. Dreyfus, G. Schapira, 1962, Nature.

Isolation and functional characterization of hemoglobin Casper: beta106(G8) Leu replaced by Pro.

D. Labie, H. Wajcman, G. Gacon, 1975, Biochemistry.

Hemoglobin Djelfa β98 (FG 5) Val → Ala: Isolation and functional properties of the heme saturated form

D. Labie, H. Wajcman, G. Gacon, 1977 .

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

D. Labie, J. Elion, H. Wajcman, 1973 .

[A case of Lepore's hemoglobin in a patient of French origin].

D. Labie, J. Pagnier, P. Boivin, 1971, Annales de biologie clinique.

Hemoglobin Cochin-Port-Royal: consequences of the replacement of the beta chain C-terminal by an arginine.

D. Labie, J. Kilmartin, H. Wajcman, 1975, Biochimica et biophysica acta.

Ca++ binding properties of human prothrombin.

D. Labie, R. Benarous, J. Elion, 1976, Biochimie.

[Child development in developing countries].

D. Labie, 2007, Medecine sciences : M/S.