Dominique Labie

Dominique Labie's AcademicInfluence.com Rankings

Dominique Labie

Biology

#7849

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#10831

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Evolutionary Biology

#178

World Rank

#199

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Molecular Biology

#937

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#960

Historical Rank

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Biology

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Dominique Labie's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Molecular evolution (1991) (2222)
Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa. (1984) (415)
Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type. (1985) (288)
Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients. (1985) (235)
[Diabetes care in sub-Saharan Africa]. (2007) (188)
Structural bases of the inhibitory effects of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S. (1979) (176)
The -158 site 5' to the G gamma gene and G gamma expression. (1985) (136)
Three-Year Follow-Up of Hydroxyurea Treatment in Severely Ill Children with Sickle Cell Disease (1997) (109)
The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF level. (1987) (106)
A novel sickle cell mutation of yet another origin in Africa: the Cameroon type (1992) (95)
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. (1989) (91)
[Conflict and emerging infectious diseases]. (2008) (88)
Alpha-thalassemia is related to prolonged survival in sickle cell anemia. (1983) (84)
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. (1988) (82)
DNA sequence variation in a negative control region 5' to the beta- globin gene correlates with the phenotypic expression of the beta s mutation (1992) (75)
β-Chain contact sites in the haemoglobin S polymer (1980) (71)
Infectious complications in sickle cell disease are influenced by HLA class II alleles. (2002) (64)
Protein titration curves by combined isoelectric focusing-electrophoresis with hemoglobin mutants as models (1978) (62)
2,3-diphosphoglycerate content and oxygen affinity as a function of red cell age in normal individuals. (1971) (62)
Increased protein binding to a −530 mutation of the human β‐globin gene associated with decreased β‐globin synthesis (1991) (62)
Covalent structures of beta and gamma autolytic derivatives of human alpha-thrombin. (1984) (62)
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. (1991) (57)
Impairment of the growth of Plasmodium falciparum in HbEE erythrocytes. (1981) (51)
Beta thalassemia due to a novel mutation in IVS 1 sequence donor site consensus sequence creating a restriction site. (1986) (51)
The amino acid sequence of the δ-β chains of hemoglobin LeporeAugusta = LeporeWashington (1966) (49)
Haemoglobin I Toulouse: β66 (E 10) Lys → Glu: a New Abnormal Haemoglobin with a Mutation localized on the E 10 Porphyrin Surrounding Zone (1969) (47)
Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. The French Study Group on Sickle Cell Disease. (1997) (46)
Preliminary report on the use of desferrioxamine in the treatment of Plasmodium falciparum malaria (1991) (45)
Anthropological approach to the heterogeneity of beta-thalassemia mutations in northern Africa. (1994) (43)
Sickle gene. Its origin and diffusion from West Africa. (1981) (41)
Atypical haplotypes linked to the βs gene in Africa are likely to be the product of recombination (1988) (39)
Fetal haemoglobin variations following hydroxyurea treatment in patients with cyanotic congenital heart disease. (1994) (38)
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 (1972) (38)
βS gene in sicily is in linkage disequilibrium with the benin haplotype: Implications for gene flow (1988) (37)
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. (1984) (37)
Quantitation of hemoglobin A1c: a rapid, automated precision-chromatography technique. (1979) (36)
HLA-E*0101 allele in homozygous state favors severe bacterial infections in sickle cell anemia. (2007) (34)
A novel beta thalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3' end of IVS 2. (1988) (32)
GENETICS OF HEMOCHROMATOSIS * (1958) (32)
Titration curves of liganded hemoglobins by combined isoelectric focusing—electrophoresis (1978) (32)
A novel sickle gene of yet another origin in Africa: The Cameroon type (1992) (31)
Hemoglobins S and C in Upper Volta (2004) (31)
The sickle gene polymorphism in North Africa. (1981) (31)
Long-term hydroxyurea treatment in young sickle cell patients. (1999) (29)
The spectrum of β‐thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy (1993) (29)
Diversity of sequence haplotypes associated with beta-thalassaemia mutations in Algeria: implications for their origin. (1998) (28)
Appearance of β globin synthesis in erythroid cells of Ferrara β°-thalassaemic patients following blood transfusion (1975) (28)
Structural and functional studies of Hb rothschild β 37 (C3) TRP → ARG A new variant of the α1β2 contact (1977) (28)
Uniparental disomy: a novel mechanism for thalassemia major [letter] (1992) (28)
Isoelectrofocusing: a method of multiple applications for hemoglobin studies. (1976) (28)
Sequence polymorphisms of potential functional relevance in the beta-globin gene locus. (1996) (28)
Unstable alpha‐chain hemoglobin variants with factitious beta‐thalassemia biosynthetic ratio: Hb questembert (α131[H14] Ser→Pro) and Hb Caen (α132[H15] Val→Gly) (1993) (27)
Hemoglobin Cochin-Port-Royal: consequences of the replacement of the beta chain C-terminal by an arginine. (1975) (26)
Isolation and partial characterization of hemoglobin A1b (1977) (26)
HAPLOTYPE-VI-ASSOCIATED MILD β+-THALASSAEMIA IN SICILY: MEDITERRANEAN TYPE? (1983) (24)
Genetic variations in human fetal globin gene microsatellites and their functional relevance (1999) (24)
Familial diphosphoglyceratemutase deficiency. Influence on the oxygen affinity curves of hemoglobin (1970) (24)
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 (1982) (23)
Uniparental disomy: a novel mechanism for thalassemia major. (1992) (23)
Two novel CD1 E alleles identified in black African individuals. (2002) (23)
Foetal Haemoglobin, Erythrocytes Containing Foetal Haemoglobin, and Hematological Features in Congolese Patients with Sickle Cell Anaemia (2012) (23)
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. (1973) (22)
Functional properties of hemoglobin Hammersmith. (1973) (22)
HÆMOGLOBINOPATHIES AND G.-6-P.D. DEFICIENCY IN LAOS (1978) (21)
DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation. (1992) (21)
DNA haplotypes and the beta s globin gene. (1989) (21)
β‐Thalassemia in Algeria (1990) (21)
Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals. (1996) (21)
Activation of prothrombin Barcelona. Evidence for active high molecular weight intermediates. (1979) (20)
Structural and functional studies of haemoglobin suresnes or α2 141 (HC3) Arg → His β2, a new high oxygen affinity mutant (1976) (20)
Titration curves of polypeptide chains by combined isoelectric focusing-electrophoresis in 8 M urea. (1979) (20)
Inter-ethnic polymorphism of the β-globin gene locus control region (LCR) in sickle-cell anemia patients (1993) (20)
Immobilized pH gradients for isoelectric focusing: Interaction between histones and histone‐like proteins with the charged polyacrylamide matrix (1983) (20)
Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem (2009) (19)
Molecular basis of α-thalassemia in Sicily (1997) (19)
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 (1973) (19)
Importation route of the sickle cell trait into Portugal: contribution of molecular epidemiology. (1992) (19)
Dissection of the association status of two polymorphisms in the β‐globin gene cluster with variations in F‐cell number in non‐anemic individuals (1997) (18)
Hemoglobin toulouse alpha 2 beta 2 66 (E 10) LysGlu. Structure and consequences in molecular pathology. (1971) (18)
Molecular Basis of β‐Thalassemia in Bahrain: An Epicenter for a Middle East Specific Mutation a (1998) (18)
Consequences of heme loss in unstable hemoglobins: A study of hemoglobin köln (1971) (17)
Structural and functional study of Hb Nancy β 145 (HC 2) Tyr → Asp a high oxygen affinity hemoglobin (1975) (17)
Isolation and functional characterization of hemoglobin Casper: beta106(G8) Leu replaced by Pro. (1975) (16)
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) (1981) (16)
A new unstable hemoglobin mutated in β 98 (FG 5) Val → Ala: Hb Djelfa (1975) (15)
DNA haplotype distribution in Algerian β thalassaemia patients (1988) (14)
Asymptomatic and mild beta-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G-->A mutation: role of the beta-globin gene haplotype. (2003) (14)
Hemoglobin J Lome β 59 (E3) Lys → Asn A new fast moving variant found in a Togolese (1977) (14)
Expression of a β thalassemi gene with abnormal splicing (1987) (14)
A new case of hemoglobin Genova α2 β228(B10) Leu → Pro further studies on the mechanism of instability and defective synthesis (1973) (13)
Known and Potential Sources for Epistatic Effects in Sickle Cell Anemia (1989) (13)
[Child development in developing countries]. (2007) (13)
Interaction between cytochrome b5 and hemoglobin: involvement of beta 66 (E10) and beta 95 (FG2) lysyl residues of hemoglobin. (1980) (13)
[Familial diphosphoglycerate mutase deficiency: hematological and biochemical study]. (1972) (13)
Disturbed hemoglobin synthesis during erythroleukemia. (1974) (13)
A gene conversion located 5' to the A gamma gene in linkage disequilibrium with the Bantu haplotype in sickle cell anemia. (1989) (13)
DNA Sequence Variation in a Negative Control Region 5 ’ to the p-Globin Gene Correlates With the Phenotypic Expression of the pS Mutation (2003) (12)
Hemoglobin fort de France (α245(CD3) HisåArg β2) A new variant with increased oxygen affinity (1977) (12)
A Silent Hemoglobin Variant: Hemoglobin Necker Enfants-Malades α 20 (Bl) His → Tyr (1980) (12)
[Molecular and cellular pathophysiology of sickle cell anemia]. (1999) (11)
Isolation And Characterization Of The Vitamin K Dependent Domain Of Human Prothrombin (1981) (11)
α-Thalassemia among sickle cell anemia patients in various African populations (2004) (11)
Structure and function of Hb Saint-Jacques (α2β2 140 (H18) Ala → Thr): A new high-oxygen-affinity variant with altered bisphosphoglycerate binding (1984) (11)
Hemoglobin M Saskatoon: further data on biophysics and oxygen equilibrium. (1971) (10)
Silent β-thalassemia associated with Hb Knossos β27(B9) Ala→Ser in Algeria (1983) (10)
Characterization of a proteolytically modified form of human prothorombin. (1980) (10)
Haemoglobin D-Ouled Rabah among the Mozabites: A Relevant Variant to Trace the Origin of Berber-Speaking Populations (1997) (10)
Purification and partial characterization of a new variant of human prothrombin: prothrombin Metz (1979) (10)
Evidence for a distinct fraction of hemoglobin, specifically associated with the young erythrocytes. (1962) (10)
Presence of an African β‐globin gene cluster haplotype in normal chromosomes in sicily (1992) (10)
Influence of thyroid status on hemoglobin A2 expression. (1983) (10)
An attempt at demonstrating the existence of a nonsense mutation in -thalassemia. (1972) (9)
Ca++ binding properties of human prothrombin. (1976) (9)
Hozygous Cases for Hemoglobin J Mexico (α50 (E3)Gln→Glu) Evidence for a Duplicated α Gene with Unequal Expression (1976) (9)
Hemoglobin Maputo : A New 6-Chain Variant (α2β2 47 (Cd6) Asp→Tyr) in Combination with Hemoglobin S, Identified by High Performance Liquid Chromatography (Hplc) (1983) (9)
Change in A3 Hæmoglobin due to β-Chain (1962) (9)
[Cheers !]. (2022) (9)
Nucleotide sequence evidence of the unicentric origin of the βC mutation in Africa (1991) (9)
Four new haplotypes observed in Algerian β-thalassemia patients (2004) (9)
Nucleotide variations in the 3' A gamma enhancer region are linked to beta-gene cluster haplotypes and are unrelated to fetal hemoglobin expression. (1989) (8)
Automated analysis of mature red blood cells and reticulocytes in SS and SC disease. (2004) (8)
Abnormal activation of a human prothrombin variant: Prothrombin barcelona (1978) (8)
Minor haemoglobin fractions in uraemic and in diabetic patients. (1981) (8)
[IL28 (interferon lambda3) gene polymorphisms and response to IFN-alpha treatment in patients infected with hepatitis virus C]. (2010) (8)
Hemoglobin E: Its oxygen affinity in relation with the ionic environment (1974) (8)
Differences in DNase I sensitivity and methylation within the human beta-globin gene domain and correlation with expression. (1986) (8)
A new case of haemoglobin Bucuresti in a Cuban family: further functional studies. (1975) (8)
Molecular basis of beta-thalassemia in Bahrain: an epicenter for a Middle East specific mutation. (1998) (7)
High genetic polymorphism of hemoglobin disorders in Laos (1979) (7)
An unusual case of leukemia with high fetal hemoglobin: demonstration of abnormal hemoglobin synthesis localized in a red cell clone (1977) (7)
Hb j mexico in algeria: Arguments for an heterogenous distribution of α genes (1976) (7)
Interspecific Hybridization of Hæmoglobin (1962) (7)
Abnormal hemoglobin synthesis in some leukemic patients. (1975) (7)
Minor hemoglobin components in diabetic and uremic patients. (1981) (7)
Common haplotype dependency of high G y-globin gene expression and high Hb F levels in . 8-thalassemia and sickle cell anemia patients ( linkage / epistatic effect / f 3 globin gene / endonuclease polymorphism / Hb F switching ) (7)
Heterogeneity of sickle cell disease as shown by density profiles: effects of fetal hemoglobin and alpha thalassemia. (1986) (6)
A haplotype-linked four base pair deletion upstream of the Aγ globin gene coincides with decreased gene expression (1992) (6)
The enhancer-like sequence 3' to the A gamma gene is polymorphic in human populations. (1989) (6)
[The problem of sickle cell disease in Africa]. (2010) (6)
A leftward deletional α+ thalassemia found in East Sicily in conjunction with heterozygous β-thalassemia (2004) (6)
Rapid and direct detection of the most frequent Mediterranean beta-thalassemic mutations by multiplex allele-specific enzymatic amplification. (1992) (6)
A Second Case of Haemoglobin Belfast (β15 [A 12] Trp→Arg) Observed in a French Patient (1976) (6)
DNA haplotype distribution in Algerian beta thalassaemia patients. An extended evaluation by family studies and representative molecular characterization. (1988) (6)
Human Prothrombin: A New Method of Preparation from a Single Individual (1973) (6)
Membrane expansion as a mechanism explaining the antisickling action of ticlopidine observed in vitro (1985) (6)
Homozygous cases for hemoglobin J Mexico (alpha54 (E3)Gln replaced by Glu) evidence for a duplicated alpha gene with unequal expression. (1976) (6)
Molecular basis of alpha-thalassemia in Sicily. (1997) (6)
Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius Island. (1995) (6)
Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia trait. (1982) (6)
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 (2003) (6)
New Variant of Haemoglobin G, Haemoglobin GParis (1966) (6)
Isolation and partial characterization of a human prothrombin variant: prothrombin Barcelona. (1974) (6)
Cinetique de l'incorporation de la [14C]arginine dans differents peptides de l'hemoglobine de lapin (1960) (5)
Detection of the Most Frequent β-Thalassemic Defect in Southeast Asia by PCR (1991) (5)
A leftward deletional alpha+ thalassemia found in East Sicily in conjunction with heterozygous beta-thalassemia. (1984) (5)
Hemoglobin Djelfa β98 (FG 5) Val → Ala: Isolation and functional properties of the heme saturated form (1977) (5)
Haemoglobin disorders among Southeast-Asian refugees in France. (1987) (5)
Heterogeneity of haplotypes among patients with severe Cooley disease in Eastern Sicily (1986) (5)
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. (1983) (5)
Multiple Molecular Bases for Thalassemia Intermedia in East Sicily a (1985) (5)
Glucose-6-Phosphate Dehydrogenase and Hemoglobin Variants in Kel Kummer Tuareg and Related Groups (1982) (5)
The consequences and implications of the multicentric origin of the Hb S gene. (1985) (5)
Sickle cell anemia in Bantu speaking Africa. (1986) (5)
Congenital Enzymopenic Methaemoglobinaemia (1976) (5)
[Genetic polymorphism of drepanocytosis]. (1985) (5)
Titration curves by combined isoelectric focusing--electrophoresis on a thin layer of agarose gel (1982) (4)
Association of Hb e with β° Thalassemia (1978) (4)
Hb J Daloa (beta 57 (E1) Asn replaced by Asp): a new variant found in Ivory Coast. (1982) (4)
[Heat stability of hemoglobin: theoretical and practical value of a kinetic method of study]. (1973) (4)
Genetics of Adaptation to High Altitude (2012) (4)
Novel and unusual deletion‐insertion thalassemic mutation in exon 1 of the β‐globin gene (1996) (4)
[A promotor polymorphism in monocyte chemoattractant is associated with increased susceptibility to pulmonary tuberculosis]. (2006) (4)
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. (1980) (4)
An unusual case of leukemia with high fetal hemoglobin: demonstration of abnormal hemoglobin synthesis localized in a red cell clone. (1977) (4)
Genetics and structure of hemoglobin lepore. (1968) (4)
Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb Questembert (alpha 131[H14]Ser-->Pro) and Hb Caen (alpha 132[H15]Val-->Gly). (1993) (3)
Interaction between cytochrome b 5 and hemoglobin : Involvement of f 66 ( El 0 ) and p 95 ( FG 2 ) lysyl residues of hemoglobin (3)
Homozygous deletional α+ thalassaemia associated with unequal expression of the two remaining α1 genes (α1A and α1Q) (1982) (3)
Abnormal hemoglobins in mauritius Island (1995) (3)
Increased protein binding to a -530 mutation of the human beta-globin gene associated with decreased beta-globin synthesis. (1991) (3)
Annotated Definition of BCL11A and HMIP-2 Haplotypes Through the Analysis of Sicilian β-Thalassemia Patients with High Levels of Fetal Hemoglobin (2013) (3)
Hb J Lome β59 (E3) Lys → Asn Associated with Hpfh in a Togolese Family (1979) (3)
A silent hemoglobin variant: hemoglobin necker enfants-malades alpha 20 (B1) His leads to Tyr. (1980) (3)
Hemoglobin Maputo: a new beta-chain variant (alpha 2 beta 2 47 (CD6) Asp replaced by Tyr) in combination with hemoglobin S, identified by high performance liquid chromatography (HPLC). (1983) (3)
[Genetic aspects of sickle cell anemia]. (1992) (3)
Prothrombin Metz: Purification and Characterization of a Variant of Human Prothrombin (1979) (3)
Genetic and biosynthetic studies of families carrying hemoglobin J alpha Mexico: association of alpha-thalassemia with HbJ. (1978) (3)
[Polymorphism of hemoglobins D in Ivory Coast: Hb Korle Bu (beta 73 (E17) Asp leads to Asn), Hb Avicenna (beta 47 (CD6) Asp leads to Ala) and Hb Cocody (beta 21 (B3) Asp leads to Asn) (author's transl)]. (1981) (3)
Beta-thalassemia in Algeria. (1990) (3)
A case of hemoglobin M Boston. New data about valency hybrids brought by isoelectrofocusing study. (1976) (3)
Types of alpha+ thalassemia in Southeast Asia refugees. (1988) (3)
Genetic heterogeneity of sickle mutations. (1987) (3)
mutation globin gene correlates with the phenotypic expression of the beta s DNA sequence variation in a negative control region 5' to the beta- (2011) (3)
MOLECULAR HETEROGENEITY OF b-THALASSEMIA IN ALGERIA : HOW TO FACE UP TO A MAJOR HEALTH (2009) (3)
A Second Case of Bemoglobxn Grady, Repetitive in the Middle of the α Chain (1976) (2)
[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)]. (1979) (2)
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. (1982) (2)
[A case of Lepore's hemoglobin in a patient of French origin]. (1971) (2)
Genetics of haemochromatosis. (1958) (2)
Genetic and biosynthetic studies of families carrying hemoglobin J α Mexico: Association of α-thalassemia with Hb J (1978) (2)
[BCL11A controls the expression of the human fetal hemoglobin]. (2012) (2)
Homozygous deletional alpha + thalassaemia associated with unequal expression of the two remaining alpha 1 genes (alpha 1A and alpha 1Q). (1982) (2)
A new unstable hemoglobin mutated in beta 98 (FG 5) Val leads to Ala: hb Djelfa. (1975) (2)
[The X chromosome, fetal hemoglobin and sickle cell anemia]. (1991) (2)
Functional disorders of some haemoglobins mutated in the haem pocket. (1974) (2)
Appearance of beta globin synthesis in erythroid cells of Ferrara beta -o-thalassaemic patients following blood transfusion. (1975) (2)
[Mycobacterium tuberculosis with extensive resistance]. (2007) (2)
[Developmental neurotoxicity of industrial chemicals]. (2007) (2)
[Hemoglobin Pyrgos beta 83 (EF 7) Gly leads to Asp in a Malian: structural identification and functional properties (author's transl)]. (1978) (2)
Analysis of crossover type in the α-3·7 haplotype among sickle cell anemia patients from various parts of Africa (1988) (2)
[Hemoglobinopathies in West-African immigrant workers in France (author's transl)]. (1978) (2)
[Polycythemia resulting from abnormal hemoglobin with increased affinity for oxygen. Two cases (author's transl)]. (1980) (2)
Haemoglobin A2 is elevated in hyperthyroid patients. (1982) (2)
Hb J Lome beta 59 (E3) Lys is replaced by Asn associated with HPFH in a Togolese family. (1979) (2)
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 (1980) (2)
The amino acid sequence of the delta-beta chains of hemoglobin Lepore Augusta = Lepore Washington. (1966) (2)
Association of Hb Hope with beta (0) thalassemia. (1978) (2)
Hémoglobinopathies in France. (1986) (2)
On the diversity of beta-globin mutations, a reflection of recent historic events in Israel. (1994) (2)
Linkage between fetal A gamma globin chain polymorphism and DNA polymorphism of the human beta gene cluster in beta thalassaemia. (1984) (2)
Structural and functional studies of haemoglobin Suresnes or alpha2 141 (HC3) Arg replaced by His beta2, a new high oxygen affinity mutant. (1976) (2)
A new case of hemoglobin Genova 2 2 28(B10) Leu leads to Pro. Further studies on the mechanism of instability and defective synthesis. (1973) (1)
[Congenital non-spherocytic haemoloytic anaemia due to haemoglobin köln. clinical aspects and structural study (author's transl)]. (1975) (1)
[Frequency and distribution of hemoglobin Lepore. Application of a rapid diagnostic test (author's transl)]. (1974) (1)
Structural and functional studies of Hb Rothschild beta (C3) Trp replaced by Arg. A new variant of the alpha1beta2 contact. (1977) (1)
Activation Studies on a Human Prothrombin Variant: Prothrombin Barcelona (1977) (1)
[Haemoglobin Fannin-Lubbock (alpha 2 beta 2 119 (GH2) Gly leads to Asp). Report of the first case found in Europe)]. (1981) (1)
Structural and functional study of Hb Nancy beta 145 (HC 2) Tyr replaced by Asp. A high oxygen affinity hemoglobin. (1975) (1)
[Biochemical study of a case of erythroleukemia. Demonstration in an abnormal erythrocyte population of simultaneous anomalies of hemoglobin and glycolysis enzymes]. (1972) (1)
« Polymorphismes de Plasmodium vivax : comment les interpréter ? Quelles incidences en santé publique aujourd'hui ? / Polymorphisms in Plasmodium vivax. How to interpret ? What consequences in health cure system ? » (2005) (1)
α-Globin loci in homozygous β-thalassemia intermedia (1983) (1)
[Sickle cell anemia: model of variability in expression of monogenic disease]. (1996) (1)
[The Mycobacterium genome: biological study and evolutionary interpretation]. (2003) (1)
[The complex relations between haemoglobinopathies and malaria]. (2010) (1)
Hemoglobin Barcelona beta 94 (FG1) Asp leads to His : a new hemoglobin Variant with increased oxygen affinity. (1981) (1)
Hemoglobin J Lome beta 59 (E3) Lys leads to Asn. A new fast moving variant found in a Togolese. (1977) (1)
[Genetic control of hemoglobin biosynthesis and its abnormalities]. (1970) (1)
[Genetic adaptation of bacteria]. (2012) (1)
[Four million year neonates deaths: balance sheet and possible actions]. (2005) (1)
Hemoglobin variants in Europe. (1980) (1)
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 (1959) (1)
Hémoglobine G Coushatta (beta 22 (B4) glu leads to ala) en Algérie: description d'un cas homozygote. (1979) (1)
RAPID DETECTION OF A MEDITERRANEAN β° SPLICE JUNCTION MUTATION BY DNA AMPLIFICATION AND BsaB1 MAPPING (1990) (1)
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. (1973) (1)
[Homozygous beta-thalassemia in Algeria. Study of 50 cases]. (1985) (1)
[Abnormal hemoglobins in South Vietnam: homozygous hemoglobinosis C, E trait & a new hemoglobin]. (1958) (1)
[Hemoglobin Sétif (alpha 94(G1) Asp yields Tyr). Genetic, biochemical and hematological studies (author's transl)]. (1974) (1)
Interaction of deletional alpha-thalassaemia with sickle cell beta-thalassaemia and its influence on foetal haemoglobin expression. (1988) (1)
[Children'rights: how they are respected?]. (2006) (1)
Expression of a beta thalassemia gene with abnormal splicing. (1987) (1)
[Molecular bases of thalassemia]. (1985) (1)
Four new haplotypes observed in Algerian beta-thalassemia patients. (1983) (1)
Congenital enzymopenic methaemoglobinaemia. Clinical and biochemical study of a family with three homozygotes. (1976) (1)
[Recent data in the biology of sickle cell disease (author's transl)]. (1981) (1)
[Treatment of homozygote beta thalassemia in Algiers. A 5-year follow-up of 66 patients]. (1989) (1)
Density distribution of red cells and prognostic significance in 50 patients with homozygous sickle-cell disease. (1988) (1)
Hb J Mexico in Algeria: arguments for an heterogenous distribution of alpha genes. (1976) (1)
Haplotype-VI-associated mild beta +-thalassemia in Sicily: Mediterranean type? (1983) (1)
Thalassemia in the Southeastern Part of Sicily a (1990) (1)
Micro-RNA regulating fetal hemoglobin expression (2011) (0)
Inefficient erythropoiesis during severe sickle cell chemia (2006) (0)
Red blood cells erythrophagocytosis (2012) (0)
[Diagnosis and remote prognosis of bronchiectasis in children]. (1951) (0)
Silent beta-thalassemia associated with Hb Knossos beta 27 (B9) Ala replaced by Ser in Algeria. (1983) (0)
Change in A3 haemoglobin due to beta-chain. (1962) (0)
Structure and function of Hb Saint-Jacques (alpha 2 beta 2 140 (H18) Ala----Thr): a new high-oxygen-affinity variant with altered bisphosphoglycerate binding. (1984) (0)
[The hemolytic anemias due to erythrocyte disorders with hemoglobinopathies]. (1967) (0)
Insulators and gene expression: a simple model that becomes complicated. About some exemples in haematology (2003) (0)
[Home and leisure accidents' mortality]. (2007) (0)
Isolation and Preliminary Characterization of a Vitamin K Dependent Peptide from Human Prothrombin (1976) (0)
Genetic variation and its maintenance: The genetic origin of the variability of the phenotypic expression of the Hb S gene (1986) (0)
Trans-regulation of fetal hemoglobin production : a 20 years long research (2008) (0)
Haemoglobin Niort: a new unstable haemoglobin. (1970) (0)
[Determination of hemoglobin affinity for oxygen]. (1971) (0)
A Congenitally Abnormal Prothrombin: Prothrombin Barcelona (1975) (0)
[The unstable hemoglobins]. (1970) (0)
La résistance au paludisme. Interaction de facteurs multiples. (1997) (0)
Sequence correction and identification of a Rsa I site 3' to human G gamma globin gene. (1987) (0)
[On a new abnormal hemoglobin: hemoglobin J (alpha-54 glutamine---glutamic acid)]. (1966) (0)
[Update on RNA splicing repair: applications to beta thalassemia and other perspectives]. (2010) (0)
[Development of a pseudogene with a functional role]. (2003) (0)
Hematological and hemoglobin synthesis studies in a family with deltabeta-thalassemia trait. (1979) (0)
Fetal hemoglobin « activation » for the treatment of hemoglobinopathies (2000) (0)
A novel polymorphism 3' to the beta-globin gene. (1998) (0)
Abnormal Haemoglobins in South Vietnam. Homozygous Haemoglobin C Disease. Haemoglobin E Trait. A New Haemoglobin. (1958) (0)
Hemoglobin Fort de France (alpha2(45)(CD3) His replaced by Arg beta2). A new variant with increased oxygen affinity. (1977) (0)
[Respiratory function in pathological chemistry]. (1970) (0)
On a corrigé in vivo l'hémophilie du rat (1998) (0)
[Action of histones from various sources on acellular biosynthesis of hemoglobin and on reticulocyte RNA]. (1968) (0)
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 (beta 21 (B3) Asp leads to Asn). (1981) (0)
[Hemoglobin Köln: physiopathology of a hemoglobin with spontaneous loss of its heme]. (1971) (0)
New antisickling agents. (1983) (0)
Isoelectrofocusing as a tool for investigation of abnormal hemoglobins. (1978) (0)
Altered translation of GATA1 in Blackfan-Diamond syndrome (2014) (0)
[Glance on chiropters]. (2006) (0)
[Adaptation to high altitudes: on which genes was selective pressure exercised?]. (2010) (0)
[Abnormal hemoglobins and thalassemias in Upper-Volta (author's transl)]. (1982) (0)
further functional studies . Bucuresti in a Cuban family : A new case of haemoglobin (0)
[Problems posed by the structure of hemoglobin Lepore]. (1967) (0)
[Plasmodium's stratagems to be protected in the invaded organisms]. (2005) (0)
A genetic component of stroke in sickle-cell disease (2013) (0)
A case of the abnormal hemoglobin C. (1981) (0)
[Unstable hemoglobins]. (1972) (0)
Hemoglobin Cocody [β21(B3)Asp→Asn] Hematologic Aspects of Heterozygosity and of Hb Cocody/β+-Thalassemia (1985) (0)
[Hereditary persistence of fetal hemoglobin associated with mutation above the gamma gene]. (1988) (0)
Purification of Chromosomal Hmg Proteins by HPLC Characterization of Two New Species: HMG O and HMG X (1985) (0)
[Tuberculosis and HIV: The drama of Africa]. (2006) (0)
[A new hemoglobin by mutation on the beta chain, hemoglobin, I-Toulouse (alpha2-beta2 66 lysglu)]. (1969) (0)
[Recent data concerning abnormal hemoglobins (author's transl)]. (1981) (0)
Sequence variations in the 3' A gamma enhancer are silent polymorphisms. (1989) (0)
[A rice resistant to the floods]. (2006) (0)
Should the therapeutic use of hydroxyurea be more cautiously evaluated (2011) (0)
Nucleotide Variations inthe3'A'y Enhancer RegionAreLinked to IB-Gene Cluster Haplotypes andAreUnrelated to Fetal Hemoglobin Expression (1989) (0)
Fetal Hemoglobin Expression (2006) (0)
[Rice poisoning by arsenic]. (2008) (0)
Snifer un vaccin antirougeole (2011) (0)
Study of Haemoglobin A in Normal Subjects and in those with Thalassaemia, made by means of Electrophoresis in Starch Gels. (1958) (0)
L'invalidation ciblée de BCL11A guérit la souris drépanocytaire Correction of sickle cell disease in mice by knock-out of BCL11A (2011) (0)
Detection of the most frequent beta-thalassemic defect in Southeast Asia by PCR. (1991) (0)
[Glycosylated hemoglobin: résults of 550 cases (author's transl)]. (1979) (0)
Tropisme placentaire du Plasmodium et acide hyaluronique. (2000) (0)
[Familial case of Genova 28 (B10) Leu-Pro hemoglobin. Clinical, hematological, genetic and biochemical study of a French family]. (1972) (0)
[Pyloric stenosis and neuronal nitric oxide synthase]. (2004) (0)
Hemoglobin Djelfa beta98 (FG 5) Val leads to Ala: isolation and functional properties of the heme saturated form. (1977) (0)
[A NEW NORMAL HEMOGLOBIN: HEMOGLOBIN A4]. (1964) (0)
Unstable Haemoglobin with a Modified Affinity for Oxygen in a French Patient (1970) (0)
[Structure and genetics of the Lepore hemoglobins]. (1967) (0)
Des moustiques capables d’interrompre le cycle du Plasmodium (2002) (0)
Correction of Down syndrome in vitro: the third chromosome 21 is invalidated by XIST RNA (2013) (0)
[Emerging infectious diseases in Myanmar]. (2007) (0)
VIIe symposium sur l'anémie de Cooley Cambridge (MA, Etats-Unis), 30 mai-2 juin 1997 (1997) (0)
[Measure of glycosylated hemoglobin A1c: its value in the control of juvenile insulin-dependent diabetes (author's transl)]. (1980) (0)
A strategic approach to haemoglobinopathies in 2002 (2002) (0)
Lapoumer Haplo Cameroun 92 (2013) (0)
Clonal cell populations with paroxysmal nocturnal hemoglobinuria phenotype and genotype in normal individuals (1999) (0)
[Determination of hemoglobin A2 of the normal subject & during various forms of thalassemia by electrophoresis in starch gel]. (1958) (0)
[Malaria: is there a role for the iron-hepcidin axis?]. (2012) (0)
Rapid detection of a Mediterranean beta (0) beta-thalassemic splice junction mutation by DNA amplification and BsaB1 mapping. (1990) (0)
[Biologic factors which influence the severity of drepanocytosis]. (1985) (0)
A second case of hemoglobin Grady, repetitive in the middle of the alpha chain. (1976) (0)
[Sickle cell disease is one century old: what about therapeutics?]. (2011) (0)
EKLF : a key factor in the expression of ß-globin gene and the switch of globin gene during the development (2000) (0)
[Hemoglobin synthesis in acute leukemia and refractory anemia]. (1973) (0)
[Analysis of the recombination zone in hereditary persistence of fetal hemoglobin with fetal gene rearrangement of the G gamma-G gamma-A gamma type]. (1987) (0)
In vitro study of ticlopidine, as a model of antisickling action of platelet antiaggregant. (1984) (0)
[Fetal proteins and proteins of the fetus]. (1965) (0)
[Plasmodium chloroquine resistance: towards a specific attack?]. (2005) (0)
Hemoglobin Fannin-Lubbock alpha 2 beta 2 119 (GH2) Gly replaced by Asp in Spain. (1981) (0)
[A new case of hemoglobin J Capetown alpha 92 (FG 4) Arg replaced by gln]. (1977) (0)
[Chronic diseases, a planetary urgency]. (2006) (0)
[Hemoglobin D Los Angeles. Evidence of the structural anomaly obtained by various methods]. (1969) (0)
Nucleic Acids Research (2008) (0)
[When Staphylococcus needs iron, it prefers heme's]. (2004) (0)
[Sickle cell disease: pneumococcus escapes prevention and adapts to the disease. Consequences on vaccine design]. (2014) (0)
[Tropical anemia in the south of India]. (1960) (0)
Sir David Weatherall: un grand médecin récompensé (2011) (0)
[On a new minor fraction of normal hemoglobin characterized by its chromatographic and metabolic properties (hemoglobin A4)]. (1965) (0)
Transfusion et accidents respiratoires aigus (2010) (0)
[BCL11A represses HbF expression and varies during ontogeny]. (2009) (0)
[Fire-related deaths in India: a retrospective survey]. (2010) (0)
A 2d case of haemoglobin Belfast (beta 15 (A 12) Trp replaced by Arg) observed in a French patient. (1976) (0)
Polymorphisms of the Inducible NO synthase as factors of malaria severity (2004) (0)
[Hemoglobinopathies and Plasmodium falciparum malaria: an example of negative epistatic effect]. (2006) (0)
How quality control pathways regulate elimination of free α-globin during β-thalassemias (2012) (0)
[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)]. (1974) (0)
[Clinical and biological aspects of beta-thalassemia. Apropos of 176 cases]. (1977) (0)
[14C] arginine into different peptides of rabbit hemoglobin]. (1960) (0)
Ex vivo maturation of red blood cells: from cellular culture to transfusion (2005) (0)
Anticorps anti-INF et Mycobacterium tuberculosis (2009) (0)
[Niort hemoglobin: a new unstable hemoglobin]. (1970) (0)
[Thalassemia: therapeutic hopes carried by hepcidin]. (2011) (0)
Inter-specific hybridization of haemoglobin. (1962) (0)
[A novel mechanism for genetic diseases: transcription of antisense RNA may silence a gene]. (2004) (0)
Hemoglobin Cocody [beta 21 (B3)Asp----Asn] hematologic aspects of heterozygosity and of Hb Cocody/beta +-thalassemia. (1985) (0)
[Nitric oxide and haemoglobin]. (2009) (0)
[Recurrent fever in malaria: a main advantage for Plasmodium falciparum?]. (2005) (0)
[Erythrocytosis due to a high-affinity hemoglobulin: mutant hemoglobin Saint-Jacques beta 140 (H18) Ala----Thr with a change in the 2,3-diphosphoglycerate binding site]. (1984) (0)
[Family and professional life: the women take the rap]. (2006) (0)
Sickle cell disease and cellular adherence (1998) (0)
[How skin and astrocytes influence the organism systemic erythropoietin response to hypoxia]. (2010) (0)
[Unstable hemoglobins]. (1972) (0)
[Hemoglobin lepore Boston in a Spanish heterozygote (author's transl)]. (1980) (0)
[Polymorphisms in Plasmodium vivax. How to interpret them? What are their consequences in the health care system?]. (2005) (0)
[Intermediate homozygous beta-thalassemia with high fetal hemoglobin synthesis. Molecular analysis]. (1989) (0)
[Erythroblasts-derived GDF15 supresses hepcidin in thalassemia]. (2008) (0)
[Non-enzymatic hemoglobin glycosylation in the normal and diabetic patient]. (1979) (0)
[Influence of alpha-thalassemia on the hematologic expression of homozygote drepanocytosis]. (1987) (0)
[The hemoglobinopathies due to a disturbance of hemoglobin synthesis]. (1971) (0)
Haemoglobin's abnormalities granting innate resitance to malaria (2003) (0)
Novel and Unusual Mutation in Exon 1 Deletion-Insertion Thalassemic of the P-Globin Gene (1996) (0)
Sequence correction and identification of a Rsa I site 3' to human Gγ globin gene (1987) (0)
Origine multicentrique de la mutation S (1987) (0)
[Structure of some abnormal hemoglobins]. (1969) (0)
[Hemolytic anaemia due to unstable hemoglobin with deletion, study of two new cases: Hb Tours (Thr beta87 (F3) deleted) and Hb St.-Antoine (Gly-Leu beta74-75 (E18-19) deleted) (author's transl)]. (1973) (0)
[Clinical tribulations of Toulouse I hemoglobin]. (1972) (0)
Hematological and Hemoglobin Synthesis Studies in a Family with Hδβ -Thalassemia Trait (1979) (0)
Multiple facets of the ATRX gene: from α-thalassemia with mental retardation to myeloproliferatve syndromes (2006) (0)
Déficit en PK et Salmonella typhimurium (2008) (0)
Association of HLA-E Polymorphism with the Incidence of Severe Bacterial Infections in Sickle Cell Anemia. (2005) (0)
The N-acetylcystein, its antioxydative action against drepanocytosis (1999) (0)
[Ayurvedic medicine and Chinese traditional medicine: first molecular bases]. (2008) (0)
[Biotechnology, role in health in developing countries]. (2003) (0)
Molecular and cellular pathophysiologic bases to the treatment of sickle cell disease (1996) (0)
[Hemoglobin G Coushatta (beta 22 (B4) glu leads to ala) in Algeria: an homozygous case]. (1979) (0)

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