Dominique Labie
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(Suggest an Edit or Addition)Dominique Labie's Published Works
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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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What Schools Are Affiliated With Dominique Labie?
Dominique Labie is affiliated with the following schools: