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Dominique Labie

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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TOP 3
Labie Dominique
[BCL11A represses HbF expression and varies during ontogeny]
Labie Dominique
[Nitric oxide and haemoglobin]
Boudrahem-Addour Nassima; Zidani Nadia; Carion Nathalie; Labie Dominique; Belhani Meriem; Beldjord Cherif
Molecular heterogeneity of beta-thalassemia in Algeria: how to face up to a major health problem.

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All Publications

2009: Labie Dominique
[BCL11A represses HbF expression and varies during ontogeny]
Médecine sciences : M/S 2009;25(5):457-60.
2009: Labie Dominique
[Nitric oxide and haemoglobin]
Médecine sciences : M/S 2009;25(2):132-5.
2009: Boudrahem-Addour Nassima; Zidani Nadia; Carion Nathalie; Labie Dominique; Belhani Meriem; Beldjord Cherif
Molecular heterogeneity of beta-thalassemia in Algeria: how to face up to a major health problem.
Hemoglobin 2009;33(1):24-36.
2008: Labie Dominique
[Conflict and emerging infectious diseases]
Médecine sciences : M/S 2008;24(12):1089-91.
2008: Labie Dominique
[Rice poisoning by arsenic]
Médecine sciences : M/S 2008;24(11):911-2.
2008: Labie Dominique
[Ayurvedic medicine and Chinese traditional medicine: first molecular bases]
Médecine sciences : M/S 2008;24(3):320-2.
2008: Vaulont Sophie; Labie Dominique
[Erythroblasts-derived GDF15 supresses hepcidin in thalassemia]
Médecine sciences : M/S 2008;24(2):139-41.
2007: Tamouza Ryad; Busson Marc; Fortier Catherine; Diagne Ibrahima; Diallo Dapa; Sloma Ivan; Contouris Hector; Krishnamoorthy Rajagopal; Labie Dominique; Girot Robert; Charron Dominique
HLA-E*0101 allele in homozygous state favors severe bacterial infections in sickle cell anemia.
Human immunology 2007;68(10):849-53.
2007: Labie Dominique
[Developmental neurotoxicity of industrial chemicals]
Médecine sciences : M/S 2007;23(10):868-72.
2007: Labie Dominique
[Child development in developing countries]
Médecine sciences : M/S 2007;23(8-9):769-71.
2007: Labie Dominique
[Diabetes care in sub-Saharan Africa]
Médecine sciences : M/S 2007;23(3):320-2.
2007: Labie Dominique
[Home and leisure accidents' mortality]
Médecine sciences : M/S 2007;23(3):317-9.
2007: Labie Dominique
[Mycobacterium tuberculosis with extensive resistance]
Médecine sciences : M/S 2007;23(2):205-9.
2007: Labie Dominique; Ferré Pascal
[Cheers !]
Médecine sciences : M/S 2007;23(2):122.
2007: Labie Dominique
[Emerging infectious diseases in Myanmar]
Médecine sciences : M/S 2007;23(1):99-101.
2006: Labie Dominique
[Family and professional life: the women take the rap]
Médecine sciences : M/S 2006;22(12):1107-9.
2006: Labie Dominique
[Hemoglobinopathies and Plasmodium falciparum malaria: an example of negative epistatic effect]
Santé (Montrouge, France) 2006;16(4):269-70.
2006: Labie Dominique
[Tuberculosis and HIV: The drama of Africa]
Médecine sciences : M/S 2006;22(10):878-80.
2006: Labie Dominique
[A rice resistant to the floods]
Médecine sciences : M/S 2006;22(8-9):778.
2006: Labie Dominique
[Children'rights: how they are respected?]
Médecine sciences : M/S 2006;22(8-9):761-5.
2006: Tamouza Ryad; Labie Dominique
[A promotor polymorphism in monocyte chemoattractant is associated with increased susceptibility to pulmonary tuberculosis]
Médecine sciences : M/S 2006;22(6-7):571-2.
2006: Labie Dominique; Gilgenkrantz Simone
[Glance on chiropters]
Médecine sciences : M/S 2006;22(1):75-7.
2006: Labie Dominique
[Chronic diseases, a planetary urgency]
Médecine sciences : M/S 2006;22(1):68-70.
2005: Labie Dominique
[Four million year neonates deaths: balance sheet and possible actions]
Médecine sciences : M/S 2005;21(8-9):768-72.
2005: Labie Dominique
[Plasmodium's stratagems to be protected in the invaded organisms]
Médecine sciences : M/S 2005;21(8-9):700-2.
2005: Labie Dominique
[Plasmodium chloroquine resistance: towards a specific attack?]
Médecine sciences : M/S 2005;21(5):463-5.
2005: Labie Dominique
[Recurrent fever in malaria: a main advantage for Plasmodium falciparum?]
Médecine sciences : M/S 2005;21(3):243-4.
2005: Labie Dominique
[Polymorphisms in Plasmodium vivax. How to interpret them? What are their consequences in the health care system?]
Médecine sciences : M/S 2005;21(2):123-4.
2004: Labie Dominique
[When Staphylococcus needs iron, it prefers heme's]
Médecine sciences : M/S 2004;20(12):1075-6.
2004: Labie Dominique
[A novel mechanism for genetic diseases: transcription of antisense RNA may silence a gene]
Médecine sciences : M/S 2004;20(11):956-7.
2004: Labie Dominique; Tamouza Ryad
[Pyloric stenosis and neuronal nitric oxide synthase]
Médecine sciences : M/S 2004;20(8-9):743-6.
2004: Maier-Redelsperger Micheline; Flahault Antoine; Neonato Maria Grazia; Girot Robert; Labie Dominique
Automated analysis of mature red blood cells and reticulocytes in SS and SC disease.
Blood cells, molecules & diseases 2004;33(1):15-24.
2003: Labie Dominique
[Development of a pseudogene with a functional role]
Médecine sciences : M/S 2003;19(11):1066-7.
2003: Ragusa Angela; Amata Silvestra; Lombardo Turi; Castiglia Lucia; Maier-Redelsperger Micheline; Labie Dominique; Bernini Luigi
Asymptomatic and mild beta-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G-->A mutation: role of the beta-globin gene haplotype.
Haematologica 2003;88(10):1099-105.
2003: Labie Dominique
[The Mycobacterium genome: biological study and evolutionary interpretation]
Médecine sciences : M/S 2003;19(3):275-7.
2003: Labie Dominique
[Biotechnology, role in health in developing countries]
Médecine sciences : M/S 2003;19(2):137-9.
2002: Tamouza R; Sghiri R; Ramasawmy R; Neonato M G; Mombo L E; Poirier J C; Schaeffer V; Fortier C; Labie D; Girot R; Toubert A; Krishnamoorthy R; Charron D
Two novel CD1 E alleles identified in black African individuals.
Tissue antigens 2002;59(5):417-20.
2002: Tamouza Ryad; Neonato Maria Grazia; Busson Marc; Marzais François; Girot Robert; Labie Dominique; Elion Jacques; Charron Dominique
Infectious complications in sickle cell disease are influenced by HLA class II alleles.
Human immunology 2002;63(3):194-9.
1999: Lapoumeroulie C; Castiglia L; Ruberto C; Fichera M; Amata S; Labie D; Ragusa A
Genetic variations in human fetal globin gene microsatellites and their functional relevance.
Human genetics 1999;104(4):307-14.
1999: Maier-Redelsperger M; Labie D; Elion J
Long-term hydroxyurea treatment in young sickle cell patients.
Current opinion in hematology 1999;6(2):115-20.
1999: Labie D; Elion J
[Molecular and cellular pathophysiology of sickle cell anemia]
Pathologie-biologie 1999;47(1):7-12.
1998: Badens C; Merghoub T; Lena-Russo D; Labie D; Elion J; Mattei J F
A novel polymorphism 3' to the beta-globin gene.
Hemoglobin 1998;22(4):387-90.
1998: Jassim N; Merghoub T; Pascaud O; al Mukharraq H; Ducrocq R; Labie D; Elion J; Krishnamoorthy R; Arrayed S A
Molecular basis of beta-thalassemia in Bahrain: an epicenter for a Middle East specific mutation.
Annals of the New York Academy of Sciences 1998;850():407-9.
1997: Merghoub T; Perichon B; Maier-Redelsperger M; Dibenedetto S P; Samperi P; Ducrocq R; Feingold N; Elion J; Schiliro G; Labie D; Krishnamoorthy R
Dissection of the association status of two polymorphisms in the beta-globin gene cluster with variations in F-cell number in non-anemic individuals.
American journal of hematology 1997;56(4):239-43.
1997: Merghoub T; Sanchez-Mazas A; Tamouza R; Lu C Y; Bouzid K; Ardjoun F Z; Labie D; Lapouméroulie C; Elion J
Haemoglobin D-Ouled Rabah among the Mozabites: a relevant variant to trace the origin of Berber-speaking populations.
European journal of human genetics : EJHG 1997;5(6):390-6.
1997: de Montalembert M; Belloy M; Bernaudin F; Gouraud F; Capdeville R; Mardini R; Philippe N; Jais J P; Bardakdjian J; Ducrocq R; Maier-Redelsperger M; Elion J; Labie D; Girot R
Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. The French Study Group on Sickle Cell Disease.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 1997;19(4):313-8.
1997: Fichera M; Spalletta A; Fiorenza F; Lombardo T; Schilirò G; Tamouza R; Lapouméroulie C; Labie D; Ragusa A
Molecular basis of alpha-thalassemia in Sicily.
Human genetics 1997;99(3):381-6.
1996: Merghoub T; Maier-Redelsperger M; Labie D; Perichon B; Feingold N; Dibenedetto S P; Schiliro G; Samperi P; Ducrocq R; Elion J; Krishnamoorthy R
Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals.
Blood 1996;87(6):2607.
1994: Triadou P; Maier-Redelsperger M; Krishnamoorty R; Deschamps A; Casadevall N; Dunda O; Ducrocq R; Elion J; Girot R; Labie D
Fetal haemoglobin variations following hydroxyurea treatment in patients with cyanotic congenital heart disease.
Nouvelle revue française d'hématologie 1994;36(5):367-72.
1994: Bennani C; Bouhass R; Perrin-Pecontal P; Tamouza R; Malou M; Elion J; Trabuchet G; Beldjord C; Benabadji M; Labie D
Anthropological approach to the heterogeneity of beta-thalassemia mutations in northern Africa.
Human biology; an international record of research 1994;66(3):369-82.
1993: Périchon B; Ragusa A; Lapouméroulie C; Romand A; Moi P; Ikuta T; Labie D; Elion J; Krishnamoorthy R
Inter-ethnic polymorphism of the beta-globin gene locus control region (LCR) in sickle-cell anemia patients.
Human genetics 1993;91(5):464-8.
1993: Bennani C; Tamouza R; Rouabhi F; Benabadji M; Malou M; Elion J; Labie D; Beldjord C
The spectrum of beta-thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy.
British journal of haematology 1993;84(2):335-7.
1992: Ragusa A; Frontini V; Lombardo M; Amata S; Lombardo T; Labie D; Krishnamoorthy R; Nagel R L
Presence of an African beta-globin gene cluster haplotype in normal chromosomes in Sicily.
American journal of hematology 1992;40(4):313-5.
1992: Beldjord C; Ducrocq R; Nadifi S; Lapoumeroulie C; Elion J; Labie D
A haplotype-linked four base pair deletion upstream of the A gamma globin gene coincides with decreased gene expression.
Human genetics 1992;89(6):625-8.
1992: Beldjord C; Henry I; Bennani C; Vanhaeke D; Labie D
Uniparental disomy: a novel mechanism for thalassemia major.
Blood 1992;80(1):287-9.
1992: Lapouméroulie C; Dunda O; Ducrocq R; Trabuchet G; Mony-Lobé M; Bodo J M; Carnevale P; Labie D; Elion J; Krishnamoorthy R
A novel sickle cell mutation of yet another origin in Africa: the Cameroon type.
Human genetics 1992;89(3):333-7.
1992: Bienvenu T; Sebillon P; Labie D; Kaplan J C; Beldjord C
Rapid and direct detection of the most frequent Mediterranean beta-thalassemic mutations by multiplex allele-specific enzymatic amplification.
Human biology; an international record of research 1992;64(1):107-13.
1992: Elion J; Berg P E; Lapouméroulie C; Trabuchet G; Mittelman M; Krishnamoorthy R; Schechter A N; Labie D
DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation.
Blood 1992;79(3):787-92.
1991: Trabuchet G; Elion J; Baudot G; Pagnier J; Bouhass R; Nigon V M; Labie D; Krishnamoorthy R
Origin and spread of beta-globin gene mutations in India, Africa, and Mediterranea: analysis of the 5' flanking and intragenic sequences of beta S and beta C genes.
Human biology; an international record of research 1991;63(3):241-52.
1991: Berg P E; Mittelman M; Elion J; Labie D; Schechter A N
Increased protein binding to a -530 mutation of the human beta-globin gene associated with decreased beta-globin synthesis.
American journal of hematology 1991;36(1):42-7.
1991: Sebillon P; Bienvenu T; Girot R; Labie D; Kaplan J C; Beldjord C
Detection of the most frequent beta-thalassemic defect in Southeast Asia by PCR.
Hemoglobin 1991;15(4):313-5.
1990: Bennani C; Sebillon P; Krishnamoorthy R; Labie D; Beldjord C
Rapid detection of a Mediterranean beta (0) beta-thalassemic splice junction mutation by DNA amplification and BsaB1 mapping.
British journal of haematology 1990;76(3):440-1.
1990: Labie D; Bennani C; Beldjord C
Beta-thalassemia in Algeria.
Annals of the New York Academy of Sciences 1990;612():43-54.
1989: Labie D; Srinivas R; Dunda O; Dode C; Lapoumeroulie C; Devi V; Devi S; Ramasami K; Elion J; Ducrocq R
Haplotypes in tribal Indians bearing the sickle gene: evidence for the unicentric origin of the beta S mutation and the unicentric origin of the tribal populations of India.
Human biology; an international record of research 1989;61(4):479-91.
1989: Ragusa A; Lombardo M; Bouhassira E; Beldjord C; Lombardo T; Nagel R L; Labie D; Krishnamoorthy R
Nucleotide variations in the 3' A gamma enhancer region are linked to beta-gene cluster haplotypes and are unrelated to fetal hemoglobin expression.
American journal of human genetics 1989;45(1):106-11.
1989: Bouhassira E E; Lachman H; Krishnamoorthy R; Labie D; Nagel R L
A gene conversion located 5' to the A gamma gene in linkage disequilibrium with the Bantu haplotype in sickle cell anemia.
The Journal of clinical investigation 1989;83(6):2070-3.
1989: Adjrad L; Amara A; Rouabhi F; Girot R; Labie D; Benabadji M
[Treatment of homozygote beta thalassemia in Algiers. A 5-year follow-up of 66 patients]
Presse médicale (Paris, France : 1983) 1989;18(20):1010-13.
1989: Bouhassira E E; Krishnamoorthy R; Ragusa A; Driscoll C; Labie D; Nagel R L
The enhancer-like sequence 3' to the A gamma gene is polymorphic in human populations.
Blood 1989;73(4):1050-3.
1989: Nagel R L; Labie D
DNA haplotypes and the beta s globin gene.
Progress in clinical and biological research 1989;316B():371-93.
1989: Ragusa A; Lombardo M; Lombardo T; Beldjord C; Nagel R L; Elion J; Labie D; Krishnamoorthy R
Sequence variations in the 3' A gamma enhancer are silent polymorphisms.
Progress in clinical and biological research 1989;316B():409-17.
1988: Srinivas R; Dunda O; Krishnamoorthy R; Fabry M E; Georges A; Labie D; Nagel R L
Atypical haplotypes linked to the beta S gene in Africa are likely to be the product of recombination.
American journal of hematology 1988;29(1):60-2.
1988: Rouabhi F; Lapouméroulie C; Amselem S; Krishnamoorthy R; Adjrad L; Girot R; Chardin P; Benabdji M; Labie D; Beldjord C
DNA haplotype distribution in Algerian beta thalassaemia patients. An extended evaluation by family studies and representative molecular characterization.
Human genetics 1988;79(4):373-6.
1988: Beldjord C; Lapoumeroulie C; Pagnier J; Benabadji M; Krishnamoorthy R; Labie D; Bank A
A novel beta thalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3' end of IVS 2.
Nucleic acids research 1988;16(11):4927-35.
1988: Chebloune Y; Pagnier J; Trabuchet G; Faure C; Verdier G; Labie D; Nigon V
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.
Proceedings of the National Academy of Sciences of the United States of America 1988;85(12):4431-5.
1988: Ragusa A; Lombardo M; Sortino G; Lombardo T; Nagel R L; Labie D
Beta S gene in Sicily is in linkage disequilibrium with the Benin haplotype: implications for gene flow.
American journal of hematology 1988;27(2):139-41.
1988: Pajot N; Maier-Redelsperger M; Dode C; Labie D; Girot R
Density distribution of red cells and prognostic significance in 50 patients with homozygous sickle-cell disease.
Haematologia 1988;21(4):189-97.
1987: Lapoumeroulie C; Acuto S; Rouabhi F; Labie D; Krishnamoorthy R; Bank A
Expression of a beta thalassemia gene with abnormal splicing.
Nucleic acids research 1987;15(20):8195-204.
1987: de Montalembert M; Dode C; Maier-Redelsperger M; Labie D; Girot R
[Influence of alpha-thalassemia on the hematologic expression of homozygote drepanocytosis]
Archives françaises de pédiatrie 1987;44(7):517-9.
1987: Nagel R L; Rao S K; Dunda-Belkhodja O; Connolly M M; Fabry M E; Georges A; Krishnamoorthy R; Labie D
The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF level.
Blood 1987;69(4):1026-30.
1986: Lapoumeroulie C; Pagnier J; Bank A; Labie D; Krishnamoorthy R
Beta thalassemia due to a novel mutation in IVS 1 sequence donor site consensus sequence creating a restriction site.
Biochemical and biophysical research communications 1986;139(2):709-13.
1986: Lombardo M; Ragusa A; Sortino G; Cacciola E; Lombardo T; Labie D
Heterogeneity of haplotypes among patients with severe Cooley disease in Eastern Sicily.
Human genetics 1986;72(2):145-7.
1985: Labie D; Dunda-Belkhodja O; Rouabhi F; Pagnier J; Ragusa A; Nagel R L
The -158 site 5' to the G gamma gene and G gamma expression.
Blood 1985;66(6):1463-5.
1985: Adjrad L; Rouabhi F; Amara A; Girot R; Labie D; Benabadji M
[Homozygous beta-thalassemia in Algeria. Study of 50 cases]
Presse médicale (Paris, France : 1983) 1985;14(41):2089-92.
1985: Labie D; Pagnier J; Lapoumeroulie C; Rouabhi F; Dunda-Belkhodja O; Chardin P; Beldjord C; Wajcman H; Fabry M E; Nagel R L
Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.
Proceedings of the National Academy of Sciences of the United States of America 1985;82(7):2111-4.
1985: Troungos C; Krishnamoorthy R; Elion J; Lombardo T; Sortino G; Cacciola E; Labie D
Multiple molecular bases for thalassemia intermedia in east Sicily.
Annals of the New York Academy of Sciences 1985;445():106-10.
1984: Beldjord C; Arbane M; Lapoumeroulie C; Rouyer-Fessard P; Benabadji M; Labie D; Beuzard Y
Linkage between fetal A gamma globin chain polymorphism and DNA polymorphism of the human beta gene cluster in beta thalassaemia.
Molecular biology & medicine 1984;2(4):301-6.
1984: Pagnier J; Mears J G; Dunda-Belkhodja O; Schaefer-Rego K E; Beldjord C; Nagel R L; Labie D
Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa.
Proceedings of the National Academy of Sciences of the United States of America 1984;81(6):1771-3.
1984: Troungos C; Krishnamoorthy R; Lombardo T; Sortino G; Cacciola E; Labie D
A leftward deletional alpha+ thalassemia found in East Sicily in conjunction with heterozygous beta-thalassemia.
Human genetics 1984;67(2):216-8.
1984: Pagnier J; Dunda-Belkhodja O; Zohoun I; Teyssier J; Baya H; Jaeger G; Nagel R L; Labie D
alpha-Thalassemia among sickle cell anemia patients in various African populations.
Human genetics 1984;68(4):318-9.
1983: Troungos C; Sartino G; Cacciola R; Lombardo T; Cacciola E; Labie D
Haplotype-VI-associated mild beta +-thalassemia in Sicily: Mediterranean type?
Lancet 1983;2(8348):509-10.
1983: Rouabhi F; Chardin P; Boissel J P; Beghoul F; Labie D; Benabadji M
Silent beta-thalassemia associated with Hb Knossos beta 27 (B9) Ala replaced by Ser in Algeria.
Hemoglobin 1983;7(6):555-61.
1983: Beldjord C; Lapouméroulie C; Baird M L; Girot R; Adjrad L; Lenoir G; Benabadji M; Labie D
Four new haplotypes observed in Algerian beta-thalassemia patients.
Human genetics 1983;65(2):204-6.
1981: Mears J G; Beldjord C; Benabadji M; Belghiti Y a; Baddou M A; Labie D; Nagel R L
The sickle gene polymorphism in North Africa.
Blood 1981;58(3):599-601.

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Dominique Labie

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