J. Godet

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Some biochemical aspects of the cuticle collagen of the nematode Caenorhabditis elegans

R. Ouazana, D. Herbage, J. Godet, 1984 .

Expression of human colony-stimulating factor-1 (CSF-1) receptor in murine pluripotent hematopoietic NFS-60 cells induces long-term proliferation in response to CSF-1 without loss of erythroid differentiation potential

F. Morlé, R. Ouazana, J. Godet, 1993 .

F. Morlé, R. Ouazana, J. Godet, 1993, Blood.

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain.

F. Morlé, L. Denoroy, L. Morlé, 1989, Blood.

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain.

F. Morlé, L. Denoroy, L. Morlé, 1989, Blood.

A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q.

J. Weissenbach, J. Hazan, H. Plauchu, 1995, Human molecular genetics.

hsp27 as a Switch between Differentiation and Apoptosis in Murine Embryonic Stem Cells*

P. Mehlen, A. Arrigo, J. Godet, 1997, The Journal of Biological Chemistry.

alpha‐Thalassaemia associated with the deletion of two nucleotides at position ‐2 and ‐3 preceding the AUG codon.

T. Henni, F. Morlé, J. Godet, 1985, The EMBO journal.

Spi-1/PU.1 Is a Positive Regulator of the Fli-1 Gene Involved in Inhibition of Erythroid Differentiation in Friend Erythroleukemic Cell Lines

I. Dusanter-Fourt, F. Morlé, C. Gonnet, 1999, Molecular and Cellular Biology.

α-Thalassemia haplotypes in the Algerian population

T. Henni, F. Morlé, J. Godet, 1987, Human Genetics.

Extent and high frequency of a short conversion between the human Aγ and Gγ fetal globin genes

F. Morlé, J. Starck, J. Godet, 2004, Human Genetics.

Mapping the α-globin genes in HB J Mexico carriers

F. Morlé, G. Trabuchet, V. Nigon, 2004, Human Genetics.

α-Globin gene deletions associated with αAand αG Philadelphiagenes in an Algerian family that includes two Hb G homozygotes

F. Morlé, J. Delaunay, J. Godet, 2004, Human Genetics.

Polymorphism of the Hinf I restriction site located 1 Kb 5′ to the human β-globin gene

N. Philippe, J. Godet, G. Kohen, 2004, Human Genetics.

Genetic analysis of cell differentiation: possible extension of the haemoglobin differon model to Drosophila morphogenesis and immunoglobulin determination.

V. Nigon, J. Godet, 1977, Journal of theoretical biology.

HbF synthesis in chicken embryonic and postnatal development: studies in various explanted erythropoietic tissues.

J. Godet, 1974, Developmental biology.

Coactivation of human α1- and α2-globin genes in single induced MEL cells containing one human α-globin locus

F. Morlé, J. Starck, J. Godet, 1997 .

Heterogeneity in β0 thalassemia from Algeria: Genetic, clinical and molecular studies

F. Morlé, J. Godet, M. Belhani, 2004, Human Genetics.

Genetic and morphogenetic factors in hemoglobin synthesis during higher vertebrate development: an approach to cell differentiation mechanisms.

V. Nigon, J. Godet, 1976, International review of cytology.

The Hb F composition in a Moroccan Family with β°-thalassaemia and Hb O-Arab

F. Morlé, J. Delaunay, F. Baklouti, 2009 .

δ°‐Thalassemia in cis of βKnossos‐globin gene Normal structure and normal transient expression of the δ‐globin gene

D. Bozon, C. Gonnet, J. Delaunay, 1989 .

The association of hemoglobin Knossos and hemoglobin Lepore in an Algerian patient.

F. Morlé, J. Delaunay, F. Baklouti, 1984, Hemoglobin.

Sickle cell β‐thalassaemia compared with sickle cell anaemia in Algeria

T. Henni, D. Bachir, J. Godet, 2009 .

Association in cis of β+‐thalassemia and hemoglobin S

A. Francina, J. Delaunay, F. Baklouti, 1987 .

Expression of human Gγ globin genes carrying a T or a C at position −158 in cos and mel cells+

F. Morlé, J. Starck, P. Charnay, 1988 .

Mapping the alpha-globin genes in an Algerian HbH patient and his family.

T. Henni, E. Whitelaw, J. Pagnier, 1980, Blood.

Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia

J. Delaunay, D. Peyramond, F. Baklouti, 1986 .

Alpha globin gene triplication in severe heterozygous beta thalassemia.

T. Henni, F. Morlé, D. Bachir, 1985, Acta haematologica.

Demonstration of two alpha-globin genes per human haploid genome for normals and Hb J Mexico.

J. Eskdale, G. Trabuchet, V. Nigon, 1977, European journal of biochemistry.

thalassemia variety of beta+-thalassemia intermedia associated with delta degree- Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new

J. Delaunay, D. Peyramond, F. Baklouti, 2013 .

Asymptomatic association of hemoglobin Dunn (α6[A4]Asp→Asn) and hemoglobin O‐Arab (β121[GH4]Glu→Lys) in a Moroccan man

H. Wajcman, H. Plauchu, A. Francina, 1988 .

Structural Characterization of the β-Globin Gene Cluster in An Individual Expressing A Very Low Ll of Gγ Globin Chains

C. Gonnet, J. Starck, R. Ouazana, 1995 .

α-Thalassemia due to the deletion of nucleotides –2 and –3 preceding the AUG initiation codon affects translation efficiency both in vitro and in vivo

F. Morlé, J. Starck, J. Godet, 1986 .

Identification of three different alpha-thalassemic haplotypes: -alpha 3.7, (--)MED and alpha Hph alpha in the same Algerian family.

F. Morlé, J. Godet, A. Bernet, 1995, Human mutation.

Hemoglobin Bart's in Northern Algeria.

T. Henni, D. Bachir, P. Jurdic, 1981, Acta haematologica.

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.

C. Petit, M. Mustapha, D. Weil, 1997, Human molecular genetics.

A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.

C. Philippe, J. Zech, J. Lambert, 2000, American journal of human genetics.

Beta thalassemic mutations recognized by DNA mapping with Hph I and Rsa I in the Algerian population.

T. Henni, N. Salomé, J. Godet, 1983, Biochemical and Biophysical Research Communications - BBRC.

A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss

P. Latour, G. Lina-Granade, H. Plauchu, 2000, Journal of medical genetics.

Identification of three different α‐thalassemic haplotypes: —α3.7, (— —)MED and αHph α in the same Algerian family

F. Morlé, P. Colonna, J. Godet, 1995 .

Evidence that expression of SpαI/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous α-spectrin allele

F. Morlé, B. Forget, J. Delaunay, 1990, Human Genetics.

Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14

C. Gonnet, J. Zech, H. Plauchu, 1999, Graefe's Archive for Clinical and Experimental Ophthalmology.

mutation on a beta s chromosome Beta+-thalassemia in cis of a sickle cell gene: occurrence of a promoter

C. Gonnet, A. Lapillonne, J. Delaunay, 2011 .

Targeted inactivation of the major positive regulatory element (HS-40) of the human alpha-globin gene locus

F. Morlé, Higgs, R. Ouazana, 1995 .

Targeted inactivation of the major positive regulatory element (HS-40) of the human alpha-globin gene locus.

D. Higgs, F. Morlé, R. Ouazana, 1995, Blood.

Non-erythroid Genes Inserted on Either Side of Human HS-40 Impair the Activation of Its Natural α-Globin Gene Targets without Being Themselves Preferentially Activated*

F. Morlé, E. Bouhassira, R. Ouazana, 2000, The Journal of Biological Chemistry.

Beta+-thalassemia in cis of a sickle cell gene: occurrence of a promoter mutation on a beta s chromosome.

C. Gonnet, A. Lapillonne, J. Delaunay, 1989, Blood.

Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss

L. Collet, K. Verhoeven, G. Lina-Granade, 1999, European Journal of Human Genetics.

Characterization of morphological and biochemical defects in the cuticle of a dumpy mutant of Caenorhabditis elegans

R. Garrone, R. Ouazana, J. Godet, 1985 .

Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families.

F. Morlé, B. Forget, K. Sahr, 1989, Blood.

Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele.

F. Morlé, B. Forget, J. Delaunay, 1990, Human genetics.

A new α chain variant Hb Sallanches [α2 104(G11) Cys→Tyr] associated with HbH disease in one homozygous patient

F. Morlé, C. Gonnet, H. Wajcman, 1995 .

Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta (+)-thalassemia intermedia associated with delta (0)-thalassemia.

J. Delaunay, D. Peyramond, F. Baklouti, 1986, Blood.