p210 reprograms transformed and normal human megakaryocytic progenitor cells into erythroid cells and suppresses FLI-1 transcription
Buet, D, Raslova, H, Geay, J-F, Jarrier, P, Lazar, V, Turhan, A, Morlé, F, Vainchenker, W, Louache, F
Published in Leukemia (01.05.2007)
Published in Leukemia (01.05.2007)
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p210BCR-ABL reprograms transformed and normal human megakaryocytic progenitor cells into erythroid cells and suppresses FLI-1 transcription
BUET, D, RASLOVA, H, GEAY, J.-F, JARRIER, P, LAZAR, V, TURHAN, A, MORLE, F, VAINCHENKER, W, LOUACHE, F
Published in Leukemia (01.05.2007)
Published in Leukemia (01.05.2007)
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A new alpha chain variant Hb Sallanches [alpha 2 104(G11) Cys-->Tyr] associated with HbH disease in one homozygous patient
Morlé, F, Francina, A, Ducrocq, R, Wajcman, H, Gonnet, C, Philippe, N, Souillet, G, Godet, J
Published in British journal of haematology (01.11.1995)
Published in British journal of haematology (01.11.1995)
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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
Espéret, Corinne, Sabatier, Sandrine, Deville, Marie-Alice, Ouazana, Roland, Bouhassira, Eric E., Godet, Jacqueline, Morlé, François, Bernet, Agnès
Published in The Journal of biological chemistry (18.08.2000)
Published in The Journal of biological chemistry (18.08.2000)
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Caspase cleavage of the transcription factor FLI-1 during preB leukemic cell death
Sarrazin, Sandrine, Bonod-Bidaud, Christelle, Remy, Pierre, Mehlen, Patrick, Morlé, François
Published in Biochimica et biophysica acta (21.10.2002)
Published in Biochimica et biophysica acta (21.10.2002)
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Targeted Inactivation of the Major Positive Regulatory Element (HS-40) of the Human α-Globin Gene Locus
Bernet, A., Sabatier, S., Picketts, D.J., Ouazana, R., Morle, F., Higgs, D.R., Godet, J.
Published in Blood (01.08.1995)
Published in Blood (01.08.1995)
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A nonsense mutation in the GPIIb heavy chain (Ser 870-->stop) impairs platelet GPIIb-IIIa expression
Vinciguerra, C, Khelif, A, Alemany, M, Morle, F, Grenier, C, Uzan, G, Gulino, D, Dechavanne, M, Negrier, C
Published in British journal of haematology (01.11.1996)
Published in British journal of haematology (01.11.1996)
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Instructive role of M‐CSF on commitment of bipotent myeloid cells involves ERK‐dependent positive and negative signaling
Carras, Sylvain, Valayer, Alexandre, Moratal, Claudine, Weiss‐Gayet, Michèle, Pages, Gilles, Morlé, Francois, Mouchiroud, Guy, Gobert, Stéphanie
Published in Journal of leukocyte biology (01.02.2016)
Published in Journal of leukocyte biology (01.02.2016)
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Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus
DE MARTINVILLE, B, KUNKEL, L. M, FRANCKE, U, BRUNS, G, MORLE, F, KOENIG, M, MANDEL, J. L, HORWICH, A, LATT, S. A, GUSELLA, J. F, HOUSMAN, D
Published in American journal of human genetics (01.03.1985)
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Published in American journal of human genetics (01.03.1985)
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Human chronic myeloid leukemic cell line with positive Philadelphia chromosome exhibits megakaryocytic and erythroid characteristics
Seigneurin, D, Champelovier, P, Mouchiroud, G, Berthier, R, Leroux, D, Prenant, M, McGregor, J, Starck, J, Morle, F, Micouin, C
Published in Experimental hematology (01.09.1987)
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Published in Experimental hematology (01.09.1987)
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Spectrin Tunis (SpαI/78), an elliptocytogenic variant, is due to the CGG→TGG codon change (Arg→Trp) at position 35 of the αI domain
MORLE, L, ROUX, A. F, GODET, J, FORGET, B. G, DENOROY, L, GARBARZ, M, DHERMY, D, KASTALLY, R, DELAUNAY, J
Published in Blood (01.08.1989)
Published in Blood (01.08.1989)
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Functional Cross-Antagonism between Transcription Factors FLI-1 and EKLF
Starck, Joëlle, Cohet, Nathalie, Gonnet, Colette, Sarrazin, Sandrine, Doubeikovskaia, Zina, Doubeikovski, Alexandre, Verger, Alexis, Duterque-Coquillaud, Martine, Morle, François
Published in Molecular and Cellular Biology (01.02.2003)
Published in Molecular and Cellular Biology (01.02.2003)
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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
Morle, L, Morle, F, Roux, AF, Godet, J, Forget, BG, Denoroy, L, Garbarz, M, Dhermy, D, Kastally, R, Delaunay, J
Published in Blood (01.08.1989)
Published in Blood (01.08.1989)
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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
Guetarni, D, Roux, A F, Alloisio, N, Morlé, F, Ducluzeau, M T, Forget, B G, Colonna, P, Delaunay, J, Godet, J
Published in Human genetics (01.10.1990)
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Published in Human genetics (01.10.1990)
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Identification of GATA-1 and NF-E2 binding sites in the flanking regions of the human alpha-globin genes
Gourdon, G, Morlé, F, Roche, J, Tourneur, N, Joulain, V, Godet, J
Published in Acta haematologica (01.01.1992)
Published in Acta haematologica (01.01.1992)
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Molecular basis of Sp αI/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the α-spectrin gene from five unrelated families
ROUX, A.-F, MORLE, F, GUETARNI, D, COLONNA, P, SAHR, K, FORGET, B. G, DELAUNAY, J, GODET, J
Published in Blood (01.06.1989)
Published in Blood (01.06.1989)
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Control of ribosome biogenesis by oncogenic ETS transcription factors
Guyot, B, Juban, G, Giraud, G, Textoris, J, Belin, S, Diaz, J.J, Guillouf, C, Moreau-Gachelin, F, Morlé, F
Published in European journal of cancer supplements (2008)
Published in European journal of cancer supplements (2008)
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