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Results:
1-14
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Results: 14
Authors:
Richard, E
Mendez, M
Mazurier, F
Morel, C
Costet, P
Xia, P
Fontanellas, A
Geronimi, F
Cario-Andre, M
Taine, L
Ged, C
Malik, P
de Verneuil, H
Moreau-Gaudry, F
Citation: E. Richard et al., Gene therapy of a mouse model of protoporphyria with a self-inactivating erythroid-specific lentiviral vector without preselection, MOL THER, 4(4), 2001, pp. 331-338
Authors:
Mangione, R
Guyon, F
Taine, L
Wen, ZQ
Roux, D
Vergnaud, A
Maugey-Laulom, B
Horovitz, J
Saura, R
Citation: R. Mangione et al., Pregnancy outcome and prognosis in fetuses with increased first-trimester nuchal translucency, FETAL DIAGN, 16(6), 2001, pp. 360-363
Authors:
Fontanellas, A
Mendez, M
Mazurier, F
Cario-Andre, M
Navarro, S
Ged, C
Taine, L
Geronimi, F
Richard, E
Moreau-Gaudry, F
de Salamanca, RE
de Verneuil, H
Citation: A. Fontanellas et al., Successful therapeutic effect in a mouse model of erythropoietic protoporphyria by partial genetic correction and fluorescence-based selection of hematopoietic cells, GENE THER, 8(8), 2001, pp. 618-626
Authors:
Giraudeau, F
Taine, L
Biancalana, V
Delobel, B
Journel, H
Missirian, C
Lacombe, D
Bonneau, D
Parent, P
Aubert, D
Hauck, Y
Croquette, MF
Toutain, A
Mattei, MG
Loiseau, HA
David, A
Vergnaud, G
Citation: F. Giraudeau et al., Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation, J MED GENET, 38(2), 2001, pp. 121-125
Authors:
Coupry, I
Taine, L
Goizet, C
Soriano, C
Mortemousque, B
Arveiler, B
Lacombe, D
Citation: I. Coupry et al., Leucodystrophy and oculocutaneous albinism in a child with an 11q14 deletion, J MED GENET, 38(1), 2001, pp. 35-38
Authors:
Frengen, E
Rocca-Serra, P
Shaposhnikov, S
Taine, L
Thorsen, J
Bepoldin, C
Krekling, M
Lafon, D
Aas, KK
Abd El Moneim, A
Johansen, H
Longy, M
Prydz, H
Dorion-Bonnet, F
Citation: E. Frengen et al., High-resolution integrated map encompassing the breast cancer loss of heterozygosity region on human chromosome 16q22.1, GENOMICS, 70(3), 2000, pp. 273-285
Authors:
Dupuy, D
Aubert, I
Duperat, VG
Petit, J
Taine, L
Stef, M
Bloch, B
Arveiler, B
Citation: D. Dupuy et al., Mapping, characterization, and expression analysis of the SM-20 human homologue, C1orf12, and identification of a novel related gene, SCAND2, GENOMICS, 69(3), 2000, pp. 348-354
Authors:
Fontanellas, A
Mazurier, F
Landry, M
Taine, L
Morel, C
Larou, M
Daniel, JY
Montagutelli, X
de Salamanca, RE
de Verneuil, H
Citation: A. Fontanellas et al., Reversion of hepatobiliary alterations by bone marrow transplantation in amurine model of erythropoietic protoporphyria, HEPATOLOGY, 32(1), 2000, pp. 73-81
Authors:
Goizet, C
Excoffier, E
Taine, L
Taupiac, E
El Moneim, AA
Arveiler, B
Bouvard, M
Lacombe, D
Citation: C. Goizet et al., Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH, AM J MED G, 96(6), 2000, pp. 839-844
Authors:
Bahuau, M
Laurendeau, I
Pelet, A
Assouline, B
Lamireau, T
Taine, L
Bail, B
Vergnes, P
Gallet, S
Vidaud, M
Lyonnet, S
Lacombe, D
Vidaud, D
Citation: M. Bahuau et al., Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia type B (IND B), J MED GENET, 37(2), 2000, pp. 146-150
Authors:
Battin, J
Lacombe, D
Taine, L
Goizet, C
Citation: J. Battin et al., Williams syndrome and behavioral phenotypes in human microdeletion syndromes, B ACA N MED, 184(1), 2000, pp. 105-116
Authors:
Fontanellas, A
Mazurier, F
Belloc, F
Taine, L
Dumain, P
Morel, C
Ged, C
de Verneuil, H
Moreau-Gaudry, F
Citation: A. Fontanellas et al., Fluorescence-based selection of retrovirally transduced cells in congenital erythropoietic porphyria: Direct selection based on the expression of thetherapeutic gene, J GENE MED, 1(5), 1999, pp. 322-330
Authors:
Mazurier, F
Fontanellas, A
Salesse, S
Taine, L
Landriau, S
Moreau-Gaudry, F
Reiffers, J
Peault, B
Di Santo, JP
de Verneuil, H
Citation: F. Mazurier et al., A novel immunodeficient mouse model - RAG2 x common cytokine receptor gamma chain double mutants - Requiring exogenous cytokine administration for human hematopoietic stem cell engraftment, J INTERF CY, 19(5), 1999, pp. 533-541
Authors:
Petit, J
Boisseau, P
Taine, L
Gauthier, B
Arveiler, B
Citation: J. Petit et al., A YAC contig encompassing the 11q14.3 breakpoint of a translocation associated with schizophrenia, and including the tyrosinase gene, MAMM GENOME, 10(6), 1999, pp. 649-652
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1-14
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