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Results: 1-20 |
Results: 20
Electrical impedance and tenderisation in bovine meat
Authors: Lepetit, J Sale, P Favier, R Dalle, R
Citation: J. Lepetit et al., Electrical impedance and tenderisation in bovine meat, MEAT SCI, 60(1), 2002, pp. 51-62
Determination of myloid antigen expression on childhood acute lymphoblastic leukaemia cells: Discrepancies using different monoclonal antibody clones
Authors: Firat, H Favier, R Adam, M Leverger, G Landman-Parker, J Cayre, Y Douay, L
Citation: H. Firat et al., Determination of myloid antigen expression on childhood acute lymphoblastic leukaemia cells: Discrepancies using different monoclonal antibody clones, LEUK LYMPH, 42(4), 2001, pp. 675-682
Determination of myeloid antigen expression on childhood acute lymphoblastic leukaemia cells: Discrepancies using different monoclonal antibody clones
Authors: Firat, H Favier, R Adam, M Leverger, G Landman-Parker, J Cayre, Y Douay, L
Citation: H. Firat et al., Determination of myeloid antigen expression on childhood acute lymphoblastic leukaemia cells: Discrepancies using different monoclonal antibody clones, LEUK LYMPH, 42(1-2), 2001, pp. 75-82
Congenital alpha(2)-plasmin inhibitor deficiencies: a review
Authors: Favier, R Aoki, N de Moerloose, P
Citation: R. Favier et al., Congenital alpha(2)-plasmin inhibitor deficiencies: a review, BR J HAEM, 114(1), 2001, pp. 4-10
Newly recognized cellular abnormalities in the gray platelet syndrome
Authors: Drouin, A Favier, R Masse, JM Debili, N Schmitt, A Elbim, C Guichard, J Adam, M Gougerot-Pocidalo, MA Cramer, EM
Citation: A. Drouin et al., Newly recognized cellular abnormalities in the gray platelet syndrome, BLOOD, 98(5), 2001, pp. 1382-1391
5 '-UTR structural organization, transcript expression, and mutational analysis of the human Rab geranylgeranyl transferase alpha-subunit (RABGGTA) gene
Authors: Li, W Detter, JC Weiss, HJ Cramer, EM Zhang, Q Novak, EK Favier, R Kingsmore, SF Swank, RT
Citation: W. Li et al., 5 '-UTR structural organization, transcript expression, and mutational analysis of the human Rab geranylgeranyl transferase alpha-subunit (RABGGTA) gene, MOL GEN MET, 71(4), 2000, pp. 599-608
Fli-1 is required for murine vascular and megakaryocytic development and is hemizygously deleted in patients with thrombocytopenia
Authors: Hart, A Melet, F Grossfeld, P Chien, K Jones, C Tunnacliffe, A Favier, R Bernstein, A
Citation: A. Hart et al., Fli-1 is required for murine vascular and megakaryocytic development and is hemizygously deleted in patients with thrombocytopenia, IMMUNITY, 13(2), 2000, pp. 167-177
Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakage
Authors: Jones, C Mullenbach, R Grossfeld, P Auer, R Favier, R Chien, K James, M Tunnacliffe, A Cotter, F
Citation: C. Jones et al., Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakage, HUM MOL GEN, 9(8), 2000, pp. 1201-1208
Comparison of thrombotic risk between 85 homozygotes and 481 heterozygotescarriers of the factor V Leiden mutation: retrospective analysis from the Procare Study
Authors: Aillaud, MF Morange, P Juhan, I Bauters, A Jude, B Biron-Andreani, C Daures, JP Schved, JF Pernod, G Polac, B Bridey, F De Prost, D Borg, JY Saladin-Theron, C Le Cam, V Denninger, MH Truchaud, F Trossaert, M Boinot, C Sultan, Y Delahousse, B Fimbel, B Gruel, Y Houbouyan, L Bihour, C Vergnes, C Dutrillaux, F Lorenzini, JL Julia, A Deschamps, A Favier, R Freyburger, G Trzeciak, MC Berruyer, M Doumergue, G Gris, JC Toulon, P Montpied, G Marques-Verdier, A Lequerrec, A Guerin, V Massignon, D
Citation: Mf. Aillaud et al., Comparison of thrombotic risk between 85 homozygotes and 481 heterozygotescarriers of the factor V Leiden mutation: retrospective analysis from the Procare Study, BL COAG FIB, 11(6), 2000, pp. 511-518
Gender differentiation of the chemoreflex during growth at high altitude: functional and neurochemical studies
Authors: Joseph, V Soliz, J Pequignot, J Sempore, B Cottet-Emard, JM Dalmaz, Y Favier, R Spielvogel, H Pequignot, JM
Citation: V. Joseph et al., Gender differentiation of the chemoreflex during growth at high altitude: functional and neurochemical studies, AM J P-REG, 278(4), 2000, pp. R806-R816
A novel point mutation of the splicing donor site in the intron 2 of the plasmin inhibitor gene
Authors: Yoshinaga, H Hirosawa, S Chung, DH Miyasaka, N Aoki, N Favier, R
Citation: H. Yoshinaga et al., A novel point mutation of the splicing donor site in the intron 2 of the plasmin inhibitor gene, THROMB HAEM, 84(2), 2000, pp. 307
Modelling the effect of sarcomere length on collagen thermal shortening incooked meat: consequence on meat toughness
Authors: Lepetit, J Grajales, A Favier, R
Citation: J. Lepetit et al., Modelling the effect of sarcomere length on collagen thermal shortening incooked meat: consequence on meat toughness, MEAT SCI, 54(3), 2000, pp. 239-250
Differential effects of endurance training and creatine depletion on regional mitochondrial adaptations in rat skeletal muscle
Authors: Roussel, D Lhenry, F Ecochard, L Sempore, B Rouanet, JL Favier, R
Citation: D. Roussel et al., Differential effects of endurance training and creatine depletion on regional mitochondrial adaptations in rat skeletal muscle, BIOCHEM J, 350, 2000, pp. 547-553
The town in European history
Authors: Favier, R
Citation: R. Favier, The town in European history, REV HIST M, 47, 2000, pp. 93-95
Skeletal muscle HSP72 level during endurance training: influence of peripheral arterial insufficiency
Authors: Ecochard, L Lhenry, F Sempore, B Favier, R
Citation: L. Ecochard et al., Skeletal muscle HSP72 level during endurance training: influence of peripheral arterial insufficiency, PFLUG ARCH, 440(6), 2000, pp. 918-924
Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female
Authors: Favier, R Lavergne, JM Costa, JM Garon, C Mazurier, C Viemont, M Delpech, M Valleix, S
Citation: R. Favier et al., Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female, BLOOD, 96(13), 2000, pp. 4373-4375
Existence of a differentiation blockage at the stage of a megakaryocyte precursor in the thrombocytopenia and absent radii (TAR) syndrome
Authors: Letestu, R Vitrat, N Masse, A Le Couedic, JP Lazar, V Rameau, P Wendling, F Vuillier, J Boutard, P Plouvier, E Plasse, M Favier, R Vainchenker, W Debili, N
Citation: R. Letestu et al., Existence of a differentiation blockage at the stage of a megakaryocyte precursor in the thrombocytopenia and absent radii (TAR) syndrome, BLOOD, 95(5), 2000, pp. 1633-1641
Incidence of G20210A mutation in severe vaso-occlusive events complicatingsickle cell anemia
Authors: Favier, R Neonato, MG Maillet, F Feingold, J Cayre, Y Girot, R
Citation: R. Favier et al., Incidence of G20210A mutation in severe vaso-occlusive events complicatingsickle cell anemia, BL COAG FIB, 10(2), 1999, pp. 111-112
Mechanical resistance of wheat straw after incubation in cultures of ruminal cellulolytic microorganisms
Authors: Fonty, G Chavarot, M Lepetit, J Canistro, J Favier, R
Citation: G. Fonty et al., Mechanical resistance of wheat straw after incubation in cultures of ruminal cellulolytic microorganisms, ANIM FEED S, 80(3-4), 1999, pp. 297-307
A case of intramedullary haematoma associated with congenital alpha(2)-plasmin inhibitor deficiency
Authors: Devaussuzenet, VMP Ducou-le-Pointe, HA Doco, AM Mary, PM Montagne, JPR Favier, R
Citation: Vmp. Devaussuzenet et al., A case of intramedullary haematoma associated with congenital alpha(2)-plasmin inhibitor deficiency, PEDIAT RAD, 28(12), 1998, pp. 978-980
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