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M Guigon

Showing results (41-50 of 60) with videos related to

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Stem Cells (Dayton, Ohio)|September 1, 1993
The tetrapeptide AcSerAspLysPro (Seraspenide), a hematopoietic inhibitor, may reduce the in vitro toxicity of 3'-azido-3'-deoxythymidine to human hematopoietic progenitorsC Grillon, D Bonnet, J Y Mary, et al.
Experimental Hematology|November 1, 1992
Reversible inhibitory effects and absence of toxicity of the tetrapeptide acetyl-N-Ser-Asp-Lys-Pro (AcSDKP) in human long-term bone marrow cultureD Bonnet, F M Lemoine, E Khoury, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Suppression of normal hematopoiesis during acute leukemiasA Najman, L Kobari, E Khoury, et al.
Advances in Experimental Medicine and Biology|January 1, 1997
In vitro HIV infection of dendritic cell precursors. Effect on dendritic cell differentiation and functionB Canque, M Rosenzwajg, S Camus, et al.
Blood|December 1, 1993
Direct and reversible inhibitory effect of the tetrapeptide acetyl-N-Ser-Asp-Lys-Pro (Seraspenide) on the growth of human CD34+ subpopulations in response to growth factorsD Bonnet, F M Lemoine, S Pontvert-Delucq, et al.
Human Gene Therapy|February 18, 1999
High level of retrovirus-mediated gene transfer into dendritic cells derived from cord blood and mobilized peripheral blood CD34+ cellsM Movassagh, C Baillou, F L Cosset, et al.
Journal of Virology|September 12, 1998
Dendritic cells route human immunodeficiency virus to lymph nodes after vaginal or intravenous administration to miceC Masurier, B Salomon, N Guettari, et al.
Experimental Hematology|November 1, 1990
Inhibition of human bone marrow progenitors by the synthetic tetrapeptide AcSDKPM Guigon, D Bonnet, F Lemoine, et al.
Experimental Hematology|September 1, 1992
Tumor necrosis factor alpha in human long-term bone marrow cultures: distinct effects on nonadherent and adherent progenitorsE Khoury, F M Lemoine, C Baillou, et al.
Human Gene Therapy|February 24, 1998
High-level gene transfer to cord blood progenitors using gibbon ape leukemia virus pseudotype retroviral vectors and an improved clinically applicable protocolM Movassagh, C Desmyter, C Baillou, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Stem Cells (Dayton, Ohio)|September 1, 1993
The tetrapeptide AcSerAspLysPro (Seraspenide), a hematopoietic inhibitor, may reduce the in vitro toxicity of 3'-azido-3'-deoxythymidine to human hematopoietic progenitorsC Grillon, D Bonnet, J Y Mary, et al.
Experimental Hematology|November 1, 1992
Reversible inhibitory effects and absence of toxicity of the tetrapeptide acetyl-N-Ser-Asp-Lys-Pro (AcSDKP) in human long-term bone marrow cultureD Bonnet, F M Lemoine, E Khoury, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Suppression of normal hematopoiesis during acute leukemiasA Najman, L Kobari, E Khoury, et al.
Advances in Experimental Medicine and Biology|January 1, 1997
In vitro HIV infection of dendritic cell precursors. Effect on dendritic cell differentiation and functionB Canque, M Rosenzwajg, S Camus, et al.
Blood|December 1, 1993
Direct and reversible inhibitory effect of the tetrapeptide acetyl-N-Ser-Asp-Lys-Pro (Seraspenide) on the growth of human CD34+ subpopulations in response to growth factorsD Bonnet, F M Lemoine, S Pontvert-Delucq, et al.
Human Gene Therapy|February 18, 1999
High level of retrovirus-mediated gene transfer into dendritic cells derived from cord blood and mobilized peripheral blood CD34+ cellsM Movassagh, C Baillou, F L Cosset, et al.
Journal of Virology|September 12, 1998
Dendritic cells route human immunodeficiency virus to lymph nodes after vaginal or intravenous administration to miceC Masurier, B Salomon, N Guettari, et al.
Experimental Hematology|November 1, 1990
Inhibition of human bone marrow progenitors by the synthetic tetrapeptide AcSDKPM Guigon, D Bonnet, F Lemoine, et al.
Experimental Hematology|September 1, 1992
Tumor necrosis factor alpha in human long-term bone marrow cultures: distinct effects on nonadherent and adherent progenitorsE Khoury, F M Lemoine, C Baillou, et al.
Human Gene Therapy|February 24, 1998
High-level gene transfer to cord blood progenitors using gibbon ape leukemia virus pseudotype retroviral vectors and an improved clinically applicable protocolM Movassagh, C Desmyter, C Baillou, et al.
Pageof 6