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Jacques Elion

Showing results (11-20 of 69) with videos related to

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Haematologica|March 8, 2005
Decreased plasma endothelin-1 levels in children with sickle cell disease treated with hydroxyureaClaudine Lapouméroulie, Malika Benkerrou, Marie Hélène Odièvre, et al.
Clinical Hemorheology and Microcirculation|September 5, 2013
Prior exposure of endothelial cells to hydroxycarbamide alters the flow dynamics and adhesion of sickle red blood cellsEmmanuelle Verger, Damien Schoëvaërt, Pascal Carrivain, et al.
Haematologica|September 8, 2006
ET-1 and ecNOS gene polymorphisms andsusceptibility to acute chest syndrome and painful vaso-occlusive crises in children with sickle cell anemiaVicky Chaar, Vanessa Tarer, Maryse Etienne-Julan, et al.
Haematologica|January 14, 2011
Differential modulation of adhesion molecule expression by hydroxycarbamide in human endothelial cells from the micro- and macrocirculation: potential implications in sickle cell disease vasoocclusive eventsSandrine Laurance, Pauline Lansiaux, François-Xavier Pellay, et al.
Human Mutation|January 12, 2005
Molecular basis of methylmalonyl-CoA mutase apoenzyme defect in 40 European patients affected by mut(o) and mut- forms of methylmalonic acidemia: identification of 29 novel mutations in the MUT geneCécile Acquaviva, Jean-François Benoist, Sabrina Pereira, et al.
Blood Cells, Molecules & Diseases|July 6, 2010
Alpha-thalassemia is associated with a decreased occurrence and a delayed age-at-onset of albuminuria in sickle cell anemia patientsDanitza Nebor, Cédric Broquere, Karine Brudey, et al.
Pediatrics|May 23, 2007
The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 geneYves Sznajer, Boris Keren, Clarisse Baumann, et al.
Microbiology (Reading, England)|June 8, 2001
Commensal Escherichia coli isolates are phylogenetically distributed among geographically distinct human populationsPatrick Duriez, Olivier Clermont, Stéphane Bonacorsi, et al.
American Journal of Hematology|April 22, 2006
UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemiaVicky Chaar, Lysiane Kéclard, Maryse Etienne-Julan, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 15, 2003
WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms' tumourChantal Loirat, Jean Luc André, Jacqueline Champigneulle, et al.
Pageof 7

Showing results (11-20 of 69) with videos related to

Sort By:
Pageof 7
Haematologica|March 8, 2005
Decreased plasma endothelin-1 levels in children with sickle cell disease treated with hydroxyureaClaudine Lapouméroulie, Malika Benkerrou, Marie Hélène Odièvre, et al.
Clinical Hemorheology and Microcirculation|September 5, 2013
Prior exposure of endothelial cells to hydroxycarbamide alters the flow dynamics and adhesion of sickle red blood cellsEmmanuelle Verger, Damien Schoëvaërt, Pascal Carrivain, et al.
Haematologica|September 8, 2006
ET-1 and ecNOS gene polymorphisms andsusceptibility to acute chest syndrome and painful vaso-occlusive crises in children with sickle cell anemiaVicky Chaar, Vanessa Tarer, Maryse Etienne-Julan, et al.
Haematologica|January 14, 2011
Differential modulation of adhesion molecule expression by hydroxycarbamide in human endothelial cells from the micro- and macrocirculation: potential implications in sickle cell disease vasoocclusive eventsSandrine Laurance, Pauline Lansiaux, François-Xavier Pellay, et al.
Human Mutation|January 12, 2005
Molecular basis of methylmalonyl-CoA mutase apoenzyme defect in 40 European patients affected by mut(o) and mut- forms of methylmalonic acidemia: identification of 29 novel mutations in the MUT geneCécile Acquaviva, Jean-François Benoist, Sabrina Pereira, et al.
Blood Cells, Molecules & Diseases|July 6, 2010
Alpha-thalassemia is associated with a decreased occurrence and a delayed age-at-onset of albuminuria in sickle cell anemia patientsDanitza Nebor, Cédric Broquere, Karine Brudey, et al.
Pediatrics|May 23, 2007
The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 geneYves Sznajer, Boris Keren, Clarisse Baumann, et al.
Microbiology (Reading, England)|June 8, 2001
Commensal Escherichia coli isolates are phylogenetically distributed among geographically distinct human populationsPatrick Duriez, Olivier Clermont, Stéphane Bonacorsi, et al.
American Journal of Hematology|April 22, 2006
UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemiaVicky Chaar, Lysiane Kéclard, Maryse Etienne-Julan, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 15, 2003
WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms' tumourChantal Loirat, Jean Luc André, Jacqueline Champigneulle, et al.
Pageof 7