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Philippe Joly

Showing results (41-50 of 148) with videos related to

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Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|November 22, 2011
Protein characterization by LC-MS/MS may be required for the DNA identification of a fusion hemoglobin: the example of Hb P-NiloticIsabelle Zanella-Cleon, Frédéric Delolme, Philippe Lacan, et al.
Blood Cells, Molecules & Diseases|May 18, 2010
The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patientsThi Khanh Tien Nguyen, Philippe Joly, Claire Bardel, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 18, 2012
Characterization of three new deletions in the β-globin gene cluster during a screening survey in two French urban areasSerge Pissard, Valérie Raclin, Philippe Lacan, et al.
Frontiers in Physiology|June 30, 2020
Mechanical Signature of Red Blood Cells Flowing Out of a Microfluidic Constriction Is Impacted by Membrane Elasticity, Cell Surface-to-Volume Ratio and DiseasesMagalie Faivre, Céline Renoux, Amel Bessaa, et al.
Hemoglobin|August 7, 2009
Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr]Isabelle Zanella-Cleon, Claude Préhu, Philippe Joly, et al.
Hemoglobin|July 26, 2008
Two new alpha-thalassemia point mutations that are undetectable by biochemical techniquesPhilippe Joly, Brigitté Pégourie, Stéphane Courby, et al.
Frontiers in Physiology|August 10, 2019
Receptor for Advanced Glycation End Products Antagonism Blunts Kidney Damage in Transgenic Townes Sickle MiceEmmanuelle Charrin, Camille Faes, Amandine Sotiaux, et al.
American Journal of Hematology|January 7, 2020
Sialic acids rather than glycosaminoglycans affect normal and sickle red blood cell rheology by binding to four major sites on fibrinogenFrank Gondelaud, Philippe Connes, Elie Nader, et al.
Haematologica|October 16, 2012
HBB loss of heterozygosity in the hemopoietic lineage gives rise to an unusual sickle-cell trait phenotypePhilippe Joly, Caroline Schluth-Bolard, Philippe Lacan, et al.
Blood Cells, Molecules & Diseases|June 13, 2025
Impact of elevated red blood cell membrane cholesterol in sickle cell anemia patients: Effects of BRN-002, a 2-hydroxypropyl-β-cyclodextrin derivate, on red blood cell lipids, deformability, sickling and hemolysisClaire Bordat, Philippe Connes, Philippe Joly, et al.
Pageof 15

Showing results (41-50 of 148) with videos related to

Sort By:
Pageof 15
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|November 22, 2011
Protein characterization by LC-MS/MS may be required for the DNA identification of a fusion hemoglobin: the example of Hb P-NiloticIsabelle Zanella-Cleon, Frédéric Delolme, Philippe Lacan, et al.
Blood Cells, Molecules & Diseases|May 18, 2010
The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patientsThi Khanh Tien Nguyen, Philippe Joly, Claire Bardel, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 18, 2012
Characterization of three new deletions in the β-globin gene cluster during a screening survey in two French urban areasSerge Pissard, Valérie Raclin, Philippe Lacan, et al.
Frontiers in Physiology|June 30, 2020
Mechanical Signature of Red Blood Cells Flowing Out of a Microfluidic Constriction Is Impacted by Membrane Elasticity, Cell Surface-to-Volume Ratio and DiseasesMagalie Faivre, Céline Renoux, Amel Bessaa, et al.
Hemoglobin|August 7, 2009
Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr]Isabelle Zanella-Cleon, Claude Préhu, Philippe Joly, et al.
Hemoglobin|July 26, 2008
Two new alpha-thalassemia point mutations that are undetectable by biochemical techniquesPhilippe Joly, Brigitté Pégourie, Stéphane Courby, et al.
Frontiers in Physiology|August 10, 2019
Receptor for Advanced Glycation End Products Antagonism Blunts Kidney Damage in Transgenic Townes Sickle MiceEmmanuelle Charrin, Camille Faes, Amandine Sotiaux, et al.
American Journal of Hematology|January 7, 2020
Sialic acids rather than glycosaminoglycans affect normal and sickle red blood cell rheology by binding to four major sites on fibrinogenFrank Gondelaud, Philippe Connes, Elie Nader, et al.
Haematologica|October 16, 2012
HBB loss of heterozygosity in the hemopoietic lineage gives rise to an unusual sickle-cell trait phenotypePhilippe Joly, Caroline Schluth-Bolard, Philippe Lacan, et al.
Blood Cells, Molecules & Diseases|June 13, 2025
Impact of elevated red blood cell membrane cholesterol in sickle cell anemia patients: Effects of BRN-002, a 2-hydroxypropyl-β-cyclodextrin derivate, on red blood cell lipids, deformability, sickling and hemolysisClaire Bordat, Philippe Connes, Philippe Joly, et al.
Pageof 15