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L French

Showing results (361-370 of 845) with videos related to

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Stem Cell Research|December 21, 2010
A high-throughput multiplexed screening assay for optimizing serum-free differentiation protocols of human embryonic stem cellsJoel T Outten, Xin Cheng, Paul Gadue, et al.
Medicine|July 1, 1984
Cavitary histoplasmosis occurring during two large urban outbreaks. Analysis of clinical, epidemiologic, roentgenographic, and laboratory featuresL J Wheat, J Wass, J Norton, et al.
Journal of Clinical Microbiology|December 17, 1997
Analysis of an outbreak of non-phage-typeable methicillin-resistant Staphylococcus aureus by using a randomly amplified polymorphic DNA assayA Tambic, E G Power, H Talsania, et al.
The Journal of Hospital Infection|September 24, 2016
Point-of-care universal screening for meticillin-resistant Staphylococcus aureus: a cluster-randomized cross-over trialP J Wu, D Jeyaratnam, O Tosas, et al.
American Journal of Infection Control|May 1, 2009
Protecting health care workers from tuberculosis: a 10-year experienceSharon F Welbel, Audrey L French, Patricia Bush, et al.
Experimental Hematology|September 4, 2004
Evidence for megakaryocyte engraftment following reduced-intensity conditioningDeborah L French, Steven Fruchtman, W Beau Mitchell, et al.
The Journal of Hospital Infection|February 1, 1990
Hong Kong strains of methicillin-resistant and methicillin-sensitive Staphylococcus aureus have similar virulenceG L French, A F Cheng, J M Ling, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 12, 1998
Cholylglycine hydrolase and 7alpha-dehydroxylase optimum assay conditions in vitro and caecal enzyme activities ex vivoL A Thomas, A King, G L French, et al.
Blood|September 1, 1996
A Cys374Tyr homozygous mutation of platelet glycoprotein IIIa (beta 3) in a Chinese patient with Glanzmann's thrombastheniaC M Grimaldi, F Chen, L E Scudder, et al.
Scientific Reports|September 1, 2016
Structural basis for early-onset neurological disorders caused by mutations in human selenocysteine synthaseAnupama K Puppala, Rachel L French, Doreen Matthies, et al.
Pageof 85

Showing results (361-370 of 845) with videos related to

Sort By:
Pageof 85
Stem Cell Research|December 21, 2010
A high-throughput multiplexed screening assay for optimizing serum-free differentiation protocols of human embryonic stem cellsJoel T Outten, Xin Cheng, Paul Gadue, et al.
Medicine|July 1, 1984
Cavitary histoplasmosis occurring during two large urban outbreaks. Analysis of clinical, epidemiologic, roentgenographic, and laboratory featuresL J Wheat, J Wass, J Norton, et al.
Journal of Clinical Microbiology|December 17, 1997
Analysis of an outbreak of non-phage-typeable methicillin-resistant Staphylococcus aureus by using a randomly amplified polymorphic DNA assayA Tambic, E G Power, H Talsania, et al.
The Journal of Hospital Infection|September 24, 2016
Point-of-care universal screening for meticillin-resistant Staphylococcus aureus: a cluster-randomized cross-over trialP J Wu, D Jeyaratnam, O Tosas, et al.
American Journal of Infection Control|May 1, 2009
Protecting health care workers from tuberculosis: a 10-year experienceSharon F Welbel, Audrey L French, Patricia Bush, et al.
Experimental Hematology|September 4, 2004
Evidence for megakaryocyte engraftment following reduced-intensity conditioningDeborah L French, Steven Fruchtman, W Beau Mitchell, et al.
The Journal of Hospital Infection|February 1, 1990
Hong Kong strains of methicillin-resistant and methicillin-sensitive Staphylococcus aureus have similar virulenceG L French, A F Cheng, J M Ling, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 12, 1998
Cholylglycine hydrolase and 7alpha-dehydroxylase optimum assay conditions in vitro and caecal enzyme activities ex vivoL A Thomas, A King, G L French, et al.
Blood|September 1, 1996
A Cys374Tyr homozygous mutation of platelet glycoprotein IIIa (beta 3) in a Chinese patient with Glanzmann's thrombastheniaC M Grimaldi, F Chen, L E Scudder, et al.
Scientific Reports|September 1, 2016
Structural basis for early-onset neurological disorders caused by mutations in human selenocysteine synthaseAnupama K Puppala, Rachel L French, Doreen Matthies, et al.
Pageof 85