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C Gaucher

Showing results (51-60 of 58) with videos related to

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Science Advances|February 19, 2025
Rift-inversion orogens are potential hot spots for natural H<sub>2</sub> generationFrank Zwaan, Sascha Brune, Anne C Glerum, et al.
Thrombosis and Haemostasis|July 1, 1997
Gene defects in 150 unrelated French cases with type 2 von Willebrand disease: from the patient to the gene. INSERM Network on Molecular Abnormalities in von Willebrand DiseaseD Meyer, E Fressinaud, C Gaucher, et al.
Toxicology and Applied Pharmacology|May 17, 2011
Automated detection of hepatotoxic compounds in human hepatocytes using HepaRG cells and image-based analysis of mitochondrial dysfunction with JC-1 dyeK Pernelle, R Le Guevel, D Glaise, et al.
The Science of the Total Environment|August 16, 2019
Geochemical and sulfate isotopic evolution of flowback and produced waters reveals water-rock interactions following hydraulic fracturing of a tight hydrocarbon reservoirF Osselin, S Saad, M Nightingale, et al.
Kidney International|April 12, 2000
Association between high von willebrand factor levels and the Thr789Ala vWF gene polymorphism but not with nephropathy in type I diabetes. The GENEDIAB Study Group and the DESIR Study GroupC Lacquemant, C Gaucher, C Delorme, et al.
Journal of Dental Research|June 3, 2017
Sclerostin Deficiency Promotes Reparative DentinogenesisA-M Collignon, N Amri, J Lesieur, et al.
Journal of Dental Research|July 28, 2025
The Absence of Claudin-10 in the Enamel Organ Alters Its IntegrityT N Nguyen, S Ribes, C Andrique, et al.
Blood|September 15, 1995
Factor VIII gene inversions in severe hemophilia A: results of an international consortium studyS E Antonarakis, J P Rossiter, M Young, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Science Advances|February 19, 2025
Rift-inversion orogens are potential hot spots for natural H<sub>2</sub> generationFrank Zwaan, Sascha Brune, Anne C Glerum, et al.
Thrombosis and Haemostasis|July 1, 1997
Gene defects in 150 unrelated French cases with type 2 von Willebrand disease: from the patient to the gene. INSERM Network on Molecular Abnormalities in von Willebrand DiseaseD Meyer, E Fressinaud, C Gaucher, et al.
Toxicology and Applied Pharmacology|May 17, 2011
Automated detection of hepatotoxic compounds in human hepatocytes using HepaRG cells and image-based analysis of mitochondrial dysfunction with JC-1 dyeK Pernelle, R Le Guevel, D Glaise, et al.
The Science of the Total Environment|August 16, 2019
Geochemical and sulfate isotopic evolution of flowback and produced waters reveals water-rock interactions following hydraulic fracturing of a tight hydrocarbon reservoirF Osselin, S Saad, M Nightingale, et al.
Kidney International|April 12, 2000
Association between high von willebrand factor levels and the Thr789Ala vWF gene polymorphism but not with nephropathy in type I diabetes. The GENEDIAB Study Group and the DESIR Study GroupC Lacquemant, C Gaucher, C Delorme, et al.
Journal of Dental Research|June 3, 2017
Sclerostin Deficiency Promotes Reparative DentinogenesisA-M Collignon, N Amri, J Lesieur, et al.
Journal of Dental Research|July 28, 2025
The Absence of Claudin-10 in the Enamel Organ Alters Its IntegrityT N Nguyen, S Ribes, C Andrique, et al.
Blood|September 15, 1995
Factor VIII gene inversions in severe hemophilia A: results of an international consortium studyS E Antonarakis, J P Rossiter, M Young, et al.
Pageof 6