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M Tager

Showing results (331-340 of 393) with videos related to

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Neurology|October 1, 1981
A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studiesM C Loonen, H F Busch, J F Koster, et al.
Biochimica Et Biophysica Acta|March 17, 1988
Glucocerebrosidase, a lysosomal enzyme that does not undergo oligosaccharide phosphorylationJ M Aerts, A W Schram, A Strijland, et al.
European Journal of Biochemistry|August 1, 1985
The occurrence of two immunologically distinguishable beta-glucocerebrosidases in human spleenJ M Aerts, W E Donker-Koopman, M K van der Vliet, et al.
The Journal of Infectious Diseases|July 1, 2016
Protection of Humanized Mice From Repeated Intravaginal HIV Challenge by Passive Immunization: A Model for Studying the Efficacy of Neutralizing Antibodies In VivoMaud Deruaz, Brian Moldt, Khoa M Le, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Age-related differences in plasmalogen content of erythrocytes from patients with the cerebro-hepato-renal (Zellweger) syndrome: implications for postnatal detection of the diseaseR J Wanders, Y R Purvis, H S Heymans, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1987
Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiencyA W Schram, S Goldfischer, C W van Roermund, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 21, 2007
Inhibited aortic aneurysm formation in BLT1-deficient miceNeil Ahluwalia, Alexander Y Lin, Andrew M Tager, et al.
American Journal of Respiratory Cell and Molecular Biology|June 19, 2004
Inhibition of pulmonary fibrosis by the chemokine IP-10/CXCL10Andrew M Tager, Richard L Kradin, Peter LaCamera, et al.
Enzyme|January 1, 1987
Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studiesR B Schutgens, R J Wanders, A Nijenhuis, et al.
Human Genetics|January 1, 1983
Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodiesR A Barneveld, W Keijzer, F P Tegelaers, et al.
Pageof 40

Showing results (331-340 of 393) with videos related to

Sort By:
Pageof 40
Neurology|October 1, 1981
A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studiesM C Loonen, H F Busch, J F Koster, et al.
Biochimica Et Biophysica Acta|March 17, 1988
Glucocerebrosidase, a lysosomal enzyme that does not undergo oligosaccharide phosphorylationJ M Aerts, A W Schram, A Strijland, et al.
European Journal of Biochemistry|August 1, 1985
The occurrence of two immunologically distinguishable beta-glucocerebrosidases in human spleenJ M Aerts, W E Donker-Koopman, M K van der Vliet, et al.
The Journal of Infectious Diseases|July 1, 2016
Protection of Humanized Mice From Repeated Intravaginal HIV Challenge by Passive Immunization: A Model for Studying the Efficacy of Neutralizing Antibodies In VivoMaud Deruaz, Brian Moldt, Khoa M Le, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Age-related differences in plasmalogen content of erythrocytes from patients with the cerebro-hepato-renal (Zellweger) syndrome: implications for postnatal detection of the diseaseR J Wanders, Y R Purvis, H S Heymans, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1987
Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiencyA W Schram, S Goldfischer, C W van Roermund, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 21, 2007
Inhibited aortic aneurysm formation in BLT1-deficient miceNeil Ahluwalia, Alexander Y Lin, Andrew M Tager, et al.
American Journal of Respiratory Cell and Molecular Biology|June 19, 2004
Inhibition of pulmonary fibrosis by the chemokine IP-10/CXCL10Andrew M Tager, Richard L Kradin, Peter LaCamera, et al.
Enzyme|January 1, 1987
Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studiesR B Schutgens, R J Wanders, A Nijenhuis, et al.
Human Genetics|January 1, 1983
Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodiesR A Barneveld, W Keijzer, F P Tegelaers, et al.
Pageof 40