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Showing results (321-330 of 393) with videos related to

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Arthritis and Rheumatism|February 10, 2011
Amelioration of dermal fibrosis by genetic deletion or pharmacologic antagonism of lysophosphatidic acid receptor 1 in a mouse model of sclerodermaFlavia V Castelino, Jon Seiders, Gretchen Bain, et al.
Nature Immunology|September 2, 2003
Leukotriene B4 receptor BLT1 mediates early effector T cell recruitmentAndrew M Tager, Shannon K Bromley, Benjamin D Medoff, et al.
Biochemical and Biophysical Research Communications|May 16, 1988
Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disordersS Brul, E A Wiemer, A Westerveld, et al.
European Journal of Biochemistry|August 15, 1983
Monoclonal antibodies against human beta-glucocerebrosidaseR A Barneveld, F P Tegelaers, E I Ginns, et al.
Biochemical and Biophysical Research Communications|September 28, 1984
Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndromeR J Wanders, M Kos, B Roest, et al.
Clinical Genetics|January 1, 1981
Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency)M C Loonen, A W Schram, J F Koster, et al.
Cell Reports|May 18, 2016
TREX1 Knockdown Induces an Interferon Response to HIV that Delays Viral Infection in Humanized MiceLee Adam Wheeler, Radiana T Trifonova, Vladimir Vrbanac, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1987
Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndromeR J Wanders, C W van Roermund, R Westra, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidationP T Clayton, B D Lake, M Hjelm, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: correlation with pyridoxine responsivenessR J Wanders, C W van Roermund, S Jurriaans, et al.
Pageof 40

Showing results (321-330 of 393) with videos related to

Sort By:
Pageof 40
Arthritis and Rheumatism|February 10, 2011
Amelioration of dermal fibrosis by genetic deletion or pharmacologic antagonism of lysophosphatidic acid receptor 1 in a mouse model of sclerodermaFlavia V Castelino, Jon Seiders, Gretchen Bain, et al.
Nature Immunology|September 2, 2003
Leukotriene B4 receptor BLT1 mediates early effector T cell recruitmentAndrew M Tager, Shannon K Bromley, Benjamin D Medoff, et al.
Biochemical and Biophysical Research Communications|May 16, 1988
Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disordersS Brul, E A Wiemer, A Westerveld, et al.
European Journal of Biochemistry|August 15, 1983
Monoclonal antibodies against human beta-glucocerebrosidaseR A Barneveld, F P Tegelaers, E I Ginns, et al.
Biochemical and Biophysical Research Communications|September 28, 1984
Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndromeR J Wanders, M Kos, B Roest, et al.
Clinical Genetics|January 1, 1981
Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency)M C Loonen, A W Schram, J F Koster, et al.
Cell Reports|May 18, 2016
TREX1 Knockdown Induces an Interferon Response to HIV that Delays Viral Infection in Humanized MiceLee Adam Wheeler, Radiana T Trifonova, Vladimir Vrbanac, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1987
Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndromeR J Wanders, C W van Roermund, R Westra, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidationP T Clayton, B D Lake, M Hjelm, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: correlation with pyridoxine responsivenessR J Wanders, C W van Roermund, S Jurriaans, et al.
Pageof 40