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L Proia

Showing results (11-20 of 203) with videos related to

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The Journal of Clinical Investigation|April 2, 2015
Emerging biology of sphingosine-1-phosphate: its role in pathogenesis and therapyRichard L Proia, Timothy Hla
La Clinica Terapeutica|April 7, 1998
[Review on renal calculosis in pregnancy]L Proia, A Lippa, A Valente
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1982
Synthesis of beta-hexosaminidase in cell-free translation and in intact fibroblasts: an insoluble precursor alpha chain in a rare form of Tay-Sachs diseaseR L Proia, E F Neufeld
Current Opinion in Structural Biology|December 5, 2002
Lubricating cell signaling pathways with gangliosidesMaria Laura Allende, Richard L Proia
Glycoconjugate Journal|October 30, 2014
Simplifying complexity: genetically resculpting glycosphingolipid synthesis pathways in mice to reveal functionMaria Laura Allende, Richard L Proia
Glycobiology|February 13, 2001
Stemming the tide: glycosphingolipid synthesis inhibitors as therapy for storage diseasesC J Tifft, R L Proia
American Journal of Human Genetics|March 1, 1995
The molecular basis of HEXA mRNA deficiency caused by the most common Tay-Sachs disease mutationD J Boles, R L Proia
Annals of Medicine|April 30, 1998
The beta-hexosaminidase deficiency disorders: development of a clinical paradigm in the mouseC J Tifft, R L Proia
The Journal of Clinical Investigation|April 16, 2004
Blood to brain to the rescueRichard L Proia, Yun-Ping Wu
The Journal of Biological Chemistry|May 5, 1989
Analysis of the glycosylation and phosphorylation of the lysosomal enzyme, beta-hexosaminidase B, by site-directed mutagenesisS Sonderfeld-Fresko, R L Proia
Pageof 21

Showing results (11-20 of 203) with videos related to

Sort By:
Pageof 21
The Journal of Clinical Investigation|April 2, 2015
Emerging biology of sphingosine-1-phosphate: its role in pathogenesis and therapyRichard L Proia, Timothy Hla
La Clinica Terapeutica|April 7, 1998
[Review on renal calculosis in pregnancy]L Proia, A Lippa, A Valente
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1982
Synthesis of beta-hexosaminidase in cell-free translation and in intact fibroblasts: an insoluble precursor alpha chain in a rare form of Tay-Sachs diseaseR L Proia, E F Neufeld
Current Opinion in Structural Biology|December 5, 2002
Lubricating cell signaling pathways with gangliosidesMaria Laura Allende, Richard L Proia
Glycoconjugate Journal|October 30, 2014
Simplifying complexity: genetically resculpting glycosphingolipid synthesis pathways in mice to reveal functionMaria Laura Allende, Richard L Proia
Glycobiology|February 13, 2001
Stemming the tide: glycosphingolipid synthesis inhibitors as therapy for storage diseasesC J Tifft, R L Proia
American Journal of Human Genetics|March 1, 1995
The molecular basis of HEXA mRNA deficiency caused by the most common Tay-Sachs disease mutationD J Boles, R L Proia
Annals of Medicine|April 30, 1998
The beta-hexosaminidase deficiency disorders: development of a clinical paradigm in the mouseC J Tifft, R L Proia
The Journal of Clinical Investigation|April 16, 2004
Blood to brain to the rescueRichard L Proia, Yun-Ping Wu
The Journal of Biological Chemistry|May 5, 1989
Analysis of the glycosylation and phosphorylation of the lysosomal enzyme, beta-hexosaminidase B, by site-directed mutagenesisS Sonderfeld-Fresko, R L Proia
Pageof 21