Zobrazeno 1 - 10 of 212 pro vyhledávání: '"M M Ponpipom"'
1
Akademický článek
Isolation of 1,3-distearoyl-glycero-2-phosphocholine (beta-lecithin) from commercial 1,2-distearoyl-sn-glycero-3-phosphocholine.
Autor: M M Ponpipom, R L Bugianesi
Publikováno v: Journal of Lipid Research, Vol 21, Iss 1, Pp 136-139 (1980)
Different batches of 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) had varying amounts of contaminants which appeared to affect systematic biological studies. This contaminant was separated by silica gel column chromatography followed by high per
Externí odkaz: https://doaj.org/article/b110944f3bcc47e9a67c064d71830818
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2
Patents and literature
Autor: T. R. Owen, S. Green, J. J. Marshall, Ralph A. Messing, J. A. Maselli, T. Inui, I. L. Calderon, H. Morise, S. Funakoshi, E. Fascetti, L. T. Davis, J. E. Blair, Y. Masuda, D. G. MacLennan, T. Sai, R. O. Horwath, A. R. Thomson, M. Rebeller, K. Nakamura, E. L. Magee, H. M. Goodman, I. L. Diaz, R. L. Mynatt, R. C. Gamble, D. J. Moore, T. Tsuchida, R. S. Leiser, C. L. Hershberger, C. P. Bahl, James D. Roberts, R. J. Wu, F. G. Bull, A. Viglia, D. L. Klass, J. E. Ahnell, S. Kawarabuki, B. Volesky, P. Zaffaroni, K. Kouno, L. Degen, D. A. Kita, P. Yout, A. Berg, M. P. Henry, M. R. Mauk, J. D. Baldeschwieler, Y. Yagi, J. Vergnault, L. Angelini, S. A. Narang, D. Lonchamp, R. Olivieri, J. A. Smith, P. A. Fedde, George T. Tsao, R. Katsumata, J. D. Baxter, H. Arimura, M. G. Busby, Z. Eckmayer, N. W. Lützen, T. Y. Shen, Y. Ooshima, M. Tsezos, K. Satou, P. H. Seeburg, J. C. Caygill, S. Nankai, Li Fu Chen, G. G. Khachatourians, R. Heady, C. Olmedo, S. Ghosh, B. J. Miles, F. J M Araujo, Cheng S. Gong, T. Saito, J. C. Ousby, N. F. Olson, N. Miwa, Y. Uemura, B. Cabane, D. M. Fenton, S. J. Luenser, M. M. Ponpipom, L. Formiconi, A. Senni, D. C. Steer, T. Iijima, T. Suyama, D. W. Hartwig, E. Gotou
Publikováno v: Applied biochemistry and biotechnology. 7(6)
Protein engineering and site-directed mutagenesis is becoming immensely important in both fundamental studies and commercial applications involving proteins and enzymes in biocatalysis. Protein engineering has become a powerful tool to help biochemis
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efa1b41de150d6864a137453a740cd70
https://pubmed.ncbi.nlm.nih.gov/24234462
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3
Purification and characterization of recombinant human farnesyl diphosphate synthase expressed in Escherichia coli
Autor: J D Bergstrom, B T Sheares, Victor D.-H. Ding, C. D. Poulter, M M Ponpipom, L B Perez
Publikováno v: Biochemical Journal. 275:61-65
We previously reported the isolation of a partial-length human fetal-liver cDNA encoding farnesyl diphosphate (FPP) synthase (EC 2.5.1.10) and the expression of an active FPP synthase fusion protein in Escherichia coli. The expressed human FPP syntha
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef62b3f8ee20f96d9a2cfb172d651622
https://doi.org/10.1042/bj2750061
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4
Cell surface carbohydrates for targeting studies
Autor: T. Y. Shen, M. M. Ponpipom, R. L. Bugianesi
Publikováno v: Canadian Journal of Chemistry. 58:214-220
Syntheses of a series of glycolipids with 6-(5-cholesten-3β-yloxy)-1-thiohexane as the aglycon and the following carbohydrates as surface determinants are described: D-glucose, D-mannose, D-galactose, 2-acetamido-2-deoxy-D-glucose, 2-acetamido-2-deo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e58a45601050305da6f58be1a2f160a9
https://doi.org/10.1139/v80-035
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5
Δ9-Tetrahydrocannabinol–Protein Conjugates
Autor: M M Ponpipom, A H Sehon, P T Tsui, K A Kelly, M Strahilevitz
Publikováno v: Canadian Journal of Biochemistry. 52:252-258
The syntheses of four distinct derivatives of Δ9-tetrahydrocannabinol (Δ9-THC), intended for subsequent coupling to proteins and for use as hapten–protein conjugates for the production of anti-THC antibodies, are described. Three of these THC der
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::06fd288758f59334758db6600d4f0296
https://doi.org/10.1139/o74-038
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7
Glycolipids as potential immunologic adjuvants
Autor: R. L. Bugianesi, Tsung-Ying Shen, A. Friedman, M. M. Ponpipom
Publikováno v: Journal of Medicinal Chemistry. 23:1184-1188
A group of 1-thio-beta-L-fucopyranosides containing hexadecane, 9-octadecene, adamantane, 1,2-diphenyltetrafluoroethane, and 3-hexynyl- and 3,6-dioxaoctylcholesterols were synthesized as potential immunologic adjuvants. Many of these fucosyl lipids a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b57cd7e458b871af50374d9422bcd1ae
https://doi.org/10.1021/jm00185a007
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8
Isolation of 1,3-distearoyl-glycero-2-phosphocholine (beta-lecithin) from commercial 1,2-distearoyl-sn-glycero-3-phosphocholine
Autor: R L Bugianesi, M M Ponpipom
Publikováno v: Journal of Lipid Research, Vol 21, Iss 1, Pp 136-139 (1980)
Different batches of 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) had varying amounts of contaminants which appeared to affect systematic biological studies. This contaminant was separated by silica gel column chromatography followed by high per
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57ec1e6fbf6419e152be96ea09ea3964
http://www.sciencedirect.com/science/article/pii/S0022227520398485
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9
The Reaction of O-Benzylidene Sugars with N-Bromosuccinimide.: VII. Stereochemical and Mechanistic Aspects in the Pyrimidine Nucleoside Series
Autor: M. M. Ponpipom, S. Hanessian
Publikováno v: Canadian Journal of Chemistry. 50:253-258
The reaction of 2′,3′-O-benzylideneuridine with N-bromosuccinimide (NBS) leads to 3'-O-benzoyl-2′,5-dibromouridine. The stereoselectivity of bromination in the sugar ring can be explained by invoking the sequential formation of benzoxonium ion
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4fd80ae26a94cb5f58e4ae7eba622f4c
https://doi.org/10.1139/v72-036
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10
The Reaction of O-Benzylidene Sugars with N-Bromosuccinimide.: VI. A New Synthesis of 2′-Deoxyuridine and some of its Selectively Substituted Derivatives
Autor: S. Hanessian, M. M. Ponpipom
Publikováno v: Canadian Journal of Chemistry. 50:246-252
A new synthesis of 2′-deoxyuridine and its selectively substituted derivatives has been developed, based on the reaction of appropriately substituted 2′,3′-O-benzylideneuridines with N-bromosuccinimide (NBS). The preponderant products are uridi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2756e898b39bdac94c202257cf84de2a
https://doi.org/10.1139/v72-035
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