Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Othmar Gabriel"'
Publikováno v:
Annals of the New York Academy of Sciences. 106:330-338
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6da3bb81bf2cc9cac40737bcb58145b0
https://doi.org/10.1111/j.1749-6632.1963.tb16649.x
https://doi.org/10.1111/j.1749-6632.1963.tb16649.x
Autor:
Douglas M. Gersten, Othmar Gabriel
Publikováno v:
Analytical Biochemistry. 203:181-186
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b9118c4eaf2b8da102ec4341841feea
https://doi.org/10.1016/0003-2697(92)90300-v
https://doi.org/10.1016/0003-2697(92)90300-v
Autor:
Othmar Gabriel, Gilbert Ashwell
Publikováno v:
Glycobiology. 2:437-443
Reduction of carbohydrates by tritiated borohydride resulted in the production of alditols or glycosides with characteristically divergent specific radioactivities. Simultaneous reduction of individual sugars in the presence of a reference standard,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d686c4bec75af9232befd324e54d2f15
https://doi.org/10.1093/glycob/2.5.437
https://doi.org/10.1093/glycob/2.5.437
Publikováno v:
Infection and Immunity. 38:993-1002
A simple model system has been developed in which lectin-mediated aggregation of glycoprotein-coated beads can be monitored by following the decrease in light scattering at 650 nm. Aggregation has been characterized with the lectin of Actinomyces vis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::587c2ad2c01152c29ab5a56af23747dd
https://doi.org/10.1128/iai.38.3.993-1002.1982
https://doi.org/10.1128/iai.38.3.993-1002.1982
Autor:
Othmar Gabriel
Publikováno v:
Journal of Biological Chemistry. 241:924-929
The biosynthesis of thymidine diphospho-l-rhamnose from thymidine diphosphoglucose specifically labeled with tritium at carbon 3 has been studied with an enzyme preparation from Escherichia coli B. Under conditions in which conversion to the 6-deoxys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdf11011390df90a598e091111cd42b4
https://doi.org/10.1016/s0021-9258(18)96853-5
https://doi.org/10.1016/s0021-9258(18)96853-5
Autor:
Gilbert Ashwell, Othmar Gabriel
Publikováno v:
Journal of Biological Chemistry. 237:1400-1404
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::294f9d6226eb634737091f978441c7bf
https://doi.org/10.1016/s0021-9258(19)83713-4
https://doi.org/10.1016/s0021-9258(19)83713-4
Publikováno v:
Journal of Biological Chemistry. 248:4635-4639
UDP-galactose-4-epimerase and TDP-glucose-oxidoreductase are shown to have analogous reaction mechanisms. TDP-glucose is a substrate for both enzymes, and when labeled with tritium at carbon 4 it displayed an isotope effect for both enzymes. Neither
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82749e01c4bc0287e9c6077ac6316c83
https://doi.org/10.1016/s0021-9258(19)43710-1
https://doi.org/10.1016/s0021-9258(19)43710-1
Autor:
Gilbert Ashwell, Othmar Gabriel
Publikováno v:
Journal of Biological Chemistry. 240:4128-4132
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dd5e7d99089c68adb3ba49255fdc803
https://doi.org/10.1016/s0021-9258(18)97035-3
https://doi.org/10.1016/s0021-9258(18)97035-3
Publikováno v:
Journal of Biological Chemistry. 248:4640-4648
A decrease in enzymatic activity during the standard assay procedure for UDP-galactose-4-epimerase (EC 5.1.3.2) led to the observation that ADP-ribose-(5) (5-(adenosine-5'-pyrophosphoryl)d-ribose), a degradation product of NAD+, is a strong inhibitor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b91ea6899d9977d8a86ded5d5b0fdd53
https://doi.org/10.1016/s0021-9258(19)43711-3
https://doi.org/10.1016/s0021-9258(19)43711-3
Autor:
Othmar Gabriel
Publikováno v:
Carbohydrate Research. 6:319-327
A method is described for the simple synthesis of D -glucose and D -galactose specifically labeled at C-4 with tritium. Methyl α- D -galactopyranoside (1) was converted into methyl 2,3,6-tri- O -benzoyl-α- D -galactopyranoside ( 2 ). Oxidation of (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0ab254e64107dcab8562a2bb0e474a2
https://doi.org/10.1016/s0008-6215(00)81453-6
https://doi.org/10.1016/s0008-6215(00)81453-6