Zobrazeno 1 - 9
of 9
pro vyhledávání: '"G C Rosso"'
Publikováno v:
Journal of Biological Chemistry. 256:8341-8347
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2605d5e3e3a92982e98927067faf0ff9
https://doi.org/10.1016/s0021-9258(19)68849-6
https://doi.org/10.1016/s0021-9258(19)68849-6
Publikováno v:
Journal of Lipid Research, Vol 16, Iss 3, Pp 235-243 (1975)
A study was conducted to determine whether retinyl phosphate would act as substrate for the enzymatic synthesis of mannosyl retinyl phosphate. Retinyl phosphate, prepared chemically, supported the growth of vitamin A-deficient rats at the same rate a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3757d7c241297d3a45bb0c222f65c6b3
http://www.sciencedirect.com/science/article/pii/S0022227520367304
http://www.sciencedirect.com/science/article/pii/S0022227520367304
Publikováno v:
Journal of Biological Chemistry. 251:6465-6467
Alkaline hydrolysis at 65 degrees converted D-mannosyl retinyl phosphate primarily into D-mannose 2-phosphate which was identified by its behavior on paper chromatography in two solvent systems, as well as by its resistance to acid hydrolysis under c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffec153a3fb380e11caa52464a7a581f
https://doi.org/10.1016/s0021-9258(20)81884-5
https://doi.org/10.1016/s0021-9258(20)81884-5
Publikováno v:
Journal of lipid research. 16(3)
A study was conducted to determine whether retinyl phosphate would act as substrate for the enzymatic synthesis of mannosyl retinyl phosphate. Retinyl phosphate, prepared chemically, supported the growth of vitamin A-deficient rats at the same rate a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::03c87f6f9af469f952eb59fb89474b24
https://pubmed.ncbi.nlm.nih.gov/236352
https://pubmed.ncbi.nlm.nih.gov/236352
Autor:
George Wolf, G C Rosso
Publikováno v:
Annals of the New York Academy of Sciences. 359
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c12147fc0f4d94e6308d5ee82d93779c
https://pubmed.ncbi.nlm.nih.gov/6942694
https://pubmed.ncbi.nlm.nih.gov/6942694
Publikováno v:
The Journal of biological chemistry. 256(16)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ae35ca821968db4c2bb9f175fa2b3fb1
https://pubmed.ncbi.nlm.nih.gov/7263657
https://pubmed.ncbi.nlm.nih.gov/7263657
Publikováno v:
World review of nutrition and dietetics. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cd3f31c00b35b19fefd635f1a2b89be6
https://pubmed.ncbi.nlm.nih.gov/735128
https://pubmed.ncbi.nlm.nih.gov/735128
Publikováno v:
The Journal of biological chemistry. 251(20)
Alkaline hydrolysis at 65 degrees converted D-mannosyl retinyl phosphate primarily into D-mannose 2-phosphate which was identified by its behavior on paper chromatography in two solvent systems, as well as by its resistance to acid hydrolysis under c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::31f11abfc77382f3ffeee35149e6aa97
https://pubmed.ncbi.nlm.nih.gov/977584
https://pubmed.ncbi.nlm.nih.gov/977584
Publikováno v:
Biochemical and biophysical research communications. 41(3)
A mannolipid synthesized by a membrane-rich fraction from rat liver in the presence of 15-14C-retinol and GDP-mannose-14C contained a polar metabolite of 14C-retinol, as well as 14C-mannose. Retinol stimulated the in vitro incorporation of 14C-mannos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39b83cafac01d526f3346174c85a419b
https://pubmed.ncbi.nlm.nih.gov/5479290
https://pubmed.ncbi.nlm.nih.gov/5479290