The stereochemistry of hexahydroprenol, ubiquinone and ergosterol biosynthesis in the mycelium of Aspergillus fumigatus Fresenius.
about
The characterization and stereochemistry of biosynthesis of dolichols in rat liverEffects of dichloroacetate on the metabolism of glucose, pyruvate, acetate, 3-hydroxybutyrate and palmitate in rat diaphragm and heart muscle in vitro and on extraction of glucose, lactate, pyruvate and free fatty acids by dog heart in vivoEvidence from mycelial studies for differences in the sterol biosynthetic pathway of Rhizoctonia solani and Phytophthora cinnamomiThe introduction of the C-22-C-23 ethylenic linkage in ergosterol biosynthesisIncorporation of tritium from [(4R)-4-3H]mevalonate into abscisic acid.Studies in phytosterol biosynthesis. Mechanism of biosynthesis of cycloartenol.The characterization and distribution of hexahydropolyprenyl esters in cultures of Aspergillus fumigatus Fresenius.Mechanisms for the formation of alanine and aspartate on rat liver in vivo after administration of ammonium chloride.The location of spermine in bacterial ribosomes as indicated by 1,5-difluoro-2,4-dinitrobenzene and by ethidium bromide.Dolichols, ubiquinones, geranylgeraniol and farnesol as the major metabolites of mevalonate in Phytophthora cactorum.Biosynthesis of geraniol and nerol and beta-D-glucosides in Pelargonium graveolens and Rosa dilecta.The biosynthesis of (+)- -pinene in Pinus species.Polyprenols of Aspergillus niger. Their characterization, biosynthesis and subcellular distribution.The stereochemistry of betulaprenol biosynthesis.The characterization of undecaprenol of Lactobacillus plantarum.Polyprenols.The stereochemistry of betulaprenol biosynthesis.
P2860
Q28239656-9E4FE7B7-6D5A-43EC-BE67-C75C7DB5DB74Q28364065-2F659C6F-15F4-4254-B069-4870AC520990Q41791246-9DA58183-03F3-4790-A443-15B458B3794BQ41857244-5D10C84F-2EC4-47C6-BED2-6B37209830BBQ41929944-1174FF41-3BCA-4BC2-98A8-1028EA2EF0F0Q41964532-421C5FBB-9B57-4751-A984-054014638A1DQ42013538-E645E411-B0B3-48F0-9978-99FFF5B3E68DQ42057394-68FB2756-546E-42A7-BB66-3C174865582CQ42918409-CBC80D43-0D30-48BF-AAF4-EA7A0AE16705Q42918783-312CCB4C-F371-4696-A76F-B89A9ADAD410Q42919646-0C9710CF-7118-4C94-A14C-06125F4DE69BQ42919649-4C4B674E-0E40-44A6-9B74-84D09EEFD779Q42924812-ED593D72-80D3-4F23-96EF-6CAA42B023A7Q42925229-C1EE4092-435D-4484-A476-A1586E620C94Q42925550-B390FB25-D888-4BAC-AF24-C9FF9753DA8DQ42934059-B6D295D3-042D-488C-87E3-FCB4524AD05BQ42952311-2EAFD2D0-C5C8-4A2D-AED5-227638830D44
P2860
The stereochemistry of hexahydroprenol, ubiquinone and ergosterol biosynthesis in the mycelium of Aspergillus fumigatus Fresenius.
description
1967 nî lūn-bûn
@nan
1967年の論文
@ja
1967年学术文章
@wuu
1967年学术文章
@zh-cn
1967年学术文章
@zh-hans
1967年学术文章
@zh-my
1967年学术文章
@zh-sg
1967年學術文章
@yue
1967年學術文章
@zh
1967年學術文章
@zh-hant
name
The stereochemistry of hexahyd ...... pergillus fumigatus Fresenius.
@en
The stereochemistry of hexahyd ...... pergillus fumigatus Fresenius.
@nl
type
label
The stereochemistry of hexahyd ...... pergillus fumigatus Fresenius.
@en
The stereochemistry of hexahyd ...... pergillus fumigatus Fresenius.
@nl
prefLabel
The stereochemistry of hexahyd ...... pergillus fumigatus Fresenius.
@en
The stereochemistry of hexahyd ...... pergillus fumigatus Fresenius.
@nl
P2860
P356
P1433
P1476
The stereochemistry of hexahyd ...... pergillus fumigatus Fresenius.
@en
P2093
P2860
P356
10.1042/BJ1040043
P407
P577
1967-07-01T00:00:00Z