about
Role of proline and GABA in sexual reproduction of angiospermsPhysiological implications of arginine metabolism in plantsSynthesis of 3-(4-Bromobenzyl)-5-(aryl methylene)-5H-furan-2-ones and their activity as inhibitors of the photosynthetic electron transport chain.Synthesis of photosynthesis-inhibiting nostoclide analogues.Molecular cloning and expression of Spirulina platensis acetohydroxy acid synthase genes in Escherichia coli.A metal-independent hydrolase from a Penicillium oxalicum strain able to use phosphonoacetic acid as the only phosphorus source.Requirement of proline synthesis during Arabidopsis reproductive development.Functional properties and structural characterization of rice δ(1)-pyrroline-5-carboxylate reductase.Functional characterization and expression analysis of rice δ(1)-pyrroline-5-carboxylate dehydrogenase provide new insight into the regulation of proline and arginine catabolismIntraspecific Variability of Floral Nectar Volume and Composition in Rapeseed (Brassica napus L. var. oleifera).Amino polyphosphonates - chemical features and practical uses, environmental durability and biodegradation.Nanostructured lipid carriers (NLC) for the delivery of natural molecules with antimicrobial activity: production, characterisation and in vitro studies.Quercetin and quercetin-3-O-glucoside interact with different components of the cAMP signaling cascade in human retinal pigment epithelial cells.High glucose-induced barrier impairment of human retinal pigment epithelium is ameliorated by treatment with Goji berry extracts through modulation of cAMP levels.Editorial: Amino Acids of the Glutamate Family: Functions beyond Primary Metabolism.Toward Unveiling the Mechanisms for Transcriptional Regulation of Proline Biosynthesis in the Plant Cell Response to Biotic and Abiotic Stress Conditions.Functional Characterization of Four Putative δ1-Pyrroline-5-Carboxylate Reductases from Bacillus subtilis.Differential responses in vitro of rice cultivars to Italian lineages of the blast pathogen Pyricularia grisea (Cooke) Sacc. 1. Oxidative burst.Plant P5C reductase as a new target for aminomethylenebisphosphonates.Differential in vitro responses of rice cultivars to Italian lineages of the blast pathogen Pyricularia grisea. 2. Aromatic biosynthesis.Amino acid content and nectar choice by forager honeybees (Apis mellifera L.).QSAR modeling of photosynthesis-inhibiting nostoclide derivatives.Effectiveness and mode of action of phosphonate inhibitors of plant glutamine synthetase.Phosphonate degradation by Spirulina strains: cyanobacterial biofilters for the removal of anticorrosive polyphosphonates from wastewater.Metabolism of the phosphonate herbicide glyphosate by a non-nitrate-utilizing strain of Penicillium chrysogenum.Development of new fungicides against Magnaporthe grisea: synthesis and biological activity of pyrazolo[3,4-d][1,3]thiazine, pyrazolo[1,5-c][1,3,5]thiadiazine, and pyrazolo[3,4-d]pyrimidine derivatives.Synthesis of pyrazole derivatives and their evaluation as photosynthetic electron transport inhibitors.Herbicidal pyridyl derivatives of aminomethylene-bisphosphonic acid inhibit plant glutamine synthetase.The role of [Delta]1-pyrroline-5-carboxylate dehydrogenase in proline degradation.Divergent properties and phylogeny of cyanobacterial 5-enol-pyruvyl-shikimate-3-phosphate synthases: evidence for horizontal gene transfer in the Nostocales.Synthesis and evaluation of effective inhibitors of plant δ1-pyrroline-5-carboxylate reductase.Synthesis and phytotoxic activity of ozonides.Biodegradation of the aminopolyphosphonate DTPMP by the cyanobacterium Anabaena variabilis proceeds via a C-P lyase-independent pathway.Tailoring the structure of aminobisphosphonates to target plant P5C reductase.Phosphonoacetate hydrolase from Penicillium oxalicum: purification and properties, phosphate starvation-independent expression, and partial sequencing.Design, synthesis, and activity of analogues of phosphinothricin as inhibitors of glutamine synthetase.Biochemical bases for a widespread tolerance of cyanobacteria to the phosphonate herbicide glyphosate.Phosphinothricin analogues as inhibitors of plant glutamine synthetases.Tailoring Natural Abenquines To Inhibit the Photosynthetic Electron Transport through Interaction with the D1 Protein in Photosystem II.Synthesis, theoretical studies, and effect on the photosynthetic electron transport of trifluoromethyl arylamides.
P50
Q26782889-9A883D25-8986-4989-9F5F-959FD9CE4941Q26797322-42708510-B4B7-4944-91AF-49B92DBB2332Q31132723-95D95291-BED2-41B6-98B2-F243EE9EA42DQ31149506-2C0AA6CC-EC8C-4A9A-BD89-7A9953FD8F74Q33388609-BBC2A5AA-FFBE-4328-8782-B5F77699EEFDQ34200454-3DF0F0ED-3EE7-4438-BBC9-5BB05FA167D4Q34444514-0FED063E-7862-4561-8042-529121D955DEQ35895886-B4B93820-1098-4C68-9F34-03837FC7DA8FQ35917725-F6E57CAA-8CC3-43F1-AA55-0A4D2C5650B8Q36689985-BFC825F7-3267-4792-ADAD-A1567892EA2BQ38236267-F248334F-0C0F-4F5E-936B-0BED64B8C904Q38720825-1BFDBA27-B97E-419B-BF0B-B16678B4B0D3Q38932106-5D4302E7-C2BC-4AFE-B220-EB824E8D86B3Q39042601-92AF7B16-2CC0-4C6F-87D9-D231403484BDQ39231213-5E1977A4-C49B-4B66-B96E-7F167499B062Q39381656-9675BA14-F965-44E3-9174-84AA818D7B74Q40086456-52E2158A-E02C-4AFD-85C3-405B6046FE0FQ42452115-F0954EEE-B3AD-4D90-8496-E2A2D699DAB7Q42619034-EA72E3C1-B491-4FFF-AF98-D1BF0AB70594Q43165186-65E02D40-13E1-4A3A-8625-25AE7701BDA1Q43187565-67887F2C-9A1A-4497-95D3-7102E6CA7796Q43268187-077FE571-E534-4EEB-AD6A-96CDB5F3D113Q43288247-E41233E0-9FB1-4BFA-82F6-C1BC0E234F89Q43336937-EF140FC3-91F0-430D-BE4E-A8FBEE91E095Q43740620-FB2A147A-B7D6-403E-9B6C-5443F071D30FQ44093616-D6E95510-E3F8-4900-9965-623F335C038BQ44821439-1817D1A8-B738-4A36-9094-CE2712E0AF73Q44908917-23ACC6EB-4A87-4C4B-9F5D-203A78B927DFQ45153601-6DFEC847-2D8E-4E61-83C1-366CDA34C640Q45738344-14820F3E-D9C4-40D0-BA35-74C5E4DF231BQ46052694-9CF3A148-37E5-4CE6-A194-DFAA278560BFQ46353665-6B6C7EB9-980A-47DF-9FF7-7DF9409DA861Q46451644-7CFDE3CC-1ECE-4123-ABA9-2B2770FDD647Q46655163-3A58AAEA-6EB5-4AD6-A2F7-ECB41BE394B5Q46675769-8B6F9EC7-4EAC-47C3-8C86-6ADDED0379FDQ46725642-09D84823-95AE-465B-A093-D6A7D07C6D71Q46761978-2FB6479F-8A29-4D44-BE59-84064B6E8BE5Q46920421-93E87DC0-DE10-4BB3-AE1B-29C154C6FA19Q47346067-E535B7FD-A9B2-40D6-8432-95AF571F11DFQ48094834-9766BFD4-F449-4BB2-84AF-6EEC571527B8
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Giuseppe Forlani
@ast
Giuseppe Forlani
@en
Giuseppe Forlani
@es
Giuseppe Forlani
@nl
Giuseppe Forlani
@sl
type
label
Giuseppe Forlani
@ast
Giuseppe Forlani
@en
Giuseppe Forlani
@es
Giuseppe Forlani
@nl
Giuseppe Forlani
@sl
prefLabel
Giuseppe Forlani
@ast
Giuseppe Forlani
@en
Giuseppe Forlani
@es
Giuseppe Forlani
@nl
Giuseppe Forlani
@sl
P1053
B-7869-2009
P106
P1153
7005906571
P21
P31
P3829
P496
0000-0003-2598-5718