| Year |
Citation |
Score |
| 2023 |
Salim V, Jarecki SA, Vick M, Miller R. Advances in Metabolic Engineering of Plant Monoterpene Indole Alkaloids. Biology. 12. PMID 37626942 DOI: 10.3390/biology12081056 |
0.323 |
|
| 2022 |
Lashley A, Miller R, Provenzano S, Jarecki SA, Erba P, Salim V. Functional Diversification and Structural Origins of Plant Natural Product Methyltransferases. Molecules (Basel, Switzerland). 28. PMID 36615239 DOI: 10.3390/molecules28010043 |
0.367 |
|
| 2018 |
Salim V, Jones AD, DellaPenna D. Camptotheca acuminata 10-hydroxycamptothecin O-methyltransferase: an alkaloid biosynthetic enzyme coopted from flavonoid metabolism. The Plant Journal : For Cell and Molecular Biology. PMID 29681057 DOI: 10.1111/Tpj.13936 |
0.351 |
|
| 2018 |
Qu Y, Easson MEAM, Simionescu R, Hajicek J, Thamm AMK, Salim V, De Luca V. Solution of the multistep pathway for assembly of corynanthean, strychnos, iboga, and aspidosperma monoterpenoid indole alkaloids from 19-geissoschizine. Proceedings of the National Academy of Sciences of the United States of America. PMID 29511102 DOI: 10.1073/pnas.1719979115 |
0.417 |
|
| 2016 |
Sadre R, Magallanes-Lundback M, Pradhan S, Salim V, Mesberg A, Jones AD, DellaPenna D. Metabolite diversity in alkaloid biosynthesis: A multi-lane (diastereomer) highway for camptothecin synthesis in Camptotheca acuminata. The Plant Cell. PMID 27432874 DOI: 10.1105/Tpc.16.00193 |
0.355 |
|
| 2014 |
De Luca V, Salim V, Thamm A, Masada SA, Yu F. Making iridoids/secoiridoids and monoterpenoid indole alkaloids: progress on pathway elucidation. Current Opinion in Plant Biology. 19: 35-42. PMID 24709280 DOI: 10.1016/j.pbi.2014.03.006 |
0.324 |
|
| 2014 |
De Luca V, Salim V, Thamm A, Masada SA, Yu F. Making iridoids/secoiridoids and monoterpenoid indole alkaloids: progress on pathway elucidation. Current Opinion in Plant Biology. 19: 35-42. PMID 24709280 DOI: 10.1016/j.pbi.2014.03.006 |
0.324 |
|
| 2014 |
Salim V, Wiens B, Masada-Atsumi S, Yu F, De Luca V. 7-deoxyloganetic acid synthase catalyzes a key 3 step oxidation to form 7-deoxyloganetic acid in Catharanthus roseus iridoid biosynthesis. Phytochemistry. 101: 23-31. PMID 24594312 DOI: 10.1016/j.phytochem.2014.02.009 |
0.323 |
|
| 2014 |
Salim V, Wiens B, Masada-Atsumi S, Yu F, De Luca V. 7-deoxyloganetic acid synthase catalyzes a key 3 step oxidation to form 7-deoxyloganetic acid in Catharanthus roseus iridoid biosynthesis. Phytochemistry. 101: 23-31. PMID 24594312 DOI: 10.1016/j.phytochem.2014.02.009 |
0.323 |
|
| 2013 |
Besseau S, Kellner F, Lanoue A, Thamm AMK, Salim V, Schneider B, Geu-Flores F, Höfer R, Guirimand G, Guihur A, Oudin A, Glevarec G, Foureau E, Papon N, Clastre M, et al. A pair of tabersonine 16-hydroxylases initiates the synthesis of vindoline in an organ-dependent manner in Catharanthus roseus Plant Physiology. 163: 1792-1803. PMID 24108213 DOI: 10.1104/Pp.113.222828 |
0.358 |
|
| 2013 |
Asada K, Salim V, Masada-Atsumi S, Edmunds E, Nagatoshi M, Terasaka K, Mizukami H, De Luca V. A 7-deoxyloganetic acid glucosyltransferase contributes a key step in secologanin biosynthesis in Madagascar periwinkle. The Plant Cell. 25: 4123-34. PMID 24104568 DOI: 10.1105/tpc.113.115154 |
0.389 |
|
| 2013 |
Asada K, Salim V, Masada-Atsumi S, Edmunds E, Nagatoshi M, Terasaka K, Mizukami H, De Luca V. A 7-deoxyloganetic acid glucosyltransferase contributes a key step in secologanin biosynthesis in Madagascar periwinkle. The Plant Cell. 25: 4123-34. PMID 24104568 DOI: 10.1105/tpc.113.115154 |
0.389 |
|
| 2013 |
Salim V, Yu F, Altarejos J, De Luca V. Virus-induced gene silencing identifies Catharanthus roseus 7-deoxyloganic acid-7-hydroxylase, a step in iridoid and monoterpene indole alkaloid biosynthesis. The Plant Journal : For Cell and Molecular Biology. 76: 754-65. PMID 24103035 DOI: 10.1111/tpj.12330 |
0.423 |
|
| 2013 |
Salim V, Yu F, Altarejos J, De Luca V. Virus-induced gene silencing identifies Catharanthus roseus 7-deoxyloganic acid-7-hydroxylase, a step in iridoid and monoterpene indole alkaloid biosynthesis. The Plant Journal : For Cell and Molecular Biology. 76: 754-65. PMID 24103035 DOI: 10.1111/tpj.12330 |
0.423 |
|
| 2012 |
De Luca V, Salim V, Levac D, Atsumi SM, Yu F. Discovery and functional analysis of monoterpenoid indole alkaloid pathways in plants Methods in Enzymology. 515: 207-229. PMID 22999176 DOI: 10.1016/B978-0-12-394290-6.00010-0 |
0.352 |
|
| 2012 |
De Luca V, Salim V, Atsumi SM, Yu F. Mining the biodiversity of plants: A revolution in the making Science. 336: 1658-1661. PMID 22745417 DOI: 10.1126/science.1217410 |
0.368 |
|
| 2010 |
Roepke J, Salim V, Wu M, Thamm AM, Murata J, Ploss K, Boland W, De Luca V. Vinca drug components accumulate exclusively in leaf exudates of Madagascar periwinkle. Proceedings of the National Academy of Sciences of the United States of America. 107: 15287-92. PMID 20696903 DOI: 10.1073/Pnas.0911451107 |
0.324 |
|
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