Regulation of HMG-CoA reductase activity in plants.

Regulation of the mevalonate pathway

Goldstein, J. L., & Brown, M. S. (1990) · Nature · doi:10.1038/343425a0 · Cited by 5,394 · see citing works

Plant antitumor agents. VI. Isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia

Wani, M. C., Taylor, H. L., Wall, M. E., COGGON, P., & McPhail, A. T. (1971) · Journal of the American Chemical Society · doi:10.1021/ja00738a045 · Cited by 4,083 · see citing works

An Introduction to Plant Biochemistry

(1934) · Nature · doi:10.1038/134795b0 · Cited by 452 · see citing works

3-Hydroxy-3-methylglutaryl Coenzyme A Reductase

Brown, M. S., Dana, S. E., Dietschy, J. M., & Siperstein, M. D. (1973) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)43725-3 · Cited by 234 · see citing works

Differential Induction and Suppression of Potato 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Genes in Response to Phytophthora infestans and to Its Elicitor Arachidonic Acid

Choi, D., Ward, B., & Bostock, R. M. (1992) · The Plant Cell · doi:10.1105/tpc.4.10.1333 · Cited by 224 · see citing works

Growth and Differentiation in Plants

Phillips, I. D. J., & Wareing, P. F. (1985) · Medical Entomology and Zoology · Cited by 221 · see citing works

The Role of Plastids in Isoprenoid Biosynthesis

Kleinig, H. (1989) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.pp.40.060189.000351 · Cited by 207 · see citing works

Introduction of plant biochemistry

Brown, E. G. (1983) · Phytochemistry · doi:10.1016/s0031-9422(00)97730-6 · Cited by 197 · see citing works

Immunological evidence for eight spans in the membrane domain of 3-hydroxy-3-methylglutaryl coenzyme A reductase: implications for enzyme degradation in the endoplasmic reticulum

Roitelman, J., Olender, E. H., Bar‐Nun, S., Dunn, W. A., & Simoni, R. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.117.5.959 · Cited by 185 · see citing works

Current Topics in Plant Biochemistry and Physiology

Randall, D. D. (1988) · Cited by 180 · see citing works

Growth and Differentiation in Plants

Johnson, C. (1982) · Phytochemistry · doi:10.1016/0031-9422(82)85235-7 · Cited by 173 · see citing works

Control of Isoprenoid Biosynthesis in Higher Plants

Gray, J. C. (1988) · Advances in botanical research · doi:10.1016/s0065-2296(08)60270-0 · Cited by 170 · see citing works

Replacement of serine-871 of hamster 3-hydroxy-3-methylglutaryl-CoA reductase prevents phosphorylation by AMP-activated kinase and blocks inhibition of sterol synthesis induced by ATP depletion.

Sato, R., Goldstein, J. L., & Brown, M. S. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.20.9261 · Cited by 164 · see citing works

Isolation and structural characterization of a cDNA encoding Arabidopsis thaliana 3-hydroxy-3-methylglutaryl coenzyme A reductase

Caelles, C., Ferrer, A., Balcells, L., Hegardt, F. G., & Boronat, A. (1989) · Plant Molecular Biology · doi:10.1007/bf00016018 · Cited by 141 · see citing works

Tomato hydroxymethylglutaryl-CoA reductase is required early in fruit development but not during ripening.

Narita, J. O., & Gruissem, W. (1989) · The Plant Cell · doi:10.1105/tpc.1.2.181 · Cited by 141 · see citing works

Three genes encode 3-hydroxy-3-methylglutaryl-coenzyme A reductase in Hevea brasiliensis: hmg1 and hmg3 are differentially expressed

Chye, M., Tan, C.-T., & Chua, N. (1992) · Plant Molecular Biology · doi:10.1007/bf00023395 · Cited by 139 · see citing works

Induction of Sesquiterpenoid Biosynthesis in Tobacco Cell Suspension Cultures by Fungal Elicitor

Chappell, J., & Nable, R. O. (1987) · PLANT PHYSIOLOGY · doi:10.1104/pp.85.2.469 · Cited by 139 · see citing works

Differential activation of potato 3-hydroxy-3-methylglutaryl coenzyme A reductase genes by wounding and pathogen challenge.

Yang, Z., Park, H., Lacy, G. H., & Cramer, C. L. (1991) · The Plant Cell · doi:10.1105/tpc.3.4.397 · Cited by 118 · see citing works

Hydroxymethylglutaryl‐CoA reductase, a key enzyme in phytosterol synthesis?

Bach, T. J. (1986) · Lipids · doi:10.1007/bf02534307 · Cited by 117 · see citing works

Evidence for a protein kinase cascade in higher plants

MacKintosh, R. W., DAVIES, S. P., Clarke, P. R., WEEKES, J., Gillespie, J. G., Gibb, B. J. M., & Hardie, D. G. (1992) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1992.tb17364.x · Cited by 111 · see citing works

3-Hydroxy-3-methylglutaryl-coenzyme A reductase from Arabidopsis thaliana is structurally distinct from the yeast and animal enzymes.

Learned, R. M., & Fink, G. R. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.8.2779 · Cited by 111 · see citing works

Inhibition of degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase in vivo by cysteine protease inhibitors

Inoue, S., Bar‐Nun, S., Roitelman, J., & Simoni, R. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)98840-x · Cited by 108 · see citing works

Terpenoid Biosynthesis: The Basic Pathway and Formation of Monoterpenes, Sesquiterpenes, and Diterpenes

Gershenzon, J., & Croteau, R. (2018) · CRC Press eBooks · doi:10.1201/9781351074070-14 · Cited by 107 · see citing works

Involvement of 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase in the Regulation of Sesquiterpenoid Phytoalexin Synthesis in Potato

Stermer, B. A., & Bostock, R. M. (1987) · PLANT PHYSIOLOGY · doi:10.1104/pp.84.2.404 · Cited by 105 · see citing works

Effect of Brassinolide on Gene Expression in Elongating Soybean Epicotyls

Clouse, S. D., Zurek, D. M., McMorris, T. C., & Baker, M. E. (1992) · PLANT PHYSIOLOGY · doi:10.1104/pp.100.3.1377 · Cited by 101 · see citing works

Isoprenylation of the plant molecular chaperone ANJ1 facilitates membrane association and function at high temperature.

Zhu, J., Bressan, R. A., & Hasegawa, P. M. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.18.8557 · Cited by 87 · see citing works

Regulatory role of microsomal 3-hydroxy-3-methylglutaryl-coenzyme a reductase in a tobacco mutant that overproduces sterols

Gondet, L., Weber, T., Maillot-Vernier, P., Benveniste, P., & Bach, T. J. (1992) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(92)90829-a · Cited by 71 · see citing works

Expression of a 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Gene from Camptotheca acuminata Is Differentially Regulated by Wounding and Methyl Jasmonate

Burnett, R. J., Maldonado‐Mendoza, I. E., McKnight, T. D., & Nessler, C. L. (1993) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.1.41 · Cited by 71 · see citing works

Plastid 3-hydroxy-3-methylglutaryl coenzyme A reductase has distinctive kinetic and regulatory features: Properties of the enzyme and positive phytochrome control of activity in pea seedlings

Wong, R. J., Cormack, D. K. M., & Russell, D. W. (1982) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(82)90253-3 · Cited by 63 · see citing works

Effects of light on terpene hydrocarbon synthesis in Pinus pinaster

Gleizes, M., Pauly, G., Bernard-Dagan, C., & Jacques, R. (1980) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1980.tb02676.x · Cited by 62 · see citing works

Properties of microsomal 3-hydroxy-3-methylglutaryl coenzyme A reductase from Pisum sativum seedlings

Brooker, J. D., & Russell, D. W. (1975) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(75)90517-2 · Cited by 59 · see citing works

Structure and nucleotide sequence of tomato HMG2 encoding 3-hydroxy-3-methyl-glutaryl coenzyme A reductase

Park, H., Denbow, C. J., & Cramer, C. L. (1992) · Plant Molecular Biology · doi:10.1007/bf00014502 · Cited by 58 · see citing works

Carotenoid synthesis in mustard seedlings as controlled by phytochrome and inhibitors

Schnarrenberger, C., & Mohr, H. (1970) · Planta · doi:10.1007/bf00385762 · Cited by 57 · see citing works

Isolation and characterization of a cDNA encoding a 3-hydroxy-3-methylglutaryl coenzyme A reductase from Nicotiana sylvestris

Genschik, P., Criqui, M., Parmentier, Y., Marbach, J., Durr, A., Fleck, J., & Jamet, É. (1992) · Plant Molecular Biology · doi:10.1007/bf00014504 · Cited by 57 · see citing works

The red light controlled production of gibberellin in etiolated wheat leaves

LOVEYS, B. R., & Wareing, P. F. (1971) · Planta · doi:10.1007/bf00385343 · Cited by 54 · see citing works

Regulation of microsomal 3-hydroxy-3-methylglutaryl coenzyme A reductase from pea seedlings: Rapid posttranslational phytochrome-mediated decrease in activity and in vivo regulation by isoprenoid products

Brooker, J. D., & Russell, D. W. (1979) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(79)90425-9 · Cited by 53 · see citing works

Isolation and Characterization of cDNAs Encoding Wheat 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase

Aoyagi, K., Beyou, A., Moon, K., Fang, L. Y., & Ulrich, T. (1993) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.2.623 · Cited by 53 · see citing works

Some Properties of Enzymes Involved in the Biosynthesis and Metabolism of 3-Hydroxy-3-Methylglutaryl-CoA in Plants

Bach, T. J., Weber, T., & Motel, A. (1990) · Springer eBooks · doi:10.1007/978-1-4684-8789-3_1 · Cited by 51 · see citing works

3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Activity in Ochromonas malhamensis

Maurey, K. M., Wolf, F., & Golbeck, J. H. (1986) · PLANT PHYSIOLOGY · doi:10.1104/pp.82.2.523 · Cited by 51 · see citing works

Regulation of cytosolic HMG-CoA reductase activity in pea seedlings: Contrasting responses to different hormones, and hormone-product interaction, suggest hormonal modulation of activity

Russell, D. W., & Davidson, H. (1982) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(82)91426-7 · Cited by 49 · see citing works

Induction of 3-Hydroxy-3-methylglutaryl CoA Reductase in Potato Tubers after Slicing, Fungal Infection or Chemical Treatment, and Some Properties of the Enzyme

Ôba, K., Kondo, K., Noriyuki Doke, A., & Uritani, I. (1985) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a076982 · Cited by 47 · see citing works

The occurrence and some properties of 3-hydroxy-3-methylglutaryl coenzyme A reductase in sweet potato roots infected by Ceratocystis fimbriata

Suzuki, H., Oba, K., & Uritani, I. (1975) · Physiological Plant Pathology · doi:10.1016/0048-4059(75)90031-4 · Cited by 45 · see citing works

Steroid glycoalkaloids and related compounds as potato quality factors

Kuć, J. (1984) · American Journal of Potato Research · doi:10.1007/bf02854034 · Cited by 38 · see citing works

Hydroxymethylglutaryl coA reductase (NADPH) in the latex of Hevea brasiliensis

Sipat, A. B. (1982) · Phytochemistry · doi:10.1016/0031-9422(82)83087-2 · Cited by 31 · see citing works

Phytochrome-mediated production of monoterpenes in thyme seedlings

Tanaka, S., Yamaura, T., 繁本, 令., & Tabata, M. (1989) · Phytochemistry · doi:10.1016/0031-9422(89)80260-2 · Cited by 31 · see citing works

Characterization of 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Activity during Maize Seed Development, Germination, and Seedling Emergence

Moore, K. B., & Oishi, K. K. (1993) · PLANT PHYSIOLOGY · doi:10.1104/pp.101.2.485 · Cited by 31 · see citing works

Differential Induction and Suppression of Potato 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Genes in Response to Phytophthora infestans and to Its Elicitor Arachidonic Acid

Choi, D., Ward, B. L., & Bostock, R. M. (1992) · The Plant Cell · doi:10.2307/3869418 · Cited by 26 · see citing works

Analysis of elicitor-inducible transcripts encoding 3-hydroxy-3-methylglutaryl coenzyme A reductase in potato

Stermer, B. A., Edwards, L. A., Edington, B. V., & Dixon, R. A. (1991) · Physiological and Molecular Plant Pathology · doi:10.1016/0885-5765(91)90024-c · Cited by 25 · see citing works

Molecular Cloning and Characterization of Plant 3-Hydroxy-3-Methylglutaryl Coenzyme a Reductase

Monfar, M., Caelles, C., Balcells, L., Ferrer, A., Hegardt, F. G., & Boronat, A. (1990) · Springer eBooks · doi:10.1007/978-1-4684-8789-3_2 · Cited by 21 · see citing works

Application of modified Lineweaver-Burk plots to studies of kinetics and regulation of radish 3-hydroxy-3-methylglutaryl-CoA reductase

Bach, T. J., & Lichtenthaler, H. K. (1984) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(84)90308-4 · Cited by 21 · see citing works

Effect of auxin on the metabolism of mevalonic acid in suspension-cultured carrot cells

Nishi, A., & Tsuritani, I. (1983) · Phytochemistry · doi:10.1016/0031-9422(83)83011-8 · Cited by 21 · see citing works

Tomato Hydroxymethylglutaryl-CoA Reductase Is Required Early in Fruit Development but Not during Ripening

Narita, J. O., & Gruissem, W. (1989) · The Plant Cell · doi:10.2307/3869034 · Cited by 21 · see citing works

Properties and Molecular Cloning of Plant HMG-CoA Reductase

Narita, J., Wettstein, A., Bach, T. J., Ferrer, A., Boronat, A., Enjuto, M., & Gruissem, W. (1992) · AOCS Publishing eBooks · doi:10.1201/9781439821831.ch2 · Cited by 20 · see citing works

Participation of Phytochrome in the Photoregulation of Terpenoid Synthesis in Thyme Seedlings

Yamaura, T., TANAKA, S. M., & Tabata, M. (1991) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a078122 · Cited by 18 · see citing works

Hevea calmodulin: Regulation of the activity of latex 3-hydroxy-3-methylglutaryl coenzyme a reductase

Wititsuwannakul, R., Wititsuwannakul, D., & Dumkong, S. (1990) · Phytochemistry · doi:10.1016/0031-9422(90)85009-5 · Cited by 18 · see citing works

Differential Activation of Potato 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Genes by Wounding and Pathogen Challenge

Yang, Z., Park, H., Lacy, G. H., & Cramer, C. L. (1991) · The Plant Cell · doi:10.2307/3869214 · Cited by 12 · see citing works

Network Analysis of the MVA and MEP Pathways for Isoprenoid Synthesis

Vranová, E., Coman, D., & Gruissem, W. (2013) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050312-120116 · Cited by 1,168 · see citing works

Cross-talk between the Cytosolic Mevalonate and the Plastidial Methylerythritol Phosphate Pathways in Tobacco Bright Yellow-2 Cells

Hemmerlin, A., Hoeffler, J., Meyer, O., Tritsch, D., Kagan, I. A., Grosdemange‐Billiard, C., Rohmer, M., & Bach, T. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302526200 · Cited by 436 · see citing works

Biosynthesis and biotechnological production of ginsenosides

Kim, Y.-J., Zhang, D., & Yang, D. (2015) · Biotechnology Advances · doi:10.1016/j.biotechadv.2015.03.001 · Cited by 387 · see citing works

A raison d’être for two distinct pathways in the early steps of plant isoprenoid biosynthesis?

Hemmerlin, A., Harwood, J. L., & Bach, T. J. (2011) · Progress in Lipid Research · doi:10.1016/j.plipres.2011.12.001 · Cited by 356 · see citing works

The potential of the mevalonate pathway for enhanced isoprenoid production

Liao, P., Hemmerlin, A., Bach, T. J., & Chye, M. (2016) · Biotechnology Advances · doi:10.1016/j.biotechadv.2016.03.005 · Cited by 332 · see citing works

Some new aspects of isoprenoid biosynthesis in plants—A review

Bach, T. J. (1995) · Lipids · doi:10.1007/bf02537822 · Cited by 301 · see citing works

Plant sterols: Diversity, biosynthesis, and physiological functions

Valitova, Y. N., Sulkarnayeva, A. G., & Minibayeva, F. V. (2016) · Biochemistry (Moscow) · doi:10.1134/s0006297916080046 · Cited by 297 · see citing works

Squalene – biochemistry, molecular biology, process biotechnology, and applications

Spanova, M., & Daum, G. (2011) · European Journal of Lipid Science and Technology · doi:10.1002/ejlt.201100203 · Cited by 268 · see citing works

Isoprenoids: Remarkable diversity of form and function

Holstein, S. A., & Hohl, R. J. (2004) · Lipids · doi:10.1007/s11745-004-1233-3 · Cited by 249 · see citing works

Terpene Specialized Metabolism inArabidopsis thaliana

Tholl, D., & Lee, S. (2011) · The Arabidopsis Book · doi:10.1199/tab.0143 · Cited by 244 · see citing works

Catharanthus terpenoid indole alkaloids: biosynthesis and regulation

El-Sayed, M., & Verpoorte, R. (2007) · Phytochemistry Reviews · doi:10.1007/s11101-006-9047-8 · Cited by 240 · see citing works

Expression of the Hevea brasiliensis (H.B.K.) Mull. Arg. 3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase 1 in Tobacco Results in Sterol Overproduction

Schaller, H., Grausem, B., Benveniste, P., Chye, M. L., Tan, C. T., Song, Y. H., & Chua, N. H. (1995) · Plant Physiology · doi:10.1104/pp.109.3.761 · Cited by 230 · see citing works

Natural rubber biosynthesis in plants, the rubber transferase complex, and metabolic engineering progress and prospects

Cherian, S., Ryu, S. B., & Cornish, K. (2019) · Plant Biotechnology Journal · doi:10.1111/pbi.13181 · Cited by 221 · see citing works

Prenylation-dependent Association of Protein-tyrosine Phosphatases PRL-1, -2, and -3 with the Plasma Membrane and the Early Endosome

Zeng, Q., Si, X., Horstmann, H., Xu, Y., Hong, W., & Pallen, C. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m000453200 · Cited by 210 · see citing works

3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase1 Interacts with NORK and Is Crucial for Nodulation in Medicago truncatula

Kevei, Z., Lougnon, G., Mergaert, P., Horváth, G. V., Kereszt, A., Jayaraman, D., Zaman, N., Marcel, F., Regulski, K., Kiss, G. B., et al. (2007) · The Plant Cell · doi:10.1105/tpc.107.053975 · Cited by 194 · see citing works

Monoterpene and sesquiterpene biosynthesis in glandular trichomes of peppermint (Mentha x piperita) rely exclusively on plastid-derived isopentenyl diphosphate

McCaskill, D. G., & Croteau, R. (1995) · Planta · doi:10.1007/bf00239938 · Cited by 179 · see citing works

Arabidopsis thaliana Contains Two Differentially Expressed Farnesyl-Diphosphate Synthase Genes

Cunillera, N., Arró, M., Delourme, D., Karst, F., Boronat, A., & Ferrer, A. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.13.7774 · Cited by 175 · see citing works

The Arabidopsis thaliana FPS1 Gene Generates a Novel mRNA That Encodes a Mitochondrial Farnesyl-diphosphate Synthase Isoform

Cunillera, N., Boronat, A., & Ferrer, A. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.24.15381 · Cited by 172 · see citing works

Functional Analysis of 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Encoding Genes in Triterpene Saponin-Producing Ginseng

Kim, Y.-J., Lee, O. R., Oh, J. Y., Jang, M.-G., & Yang, D. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.222596 · Cited by 161 · see citing works

Advances and challenges in ginseng research from 2011 to 2020: the phytochemistry, quality control, metabolism, and biosynthesis

Li, X., Liu, J., Zuo, T., Hu, Y., Li, Z., Wang, H.-D., Xu, X., Yang, W., & Guo, D. (2022) · Natural Product Reports · doi:10.1039/d1np00071c · Cited by 155 · see citing works

Towards efficient terpenoid biosynthesis: manipulating IPP and DMAPP supply

Wang, Q., Quan, S., & Xiao, H. (2019) · Bioresources and Bioprocessing · doi:10.1186/s40643-019-0242-z · Cited by 152 · see citing works

Isopentenyl diphosphate isomerase: a core enzyme in isoprenoid biosynthesis. A review of its biochemistry and function

Ramos-Valdivia, A. C., van der Heijden, R., & Verpoorte, R. (1997) · Natural Product Reports · doi:10.1039/np9971400591 · Cited by 150 · see citing works

A role for the mevalonate pathway in early plant symbiotic signaling

Venkateshwaran, M., Jayaraman, D., Chabaud, M., Genre, A., Balloon, A. J., Maëda, J., Forshey, K. L., den Os, D., Kwiecien, N. W., Coon, J. J., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1413762112 · Cited by 148 · see citing works

The biology of HMG-CoA reductase: the pros of contra-regulation

Hampton, R., Dimster-Denk, D., & Rine, J. (1996) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(96)80168-x · Cited by 147 · see citing works

Comparative proteomics of glycosomes from bloodstream form and procyclic culture form Trypanosoma brucei brucei

Colasante, C., Ellis, M., Ruppert, T., & Voncken, F. G. J. (2006) · PROTEOMICS · doi:10.1002/pmic.200500668 · Cited by 142 · see citing works

Relative expression of genes of terpene metabolism in different tissues of Artemisia annuaL

Olofsson, L., Engström, A., Lundgren, A., & Brodelius, P. E. (2011) · BMC Plant Biology · doi:10.1186/1471-2229-11-45 · Cited by 144 · see citing works

Biosynthesis of anthraquinones in cell cultures of the Rubiaceae

Han, Y.-S., van der Heijden, R., & Verpoorte, R. (2001) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1023/a:1012758922713 · Cited by 142 · see citing works

Biosynthetic pathways of triterpenoids and strategies to improve their Biosynthetic Efficiency

Noushahi, H. A., Khan, A. H., Noushahi, U. F., Hussain, M., Javed, T., Zafar, M., Batool, M., Ahmed, U., Liu, K., Harrison, M. T., et al. (2022) · Plant Growth Regulation · doi:10.1007/s10725-022-00818-9 · Cited by 140 · see citing works

Inhibition of Squalene Synthase and Squalene Epoxidase in Tobacco Cells Triggers an Up-Regulation of 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase

Wentzinger, L., Bach, T. J., & Hartmann, M.-A. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.004655 · Cited by 135 · see citing works

Why Do Plants Convert Sitosterol to Stigmasterol?

Aboobucker, S. I., & Suza, W. P. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00354 · Cited by 127 · see citing works

Bacterial Expression of the Catalytic Domain of 3–Hydroxy‐3–Methylglutaryl‐CoA Reductase (Isoform HMGR1) from Arabidopsis thaliana , and Its Inactivation by Phosphorylation at Ser577 by Brassica oleracea 3‐Hydroxy‐3‐Methylglutaryl‐CoA Reductase Kinase

Dale, S. J., Arró, M., Becerra, B., MORRICE, N. A., Boronat, A., Hardie, D. G., & Ferrer, A. (1995) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1995.506_2.x · Cited by 129 · see citing works

Laticifer-Specific cis-Prenyltransferase Silencing Affects the Rubber, Triterpene, and Inulin Content of Taraxacum brevicorniculatum

Post, J., van Deenen, N., Fricke, J., Kowalski, N., Wurbs, D., Schaller, H., Eisenreich, W., Huber, C., Twyman, R. M., Prüfer, D., et al. (2012) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.187880 · Cited by 129 · see citing works

The Isogene 1-Deoxy-D-Xylulose 5-Phosphate Synthase 2 Controls Isoprenoid Profiles, Precursor Pathway Allocation, and Density of Tomato Trichomes

Paetzold, H., Garms, S., Bartram, S., Wieczorek, J., Urós-Gracia, E.-M., Rodrı́guez-Concepción, M., Boland, W., Strack, D., Hause, B., & Walter, M. H. (2010) · Molecular Plant · doi:10.1093/mp/ssq032 · Cited by 126 · see citing works

Multilevel Control of Arabidopsis 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase by Protein Phosphatase 2A

Leivar, P., Antolín‐Llovera, M., Ferrero, S., Closa, M., Arró, M., Ferrer, A., Boronat, A., & Campos, N. (2011) · The Plant Cell · doi:10.1105/tpc.110.074278 · Cited by 124 · see citing works

Overexpression of Arabidopsis thaliana farnesyl diphosphate synthase (FPS1S) in transgenic Arabidopsis induces a cell death/senescence‐like response and reduced cytokinin levels

Masferrer, A., Arró, M., Manzano, D., Schaller, H., Fernàndez‐Busquets, X., Moncaleán, P., Fernández, B., Cunillera, N., Boronat, A., & Ferrer, A. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01273.x · Cited by 112 · see citing works

Prospects for the bioengineering of isoprenoid biosynthesis

McCaskill, D. G., & Croteau, R. (1997) · Advances in biochemical engineering, biotechnology · doi:10.1007/bfb0102064 · Cited by 111 · see citing works

Some caveats for bioengineering terpenoid metabolism in plants

McCaskill, D. G., & Croteau, R. (1998) · Trends in biotechnology · doi:10.1016/s0167-7799(98)01231-1 · Cited by 110 · see citing works

Biosynthesis of Mevalonic Acid from Acetyl-CoA

Bochar, D. A., Freisen, J., Stauffacher, C. V., & Rodwell, V. W. (1999) · Elsevier eBooks · doi:10.1016/b978-0-08-091283-7.00035-7 · Cited by 109 · see citing works

The integration of GC–MS and LC–MS to assay the metabolomics profiling in Panax ginseng and Panax quinquefolius reveals a tissue- and species-specific connectivity of primary metabolites and ginsenosides accumulation

Liu, J., Liu, Y., Wang, Y., Abozeid, A., Zu, Y., & Tang, Z. (2016) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2016.12.026 · Cited by 106 · see citing works

The Arabidopsis thaliana FPP synthase isozymes have overlapping and specific functions in isoprenoid biosynthesis, and complete loss of FPP synthase activity causes early developmental arrest

Closa, M., Vranová, E., Bortolotti, C., Bigler, L., Arró, M., Ferrer, A., & Gruissem, W. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04253.x · Cited by 106 · see citing works

Enhancement of seed phytosterol levels by expression of an N‐terminal truncated Hevea brasiliensis (rubber tree) 3‐hydroxy‐3‐methylglutaryl‐CoA reductase

Harker, M., Holmberg, N., Clayton, J. C., Gibbard, C. L., Wallace, A. D., Rawlins, S., Hellyer, S. A., Lanot, A., & Safford, R. (2003) · Plant Biotechnology Journal · doi:10.1046/j.1467-7652.2003.00011.x · Cited by 100 · see citing works

Natural rubber-producing sources, systems, and perspectives for breeding and biotechnology studies of Taraxacum kok-saghyz

Salehi, M., Cornish, K., Bahmankar, M., & Naghavi, M. R. (2021) · Industrial Crops and Products · doi:10.1016/j.indcrop.2021.113667 · Cited by 93 · see citing works

Expression of the Arabidopsis HMG2 Gene, Encoding 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase, Is Restricted to Meristematic and Floral Tissues

Enjuto, M., Lumbreras, V., Marín, C., & Boronat, A. (1995) · The Plant Cell · doi:10.1105/tpc.7.5.517 · Cited by 92 · see citing works

Cloning and characterization of cDNA encoding farnesyl diphosphate synthase from rubber tree (Hevea brasiliensis)

Adiwilaga, K. D., & Kush, A. K. (1996) · Plant Molecular Biology · doi:10.1007/bf00020805 · Cited by 89 · see citing works

The biosynthesis of steroids and triterpenoids

Brown, G. D. (1998) · Natural Product Reports · doi:10.1039/a815653y · Cited by 88 · see citing works

Resistance to Botrytis cinerea in Solanum lycopersicoides involves widespread transcriptional reprogramming

Smith, J. E., Mengesha, B., Tang, H. P., Mengiste, T. D., & Bluhm, B. H. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-334 · Cited by 86 · see citing works

Targeting and Topology in the Membrane of Plant 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase

Campos, N., & Boronat, A. (1995) · The Plant Cell · doi:10.1105/tpc.7.12.2163 · Cited by 86 · see citing works

Non-transgenic Gene Modulation via Spray Delivery of Nucleic Acid/Peptide Complexes into Plant Nuclei and Chloroplasts

Thagun, C., Horii, Y., Mori, M., Fujita, S., Ohtani, M., Tsuchiya, K., Kodama, Y., Odahara, M., & Numata, K. (2022) · ACS Nano · doi:10.1021/acsnano.1c07723 · Cited by 84 · see citing works

Potato steroidal glycoalkaloid levels and the expression of key isoprenoid metabolic genes

Krits, P., Fogelman, E., & Ginzberg, I. (2007) · Planta · doi:10.1007/s00425-007-0602-3 · Cited by 84 · see citing works

Label‐free deep shotgun proteomics reveals protein dynamics during tomato fruit tissues development

Szymański, J., Levin, Y., Savidor, A., Breitel, D., Chappell‐Maor, L., Heinig, U., Töpfer, N., & Aharoni, A. (2017) · The Plant Journal · doi:10.1111/tpj.13490 · Cited by 81 · see citing works

Secondary Metabolism

Verpoorte, R. (2000) · Springer eBooks · doi:10.1007/978-94-015-9423-3_1 · Cited by 80 · see citing works

Nuclear Calcium Signaling in Plants

Charpentier, M., & Oldroyd, G. E. D. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.220863 · Cited by 79 · see citing works

Metabolic engineering for the production of isoprene and isopentenol by Escherichia coli

Li, M., Nian, R., Xian, M., & Zhang, H. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-9200-5 · Cited by 79 · see citing works

Mevalonate Biosynthesis in Plants

Bach, T. J., Boronat, A., Campos, N., Ferrer, A., & Vollack, K. (1999) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409239991209237 · Cited by 79 · see citing works

Chapter 3 Biosynthesis of Terpenoid Indole Alkaloids in Catharanthus roseus Cells

Verpoorte, R., van der Heijden, R., & Moreno, P. R. H. (1997) · The Alkaloids. Chemistry and physiology · doi:10.1016/s0099-9598(08)60017-6 · Cited by 74 · see citing works

PLEIOTROPIC REGULATORY LOCUS 1 (PRL1) Integrates the Regulation of Sugar Responses with Isoprenoid Metabolism in Arabidopsis

Flores-Pérez, Ú., Pérez-Gil, J., Closa, M., Wright, L. P., Botella‐Pavía, P., Phillips, M. A., Ferrer, A., Gershenzon, J., & Rodrı́guez-Concepción, M. (2009) · Molecular Plant · doi:10.1093/mp/ssp100 · Cited by 74 · see citing works

Effects of mevinolin on cell cycle progression and viability of tobacco BY‐2 cells

Hemmerlin, A., & Bach, T. J. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00095.x · Cited by 69 · see citing works

Cloning and Characterization of a Root-specific Expressing Gene Encoding 3-hydroxy-3-methylglutaryl Coenzyme a Reductase from Ginkgo biloba

Shen, G., Pang, Y., Wu, W., Liao, Z., Zhao, L., Sun, X., & Tang, K. (2006) · Molecular Biology Reports · doi:10.1007/s11033-006-0014-7 · Cited by 68 · see citing works

Stable heterologous expression of biologically active terpenoids in green plant cells

Ikram, N. K. K., Zhan, X., Pan, X., King, B. C., & Simonsen, H. T. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00129 · Cited by 68 · see citing works

Chemopreventive effects of β-ionone and geraniol during rat hepatocarcinogenesis promotion: distinct actions on cell proliferation, apoptosis, HMGCoA reductase, and RhoA

Cardozo, M. T., de Conti, A., Ong, T. P., Scolastici, C., Purgatto, E., Horst, M. A., Bassoli, B. K., & Moreno, F. S. (2010) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2009.12.007 · Cited by 68 · see citing works

Farnesol-Induced Cell Death and Stimulation of 3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase Activity in Tobacco cv Bright Yellow-2 Cells,

Hemmerlin, A., & Bach, T. J. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.123.4.1257 · Cited by 66 · see citing works

Cloning of cDNAs or genes encoding enzymes of sterol biosynthesis from plants and other eukaryotes: Heterologous expression and complementation analysis of mutations for functional characterization

Bach, T. J., & Benveniste, P. (1997) · Progress in Lipid Research · doi:10.1016/s0163-7827(97)00009-x · Cited by 65 · see citing works

Developmental and light‐regulated post‐translational control of 3‐hydroxy‐3‐methylglutaryl‐CoA reductase levels in potato

Korth, K. L., Jaggard, D. A. W., & Dixon, R. A. (2000) · The Plant Journal · doi:10.1046/j.1365-313x.2000.00821.x · Cited by 63 · see citing works

The Morphoregulatory Role of Thidiazuron: Metabolomics-Guided Hypothesis Generation for Mechanisms of Activity

Erland, L. A. E., Giebelhaus, R. T., Victor, J. M. R., Murch, S. J., & Saxena, P. K. (2020) · Biomolecules · doi:10.3390/biom10091253 · Cited by 60 · see citing works

Molecular cloning and expression analysis of the mevalonate kinase gene from Arabidopsis thaliana

Lluch, M., Masferrer, A., Arró, M., Boronat, A., & Ferrer, A. (2000) · Plant Molecular Biology · doi:10.1023/a:1006325630792 · Cited by 59 · see citing works

Induction of potato steroidal glycoalkaloid biosynthetic pathway by overexpression of cDNA encoding primary metabolism HMG-CoA reductase and squalene synthase

Ginzberg, I., Thippeswamy, M., Fogelman, E., Demirel, U., Mweetwa, A. M., Tokuhisa, J. G., & Veilleux, R. E. (2011) · Planta · doi:10.1007/s00425-011-1578-6 · Cited by 59 · see citing works

Sterol partitioning by HMGR and DXR for routing intermediates toward withanolide biosynthesis

Singh, S., Pal, S., Shanker, K., Chanotiya, C. S., Gupta, M. M., Dwivedi, U. N., & Shasany, A. K. (2014) · Physiologia Plantarum · doi:10.1111/ppl.12213 · Cited by 59 · see citing works

Arabidopsis 3-hydroxy-3-methylglutaryl-CoA reductase is regulated at the post-translational level in response to alterations of the sphingolipid and the sterol biosynthetic pathways

Nieto, B., Forés, O., Arró, M., & Ferrer, A. (2008) · Phytochemistry · doi:10.1016/j.phytochem.2008.10.010 · Cited by 59 · see citing works

Analysis of the first Taraxacum kok-saghyz transcriptome reveals potential rubber yield related SNPs

Luo, Z., Iaffaldano, B. J., Zhuang, X., Fresnedo‐Ramírez, J., & Cornish, K. (2017) · Scientific Reports · doi:10.1038/s41598-017-09034-2 · Cited by 58 · see citing works

Expression of 3-hydroxy-3-methylglutaryl-CoA reductase, p-hydroxybenzoate-m-geranyltransferase and genes of phenylpropanoid pathway exhibits positive correlation with shikonins content in arnebia [Arnebia euchroma (Royle) Johnston]

Singh, R. S., Gara, R. K., Bhardwaj, P. K., Kaachra, A., Malik, S., Kumar, R. S., Sharma, M., Ahuja, P. S., & Kumar, S. (2010) · BMC Molecular Biology · doi:10.1186/1471-2199-11-88 · Cited by 55 · see citing works

HMG-CoA reductase gene families that differentially accumulate transcripts in potato tubers are developmentally expressed in floral tissues

Korth, K. L., Stermer, B. A., Bhattacharyya, M. K., & Dixon, R. A. (1997) · Plant Molecular Biology · doi:10.1023/a:1005743011651 · Cited by 55 · see citing works

Harnessing evolutionary diversification of primary metabolism for plant synthetic biology

Maeda, H. A. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.rev119.006132 · Cited by 54 · see citing works

Molecular characterization of three 3-hydroxy-3-methylglutaryl-CoA reductase genes including pathogen-induced Hmg2 from pepper (Capsicum annuum)

Ha, S., Kim, J., Hwang, Y.-S., & Lee, S.-W. (2003) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/s0167-4781(02)00624-3 · Cited by 53 · see citing works

Biosynthetic Pathway of Insect Juvenile Hormone III in Cell Suspension Cultures of the Sedge Cyperus iria

Bede, J. C., Teal, P. E. A., Goodman, W. G., & Tobe, S. S. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.010264 · Cited by 52 · see citing works

Co-ordinate regulation of sterol biosynthesis enzyme activity during accumulation of sterols in developing rape and tobacco seed

Harker, M., Hellyer, A., Clayton, J. C., Duvoix, A., Lanot, A., & Safford, R. (2003) · Planta · doi:10.1007/s00425-002-0913-3 · Cited by 51 · see citing works

Regulatory role of microsomal 3-hydroxy-3-methylglutaryl-coenzyme A reductase for shikonin biosynthesis in Lithospermum erythrorhizon cell suspension cultures

Lange, B. M., Severin, K., Bechthold, A., & Heide, L. E. (1998) · Planta · doi:10.1007/s004250050252 · Cited by 51 · see citing works

Mitochondrial Localization of the Mevalonate Pathway Enzyme 3-Hydroxy-3-methyl-glutaryl-CoA Reductase in the Trypanosomatidae

Peña-Dı́az, J., Montalvetti, A., Flores, C., Constán, A., Hurtado‐Guerrero, R., de Souza, W., Gancedo, C., Ruiz-Pérez, L. M., & González‐Pacanowska, D. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-10-0720 · Cited by 48 · see citing works

Molecular characterization of three differentially expressed members of the Camptotheca acuminata 3-hydroxy-3-methylglutaryl CoA reductase (HMGR) gene family

Maldonado‐Mendoza, I. E., Vincent, R. M., & Nessler, C. L. (1997) · Plant Molecular Biology · doi:10.1023/a:1005866813347 · Cited by 47 · see citing works

Uncovering mechanisms of rubber biosynthesis in Taraxacum koksaghyz – role of cis‐prenyltransferase‐like 1 protein

Niephaus, E., Müller, B., van Deenen, N., Lassowskat, I., Bonin, M., Finkemeier, I., Prüfer, D., & Gronover, C. S. (2019) · The Plant Journal · doi:10.1111/tpj.14471 · Cited by 46 · see citing works

Enhancement of triterpenoid saponins biosynthesis in Panax notoginseng cells by co-overexpressions of 3-hydroxy-3-methylglutaryl CoA reductase and squalene synthase genes

Deng, B., Zhang, P., Ge, F., Liu, D., & Chen, C. (2017) · Biochemical Engineering Journal · doi:10.1016/j.bej.2017.03.001 · Cited by 45 · see citing works

From Soybean Phytosterols to Steroid Hormones

Wang, F., Kang, Y., & Wei, D. (2011) · InTech eBooks · doi:10.5772/18808 · Cited by 45 · see citing works

Cloning of hmg1 and hmg2 cDNAs encoding 3-hydroxy-3-methylglutaryl coenzyme A reductase and their expression and activity in relation to α-farnesene synthesis in apple

Rupasinghe, H. P. V., Almquist, K. C., Paliyath, G., & Murr, D. P. (2001) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(01)01316-x · Cited by 43 · see citing works

Biochemistry of Terpenoids: Monoterpenes, Sesquiterpenes, Diterpenes, Sterols, Cardiac Glycosides and Steroid Saponins

Gershenzon, J., & Kreis, W. (2017) · Annual Plant Reviews online · doi:10.1002/9781119312994.apr0016 · Cited by 42 · see citing works

Expressional diversity of grapevine 3-Hydroxy-3-methylglutaryl-CoA reductase (VvHMGR) in different grapes genotypes

Zheng, T., Guan, L., Yu, K., Haider, M. S., Nasim, M., Liu, Z., Li, T., Zhang, K., Jiu, S., Jia, H., et al. (2021) · BMC Plant Biology · doi:10.1186/s12870-021-03073-8 · Cited by 40 · see citing works

Cloning of a cDNA Encoding Cytosolic Acetoacetyl-Coenzyme A Thiolase from Radish by Functional Expression in Saccharomyces cerevisiae

Vollack, K., & Bach, T. J. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.4.1097 · Cited by 40 · see citing works

Activation of the cholesterol pathway and Ras maturation in response to stress

Shack, S., Gorospe, M., Fawcett, T. W., Hudgins, W. R., & Holbrook, N. J. (1999) · Oncogene · doi:10.1038/sj.onc.1203002 · Cited by 39 · see citing works

The history, beneficial ingredients, mechanism, processing, and products of Panax ginseng for medicinal and edible value

Zhang, Z.-B., Chen, Y., Wang, H., Jia, X., Wu, W., Pang, S.-T., Li, W., Zahoor, S., Khan, W., Liu, Y.-C., et al. (2024) · Food & medicine homology. · doi:10.26599/fmh.2025.9420059 · Cited by 38 · see citing works

Cloning and characterisation of the gene encoding HMG-CoA reductase from Taxus media and its functional identification in yeast

Liao, Z., Tan, Q., Chai, Y., Zuo, K., Chen, M., Gong, Y., Wang, P., ., Y. P., Tan, F., Sun, X., et al. (2004) · Functional Plant Biology · doi:10.1071/fp03153 · Cited by 38 · see citing works

5 Sterol metabolism and functions in higher plants

Hartmann, M.-A. (2003) · Topics in current genetics · doi:10.1007/978-3-540-40999-1_6 · Cited by 38 · see citing works

Expression Profiling in Pinus pinaster in Response to Infection with the Pine Wood Nematode Bursaphelenchus xylophilus

Gaspar, D., Trindade, C. S., Usié, A., Meireles, B., Barbosa, P., Fortes, A. M., Pesquita, C., Costa, R. M. L., & Ramos, A. M. (2017) · Forests · doi:10.3390/f8080279 · Cited by 37 · see citing works

CRISPR-Cas9-mediated disruption of the HMG-CoA reductase genes of Mucor circinelloides and subcellular localization of the encoded enzymes

Nagy, G., Vaz, A. G., Szebenyi, C., Takó, M., Tóth, E. J., Csernetics, Á., Bencsik, O., Szekeres, A., Homa, M., Ayaydin, F., et al. (2019) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2019.04.008 · Cited by 37 · see citing works

Enzymology of Phytosterol Transformations

Nes, W. D., & Venkatramesh, M. (1999) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409239991209219 · Cited by 37 · see citing works

Integrative Network Analysis of the Signaling Cascades in Seedling Leaves of Bread Wheat by Large-Scale Phosphoproteomic Profiling

Lv, D., Ge, P., Zhang, M., Cheng, Z., Li, X., & Yan, Y. (2014) · Journal of Proteome Research · doi:10.1021/pr401184v · Cited by 36 · see citing works

Molecular cloning of mevalonate pathway genes from Taraxacum brevicorniculatum and functional characterisation of the key enzyme 3-hydroxy-3-methylglutaryl-coenzyme A reductase

van Deenen, N., Bachmann, A., Schmidt, T. J., Schaller, H., Sand, J., Prüfer, D., & Gronover, C. S. (2011) · Molecular Biology Reports · doi:10.1007/s11033-011-1221-4 · Cited by 36 · see citing works

Interaction of Farnesylated PRL-2, a Protein-tyrosine Phosphatase, with the β-Subunit of Geranylgeranyltransferase II

Si, X., Zeng, Q., Ng, C. H., Hong, W., & Pallen, C. J. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m010400200 · Cited by 36 · see citing works

Role of Peroxisomes in Isoprenoid Biosynthesis

Aboushadi, N., Engfelt, W. H., Paton, V. G., & Krisans, S. K. (1999) · Journal of Histochemistry & Cytochemistry · doi:10.1177/002215549904700904 · Cited by 36 · see citing works

Powdery Mildew Resistance Genes in Vines: An Opportunity to Achieve a More Sustainable Viticulture

Sosa-Zuniga, V., Valenzuela, Á. V., Barba, P., Espinoza, C., Romero-Romero, J. L., & Arce‐Johnson, P. (2022) · Pathogens · doi:10.3390/pathogens11060703 · Cited by 35 · see citing works

Modulation of plant HMG-CoA reductase by protein phosphatase 2A

Antolín‐Llovera, M., Leivar, P., Arró, M., Ferrer, A., Boronat, A., & Campos, N. (2011) · Plant Signaling & Behavior · doi:10.4161/psb.6.8.16363 · Cited by 35 · see citing works

Chapter 12 Plant Biotechnology and the Production of Alkaloids: Prospects of Metabolic Engineering

Verpoorte, R., van der Heijden, R., & Memelink, J. (1998) · The Alkaloids. Chemistry and biology/The alkaloids. Chemistry and biology · doi:10.1016/s1099-4831(08)60050-4 · Cited by 35 · see citing works

Biochemistry of Terpenoids: Monoterpenes, Sesquiterpenes and Diterpenes

Ashour, M. L., Wink, M., & Gershenzon, J. (2017) · Wiley eBooks · doi:10.1002/9781119312994.apr0427 · Cited by 36 · see citing works

Modulation of plant HMG-CoA reductase by protein phosphatase 2A

Antolín‐Llovera, M., Leivar, P., Arró, M., Ferrer, A., Boronat, A., & Campos, N. (2011) · Plant Signaling & Behavior · doi:10.4161/psb.6.8.16363 · Cited by 35 · see citing works

An Overview of 3-Hydroxy-3-Methylglutaryl CoA Reductase (HMGR) in Plants

Teha, K. Y., & Abdullah, J. O. (2016) · Universiti Putra Malaysia Institutional Repository (Universiti Putra Malaysia) · Cited by 1 · see citing works

Anàlisi de l’HMG-CoA reductasa d’Arabidopsis thaliana: implicació en la morfogènesi del reticle endoplasmàtic

Torrero, S. F. (2010) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Regulated accumulation of 3-hydroxy-3-methylglutaryl CoA reductase protein in potato cell cultures: effects of calcium and enzyme inhibitors

Crane, C. F., & Korth, K. L. (2002) · Journal of Plant Physiology · doi:10.1078/0176-1617-00874 · Cited by 5 · see citing works

Is the Reaction Catalyzed by 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase a Rate-Limiting Step for Isoprenoid Biosynthesis in Plants?

Chappell, J., Wolf, F., Proulx, J., Cuellar, R., & Saunders, C. (1995) · Plant Physiology · doi:10.1104/pp.109.4.1337 · Cited by 335 · see citing works