Metal transporters in organelles and their roles in heavy metal transportation and sequestration mechanisms in plants

The Proceedings of the National Academy of Sciences

Richards, J. W. (1915) · Science · doi:10.1126/science.42.1074.161 · Cited by 13,941 · see citing works

Heavy metals, occurrence and toxicity for plants: a review

Nagajyoti, P. C., Lee, K. D., & Sreekanth, T. V. M. (2010) · Environmental Chemistry Letters · doi:10.1007/s10311-010-0297-8 · Cited by 3,962 · see citing works

Cellular mechanisms for heavy metal detoxification and tolerance

Hall, J. L. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.366.1 · Cited by 2,968 · see citing works

Zinc in plants

Broadley, M. R., White, P. J., Hammond, J. P., Zelko, I., & Lux, A. (2007) · New Phytologist · doi:10.1111/j.1469-8137.2007.01996.x · Cited by 2,112 · see citing works

Contrasting Computational Models of Mate Preference Integration Across 45 Countries

Conroy‐Beam, D., Buss, D. M., Asao, K., Sorokowska, A., Sorokowski, P., Aavik, T., Akello, G., Alhabahba, M. M., Alm, C., Amjad, N., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-52748-8 · Cited by 1,771 · see citing works

Heavy metals toxicity in plants: An overview on the role of glutathione and phytochelatins in heavy metal stress tolerance of plants

Yadav, S. K. (2009) · South African Journal of Botany · doi:10.1016/j.sajb.2009.10.007 · Cited by 1,611 · see citing works

Molecular mechanisms of plant metal tolerance and homeostasis

Clemens, S. (2001) · Planta · doi:10.1007/s004250000458 · Cited by 1,417 · see citing works

Transporters of arsenite in rice and their role in arsenic accumulation in rice grain

Feng, J. X., Yamaji, N., Mitani, N., Xu, X., Su, Y., McGrath, S. P., & Zhao, F. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802361105 · Cited by 1,414 · see citing works

Nramp5 Is a Major Transporter Responsible for Manganese and Cadmium Uptake in Rice

Sasaki, A., Yamaji, N., Yokosho, K., & Feng, J. X. (2012) · The Plant Cell · doi:10.1105/tpc.112.096925 · Cited by 1,316 · see citing works

Heavy Metal Stress and Some Mechanisms of Plant Defense Response

Emamverdian, A., Ding, Y., Mokhberdoran, F., & Xie, Y. (2015) · The Scientific World JOURNAL · doi:10.1155/2015/756120 · Cited by 1,136 · see citing works

Correction: Corrigendum: Assembling Composite Dermal Papilla Spheres with Adipose-derived Stem Cells to Enhance Hair Follicle Induction

Huang, C.-F., Chang, Y., Hsueh, Y., Huang, C.-W., Wang, D.-H., Huang, T.-C., Wu, Y.-T., Su, F., Hughes, M. W., Chuong, C., et al. (2016) · Scientific Reports · doi:10.1038/srep31257 · Cited by 941 · see citing works

Photosynthetic Response of Plants Under Different Abiotic Stresses: A Review

Sharma, A., Kumar, V., Shahzad, B., Ramakrishnan, M., Sidhu, G. P. S., Bali, A. S., Handa, N., Kapoor, D., Yadav, P., Khanna, K., et al. (2019) · Journal of Plant Growth Regulation · doi:10.1007/s00344-019-10018-x · Cited by 889 · see citing works

Manganese in Plants: From Acquisition to Subcellular Allocation

Alejandro, S., Höller, S., Meier, B., & Peiter, E. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00300 · Cited by 859 · see citing works

The ABC transporter AtPDR8 is a cadmium extrusion pump conferring heavy metal resistance

Kim, D., Bovet, L., Maeshima, M., Martinoia, E., & Lee, Y. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03044.x · Cited by 721 · see citing works

Localization of Iron in Arabidopsis Seed Requires the Vacuolar Membrane Transporter VIT1

Kim, S. A., Punshon, T., Lanzirotti, A., Li, L., Alonso, J. M., Ecker, J. R., Kaplan, J., & Guerinot, M. L. (2006) · Science · doi:10.1126/science.1132563 · Cited by 682 · see citing works

AtHMA3, a P1B-ATPase Allowing Cd/Zn/Co/Pb Vacuolar Storage in Arabidopsis

Morel‐Rouhier, M., Crouzet, J., Gravot, A., Auroy, P., Leonhardt, N., Vavasseur, A., & Richaud, P. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.130294 · Cited by 677 · see citing works

Arsenic tolerance in Arabidopsis is mediated by two ABCC-type phytochelatin transporters

Song, W., Park, J.-Y., Mendoza‐Cózatl, D. G., Grotemeyer, M. S., Shim, D., Hörtensteiner, S., Geisler, M. M., Weder, B., Rea, P. A., Rentsch, D., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013964107 · Cited by 675 · see citing works

Facing the challenges of Cu, Fe and Zn homeostasis in plants

Palmer, C. M., & Guerinot, M. L. (2009) · Nature Chemical Biology · doi:10.1038/nchembio.166 · Cited by 633 · see citing works

Emerging mechanisms for heavy metal transport in plants

Williams, L. E., Pittman, J. K., & Hall, J. L. (2000) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(00)00133-4 · Cited by 631 · see citing works

Mobilization of vacuolar iron by AtNRAMP3 and AtNRAMP4 is essential for seed germination on low iron

Lanquar, V., Lelièvre, F., Bolte, S., Hamès, C., Alcon, C., Neumann, D., Vansuyt, G., Curie, C., Schröder, A., Krämer, U., et al. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600864 · Cited by 631 · see citing works

The OsNRAMP1 iron transporter is involved in Cd accumulation in rice

Takahashi, R., Ishimaru, Y., Senoura, T., Shimo, H., Ishikawa, S., Arao, T., Nakanishi, H., & Nishizawa, N. K. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err136 · Cited by 591 · see citing works

Vacuolar compartmentalization as indispensable component of heavy metal detoxification in plants

Sharma, S. S., Dietz, K., & Mimura, T. (2016) · Plant Cell & Environment · doi:10.1111/pce.12706 · Cited by 579 · see citing works

Chromium Bioaccumulation and Its Impacts on Plants: An Overview

Sharma, A., Kapoor, D., Wang, J., Shahzad, B., Kumar, V., Bali, A. S., Jasrotia, S., Zheng, B., Yuan, H., & Yan, D. (2020) · Plants · doi:10.3390/plants9010100 · Cited by 533 · see citing works

A rice ABC transporter, OsABCC1, reduces arsenic accumulation in the grain

Song, W., Yamaki, T., Yamaji, N., Ko, D., Jung, K., Fujii‐Kashino, M., An, G., Martinoia, E., Lee, Y., & Ma, J. F. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414968111 · Cited by 513 · see citing works

Heavy Metal Stress, Signaling, and Tolerance Due to Plant-Associated Microbes: An Overview

Tiwari, S., & Lata, C. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00452 · Cited by 491 · see citing works

AtNRAMP3, a multispecific vacuolar metal transporter involved in plant responses to iron deficiency

Thomine, S., Lelièvre, F., Debarbieux, E., Schroeder, J. I., & Barbier‐Brygoo, H. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01760.x · Cited by 480 · see citing works

Transport properties of members of the ZIP family in plants and their role in Zn and Mn homeostasis

Milner, M. J., Seamon, J., Craft, E. J., & Kochian, L. V. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers315 · Cited by 470 · see citing works

Monoubiquitin-dependent endocytosis of the IRON-REGULATED TRANSPORTER 1 (IRT1) transporter controls iron uptake in plants

Barberon, M., Zelazny, E., Robert, S., Conéjéro, G., Curie, C., Friml, J., & Vert, G. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1100659108 · Cited by 469 · see citing works

Mutations in Rice (Oryza sativa) Heavy Metal ATPase 2 (OsHMA2) Restrict the Translocation of Zinc and Cadmium

Satoh‐Nagasawa, N., Mori, M., Nakazawa, N., Kawamoto, T., Nagato, Y., Sakurai, K., Takahashi, H., Watanabe, A., & Akagi, H. (2011) · Plant and Cell Physiology · doi:10.1093/pcp/pcr166 · Cited by 455 · see citing works

Heavy Metal Stress. Activation of Distinct Mitogen-Activated Protein Kinase Pathways by Copper and Cadmium

Jonak, C., Nakagami, H., & Heribert Hirt, A. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.045724 · Cited by 432 · see citing works

Crosstalk between phytohormones and secondary metabolites in the drought stress tolerance of crop plants: A review

Jogawat, A., Yadav, B., Chhaya, Lakra, N., Singh, A. K., & Narayan, O. P. (2021) · Physiologia Plantarum · doi:10.1111/ppl.13328 · Cited by 431 · see citing works

Put the metal to the petal: metal uptake and transport throughout plants

Colangelo, E. P., & Guerinot, M. L. (2006) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2006.03.015 · Cited by 429 · see citing works

Biotic and heavy metal stress response in plants: evidence for common signals

Mithöfer, A., Schulze, B., & Boland, W. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.04.011 · Cited by 423 · see citing works

Overexpression of OsHMA3 enhances Cd tolerance and expression of Zn transporter genes in rice

Sasaki, A., Yamaji, N., & Feng, J. X. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru340 · Cited by 421 · see citing works

OsNRAMP1 transporter contributes to cadmium and manganese uptake in rice

Chang, J., Huang, S., Yamaji, N., Zhang, W., Feng, J. X., & Zhao, F. J. (2020) · Plant Cell & Environment · doi:10.1111/pce.13843 · Cited by 421 · see citing works

The Arabidopsis metal tolerance protein AtMTP3 maintains metal homeostasis by mediating Zn exclusion from the shoot under Fe deficiency and Zn oversupply

Arrivault, S., Senger, T., & Krämer, U. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02746.x · Cited by 418 · see citing works

Cadmium-inducible expression of the ABC-type transporter AtABCC3 increases phytochelatin-mediated cadmium tolerance in Arabidopsis

Brunetti, P., Zanella, L., Paolis, A. D., Litta, D. D., Cecchetti, V., Falasca, G., Barbieri, M., Altamura, M. M., Costantino, P., & Cardarelli, M. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv185 · Cited by 408 · see citing works

Correction: Corrigendum: Rapid antibiotic-resistance predictions from genome sequence data for Staphylococcus aureus and Mycobacterium tuberculosis

Bradley, P., Gordon, N. C., Walker, T. M., Dunn, L. E. M., Heys, S., Huang, B., Earle, S. G., Pankhurst, L. J., Anson, L. W., de Cesare, M., et al. (2016) · Nature Communications · doi:10.1038/ncomms11465 · Cited by 370 · see citing works

Investigating the Contribution of the Phosphate Transport Pathway to Arsenic Accumulation in Rice

Wu, Z., Ren, H., McGrath, S. P., et al. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.178921 · Cited by 360 · see citing works

OsZIP1 functions as a metal efflux transporter limiting excess zinc, copper and cadmium accumulation in rice

Liu, X. S., Feng, S. J., Zhang, B. Q., Wang, M. Q., Cao, H. W., Rono, J. K., Chen, X., & Yang, Z. M. (2019) · BMC Plant Biology · doi:10.1186/s12870-019-1899-3 · Cited by 351 · see citing works

The Role of Salicylic Acid in Plants Exposed to Heavy Metals

Sharma, A., Sidhu, G. P. S., Araniti, F., Bali, A. S., Shahzad, B., Tripathi, D. K., Brestič, M., Skalický, M., & Landi, M. (2020) · Molecules · doi:10.3390/molecules25030540 · Cited by 349 · see citing works

The Ferroportin Metal Efflux Proteins Function in Iron and Cobalt Homeostasis in Arabidopsis

Morrissey, J., Baxter, I. R., Lee, J., Li, L., Lahner, B., Grotz, N., Kaplan, J., Salt, D. E., & Guerinot, M. L. (2009) · The Plant Cell · doi:10.1105/tpc.109.069401 · Cited by 345 · see citing works

Ancient and essential: the assembly of iron–sulfur clusters in plants

Balk, J., & Pilon, M. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2010.12.006 · Cited by 344 · see citing works

Two P-Type ATPases Are Required for Copper Delivery in Arabidopsis thaliana Chloroplasts

Abdel‐Ghany, S. E., Müller-Moulé, P., Niyogi, K., Pilon, M., & Shikanai, T. (2005) · The Plant Cell · doi:10.1105/tpc.104.030452 · Cited by 325 · see citing works

Identification of a copper transporter family in Arabidopsis thaliana

Sancenón, V., Puig, S., Mira, H., Thiele, D. J., & Peñarrubia, L. (2003) · Plant Molecular Biology · doi:10.1023/a:1022345507112 · Cited by 323 · see citing works

The heavy metal paradox in arbuscular mycorrhizas: from mechanisms to biotechnological applications

Ferrol, N., Tamayo, E., & Vargas, P. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw403 · Cited by 318 · see citing works

AtATM3 Is Involved in Heavy Metal Resistance in Arabidopsis

Kim, D.-Y., Bovet, L., Kushnir, S., Noh, E. W., Martinoia, E., & Lee, Y. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.074146 · Cited by 315 · see citing works

Secondary metabolites in the drought stress tolerance of crop plants: A review

Yadav, B., Jogawat, A., Rahman, M. S., & Narayan, O. P. (2021) · Gene Reports · doi:10.1016/j.genrep.2021.101040 · Cited by 315 · see citing works

Zinc Transporter of Arabidopsis thaliana AtMTP1 is Localized to Vacuolar Membranes and Implicated in Zinc Homeostasis

Kobae, Y., Uemura, T., Sato, M. H., Ohnishi, M., Mimura, T., Nakagawa, T., & Maeshima, M. (2004) · Plant and Cell Physiology · doi:10.1093/pcp/pci015 · Cited by 310 · see citing works

A Mutant of the Arabidopsis Phosphate Transporter PHT1;1 Displays Enhanced Arsenic Accumulation

Catarecha, P., Segura, M. D., Franco‐Zorrilla, J. M., et al. (2007) · The Plant Cell · doi:10.1105/tpc.106.041871 · Cited by 309 · see citing works

Metal Sensing by the IRT1 Transporter-Receptor Orchestrates Its Own Degradation and Plant Metal Nutrition

Dubeaux, G., Neveu, J., Zelazny, E., & Vert, G. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.02.009 · Cited by 307 · see citing works

A Major Quantitative Trait Locus for Cadmium Tolerance in <i>Arabidopsis halleri</i> Colocalizes with <i>HMA4</i>, a Gene Encoding a Heavy Metal ATPase

Courbot, M., Willems, G., Motte, P., Arvidsson, S., Roosens, N., Saumitou-Laprade, P., & Verbruggen, N. (2007) · Plant Physiology · doi:10.1104/pp.106.095133 · Cited by 303 · see citing works

Very high density EEG elucidates spatiotemporal aspects of early visual processing

Robinson, A. K., Venkatesh, P., Boring, M. J., Tarr, M. J., Grover, P., & Behrmann, M. (2017) · Scientific Reports · doi:10.1038/s41598-017-16377-3 · Cited by 302 · see citing works

The ABC transporter ABCG36 is required for cadmium tolerance in rice

Fu, S., Lu, Y., Xiang, Z., Yang, G., Chao, D., Wang, Z., Shi, M., Chen, J., Chao, D., Li, R., et al. (2019) · Journal of Experimental Botany · doi:10.1093/jxb/erz335 · Cited by 299 · see citing works

A secretory pathway-localized cation diffusion facilitator confers plant manganese tolerance

Peiter, E., Montanini, B., Gobert, A., Pedas, P., Husted, S., Maathuis, F. J. M., Blaudez, D., Chalot, M., & Sanders, D. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609507104 · Cited by 287 · see citing works

Vacuolar Nicotianamine Has Critical and Distinct Roles under Iron Deficiency and for Zinc Sequestration in Arabidopsis

Haydon, M. J., Kawachi, M., Wirtz, M., Hillmer, S., Hell, R., & Krämer, U. (2012) · The Plant Cell · doi:10.1105/tpc.111.095042 · Cited by 281 · see citing works

The Arabidopsis Copper Transporter COPT1 Functions in Root Elongation and Pollen Development

Sancenón, V., Puig, S., Mateu‐Andrés, I., Dorcey, E., Thiele, D. J., & Peñarrubia, L. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313321200 · Cited by 279 · see citing works

OPT3 Is a Phloem-Specific Iron Transporter That Is Essential for Systemic Iron Signaling and Redistribution of Iron and Cadmium inArabidopsis

Zhai, Z., Gayomba, S. R., Jung, H., Vimalakumari, N. K., Piñeros, M. A., Craft, E. J., Rutzke, M. A., Danku, J., Lahner, B., Punshon, T., et al. (2014) · The Plant Cell · doi:10.1105/tpc.114.123737 · Cited by 272 · see citing works

PIC1, an Ancient Permease in Arabidopsis Chloroplasts, Mediates Iron Transport

Duy, D., Wanner, G., Meda, A. R., von Wirén, N., Soll, J., & Philippar, K. (2007) · The Plant Cell · doi:10.1105/tpc.106.047407 · Cited by 268 · see citing works

The role of heavy-metal ATPases, HMAs, in zinc and cadmium transport in rice

Takahashi, R., Bashir, K., Ishimaru, Y., Nishizawa, N. K., & Nakanishi, H. (2012) · Plant Signaling & Behavior · doi:10.4161/psb.22454 · Cited by 265 · see citing works

The NRAMP6 metal transporter contributes to cadmium toxicity

Cailliatte, R., Lapeyre, B., Briat, J., Mari, S., & Curie, C. (2009) · Biochemical Journal · doi:10.1042/bj20090655 · Cited by 264 · see citing works

Copper and Iron Homeostasis in Plants: The Challenges of Oxidative Stress

Ravet, K., & Pilon, M. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.5084 · Cited by 261 · see citing works

Variation in Molybdenum Content Across Broadly Distributed Populations of Arabidopsis thaliana Is Controlled by a Mitochondrial Molybdenum Transporter (MOT1)

Baxter, I. R., Balasubramaniam, M., Park, H. C., Büchner, P., Lahner, B., Danku, J., Zhao, K., Lee, J., Hawkesford, M. J., Guerinot, M. L., et al. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000004 · Cited by 245 · see citing works

A Strong Loss-of-Function Mutation in RAN1 Results in Constitutive Activation of the Ethylene Response Pathway as Well as a Rosette-Lethal Phenotype

Woeste, K., & Kieber, J. J. (2000) · The Plant Cell · doi:10.1105/tpc.12.3.443 · Cited by 244 · see citing works

Arabidopsis HMA2, a Divalent Heavy Metal-Transporting PIB-Type ATPase, Is Involved in Cytoplasmic Zn2+ Homeostasis

Eren, E., & ARGÜELLO, J. M. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.046292 · Cited by 240 · see citing works

A heavy metal P-type ATPase OsHMA4 prevents copper accumulation in rice grain

Huang, X., Deng, F., Yamaji, N., Pinson, S. R. M., Fujii‐Kashino, M., Danku, J., Douglas, A., Guerinot, M. L., Salt, D. E., & Feng, J. X. (2016) · Nature Communications · doi:10.1038/ncomms12138 · Cited by 237 · see citing works

Role of Ethylene and Its Cross Talk with Other Signaling Molecules in Plant Responses to Heavy Metal Stress

Thảo, N. P., Khan, M., Thư, N. B. A., Hoang, X. L. T., Asgher, M., Khan, N. A., & Tran, L. P. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.00663 · Cited by 236 · see citing works

Divalent Metal Ions in Plant Mitochondria and Their Role in Interactions with Proteins and Oxidative Stress-Induced Damage to Respiratory Function

Tan, Y., O’Toole, N., Taylor, N. L., & Millar, A. H. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.147942 · Cited by 229 · see citing works

Hydrogen peroxide as a signalling molecule in plants and its crosstalk with other plant growth regulators under heavy metal stress

Nazir, F., Fariduddin, Q., & Khan, T. A. (2020) · Chemosphere · doi:10.1016/j.chemosphere.2020.126486 · Cited by 229 · see citing works

A Member of the Heavy Metal P-Type ATPase OsHMA5 Is Involved in Xylem Loading of Copper in Rice

Deng, F., Yamaji, N., Xia, J., & Feng, J. X. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.226225 · Cited by 220 · see citing works

Heavy Metal Stress and Sulfate Uptake in Maize Roots

Nocito, F. F., Lancilli, C., Crema, B., et al. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.076240 · Cited by 208 · see citing works

The Vacuolar Manganese Transporter MTP8 Determines Tolerance to Iron Deficiency-Induced Chlorosis in Arabidopsis

Eroğlu, S., Meier, B., von Wirén, N., & Peiter, E. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.01194 · Cited by 202 · see citing works

Arabidopsis IRT2 cooperates with the high-affinity iron uptake system to maintain iron homeostasis in root epidermal cells

Vert, G., Barberon, M., Zelazny, E., Séguéla-Arnaud, M., Briat, J., & Curie, C. (2009) · Planta · doi:10.1007/s00425-009-0904-8 · Cited by 190 · see citing works

Functional analysis of the rice vacuolar zinc transporter OsMTP1

Menguer, P. K., Farthing, E. C., Peaston, K. A., et al. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert136 · Cited by 181 · see citing works

ECA3, a Golgi-Localized P2A-Type ATPase, Plays a Crucial Role in Manganese Nutrition in Arabidopsis

Mills, R. F., Doherty, M. L., López‐Marqués, R. L., Weimar, T., Dupree, P., Palmgren, M. B., Pittman, J. K., & Williams, L. E. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.110817 · Cited by 180 · see citing works

The high-affinity metal Transporters NRAMP1 and IRT1 Team up to Take up Iron under Sufficient Metal Provision

Castaings, L., Caquot, A., Loubet, S., & Curie, C. (2016) · Scientific Reports · doi:10.1038/srep37222 · Cited by 176 · see citing works

The rice mitochondrial iron transporter is essential for plant growth

Bashir, K., Ishimaru, Y., Shimo, H., Nagasaka, S., Fujimoto, M., Takanashi, H., Tsutsumi, N., An, G., Nakanishi, H., & Nishizawa, N. K. (2011) · Nature Communications · doi:10.1038/ncomms1326 · Cited by 172 · see citing works

Chloroplastic and mitochondrial metal homeostasis

Nouet, C., Motté, P., & Hanikenne, M. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2011.03.005 · Cited by 172 · see citing works

OPT3 Is a Component of the Iron-Signaling Network between Leaves and Roots and Misregulation of OPT3 Leads to an Over-Accumulation of Cadmium in Seeds

Mendoza‐Cózatl, D. G., Xie, Q., Akmakjian, G. Z., Jobe, T. O., Patel, A., Stacey, M. G., Song, L., Demoin, D. W., Jurisson, S. S., Stacey, G. S., et al. (2014) · Molecular Plant · doi:10.1093/mp/ssu067 · Cited by 167 · see citing works

Translocation of copper and other micronutrients in tomato plants (Lycopersicon esculentumMill.): nicotianamine-stimulated copper transport in the xylem

Pich, A., & Scholz, G. (1996) · Journal of Experimental Botany · doi:10.1093/jxb/47.1.41 · Cited by 162 · see citing works

Expression of BjMT2, a metallothionein 2 from Brassica juncea, increases copper and cadmium tolerance in Escherichia coli and Arabidopsis thaliana, but inhibits root elongation in Arabidopsis thaliana seedlings

An, Z., Cuijie, L., Yuan‐Gang, Z., Yejie, D., Wachter, A., Gromes, R., & Rausch, T. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl102 · Cited by 157 · see citing works

The tonoplast copper transporter COPT5 acts as an exporter and is required for interorgan allocation of copper in Arabidopsis thaliana

Klaumann, S., Nickolaus, S. D., Fürst, S. H., Starck, S., Schneider, S., Neuhaus, H. E., & Trentmann, O. (2011) · New Phytologist · doi:10.1111/j.1469-8137.2011.03798.x · Cited by 155 · see citing works

Nitric oxide‐mediated regulation of oxidative stress in plants under metal stress: a review on molecular and biochemical aspects

Sharma, A., Soares, C., Sousa, B., Martins, M., Kumar, V., Shahzad, B., Sidhu, G. P. S., Bali, A. S., Asgher, M., Bhardwaj, R., et al. (2019) · Physiologia Plantarum · doi:10.1111/ppl.13004 · Cited by 155 · see citing works

OsPT4 Contributes to Arsenate Uptake and Transport in Rice

Ye, Y., Li, P., Xu, T., Zeng, L., Cheng, D., Yang, M., Luo, J., & Lian, X. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.02197 · Cited by 145 · see citing works

The Arabidopsis YELLOW STRIPE LIKE4 and 6 Transporters Control Iron Release from the Chloroplast

Divol, F., Couch, D., Conéjéro, G., et al. (2013) · The Plant Cell · doi:10.1105/tpc.112.107672 · Cited by 144 · see citing works

An overview of recent advancement in phytohormones-mediated stress management and drought tolerance in crop plants

Chhaya, Yadav, B., Jogawat, A., Gnanasekaran, P., Kumari, P., Lakra, N., Lal, S. K., Pawar, J. S., & Narayan, O. P. (2020) · Plant Gene · doi:10.1016/j.plgene.2020.100264 · Cited by 143 · see citing works

Arabidopsis Copper Transport Protein COPT2 Participates in the Cross Talk between Iron Deficiency Responses and Low-Phosphate Signaling

Perea‐García, A., Garcia‐Molina, A., Andrés‐Colás, N., Vera‐Sirera, F., Perez-Amador, M. A., Puig, S., & Peñarrubia, L. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.212407 · Cited by 137 · see citing works

The rhizobacterium Variovorax paradoxus 5C-2, containing ACC deaminase, promotes growth and development of Arabidopsis thaliana via an ethylene-dependent pathway

Chen, L., Dodd, I. C., Theobald, J. C., et al. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert031 · Cited by 136 · see citing works

Co-expression of multiple heavy metal transporters changes the translocation, accumulation, and potential oxidative stress of Cd and Zn in rice (Oryza sativa)

Tian, S., Liang, S., Qiao, K., Wang, F., Zhang, Y., & Chai, T. (2019) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2019.120853 · Cited by 132 · see citing works

Science in China. Series C, Life sciences

中国科学院 (1996) · Medical Entomology and Zoology · Cited by 131 · see citing works

A Novel Role for Arabidopsis Mitochondrial ABC Transporter ATM3 in Molybdenum Cofactor Biosynthesis

Teschner, J., Lachmann, N., Schulze, J., Geisler, M., Selbach, K., Santamaria‐Araujo, J. A., Balk, J., Mendel, R. R., & Bittner, F. (2010) · The Plant Cell · doi:10.1105/tpc.109.068478 · Cited by 131 · see citing works

Vacuolar Transporters for Cadmium and Arsenic in Plants and their Applications in Phytoremediation and Crop Development

Zhang, J., Martinoia, E., & Lee, Y. (2018) · Plant and Cell Physiology · doi:10.1093/pcp/pcy006 · Cited by 130 · see citing works

Chloroplast Transition Metal Regulation for Efficient Photosynthesis

Schmidt, S. B., Eisenhut, M., & Schneider, A. (2020) · Trends in Plant Science · doi:10.1016/j.tplants.2020.03.003 · Cited by 129 · see citing works

Intron Retention in the 5′UTR of the Novel ZIF2 Transporter Enhances Translation to Promote Zinc Tolerance in Arabidopsis

Rémy, E., Cabrito, T. R., Batista, R. A., Hussein, M. A., Teixeira, M. C., Athanasiadis, A., Sá‐Correia, I., & Duque, P. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004375 · Cited by 126 · see citing works

Metal Tolerance Protein 8 Mediates Manganese Homeostasis and Iron Reallocation during Seed Development and Germination

Eroğlu, S., Giehl, R. F. H., Meier, B., Takahashi, M., Terada, Y., Ignatyev, K., Andresen, E., Küpper, H., Peiter, E., & Nicolaus Von Wirén, A. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.01646 · Cited by 125 · see citing works

Vacuolar-Iron-Transporter1-Like Proteins Mediate Iron Homeostasis in Arabidopsis

Gollhofer, J., Timofeev, R. V., Lan, P., Schmidt, W., & Buckhout, T. J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0110468 · Cited by 123 · see citing works

Deregulated Copper Transport Affects Arabidopsis Development Especially in the Absence of Environmental Cycles

Andrés‐Colás, N., Perea‐García, A., Puig, S., & Peñarrubia, L. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.153676 · Cited by 122 · see citing works

Root development under metal stress in Arabidopsis thaliana requires the H + /cation antiporter CAX4

Mei, H., Cheng, N. H., Zhao, J. H., Park, S., Escareno, R. A., Pittman, J. K., & Hirschi, K. D. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2009.02831.x · Cited by 121 · see citing works

The metal transporter PgIREG1 from the hyperaccumulator Psychotria gabriellae is a candidate gene for nickel tolerance and accumulation

Merlot, S., Hannibal, L., Martins, S., Martinelli, L., Amir, H., Lebrun, M., & Thomine, S. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru025 · Cited by 119 · see citing works

Systemic Upregulation of MTP2- and HMA2-Mediated Zn Partitioning to the Shoot Supplements Local Zn Deficiency Responses

Sinclair, S. A., Senger, T., Talke, I. N., et al. (2018) · The Plant Cell · doi:10.1105/tpc.18.00207 · Cited by 115 · see citing works

The intracellular Arabidopsis COPT5 transport protein is required for photosynthetic electron transport under severe copper deficiency

Garcia‐Molina, A., Andrés‐Colás, N., Perea‐García, A., del Valle-Tascón, S., Peñarrubia, L., & Puig, S. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04472.x · Cited by 114 · see citing works

Heavy metal signalling in plants: linking cellular and organismic responses

Polle, A., & Schützendübel, A. (2003) · Topics in current genetics · doi:10.1007/978-3-540-39402-0_8 · Cited by 109 · see citing works

Genome-wide identification of Cd-responsive NRAMP transporter genes and analyzing expression of NRAMP 1 mediated by miR167 in Brassica napus

Meng, J. G., Zhang, X. D., Tan, S. K., Zhao, K. X., & Yang, Z. M. (2017) · BioMetals · doi:10.1007/s10534-017-0057-3 · Cited by 107 · see citing works

The Chloroplast Permease PIC1 Regulates Plant Growth and Development by Directing Homeostasis and Transport of Iron

Duy, D., Stübe, R., Wanner, G., & Philippar, K. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.170233 · Cited by 103 · see citing works

Functional and regulatory analysis of the Arabidopsis thaliana CAX2 cation transporter

Pittman, J. K., Shigaki, T., Marshall, J., Morris, J., Cheng, N., & Hirschi, K. D. (2004) · Plant Molecular Biology · doi:10.1007/s11103-004-6446-3 · Cited by 102 · see citing works

Exposure to heavy metal stress triggers changes in plasmodesmatal permeability via deposition and breakdown of callose

O’Lexy, R., Kasai, K., Clark, N. M., Fujiwara, T., Sozzani, R., & Gallagher, K. L. (2018) · Journal of Experimental Botany · doi:10.1093/jxb/ery171 · Cited by 102 · see citing works

The Arabidopsis COPT6 Transport Protein Functions in Copper Distribution Under Copper-Deficient Conditions

Garcia‐Molina, A., Andrés‐Colás, N., Perea‐García, A., Neumann, U., Dodani, S. C., Huijser, P., Peñarrubia, L., & Puig, S. (2013) · Plant and Cell Physiology · doi:10.1093/pcp/pct088 · Cited by 99 · see citing works

Iron-Nicotianamine Transporters Are Required for Proper Long Distance Iron Signaling

Kumar, R. K., Chu, H.-H., Abundis, C., Vasques, K. A., Chan-Rodríguez, D., Chia, J., Huang, R., Vatamaniuk, O. K., & Walker, E. L. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.00821 · Cited by 97 · see citing works

Expression of TpNRAMP5, a metal transporter from Polish wheat (Triticum polonicum L.), enhances the accumulation of Cd, Co and Mn in transgenic Arabidopsis plants

Peng, F., Wang, C., Zhu, J., Zeng, J., Kang, H., Fan, X., Sha, L., Zhang, H., Zhou, Y., & Wang, Y. (2018) · Planta · doi:10.1007/s00425-018-2872-3 · Cited by 96 · see citing works

Root‐selective expression of AtCAX4 and AtCAX2 results in reduced lamina cadmium in field‐grown Nicotiana tabacum L.

Korenkov, V. D., King, B., Hirschi, K. D., & Wagner, G. J. (2009) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2008.00390.x · Cited by 94 · see citing works

Barley HvHMA1 Is a Heavy Metal Pump Involved in Mobilizing Organellar Zn and Cu and Plays a Role in Metal Loading into Grains

Mikkelsen, M. D., Pedas, P., Schiller, M., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049027 · Cited by 91 · see citing works

The Plastid Envelope CHLOROPLAST MANGANESE TRANSPORTER1 Is Essential for Manganese Homeostasis in Arabidopsis

Eisenhut, M., Hoecker, N., Schmidt, S. B., et al. (2018) · Molecular Plant · doi:10.1016/j.molp.2018.04.008 · Cited by 91 · see citing works

Functional Characterization of AtATM1, AtATM2, and AtATM3, a Subfamily of Arabidopsis Half-molecule ATP-binding Cassette Transporters Implicated in Iron Homeostasis

Chen, S., Sánchez-Fernández, R., Lyver, E. R., et al. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702383200 · Cited by 89 · see citing works

Multiple Antibiotic Resistance in Arabidopsis Is Conferred by Mutations in a Chloroplast-Localized Transport Protein

Conte, S. S., Stevenson, D. S., Furner, I. J., & Lloyd, A. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.143487 · Cited by 89 · see citing works

Antioxidant enzymes in chickpea colonized by Piriformospora indica participate in defense against the pathogen Botrytis cinerea

Narayan, O. P., Verma, N., Singh, A. K., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-12944-w · Cited by 89 · see citing works

HMA1 and PAA1, two chloroplast-envelope PIB-ATPases, play distinct roles in chloroplast copper homeostasis

Boutigny, S., Sautron, E., Finazzi, G., et al. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru020 · Cited by 86 · see citing works

Calcium-dependent protein kinase CPK31 interacts with arsenic transporter AtNIP1;1 and regulates arsenite uptake in Arabidopsis thaliana

Ji, R., Zhou, L., Liu, J., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0173681 · Cited by 82 · see citing works

Inner Envelope CHLOROPLAST MANGANESE TRANSPORTER 1 Supports Manganese Homeostasis and Phototrophic Growth in Arabidopsis

Zhang, B., Zhang, C., Liu, C., Jing, Y., Wang, Y., Jin, L., Yang, L., Fu, A., Shi, J., Zhao, F., et al. (2018) · Molecular Plant · doi:10.1016/j.molp.2018.04.007 · Cited by 80 · see citing works

Plant mineral transport systems and the potential for crop improvement

Yadav, B., Jogawat, A., Lal, S. K., Lakra, N., Mehta, S., Shabek, N., & Narayan, O. P. (2021) · Planta · doi:10.1007/s00425-020-03551-7 · Cited by 79 · see citing works

Poplar maintains zinc homeostasis with heavy metal genes HMA4 and PCS1

Adams, J. P., Adeli, A., Hsu, C., Harkess, R. L., Page, G. P., dePamphilis, C. W., Schultz, E. B., & Yüceer, Ç. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err025 · Cited by 75 · see citing works

The Intracellular Transporter AtNRAMP6 Is Involved in Fe Homeostasis in Arabidopsis

Li, J., Wang, Y., Zheng, L., Li, Y., Zhou, X., Li, J., Gu, D., Xu, E., Lu, Y., Chen, X., et al. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01124 · Cited by 74 · see citing works

Sulfur transfer from the endophytic fungus Serendipita indica improves maize growth and requires the sulfate transporter SiSulT

Narayan, O. P., Verma, N., Jogawat, A., et al. (2021) · The Plant Cell · doi:10.1093/plcell/koab006 · Cited by 71 · see citing works

Over-expression of chickpea glutaredoxin (CaGrx) provides tolerance to heavy metals by reducing metal accumulation and improved physiological and antioxidant defence system

Kumar, A., Dubey, A. K., Kumar, V., et al. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2020.110252 · Cited by 70 · see citing works

Mutation at Different Sites of Metal Transporter Gene OsNramp5 Affects Cd Accumulation and Related Agronomic Traits in Rice (Oryza sativa L.)

Wang, T., Li, Y., Fu, Y., Xie, H., Song, S., Qiu, M., Wen, J., Chen, M., Chen, G., Tian, Y., et al. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01081 · Cited by 69 · see citing works

LPCAT1 controls phosphate homeostasis in a zinc-dependent manner

Kisko, M. F. K., Bouain, N., Safi, A., et al. (2018) · eLife · doi:10.7554/elife.32077 · Cited by 68 · see citing works

Endomembrane Reorganization Induced by Heavy Metals

Caroli, M. D., Furini, A., DalCorso, G., Rojas, M., & Sansebastiano, G. P. D. (2020) · Plants · doi:10.3390/plants9040482 · Cited by 68 · see citing works

Chloroplast targeting of phytochelatin synthase in Arabidopsis: effects on heavy metal tolerance and accumulation

Picault, N., Cazalé, A., Beyly, A., Cuiné, S., Carrier, P., Luu, D., Forestier, C., & Peltier, G. (2006) · Biochimie · doi:10.1016/j.biochi.2006.04.016 · Cited by 66 · see citing works

Enhanced vacuole compartmentalization of cadmium in root cells contributes to glutathione-induced reduction of cadmium translocation from roots to shoots in pakchoi (Brassica chinensis L.)

Huang, Y., Chen, J., Zhang, D., Fang, B., YangJin, T., Zou, J., Chen, Y., Su, N., & Cui, J. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2020.111616 · Cited by 66 · see citing works

The putative Arabidopsis zinc transporter ZTP29 is involved in the response to salt stress

Wang, M., Xu, Q., Yu, J., & Yuan, M. (2010) · Plant Molecular Biology · doi:10.1007/s11103-010-9633-4 · Cited by 65 · see citing works

The bifunctional transporter‐receptor IRT 1 at the heart of metal sensing and signalling

Cointry, V., & Vert, G. (2019) · New Phytologist · doi:10.1111/nph.15826 · Cited by 63 · see citing works

Calcium-Dependent Hydrogen Peroxide Mediates Hydrogen-Rich Water-Reduced Cadmium Uptake in Plant Roots

Wu, Q., Huang, L., Su, N., et al. (2020) · PLANT PHYSIOLOGY · doi:10.1104/pp.20.00377 · Cited by 63 · see citing works

Overexpression of the transporters AtZIP1 and AtMTP1 in cassava changes zinc accumulation and partitioning

Gaitán‐Solís, E., Taylor, N. J., Siritunga, D., Stevens, W., & Schachtman, D. P. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00492 · Cited by 61 · see citing works

Functional Characterization of a Magnesium Transporter of Root Endophytic Fungus Piriformospora indica

Prasad, D., Verma, N., Bakshi, M., et al. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.03231 · Cited by 60 · see citing works

Maize YSL2 is required for iron distribution and development in kernels

Zang, J., Huo, Y., Liu, J., et al. (2020) · Journal of Experimental Botany · doi:10.1093/jxb/eraa332 · Cited by 58 · see citing works

GmHMA3 sequesters Cd to the root endoplasmic reticulum to limit translocation to the stems in soybean

Wang, Y., Wang, C., Liu, Y., Yu, K., & Zhou, Y. (2018) · Plant Science · doi:10.1016/j.plantsci.2018.02.007 · Cited by 57 · see citing works

The two copies of the zinc and cadmium ZIP6 transporter ofArabidopsis hallerihave distinct effects on cadmium tolerance

Spielmann, J., Ahmadi, H., Scheepers, M., Weber, M., Nitsche, S., Carnol, M., Bosman, B., Kroymann, J., Motté, P., Clemens, S., et al. (2020) · Plant Cell & Environment · doi:10.1111/pce.13806 · Cited by 55 · see citing works

CAX3 (cation/proton exchanger) mediates a Cd tolerance by decreasing ROS through Ca elevation in Arabidopsis

Modareszadeh, M., Bahmani, R., Kim, D.-G., et al. (2020) · Plant Molecular Biology · doi:10.1007/s11103-020-01072-1 · Cited by 55 · see citing works

Identification and subcellular localization of the soybean copper P1B-ATPase GmHMA8 transporter

Bernal, M., Testillano, P. S., Alfonso, M., Risueño, M. D. C., Picorel, R., & Yruela, I. (2006) · Journal of Structural Biology · doi:10.1016/j.jsb.2006.10.016 · Cited by 54 · see citing works

The Medicago truncatula Vacuolar iron Transporter‐Like proteins VTL4 and VTL8 deliver iron to symbiotic bacteria at different stages of the infection process

Walton, J. H., Kontra‐Kováts, G. Z., Green, R. T., Domonkos, Á., Horváth, B., Brear, E. M., Franceschetti, M., Kaló, P., & Balk, J. (2020) · New Phytologist · doi:10.1111/nph.16735 · Cited by 54 · see citing works

Zn2+-induced changes at the root level account for the increased tolerance of acclimated tobacco plants

Bazihizina, N., Taiti, C., Marti, L., Rodrigo-Moreno, A., Spinelli, F., Giordano, C., Caparrotta, S., Gori, M., Azzarello, E., & Mancuso, S. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru251 · Cited by 53 · see citing works

Disruption of Nap14, a plastid‐localized non‐intrinsic ABC protein in Arabidopsis thaliana results in the over‐accumulation of transition metals and in aberrant chloroplast structures

Shimoni-Shor, E., Hassidim, M., Yuval-Naeh, N., et al. (2010) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2010.02124.x · Cited by 51 · see citing works

IDI7, a new iron‐regulated ABC transporter from barley roots, localizes to the tonoplast

Yamaguchi, H., Nishizawa, N., Nakanishi, H., et al. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.369.727 · Cited by 51 · see citing works

Plastocyanin Controls the Stabilization of the Thylakoid Cu-transporting P-type ATPase PAA2/HMA8 in Response to Low Copper in Arabidopsis

Tapken, W., Ravet, K., & Pilon, M. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.318204 · Cited by 51 · see citing works

A Novel Prokaryote-Type ECF/ABC Transporter Module in Chloroplast Metal Homeostasis

von Voithenberg, L. V., Park, J., Stübe, R., Lux, C., Lee, Y., & Philippar, K. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01264 · Cited by 50 · see citing works

Functional characterization of BjCET3 and BjCET4, two new cation-efflux transporters from Brassica juncea L.

Lang, M., Hao, M., Fan, Q., Wang, W., Mo, S., Zhao, W., & Zhou, J. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err137 · Cited by 49 · see citing works

Identification of MTP gene family in tea plant (Camellia sinensis L.) and characterization of CsMTP8.2 in manganese toxicity

Zhang, X., Li, Q., Xu, W., et al. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2020.110904 · Cited by 48 · see citing works

Triplin, a small molecule, reveals copper ion transport in ethylene signaling from ATX1 to RAN1

Li, W., Lacey, R. F., Ye, Y., Lu, J. J., Yeh, K., Xiao, Y., Li, L., Wen, C., Binder, B. M., & Zhao, Y. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006703 · Cited by 47 · see citing works

A Single Point Mutation in GmHMA3 Affects Cadimum (Cd) Translocation and Accumulation in Soybean Seeds

Wang, Y., Yu, K., Poysa, V. W., et al. (2012) · Molecular Plant · doi:10.1093/mp/sss069 · Cited by 44 · see citing works

Ferroportin 3 is a dual‐targeted mitochondrial/chloroplast iron exporter necessary for iron homeostasis in Arabidopsis

Kim, L. J., Tsuyuki, K. M., Hu, F., Park, E. Y., Zhang, J., Iraheta, J. G., Chia, J., Huang, R., Tucker, A. E., Clyne, M., et al. (2021) · The Plant Journal · doi:10.1111/tpj.15286 · Cited by 44 · see citing works

A rice chloroplast‐localized ABC transporter ARG1 modulates cobalt and nickel homeostasis and contributes to photosynthetic capacity

Li, H., Liu, Y., Qin, H., Lin, X., Tang, D., Wu, Z., Luo, W., Shen, Y. X., Dong, F., Wang, Y., et al. (2020) · New Phytologist · doi:10.1111/nph.16708 · Cited by 43 · see citing works

Mitochondrial Iron Transporters (MIT1 and MIT2) Are Essential for Iron Homeostasis and Embryogenesis in Arabidopsis thaliana

Jain, A., Dashner, Z. S., & Connolly, E. L. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01449 · Cited by 42 · see citing works

Knocking down mitochondrial iron transporter (MIT) reprograms primary and secondary metabolism in rice plants

Vigani, G., Bashir, K., Ishimaru, Y., Lehmann, M., Casiraghi, F. M., Nakanishi, H., Seki, M., Geigenberger, P., Zocchi, G., & Nishizawa, N. K. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv531 · Cited by 41 · see citing works

Mitochondrial ABC Transporter ATM3 Is Essential for Cytosolic Iron-Sulfur Cluster Assembly

Zuo, J., Wu, Z., Li, Y., et al. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.01760 · Cited by 41 · see citing works

The Clp protease system is required for copper ion‐dependent turnover of the PAA 2/ HMA 8 copper transporter in chloroplasts

Tapken, W., Kim, J., Nishimura, K. J., et al. (2014) · New Phytologist · doi:10.1111/nph.13093 · Cited by 40 · see citing works

The ratio of Zn to Cd supply as a determinant of metal-homeostasis gene expression in tobacco and its modulation by overexpressing the metal exporter AtHMA4

Barabasz, A., Klimecka, M. M., Kendziorek, M., Weremczuk, A., Ruszczyńska, A., Bulska, E., & Antosiewicz, D. M. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw389 · Cited by 40 · see citing works

Gene Expression Pattern of Vacuolar-Iron Transporter-Like (VTL) Genes in Hexaploid Wheat during Metal Stress

Sharma, S., Kaur, G., Kumar, A., Meena, V., Ram, H., Kaur, J., & Pandey, A. K. (2020) · Plants · doi:10.3390/plants9020229 · Cited by 40 · see citing works

Phosphorylation of a malate transporter promotes malate excretion and reduces cadmium uptake in apple

Ma, Q., Sun, M., Lü, J., Hu, D., Kang, H., You, C., & Hao, Y. (2020) · Journal of Experimental Botany · doi:10.1093/jxb/eraa121 · Cited by 38 · see citing works

Copper transporter COPT5 participates in the crosstalk between vacuolar copper and iron pools mobilisation

Carrió-Seguí, À., Romero, P., Curie, C., et al. (2019) · Scientific Reports · doi:10.1038/s41598-018-38005-4 · Cited by 35 · see citing works

Expression of a Brassica napus metal transport protein (BnMTP3) in Arabidopsis thaliana confers tolerance to Zn and Mn

Gu, D., Zhou, X., Ma, Y., Xu, E., Yu, Y., Liu, Y., Chen, X., & Zhang, W. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110754 · Cited by 35 · see citing works

Elevated Expression of Vacuolar Nickel Transporter Gene IREG2 Is Associated With Reduced Root-to-Shoot Nickel Translocation in Noccaea japonica

Nishida, S., Tanikawa, R., Ishida, S., Yoshida, J., Mizuno, T., Nakanishi, H., & Furuta, N. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00610 · Cited by 32 · see citing works

Homology modeling andin vivofunctional characterization of the zinc permeation pathway in a heavy metal P-type ATPase

Lekeux, G., Crowet, J., Nouet, C., Joris, M., Jadoul, A., Bosman, B., Carnol, M., Motté, P., Lins, L., Galleni, M., et al. (2018) · Journal of Experimental Botany · doi:10.1093/jxb/ery353 · Cited by 29 · see citing works

Tobacco PIC1 Mediates Iron Transport and Regulates Chloroplast Development

Gong, X., Guo, C., Terachi, T., Cai, H., & Yu, D. (2014) · Plant Molecular Biology Reporter · doi:10.1007/s11105-014-0758-5 · Cited by 23 · see citing works

Identification and characterization of a novel copper transporter gene family TaCT 1 in common wheat

Li, H., Fan, R., Li, L., et al. (2013) · Plant Cell & Environment · doi:10.1111/pce.12263 · Cited by 23 · see citing works

Maize ZmFDR3 localized in chloroplasts is involved in iron transport

Jian-hui, H., Song, X., Li, P., Yang, H., & Yin, L. (2009) · Science in China Series C Life Sciences · doi:10.1007/s11427-009-0108-2 · Cited by 21 · see citing works

Cloning and characterisation of ZmZLP1, a gene encoding an endoplasmic reticulum-localised zinc transporter in Zea mays

Xu, Y., Wang, B., Yu, J., Ao, G., & Zhao, Q. (2010) · Functional Plant Biology · doi:10.1071/fp09045 · Cited by 21 · see citing works

COPT2, a plasma membrane located copper transporter, is involved in the uptake of Au in Arabidopsis

Tiwari, M., Venkatachalam, P., Peñarrubia, L., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-11896-5 · Cited by 21 · see citing works

Homologous Proteins of the Manganese Transporter PAM71 Are Localized in the Golgi Apparatus and Endoplasmic Reticulum

Hoecker, N., Honke, A., Frey, K., et al. (2020) · Plants · doi:10.3390/plants9020239 · Cited by 20 · see citing works

Pear metal transport protein PbMTP8.1 confers manganese tolerance when expressed in yeast and Arabidopsis thaliana

Li, J., Zheng, L., Fan, Y., et al. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2020.111687 · Cited by 19 · see citing works

Identification and characterization of a tobacco metal tolerance protein, NtMTP2

Papierniak, A., Kozak, K., Barabasz, A., Palusińska, M., Całka-Kresa, M., Maślińska-Gromadka, K., & Antosiewicz, D. M. (2020) · Metallomics · doi:10.1039/d0mt00210k · Cited by 17 · see citing works

Zea mays Fe deficiency‐related 4 (Zm FDR 4) functions as an iron transporter in the plastids of monocots

Zhang, X., Zhang, X., Zhang, Q., et al. (2017) · The Plant Journal · doi:10.1111/tpj.13482 · Cited by 15 · see citing works

Investigation of PIC1 (permease in chloroplasts 1) gene’s role in iron homeostasis: bioinformatics and expression analyses in tomato and sorghum

Filiz, E., & Akbudak, M. A. (2019) · BioMetals · doi:10.1007/s10534-019-00228-x · Cited by 12 · see citing works

Role of Sulphate Transporter (PiSulT) of Endophytic Fungus Serendipita indica in Plant Growth and DevelopmentPreprint

Narayan, O. P., Verma, N., Jogawat, A., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.01.07.897710 · Cited by 10 · see citing works

Functional characterization of a chloroplast-localized Mn2+(Ca2+)/H+ antiporter, ZmmCCHA1 from Zea mays ssp. mexicana L

Wang, C., Ou, D., Wang, C., et al. (2020) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2020.08.002 · Cited by 5 · see citing works

Analysis of Heavy Metal Impacts on Cereal Crop Growth and Development in Contaminated Soils

Vasilachi, I. C., Stoleru, V., & Gavrilescu, M. (2023) · Agriculture · doi:10.3390/agriculture13101983 · Cited by 210 · see citing works

Plant hyperaccumulators: a state-of-the-art review on mechanism of heavy metal transport and sequestration

Bhat, B. A., Rather, M. A., Bilal, T., Nazir, R., Qadir, R. U., & Mir, R. A. (2025) · Frontiers in Plant Science · doi:10.3389/fpls.2025.1631378 · Cited by 68 · see citing works

Selective Determination of the Doxorubicin Content of Individual Acidic Organelles in Impure Subcellular Fractions

Chen, Y., Walsh, R. J., & Arriaga, E. A. (2005) · Analytical Chemistry · doi:10.1021/ac0480996 · Cited by 35 · see citing works

Simultaneous isolation of intact mitochondria and chloroplasts from a single pulping of plant tissue

Rödiger, A., Baudisch, B., & Klösgen, R. B. (2010) · Journal of Plant Physiology · doi:10.1016/j.jplph.2009.11.013 · Cited by 52 · see citing works

Sheets, ribbons and tubules — how organelles get their shape

Voeltz, G. K., & Prinz, W. A. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2119 · Cited by 154 · see citing works

Cell Organelles: DNA

Kadam, N. R., & Kasar, P. M. (2023) · Asian Journal of Research in Pharmaceutical Sciences · doi:10.52711/2231-5659.2023.00045

Identifying Bona Fide Components of an Organelle by Isotope-Coded Labeling of Subcellular Fractions

Marelli, M., Nesvizhskii, A. I., & Aitchison, J. D. (2008) · Methods in molecular biology · doi:10.1007/978-1-59745-028-7_24 · Cited by 5 · see citing works