Aquaglyceroporins: ancient channels for metalloids
Open accessAbstract
The identification of aquaglyceroporins as uptake channels for arsenic and antimony shows how these toxic elements can enter the food chain, and suggests that food plants could be genetically modified to exclude arsenic while still accumulating boron and silicon.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
All seafoods contain arsenic, which enters cells through phosphate transporters and aquaglyceroporins.
“All seafoods contain arsenic, which enters cells through phosphate transporters and aquaglyceroporins (Bhattacharjee et al. 2008; Cooney et al. 1978; Zhao et al. 2010).”
From Algae as nutritional and functional food sources: revisiting our understanding. (2017) · cites this paper as Bhattacharjee et al. 2008
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Feng, J. X., Tamai, K., Yamaji, N., Mitani, N., Konishi, S., Katsuhara, M., Ishiguro, M., Murata, Y., & Yano, M. (2006) · Nature · doi:10.1038/nature04590 · Cited by 1,644 · 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
Structural mechanism of plant aquaporin gating
Törnroth‐Horsefield, S., Wang, Y., Hedfalk, K., Johanson, U., Karlsson, M. E., Tajkhorshid, E., Neutze, R., & Kjellbom, P. O. (2005) · Nature · doi:10.1038/nature04316 · Cited by 863 · see citing works
Takano, J., Wada, M., Ludewig, U., Schaaf, G., Nicolaus Von Wirén, A., & Fujiwara, T. (2006) · The Plant Cell · doi:10.1105/tpc.106.041640 · Cited by 730 · see citing works
Arsenic hazards: strategies for tolerance and remediation by plants
Tripathi, R. D., Srivastava, S., Mishra, S., Singh, N., Tuli, R., Gupta, D. K., & Maathuis, F. J. M. (2007) · Trends in biotechnology · doi:10.1016/j.tibtech.2007.02.003 · Cited by 665 · see citing works
Bienert, G. P., Thorsen, M. K., Bienert, M. D., Nilsson, R. H., Wagner, A., Tamás, M. J., & Jahn, T. P. (2008) · BMC Biology · doi:10.1186/1741-7007-6-26 · Cited by 414 · see citing works
Unexpected complexity of the Aquaporin gene family in the moss Physcomitrella patens
Danielson, J. Å., & Johanson, U. (2008) · BMC Plant Biology · doi:10.1186/1471-2229-8-45 · Cited by 409 · see citing works
Wysocki, R., Chéry, C. C., Wawrzycka, D., Hulle, M. V., Cornelis, R., Thevelein, J. M., & Tamás, M. J. (2001) · Molecular Microbiology · doi:10.1046/j.1365-2958.2001.02485.x · Cited by 327 · see citing works
Identification of Maize Silicon Influx Transporters
Mitani, N., Yamaji, N., & Ma, J. F. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn110 · Cited by 300 · see citing works
As(III) and Sb(III) Uptake by GlpF and Efflux by ArsB in Escherichia coli
Meng, Y., Liu, Z., & Rosen, B. P. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m400037200 · Cited by 297 · see citing works
Self-citationAntimonite is accumulated by the glycerol facilitator GlpF in Escherichia coli
Sanders, O. I., Rensing, C., Kuroda, M., Mitra, B., & Rosen, B. P. (1997) · Journal of Bacteriology · doi:10.1128/jb.179.10.3365-3367.1997 · Cited by 235 · see citing works
Self-citationThe Arabidopsis thaliana aquaglyceroporin AtNIP7;1 is a pathway for arsenite uptake
Isayenkov, S. V., & Maathuis, F. J. M. (2008) · FEBS Letters · doi:10.1016/j.febslet.2008.04.022 · Cited by 205 · see citing works
Allen, F. H., & Hoy, V. J. (1998) · Encyclopedia of Computational Chemistry · doi:10.1002/0470845015.cca059s · Cited by 189 · see citing works
Arsenic and Paddy Rice: A Neglected Cancer Risk?
Stone, R. A. (2008) · Science · doi:10.1126/science.321.5886.184 · Cited by 153 · see citing works
Porquet, A., & Filella, M. (2007) · Chemical Research in Toxicology · doi:10.1021/tx700110m · Cited by 90 · see citing works
Aquaglyceroporins and Metalloid Transport: Implications in Human Diseases
Bhattacharjee, H., Rosen, B. P., & Mukhopadhyay, R. (2008) · Handbook of experimental pharmacology · doi:10.1007/978-3-540-79885-9_16 · Cited by 52 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Algae as nutritional and functional food sources: revisiting our understanding.
Wells, M. L., Potin, P., Craigie, J. S., Raven, J. A., Merchant, S. S., Helliwell, K. E., Smith, A. G., Camire, M. E., & Brawley, S. H. (2017) · Journal of Applied Phycology · doi:10.1007/s10811-016-0974-5 · Cited by 1,562 · see citing works
Earth Abides Arsenic Biotransformations
Zhu, Y.-G., Yoshinaga, M., Zhao, F.-J., & Rosen, B. P. (2014) · Annual Review of Earth and Planetary Sciences · doi:10.1146/annurev-earth-060313-054942 · Cited by 550 · see citing works
Self-citationPathways of arsenic uptake and efflux
Garbinski, L. D., Rosen, B. P., & Chen, J. (2019) · Environment International · doi:10.1016/j.envint.2019.02.058 · Cited by 341 · see citing works
Self-citationPathways of Arsenic Uptake and Efflux
Yang, H.-C., Fu, H.-L., Lin, Y., & Rosen, B. P. (2012) · Current topics in membranes · doi:10.1016/b978-0-12-394390-3.00012-4 · Cited by 303 · see citing works
Self-citationAquaglyceroporins: Generalized metalloid channels
Mukhopadhyay, R., Bhattacharjee, H., & Rosen, B. P. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.11.021 · Cited by 193 · see citing works
Self-citationReview of arsenic speciation, toxicity and metabolism in microalgae
Wang, Y., Wang, S., Xu, P., Liu, C., Liu, M., Wang, Y., Wang, C., Zhang, C., & Ge, Y. (2015) · Reviews in Environmental Science and Bio/Technology · doi:10.1007/s11157-015-9371-9 · Cited by 186 · see citing works
Schnurbusch, T., Hayes, J. E., Hrmová, M., Baumann, U., Ramesh, S. A., Tyerman, S. D., Langridge, P., & Sutton, T. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.158832 · Cited by 181 · see citing works
Fate of arsenic in living systems: Implications for sustainable and safe food chains
Rehman, M. U., Khan, R., Khan, A., Qamar, W., Arafah, A. M., Ahmad, A., Ahmad, A., Akhter, R., Rinklebe, J., & Ahmad, P. (2021) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2021.126050 · Cited by 173 · see citing works
The Environmental Geochemistry of Arsenic -- An Overview --
Bowell, R. J., Alpers, C. N., Jamieson, H. E., Nordstrom, D. K., & Majzlan, J. (2014) · Reviews in Mineralogy and Geochemistry · doi:10.2138/rmg.2014.79.1 · Cited by 169 · see citing works
How prokaryotes deal with arsenic †
Slyemi, D., & Bonnefoy, V. (2011) · Environmental Microbiology Reports · doi:10.1111/j.1758-2229.2011.00300.x · Cited by 162 · see citing works
Arsenic and Antimony Transporters in Eukaryotes
Maciaszczyk-Dziubińska, E., Wawrzycka, D., & Wysocki, R. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms13033527 · Cited by 154 · see citing works
Ma, Z., Lin, L., Wu, M., Yu, H., Shang, T., Zhang, T., & Zhao, M. (2018) · Aquaculture · doi:10.1016/j.aquaculture.2018.07.040 · Cited by 120 · see citing works
Phytoremediation potential of Arundo donax in arsenic-contaminated synthetic wastewater
Mirza, N., Mahmood, Q., Pervez, A., Ahmad, R., Farooq, R., Shah, M. M., & Azim, M. R. (2010) · Bioresource Technology · doi:10.1016/j.biortech.2010.03.012 · Cited by 118 · see citing works
Zhu, Y., & Rosen, B. P. (2009) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2009.02.011 · Cited by 108 · see citing works
Self-citationPlants as Useful Vectors to Reduce Environmental Toxic Arsenic Content
Mirza, N., Mahmood, Q., Shah, M. M., Pervez, A., & Sultan, S. (2014) · The Scientific World JOURNAL · doi:10.1155/2014/921581 · Cited by 104 · see citing works
Transport routes of metalloids into and out of the cell: A review of the current knowledge
Zangi, R., & Filella, M. (2012) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2012.02.001 · Cited by 103 · see citing works
Ecological restoration of arsenic contaminated soil by Arundo donax L
Mirza, N., Pervez, A., Mahmood, Q., Shah, M. M., & Shafqat, M. N. (2011) · Ecological Engineering · doi:10.1016/j.ecoleng.2011.07.006 · Cited by 100 · see citing works
Katsuhara, M., Sasano, S., Horie, T., Matsumoto, T., Rhee, J., & Shibasaka, M. (2014) · Plant Biotechnology · doi:10.5511/plantbiotechnology.14.0421a · Cited by 96 · see citing works
Antimony toxicity in soils and plants, and mechanisms of its alleviation
Vidya, C. S.-N., Shetty, R., Vaculíková, M., & Vaculík, M. (2022) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2022.104996 · Cited by 92 · see citing works
Biogeochemistry of antimony in soil-plant system: Ecotoxicology and human health
Natasha, N., Shahid, M. A. R., Khalid, S., Dumat, C., Pierart, A., & Niazi, N. K. (2019) · Applied Geochemistry · doi:10.1016/j.apgeochem.2019.04.006 · Cited by 82 · see citing works
Antimony uptake, efflux and speciation in arsenic hyperaccumulator Pteris vittata
Tisarum, R., Lessl, J. T., Dong, X., de Oliveira, L. M., Rathinasabapathi, B., & Ma, L. Q. (2013) · Environmental Pollution · doi:10.1016/j.envpol.2013.11.033 · Cited by 62 · see citing works
tassel-less1 Encodes a Boron Channel Protein Required for Inflorescence Development in Maize
Leonard, A., Holloway, B. A., Guo, M., Rupe, M. A., Yu, G.-X., Beatty, M. K., Zastrow‐Hayes, G., Meeley, R. B., Llaca, V., Butler, K., et al. (2014) · Plant and Cell Physiology · doi:10.1093/pcp/pcu036 · Cited by 60 · see citing works
Müller, K., Daus, B., Mattusch, J., Vetterlein, D., Merbach, I., & Wennrich, R. (2012) · Environmental Pollution · doi:10.1016/j.envpol.2012.10.024 · Cited by 57 · see citing works
How Plants Handle Trivalent (+3) Elements
Poschenrieder, C., Busoms, S., & Barceló, J. A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20163984 · Cited by 54 · see citing works
The plasma membrane proteome of maize roots grown under low and high iron conditions
Hopff, D., Wienkoop, S., & Lüthje, S. (2013) · Journal of Proteomics · doi:10.1016/j.jprot.2013.01.006 · Cited by 53 · see citing works
Plant aquaporins: Their roles beyond water transport
Sun, Q., Liu, X., Kitagawa, Y., Calamita, G., & Ding, X. (2024) · The Crop Journal · doi:10.1016/j.cj.2024.04.005 · Cited by 52 · see citing works
Paul, T., & Saha, N. C. (2019) · Pedosphere · doi:10.1016/s1002-0160(19)60829-5 · Cited by 47 · see citing works
Deng, F., Liu, X., Chen, Y., Rathinasabapathi, B., Rensing, C., Chen, J., Bi, J., Xiang, P., & Ma, L. Q. (2019) · Critical Reviews in Environmental Science and Technology · doi:10.1080/10643389.2019.1662704 · Cited by 43 · see citing works
Transcriptomic Response of Purple Willow (Salix purpurea) to Arsenic Stress
Yanitch, A., Brereton, N. J. B., González, E., Labrecque, M., Joly, S., & Pitre, F. E. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.01115 · Cited by 42 · see citing works
Arsenic stress in Rice (Oryza sativa) and its amelioration approaches
Khan, Z., Thounaojam, T. C., & Upadhyaya, H. (2022) · Plant Stress · doi:10.1016/j.stress.2022.100076 · Cited by 41 · see citing works
Unravelling molecular mechanisms for enhancing arsenic tolerance in plants: A review
Gautam, A., Pandey, A. K., & Dubey, R. S. (2020) · Plant Gene · doi:10.1016/j.plgene.2020.100240 · Cited by 40 · see citing works
Mathews, S., Rathinasabapathi, B., & Ma, L. Q. (2011) · Environmental Pollution · doi:10.1016/j.envpol.2011.08.027 · Cited by 40 · see citing works
Jung, D., Sato, J. D., Shaw, J. R., & Stanton, B. A. (2011) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2011.11.014 · Cited by 38 · see citing works
Tisarum, R., Chen, Y., Dong, X., Lessl, J. T., & Ma, L. Q. (2015) · Environmental Pollution · doi:10.1016/j.envpol.2015.06.029 · Cited by 38 · see citing works
Dhuldhaj, U. P., Yadav, I. C., Singh, S., & Sharma, N. K. (2012) · Reviews of Environmental Contamination and Toxicology · doi:10.1007/978-1-4614-5882-1_1 · Cited by 36 · see citing works
Geng, A., Lian, W., Wang, Y., Liu, M., Zhang, Y., Wang, X., & Chen, G. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25052861 · Cited by 29 · see citing works
Germanium as a tool to dissect boron toxicity effects in barley and wheat
Hayes, J. E., Pallotta, M. A., Baumann, U., Berger, B., Langridge, P., & Sutton, T. (2013) · Functional Plant Biology · doi:10.1071/fp12329 · Cited by 29 · see citing works
Rubinos, D. A., Calvo, V., Iglesias, L., & Barral, M. T. (2014) · Environmental Science and Pollution Research · doi:10.1007/s11356-014-2715-0 · Cited by 29 · see citing works
Physiological responses, tolerance, and remediation strategies in plants exposed to metalloids
Singh, S., Kumar, V., Datta, S., Dhanjal, D. S., Singh, S., Kumar, S., Kapoor, D., Prasad, R., & Singh, J. (2020) · Environmental Science and Pollution Research · doi:10.1007/s11356-020-10293-2 · Cited by 26 · see citing works
Usage of Si, P, Se, and Ca Decrease Arsenic Concentration/Toxicity in Rice, a Review
Boorboori, M. R., Gao, Y., Wang, H. E., & Fang, C. (2021) · Applied Sciences · doi:10.3390/app11178090 · Cited by 25 · see citing works
Hockmann, K., Tandy, S., Studer, B., Evangelou, M. W. H., & Schulin, R. (2018) · Environmental Pollution · doi:10.1016/j.envpol.2018.03.014 · Cited by 23 · see citing works
Freshwater phytoplankton: Salinity stress on arsenic biotransformation
Papry, R. I., Fujisawa, S., Zai, Y., Akhyar, O., Mashio, A. S., & Hasegawa, H. (2020) · Environmental Pollution · doi:10.1016/j.envpol.2020.116090 · Cited by 22 · see citing works
Chan, W. K., Wildeboer, D., Garelick, H., & Purchase, D. (2016) · Fungal biology · doi:10.1007/978-3-319-42852-9_10 · Cited by 21 · see citing works
Ngo, L. K., Price, H. L., Bennett, W. W., Teasdale, P. R., & Jolley, D. F. (2019) · Environmental Pollution · doi:10.1016/j.envpol.2019.113815 · Cited by 21 · see citing works
Huang, Y., Yan, X., Zheng, X., Xu, K., Zhong, Q., Yang, T., Liu, F., Wang, C., Shu, L., He, Z., et al. (2020) · Environmental Geochemistry and Health · doi:10.1007/s10653-020-00658-4 · Cited by 21 · see citing works
Mourão, J., Rebelo, A., Ribeiro, S., Peixe, L. M. S. V., Novais, C., & Antunes, P. (2020) · Environmental Microbiology · doi:10.1111/1462-2920.15016 · Cited by 20 · see citing works
MtNIP5;1, a novel Medicago truncatula boron diffusion facilitator induced under deficiency
Granado‐Rodríguez, S., Bolaños, L., & Reguera, M. (2020) · BMC Plant Biology · doi:10.1186/s12870-020-02750-4 · Cited by 19 · see citing works
Geochemical Characteristics of Mineral Elements: Arsenic, Fluorine, Lead, Nitrogen, and Carbon
Kar, S. (2022) · Springer eBooks · doi:10.1007/978-981-16-8770-9_10 · Cited by 18 · see citing works
Liu, X., Wei, Y., Zhou, X., Pei, X., & Zhang, S. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.02127-15 · Cited by 18 · see citing works
Structure and function of a silicic acid channel Lsi1
Saitoh, Y., & Suga, M. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.982068 · Cited by 17 · see citing works
Antimony induced structural and ultrastructural changes in Trapa natans
Baruah, S., Bora, M. S., Dutta, S., Hazarika, K. K., Mudoi, P., & Sarma, K. P. (2021) · Scientific Reports · doi:10.1038/s41598-021-89865-2 · Cited by 17 · see citing works
Ahmad, J., Beg, M. A., Ali, A. A., Al‐Huqail, A. A., & Qureshi, M. I. (2022) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2022.114128 · Cited by 17 · see citing works
Cation transporters in plants: an overview
Sharma, A., Sharma, H., & Upadhyay, S. K. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-85790-1.00011-7 · Cited by 16 · see citing works
Uzcategui, N. L., Figarella, K., Bassarak, B., Meza, N. W., Mukhopadhyay, R., Ramı́rez, J. L., & Duszenko, M. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000354490 · Cited by 16 · see citing works
Self-citationLu, Y., Ran, M., Jiao, Y., Wu, J., & Li, J. (2023) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2023.105601 · Cited by 14 · see citing works
Trypanosomatid Aquaporins: Roles in Physiology and Drug Response
Mandal, G., Orta, J., Sharma, M., & Mukhopadhyay, R. (2013) · Diseases · doi:10.3390/diseases2010003 · Cited by 14 · see citing works
Self-citationA Novel Aquaporin 3 in Killifish (Fundulus heteroclitus) Is Not An Arsenic Channel
Jung, D., MacIver, B., Jackson, B. P., Barnaby, R., Sato, J. D., Zeidel, M. L., Shaw, J. R., & Stanton, B. A. (2012) · Toxicological Sciences · doi:10.1093/toxsci/kfs078 · Cited by 14 · see citing works
Biosilica-Based Strategies for Treatment of Osteoporosis and Other Bone Diseases
Schröder, H. C., Wiens, M., Wang, X., Schloßmacher, U., & Müller, W. E. G. (2011) · Progress in molecular and subcellular biology · doi:10.1007/978-3-642-21230-7_10 · Cited by 13 · see citing works
Patel, A., Tiwari, S., & Prasad, S. M. (2021) · Environmental Science and Pollution Research · doi:10.1007/s11356-021-13800-1 · Cited by 13 · see citing works
Qian, W., Chen, C. C., Huang, Y., & Zhu, X. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.168508 · Cited by 12 · see citing works
Mechanisms of Arsenic Transport, Accumulation, and Distribution in Rice
Shinde, A., & Kumar, K. (2021) · Springer eBooks · doi:10.1007/978-981-33-6068-6_11 · Cited by 12 · see citing works
Metalloids and Their Role in the Biological System
Kesawat, M. S., Shivaraj, S. M., Kim, D. K., Kumar, M., Hahn, B.-S., & Deshmukh, R. K. (2020) · Wiley eBooks · doi:10.1002/9781119487210.ch1 · Cited by 12 · see citing works
Han, Y., Liu, B., Yin, Z., Shan, X., Zhang, M., Jing, C., & Jiang, W. (2025) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2025.138820 · Cited by 10 · see citing works
A novel variant of aquaporin 3 is expressed in killifish (Fundulus heteroclitus) intestine
Jung, D., Adamo, M. A., Lehman, R. M., Barnaby, R., Jackson, C. E., Jackson, B. P., Shaw, J. R., & Stanton, B. A. (2015) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2015.03.001 · Cited by 10 · see citing works
Wan, X., Yang, J., & Lei, M. (2018) · Environmental Science and Pollution Research · doi:10.1007/s11356-018-3228-z · Cited by 10 · see citing works
Influence of titanium dioxide nanoparticles on the toxicity of arsenate in Nannochloropsis maritima
Yang, F., & Yan, C. (2018) · Chemosphere · doi:10.1016/j.chemosphere.2018.06.097 · Cited by 9 · see citing works
Jiao, Y., Ran, M., Wu, J., & Li, J. (2025) · Journal of Environmental Management · doi:10.1016/j.jenvman.2025.124100 · Cited by 8 · see citing works
Hu, Y., Xiang, X., Jiang, W., Meng, G., Jing, Z., Guo, Z., Zhou, J., Tang, H., Miao, J., & Morsy, K. (2024) · Agronomy · doi:10.3390/agronomy14091887 · Cited by 7 · see citing works
Yoon, H., Giometto, A., Pothier, M. P., Zhang, X., Poulain, A. J., & Reid, M. C. (2022) · Applied and Environmental Microbiology · doi:10.1128/aem.00891-22 · Cited by 7 · see citing works
Pozzolini, M., Ferrando, S., Gallus, L., Gambardella, C., Ghignone, S., & Giovine, M. (2016) · Biological Bulletin · doi:10.1086/bblv230n3p220 · Cited by 6 · see citing works
Endogenous factors involved in regulating arsenic uptake and toxicity in plant
Kumar, M., Singh, S., Maury, J., Ahmad, I., Kushwaha, A. S., Shukla, J., Gill, S. S., & Tuteja, N. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99600-6.00019-0 · Cited by 6 · see citing works
Plant responses to arsenic: uptake, metabolism and resistance to arsenic toxicity – a review
Heidari, M. (2017) · Zemdirbyste-Agriculture · doi:10.13080/z-a.2017.104.047 · Cited by 6 · see citing works
Transgenics for Arsenic and Chromium Phytoremediation
Tiwari, S., & Sarangi, B. K. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814389-6.00009-2 · Cited by 6 · see citing works
Bihmidine, S., Cao, M., Kang, M., Awada, T. N., Etten, J. L. V., Dunigan, D. D., & Clemente, T. E. (2014) · Planta · doi:10.1007/s00425-014-2075-5 · Cited by 5 · see citing works
Anti-Oxidative Response of Cyanobacterium Anabaena sp. strain PCC 7120 to Arsenite (As(III))
Dhuldhaj, U. P., Pandya, U., & Singh, S. (2018) · Microbiology · doi:10.1134/s0026261718060097 · Cited by 5 · see citing works
Salicylic Acid‐Mediated Physiological and Molecular Mechanism in Plants Under Metal(loid) Stress
Kour, J., Khanna, K., Sharma, P., Singh, A. D., Bhardwaj, T., Sharma, N., Sharma, A., Kaur, R., & Bhardwaj, R. (2022) · Wiley eBooks · doi:10.1002/9781119671107.ch8 · Cited by 5 · see citing works
Ali, W. (2012) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York) · Cited by 4 · see citing works
Kumar, U., Jha, A. K., & Singh, R. S. (2021) · Springer eBooks · doi:10.1007/978-981-33-6068-6_14 · Cited by 3 · see citing works
Fu, H., Jiang, X. J., & Rosen, B. P. (2010) · Wiley eBooks · doi:10.1002/9780470975503.ch8 · Cited by 3 · see citing works
Self-citationFrom Utility to Toxicity: Managing Metalloid Pollution Through Innovative Remediation Technologies
Davamani, V., Arulmani, S., Poornima, R., Premalatha, R. P., Deepasri, M., Kalaiselvi, P., Gopalakrishnan, M., Moon, C. J., Theerthagiri, J., & Choi, M. Y. (2025) · The Chemical Record · doi:10.1002/tcr.202500191 · Cited by 2 · see citing works
Dhuldhaj, U. P., & Pandya, U. (2021) · Archives of Microbiology · doi:10.1007/s00203-021-02405-4 · Cited by 2 · see citing works
Do Antimonite and Silicon Share the Same Root Uptake Pathway by Lsi1 in Sorghum bicolor L. Moench?
Vidya, C. S.-N., Shetty, R., Bokor, B., Fialová, I., Luxová, M., Jašková, K., & Vaculík, M. (2023) · Plants · doi:10.3390/plants12122368 · Cited by 2 · see citing works
D’Eusanio, V., Frignani, E., Marchetti, A., Pigani, L., Rivi, M., & Roncaglia, F. (2025) · Molecules · doi:10.3390/molecules30040908 · Cited by 2 · see citing works
Chan, Y.-H., Lin, C.-Y., Pai, S. H., Huang, J., & Lin, C. (2011) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf1040542 · Cited by 2 · see citing works
Arsenic Tolerance in Plants: Cellular Maneuvering Through Sulfur Metabolites
Talukdar, D. (2016) · Springer eBooks · doi:10.1007/978-3-319-44081-1_14 · Cited by 2 · see citing works
Role of microorganisms in alleviation of arsenic toxicity in plants
Khan, A. A., Kukreti, B., Makarana, G., Suyal, D. C., Singh, A. V., & Kumar, S. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99896-3.00007-2 · Cited by 2 · see citing works
Plant aquaporins: the origin of NIPsPreprint
Borstlap, A. C. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/351064 · Cited by 2 · see citing works
Azam, S. M., Huang, K., Yuan, J., Bai, Y., Chen, Q., Dang, P., Alwathnani, H. A., Zayid, H. F. B., Feng, R., & Rensing, C. (2025) · Plants · doi:10.3390/plants14101475 · Cited by 1 · see citing works
Shorif, M. J. U., Rahman, M. A., & Chowdhury, S. (2025) · Arabian Journal for Science and Engineering · doi:10.1007/s13369-025-10920-5 · Cited by 1 · see citing works
Gawade, N. S., Pagariya, M. C., Jadhav, P., Muhammed, P. K. M., Shinde, N. A., Mandlik, R., Madhavan, S., Jadhav, P. V., Sonah, H., Patil, G., et al. (2025) · Plant Science · doi:10.1016/j.plantsci.2025.112971 · Cited by 1 · see citing works
Das, A., Das, R., & Bhattacharjee, C. (2020) · Lecture notes in bioengineering · doi:10.1007/978-981-15-7409-2_23 · Cited by 1 · see citing works
Beamer, Z. G., Routray, P., Agrawal, R., Li, T., Gibson, K. M., Ostrouchov, K. E., Smith, J. C., & Roberts, D. M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.05.510970 · Cited by 1 · see citing works
Biogeochemical Processes of Arsenic in Paddy Soils
Zhu, Y., Liu, W., Duan, G., Williams, P. N., & Sun, G. (2010) · Springer eBooks · doi:10.1007/978-3-642-05297-2_14
Managing arsenic in paddy soils to reduce human exposure to arsenic in rice
Zhu, Y. (2010) · CRC Press eBooks · doi:10.1201/b10548-74
B. Rosen, K. M. (2012) · CRC Press eBooks · doi:10.1201/b12522-78
Alowaifeer, A. M. (2019) · Montana State University ScholarWorks (Montana State University)
Lu, Y. C., Peng, F., Wang, Y., Li, H., & Yang, Z. (2023) · Toxics · doi:10.3390/toxics11100860
Granado‐Rodríguez, S., Bolaños, L., & Reguera, M. (2020) · Figshare · doi:10.6084/m9.figshare.13357151
Granado‐Rodríguez, S., Bolaños, L., & Reguera, M. (2020) · Figshare · doi:10.6084/m9.figshare.13357154
- Authors
- Bhattacharjee, H., Mukhopadhyay, R., Thiyagarajan, S., & Rosen, B. P.
- Affiliations
- Wayne State University (US)
- Corresponding author
- Rosen, Barry P
- Venue
- Journal of Biology
- Published
- 2008
- Volume
- 7
- Issue
- 9
- Pages
- 33
- ISSN
- 1475-4924 (ISSN-L)
- PMC
- PMC2776386
- OpenAlex
- W2145039095
- Cited by
- 107
- References
- 16
- Citations by year
- 2026: 3 · 2025: 7 · 2024: 3 · 2023: 6 · 2022: 9 · 2021: 7 · 2020: 14 · 2019: 8 · 2018: 6 · 2017: 2 · 2016: 4 · 2015: 5 · 2014: 7 · 2013: 6 · 2012: 8
- FWCI
- 1.63
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Journal of Biology (publishedVersion, cc-by)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (R37GM055425)
- National Institute of Allergy and Infectious Diseases (R01AI058170)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Physical Sciences › Environmental Science › Environmental Chemistry › Arsenic contamination and mitigation
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Heavy Metal Exposure and Toxicity
- Keywords
- aquaglyceroporins, arsenic uptake, metalloid toxicity, food chain contamination, transgenic plants, boron accumulation, silicon accumulation
- MeSH terms
- Antimony, Arsenic, Biological Transport, Genetic Engineering, Plant Proteins, Crops, Agricultural, Food Chain, Aquaglyceroporins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review