silver (BioDeep_00000732062)

Main id: BioDeep_00000006290

 


代谢物信息卡片


silver

化学式: Ag (106.9051)
中文名称: 银标准溶液, 蛋白银
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: [Ag]
InChI: InChI=1S/Ag

描述信息

D - Dermatologicals > D08 - Antiseptics and disinfectants > D08A - Antiseptics and disinfectants > D08AL - Silver compounds
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Coronavirus
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COVID-19
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SARS

同义名列表

2 个代谢物同义名

silver; Silver



数据库引用编号

12 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(6)

PlantCyc(1)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

0 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 7 ALB, CA1, CA3, ENO2, PFDN5, TH, VIM
Peripheral membrane protein 1 MBP
Endosome membrane 1 TF
Endoplasmic reticulum membrane 1 PMEL
Nucleus 6 ALB, KLK3, MBP, NCL, PFDN5, TH
cytosol 10 ALB, CA1, CA3, ENO2, MBP, PFDN5, SST, TH, UAP1, VIM
dendrite 1 TH
phagocytic vesicle 1 VIM
centrosome 1 ALB
nucleoplasm 2 NCL, UAP1
Cell membrane 3 AGTR1, ENO2, VIM
Cytoplasmic side 1 MBP
Cell projection, axon 1 TH
Multi-pass membrane protein 2 AGTR1, SYP
Synapse 2 MBP, TAC1
cell cortex 1 NCL
cell surface 2 MBP, TF
Golgi apparatus 2 ALB, PMEL
neuromuscular junction 1 SYP
neuronal cell body 3 MBP, SST, TAC1
presynaptic membrane 1 SYP
smooth endoplasmic reticulum 1 TH
synaptic vesicle 2 SYP, TH
Cytoplasm, cytosol 1 UAP1
plasma membrane 10 AGTR1, ENO2, KLK3, MBP, NCL, PMEL, REN, TF, UAP1, VIM
presynaptic active zone 1 SYP
synaptic vesicle membrane 1 SYP
terminal bouton 2 SYP, TH
Membrane 6 AGTR1, ENO2, NCL, PMEL, REN, SYP
apical plasma membrane 1 TF
axon 3 TAC1, TH, VIM
extracellular exosome 9 ALB, CA1, ENO2, KLK3, MBP, NCL, PMEL, TF, VIM
endoplasmic reticulum 3 AGR3, ALB, PMEL
extracellular space 7 ALB, ENO2, KLK3, REN, SST, TAC1, TF
perinuclear region of cytoplasm 3 SYP, TF, TH
Schaffer collateral - CA1 synapse 1 SYP
mitochondrion 1 TH
protein-containing complex 3 ALB, KLK3, MBP
intracellular membrane-bounded organelle 1 AGR3
Single-pass type I membrane protein 1 PMEL
Secreted 5 ALB, PMEL, REN, SST, TF
extracellular region 7 ALB, KLK3, MBP, REN, SST, TAC1, TF
cytoplasmic side of plasma membrane 1 TH
basal part of cell 1 TF
excitatory synapse 1 SYP
anchoring junction 1 ALB
photoreceptor inner segment 1 ENO2
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 SYP
Endosome, multivesicular body 1 PMEL
Extracellular vesicle 1 PMEL
perikaryon 2 ENO2, TH
cytoplasmic vesicle 2 TF, TH
nucleolus 1 NCL
Melanosome membrane 2 PMEL, TH
Early endosome 1 TF
apical part of cell 1 REN
clathrin-coated pit 1 TF
recycling endosome 1 TF
vesicle 1 TF
Cytoplasm, perinuclear region 1 TH
Cytoplasm, cytoskeleton 1 VIM
focal adhesion 1 VIM
GABA-ergic synapse 1 SST
Peroxisome 1 VIM
collagen-containing extracellular matrix 1 MBP
secretory granule 1 KLK3
intermediate filament 1 VIM
Late endosome 1 TF
neuron projection 3 SYP, TH, VIM
ciliary basal body 1 ALB
cell leading edge 1 VIM
cell periphery 1 MBP
Chromosome 1 NCL
cytoskeleton 1 VIM
[Isoform 3]: Nucleus 1 MBP
centriole 1 ALB
cytoplasmic ribonucleoprotein granule 1 NCL
Nucleus, nucleolus 1 NCL
spindle pole 1 ALB
blood microparticle 2 ALB, TF
spliceosomal complex 1 NCL
Endomembrane system 1 SYP
Cornified envelope 1 NCL
microtubule organizing center 1 VIM
Melanosome 1 PMEL
myelin sheath 1 MBP
intermediate filament cytoskeleton 2 PFDN5, VIM
basal plasma membrane 1 TF
multivesicular body membrane 1 PMEL
ficolin-1-rich granule lumen 1 MBP
secretory granule lumen 1 TF
HFE-transferrin receptor complex 1 TF
endoplasmic reticulum lumen 2 ALB, TF
nuclear matrix 1 VIM
platelet alpha granule lumen 1 ALB
endocytic vesicle 1 TF
transport vesicle 1 MBP
neuronal dense core vesicle 1 SST
Golgi apparatus, cis-Golgi network membrane 1 PMEL
Nucleus matrix 1 VIM
clathrin-coated endocytic vesicle membrane 1 TF
ribonucleoprotein complex 1 NCL
Synapse, synaptosome 1 SYP
prefoldin complex 1 PFDN5
cis-Golgi network membrane 1 PMEL
vesicle coat 1 TF
multivesicular body, internal vesicle 1 PMEL
compact myelin 1 MBP
internode region of axon 1 MBP
phosphopyruvate hydratase complex 1 ENO2
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle 1 TH
[Bone marrow proteoglycan]: Secreted 1 MBP
macropinosome membrane 1 NCL
ciliary transition fiber 1 ALB
Myelin membrane 1 MBP
dense body 1 TF


文献列表

  • Min Kim, Jung-Suk Sung, Raji Atchudan, Asad Syed, Ashok Kumar Nadda, Dae-Young Kim, Gajanan Sampatrao Ghodake. A rapid, high-yield and bioinspired synthesis of colloidal silver nanoparticles using Glycyrrhiza glabra root extract and assessment of antibacterial and phytostimulatory activity. Microscopy research and technique. 2023 Sep; 86(9):1154-1168. doi: 10.1002/jemt.24389. [PMID: 37421302]
  • Yan Liu, Lijuan He, Yunli Zhao, Yongbing Cao, Zhiguo Yu, Feng Lu. Optimization of Surface-Enhanced Raman Spectroscopy Detection Conditions for Interaction between Gonyautoxin and Its Aptamer. Toxins. 2022 01; 14(1):. doi: 10.3390/toxins14010049. [PMID: 35051026]
  • Lu Li, Zhenfei Bi, Yuzhu Hu, Lu Sun, Yanlin Song, Siyuan Chen, Fei Mo, Jingyun Yang, Yuquan Wei, Xiawei Wei. Silver nanoparticles and silver ions cause inflammatory response through induction of cell necrosis and the release of mitochondria in vivo and in vitro. Cell biology and toxicology. 2021 04; 37(2):177-191. doi: 10.1007/s10565-020-09526-4. [PMID: 32367270]
  • Ru Jiang, Hua-Yue Zhu, Yong-Qian Fu, Sheng-Tao Jiang, En-Min Zong, Jian-Qiang Zhu, Ying-Ying Zhu, Li-Fan Chen. Colloidal CdS sensitized nano-ZnO/chitosan hydrogel with fast and efficient photocatalytic removal of congo red under solar light irradiation. International journal of biological macromolecules. 2021 Mar; 174(?):52-60. doi: 10.1016/j.ijbiomac.2021.01.077. [PMID: 33460656]
  • Shweta Rajawat, Manzar M Malik. Targeted Delivery of Colloidal Silver for MCF-7 Breast Cancer Treatment. Current drug delivery. 2020; 17(7):613-621. doi: 10.2174/1567201817666200508095241. [PMID: 32384028]
  • Lourdes Marchante, Lucía Loarce, Pedro M Izquierdo-Cañas, M Elena Alañón, Esteban García-Romero, M Soledad Pérez-Coello, M Consuelo Díaz-Maroto. Natural extracts from grape seed and stem by-products in combination with colloidal silver as alternative preservatives to SO2 for white wines: Effects on chemical composition and sensorial properties. Food research international (Ottawa, Ont.). 2019 11; 125(?):108594. doi: 10.1016/j.foodres.2019.108594. [PMID: 31554048]
  • Lourdes Marchante, Pedro M Izquierdo-Cañas, Sergio Gómez-Alonso, M Elena Alañón, Esteban García-Romero, M Soledad Pérez-Coello, M Consuelo Díaz-Maroto. Oenological potential of extracts from winery and cooperage by-products in combination with colloidal silver as natural substitutes to sulphur dioxide. Food chemistry. 2019 Mar; 276(?):485-493. doi: 10.1016/j.foodchem.2018.10.072. [PMID: 30409623]
  • Martina Varga, Janja Horvatić, Lara Barišić, Zdenko Lončarić, Maja Dutour Sikirić, Ina Erceg, Aleksandra Kočić, Ivna Štolfa Čamagajevac. Physiological and biochemical effect of silver on the aquatic plant Lemna gibba L.: Evaluation of commercially available product containing colloidal silver. Aquatic toxicology (Amsterdam, Netherlands). 2019 Feb; 207(?):52-62. doi: 10.1016/j.aquatox.2018.11.018. [PMID: 30521985]
  • Naiyf S Alharbi, Marimuthu Govindarajan, Shine Kadaikunnan, Jamal M Khaled, Taghreed N Almanaa, Sami A Alyahya, Mohammed N Al-Anbr, Kasi Gopinath, Arumugam Sudha. Nanosilver crystals capped with Bauhinia acuminata phytochemicals as new antimicrobials and mosquito larvicides. Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS). 2018 Dec; 50(?):146-153. doi: 10.1016/j.jtemb.2018.06.016. [PMID: 30262272]
  • Daqiu Zhao, Menglin Cheng, Wenhui Tang, Ding Liu, Siyu Zhou, Jiasong Meng, Jun Tao. Nano-silver modifies the vase life of cut herbaceous peony (Paeonia lactiflora Pall.) flowers. Protoplasma. 2018 Jul; 255(4):1001-1013. doi: 10.1007/s00709-018-1209-1. [PMID: 29359232]
  • Oğuz Eryılmaz, Perihan Seda Ateş, İsmail Ünal, Ünsal Veli Üstündağ, Sadık Bay, Ahmet Ata Alturfan, Türkan Yiğitbaşı, Ebru Emekli-Alturfan, Mehmet Akalın. Evaluation of the interaction between proliferation, oxidant-antioxidant status, Wnt pathway, and apoptosis in zebrafish embryos exposed to silver nanoparticles used in textile industry. Journal of biochemical and molecular toxicology. 2018 Jan; 32(1):. doi: 10.1002/jbt.22015. [PMID: 29283201]
  • Masumeh Mirzaei, Mazdak Razi, Rajabali Sadrkhanlou. Nanosilver particles increase follicular atresia: Correlation with oxidative stress and aromatization. Environmental toxicology. 2017 Oct; 32(10):2244-2255. doi: 10.1002/tox.22440. [PMID: 28646569]
  • Foysal Kabir Tareq, Mst Fayzunnesa, Md Shahariar Kabir. Antimicrobial activity of plant-median synthesized silver nanoparticles against food and agricultural pathogens. Microbial pathogenesis. 2017 Aug; 109(?):228-232. doi: 10.1016/j.micpath.2017.06.002. [PMID: 28583887]
  • Anica Simić, Ailin Falkmo Hansen, Bjørn Olav Åsvold, Pål Richard Romundstad, Kristian Midthjell, Tore Syversen, Trond Peder Flaten. Trace element status in patients with type 2 diabetes in Norway: The HUNT3 Survey. Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS). 2017 May; 41(?):91-98. doi: 10.1016/j.jtemb.2017.03.001. [PMID: 28347468]
  • Ailin Falkmo Hansen, Anica Simić, Bjørn Olav Åsvold, Pål Richard Romundstad, Kristian Midthjell, Tore Syversen, Trond Peder Flaten. Trace elements in early phase type 2 diabetes mellitus-A population-based study. The HUNT study in Norway. Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS). 2017 Mar; 40(?):46-53. doi: 10.1016/j.jtemb.2016.12.008. [PMID: 28159221]
  • Guangqiu Qin, Song Tang, Shibin Li, Haoliang Lu, Yanwu Wang, Peng Zhao, Bin Li, Jiehong Zhang, Liang Peng. Toxicological evaluation of silver nanoparticles and silver nitrate in rats following 28 days of repeated oral exposure. Environmental toxicology. 2017 Feb; 32(2):609-618. doi: 10.1002/tox.22263. [PMID: 26996539]
  • K Dziendzikowska, A Krawczyńska, M Oczkowski, T Królikowski, K Brzóska, A Lankoff, M Dziendzikowski, T Stępkowski, M Kruszewski, J Gromadzka-Ostrowska. Progressive effects of silver nanoparticles on hormonal regulation of reproduction in male rats. Toxicology and applied pharmacology. 2016 Dec; 313(?):35-46. doi: 10.1016/j.taap.2016.10.013. [PMID: 27746313]
  • Sufang Qiu, Chao Li, Jinyong Lin, Yuanji Xu, Jun Lu, Qingting Huang, Changyan Zou, Chao Chen, Nanyang Xiao, Duo Lin, Rong Chen, Jianji Pan, Shangyuan Feng. Early discrimination of nasopharyngeal carcinoma based on tissue deoxyribose nucleic acid surface-enhanced Raman spectroscopy analysis. Journal of biomedical optics. 2016 12; 21(12):125003. doi: 10.1117/1.jbo.21.12.125003. [PMID: 27936269]
  • María Soledad Morales-Covarrubias, Noemí García-Aguilar, María Del Bolan-Mejía, Ana Carmela Puello-Cruz. Evaluation of medicinal plants and colloidal silver efficiency against Vibrio parahaemolyticus infection in Litopenaeus vannamei cultured at low salinity. Diseases of aquatic organisms. 2016 Nov; 122(1):57-65. doi: 10.3354/dao03060. [PMID: 27901504]
  • Anastasia Georgantzopoulou, Sébastien Cambier, Tommaso Serchi, Marcin Kruszewski, Yekkuni L Balachandran, Patrick Grysan, Jean-Nicolas Audinot, Johanna Ziebel, Cédric Guignard, Arno C Gutleb, AlberTinka J Murk. Inhibition of multixenobiotic resistance transporters (MXR) by silver nanoparticles and ions in vitro and in Daphnia magna. The Science of the total environment. 2016 Nov; 569-570(?):681-689. doi: 10.1016/j.scitotenv.2016.06.157. [PMID: 27376922]
  • R Pradeep Kumar, Annie Abraham. PVP- coated naringenin nanoparticles for biomedical applications - In vivo toxicological evaluations. Chemico-biological interactions. 2016 Sep; 257(?):110-8. doi: 10.1016/j.cbi.2016.07.012. [PMID: 27417253]
  • Zia-Ur-Rehman Mashwani, Mubarak Ali Khan, Tariq Khan, Akhtar Nadhman. Applications of plant terpenoids in the synthesis of colloidal silver nanoparticles. Advances in colloid and interface science. 2016 Aug; 234(?):132-141. doi: 10.1016/j.cis.2016.04.008. [PMID: 27181393]
  • Andreas Schnapp, Ann-Christin Niehoff, Annika Koch, Klaus Dreisewerd. Laser desorption/ionization mass spectrometry of lipids using etched silver substrates. Methods (San Diego, Calif.). 2016 07; 104(?):194-203. doi: 10.1016/j.ymeth.2016.01.014. [PMID: 26827933]
  • Alina Martirosyan, Konstantinos Grintzalis, Madeleine Polet, Laurie Laloux, Yves-Jacques Schneider. Tuning the inflammatory response to silver nanoparticles via quercetin in Caco-2 (co-)cultures as model of the human intestinal mucosa. Toxicology letters. 2016 Jun; 253(?):36-45. doi: 10.1016/j.toxlet.2016.04.018. [PMID: 27113704]
  • Kadarkarai Murugan, Devakumar Dinesh, Manickam Paulpandi, Abdulaziz Dakhellah Meqbel Althbyani, Jayapal Subramaniam, Pari Madhiyazhagan, Lan Wang, Udaiyan Suresh, Palanisamy Mahesh Kumar, Jagathish Mohan, Rajapandian Rajaganesh, Hui Wei, Kandasamy Kalimuthu, Megha N Parajulee, Heinz Mehlhorn, Giovanni Benelli. Nanoparticles in the fight against mosquito-borne diseases: bioactivity of Bruguiera cylindrica-synthesized nanoparticles against dengue virus DEN-2 (in vitro) and its mosquito vector Aedes aegypti (Diptera: Culicidae). Parasitology research. 2015 Dec; 114(12):4349-61. doi: 10.1007/s00436-015-4676-8. [PMID: 26290219]
  • Agata Krawczyńska, Katarzyna Dziendzikowska, Joanna Gromadzka-Ostrowska, Anna Lankoff, Andrzej Przemysław Herman, Michał Oczkowski, Tomasz Królikowski, Jacek Wilczak, Maria Wojewódzka, Marcin Kruszewski. Silver and titanium dioxide nanoparticles alter oxidative/inflammatory response and renin-angiotensin system in brain. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2015 Nov; 85(?):96-105. doi: 10.1016/j.fct.2015.08.005. [PMID: 26277626]
  • Leonardo P Franchi, Bella B Manshian, Tiago A J de Souza, Stefaan J Soenen, Elaine Y Matsubara, J Mauricio Rosolen, Catarina S Takahashi. Cyto- and genotoxic effects of metallic nanoparticles in untransformed human fibroblast. Toxicology in vitro : an international journal published in association with BIBRA. 2015 Oct; 29(7):1319-31. doi: 10.1016/j.tiv.2015.05.010. [PMID: 26028148]
  • Seied Mahdi Pourmortazavi, Mehdi Taghdiri, Vajihe Makari, Mehdi Rahimi-Nasrabadi. Procedure optimization for green synthesis of silver nanoparticles by aqueous extract of Eucalyptus oleosa. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2015 Feb; 136 Pt C(?):1249-54. doi: 10.1016/j.saa.2014.10.010. [PMID: 25456666]
  • Yuta Arai, Takamitsu Miyayama, Seishiro Hirano. Difference in the toxicity mechanism between ion and nanoparticle forms of silver in the mouse lung and in macrophages. Toxicology. 2015 Feb; 328(?):84-92. doi: 10.1016/j.tox.2014.12.014. [PMID: 25527144]
  • Al Omar Suliman Y, Daoud Ali, Saud Alarifi, Abdul Halim Harrath, Lamjed Mansour, Saleh Hamad Alwasel. Evaluation of cytotoxic, oxidative stress, proinflammatory and genotoxic effect of silver nanoparticles in human lung epithelial cells. Environmental toxicology. 2015 Feb; 30(2):149-60. doi: 10.1002/tox.21880. [PMID: 23804405]
  • Thomas X Garcia, Guilherme M J Costa, Luiz R França, Marie-Claude Hofmann. Sub-acute intravenous administration of silver nanoparticles in male mice alters Leydig cell function and testosterone levels. Reproductive toxicology (Elmsford, N.Y.). 2014 Jun; 45(?):59-70. doi: 10.1016/j.reprotox.2014.01.006. [PMID: 24447867]
  • Raju Y Prasad, John K McGee, Micaela G Killius, Danielle A Suarez, Carl F Blackman, David M DeMarini, Steven O Simmons. Investigating oxidative stress and inflammatory responses elicited by silver nanoparticles using high-throughput reporter genes in HepG2 cells: effect of size, surface coating, and intracellular uptake. Toxicology in vitro : an international journal published in association with BIBRA. 2013 Sep; 27(6):2013-21. doi: 10.1016/j.tiv.2013.07.005. [PMID: 23872425]
  • Polina S Babich, Alexey N Skvortsov, Paolo Rusconi, Nadezhda V Tsymbalenko, Marja Mutanen, Ludmila V Puchkova, Massimo Broggini. Non-hepatic tumors change the activity of genes encoding copper trafficking proteins in the liver. Cancer biology & therapy. 2013 Jul; 14(7):614-24. doi: 10.4161/cbt.24594. [PMID: 23792645]
  • Johnson J Liu, Yaeseul Kim, Fang Yan, Qi Ding, Virginia Ip, Nancy N Jong, Julian F B Mercer, Mark J McKeage. Contributions of rat Ctr1 to the uptake and toxicity of copper and platinum anticancer drugs in dorsal root ganglion neurons. Biochemical pharmacology. 2013 Jan; 85(2):207-15. doi: 10.1016/j.bcp.2012.10.023. [PMID: 23123662]
  • F Gagné, C André, R Skirrow, M Gélinas, J Auclair, G van Aggelen, P Turcotte, C Gagnon. Toxicity of silver nanoparticles to rainbow trout: a toxicogenomic approach. Chemosphere. 2012 Oct; 89(5):615-22. doi: 10.1016/j.chemosphere.2012.05.063. [PMID: 22727896]
  • Su Jin Kang, Young Joon Lee, Eun-Kyung Lee, Mi-Kyoung Kwak. Silver nanoparticles-mediated G2/M cycle arrest of renal epithelial cells is associated with NRF2-GSH signaling. Toxicology letters. 2012 Jun; 211(3):334-41. doi: 10.1016/j.toxlet.2012.04.016. [PMID: 22546375]
  • Jonghoon Choi, Vytas Reipa, Victoria M Hitchins, Peter L Goering, Richard A Malinauskas. Physicochemical characterization and in vitro hemolysis evaluation of silver nanoparticles. Toxicological sciences : an official journal of the Society of Toxicology. 2011 Sep; 123(1):133-43. doi: 10.1093/toxsci/kfr149. [PMID: 21652737]
  • Ekaterina Ilyechova, Alexej Skvortsov, Euvgeny Zatulovsky, Nadezhda Tsymbalenko, Michael Shavlovsky, Massimo Broggini, Ludmila Puchkova. Experimental switching of copper status in laboratory rodents. Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS). 2011 Jan; 25(1):27-35. doi: 10.1016/j.jtemb.2010.08.002. [PMID: 20965708]
  • Tessa M Scown, Eduarda M Santos, Blair D Johnston, Birgit Gaiser, Mohammed Baalousha, Svetlin Mitov, Jamie R Lead, Vicki Stone, Teresa F Fernandes, Mark Jepson, Ronny van Aerle, Charles R Tyler. Effects of aqueous exposure to silver nanoparticles of different sizes in rainbow trout. Toxicological sciences : an official journal of the Society of Toxicology. 2010 Jun; 115(2):521-34. doi: 10.1093/toxsci/kfq076. [PMID: 20219766]
  • Alan B G Lansdown. A pharmacological and toxicological profile of silver as an antimicrobial agent in medical devices. Advances in pharmacological sciences. 2010; 2010(?):910686. doi: 10.1155/2010/910686. [PMID: 21188244]
  • S Arora, J Jain, J M Rajwade, K M Paknikar. Interactions of silver nanoparticles with primary mouse fibroblasts and liver cells. Toxicology and applied pharmacology. 2009 May; 236(3):310-8. doi: 10.1016/j.taap.2009.02.020. [PMID: 19269301]
  • Jae Hyuck Sung, Jun Ho Ji, Jung Duck Park, Jin Uk Yoon, Dae Sung Kim, Ki Soo Jeon, Moon Yong Song, Jayoung Jeong, Beom Seok Han, Jeong Hee Han, Yong Hyun Chung, Hee Kyung Chang, Ji Hyun Lee, Myung Haing Cho, Bruce J Kelman, Il Je Yu. Subchronic inhalation toxicity of silver nanoparticles. Toxicological sciences : an official journal of the Society of Toxicology. 2009 Apr; 108(2):452-61. doi: 10.1093/toxsci/kfn246. [PMID: 19033393]
  • Jesse Bertinato, Eleonora Swist, Louise J Plouffe, Stephen P J Brooks, Mary R L'abbé. Ctr2 is partially localized to the plasma membrane and stimulates copper uptake in COS-7 cells. The Biochemical journal. 2008 Feb; 409(3):731-40. doi: 10.1042/bj20071025. [PMID: 17944601]
  • Gülüzar Atli, Ozlem Alptekin, Seyhan Tükel, Mustafa Canli. Response of catalase activity to Ag+, Cd2+, Cr6+, Cu2+ and Zn2+ in five tissues of freshwater fish Oreochromis niloticus. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2006 Jun; 143(2):218-24. doi: 10.1016/j.cbpc.2006.02.003. [PMID: 16581305]
  • Marija Trop, Michael Novak, Siegfried Rodl, Bengt Hellbom, Wolfgang Kroell, Walter Goessler. Silver-coated dressing acticoat caused raised liver enzymes and argyria-like symptoms in burn patient. The Journal of trauma. 2006 Mar; 60(3):648-52. doi: 10.1097/01.ta.0000208126.22089.b6. [PMID: 16531870]
  • Jean-François Monty, Roxana M Llanos, Julian F B Mercer, David R Kramer. Copper exposure induces trafficking of the menkes protein in intestinal epithelium of ATP7A transgenic mice. The Journal of nutrition. 2005 Dec; 135(12):2762-6. doi: 10.1093/jn/135.12.2762. [PMID: 16317117]