Glufosinate (BioDeep_00000014870)

Main id: BioDeep_00000005604

 

human metabolite blood metabolite natural product


代谢物信息卡片


2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid

化学式: C5H12NO4P (181.0504)
中文名称: DL-磷化酶
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CP(=O)(CCC(C(=O)O)N)O
InChI: InChI=1S/C5H12NO4P/c1-11(9,10)3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)(H,9,10)



数据库引用编号

14 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

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)

9 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 9 ALB, ARHGAP45, CAT, DAO, GLUL, HMGB1, HPD, HPGDS, PMM2
Peripheral membrane protein 7 ACHE, CYP1B1, DAO, HMGB1, HPD, HSD17B6, PPOX
Endoplasmic reticulum membrane 3 CYP1B1, HPD, SFTPD
Nucleus 4 ACHE, ALB, GLUL, HMGB1
cytosol 10 ALB, ARHGAP45, CAT, DAO, GFER, GLUL, GSR, HPD, HPGDS, PMM2
mitochondrial membrane 1 PPOX
centrosome 1 ALB
nucleoplasm 3 HMGB1, HPGDS, PMM2
Cell membrane 6 ACHE, DAO, GLUL, GRID1, HMGB1, SLC1A2
Lipid-anchor 1 GLUL
ruffle membrane 1 ARHGAP45
Early endosome membrane 1 HSD17B6
Multi-pass membrane protein 2 GRID1, SLC1A2
Golgi apparatus membrane 1 HPD
Synapse 2 ACHE, PPOX
cell surface 3 ACHE, HMGB1, SLC1A2
glutamatergic synapse 2 GRID1, SLC1A2
Golgi apparatus 2 ACHE, ALB
Golgi membrane 1 HPD
mitochondrial inner membrane 1 PPOX
neuromuscular junction 1 ACHE
neuronal cell body 1 PMM2
postsynapse 1 PPOX
presynaptic membrane 1 SLC1A2
synaptic vesicle 1 PPOX
Cytoplasm, cytosol 2 DAO, GLUL
Lysosome 1 SFTPD
endosome 1 HMGB1
plasma membrane 9 ACHE, ARHGAP45, BCHE, DAO, GLUL, GRID1, HMGB1, NPR1, SLC1A2
presynaptic active zone 1 DAO
Membrane 6 ACHE, ARHGAP45, CAT, CYP1B1, NPR1, SLC1A2
extracellular exosome 7 ALB, CAT, DAO, GLUL, GRID1, GSR, HPD
Lumenal side 1 HSD17B6
endoplasmic reticulum 4 ALB, GLUL, HMGB1, HSD17B6
extracellular space 7 ACHE, ALB, BCHE, DAO, GFER, HMGB1, SFTPD
perinuclear region of cytoplasm 2 ACHE, PPOX
bicellular tight junction 1 DAO
mitochondrion 6 CAT, CYP1B1, GFER, GLUL, GSR, PPOX
protein-containing complex 2 ALB, CAT
intracellular membrane-bounded organelle 4 CAT, CYP1B1, HPGDS, HSD17B6
Microsome membrane 2 CYP1B1, HSD17B6
Secreted 5 ACHE, ALB, BCHE, DAO, HMGB1
extracellular region 9 ACHE, ALB, ARHGAP45, BCHE, CAT, DAO, HMGB1, PPOX, SFTPD
mitochondrial matrix 2 CAT, GSR
Extracellular side 3 ACHE, DAO, HMGB1
anchoring junction 1 ALB
external side of plasma membrane 1 GSR
multivesicular body 1 SFTPD
neuronal dense core vesicle lumen 1 PPOX
cytoplasmic vesicle 1 PPOX
vesicle 1 SLC1A2
postsynaptic membrane 1 GRID1
Cell projection, ruffle membrane 1 ARHGAP45
Mitochondrion inner membrane 1 PPOX
Membrane raft 1 SLC1A2
focal adhesion 1 CAT
axolemma 1 SLC1A2
GABA-ergic synapse 1 GRID1
Peroxisome 2 CAT, DAO
basement membrane 1 ACHE
collagen trimer 1 SFTPD
Peroxisome matrix 2 CAT, DAO
peroxisomal matrix 2 CAT, DAO
peroxisomal membrane 1 CAT
mitochondrial intermembrane space 2 GFER, PPOX
Postsynaptic cell membrane 1 GRID1
receptor complex 1 NPR1
ciliary basal body 1 ALB
cell projection 1 DAO
Chromosome 1 HMGB1
centriole 1 ALB
Secreted, extracellular space 1 DAO
spindle pole 1 ALB
blood microparticle 2 ALB, BCHE
Lipid-anchor, GPI-anchor 1 ACHE
cell body 2 GLUL, SLC1A2
side of membrane 1 ACHE
Microsome 1 GLUL
ficolin-1-rich granule lumen 2 CAT, HMGB1
secretory granule lumen 3 ARHGAP45, CAT, HMGB1
endoplasmic reticulum lumen 2 ALB, BCHE
transcription repressor complex 1 HMGB1
platelet alpha granule lumen 1 ALB
specific granule lumen 1 DAO
endocytic vesicle 1 SFTPD
azurophil granule lumen 1 ARHGAP45
postsynaptic density membrane 1 GRID1
clathrin-coated endocytic vesicle 1 SFTPD
nuclear envelope lumen 1 BCHE
endoplasmic reticulum-Golgi intermediate compartment 1 HMGB1
synaptic cleft 1 ACHE
Rough endoplasmic reticulum 1 PPOX
condensed chromosome 1 HMGB1
Intermembrane side 1 PPOX
astrocyte projection 1 SLC1A2
glial cell projection 1 GLUL
catalase complex 1 CAT
alphav-beta3 integrin-HMGB1 complex 1 HMGB1
neuron projection terminus 1 SLC1A2
ANPR-A receptor complex 1 NPR1
[Isoform H]: Cell membrane 1 ACHE
membrane protein complex 1 SLC1A2
ciliary transition fiber 1 ALB


文献列表

  • Jin-Qiu Xia, Qin-Yu Liang, Da-Yu He, Zheng-Yi Zhang, Jie Wu, Jing Zhang, Ping-Xia Zhao, Zi-Sheng Zhang, Cheng-Bin Xiang. Knockout of OsSPL10 confers enhanced glufosinate resistance in rice. Plant communications. 2024 Feb; 5(2):100731. doi: 10.1016/j.xplc.2023.100731. [PMID: 37828741]
  • Yangliu Wu, Yilu Zhou, Xun Jiao, Yongxin She, Wenbo Zeng, Hailan Cui, Canping Pan. Development and inter-laboratory validation of analytical methods for glufosinate and its two metabolites in foods of plant origin. Analytical and bioanalytical chemistry. 2024 Jan; 416(3):663-674. doi: 10.1007/s00216-023-04542-9. [PMID: 36693955]
  • Vadim G Lebedev, Alla V Korobova, Galina V Shendel, Konstantin A Shestibratov. Hormonal Status of Transgenic Birch with a Pine Glutamine Synthetase Gene during Rooting In Vitro and Budburst Outdoors. Biomolecules. 2023 12; 13(12):. doi: 10.3390/biom13121734. [PMID: 38136605]
  • Yan Ren, Binmei Liu, Hongrui Jiang, Weimin Cheng, Liangzhi Tao, Kun Wu, Hui Wang, Guangle Shen, Yu Fang, Conghe Zhang, Yuejin Wu, Xiangdong Fu, Yafeng Ye. Precision editing of GLR1 confers glufosinate resistance without yield penalty in rice. Plant biotechnology journal. 2023 Sep; ?(?):. doi: 10.1111/pbi.14168. [PMID: 37688553]
  • Jin-Qiu Xia, Da-Yu He, Qin-Yu Liang, Zheng-Yi Zhang, Jie Wu, Zi-Sheng Zhang, Jing Zhang, Lin Wang, Cong-He Zhang, Ping-Xia Zhao, Cheng-Bin Xiang. Loss of OsARF18 function confers glufosinate resistance in rice. Molecular plant. 2023 09; 16(9):1355-1358. doi: 10.1016/j.molp.2023.08.016. [PMID: 37660256]
  • Daisuke Watanabe, Shuhei Sonoda, Hikoto Ohta. Simultaneous determination of water-soluble herbicides using hydrophilic interaction liquid chromatography-mass spectrometry. Forensic toxicology. 2023 Jul; ?(?):. doi: 10.1007/s11419-023-00669-7. [PMID: 37480483]
  • Feng Zhu, Yu Yan, Xi-Mei Xue, Rui-Lian Yu, Jun Ye. Identification and characterization of a phosphinothricin N-acetyltransferase from Enterobacter LSJC7. Pesticide biochemistry and physiology. 2023 Jun; 193(?):105464. doi: 10.1016/j.pestbp.2023.105464. [PMID: 37247996]
  • Xu Zhao, Kan Fu, Kai-Ping Xiang, Lan-Ying Wang, Yun-Fei Zhang, Yan-Ping Luo. Comparison of the chronic and multigenerational toxicity of racemic glufosinate and l-glufosinate to Caenorhabditis elegans at environmental concentrations. Chemosphere. 2023 Mar; 316(?):137863. doi: 10.1016/j.chemosphere.2023.137863. [PMID: 36649895]
  • Buddhadev Mallick, Sukanta Rana, Tuhin S Ghosh. Role of herbicides in the decline of butterfly population and diversity. Journal of experimental zoology. Part A, Ecological and integrative physiology. 2023 Feb; ?(?):. doi: 10.1002/jez.2688. [PMID: 36789524]
  • Eliška Kobercová, Miroslav Srba, Lukáš Fischer. Sulfadiazine and phosphinothricin selection systems optimised for the transformation of tobacco BY-2 cells. Plant cell reports. 2023 Jan; ?(?):. doi: 10.1007/s00299-022-02975-7. [PMID: 36609768]
  • Martin Andreas Amberger, Markus Schröder, Jürgen Kuballa, Eckard Jantzen. Direct determination of glyphosate, aminomethylphosphonic acid and glufosinate in food samples with ion chromatography coupled to electrospray ionization tandem mass spectrometry. Journal of chromatography. A. 2023 Jan; 1687(?):463631. doi: 10.1016/j.chroma.2022.463631. [PMID: 36446262]
  • Vipin Kumar, Vijay Singh, Michael L Flessner, Joseph Haymaker, Mark S Reiter, Steven B Mirsky. Cover crop termination options and application of remote sensing for evaluating termination efficiency. PloS one. 2023; 18(4):e0284529. doi: 10.1371/journal.pone.0284529. [PMID: 37079528]
  • Kuan Wang, Yue Geng, Zhe Dong, Xinglu Pan, Xiaohu Wu, Jun Xu, Haixiang Gao, Fengshou Dong, Yongquan Zheng. Simultaneous determination of glyphosate, glufosinate ammonium and their metabolites in maize and soybean by ultra-performance liquid chromatography with tandem mass spectrometry. Analytical methods : advancing methods and applications. 2022 10; 14(39):3850-3858. doi: 10.1039/d2ay01298g. [PMID: 36128953]
  • Jianxi Bao, Yuexin Gao, Yanan Li, Suowei Wu, Jinping Li, Zhenying Dong, Xiangyuan Wan. Genetic Analysis and Fine Mapping of ZmGHT1 Conferring Glufosinate Herbicide Tolerance in Maize (Zea mays L.). International journal of molecular sciences. 2022 Sep; 23(19):. doi: 10.3390/ijms231911481. [PMID: 36232781]
  • Beatriz Sierra-Serrano, Amalia García-García, Tania Hidalgo, Daniel Ruiz-Camino, Antonio Rodríguez-Diéguez, Georgiana Amariei, Roberto Rosal, Patricia Horcajada, Sara Rojas. Copper Glufosinate-Based Metal-Organic Framework as a Novel Multifunctional Agrochemical. ACS applied materials & interfaces. 2022 Aug; 14(30):34955-34962. doi: 10.1021/acsami.2c07113. [PMID: 35853100]
  • Sanhe Li, Wenjun Zha, Kai Liu, Chen Li, Lei Zhou, Guangcun He, Huashan Xu, Peide Li, Junxiao Chen, Zhijun Chen, Aiqing You. Molecular identification and efficacy assessment of a glufosinate-tolerant and brown planthopper-resistant transgenic rice line. Journal of plant physiology. 2022 Jun; 273(?):153688. doi: 10.1016/j.jplph.2022.153688. [PMID: 35462224]
  • Zhong-Min Li, Kurunthachalam Kannan. A Method for the Analysis of Glyphosate, Aminomethylphosphonic Acid, and Glufosinate in Human Urine Using Liquid Chromatography-Tandem Mass Spectrometry. International journal of environmental research and public health. 2022 04; 19(9):. doi: 10.3390/ijerph19094966. [PMID: 35564359]
  • Chun Zhang, Qin Yu, Heping Han, Chaojie Yu, Alex Nyporko, Xingshan Tian, Hugh Beckie, Stephen Powles. A naturally evolved mutation (Ser59Gly) in glutamine synthetase confers glufosinate resistance in plants. Journal of experimental botany. 2022 04; 73(7):2251-2262. doi: 10.1093/jxb/erac008. [PMID: 35029685]
  • Seonghoon Yeon, Sung Hwa Kim, Juhyun Sim, Sunchun Kim, Yoonsuk Lee, Hyun Kim, Yong Sung Cha. Major component causing neurological toxicity in acute glufosinate ammonium poisoning: determination of glufosinate, 1-methoxy-2-propanol, and ammonia in serum and cerebrospinal fluid. Clinical toxicology (Philadelphia, Pa.). 2022 Mar; 60(3):286-292. doi: 10.1080/15563650.2021.1952215. [PMID: 34269144]
  • Leesun Kim, Sujn Baek, Kyungae Son, Hee-Dong Lee, Dal-Soon Choi, Chang Jo Kim, Hyun Ho Noh. Effective and rugged analysis of glyphosate, glufosinate, and metabolites in Tenebrio molitor larva (mealworms) using liquid chromatography tandem mass spectrometry. Scientific reports. 2021 09; 11(1):17597. doi: 10.1038/s41598-021-96529-8. [PMID: 34475419]
  • Tomomi Ohara, Takashi Yoshimoto, Yujin Natori, Akira Ishii. A simple method for the determination of glyphosate, glufosinate and their metabolites in biological specimen by liquid chromatography/tandem mass spectrometry: an application for forensic toxicology. Nagoya journal of medical science. 2021 Aug; 83(3):567-587. doi: 10.18999/nagjms.83.3.567. [PMID: 34552290]
  • Yong Wang, Wanjun Gao, Yeyun Li, Yu Xiao, Wei Song, Ting Yao, Manhuan Cheng, Wenjuan Wang, Ruyan Hou. Establishment of a HPLC-MS/MS Detection Method for Glyphosate, Glufosinate-Ammonium, and Aminomethyl Phosphoric Acid in Tea and Its Use for Risk Exposure Assessment. Journal of agricultural and food chemistry. 2021 Jul; 69(28):7969-7978. doi: 10.1021/acs.jafc.1c01757. [PMID: 34232658]
  • Martins Jansons, Iveta Pugajeva, Vadims Bartkevics, Hark Bahadur Karkee. LC-MS/MS characterisation and determination of dansyl chloride derivatised glyphosate, aminomethylphosphonic acid (AMPA), and glufosinate in foods of plant and animal origin. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2021 Jul; 1177(?):122779. doi: 10.1016/j.jchromb.2021.122779. [PMID: 34098182]
  • X M Zhang, H Sun, J S Zhang, D L Hu, Q Zhang. [A case of glufosinate-ammonium poisoning in a patient with total gastrectomy]. Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases. 2021 May; 39(5):366-367. doi: 10.3760/cma.j.cn121094-20201127-00653. [PMID: 34074083]
  • Min-Jung Yook, Hae-Rim Park, Chuan-Jie Zhang, Soo-Hyun Lim, Soon-Chun Jeong, Young Soo Chung, Do-Soon Kim. Environmental risk assessment of glufosinate-resistant soybean by pollen-mediated gene flow under field conditions in the region of the genetic origin. The Science of the total environment. 2021 Mar; 762(?):143073. doi: 10.1016/j.scitotenv.2020.143073. [PMID: 33189381]
  • Jean-François Bienvenu, Patrick Bélanger, Éric Gaudreau, Gilles Provencher, Normand Fleury. Determination of glyphosate, glufosinate and their major metabolites in urine by the UPLC-MS/MS method applicable to biomonitoring and epidemiological studies. Analytical and bioanalytical chemistry. 2021 Mar; 413(8):2225-2234. doi: 10.1007/s00216-021-03194-x. [PMID: 33547480]
  • Siriwat Boonchaisri, Simone Rochfort, Trevor Stevenson, Daniel A Dias. LC-MS untargeted metabolomics assesses the delayed response of glufosinate treatment of transgenic glufosinate resistant (GR) buffalo grasses (Stenotaphrum secundatum L.). Metabolomics : Official journal of the Metabolomic Society. 2021 02; 17(3):28. doi: 10.1007/s11306-021-01776-5. [PMID: 33609206]
  • Samuel Ferrari, Odin Serodio Mettifogo, Matheus Luís Oliveira Cunha, Luis Fernando Dos Santos Cordeiro, Sony Anderson Cidreira Bastos, Luís Guilherme Delovo Carara, Lara Caroline Alves de Oliveira. Does the glufosinate-ammonium herbicide have the potential to induce the hormesis effect in upland rice?. Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes. 2021; 56(11):969-976. doi: 10.1080/03601234.2021.1994287. [PMID: 34678127]
  • Adrian A Franke, Xingnan Li, Jennifer F Lai. Analysis of glyphosate, aminomethylphosphonic acid, and glufosinate from human urine by HRAM LC-MS. Analytical and bioanalytical chemistry. 2020 Dec; 412(30):8313-8324. doi: 10.1007/s00216-020-02966-1. [PMID: 33011839]
  • Hudson K Takano, Franck E Dayan. Glufosinate-ammonium: a review of the current state of knowledge. Pest management science. 2020 Dec; 76(12):3911-3925. doi: 10.1002/ps.5965. [PMID: 32578317]
  • Hudson K Takano, Roland Beffa, Christopher Preston, Philip Westra, Franck E Dayan. A novel insight into the mode of action of glufosinate: how reactive oxygen species are formed. Photosynthesis research. 2020 Jun; 144(3):361-372. doi: 10.1007/s11120-020-00749-4. [PMID: 32372199]
  • Chengzeng Zhou, Xiaoxia Luo, Nengyi Chen, Lili Zhang, Jiangtao Gao. C-P Natural Products as Next-Generation Herbicides: Chemistry and Biology of Glufosinate. Journal of agricultural and food chemistry. 2020 Mar; 68(11):3344-3353. doi: 10.1021/acs.jafc.0c00052. [PMID: 32125843]
  • Hudson K Takano, Roland Beffa, Christopher Preston, Philip Westra, Franck E Dayan. Physiological Factors Affecting Uptake and Translocation of Glufosinate. Journal of agricultural and food chemistry. 2020 Mar; 68(10):3026-3032. doi: 10.1021/acs.jafc.9b07046. [PMID: 32049526]
  • Guo-Qing Song, Xue Han, Andrew T Wiersma, Xiaojuan Zong, Halima E Awale, James D Kelly. Induction of competent cells for Agrobacterium tumefaciens-mediated stable transformation of common bean (Phaseolus vulgaris L.). PloS one. 2020; 15(3):e0229909. doi: 10.1371/journal.pone.0229909. [PMID: 32134988]
  • Kiyotaka Usui, Eriko Minami, Yuji Fujita, Eito Kubota, Haruka Kobayashi, Tomoki Hanazawa, Tomohiro Yoshizawa, Yoshito Kamijo, Masato Funayama. Application of probe electrospray ionization-tandem mass spectrometry to ultra-rapid determination of glufosinate and glyphosate in human serum. Journal of pharmaceutical and biomedical analysis. 2019 Sep; 174(?):175-181. doi: 10.1016/j.jpba.2019.05.040. [PMID: 31170631]
  • Hudson K Takano, Eric L Patterson, Scott J Nissen, Franck E Dayan, Todd A Gaines. Predicting herbicide movement across semi-permeable membranes using three phase partitioning. Pesticide biochemistry and physiology. 2019 Sep; 159(?):22-26. doi: 10.1016/j.pestbp.2019.05.009. [PMID: 31400780]
  • Marilda Chiarello, María Luisa Jiménez-Medina, Jesús Marín Saéz, Sidnei Moura, Antonia Garrido Frenich, Roberto Romero-González. Fast analysis of glufosinate, glyphosate and its main metabolite, aminomethylphosphonic acid, in edible oils, by liquid chromatographycoupled with electrospray tandem mass spectrometry. Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment. 2019 Sep; 36(9):1376-1384. doi: 10.1080/19440049.2019.1631493. [PMID: 31287383]
  • J Lee, Y Lee, Y S Kim, J G Choi, T H Go, H Kim, Y S Cha. Serum ammonia as an early predictor of in-hospital mortality in patients with glufosinate poisoning. Human & experimental toxicology. 2019 Sep; 38(9):1007-1013. doi: 10.1177/0960327119855124. [PMID: 31146590]
  • Caio A C G Brunharo, Hudson K Takano, Carol A Mallory-Smith, Franck E Dayan, Bradley D Hanson. Role of Glutamine Synthetase Isogenes and Herbicide Metabolism in the Mechanism of Resistance to Glufosinate in Lolium perenne L. spp. multiflorum Biotypes from Oregon. Journal of agricultural and food chemistry. 2019 Aug; 67(31):8431-8440. doi: 10.1021/acs.jafc.9b01392. [PMID: 31067047]
  • Elumalai Sivamani, Samson Nalapalli, Anna Prairie, David Bradley, Lee Richbourg, Tim Strebe, Tara Liebler, Daolong Wang, Qiudeng Que. A study on optimization of pat gene expression cassette for maize transformation. Molecular biology reports. 2019 Jun; 46(3):3009-3017. doi: 10.1007/s11033-019-04737-3. [PMID: 30859449]
  • Hudson K Takano, Roland Beffa, Christopher Preston, Philip Westra, Franck E Dayan. Reactive oxygen species trigger the fast action of glufosinate. Planta. 2019 Jun; 249(6):1837-1849. doi: 10.1007/s00425-019-03124-3. [PMID: 30850862]
  • Slavica Dmitrović, Milan Dragićević, Jelena Savić, Milica Milutinović, Suzana Živković, Vuk Maksimović, Dragana Matekalo, Danijela Mišić. Nepetalactone-rich essential oil mitigates phosphinothricin-induced ammonium toxicity in Arabidopsis thaliana (L.) Heynh. Journal of plant physiology. 2019 Jun; 237(?):87-94. doi: 10.1016/j.jplph.2019.04.006. [PMID: 31034969]
  • Luyao Zhang, Jinling Diao, Li Chen, Zikang Wang, Wenjun Zhang, Yao Li, Zhongnan Tian, Zhiqiang Zhou. Hepatotoxicity and reproductive disruption in male lizards (Eremias argus) exposed to glufosinate-ammonium contaminated soil. Environmental pollution (Barking, Essex : 1987). 2019 Mar; 246(?):190-197. doi: 10.1016/j.envpol.2018.12.004. [PMID: 30543945]
  • Siwei Wang, Guangfeng Zeng, Yanping Liu, Xiaonan Wang, Haibin Sun. [Determination of glufosinate-ammonium and its three metabolites in litchi and banana by high performance liquid chromatography coupled with triple quadrupole mass spectrometry]. Se pu = Chinese journal of chromatography. 2019 Jan; 37(1):93-99. doi: 10.3724/sp.j.1123.2018.08002. [PMID: 30693715]
  • Quan Zhang, Qingmiao Cui, Siqing Yue, Zhengbiao Lu, Meirong Zhao. Enantioselective effect of glufosinate on the growth of maize seedlings. Environmental science and pollution research international. 2019 Jan; 26(1):171-178. doi: 10.1007/s11356-018-3576-8. [PMID: 30387058]
  • Fabio H Krenchinski, Caio A Carbonari, Victor J S Cesco, Alfredo J P Albrecht, Mariana de Lara Campos Arcuri, Ivan de Godoy Maia, Edivaldo D Velini. Glufosinate Resistance Level is Proportional to Phosphinothricin Acetyltransferase Gene Expression in Glufosinate-Resistant Maize. Journal of agricultural and food chemistry. 2018 Dec; 66(48):12641-12650. doi: 10.1021/acs.jafc.8b04823. [PMID: 30418770]
  • Dhirendra Fartyal, Aakrati Agarwal, Donald James, Bhabesh Borphukan, Babu Ram, Vijay Sheri, Pawan K Agrawal, V Mohan Murali Achary, M K Reddy. Developing dual herbicide tolerant transgenic rice plants for sustainable weed management. Scientific reports. 2018 08; 8(1):11598. doi: 10.1038/s41598-018-29554-9. [PMID: 30072810]
  • Jingxu Zhang, Ye Kang, Bernal E Valverde, Weimin Dai, Xiaoling Song, Sheng Qiang. Feral rice from introgression of weedy rice genes into transgenic herbicide-resistant hybrid-rice progeny. Journal of experimental botany. 2018 07; 69(16):3855-3865. doi: 10.1093/jxb/ery210. [PMID: 29873749]
  • Y S Cha, H Kim, Y Lee, E H Choi, H I Kim, O H Kim, K-C Cha, K H Lee, S O Hwang. The relationship between serum ammonia level and neurologic complications in patients with acute glufosinate ammonium poisoning: A prospective observational study. Human & experimental toxicology. 2018 Jun; 37(6):571-579. doi: 10.1177/0960327117715902. [PMID: 28741381]
  • Adam Jalaludin, Qin Yu, Peter Zoellner, Roland Beffa, Stephen B Powles. Characterisation of glufosinate resistance mechanisms in Eleusine indica. Pest management science. 2017 Jun; 73(6):1091-1100. doi: 10.1002/ps.4528. [PMID: 28094896]
  • Jung-Won Lee, Young-Jin Choi, Samel Park, Hyo-Wook Gil, Ho-Yeon Song, Sae-Yong Hong. Serum S100 protein could predict altered consciousness in glyphosate or glufosinate poisoning patients. Clinical toxicology (Philadelphia, Pa.). 2017 Jun; 55(5):357-359. doi: 10.1080/15563650.2017.1286013. [PMID: 28301275]
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