scholarly article | Q13442814 |
P356 | DOI | 10.1039/B307945G |
P50 | author | Jörg Feldmann | Q54652880 |
Andrea Raab | Q90783627 | ||
P2093 | author name string | Marcel Jaspars | |
Andrew A. Meharg | |||
David R. Genney | |||
P2860 | cites work | Enzymatic reduction of arsenic compounds in mammalian systems: the rate-limiting enzyme of rabbit liver arsenic biotransformation is MMA(V) reductase | Q28377855 |
The MRP2/cMOAT transporter and arsenic-glutathione complex formation are required for biliary excretion of arsenic | Q30607266 | ||
Speciation of key arsenic metabolic intermediates in human urine. | Q33925487 | ||
Methylated trivalent arsenic species are genotoxic | Q33942554 | ||
Antimonite is accumulated by the glycerol facilitator GlpF in Escherichia coli | Q39845794 | ||
Glutathione-conjugated arsenics in the potential hepato-enteric circulation in rats | Q43822900 | ||
Arsenic-speciation in arsenate-resistant and non-resistant populations of the earthworm, Lumbricus rubellus. | Q44114441 | ||
Glutathione-dependent biliary excretion of arsenic | Q45777659 | ||
Reactions of arsenic(III) and arsenic(V) species with glutathione | Q46619791 | ||
Families of arsenic transporters | Q67523987 | ||
Effect of arsenicals on biliary excretion of endogenous glutathione and xenobiotics with glutathione-dependent hepatobiliary transport | Q70126848 | ||
Reduction and binding of arsenate and dimethylarsinate by glutathione: a magnetic resonance study | Q72360120 | ||
Role of glutathione in the biliary excretion of the arsenical drugs trimelarsan and melarsoprol | Q73634927 | ||
Enzymatic methylation of arsenic compounds. VI. Characterization of hamster liver arsenite and methylarsonic acid methyltransferase activities in vitro | Q77681451 | ||
P433 | issue | 1 | |
P921 | main subject | arsenic | Q871 |
P304 | page(s) | 183-190 | |
P577 | publication date | 2004-01-01 | |
P1433 | published in | Journal of Analytical Atomic Spectrometry | Q3013649 |
P1476 | title | Arsenic–glutathione complexes—their stability in solution and during separation by different HPLC modes | |
P478 | volume | 19 |
Q55593711 | Condensation cascades and methylgroup transfer reactions during the formation of arsane, methyl- and dimethylarsane by aqueous borohydride and (methyl) arsenates |
Q33775663 | Elemental Characterization of Romanian Crop Medicinal Plants by Neutron Activation Analysis |
Q59003964 | Enhanced determination of As–phytochelatin complexes in Chlorella vulgaris using focused sonication for extraction of water-soluble species |
Q50211882 | Green Luminescent CdTe Quantum Dot Based Fluorescence Nano-Sensor for Sensitive Detection of Arsenic (III). |
Q55593796 | Integrated mass spectrometry in (semi-)metal speciation and its potential in phytochemistry |
Q39098278 | Mass spectrometric detection, identification, and fragmentation of arseno-phytochelatins |
Q38620066 | Methylated trivalent arsenic-glutathione complexes are more stable than their arsenite analog |
Q39139847 | Monomethylated trivalent arsenic species disrupt steroid receptor interactions with their DNA response elements at non-cytotoxic cellular concentrations |
Q59106509 | Phytotoxicity and detoxification mechanism differ among inorganic and methylated arsenic species in Arabidopsis thaliana |
Q56839582 | Review: The role of atomic spectrometry in plant science |
Q59003950 | Selenopeptides and elemental selenium in Thunbergia alata after exposure to selenite: quantification method for elemental selenium |
Q46824425 | Uptake, translocation and transformation of arsenate and arsenite in sunflower (Helianthus annuus): formation of arsenic-phytochelatin complexes during exposure to high arsenic concentrations. |
Q59004317 | What can the different current-detection methods offer for element speciation? |