Q72716912 | A molecular mechanism for qE-quenching |
Q80287534 | A non-invasive assay of the plastoquinone pool redox state based on the OJIP-transient |
Q37808571 | Alternative Electron Flows (Water–Water Cycle and Cyclic Electron Flow Around PSI) in Photosynthesis: Molecular Mechanisms and Physiological Functions |
Q81575883 | An Analysis of the Mechanism of the Low-wave Phenomenon of Chlorophyll Fluorescence |
Q86898522 | An active Mehler-peroxidase reaction sequence can prevent cyclic PS I electron transport in the presence of dioxygen in intact spinach chloroplasts |
Q48572231 | Analysis of fluorescence induction in thylakoids with the method of moments reveals two different active Photosystem II centres |
Q39006402 | Analysis of the relative increase in photosynthetic O(2) uptake when photosynthesis in grapevine leaves is inhibited following low night temperatures and/or water stress |
Q43916202 | Ascorbate deficiency can limit violaxanthin de-epoxidase activity in vivo |
Q86914041 | Can charge recombination as caused by pH-dependent donor-side limitation in PS 2 account for high-energy-state quenching? |
Q86656903 | Changes in xanthophyll-cycle components and in fluorescence yield in leaves of a crassulacean-acid-metabolism plant, Clusia rosea Jacq., throughout a 12-hour photoperiod of constant irradiance |
Q86885618 | Characterisation of a H2O 2-oxidisable cytochrome b-559 in intact chloroplasts with a new type of LED Array Spectrophotometer |
Q87067010 | Characterization of the reversible state of photoinhibition occurring in vitro under anaerobic conditions |
Q40975923 | Chilling-enhanced photooxidation: The production, action and study of reactive oxygen species produced during chilling in the light |
Q95301939 | Chlorophyll a fluorescence induction1 |
Q38027427 | Chlorophyll a fluorescence induction: a personal perspective of the thermal phase, the J-I-P rise |
Q38086088 | Chlorophyll a fluorescence: beyond the limits of the Q(A) model |
Q81358426 | Chlorophyll fluorescence transients of Photosystem II membrane particles as a tool for studying photosynthetic oxygen evolution |
Q64884863 | Chloroplast energization and oxidation of P700/plastocyanin in illuminated leaves at reduced levels of CO2 or oxygen. |
Q46905431 | Chloroplastic NAD(P)H dehydrogenase in tobacco leaves functions in alleviation of oxidative damage caused by temperature stress |
Q43540549 | Chloroplastic ascorbate peroxidase is the primary target of methylviologen-induced photooxidative stress in spinach leaves: its relevance to monodehydroascorbate radical detected with in vivo ESR. |
Q86894183 | Competition between electron acceptors in photosynthesis: Regulation of the malate valve during CO2 fixation and nitrite reduction |
Q87067547 | Concerning oscillations |
Q42910431 | Continuous ECS-indicated recording of the proton-motive charge flux in leaves |
Q86884744 | Coregulation of electron transport through PS I by Cyt b 6 f, excitation capture by P700 and acceptor side reduction. Time kinetics and electron transport requirement |
Q40380824 | Dark-interval relaxation kinetics (DIRK) of absorbance changes as a quantitative probe of steady-state electron transfer |
Q86912301 | Effects of inorganic carbon accumulation on photosynthetic oxygen reduction and cyclic electron flow in the cyanobacterium Synechococcus PCC7942 |
Q50751934 | Effects of severe CO(2) starvation on the photosynthetic electron transport chain in tobacco plants. |
Q60323617 | Electron acceptors in isolated intact spinach chloroplasts act hierarchically to prevent over-reduction and competition for electrons |
Q31689737 | Electron pathways involved in H(2)-metabolism in the green alga Scenedesmus obliquus |
Q47703375 | Electron transport and photophosphorylation by Photosystem I in vivo in plants and cyanobacteria |
Q86837604 | Electron transport to oxygen mitigates against the photoinactivation of Photosystem II in vivo |
Q54052963 | End product feedback effects on photosynthetic electron transport. |
Q30320161 | Estimation of chlorophyll content and daily primary production of the major algal groups by means of multiwavelength-excitation PAM chlorophyll fluorometry: performance and methodological limits |
Q44842843 | Experimental evidence for ascorbate-dependent electron transport in leaves with inactive oxygen-evolving complexes. |
Q84061974 | Grafting of Cucumis sativus onto Cucurbita ficifolia leads to improved plant growth, increased light utilization and reduced accumulation of reactive oxygen species in chilled plants |
Q86623493 | Growth of cotton under continuous salinity stress: influence on allocation pattern, stomatal and non-stomatal components of photosynthesis and dissipation of excess light energy |
Q46988753 | Heat-induced changes in the EPR signal of tyrosine D (Y(D)OX) a possible role of Cytochrome b559. |
Q51958835 | High-Temperature Induced Chlorophyll Fluorescence Rise in Plants at 40-50 degrees C: Experimental and Theoretical Approach. |
Q28362438 | Increased sensitivity of photosynthesis to antimycin A induced by inactivation of the chloroplast ndhB gene. Evidence for a participation of the NADH-dehydrogenase complex to cyclic electron flow around photosystem I |
Q79811365 | Infection with virulent and avirulent P. syringae strains differentially affects photosynthesis and sink metabolism in Arabidopsis leaves |
Q41015624 | Inhibition by ethoxyzolamide of a photoacoustic uptake signal in leaves: Evidence for carbonic anhydrase catalyzed CO2-solubilisation |
Q86911969 | Intact chloroplasts display pH 5 optimum of O2-reduction in the absence of methyl viologen: Indirect evidence for a regulatory role of superoxide protonation |
Q34462308 | Irrungen, Wirrungen? The Mehler reaction in relation to cyclic electron transport in C3 plants |
Q86898512 | Measurements of mesophyll conductance, photosynthetic electron transport and alternative electron sinks of field grown wheat leaves |
Q60323722 | Mechanisms for controlling balance between light input and utilisation in the salt tolerant alga Dunaliella C9AA |
Q86900814 | Membrane barriers and Mehler-peroxidase reaction limit the ascorbate available for violaxanthin de-epoxidase activity in intact chloroplasts |
Q56954963 | Monitoring photosynthetic activity of crustose lichens using a PAM-2000 fluorescence system |
Q48571335 | On the rates of cyclic electron transport around Photosystem II in the presence of donor side limitation |
Q86901115 | On the relationship between chlorophyll fluorescence quenching and the quantum yield of electron transport in isolated thylakoids |
Q54766716 | Oscillations in photosynthesis are initiated and supported by imbalances in the supply of ATP and NADPH to the Calvin cycle. |
Q61831908 | Overexpression of Iron Superoxide Dismutase in Transformed Poplar Modifies the Regulation of Photosynthesis at Low CO2Partial Pressures or Following Exposure to the Prooxidant Herbicide Methyl Viologen |
Q59136393 | Oxidation of P700 Ensures Robust Photosynthesis |
Q39190943 | Oxygen-dependent electron transport and protection from photoinhibition in leaves of tropical tree species. |
Q58073252 | PAM Chlorophyll Fluorometry: a New in situ Technique for Stress Assessment in Scleractinian Corals, used to Examine the Effects of Cyanide from Cyanide Fishing |
Q47708627 | Photoinactivation of photosystem II by cumulative exposure to short light pulses during the induction period of photosynthesis |
Q46625293 | Photoinhibition of photosynthesis in Macrocystis pyrifera (Phaeophyceae), Chondrus crispus (Rhodophyceae) and Ulva lactuca (Chlorophyceae) in outdoor culture systems |
Q86624461 | Photoinhibition of photosystem II in vivo is preceded by down-regulation through light-induced acidification of the lumen: Consequences for the mechanism of photoinhibition in vivo |
Q53123385 | Photorespiration provides the chance of cyclic electron flow to operate for the redox-regulation of P700 in photosynthetic electron transport system of sunflower leaves. |
Q50750815 | Photosynthetic acclimation to photon irradiance and its relation to chlorophyll fluorescence and carbon assimilation in the halotolerant green alga Dunaliella viridis. |
Q87067560 | Photosystem I-dependent cyclic electron transport is important in controlling Photosystem II activity in leaves under conditions of water stress |
Q35864219 | Photosystem II cycle activity and alternative electron transport in the diatom Phaeodactylum tricornutum under dynamic light conditions and nitrogen limitation. |
Q37280758 | Photosystem II reaction centre quenching: mechanisms and physiological role |
Q74285485 | Physiological response of Pinus halepensis needles under ozone and water stress conditions |
Q95288830 | Proton to electron stoichiometry in electron transport of spinach thylakoids |
Q87065364 | Pulse-modulated photoacoustic measurements reveal strong gas-uptake component at high CO2-concentrations |
Q86898518 | Rates of vectorial proton transport supported by cyclic electron flow during oxygen reduction by illuminated intact chloroplasts |
Q47166960 | Redox changes of ferredoxin, P700, and plastocyanin measured simultaneously in intact leaves |
Q55003496 | Reduction-Induced Suppression of Electron Flow (RISE) Is Relieved by Non-ATP-Consuming Electron Flow in Synechococcus elongatus PCC 7942. |
Q86892320 | Regulation and possible function of the violaxanthin cycle |
Q60323725 | Regulation of Photosystem II |
Q34725584 | Regulation of photosynthesis of C3 plants in response to progressive drought: stomatal conductance as a reference parameter |
Q47704857 | Spectroscopy of non-photochemical and photochemical quenching of chlorophyll fluorescence in leaves; evidence for a role of the light harvesting complex of Photosystem II in the regulation of energy dissipation |
Q62634615 | Steady-state chlorophyll fluorescence (Fs) measurements as a tool to follow variations of net CO2 assimilation and stomatal conductance during water-stress in C3 plants |
Q44399880 | Study of the effect of reducing conditions on the initial chlorophyll fluorescence rise in the green microalgae Chlamydomonas reinhardtii |
Q43528508 | Systems-wide analysis of acclimation responses to long-term heat stress and recovery in the photosynthetic model organism Chlamydomonas reinhardtii. |
Q45298817 | The multiphasic nature of nonphotochemical quenching: implications for assessment of photosynthetic electron transport based on chlorophyll fluorescence |
Q60323710 | The relationship between Photosystem II intrinsic quantum yield and millisecond luminescence in thylakoids |
Q51293085 | The role of O2 as an electron acceptor alternative to CO2 in photosynthesis of the common marine angiosperm Zostera marina L. |
Q86912137 | The role of calcium in the pH-dependent control of Photosystem II |
Q47349516 | The size of the lumenal proton pool in leaves during induction and steady-state photosynthesis |
Q86901101 | The use of photothermal radiometry in assessing leaf photosynthesis: II. Correlation of energy storage to Photosystem II fluorescence parameters |
Q71860383 | Two fundamentally different types of variable chlorophyll fluorescence in vivo |
Q86639649 | Vacuolar pH oscillations in mesophyll cells accompany oscillations of photosynthesis in leaves: Interdependence of cellular compartments, and regulation of electron flow in photosynthesis |
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