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Desiccation-induced ultrastructural and biochemical changes in the leaves of the resurrection plant Myrothamnus flabellifolia
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00348713openalex-snapshot
Desiccation tolerant vascular plants of southern Africa
inferredcites →https://doi.org/10.1007/bf00392810openalex-snapshot
Response of photosynthesis and respiration of resurrection plants to desiccation and rehydration
inferredcites →https://doi.org/10.1007/bf02860532openalex-snapshot
Calcium oxalate crystals in plants
inferredcites →https://doi.org/10.1007/s004100100273openalex-snapshot
Lithospheric thickness beneath the southern Kenya Rift: implications from basalt geochemistry
inferredcites →https://doi.org/10.1007/s10886-005-8396-xopenalex-snapshot
The South African and Namibian Populations of the Resurrection Plant Myrothamnus flabellifolius are Genetically Distinct and Display Variation in Their Galloylquinic Acid Composition
inferredcites →https://doi.org/10.1016/0031-9422(90)85257-gopenalex-snapshot
Loss of colour, a prerequisite to plant pigmentation by flavonoids
inferredcites →https://doi.org/10.1016/0031-9422(90)85411-8openalex-snapshot
The mechanism of co-pigmentation of anthocyanins in aqueous solutions
inferredcites →https://doi.org/10.1016/0076-6879(87)48036-1openalex-snapshot
[34] Chlorophylls and carotenoids: Pigments of photosynthetic biomembranes
inferredcites →https://doi.org/10.1016/0308-8146(94)90254-2openalex-snapshot
Effect of light and tannic acid on the stability of anthocyanin in DMSO and in water
inferredcites →https://doi.org/10.1016/b978-0-12-318880-9.x5001-7openalex-snapshot
Electron Microscopy of Plant Cells
inferredcites →https://doi.org/10.1016/b978-0-12-333920-1.x5001-0openalex-snapshot
Fixation for Electron Microscopy
inferredcites →https://doi.org/10.1016/b978-0-12-472550-8.50011-1openalex-snapshot
Analysis of Anthocyanins
inferredcites →https://doi.org/10.1016/s0022-5320(69)90033-1openalex-snapshot
A low-viscosity epoxy resin embedding medium for electron microscopy
inferredcites →https://doi.org/10.1016/s0031-9422(98)00087-9openalex-snapshot
Maldi-tof analysis of mixtures of 3-deoxyanthocyanidins and anthocyanins
inferredcites →https://doi.org/10.1016/s0176-1617(86)80148-1openalex-snapshot
Sugar and Ion Content in Leaf Tissues of Several Drought Tolerant Plants under Water Stress
inferredcites →https://doi.org/10.1016/s0254-6299(16)30464-1openalex-snapshot
The composition and antimicrobial activity of the essential oil of the resurrection plant Myrothamnus flabellifolius
inferredcites →https://doi.org/10.1021/jf991089zopenalex-snapshot
Monosaccharide Composition of Sweetpotato Fiber and Cell Wall Polysaccharides from Sweetpotato, Cassava, and Potato Analyzed by the High-Performance Anion Exchange Chromatography with Pulsed Amperometric Detection Method
inferredcites →https://doi.org/10.1023/a:1005801610891openalex-snapshot
Protection mechanisms against excess light in the resurrection plants Craterostigma wilmsii and Xerophyta viscosa
inferredcites →https://doi.org/10.1023/a:1026565817218openalex-snapshot
Granitic and gneissic outcrops (inselbergs) as centers of diversity for desiccation-tolerant vascular plants
inferredcites →https://doi.org/10.1042/bj20040499openalex-snapshot
The predominant polyphenol in the leaves of the resurrection plantMyrothamnus flabellifolius, 3,4,5 tri-O-galloylquinic acid, protects membranes against desiccation and free radical-induced oxidation
inferredcites →https://doi.org/10.1046/j.0016-8025.2003.01052.xopenalex-snapshot
An investigation into the role of light during desiccation of three angiosperm resurrection plants
inferredcites →https://doi.org/10.1046/j.0028-646x.2001.00206.xopenalex-snapshot
Restoration of the hydraulic system in a resurrection plant: fitting the theory with the facts
inferredcites →https://doi.org/10.1046/j.1469-8137.1999.00483.xopenalex-snapshot
Diurnal changes in xylem pressure of the hydrated resurrection plant Myrothamnus flabellifolia: evidence for lipid bodies in conducting xylem vessels
inferredcites →https://doi.org/10.1046/j.1469-8137.2000.00755.xopenalex-snapshot
Xylem conduits of a resurrection plant contain a unique lipid lining and refill following a distinct pattern after desiccation
inferredcites →https://doi.org/10.1046/j.1469-8137.2000.00759.xopenalex-snapshot
Water rise kinetics in refilling xylem after desiccation in a resurrection plant
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00814.xopenalex-snapshot
The impact of lipid distribution, composition and mobility on xylem water refilling of the resurrection plantMyrothamnus flabellifolia
inferredcites →https://doi.org/10.1093/aob/mcl269openalex-snapshot
An Overview of the Biology of the Desiccation-tolerant Resurrection Plant Myrothamnus flabellifolia
inferredcites →https://doi.org/10.1093/jxb/29.3.757openalex-snapshot
The Ultrastructure of Phenolic-Storing Cells Fixed with Caffeine
inferredcites →https://doi.org/10.1093/jxb/erf028openalex-snapshot
Recovery of the resurrection plant Craterostigma wilmsii from desiccation: protection versus repair
inferredcites →https://doi.org/10.1094/phyto-67-592openalex-snapshot
Indicator Hosts for Pear Decline: Symptomatology, Histopathology, and Distribution of Mycoplasmalike Organisms in Leaf Veins
inferredcites →https://doi.org/10.1104/pp.106.077701openalex-snapshot
Response of the Leaf Cell Wall to Desiccation in the Resurrection Plant Myrothamnus flabellifolius
inferredcites →https://doi.org/10.1105/tpc.021642openalex-snapshot
Overexpression of GLUTAMINE DUMPER1 Leads to Hypersecretion of Glutamine from Hydathodes of Arabidopsis Leaves[W]
inferredcites →https://doi.org/10.1105/tpc.11.4.751openalex-snapshot
Cell-Mediated Crystallization of Calcium Oxalate in Plants
inferredcites →https://doi.org/10.1111/j.1365-2621.2000.tb16007.xopenalex-snapshot
Changes in Anthocyanins and Polyphenolics During Juice Processing of Highbush Blueberries ( Vaccinium corymbosum L.)
inferredcites →https://doi.org/10.1111/j.1365-3040.2004.01212.xopenalex-snapshot
Insights into the cellular mechanisms of desiccation tolerance among angiosperm resurrection plant species
inferredcites →https://doi.org/10.1111/j.1751-1097.1999.tb01944.xopenalex-snapshot
Environmental Significance of Anthocyanins in Plant Stress Responses
inferredcites →https://doi.org/10.1126/science.174.4013.1033openalex-snapshot
Desiccation-Tolerant Flowering Plants in Southern Africa
inferredcites →https://doi.org/10.5897/ajb2002.000-006openalex-snapshot
Physiological and molecular insights into drought tolerance
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.12.016zenodo-depositor-declared
Metabolomics as a complement to phylogenetics for assessing intraspecific boundaries in the desiccation-tolerant medicinal shrub Myrothamnus flabellifolia (Myrothamnaceae)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112323zenodo-depositor-declared
The phenolic profile extracted from the desiccation-tolerant medicinal shrub Myrothamnus flabellifolia using Natural Deep Eutectic Solvents varies according to the solvation conditions
inferred← citeshttps://doi.org/10.1002/9780470376881.ch3openalex-snapshot
Mechanisms of Desiccation Tolerance in Angiosperm Resurrection Plants
inferred← citeshttps://doi.org/10.1002/9783527632930.ch17openalex-snapshot
A Systems‐Based Molecular Biology Analysis of Resurrection Plants for Crop and Forage Improvement in Arid Environments
inferred← citeshttps://doi.org/10.1007/s10725-010-9498-1openalex-snapshot
The use of aeroponics to investigate antioxidant activity in the roots of Xerophyta viscosa
inferred← citeshttps://doi.org/10.1007/s11103-016-0468-5openalex-snapshot
New features of desiccation tolerance in the lichen photobiont Trebouxia gelatinosa are revealed by a transcriptomic approach
inferred← citeshttps://doi.org/10.1016/b978-0-12-387692-8.00004-7openalex-snapshot
Plants in Extreme Environments
inferred← citeshttps://doi.org/10.1016/b978-0-12-387692-8.00009-6openalex-snapshot
An Overview of the Current Understanding of Desiccation Tolerance in the Vegetative Tissues of Higher Plants
inferred← citeshttps://doi.org/10.1016/bs.abr.2020.09.007openalex-snapshot
NADES formation in vegetative desiccation tolerance: Prospects and challenges
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2017.09.003openalex-snapshot
The dual strategy of the bromeliad Pitcairnia burchellii Mez to cope with desiccation
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.09.027openalex-snapshot
Chloroplast breakdown during dehydration of a homoiochlorophyllous resurrection plant proceeds via senescence-like processes
inferred← citeshttps://doi.org/10.1016/j.fitote.2016.08.013openalex-snapshot
Qualitative and quantitative phytochemical characterization of Myrothamnus flabellifolia Welw.
inferred← citeshttps://doi.org/10.1016/j.pbi.2023.102410openalex-snapshot
A review of the role of metabolites in vegetative desiccation tolerance of angiosperms
inferred← citeshttps://doi.org/10.1016/j.sajb.2010.10.003openalex-snapshot
An ultrastructural investigation of the surface microbiota present on the leaves and reproductive structures of the resurrection plant Myrothamnus flabellifolia
inferred← citeshttps://doi.org/10.1016/j.tplants.2008.11.007openalex-snapshot
Towards a systems-based understanding of plant desiccation tolerance
inferred← citeshttps://doi.org/10.1038/hortres.2015.34openalex-snapshot
Transcriptomic analysis reveals numerous diverse protein kinases and transcription factors involved in desiccation tolerance in the resurrection plant Myrothamnus flabellifolia
inferred← citeshttps://doi.org/10.1071/bt11148openalex-snapshot
Ultrastructure and anatomy of Macadamia (Proteaceae) kernels
inferred← citeshttps://doi.org/10.1071/fp07142_coopenalex-snapshot
Corrigendum to : Protection mechanisms in the resurrection plant Xerophyta viscosa : cloning, expression, characterisation and role of XvINO1 , a gene coding for a myo -inositol 1-phosphate synthase
inferred← citeshttps://doi.org/10.1093/jxb/ern226openalex-snapshot
Expression of Xhdsi-1VOC, a novel member of the vicinal oxygen chelate (VOC) metalloenzyme superfamily, is up-regulated in leaves and roots during desiccation in the resurrection plant Xerophyta humilis (Bak) Dur and Schinz
inferred← citeshttps://doi.org/10.1093/jxb/erz472openalex-snapshot
Positive root pressure is critical for whole-plant desiccation recovery in two species of terrestrial resurrection ferns
inferred← citeshttps://doi.org/10.1111/j.1399-3054.2008.01134.xopenalex-snapshot
Adaptations of higher plant cell walls to water loss: drought vs desiccation
inferred← citeshttps://doi.org/10.1111/j.1438-8677.2011.00546.xopenalex-snapshot
A morpho‐anatomical characterisation of Myrothamnus moschatus (Myrothamnaceae) under the aspect of desiccation tolerance
inferred← citeshttps://doi.org/10.1111/nph.16067openalex-snapshot
High‐resolution computed tomography reveals dynamics of desiccation and rehydration in fern petioles of a desiccation‐tolerant fern
inferred← citeshttps://doi.org/10.1111/nph.71466openalex-snapshot
Desiccation tolerance mechanisms in the green lineage and beyond
inferred← citeshttps://doi.org/10.1139/cjb-2013-0082openalex-snapshot
Asymbiotic germination of mature seeds and protocorm development ofPseudorchis albida(Orchidaceae) are inhibited by nitrates even at extremely low concentrations
inferred← citeshttps://doi.org/10.1146/annurev-arplant-071219-105542openalex-snapshot
Desiccation Tolerance: Avoiding Cellular Damage During Drying and Rehydration
inferred← citeshttps://doi.org/10.11606/d.41.2012.tde-21012013-141040openalex-snapshot
Microgramma squamulosa (Kaulf.) de la Sota e Pleopeltis hirsutissima (Raddi) de la Sota: estratégias contrastantes de uso da água em um ambiente epifítico
inferred← citeshttps://doi.org/10.3109/07388551.2012.659174openalex-snapshot
Systems biology-based approaches toward understanding drought tolerance in food crops
inferred← citeshttps://doi.org/10.3389/fpls.2014.00036openalex-snapshot
Drying without senescence in resurrection plants
inferred← citeshttps://doi.org/10.3390/horticulturae9121339openalex-snapshot
Effect of Osmolytes on Photoassembly of Functionally Active Mn4CaO5 Cluster in Mn-Depleted Photosystem II Preparations Isolated from Spinach Leaves
inferred← citeshttps://doi.org/10.3390/ijms23158155openalex-snapshot
Overexpressing PhytochromeInteractingFactor 8 of Myrothamnus flabellifolia Enhanced Drought and Salt Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3390/plants13060847openalex-snapshot
Evaluation of the Antioxidant, Cytotoxicity, Antibacterial, Anti-Motility, and Anti-Biofilm Effects of Myrothamnus flabellifolius Welw. Leaves and Stem Defatted Subfractions
inferred← citeshttps://doi.org/10.3390/proteomes4040040openalex-snapshot
Enzymes and Metabolites in Carbohydrate Metabolism of Desiccation Tolerant Plants
inferred← citeshttps://doi.org/10.3390/rs14112596openalex-snapshot
Machine Learning in the Analysis of Multispectral Reads in Maize Canopies Responding to Increased Temperatures and Water Deficit
inferred← citeshttps://doi.org/10.3732/ajb.0900285openalex-snapshot
Dehydration‐induced expression of a 31‐kDa dehydrin in Polypodium polypodioides (Polypodiaceae) may enable large, reversible deformation of cell walls
inferred← citeshttps://doi.org/10.5897/ajb.9000398openalex-snapshot
Physiological response of selected eragrostis species to water-deficit stress
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