연구동향 분석
박사

Functional characterization of 3-ketoacyl-CoA synthase 9 and 4 in Arabidopsis thaliana = 애기장대 3-ketoacyl-CoA synthase 9과 4의 기능연구

김주영 2020년

논문상세정보
인용/피인용
' Functional characterization of 3-ketoacyl-CoA synthase 9 and 4 in Arabidopsis thaliana = 애기장대 3-ketoacyl-CoA synthase 9과 4의 기능연구' 의 주제별 논문영향력
논문영향력 선정 방법
논문영향력 요약
주제
  • 기술과 연합작용
  • 3-ketoacyl-CoA synthase
  • Lipids
  • Suberin
  • Wax
  • arabidopsis
  • kcs
  • phospholipid
  • sphingolipid
동일주제 총논문수 논문피인용 총횟수 주제별 논문영향력의 평균
7,424 0

0.0%

' Functional characterization of 3-ketoacyl-CoA synthase 9 and 4 in Arabidopsis thaliana = 애기장대 3-ketoacyl-CoA synthase 9과 4의 기능연구' 의 참고문헌

  • Wax Crystal-Sparse Leaf 1 encodes a beta-ketoacyl CoA synthase involved in biosynthesis of cuticular waxes on rice leaf .
    [2008]
  • WRINKLED1 encodes an AP2/EREB domain protein involved in the control of storage compound biosynthesis in Arabidopsis
    40 ( 4 ) :575-85 [2004]
  • Very-long-chain fatty acids restrict regeneration capacity by confining pericycle competence for callus formation in Arabidopsis .
    113 ( 18 ) :5101-6 . [2016]
  • Very-long-chain fatty acids are required for cell plate formation during cytokinesis in Arabidopsis thaliana
    124 ( Pt 19 ) :3223-34 [2011]
  • Very-long-chain fatty acids are involved in polar auxin transport and developmental patterning in Arabidopsis
    22 : 364-375 [2010]
  • Very long chain fatty acid and lipid signaling in the response of plants to pathogens
    4 ( 2 ) :94-9. Review [2009]
  • Very Long Chain Fatty Acids Are Functionally Involved in Necroptosis
    24 ( 12 ) :1445-1454 [2017]
  • Two Arabidopsis 3-ketoacyl CoA synthase genes , KCS20 and KCS2/DAISY , are functionally redundant in cuticular wax and root suberin biosynthesis , but differentially controlled by osmotic stress
    60 ( 3 ) : 462-475 . [2009]
  • Transcriptome analysis of haploid male gametophyte development in Arabidopsis
    5 ( 11 ) : R85 . [2004]
  • To branch or not to branch : the role of pre-patterning in lateral root formation
    140 ( 21 ) , 4301 ? 4310 [2013]
  • The small , versatile pPZP family of Agrobacterium binary vectors for plant transformation .
    25 : 989-994 [1994]
  • The lack of a systematic validation of reference genes : a serious pitfall undervalued in reverse transcription polymerase chain reaction ( RT-PCR ) analysis in plants
    [2008]
  • The essential nature of sphingolipids in plants as revealed by the functional identification and characterization of the Arabidopsis LCB1 subunit of serine palmitoyltransferase .
    18 ( 12 ) :3576 ? 3593 [2006]
  • The effect of lectins on germinating pollen of Lilium longiflorum II . Effect of concanavalin A on phospholipid turnover and on biosynthesis of pectic polysaccharides
    35 ( 3 ) , p. 257-263 [1986]
  • The cytochrome P450 enzyme CYP96A15 is the midchain alkane hydroxylase responsible for formation of secondary alcohols and ketones in stem cuticular wax of Arabidopsis
    145 ( 3 ) : 653-667 [2007]
  • The acyltransferase GPAT5 is required for the synthesis of suberin in seed coat and root of Arabidopsis
    [2007]
  • The VLCFA elongase gene family in Arabidopsis thaliana : phylogenetic analysis , 3D modeling and expression profiling .
    67 : 547-566 [2008]
  • The CER3 wax biosynthetic gene from Arabidopsis thaliana is allelic to WAX2/YRE/FLP1 .
    581 ( 18 ) : 3538-3544 [2007]
  • The Arabidopsis cer26 mutant , like the cer2 mutant , is specifically affected in the very long chain fatty acid elongation process
    73 ( 5 ) : 733-746 [2013]
  • The ABC transporter ABCG1 is required for suberin formation in potato tuber periderm
    26 ( 8 ) :3403-15 . [2014]
  • Synthesis of very-long-chain fatty acids in the epidermis controls plant organ growth by restricting cell proliferation
    11 ( 4 ) : e1001531 [2013]
  • Substrate specificity of Arabidopsis 3-ketoacyl-CoA synthases .
    346 : 583 ? 590 [2006]
  • Suberin goes genomics : use of a short living plant to investigate a long lasting polymer
    [2012]
  • Sturbois B. Biosynthesis of very long chain fatty acids in higher plants
    33 ( 1-2 ) :55-69. Review [1994]
  • SphingolipidsContaining Very-Long-Chain Fatty Acids Define a Secretory Pathway for Specific Polar Plasma Membrane Protein Targeting in Arabidopsis
    23 ( 6 ) , 2362 ? 2378 [2011]
  • Sphingolipid metabolism is strikingly different between pollen and leaf in Arabidopsis as revealed byCompositional and gene expression profiling .
    [2015]
  • Sphingolipid long-chain base hydroxylation is important for growth and regulation of sphingolipidContent andComposition in Arabidopsis .
    20 ( 7 ) :1862 ? 1878 . [2008]
  • Sphingolipid Delta8 unsaturation is important for glucosylceramide biosynthesis and low-temperature performance in Arabidopsis
    69 ( 5 ) :769 ? 781 [2012]
  • Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides
    101 : 11903 ? 11908 [2004]
  • Solving the puzzles ofCutin and suberin polymer biosynthesis .
    15 ( 3 ) :329-337 [2012]
  • Significance of the expression of theCER6Condensing enzyme forCuticular wax production in Arabidopsis
    129 ( 4 ) :1568-80 . [2002]
  • Serine palmitoyltransferase , a key enzyme for de novo synthesis of sphingolipids , is essential for male gametophyte development in Arabidopsis
    146 ( 3 ) :1322-32 [2008]
  • Resolution and purification of an aldehyde-generating and an alcohol-generating fatty acyl-CoA reductase from pea leaves ( Pisum sativum L. )
    340 : 64-72 . [1997]
  • Rennie EA, Ebert B, Miles GP, Cahoon RE, Christiansen KM, Stonebloom S, Khatab H, Twell D, Petzold CJ, Adams PD, Dupree P, Heazlewood JL, Cahoon EB, Scheller HV. (2014) Identification of a sphingolipid メ-glucuronosyltransferase that is essential for pollen function in Arabidopsis. Plant Cell. 26(8):3314-25.
  • Reconstitution of plant alkane biosynthesis in yeast demonstrates that Arabidopsis ECERIFERUM1 and ECERIFERUM3 areCoreComponents of a very-long-chain alkane synthesisComplex
    24 ( 7 ) :3106-3118 [2012]
  • Rapid measurement of sphingolipids from Arabidopsis thaliana by reversed-phase high-performance liquidChromatographyCoupled to electrospray ionization tandem mass spectrometry
    21 : 1304-1314 [2007]
  • Purity of the sacred lotus , or escape fromContamination in biological surfaces
    202 ( 1 ) : 1-8 [1997]
  • Protein oligomerization modulates raft partitioning and apical sorting of GPI-anchored proteins .
    167 , 699-709 . [2004]
  • Protecting against water loss : Analysis of the barrier properties of plantCuticles
    52 : 2023-2032 [2001]
  • ProfilingCandidate genes involved in wax biosynthesis in Arabidopsis thaliana by microarray analysis
    1734 ( 3 ) :247-58 . [2005]
  • Pollen lipidomics : lipid profiling exposes a notable diversity in 22 allergenic pollen and potential biomarkers of the allergic immune response
    8 ( 2 ) : e57566 . [2013]
  • PlantCuticular lipid export requires an ABC transporter
    306 ( 5696 ) : 702-704 [2004]
  • Plant sphingolipids : Their importance inCellular organization and adaption . Biochimica et Biophysica Acta , 1861 ( 9Part B ) , 1329 ? 1335
    [2016]
  • Physiological effects of surface waxes
    62 : 101-104 [1978]
  • Phospholipids as Plant Growth Regulators
    48 ( 2 ) , 97-109 [2006]
  • Phosphatidylserine delivery to endoplasmic reticulum-derived vesicles of plant cells depends on two biosynthetic pathways
    498 ( 1 ) :32-6 . [2001]
  • Paul S, Gable K, Beaudoin F, Cahoon E, Jaworski J, Napier JA, Dunn TM (2006)
    [2006]
  • PHOSPHATIDYLSERINE SYNTHASE1 is required for microspore development in Arabidopsis thaliana
    67 ( 4 ) :648-61 . [2011]
  • Overexpression of the novel Arabidopsis gene At5g02890 alters inflorescence stem wax composition and affects phytohormone homeostasis
    26 : 8-68 [2017]
  • Overexpression of Arabidopsis ECERIFERUM1 promotes wax very-long-chain alkane biosynthesis and influences plant response to biotic and abiotic stresses .
    156 : 29-45 [2011]
  • One of the origins of plasma membrane phosphatidylserine in plant cells is a local synthesis by a serine exchange activityFEBS Lett.4648084
    [1999]
  • Oligomerization is a specific requirement for apical sorting of glycosyl-phosphatidylinositol-anchored proteins but not for non-raft-associated apical proteins .
    8 , 251-258 . [2007]
  • New Phytol . Plant sphingolipids : decoding the enigma of the Sphinx
    185 ( 3 ) :611-30.185 ( 30 ) . [2010]
  • Nanoridges that characterize the surface morphology of flowers require the synthesis of cutin polyester
    106 ( 51 ) :22008-22013 . [2009]
  • Multifunctional acetyl-CoA carboxylase1 is essential for very long chain fatty acid elongation and embryo development in Arabidopsis
    336 ( 1 ) :75 ? 86 [2003]
  • Molecular characterization of the CER1 gene of arabidopsis involved in epicuticular wax biosynthesis and pollen fertility .
    7 ( 12 ) :2115-2127 [1995]
  • Membrane microdomains : from seeing to understanding .
    [2014]
  • Members of the Arabidopsis FAE1-like 3-ketoacyl-CoA synthase gene family substitute for the Elop proteins of Saccharomyces cerevisiae. J Biol Chem. 281(14):9018-29.
  • McDowell GS, Blanchard AP, Valenzuela N, Xu H, Gelbard S, Bertrand M, Slater GW, Figeys D, Fai S, Bennett SA. (2013) Visualization and Phospholipid Identification (VaLID): online integrated search engine capable of identifying and visualizing glycerophospholipids with given mass. Bioinformatics. 29(2):284-5.
  • Loss-of-function mutations and inducible RNAi suppression of Arabidopsis LCB2 genes reveal the critical role of sphingolipids in gametophytic and sporophytic cell viability
    54 ( 2 ) :284-98 . [2008]
  • Loss of the Arabidopsis thaliana P4-ATPases ALA6 and ALA7 impairs pollen fitness and alters the pollen tube plasma membrane
    [2015]
  • Lipids in pollen - They are different
    1861 ( 9 Pt B ) :1315-1328 [2016]
  • Lipids are required for directional pollen-tube growth
    392 ( 6678 ) :818-21 [1998]
  • Li-Beisson Y, Shorrosh B, Beisson F, Andersson MX, Arondel V, Bates PD, Baud S, Bird D, Debono A, Durrett TP, Franke RB, Graham IA, Katayama K, Kelly AA, Larson T, Markham JE, Miquel M, Molina I, Nishida I, Rowland O, Samuels L, Schmid KM, Wada H, Welti R, Xu C, Zallot R, and Ohlrogge J (2013) Acyl-Lipid Metabolism. The Arabidopsis Book 11: e0161
  • LATERAL ORGAN BOUNDARIES DOMAIN ( LBD ) 10 interacts with SIDECAR POLLEN/LBD27 to control pollen development in Arabidopsis
    81 ( 5 ) :794-809 . [2015]
  • KCS1encodes a fatty acid elongase 3-ketoacyl-CoA synthase affecting wax biosynthesis in Arabidopsis thaliana
    17 ( 2 ) : 119-130 [1999]
  • Involvement of Arabidopsis ACYL-COENZYME A DESATURASE-LIKE2 ( At2g31360 ) in the biosynthesis of the very-long-chain monounsaturated fatty acid components of membrane lipids
    161 ( 1 ) :81-96 . [2013]
  • Intra- and extracellular lipid composition and associated gene expression patterns during pollen development in Brassica napus
    11 ( 3 ) :549-62 . [1997]
  • Inhibition of saturated very-long-chain fatty acid biosynthesis by mefluidide and perfluidone , selective inhibitors of 3-ketoacyl-CoA synthases
    [2012]
  • In planta Agrobacterium mediated gene transfer by infiltration of adult Arabidopsis thaliana plants
    Serie III 316 : 1194-1199 [1993]
  • Identification of the wax ester synthase/acyl-coenzyme A : diacylglycerol acyltransferase WSD1 required for stem wax ester biosynthesis in Arabidopsis
    148 ( 1 ) : 97-107 [2008]
  • Identification of functional BrFAD2-1 gene encoding microsomal delta-12 fatty acid desaturase from Brassica rapa and development of Brassica napus containing high oleic acid contents .
    30 : 1881-1892 [2011]
  • Identification of an Arabidopsis feruloyl-coenzyme A transferase required for suberin synthesis
    151 : 1317-1328 . [2009]
  • Identification of acyltransferases required for cutin biosynthesis and production of cutin with suberin-like monomers
    104 ( 46 ) : 18339-18344 [2007]
  • How Very-Long-Chain Fatty Acids Could Signal Stressful Conditions in Plants ?
    [2016]
  • Glucosylceramides are critical for cell-type differentiation and organogenesis , but not for cell viability in Arabidopsis
    84 ( 1 ) :188-201 .
  • Genetic and biochemical evidence for involvement of HOTHEAD in the biosynthesis of long-chain alphaomega-dicarboxylic fatty acids and formation of extracellular matrix
    224 ( 2 ) : 315-329 [2006]
  • Genetic and Biochemical Mechanisms of Pollen Wall Development
    20 ( 11 ) :741-753 [2015]
  • Functional characterization of the Arabidopsis beta-ketoacyl-coenzyme A reductase candidates of the fatty acid elongase
    150 ( 3 ) :1174-1191 [2009]
  • Franke R, Hofer R, Briesen I, Emsermann M, Efremova N, Yephremov A, Schreiber
  • Faure, J.D., Vittorioso, P., Santoni, V., Fraisier, V., Prinsen, E., Barlier, I., Vanonckelen, H., Caboche, M., and Bellini, C. (1998). The PASTICCINO genes of Arabidopsis thaliana are involved in the control of cell division and differentiation. Development 125: 909?918.
  • Fatty Acids : Structures and Properties
    DOI : 10.1038/npg.els.0003894 [2005]
  • Extending the story of very-long-chain fatty acid elongation
    210 : 93-107 [2013]
  • Enrichment of hydroxylated C24and C26-acyl-chain sphingolipids mediates PIN2 apical sorting at trans-Golgi network subdomains .
    [2016]
  • Effective lipid staining in plant material with Sudan red 78 or Fluorol yellow O88 in polyethylene glycol-glycerol .
    66 ( 3 ) :111-6 . [1990]
  • Early flower development in Arabidopsis
    [1990]
  • ELO2 and ELO3 , homologues of the Saccharomyces cerevisiae ELO1 gene , function in fatty acid elongation and are required for sphingolipid formation
    272 : 17376-17384 [1997]
  • ECERIFERUM2-LIKE proteins have unique biochemical and physiological functions in very-long-chain fatty acid elongation
    167 ( 3 ) : 682-692 [2015]
  • Dual fatty acid elongase complex interactions in Arabidopsis
    11 ( 9 ) : e0160631 . doi : 10.1371/journal.pone.0160631 . [2016]
  • Disruptions of the Arabidopsis enoyl-CoA reductase gene reveal an essential role for very-long-chain fatty acid synthesis in cell expansion during plant morphogenesis
    17 ( 5 ) : 1467-1481 [2005]
  • Disruption of glycosylphosphatidylinositol-anchored lipid transfer protein 15 affects seed coat permeability in Arabidopsis
    96 ( 6 ) :1206-1217 [2018]
  • Discovery of new cargo proteins that enter cells through clathrin-independent endocytosis
    10 ( 5 ) :590-9 . [2009]
  • Directed tagging of the Arabidopsis FATTY ACID ELONGATION1 ( FAE1 ) gene with the maize transposon activator .
    7 : 309-319 [1995]
  • Deposition and localization of lipid polyester in developing seeds of Brassica napus and Arabidopsis thaliana
    53 ( 3 ) : 437-449 [2008]
  • Deficiency in phosphatidylserine decarboxylase activity in the psd1 psd2 psd3 triple mutant of Arabidopsis affects phosphatidylethanolamine accumulation in mitochondria .
    144 : 904-914 . [2007]
  • Defects in CTP : PHOSPHORYLETHANOLAMINE CYTIDYLYLTRANSFERASE affect embryonic and postembryonic development in Arabidopsis
    18 ( 12 ) :3370-85 . [2016]
  • Cytochemical Analysis of Pollen Development in Wild-Type Arabidopsis and a Male-Sterile Mutant
    2 ( 9 ) :877-889 . [1990]
  • Cuticular lipid composition , surface structure , and gene expression in Arabidopsis stem epidermis
    139 ( 4 ) : 1649-1665 [2005]
  • Comprehensive cell-specific protein analysis in early and late pollen development from diploid microsporocytes to pollen tube growth
    13 ( 1 ) :295-310 [2014]
  • Composition of secondary alcohols , ketones , alkanediols , and ketols in Arabidopsis thaliana cuticular waxes
    [2009]
  • Cloning and characterization of the WAX2 gene of Arabidopsis involved in cuticle membrane and wax production .
    15 ( 5 ) :1170-1185 [2003]
  • Clathrin-independent endocytosis : new insights into caveolae and non-caveolar lipid raft carriers .
    1745 ( 3 ) :273-86 . [2005]
  • Characterization of the FIDDLEHEAD gene of Arabidopsis reveals a link between adhesion response and cell differentiation in the dpidermis
    11 ( 11 ) : 2187-2201 [1999]
  • Characterization of glycosylphosphatidylinositol-anchored lipid transfer protein 2 ( LTPG2 ) and overlapping function between LTPG/LTPG1 and LTPG2 in cuticular wax export or accumulation in Arabidopsis thaliana
    53 ( 8 ) :1391-1403 [2012]
  • Characterization of Arabidopsis ABCG11/WBC11 , an ATP binding cassette ( ABC ) transporter that is required for cuticular lipid secretion
    52 ( 3 ) :485-498 [2007]
  • Characterisation of detergent-insoluble membranes in pollen tubes of Nicotiana tabacum ( L. )
    4 ( 3 ) , 378 ? 399 . [2015]
  • Chao D, Gable K, Chen M, Baxter I, Dietrich CR, Cahoon EB, Guerinot ML, Lahner B, Lu S, Markham JE, Morrissey J, Han G, Gupta SD, Harmon JM, Jaworski JG, Dunn TM, Salta DE (2011) Sphingolipids in the root play an important role in regulating the leaf ionome in Arabidopsis thaliana. Plant Cell 23: 1061-1081
  • Cassagne C. Nature of the reaction product of stearoyl-CoA elongation by etiolated leek seeding microsomes .
    15 ; 239 ( 1 ) :260-9 . [1985]
  • Casparian strip diffusion barrier in Arabidopsis is made of a lignin polymer without suberin
    109 ( 25 ) :10101-6 [2012]
  • CUT1 , an Arabidopsis gene required for cuticular wax biosynthesis and pollen fertility , encodes a very-long-chain fatty acid condensing enzyme
    11 : 825-838 [1999]
  • CO2 and water vapor exchange across leaf cuticle ( epidermis ) at various water potentials
    114 ( 1 ) :185-191 [1997]
  • CER4 encodes an alcohol-forming fatty acyl-coenzyme A reductase involved in cuticular wax production in Arabidopsis
    142 ( 3 ) : 866-877 [2006]
  • Building lipid barriers : biosynthesis of cutin and suberin
    13 ( 5 ) : 236-246 [2008]
  • Biosynthesis of saturated very long chain fatty acids by purified membrane fractions from leek epidermal cells
    191 ( 1 ) :146-52 . [1978]
  • Biosynthesis of phosphatidyl ethanolamine and phosphatidyl choline in spinach leaves
    [1973]
  • Biosynthesis of Sphingolipids in Plants ( and Some of Their Functions
    [2013]
  • Biosynthesis and secretion of plant cuticular wax
    42 ( 1 ) : 51-80 [2003]
  • Biosynthesis and Elongation of Short- and Medium-Chain-Length Fatty Acids
    122 ( 1 ) 275-282 ; DOI : 10.1104/pp.122.1.275 [2000]
  • Binary ti vectors for plant transformation and promoter analysis .
    153 : 292-305 [1987]
  • Behavior of storage lipids during development and germination of olive ( Olea europaea L. ) pollen . Protoplasma
    221 ( 3-4 ) :237-44 [2003]
  • Bach L, Michaelson LV, Haslam R, Bellec Y, Gissot L, Marion J, Da Costa M, Boutin JP, Miquel M, Tellier F, Domergue F, Markham JE, Beaudoin F, Napier JA, and Faure JD (2008) The very-long-chain hydroxy fatty acyl-CoA dehydratase PASTICCINO2 is essential and limiting for plant development. Proc Natl. Acad. Sci. USA 105(38):14727-14731
  • Arabidopsis thaliana polar glycerolipid profiling by thin layer chromatography ( TLC ) coupled with gas-liquid chromatography ( GLC )
    49 ) [2011]
  • Arabidopsis mutants of sphingolipid fatty acid メ-hydroxylases accumulate ceramides and salicylates .
    196 ( 4 ) :1086-97 . [2012]
  • Arabidopsis ketoacyl-CoA synthase 16 ( KCS16 ) forms C36 /C38 acyl precursors for leaf trichome and pavement surface wax .
    40 ( 9 ) :1761-1776 . [2017]
  • Arabidopsis LTPG is a glycosylphosphatidylinositol-anchored lipid transfer protein required for export of lipids to the plant surface
    21 ( 4 ) :1230-1238 [2009]
  • Arabidopsis ECERIFERUM2 is a component of the fatty acid elongation machinery required for fatty acid extension to exceptional lengths
    160 ( 3 ) : 1164-1174 [2012]
  • Arabidopsis CYP86A2 represses Pseudomonas syringae type III genes and is required for cuticle development
    23 ( 14 ) : 2903-2913 [2004]
  • Arabidopsis ABCG transporters , which are required for export of diverse cuticular lipids , dimerize in different combinations
    22 ( 9 ) : 3066-3075 [2010]
  • Arabidopsis 3-ketoacyl-coenzyme a synthase9 is involved in the synthesis of tetracosanoic acids as precursors of cuticular waxes , suberins , sphingolipids , and phospholipids
    162 ( 2 ) : 567-580 [2013]
  • Apoplastic polyesters in Arabidopsis surface tissues : a typical suberin and a particular cutin
    66 ( 22 ) :2643-58 . [2005]
  • An introduction to plant sphingolipids and a review of recent advances in understanding their metabolism and function
    161 : 677-702 [2004]
  • An Electronic Fluorescent Pictograph browser for exploring and analyzing large-scale biological data sets
    2 ( 8 ) : e718 . [2007]
  • Alterations in CER6 , a gene identical to CUT1 , differentially affect long-chain lipid content on the surface of pollen and stems
    [2000]
  • Adaptation of Root Function by Nutrient-Induced Plasticity of Endodermal Differentiation
    164 ( 3 ) :447-59 . [2016]
  • AUX1 acts upstream of PIN2 in regulating root gravitropism .
    507 ( 1-4 ) :433-436 [2018]
  • ABCG1 contributes to suberin formation in Arabidopsis thaliana roots
    9 ( 1 ) :11381 . [2019]
  • ABCB19/PGP19 stabilises PIN1 in membrane microdomains in Arabidopsis .
    57 ( 1 ) :27-44 .
  • A molecular caliper mechanism for determining very long-chain fatty acid length
    [2007]
  • A distinct type of glycerol-3-phosphate acyltransferase with sn-2 preference and phosphatase activity producing 2-monoacylglycerol
    107 ( 26 ) : 12040-12045 [2010]
  • A MYB transcription factor regulates very-long-chain fatty acid biosynthesis for activation of the hypersensitive cell death response in Arabidopsis
    20 : 752-767 [2008]
  • 70 L.C. Geonzon, R.G. Bacabac, S. Matsukawa, J. Electrochem. Soc., 166 (2019) B3228- B3234.