On the public citation graph
Biogenesis and homeostasis of chloroplasts and other plastids
0 signed · 924 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-61779-234-2_5openalex-snapshot
Visualisation of Stromules on Arabidopsis Plastids
inferredcites →https://doi.org/10.1007/s00425-012-1739-2openalex-snapshot
Divide and shape: an endosymbiont in action
inferredcites →https://doi.org/10.1007/s00425-012-1743-6openalex-snapshot
Emerging facets of plastid division regulation
inferredcites →https://doi.org/10.1007/s10265-010-0309-6openalex-snapshot
Cytoplasmic inheritance in green algae: patterns, mechanisms and relation to sex type
inferredcites →https://doi.org/10.1007/s10577-013-9349-9openalex-snapshot
DNA abandonment and the mechanisms of uniparental inheritance of mitochondria and chloroplasts
inferredcites →https://doi.org/10.1007/s11120-007-9183-zopenalex-snapshot
Chloroplast translation regulation
inferredcites →https://doi.org/10.1016/b978-0-12-386037-8.00002-8openalex-snapshot
Retrograde Signaling Pathway from Plastid to Nucleus
inferredcites →https://doi.org/10.1016/j.bbabio.2010.12.003openalex-snapshot
The Clp protease system; a central component of the chloroplast protease network
inferredcites →https://doi.org/10.1016/j.bbamcr.2012.03.006openalex-snapshot
Cytosolic events involved in chloroplast protein targeting
inferredcites →https://doi.org/10.1016/j.bbamcr.2012.03.012openalex-snapshot
Processing peptidases in mitochondria and chloroplasts
inferredcites →https://doi.org/10.1016/j.bbamcr.2012.03.019openalex-snapshot
Molecular chaperone involvement in chloroplast protein import
inferredcites →https://doi.org/10.1016/j.bbamcr.2012.04.004openalex-snapshot
Protein targeting to subcellular organelles via mRNA localization
inferredcites →https://doi.org/10.1016/j.bbamcr.2012.06.028openalex-snapshot
Intra-plastid protein trafficking: How plant cells adapted prokaryotic mechanisms to the eukaryotic condition
inferredcites →https://doi.org/10.1016/j.bbamcr.2012.10.002openalex-snapshot
The chloroplast protein import system: From algae to trees
inferredcites →https://doi.org/10.1016/j.ceb.2009.03.004openalex-snapshot
Chloroplast biogenesis: diversity and regulation of the protein import apparatus
inferredcites →https://doi.org/10.1016/j.ceb.2013.04.006openalex-snapshot
FtsZ in chloroplast division: structure, function and evolution
inferredcites →https://doi.org/10.1016/j.cell.2010.05.007openalex-snapshot
Arabidopsis HEMERA/pTAC12 Initiates Photomorphogenesis by Phytochromes
inferredcites →https://doi.org/10.1016/j.cell.2012.04.038openalex-snapshot
Retrograde Signaling by the Plastidial Metabolite MEcPP Regulates Expression of Nuclear Stress-Response Genes
inferredcites →https://doi.org/10.1016/j.cub.2008.12.018openalex-snapshot
Plant-Specific Protein MCD1 Determines the Site of Chloroplast Division in Concert with Bacteria-Derived MinD
inferredcites →https://doi.org/10.1016/j.cub.2011.04.004openalex-snapshot
Heme Synthesis by Plastid Ferrochelatase I Regulates Nuclear Gene Expression in Plants
inferredcites →https://doi.org/10.1016/j.cub.2012.01.027openalex-snapshot
Mechanosensitive Channels Protect Plastids from Hypoosmotic Stress During Normal Plant Growth
inferredcites →https://doi.org/10.1016/j.devcel.2011.11.011openalex-snapshot
Exit from Proliferation during Leaf Development in Arabidopsis thaliana: A Not-So-Gradual Process
inferredcites →https://doi.org/10.1016/j.pbi.2008.10.001openalex-snapshot
Plastid division: across time and space
inferredcites →https://doi.org/10.1016/j.pbi.2012.07.002openalex-snapshot
The plastid-dividing machinery: formation, constriction and fission
inferredcites →https://doi.org/10.1016/j.tcb.2013.04.008openalex-snapshot
Dynamic regulation of endosymbiotic organelles by ubiquitination
inferredcites →https://doi.org/10.1016/j.tem.2012.06.006openalex-snapshot
Transcriptional integration of mitochondrial biogenesis
inferredcites →https://doi.org/10.1016/j.tplants.2005.07.009openalex-snapshot
Chloroplast outer membrane protein targeting and insertion
inferredcites →https://doi.org/10.1016/j.tplants.2005.12.004openalex-snapshot
Why are plastid genomes retained in non-photosynthetic organisms?
inferredcites →https://doi.org/10.1016/j.tplants.2008.09.003openalex-snapshot
The plastidial MEP pathway: unified nomenclature and resources
inferredcites →https://doi.org/10.1016/j.tplants.2008.10.001openalex-snapshot
Pentatricopeptide repeat proteins: a socket set for organelle gene expression
inferredcites →https://doi.org/10.1016/j.tplants.2010.06.002openalex-snapshot
Redox extends its regulatory reach to chloroplast protein import
inferredcites →https://doi.org/10.1016/j.tplants.2011.10.004openalex-snapshot
A structural phylogenetic map for chloroplast photosynthesis
inferredcites →https://doi.org/10.1016/j.tplants.2013.04.003openalex-snapshot
Transit peptide design and plastid import regulation
inferredcites →https://doi.org/10.1016/s0167-4889(01)00149-5openalex-snapshot
The paradox of plastid transit peptides: conservation of function despite divergence in primary structure
inferredcites →https://doi.org/10.1016/s1937-6448(10)80004-8openalex-snapshot
New Insights into the Types and Function of Proteases in Plastids
inferredcites →https://doi.org/10.1038/17624openalex-snapshot
Photosynthetic control of chloroplast gene expression
inferredcites →https://doi.org/10.1038/279816a0openalex-snapshot
Cytoplasmic synthesis of plastid polypeptides may be controlled by plastid-synthesised RNA
inferredcites →https://doi.org/10.1038/35003214openalex-snapshot
The major protein import receptor of plastids is essential for chloroplast biogenesis
inferredcites →https://doi.org/10.1038/nature01204openalex-snapshot
Chloroplast to nucleus communication triggered by accumulation of Mg-protoporphyrinIX
inferredcites →https://doi.org/10.1038/nature01435openalex-snapshot
Direct measurement of the transfer rate of chloroplast DNA into the nucleus
inferredcites →https://doi.org/10.1038/nature03229openalex-snapshot
A pentatricopeptide repeat protein is essential for RNA editing in chloroplasts
inferredcites →https://doi.org/10.1038/nature04016openalex-snapshot
Photosystem II core phosphorylation and photosynthetic acclimation require two different protein kinases
inferredcites →https://doi.org/10.1038/ncb1321openalex-snapshot
Phosphatidylinositol transfer protein-α in netrin-1-induced PLC signalling and neurite outgrowth
inferredcites →https://doi.org/10.1038/ncb1330openalex-snapshot
Evidence for a protein transported through the secretory pathway en route to the higher plant chloroplast
inferredcites →https://doi.org/10.1038/ncomms1278openalex-snapshot
LTD is a protein required for sorting light-harvesting chlorophyll-binding proteins to the chloroplast SRP pathway
inferredcites →https://doi.org/10.1038/ncomms1486openalex-snapshot
A chloroplast envelope-bound PHD transcription factor mediates chloroplast signals to the nucleus
inferredcites →https://doi.org/10.1038/ng.703openalex-snapshot
The developmental dynamics of the maize leaf transcriptome
inferredcites →https://doi.org/10.1038/nrg1271openalex-snapshot
Endosymbiotic gene transfer: organelle genomes forge eukaryotic chromosomes
inferredcites →https://doi.org/10.1038/nrg2049openalex-snapshot
Light-regulated transcriptional networks in higher plants
inferredcites →https://doi.org/10.1038/nrm3027openalex-snapshot
Common ground for protein translocation: access control for mitochondria and chloroplasts
inferredcites →https://doi.org/10.1038/nsmb.1836openalex-snapshot
ATP-independent reversal of a membrane protein aggregate by a chloroplast SRP subunit
inferredcites →https://doi.org/10.1038/sj.embor.7400902openalex-snapshot
ARC3 is a stromal Z‐ring accessory protein essential for plastid division
inferredcites →https://doi.org/10.1042/bst0380789openalex-snapshot
Mitochondrial fusion, division and positioning in plants
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01755.xopenalex-snapshot
A polyglycine stretch is necessary for proper targeting of the protein translocation channel precursor to the outer envelope membrane of chloroplasts
inferredcites →https://doi.org/10.1073/pnas.0308362101openalex-snapshot
Blue light-induced transcription of plastid-encoded psbD gene is mediated by a nuclear-encoded transcription initiation factor, AtSig5
inferredcites →https://doi.org/10.1073/pnas.0502564102openalex-snapshot
Cell and plastid division are coordinated through the prereplication factor AtCDT1
inferredcites →https://doi.org/10.1073/pnas.0702061104openalex-snapshot
EXECUTER1- and EXECUTER2-dependent transfer of stress-related signals from the plastid to the nucleus of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0803054105openalex-snapshot
Tetrapyrrole profiling in Arabidopsis seedlings reveals that retrograde plastid nuclear signaling is not due to Mg-protoporphyrin IX accumulation
inferredcites →https://doi.org/10.1073/pnas.0803245105openalex-snapshot
The steady-state level of Mg-protoporphyrin IX is not a determinant of plastid-to-nucleus signaling in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0803928105openalex-snapshot
The ancestral symbiont sensor kinase CSK links photosynthesis with gene expression in chloroplasts
inferredcites →https://doi.org/10.1073/pnas.0811684106openalex-snapshot
PIF3 is a repressor of chloroplast development
inferredcites →https://doi.org/10.1073/pnas.0911692107openalex-snapshot
Sigma factor phosphorylation in the photosynthetic control of photosystem stoichiometry
inferredcites →https://doi.org/10.1073/pnas.1103442108openalex-snapshot
Plastid gene expression and plant development require a plastidic protein of the mitochondrial transcription termination factor family
inferredcites →https://doi.org/10.1073/pnas.1114297109openalex-snapshot
Cell-to-cell movement of plastids in plants
inferredcites →https://doi.org/10.1073/pnas.1115886110openalex-snapshot
Energetic cost of protein import across the envelope membranes of chloroplasts
inferredcites →https://doi.org/10.1073/pnas.1115982109openalex-snapshot
Carotenoid oxidation products are stress signals that mediate gene responses to singlet oxygen in plants
inferredcites →https://doi.org/10.1073/pnas.1219229110openalex-snapshot
An essential role for chloroplast heat shock protein 90 (Hsp90C) in protein import into chloroplasts
inferredcites →https://doi.org/10.1074/jbc.m110.109744openalex-snapshot
Determinants for Stop-transfer and Post-import Pathways for Protein Targeting to the Chloroplast Inner Envelope Membrane
inferredcites →https://doi.org/10.1074/jbc.m611112200openalex-snapshot
Toc159- and Toc75-independent Import of a Transit Sequence-less Precursor into the Inner Envelope of Chloroplasts
inferredcites →https://doi.org/10.1074/jbc.m807134200openalex-snapshot
Characterization of Tic110, a Channel-forming Protein at the Inner Envelope Membrane of Chloroplasts, Unveils a Response to Ca2+ and a Stromal Regulatory Disulfide Bridge
inferredcites →https://doi.org/10.1083/jcb.200609172openalex-snapshot
Stimulation of transit-peptide release and ATP hydrolysis by a cochaperone during protein import into chloroplasts
inferredcites →https://doi.org/10.1083/jcb.200803034openalex-snapshot
The role of GTP binding and hydrolysis at the atToc159 preprotein receptor during protein import into chloroplasts
inferredcites →https://doi.org/10.1083/jcb.201205114openalex-snapshot
Distinct functions of chloroplast FtsZ1 and FtsZ2 in Z-ring structure and remodeling
inferredcites →https://doi.org/10.1093/emboj/16.13.4041openalex-snapshot
The two RNA polymerases encoded by the nuclear and the plastid compartments transcribe distinct groups of genes in tobacco plastids
inferredcites →https://doi.org/10.1093/jxb/erj144openalex-snapshot
The suffulta mutation in tomato reveals a novel method of plastid replication during fruit ripening
inferredcites →https://doi.org/10.1093/jxb/err357openalex-snapshot
Vipp1: a very important protein in plastids?!
inferredcites →https://doi.org/10.1093/jxb/err444openalex-snapshot
Targeting of lumenal proteins across the thylakoid membrane
inferredcites →https://doi.org/10.1093/mp/ssp082openalex-snapshot
Chloroplast Proteins without Cleavable Transit Peptides: Rare Exceptions or a Major Constituent of the Chloroplast Proteome?
inferredcites →https://doi.org/10.1093/pcp/pcp035openalex-snapshot
Light-Independent Cell Death Induced by Accumulation of Pheophorbide a in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcp047openalex-snapshot
Plant Cells Without Detectable Plastids are Generated in the crumpled leaf Mutant of Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcp138openalex-snapshot
Ectopic Overexpression of The Transcription Factor OsGLK1 Induces Chloroplast Development in Non-Green Rice Cells
inferredcites →https://doi.org/10.1093/pcp/pcr054openalex-snapshot
Two Novel Proteins, MRL7 and Its Paralog MRL7-L, Have Essential but Functionally Distinct Roles in Chloroplast Development and Are Involved in Plastid Gene Expression Regulation in Arabidopsis
inferredcites →https://doi.org/10.1098/rstb.2009.0103openalex-snapshot
The endosymbiotic origin, diversification and fate of plastids
inferredcites →https://doi.org/10.1104/pp.106.080069openalex-snapshot
The SCABRA3 Nuclear Gene Encodes the Plastid RpoTp RNA Polymerase, Which Is Required for Chloroplast Biogenesis and Mesophyll Cell Proliferation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.122770openalex-snapshot
Mobilization of Rubisco and Stroma-Localized Fluorescent Proteins of Chloroplasts to the Vacuole by anATGGene-Dependent Autophagic Process
inferredcites →https://doi.org/10.1104/pp.109.140483openalex-snapshot
Genome-Wide Analysis of Plastid Gene Expression in Potato Leaf Chloroplasts and Tuber Amyloplasts: Transcriptional and Posttranscriptional Control
inferredcites →https://doi.org/10.1104/pp.109.145987openalex-snapshot
Coordination of Plastid Protein Import and Nuclear Gene Expression by Plastid-to-Nucleus Retrograde Signaling
inferredcites →https://doi.org/10.1104/pp.110.166546openalex-snapshot
Plastids Contain a Second Sec Translocase System with Essential Functions
inferredcites →https://doi.org/10.1104/pp.110.170647openalex-snapshot
Three-Dimensional Architecture of Grana and Stroma Thylakoids of Higher Plants as Determined by Electron Tomography
inferredcites →https://doi.org/10.1104/pp.110.170852openalex-snapshot
Stromules: Recent Insights into a Long Neglected Feature of Plastid Morphology and Function
inferredcites →https://doi.org/10.1104/pp.111.172932openalex-snapshot
Plastid Proteomics in Higher Plants: Current State and Future Goals
inferredcites →https://doi.org/10.1104/pp.111.181891openalex-snapshot
In Vivo Analyses of the Roles of Essential Omp85-Related Proteins in the Chloroplast Outer Envelope Membrane
inferredcites →https://doi.org/10.1104/pp.111.188474openalex-snapshot
Nucleoid-Enriched Proteomes in Developing Plastids and Chloroplasts from Maize Leaves: A New Conceptual Framework for Nucleoid Functions
inferredcites →https://doi.org/10.1104/pp.112.198705openalex-snapshot
Functional Characterization of the GATA Transcription Factors GNC and CGA1 Reveals Their Key Role in Chloroplast Development, Growth, and Division in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.112.203810openalex-snapshot
Characterizing Regulatory and Functional Differentiation between Maize Mesophyll and Bundle Sheath Cells by Transcriptomic Analysis
inferredcites →https://doi.org/10.1104/pp.112.212654openalex-snapshot
Network Inference Analysis Identifies an APRR2-Like Gene Linked to Pigment Accumulation in Tomato and Pepper Fruits
inferredcites →https://doi.org/10.1104/pp.84.3.911openalex-snapshot
Changes in Photosynthetic Capacity and Photosynthetic Protein Pattern during Tomato Fruit Ripening
inferredcites →https://doi.org/10.1105/tpc.010397openalex-snapshot
HCF152, an Arabidopsis RNA Binding Pentatricopeptide Repeat Protein Involved in the Processing of Chloroplast psbB-psbT-psbH-petB-petD RNAs
inferredcites →https://doi.org/10.1105/tpc.105.036392openalex-snapshot
pTAC2, -6, and -12 Are Components of the Transcriptionally Active Plastid Chromosome That Are Required for Plastid Gene Expression
inferredcites →https://doi.org/10.1105/tpc.106.046417openalex-snapshot
The CauliflowerOrGene Encodes a DnaJ Cysteine-Rich Domain-Containing Protein That Mediates High Levels of β-Carotene Accumulation
inferredcites →https://doi.org/10.1105/tpc.107.054312openalex-snapshot
Plastid Signals Remodel Light Signaling Networks and Are Essential for Efficient Chloroplast Biogenesis inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.057075openalex-snapshot
Distinct Light-Initiated Gene Expression and Cell Cycle Programs in the Shoot Apex and Cotyledons ofArabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.061507openalex-snapshot
The High Light Response inArabidopsisInvolves ABA Signaling between Vascular and Bundle Sheath Cells
inferredcites →https://doi.org/10.1105/tpc.108.062018openalex-snapshot
Dynamic Plastid Redox Signals Integrate Gene Expression and Metabolism to Induce Distinct Metabolic States in Photosynthetic Acclimation inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.064964openalex-snapshot
Arabidopsis STN7 Kinase Provides a Link between Short- and Long-Term Photosynthetic Acclimation
inferredcites →https://doi.org/10.1105/tpc.108.065250openalex-snapshot
GLK Transcription Factors Coordinate Expression of the Photosynthetic Apparatus in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.067785openalex-snapshot
The PLASTID DIVISION1 and 2 Components of the Chloroplast Division Machinery Determine the Rate of Chloroplast Division in Land Plant Cell Differentiation
inferredcites →https://doi.org/10.1105/tpc.109.071548openalex-snapshot
Heat Shock Protein Cognate 70-4 and an E3 Ubiquitin Ligase, CHIP, Mediate Plastid-Destined Precursor Degradation through the Ubiquitin-26S Proteasome System in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.11.4.549openalex-snapshot
Plastid Division and Development
inferredcites →https://doi.org/10.1105/tpc.110.073866openalex-snapshot
Integrative Transcript and Metabolite Analysis of Nutritionally Enhanced DE-ETIOLATED1 Downregulated Tomato Fruit
inferredcites →https://doi.org/10.1105/tpc.110.079442openalex-snapshot
AnArabidopsisE3 Ligase, SHOOT GRAVITROPISM9, Modulates the Interaction between Statoliths and F-Actin in Gravity Sensing
inferredcites →https://doi.org/10.1105/tpc.110.079764openalex-snapshot
Structural and Metabolic Transitions of C4 Leaf Development and Differentiation Defined by Microscopy and Quantitative Proteomics in Maize
inferredcites →https://doi.org/10.1105/tpc.111.090324openalex-snapshot
Systems Analysis of a Maize Leaf Developmental Gradient Redefines the Current C4 Model and Provides Candidates for Regulation
inferredcites →https://doi.org/10.1105/tpc.111.091033openalex-snapshot
Evidence for a SAL1-PAP Chloroplast Retrograde Pathway That Functions in Drought and High Light Signaling in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.092254openalex-snapshot
Regulation of Root Greening by Light and Auxin/Cytokinin Signaling in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.092692openalex-snapshot
Evidence for a Role of VIPP1 in the Structural Organization of the Photosynthetic Apparatus in Chlamydomonas
inferredcites →https://doi.org/10.1105/tpc.111.094458openalex-snapshot
Gain and Loss of Photosynthetic Membranes during Plastid Differentiation in the Shoot Apex of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.095398openalex-snapshot
Differential Coloring Reveals That Plastids Do Not Form Networks for Exchanging Macromolecules
inferredcites →https://doi.org/10.1105/tpc.112.103606openalex-snapshot
Essential Role of VIPP1 in Chloroplast Envelope Maintenance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.111047openalex-snapshot
Chloroplast Division Protein ARC3 Regulates Chloroplast FtsZ-Ring Assembly and Positioning in Arabidopsis through Interaction with FtsZ2
inferredcites →https://doi.org/10.1105/tpc.113.113118openalex-snapshot
Arabidopsis CURVATURE THYLAKOID1 Proteins Modify Thylakoid Architecture by Inducing Membrane Curvature
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01630.xopenalex-snapshot
Variegation mutants and mechanisms of chloroplast biogenesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02736.xopenalex-snapshot
Isolation of precise plastid deletion mutants by homology‐based excision: a resource for site‐directed mutagenesis, multi‐gene changes and high‐throughput plastid transformation
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03035.xopenalex-snapshot
crinkled leaves 8 – A mutation in the large subunit of ribonucleotide reductase – leads to defects in leaf development and chloroplast division in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03279.xopenalex-snapshot
A novel serine/proline‐rich domain in combination with a transmembrane domain is required for the insertion of AtTic40 into the inner envelope membrane of chloroplasts
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03905.xopenalex-snapshot
PARC6, a novel chloroplast division factor, influences FtsZ assembly and is required for recruitment of PDV1 during chloroplast division in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04798.xopenalex-snapshot
Exclusion of plastid nucleoids and ribosomes from stromules in tobacco and Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05118.xopenalex-snapshot
Gibberellin indirectly promotes chloroplast biogenesis as a means to maintain the chloroplast population of expanded cells
inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01343.xopenalex-snapshot
In‐depth analysis of the distinctive effects of norflurazon implies that tetrapyrrole biosynthesis, organellar gene expression and ABA cooperate in the GUN‐type of plastid signalling
inferredcites →https://doi.org/10.1111/j.1469-8137.1978.tb01581.xopenalex-snapshot
A SUGGESTED CYCLE OF PLASTID DEVELOPMENTAL INTERRELATIONSHIPS
inferredcites →https://doi.org/10.1111/j.1751-1097.2008.00459.xopenalex-snapshot
The Plastoglobule: A Bag Full of Lipid Biochemistry Tricks †
inferredcites →https://doi.org/10.1111/tpj.12011openalex-snapshot
Sigma factor‐mediated plastid retrograde signals control nuclear gene expression
inferredcites →https://doi.org/10.1111/tpj.12249openalex-snapshot
Structural characterizations of the chloroplast translocon protein Tic110
inferredcites →https://doi.org/10.1126/science.1129689openalex-snapshot
Isolated Chloroplast Division Machinery Can Actively Constrict After Stretching
inferredcites →https://doi.org/10.1126/science.1140516openalex-snapshot
Signals from chloroplasts converge to regulate nuclear gene expression.
inferredcites →https://doi.org/10.1126/science.1170397openalex-snapshot
Exchange of Genetic Material Between Cells in Plant Tissue Grafts
inferredcites →https://doi.org/10.1126/science.1190791openalex-snapshot
Chloroplasts Divide by Contraction of a Bundle of Nanofilaments Consisting of Polyglucan
inferredcites →https://doi.org/10.1126/science.1222218openalex-snapshot
Uniform ripening Encodes a Golden 2-like Transcription Factor Regulating Tomato Fruit Chloroplast Development
inferredcites →https://doi.org/10.1126/science.1225053openalex-snapshot
Chloroplast Biogenesis Is Regulated by Direct Action of the Ubiquitin-Proteasome System
inferredcites →https://doi.org/10.1126/science.1229262openalex-snapshot
Uncovering the Protein Translocon at the Chloroplast Inner Envelope Membrane
inferredcites →https://doi.org/10.1126/science.1230397openalex-snapshot
Circadian Control of Chloroplast Transcription by a Nuclear-Encoded Timing Signal
inferredcites →https://doi.org/10.1126/science.282.5386.100openalex-snapshot
An Arabidopsis Mutant Defective in the Plastid General Protein Import Apparatus
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112222openalex-snapshot
Protein Transport into Chloroplasts
inferredcites →https://doi.org/10.1146/annurev-genet-110410-132544openalex-snapshot
The Biosynthetic Capacities of the Plastids and Integration Between Cytoplasmic and Chloroplast Processes
inferredcites →https://doi.org/10.1146/annurev.arplant.51.1.111openalex-snapshot
N ONPHOTOSYNTHETIC M ETABOLISM IN P LASTIDS
inferredcites →https://doi.org/10.1146/annurev.cellbio.042308.113414openalex-snapshot
Mechanisms of Lipid Transport Involved in Organelle Biogenesis in Plant Cells
inferredcites →https://doi.org/10.1146/annurev.genet.41.110306.130134openalex-snapshot
The Origin and Establishment of the Plastid in Algae and Plants
inferredcites →https://doi.org/10.1146/annurev.genet.42.110807.091452openalex-snapshot
The Dynamics of Photosynthesis
inferredcites →https://doi.org/10.1199/tab.0110openalex-snapshot
Chloroplast Biogenesis: Control of Plastid Development, Protein Import, Division and Inheritance
inferredcites →https://doi.org/10.1199/tab.0145openalex-snapshot
Tetrapyrrole Metabolism in Arabidopsis thaliana
inferredcites →https://doi.org/10.1271/bbb.68.2215openalex-snapshot
Roles of Chloroplast RNA Polymerase Sigma Factors in Chloroplast Development and Stress Response in Higher Plants
inferredcites →https://doi.org/10.1371/journal.pbio.1001416openalex-snapshot
Differential Age-Dependent Import Regulation by Signal Peptides
inferredcites →https://doi.org/10.1371/journal.pone.0063863openalex-snapshot
Evolutionary, Molecular and Genetic Analyses of Tic22 Homologues in Arabidopsis thaliana Chloroplasts
inferredcites →https://doi.org/10.1387/ijdb.051997elopenalex-snapshot
Plastids unleashed: their development and their integration in plant development
inferredcites →https://doi.org/10.1515/bc.2007.111openalex-snapshot
Mechanisms of protein import into thylakoids of chloroplasts
inferredcites →https://doi.org/10.3389/fpls.2013.00014openalex-snapshot
A model for tetrapyrrole synthesis as the primary mechanism for plastid-to-nucleus signaling during chloroplast biogenesis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4780645openalex-extracted
A Novel Pls-Dyw Type Ppr Protein Osasl Is Essential for Chloroplast Development in Rice
inferred← citeshttps://doi.org/10.2139/ssrn.4798882openalex-extracted
Genome-Wide Identification of the Toc Gtpase Gene Family and Screening for Substrate Specificity of Sltoc34-1 in Tomato
inferred← citeshttps://doi.org/10.1002/2211-5463.12791openalex-snapshot
Toc75‐V/OEP80 is processed during translocation into chloroplasts, and the membrane‐embedded form exposes its POTRA domain to the intermembrane space
inferred← citeshttps://doi.org/10.1002/9780470015902.a0001314.pub3openalex-snapshot
C 3 Carbon Reduction Cycle
inferred← citeshttps://doi.org/10.1002/9780470015902.a0029282openalex-snapshot
Plant Chloroplasts and Other Plastids
inferred← citeshttps://doi.org/10.1002/9781119079972.ch9openalex-snapshot
Improvement of Carotenoid Accumulation in Tomato Fruit
inferred← citeshttps://doi.org/10.1002/adma.73889openalex-snapshot
Bioinspired Artificial Bioenergetic Organelles: Design Principles, Nanofabrication and Therapeutic Translation
inferred← citeshttps://doi.org/10.1002/advs.77268openalex-snapshot
OsCPK12‐OsATPD1 Module Regulates Photosynthetic Acclimation to Light Stress in Rice
inferred← citeshttps://doi.org/10.1002/agj2.70116openalex-snapshot
Production and scavenging of reactive oxygen species in plant cells under cadmium stress
inferred← citeshttps://doi.org/10.1002/bies.202100041openalex-snapshot
Modern cities modelled as “super‐cells” rather than multicellular organisms: Implications for industry, goods and services
inferred← citeshttps://doi.org/10.1002/cpz1.360openalex-snapshot
Chromatin Immunoprecipitation in Chloroplasts
inferred← citeshttps://doi.org/10.1002/ece3.72129openalex-snapshot
Complete Chloroplast Genome of Enkianthus Lour. (Ericaceae): Comparative Analysis, Phylogenetic Relationships, Divergence History, and Adaptive Evolution
inferred← citeshttps://doi.org/10.1002/imt2.252openalex-snapshot
Polyploidy drives autophagy to participate in plant‐specific functions
inferred← citeshttps://doi.org/10.1002/pld3.537openalex-snapshot
Photosynthetically active radiation is required for seedling growth promotion by volcanic dacitic tuff breccia (Azomite)
inferred← citeshttps://doi.org/10.1002/pld3.70111openalex-snapshot
Rapid and Cost‐Effective Digital Quantification of RNA Editing and Maturation in Organelle Transcripts by Oxford Nanopore Target‐Indexed‐PCR (TIP) Sequencing
inferred← citeshttps://doi.org/10.1002/ppap.70262openalex-snapshot
Nonthermal Plasma Regulation of Photosynthetic Performance: Molecular Mechanisms, Chloroplast Responses, and Crop Improvement
inferred← citeshttps://doi.org/10.1007/978-1-0716-0743-5_10openalex-snapshot
Purification and Analysis of Chloroplast RNAs in Arabidopsis
inferred← citeshttps://doi.org/10.1007/978-1-0716-0880-7_8openalex-snapshot
Arabidopsis Photosynthetic and Heterotrophic Cell Suspension Cultures
inferred← citeshttps://doi.org/10.1007/978-1-0716-1186-9_34openalex-snapshot
Chloroplast Isolation and Enrichment of Low-Abundance Proteins by Affinity Chromatography for Identification in Complex Proteomes
inferred← citeshttps://doi.org/10.1007/978-1-0716-1472-3_3openalex-snapshot
Engineering Chloroplasts for High-Level Constitutive or Inducible Transgene Expression
inferred← citeshttps://doi.org/10.1007/978-1-0716-3726-5_18openalex-snapshot
Isolation of Cytosolic Ribosomes Associated with Plant Mitochondria and Chloroplasts
inferred← citeshttps://doi.org/10.1007/978-1-0716-5245-9_3openalex-snapshot
Albinism in Cereal Androgenesis—Shedding Light on Molecular Mechanisms and Possible Solutions
inferred← citeshttps://doi.org/10.1007/978-1-4939-2550-6_16openalex-snapshot
Chloroplast Isolation and Affinity Chromatography for Enrichment of Low-Abundant Proteins in Complex Proteomes
inferred← citeshttps://doi.org/10.1007/978-1-4939-7411-5_8openalex-snapshot
Preparation of Membrane Fractions (Envelope, Thylakoids, Grana, and Stroma Lamellae) from Arabidopsis Chloroplasts for Quantitative Proteomic Investigations and Other Studies
inferred← citeshttps://doi.org/10.1007/978-1-4939-8654-5_10openalex-snapshot
Purification of Nongreen Plastids (Proplastids and Amyloplasts) from Angiosperms, and Isolation of Their Envelope Membranes
inferred← citeshttps://doi.org/10.1007/978-1-4939-8654-5_17openalex-snapshot
Determination of the DNA/RNA-Associated Subproteome from Chloroplasts and Other Plastid Types
inferred← citeshttps://doi.org/10.1007/978-1-4939-8654-5_23openalex-snapshot
Genetic Analysis of Chloroplast Biogenesis, and Function and Mutant Collections
inferred← citeshttps://doi.org/10.1007/978-1-4939-8654-5_26openalex-snapshot
AT_CHLORO: The First Step When Looking for Information About Subplastidial Localization of Proteins
inferred← citeshttps://doi.org/10.1007/978-1-4939-8654-5_5openalex-snapshot
The Main Functions of Plastids
inferred← citeshttps://doi.org/10.1007/978-1-4939-9952-1_18openalex-snapshot
Visualization of Carotenoid-Storage Structures in Fruits by Transmission Electron Microscopy
inferred← citeshttps://doi.org/10.1007/978-3-031-57446-7_12openalex-snapshot
What Has Paulinella Taught us About Endosymbiont Metabolic Integration?
inferred← citeshttps://doi.org/10.1007/978-3-031-57446-7_13openalex-snapshot
Translocation of Proteins into Primary Plastids
inferred← citeshttps://doi.org/10.1007/978-3-031-65003-1_8openalex-snapshot
Molecular Breeding of Carotenoids in Sweetpotato
inferred← citeshttps://doi.org/10.1007/978-3-031-70098-9_3openalex-snapshot
The Roles of mTERF Proteins in Chloroplast Gene Expression
inferred← citeshttps://doi.org/10.1007/978-3-031-70098-9_4openalex-snapshot
Chloroplast Translation Machinery
inferred← citeshttps://doi.org/10.1007/978-3-031-70098-9_5openalex-snapshot
Chloroplast Stress Signals: Control of Retrograde Signaling, Chloroplast Turn-Over, and Cell Fate Decisions
inferred← citeshttps://doi.org/10.1007/978-3-031-70098-9_6openalex-snapshot
The Genetic Engineering Toolbox for Transformation of Higher Plant Plastids
inferred← citeshttps://doi.org/10.1007/978-3-319-43694-4_9openalex-snapshot
Brassica Mitochondrial and Chloroplast Genomes
inferred← citeshttps://doi.org/10.1007/978-3-319-69944-8_9openalex-snapshot
Evolving Views on Plastid Pleomorphy
inferred← citeshttps://doi.org/10.1007/978-981-95-0772-6_1openalex-snapshot
Plastids and Their Interconversions
inferred← citeshttps://doi.org/10.1007/978-981-95-0772-6_10openalex-snapshot
Amyloplasts: Starch-Synthesising Plastids
inferred← citeshttps://doi.org/10.1007/978-981-95-0772-6_11openalex-snapshot
Elaioplast Development: Insights into Lipid Storage Organelle Biogenesis
inferred← citeshttps://doi.org/10.1007/978-981-95-0772-6_2openalex-snapshot
Chloroplasts: Genetic Machinery and Regulatory Mechanisms in Plant Function and Adaptation
inferred← citeshttps://doi.org/10.1007/978-981-95-0772-6_9openalex-snapshot
Chromoplast Biogenesis: A Journey from Chloroplasts
inferred← citeshttps://doi.org/10.1007/978-981-99-4890-1_11openalex-snapshot
Exploring Plant-Pathogen Interactions through Subcellular Proteomics: Insights and Challenges
inferred← citeshttps://doi.org/10.1007/s00122-019-03437-7openalex-snapshot
Quantitative trait loci and differential gene expression analyses reveal the genetic basis for negatively associated β-carotene and starch content in hexaploid sweetpotato [Ipomoea batatas (L.) Lam.]
inferred← citeshttps://doi.org/10.1007/s00122-021-03905-zopenalex-snapshot
RETRACTED ARTICLE: BrRNE cleaves RNA in chloroplasts, regulating retrograde signals in Brassica rapa L. ssp. pekinensis
inferred← citeshttps://doi.org/10.1007/s00122-025-04994-wopenalex-snapshot
Chlorophyll deficient 5 encodes a DNA helicase and is essential for chloroplast development in rice
inferred← citeshttps://doi.org/10.1007/s00299-017-2136-xopenalex-snapshot
Lethal albinic seedling, encoding a threonyl-tRNA synthetase, is involved in development of plastid protein synthesis system in rice
inferred← citeshttps://doi.org/10.1007/s00299-018-2323-4openalex-snapshot
The plastid genome as a chassis for synthetic biology-enabled metabolic engineering: players in gene expression
inferred← citeshttps://doi.org/10.1007/s00299-019-02420-2openalex-snapshot
Differentiation of chromoplasts and other plastids in plants
inferred← citeshttps://doi.org/10.1007/s00299-023-03020-xopenalex-snapshot
Plastid engineering using episomal DNA
inferred← citeshttps://doi.org/10.1007/s00299-024-03350-4openalex-snapshot
Hydrogen peroxide participates in leaf senescence by inhibiting CHLI1 activity
inferred← citeshttps://doi.org/10.1007/s00299-025-03500-2openalex-snapshot
GET3B is involved in chloroplast biogenesis and interacts with the thylakoidal ALB3 and ALB4 insertases
inferred← citeshttps://doi.org/10.1007/s00299-026-03806-9openalex-snapshot
Selective degradation processes in plants are not limited to autophagy
inferred← citeshttps://doi.org/10.1007/s00344-018-9889-5openalex-snapshot
Functional Identification of Apple MdGLK1 Which Regulates Chlorophyll Biosynthesis in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00344-025-11911-4openalex-snapshot
An Improved Method for Isolating Intact Chloroplasts from Different Plant Species
inferred← citeshttps://doi.org/10.1007/s00425-014-2137-8openalex-snapshot
Rapid identification of angulata leaf mutations using next-generation sequencing
inferred← citeshttps://doi.org/10.1007/s00425-021-03773-3openalex-snapshot
Occurrence of albinism during wheat androgenesis is correlated with repression of the key genes required for proper chloroplast biogenesis
inferred← citeshttps://doi.org/10.1007/s00425-021-03812-zopenalex-snapshot
Comprehensive analysis of chloroplast genome of Albizia julibrissin Durazz. (Leguminosae sp.)
inferred← citeshttps://doi.org/10.1007/s00425-022-04016-9openalex-snapshot
Plastid diversity and chromoplast biogenesis in differently coloured carrots: role of the DcOR3Leu gene
inferred← citeshttps://doi.org/10.1007/s00425-025-04874-zopenalex-snapshot
Far-red light induces ultrastructural reorganization of chloroplasts in Marchantia polymorpha to compensate for reduced photosynthetic efficiency
inferred← citeshttps://doi.org/10.1007/s00425-026-05173-xopenalex-snapshot
Cold-sensitive chloroplast development: advances from chloroplast ribosome-deficient mutants
inferred← citeshttps://doi.org/10.1007/s00497-016-0274-xopenalex-snapshot
Importance of organellar proteins, protein translocation and vesicle transport routes for pollen development and function
inferred← citeshttps://doi.org/10.1007/s00497-016-0276-8openalex-snapshot
Unfolded protein response in pollen development and heat stress tolerance
inferred← citeshttps://doi.org/10.1007/s00709-017-1096-xopenalex-snapshot
Three rings for the evolution of plastid shape: a tale of land plant FtsZ
inferred← citeshttps://doi.org/10.1007/s00709-019-01406-xopenalex-snapshot
Different colored Chrysanthemum × morifolium cultivars represent distinct plastid transformation and carotenoid deposit patterns
inferred← citeshttps://doi.org/10.1007/s00709-022-01766-xopenalex-snapshot
Dynamics of endogenous levels and subcellular localization of ABA and cytokinins during pollen germination in spruce and tobacco
inferred← citeshttps://doi.org/10.1007/s10265-018-1050-9openalex-snapshot
The cellular machineries responsible for the division of endosymbiotic organelles
inferred← citeshttps://doi.org/10.1007/s10265-022-01371-2openalex-snapshot
Strigolactone is involved in nitric oxide-enhanced the salt resistance in tomato seedlings
inferred← citeshttps://doi.org/10.1007/s10646-017-1821-4openalex-snapshot
Evaluation of ecotoxicological impact of new pyrrole-derived aminophosphonates using selected bioassay battery
inferred← citeshttps://doi.org/10.1007/s10722-023-01818-yopenalex-snapshot
Regardless of having identical photosynthetic pathways, chloroplast genomes vary depending on whether the host plant is monocotyledonous or dicotyledonous
inferred← citeshttps://doi.org/10.1007/s10725-017-0336-6openalex-snapshot
OsSLA4 encodes a pentatricopeptide repeat protein essential for early chloroplast development and seedling growth in rice
inferred← citeshttps://doi.org/10.1007/s10725-020-00661-wopenalex-snapshot
Environmental impacts on carotenoid metabolism in leaves
inferred← citeshttps://doi.org/10.1007/s10725-023-01109-7openalex-snapshot
Significance of the plastidial stringent response for plant growth on soil
inferred← citeshttps://doi.org/10.1007/s10725-025-01283-wopenalex-snapshot
OsOZ1, a zinc finger motif-containing protein, is essential for chloroplast development through RNA editing and intron splicing in rice
inferred← citeshttps://doi.org/10.1007/s10930-019-09846-3openalex-snapshot
The TOC GTPase Receptors: Regulators of the Fidelity, Specificity and Substrate Profiles of the General Protein Import Machinery of Chloroplasts
inferred← citeshttps://doi.org/10.1007/s11032-024-01468-7openalex-snapshot
OsPGL3A encodes a DYW-type pentatricopeptide repeat protein involved in chloroplast RNA processing and regulated chloroplast development
inferred← citeshttps://doi.org/10.1007/s11032-025-01621-wopenalex-snapshot
P-type pentatricopeptide repeat protein OsYS6 is essential for chloroplast development in rice through its role in chloroplast RNA processing
inferred← citeshttps://doi.org/10.1007/s11033-020-05337-2openalex-snapshot
In silico characterization, and expression analysis of rice golden 2-like (OsGLK) members in response to low phosphorous
inferred← citeshttps://doi.org/10.1007/s11099-018-0785-9openalex-snapshot
Improved photosynthesis in Arabidopsis roots by activation of GATA transcription factors
inferred← citeshttps://doi.org/10.1007/s11103-019-00841-xopenalex-snapshot
Comparative sequence and methylation analysis of chloroplast and amyloplast genomes from rice
inferred← citeshttps://doi.org/10.1007/s11103-020-01022-xopenalex-snapshot
GSM2, a transaldolase, contributes to reactive oxygen species homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11105-018-1109-8openalex-snapshot
Chlorophyll deficient 3, Encoding a Putative Potassium Efflux Antiporter, Affects Chloroplast Development Under High Temperature Conditions in Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s11120-015-0154-5openalex-snapshot
Organization of chlorophyll biosynthesis and insertion of chlorophyll into the chlorophyll-binding proteins in chloroplasts
inferred← citeshttps://doi.org/10.1007/s11120-017-0477-5openalex-snapshot
UMP kinase activity is involved in proper chloroplast development in rice
inferred← citeshttps://doi.org/10.1007/s11248-014-9845-5openalex-snapshot
The HIV-1 Pr55gag polyprotein binds to plastidial membranes and leads to severe impairment of chloroplast biogenesis and seedling lethality in transplastomic tobacco plants
inferred← citeshttps://doi.org/10.1007/s11295-017-1104-5openalex-snapshot
Comparative iTRAQ proteomic profiling of susceptible and resistant apple cultivars infected by Alternaria alternata apple pathotype
inferred← citeshttps://doi.org/10.1007/s11738-023-03638-0openalex-snapshot
Transcriptome analysis of Iris japonica var. variegata for chlorophyll and photosynthesis-related pathways involved in white–green striped leaves
inferred← citeshttps://doi.org/10.1007/s12010-022-03930-8openalex-snapshot
Chloroplast Engineering: Fundamental Insights and Its Application in Amelioration of Environmental Stress
inferred← citeshttps://doi.org/10.1007/s12035-018-1342-zopenalex-snapshot
Amyloid β Peptide Compromises Neural Stem Cell Fate by Irreversibly Disturbing Mitochondrial Oxidative State and Blocking Mitochondrial Biogenesis and Dynamics
inferred← citeshttps://doi.org/10.1007/s12230-018-9648-yopenalex-snapshot
Potato Tuber Greening: a Review of Predisposing Factors, Management and Future Challenges
inferred← citeshttps://doi.org/10.1007/s12298-019-00651-xopenalex-snapshot
Structure and features of the complete chloroplast genome of Melastoma dodecandrum
inferred← citeshttps://doi.org/10.1007/s12374-017-0294-6openalex-snapshot
Domain of Unknown Function 143 is required for the functioning of PEP-associated protein DG238 in the chloroplast
inferred← citeshttps://doi.org/10.1007/s12374-018-0373-3openalex-snapshot
Structural Analysis of Tha4, a Twin-arginine Translocase Protein Localized in Plant Thylakoid Membranes
inferred← citeshttps://doi.org/10.1007/s12374-019-0213-0openalex-snapshot
Autophagy-mediated Nutrient Recycling and Regulation in Plants: A Molecular View
inferred← citeshttps://doi.org/10.1007/s13205-019-1893-3openalex-snapshot
Identification and analysis of RNA editing sites in chloroplast transcripts of kenaf (Hibiscus cannabinus L.)
inferred← citeshttps://doi.org/10.1007/s40626-018-0133-2openalex-snapshot
The proteOMIC era: a useful tool to gain deeper insights into plastid physiology
inferred← citeshttps://doi.org/10.1007/s40626-019-00140-2openalex-snapshot
Proteomics: A tool to decipher cold tolerance
inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00180-2openalex-snapshot
Plastids: The Versatile Anabolic Factories of Plant Cells
inferred← citeshttps://doi.org/10.1016/b978-0-323-34126-4.00019-0openalex-snapshot
Mitochondria, Chloroplasts, Peroxisomes
inferred← citeshttps://doi.org/10.1016/b978-0-443-36542-3.00014-1openalex-snapshot
Chemical synthesis as design and construction of molecular architectures: a brief history
inferred← citeshttps://doi.org/10.1016/b978-0-443-44376-3.00004-5openalex-snapshot
Nanomaterials for improving photosynthetic efficiency: current innovations
inferred← citeshttps://doi.org/10.1016/bs.abr.2017.11.011openalex-snapshot
Plastid Autonomy vs Nuclear Control Over Plastid Function
inferred← citeshttps://doi.org/10.1016/bs.abr.2019.05.002openalex-snapshot
The role of tetrapyrroles in chloroplast-to-nucleus retrograde signaling
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2016.02.007openalex-snapshot
New Insights Into Roles of Ubiquitin Modification in Regulating Plastids and Other Endosymbiotic Organelles
inferred← citeshttps://doi.org/10.1016/j.aoas.2019.10.002openalex-snapshot
Saffron extract stimulates growth, improves the antioxidant components of Solanum lycopersicum L., and has an antifungal effect
inferred← citeshttps://doi.org/10.1016/j.bamboo.2025.100169openalex-snapshot
Effects of spectral quality on the micropropagation of Dendrocalamus asper (Schult. & Schult.f.) Backer and genetic fidelity analysis by ISSR
inferred← citeshttps://doi.org/10.1016/j.bbabio.2014.11.012openalex-snapshot
Organization, function and substrates of the essential Clp protease system in plastids
inferred← citeshttps://doi.org/10.1016/j.bbabio.2015.02.003openalex-snapshot
Insights into chloroplast biogenesis and development
inferred← citeshttps://doi.org/10.1016/j.bbabio.2015.02.004openalex-snapshot
Chloroplast RNA polymerases: Role in chloroplast biogenesis
inferred← citeshttps://doi.org/10.1016/j.bbabio.2015.02.011openalex-snapshot
The TIC complex uncovered: The alternative view on the molecular mechanism of protein translocation across the inner envelope membrane of chloroplasts
inferred← citeshttps://doi.org/10.1016/j.bbabio.2015.02.014openalex-snapshot
Large-scale genetic analysis of chloroplast biogenesis in maize
inferred← citeshttps://doi.org/10.1016/j.bbabio.2015.02.017openalex-snapshot
Functions of plastid protein import and the ubiquitin–proteasome system in plastid development
inferred← citeshttps://doi.org/10.1016/j.bbabio.2015.05.008openalex-snapshot
Translational regulation in chloroplasts for development and homeostasis
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2023.108258openalex-snapshot
Subcellular compartmentalization in the biosynthesis and engineering of plant natural products
inferred← citeshttps://doi.org/10.1016/j.ceb.2015.03.004openalex-snapshot
Lipid trafficking at endoplasmic reticulum–chloroplast membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.ceca.2014.10.012openalex-snapshot
Targeting and biogenesis of transporters and channels in chloroplast envelope membranes: Unsolved questions
inferred← citeshttps://doi.org/10.1016/j.cej.2026.178786openalex-snapshot
Bio-inspired catalytic hydrogel with structural color-coding for synergistic therapy of diabetic foot ulcers
inferred← citeshttps://doi.org/10.1016/j.cell.2020.02.045openalex-snapshot
Liquid-Liquid Phase Transition Drives Intra-chloroplast Cargo Sorting
inferred← citeshttps://doi.org/10.1016/j.cell.2022.10.030openalex-snapshot
Structure of a TOC-TIC supercomplex spanning two chloroplast envelope membranes
inferred← citeshttps://doi.org/10.1016/j.cell.2024.01.026openalex-snapshot
Cryo-EM structures of the plant plastid-encoded RNA polymerase
inferred← citeshttps://doi.org/10.1016/j.cell.2024.06.039openalex-snapshot
MYB-related transcription factors control chloroplast biogenesis
inferred← citeshttps://doi.org/10.1016/j.cell.2024.08.002openalex-snapshot
Conservation and specialization of the Ycf2-FtsHi chloroplast protein import motor in green algae
inferred← citeshttps://doi.org/10.1016/j.cell.2024.08.003openalex-snapshot
Structural insights into the chloroplast protein import in land plants
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110664openalex-snapshot
The CDC48 complex mediates ubiquitin-dependent degradation of intra-chloroplast proteins in plants
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114696openalex-snapshot
Streamlined regulation of chloroplast development in the liverwort Marchantia polymorpha
inferred← citeshttps://doi.org/10.1016/j.chmed.2026.06.013openalex-snapshot
Herb-microbiome interaction breeding: A new pathway to ideal medicinal plant phenotypes
inferred← citeshttps://doi.org/10.1016/j.cj.2020.10.015openalex-snapshot
Bn.YCO affects chloroplast development in Brassica napus L.
inferred← citeshttps://doi.org/10.1016/j.cj.2023.04.009openalex-snapshot
OsTHA8 encodes a pentatricopeptide repeat protein required for RNA editing and splicing during rice chloroplast development
inferred← citeshttps://doi.org/10.1016/j.copbio.2017.07.004openalex-snapshot
Plastid transformation and its application in metabolic engineering
inferred← citeshttps://doi.org/10.1016/j.coviro.2015.11.002openalex-snapshot
The altered photosynthetic machinery during compatible virus infection
inferred← citeshttps://doi.org/10.1016/j.cpb.2021.100203openalex-snapshot
Vital roles of carotenoids in plants and humans to deteriorate stress with its structure, biosynthesis, metabolic engineering and functional aspects
inferred← citeshttps://doi.org/10.1016/j.cub.2015.08.015openalex-snapshot
Regulation of Chloroplast Protein Import by the Ubiquitin E3 Ligase SP1 Is Important for Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1016/j.cub.2015.11.022openalex-snapshot
Plant Signaling: Ubiquitin Pulls the Trigger on Chloroplast Degradation
inferred← citeshttps://doi.org/10.1016/j.cub.2018.06.006openalex-snapshot
Chloroplast Biogenesis Controlled by DELLA-TOC159 Interaction in Early Plant Development
inferred← citeshttps://doi.org/10.1016/j.cub.2023.01.060openalex-snapshot
Multiple ubiquitin E3 ligase genes antagonistically regulate chloroplast-associated protein degradation
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.10.005openalex-snapshot
The Arabidopsis mature endosperm promotes seedling cuticle formation via release of sulfated peptides
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.110331openalex-snapshot
Ecotoxicological effects of new C-substituted derivatives of N-phosphonomethylglycine (glyphosate) and their preliminary evaluation towards herbicidal application in agriculture
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105009openalex-snapshot
Chloroplast proteomics reveals transgenerational cross-stress priming in Pinus radiata
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105429openalex-snapshot
Sep2, a light-harvesting complex-like protein, is involved in light stress response by binding to free chlorophylls
inferred← citeshttps://doi.org/10.1016/j.envres.2024.118635openalex-snapshot
Carbon nanosol promotes plant growth and broad-spectrum resistance
inferred← citeshttps://doi.org/10.1016/j.hpj.2023.05.011openalex-snapshot
PtrDJ1C, an atypical member of the DJ-1 superfamily, is essential for early chloroplast development and lignin deposition in poplar
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.136354openalex-snapshot
The role of SlCHRC in carotenoid biosynthesis and plastid development in tomato fruit
inferred← citeshttps://doi.org/10.1016/j.indcrop.2021.113248openalex-snapshot
The complete chloroplast genome sequences of five Miscanthus species, and comparative analyses with other grass plastomes
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.116964openalex-snapshot
Integrated cytological, physiological, and transcriptome analysis of the bud mutant of jujube (Ziziphus jujuba Mill.) with non-lethal albino phenotype
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.120488openalex-snapshot
Silencing of PDC-E1β genes affects chloroplast development and amino acid metabolism in tobacco
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.121621openalex-snapshot
The molecular mechanisms underlying flowering-induced aberrant rhizome development in Phyllostachys nigra
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104974openalex-snapshot
Loss of key endosymbiont genes may facilitate early host control of the chromatophore in Paulinella
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106216openalex-snapshot
RETRACTED: UPL5 modulates WHY2 protein distribution in a Kub-site dependent ubiquitination in response to [Ca2+]cyt-induced leaf senescence
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.100338openalex-snapshot
Structure, function, and substrates of Clp AAA+ protease systems in cyanobacteria, plastids, and apicoplasts: A comparative analysis
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.101609openalex-snapshot
Proteomics, phylogenetics, and coexpression analyses indicate novel interactions in the plastid CLP chaperone-protease system
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.102489openalex-snapshot
Chloroplast envelope ATPase PGA1/AtFtsH12 is required for chloroplast protein accumulation and cytosol-chloroplast protein homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jcs.2021.103317openalex-snapshot
GUN4-mediated tetrapyrrole metabolites regulates starch biosynthesis during early seed development in rice
inferred← citeshttps://doi.org/10.1016/j.jgg.2022.04.006openalex-snapshot
Nuclear EPL-HAM complex is essential for the development of chloroplasts
inferred← citeshttps://doi.org/10.1016/j.jgg.2023.02.010openalex-snapshot
Regulation of chloroplast protein degradation
inferred← citeshttps://doi.org/10.1016/j.jgg.2025.11.006openalex-snapshot
Ribosomal protein bL31c interacts with translation elongation factor RAB8D to regulate chloroplast translation elongation and PSI-LHCI-LHCII assembly in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jgg.2026.09.014openalex-snapshot
OsToc159 is essential for amyloplast development and starch granule initiation in rice endosperm
inferred← citeshttps://doi.org/10.1016/j.jia.2023.06.020openalex-snapshot
A Golden2-like transcription factor, BnGLK1a, improves chloroplast development, photosynthesis, and seed weight in rapeseed
inferred← citeshttps://doi.org/10.1016/j.jia.2026.05.051openalex-snapshot
The mRNA-miRNA networks regulate juvenile leaves yellowing in Chinese cabbage jly mutant caused by BrRNE alternative splicing variants
inferred← citeshttps://doi.org/10.1016/j.jmb.2014.08.016openalex-snapshot
New Insights into the Mechanism of Chloroplast Protein Import and Its Integration with Protein Quality Control, Organelle Biogenesis and Development
inferred← citeshttps://doi.org/10.1016/j.jplph.2016.04.006openalex-snapshot
Photosynthetic acclimation, vernalization, crop productivity and ‘the grand design of photosynthesis’
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154819openalex-snapshot
Horse chestnut (Aesculus hippocastanum L.) bud scales harbor photosynthetically active chloroplasts during their entire lifespan
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154863openalex-snapshot
An integrated transcriptomic and proteomics analysis reveals the impact of drought stress on Pisum sativum
inferred← citeshttps://doi.org/10.1016/j.molcel.2024.02.003openalex-snapshot
Structure of the multi-subunit chloroplast RNA polymerase
inferred← citeshttps://doi.org/10.1016/j.molp.2014.11.006openalex-snapshot
Regulation of Carotenoid Metabolism in Tomato
inferred← citeshttps://doi.org/10.1016/j.molp.2015.12.004openalex-snapshot
Ion Channels in Plant Bioenergetic Organelles, Chloroplasts and Mitochondria: From Molecular Identification to Function
inferred← citeshttps://doi.org/10.1016/j.molp.2016.06.008openalex-snapshot
PTOX Mediates Novel Pathways of Electron Transport in Etioplasts of Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.molp.2016.08.005openalex-snapshot
Essentials of Proteolytic Machineries in Chloroplasts
inferred← citeshttps://doi.org/10.1016/j.molp.2016.10.011openalex-snapshot
Surveying the Oligomeric State of Arabidopsis thaliana Chloroplasts
inferred← citeshttps://doi.org/10.1016/j.molp.2017.02.009openalex-snapshot
SNOWY COTYLEDON 2 Promotes Chloroplast Development and Has a Role in Leaf Variegation in Both Lotus japonicus and Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.molp.2017.09.010openalex-snapshot
Carotenoid Metabolism in Plants: The Role of Plastids
inferred← citeshttps://doi.org/10.1016/j.molp.2018.11.002openalex-snapshot
Tension and Resolution: Dynamic, Evolving Populations of Organelle Genomes within Plant Cells
inferred← citeshttps://doi.org/10.1016/j.molp.2019.03.002openalex-snapshot
CHLORAD: Eradicating Translocon Components from the Outer Membrane of the Chloroplast
inferred← citeshttps://doi.org/10.1016/j.molp.2020.03.007openalex-snapshot
ORHis, a Natural Variant of OR, Specifically Interacts with Plastid Division Factor ARC3 to Regulate Chromoplast Number and Carotenoid Accumulation
inferred← citeshttps://doi.org/10.1016/j.molp.2024.08.004openalex-snapshot
Efficient control of root-knot nematodes by expressing Bt nematicidal proteins in root leucoplasts
inferred← citeshttps://doi.org/10.1016/j.molp.2025.08.013openalex-snapshot
The chloroplast translocon subunit TOC33 relays singlet oxygen-induced chloroplast-to-nucleus retrograde signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.ncrops.2024.100026openalex-snapshot
Exploring the frontier of plant phase separation: Current insights and future prospects
inferred← citeshttps://doi.org/10.1016/j.optlastec.2025.113413openalex-snapshot
Cascaded optical tweezers with high-order beams for three-dimensional manipulation of cellular arrays
inferred← citeshttps://doi.org/10.1016/j.plantsci.2017.02.007openalex-snapshot
The rice TCD11 encoding plastid ribosomal protein S6 is essential for chloroplast development at low temperature
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.04.020openalex-snapshot
Features of cues and processes during chloroplast-mediated retrograde signaling in the alga Chlamydomonas
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.09.020openalex-snapshot
FLOURY ENDOSPERM11 encoding a plastid heat shock protein 70 is essential for amyloplast development in rice
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110321openalex-snapshot
Plastid differentiation during microgametogenesis determines green plant regeneration in barley microspore culture
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110585openalex-snapshot
Characterization of a novel allele of bc12/gdd1 indicates a differential leaf color function for BC12/GDD1 in Indica and Japonica backgrounds
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111395openalex-snapshot
STRIPE3, encoding a human dNTPase SAMHD1 homolog, regulates chloroplast development in rice
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111925openalex-snapshot
Disruption of the rice ALS1 localized in chloroplast causes seedling-lethal albino phenotype
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112053openalex-snapshot
Functional conservation of GENOMES UNCOUPLED1 in plastid-to-nucleus retrograde signaling in tomato
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112134openalex-snapshot
A novel PLS-DYW type PPR protein OsASL is essential for chloroplast development in rice
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112208openalex-snapshot
The yellow-cotyledon gene (ATYCO) is a crucial factor for thylakoid formation and photosynthesis regulation in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112901openalex-snapshot
Chlorophyll deficient barley xan-n mutants are defective in an essential superoxide dismutase
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113328openalex-snapshot
The nuclear-encoded plastid ribosomal protein bL31c of Arabidopsis thaliana functions in chloroplast biogenesis and leaf development
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113493openalex-snapshot
Thylakoid membrane transporter SecE1 is required for chloroplast development and photosynthetic function in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2014.12.018openalex-snapshot
The TOC159 mutant of Arabidopsis thaliana accumulates altered levels of saturated and polyunsaturated fatty acids
inferred← citeshttps://doi.org/10.1016/j.plaphy.2015.09.006openalex-snapshot
The toc132toc120 heterozygote mutant of Arabidopsis thaliana accumulates reduced levels of hexadecatrienoic acid
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.11.034openalex-snapshot
Dehydration-induced alterations in chloroplast proteome and reprogramming of cellular metabolism in developing chickpea delineate interrelated adaptive responses
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.12.011openalex-snapshot
The TOC159 null mutant of Arabidopsis thaliana is impaired in the accumulation of plastid lipids and phosphatidylcholine
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108868openalex-snapshot
Temporal dynamics of chloroplast biogenesis revealed initiation of photosynthesis-related gene expression and protein complexes during alfalfa seed germination
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109327openalex-snapshot
Comparative transcriptome and metabolomic analysis reveal key genes and mechanisms responsible for the dark-green leaf color of a strawberry mutant
showing the first 200 of 767 · page through all 767
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.