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Gene silencing in the marine diatom Phaeodactylum tricornutum

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1460-2075.1987.tb02730.xopenalex-snapshot

GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.

inferredcites →https://doi.org/10.1007/1-59745-466-4_17openalex-snapshot

Genetic Transformation

inferredcites →https://doi.org/10.1007/978-1-4615-8714-9openalex-snapshot

Culture of Marine Invertebrate Animals

inferredcites →https://doi.org/10.1007/978-1-4615-8714-9_3openalex-snapshot

Culture of Phytoplankton for Feeding Marine Invertebrates

inferredcites →https://doi.org/10.1007/bf02172403openalex-snapshot

Stable nuclear transformation of the diatomPhaeodactylum tricornutum

inferredcites →https://doi.org/10.1007/pl00011773openalex-snapshot

Transformation of Nonselectable Reporter Genes in Marine Diatoms

inferredcites →https://doi.org/10.1007/s00294-005-0042-1openalex-snapshot

RNA silencing in Chlamydomonas: mechanisms and tools

inferredcites →https://doi.org/10.1007/s00294-006-0078-xopenalex-snapshot

On the origin and functions of RNA-mediated silencing: from protists to man

inferredcites →https://doi.org/10.1016/0378-1119(88)90126-6openalex-snapshot

Antisense genes in plants: an overview

inferredcites →https://doi.org/10.1016/0968-0004(93)90137-copenalex-snapshot

What makes an mRNA anti-sensi-itive?

inferredcites →https://doi.org/10.1016/j.cell.2009.01.035openalex-snapshot

Origins and Mechanisms of miRNAs and siRNAs

inferredcites →https://doi.org/10.1016/j.cell.2009.01.046openalex-snapshot

Origin, Biogenesis, and Activity of Plant MicroRNAs

inferredcites →https://doi.org/10.1016/j.cub.2008.05.037openalex-snapshot

A Diatom Gene Regulating Nitric-Oxide Signaling and Susceptibility to Diatom-Derived Aldehydes

inferredcites →https://doi.org/10.1016/j.febslet.2004.04.043openalex-snapshot

Effectiveness of RNA interference in transgenic plants

inferredcites →https://doi.org/10.1016/j.febslet.2005.08.014openalex-snapshot

RNA silencing platforms in plants

inferredcites →https://doi.org/10.1016/j.gene.2007.05.022openalex-snapshot

Molecular toolbox for studying diatom biology in Phaeodactylum tricornutum

inferredcites →https://doi.org/10.1016/j.molcel.2005.07.011openalex-snapshot

Crystal Structure of A. aeolicus Argonaute, a Site-Specific DNA-Guided Endoribonuclease, Provides Insights into RISC-Mediated mRNA Cleavage

inferredcites →https://doi.org/10.1016/j.pbi.2007.06.007openalex-snapshot

Targets of RNA-directed DNA methylation

inferredcites →https://doi.org/10.1016/j.tig.2006.03.003openalex-snapshot

The diversity of RNA silencing pathways in plants

inferredcites →https://doi.org/10.1016/j.tplants.2006.01.003openalex-snapshot

Nomenclature and functions of RNA-directed RNA polymerases

inferredcites →https://doi.org/10.1016/j.tplants.2008.04.007openalex-snapshot

Plant ARGONAUTES

inferredcites →https://doi.org/10.1016/j.tplants.2008.05.001openalex-snapshot

Inputs and outputs for chromatin-targeted RNAi

inferredcites →https://doi.org/10.1016/s0168-9525(01)02276-4openalex-snapshot

Broadcast interference – functional genomics

inferredcites →https://doi.org/10.1016/s0969-2126(01)00685-2openalex-snapshot

Crystallographic and Modeling Studies of RNase III Suggest a Mechanism for Double-Stranded RNA Cleavage

inferredcites →https://doi.org/10.1016/s1434-4610(99)70006-4openalex-snapshot

Diatoms and the Ocean Carbon Cycle

inferredcites →https://doi.org/10.1038/35030305openalex-snapshot

Total silencing by intron-spliced hairpin RNAs

inferredcites →https://doi.org/10.1038/35036500openalex-snapshot

Phytochromes and light signal perception by plants—an emerging synthesis

inferredcites →https://doi.org/10.1038/emboj.2008.260openalex-snapshot

A stepwise pathway for biogenesis of 24‐nt secondary siRNAs and spreading of DNA methylation

inferredcites →https://doi.org/10.1038/embor.2009.59openalex-snapshot

Diatom PtCPF1 is a new cryptochrome/photolyase family member with DNA repair and transcription regulation activity

inferredcites →https://doi.org/10.1038/nature02874openalex-snapshot

RNA silencing in plants

inferredcites →https://doi.org/10.1038/nature07410openalex-snapshot

The Phaeodactylum genome reveals the evolutionary history of diatom genomes

inferredcites →https://doi.org/10.1038/nprot.2007.250openalex-snapshot

Design and implementation of high-throughput RNAi screens in cultured Drosophila cells

inferredcites →https://doi.org/10.1038/nrg2179openalex-snapshot

Specialization and evolution of endogenous small RNA pathways

inferredcites →https://doi.org/10.1038/nrg982openalex-snapshot

Exploring plant genomes by RNA-induced gene silencing

inferredcites →https://doi.org/10.1038/nrm1129openalex-snapshot

Killing the messenger: short RNAs that silence gene expression

inferredcites →https://doi.org/10.1038/nrm2321openalex-snapshot

Argonaute proteins: key players in RNA silencing

inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01105.xopenalex-snapshot

Construct design for efficient, effective and high‐throughput gene silencing in plants

inferredcites →https://doi.org/10.1073/pnas.0707946105openalex-snapshot

Whole-genome expression profiling of the marine diatom Thalassiosira pseudonana identifies genes involved in silicon bioprocesses

inferredcites →https://doi.org/10.1073/pnas.95.23.13959openalex-snapshot

Virus resistance and gene silencing in plants can be induced by simultaneous expression of sense and antisense RNA

inferredcites →https://doi.org/10.1093/molbev/msm092openalex-snapshot

MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0

inferredcites →https://doi.org/10.1093/nar/gkn905openalex-snapshot

Update of the Diatom EST Database: a new tool for digital transcriptomics

inferredcites →https://doi.org/10.1093/nar/gng085openalex-snapshot

Stable and heritable gene silencing in the malaria vector Anopheles stephensi

inferredcites →https://doi.org/10.1101/gad.1265105openalex-snapshot

A Dicer-like protein in Tetrahymena has distinct functions in genome rearrangement, chromosome segregation, and meiotic prophase

inferredcites →https://doi.org/10.1104/pp.104.052829openalex-snapshot

Comparative Genomics of the Pennate Diatom Phaeodactylum tricornutum

inferredcites →https://doi.org/10.1105/tpc.010480openalex-snapshot

Spreading of RNA Targeting and DNA Methylation in RNA Silencing Requires Transcription of the Target Gene and a Putative RNA-Dependent RNA Polymerase

inferredcites →https://doi.org/10.1105/tpc.11.12.2291openalex-snapshot

RNA–DNA Interactions and DNA Methylation in Post-Transcriptional Gene Silencing

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02227.xopenalex-snapshot

Tandem inverted repeat system for selection of effective transgenic RNAi strains in Chlamydomonas

inferredcites →https://doi.org/10.1111/j.1529-8817.2006.00269.xopenalex-snapshot

MOLECULAR GENETIC MANIPULATION OF THE DIATOM THALASSIOSIRA PSEUDONANA (BACILLARIOPHYCEAE)1

inferredcites →https://doi.org/10.1111/j.1529-8817.2007.00342.xopenalex-snapshot

IDENTIFICATION AND COMPARATIVE GENOMIC ANALYSIS OF SIGNALING AND REGULATORY COMPONENTS IN THE DIATOM THALASSIOSIRA PSEUDONANA1

inferredcites →https://doi.org/10.1126/science.1079695openalex-snapshot

ARGONAUTE4 Control of Locus-Specific siRNA Accumulation and DNA and Histone Methylation

inferredcites →https://doi.org/10.1126/science.1101156openalex-snapshot

The Genome of the Diatom Thalassiosira Pseudonana : Ecology, Evolution, and Metabolism

inferredcites →https://doi.org/10.1126/science.1121638openalex-snapshot

Structural Basis for Double-Stranded RNA Processing by Dicer

inferredcites →https://doi.org/10.1126/science.281.5374.200openalex-snapshot

Biogeochemical Controls and Feedbacks on Ocean Primary Production

inferredcites →https://doi.org/10.1126/science.286.5441.950openalex-snapshot

A Species of Small Antisense RNA in Posttranscriptional Gene Silencing in Plants

inferredcites →https://doi.org/10.1261/rna.246906openalex-snapshot

An unusual Dicer-like1 protein fuels the RNA interference pathway in Trypanosoma brucei

inferredcites →https://doi.org/10.1261/rna.599107openalex-snapshot

Defining the optimal parameters for hairpin-based knockdown constructs

inferredcites →https://doi.org/10.1385/1-59259-775-0:003openalex-snapshot

RNA Interference

inferredcites →https://doi.org/10.1385/1-59745-151-7:127openalex-snapshot

Functional Genomic Approaches in C. elegans

inferredcites →https://doi.org/10.1385/1-59745-466-4:257openalex-snapshot

Genetic Transformation: A Tool to Study Protein Targeting in Diatoms

inferredcites →https://doi.org/10.1534/genetics.107.086546openalex-snapshot

Diversification of the Core RNA Interference Machinery in Chlamydomonas reinhardtii and the Role of DCL1 in Transposon Silencing

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.4774683openalex-extracted

Characterization of Red Light Inducible Promoter from Marine Diatom Phaeodactylum Tricornutum and its Application in Synthetic Biology

inferred← citeshttps://doi.org/10.1002/9780470979365.ch5openalex-snapshot

Studying Ecologically Important Traits: Ecogenomics, QTL Analysis, and Reverse Genetics

inferred← citeshttps://doi.org/10.1002/9780470979365.refsopenalex-snapshot

References

inferred← citeshttps://doi.org/10.1002/9781118567166.ch10openalex-snapshot

Molecular Genetic Manipulation of Microalgae: Principles and Applications

inferred← citeshttps://doi.org/10.1002/9781119370741.ch20openalex-snapshot

Diatom Silica for Biomedical Applications

inferred← citeshttps://doi.org/10.1002/9781119842156.ch7openalex-snapshot

Sensing Light Underwater

inferred← citeshttps://doi.org/10.1002/adhm.201800552openalex-snapshot

Diatom Silica for Biomedical Applications: Recent Progress and Advances

inferred← citeshttps://doi.org/10.1002/cm.20431openalex-snapshot

Myosin diversity in the diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1002/cphc.200900894openalex-snapshot

A Brief History of Phytochromes

inferred← citeshttps://doi.org/10.1002/ece3.72754openalex-snapshot

Transcriptomic Responses of the Marine Diatom Phaeodactylum tricornutum to High Carbon and Low Nitrogen Stress

inferred← citeshttps://doi.org/10.1002/ep.11849openalex-snapshot

Biocommodities from photosynthetic microorganisms

inferred← citeshttps://doi.org/10.1002/mbo3.1239openalex-snapshot

Characterization of endogenous promoters of GapC1 and GS for recombinant protein expression in Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1002/wnan.1284openalex-snapshot

Complex‐shaped microbial biominerals for nanotechnology

inferred← citeshttps://doi.org/10.1007/978-1-4419-7823-3_11openalex-snapshot

Turnover of Mature miRNAs and siRNAs in Plants and Algae

inferred← citeshttps://doi.org/10.1007/978-3-030-92499-7_21openalex-snapshot

Sensing and Signalling in Diatom Responses to Abiotic Cues

inferred← citeshttps://doi.org/10.1007/978-3-030-92499-7_25openalex-snapshot

Genetic Engineering in Marine Diatoms: Current Practices and Emerging Technologies

inferred← citeshttps://doi.org/10.1007/978-3-030-92499-7_5openalex-snapshot

Structure and Evolution of Diatom Nuclear Genes and Genomes

inferred← citeshttps://doi.org/10.1007/978-3-030-92499-7_7openalex-snapshot

Epigenetic Control of Diatom Genomes: An Overview from In Silico Characterization to Functional Studies

inferred← citeshttps://doi.org/10.1007/978-3-030-94074-4_1openalex-snapshot

Introduction: Values of Pollution-Free Atmosphere

inferred← citeshttps://doi.org/10.1007/978-3-319-16640-7_11openalex-snapshot

Genetic Engineering for Microalgae Strain Improvement in Relation to Biocrude Production Systems

inferred← citeshttps://doi.org/10.1007/978-3-319-16640-7_8openalex-snapshot

Prospective Applications of Synthetic Biology for Algal Bioproduct Optimization

inferred← citeshttps://doi.org/10.1007/978-3-319-24945-2_23openalex-snapshot

Algal Physiology and Large-Scale Outdoor Cultures of Microalgae

inferred← citeshttps://doi.org/10.1007/978-3-319-27216-0_16openalex-snapshot

Microalgae as Solar-Powered Protein Factories

inferred← citeshttps://doi.org/10.1007/978-3-319-57057-0_14openalex-snapshot

Polar Microalgae: Functional Genomics, Physiology, and the Environment

inferred← citeshttps://doi.org/10.1007/978-3-642-53971-8_5openalex-snapshot

Marine Microalgae

inferred← citeshttps://doi.org/10.1007/978-81-322-1683-4_12openalex-snapshot

Third Generation Green Energy: Cyanobacteria, Key to Production of Sustainable Energy Through Metabolic Engineering

inferred← citeshttps://doi.org/10.1007/978-94-007-5479-9_6openalex-snapshot

Genetic Engineering to Improve Algal Biofuels Production

inferred← citeshttps://doi.org/10.1007/978-94-017-8742-0_18openalex-snapshot

Carbon Fixation in Diatoms

inferred← citeshttps://doi.org/10.1007/s00253-018-8925-5openalex-snapshot

Transformation techniques for metabolic engineering of diatoms and haptophytes: current state and prospects

inferred← citeshttps://doi.org/10.1007/s00299-018-2270-0openalex-snapshot

Advanced genetic tools enable synthetic biology in the oleaginous microalgae Nannochloropsis sp.

inferred← citeshttps://doi.org/10.1007/s00299-018-2334-1openalex-snapshot

Genome editing in diatoms: achievements and goals

inferred← citeshttps://doi.org/10.1007/s00343-014-3173-8openalex-snapshot

Association of triacylglyceride content and transcript abundance of genes involving in lipid synthesis of nitrogen deficient Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1007/s00425-013-1962-5openalex-snapshot

Algal photoreceptors: in vivo functions and potential applications

inferred← citeshttps://doi.org/10.1007/s10126-014-9570-3openalex-snapshot

Construction of Novel Chloroplast Expression Vector and Development of an Efficient Transformation System for the Diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1007/s10126-014-9593-9openalex-snapshot

Reduction in Carotenoid Levels in the Marine Diatom Phaeodactylum tricornutum by Artificial MicroRNAs Targeted Against the Endogenous Phytoene Synthase Gene

inferred← citeshttps://doi.org/10.1007/s10126-015-9633-0openalex-snapshot

Establishment of Genetic Transformation in the Sexually Reproducing Diatoms Pseudo-nitzschia multistriata and Pseudo-nitzschia arenysensis and Inheritance of the Transgene

inferred← citeshttps://doi.org/10.1007/s10126-023-10273-wopenalex-snapshot

Nuclear Transformation of the Marine Pennate Diatom Nitzschia sp. Strain NIES-4635 by Multi-Pulse Electroporation

inferred← citeshttps://doi.org/10.1007/s10811-013-0047-yopenalex-snapshot

The first evidence for genotypic stability in a cryopreserved transgenic diatom

inferred← citeshttps://doi.org/10.1007/s10811-017-1335-8openalex-snapshot

Novel promoters for constitutive and inducible expression of transgenes in the diatom Phaeodactylum tricornutum under varied nitrate availability

inferred← citeshttps://doi.org/10.1007/s10811-022-02795-yopenalex-snapshot

Phosphate-inducible poly-hydroxy butyrate production dynamics in CO2 supplemented upscaled cultivation of engineered Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1007/s11120-014-0048-yopenalex-snapshot

A stable and efficient nuclear transformation system for the diatom Chaetoceros gracilis

inferred← citeshttps://doi.org/10.1007/s11802-014-2442-7openalex-snapshot

Predicting the reproduction strategies of several microalgae through their genome sequences

inferred← citeshttps://doi.org/10.1007/s11802-015-2442-2openalex-snapshot

Predicting the reproduction strategies of several microalgae through their genome sequences

inferred← citeshttps://doi.org/10.1007/s11816-016-0408-5openalex-snapshot

Characterization of PyGUS gene silencing in the red macroalga, Pyropia yezoensis

inferred← citeshttps://doi.org/10.1007/s12010-012-9602-2openalex-snapshot

A Potential Commercial Source of Fucoxanthin Extracted from the Microalga Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1007/s13765-016-0235-yopenalex-snapshot

Cloning of a novel endogenous promoter for foreign gene expression in Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1007/s40502-018-0423-3openalex-snapshot

Targeted genome editing in algae using CRISPR/Cas9

inferred← citeshttps://doi.org/10.1007/s42977-025-00301-2openalex-snapshot

The future of food: seaweed farming, biotechnology, and global sustainability

inferred← citeshttps://doi.org/10.1016/b978-0-12-800776-1.00024-8openalex-snapshot

Genetic Engineering of Marine Microalgae to Optimize Bioenergy Production

inferred← citeshttps://doi.org/10.1016/b978-0-12-820084-1.00008-9openalex-snapshot

Unraveling the diversity of algae and its biomacromolecules

inferred← citeshttps://doi.org/10.1016/b978-0-12-821601-9.00008-xopenalex-snapshot

Biofuel production from microalgae and process enhancement by metabolic engineering and ultrasound

inferred← citeshttps://doi.org/10.1016/b978-0-12-823764-9.00019-4openalex-snapshot

Genetic manipulation of microalgae for enhanced biotechnological applications

inferred← citeshttps://doi.org/10.1016/b978-0-323-95332-0.00011-9openalex-snapshot

Microalgae as biofuel: current perspectives and technological progress

inferred← citeshttps://doi.org/10.1016/b978-0-444-63475-7.00014-5openalex-snapshot

Photosynthetic Platform Strain Selection

inferred← citeshttps://doi.org/10.1016/bs.mcb.2016.04.003openalex-snapshot

The nonopisthokont septins

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Knockdown of phosphoenolpyruvate carboxykinase increases carbon flux to lipid synthesis in Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.algal.2016.07.002openalex-snapshot

Inducible expression of Haematococcus oil globule protein in the diatom Phaeodactylum tricornutum : Association with lipid droplets and enhancement of TAG accumulation under nitrogen starvation

inferred← citeshttps://doi.org/10.1016/j.algal.2016.10.018openalex-snapshot

Addressing various compartments of the diatom model organism Phaeodactylum tricornutum via sub-cellular marker proteins

inferred← citeshttps://doi.org/10.1016/j.algal.2017.02.005openalex-snapshot

A fast and reliable strategy to generate TALEN-mediated gene knockouts in the diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.algal.2017.07.028openalex-snapshot

A lipid droplet-associated protein involved in lipid droplet biogenesis and triacylglycerol accumulation in the oleaginous microalga Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.algal.2017.08.009openalex-snapshot

The inhibition of TOR in the model diatom Phaeodactylum tricornutum promotes a get-fat growth regime

inferred← citeshttps://doi.org/10.1016/j.algal.2018.06.023openalex-snapshot

Identification of the triacylglycerol lipase in the chloroplast envelope of the diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.algal.2018.08.012openalex-snapshot

Orchestration of transcriptome, proteome and metabolome in the diatom Phaeodactylum tricornutum during nitrogen limitation

inferred← citeshttps://doi.org/10.1016/j.algal.2019.101469openalex-snapshot

A strategy to complement PtAUREO1a in TALEN knockout strains of Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.algal.2019.101772openalex-snapshot

Microalgae: A potential sustainable commercial source of sterols

inferred← citeshttps://doi.org/10.1016/j.algal.2020.102159openalex-snapshot

Characterisation of novel regulatory sequences compatible with modular assembly in the diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.algal.2022.102728openalex-snapshot

A DUF4281 domain-containing protein (homologue of ABA4) of Phaeodactylum tricornutum regulates the biosynthesis of fucoxanthin

inferred← citeshttps://doi.org/10.1016/j.algal.2022.102827openalex-snapshot

Silencing 1,3-β-glucan synthase gene promotes total lipid production and changes fatty acids composition by affecting carbon flow distribution in Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.algal.2022.102960openalex-snapshot

NmrA acts as a positive regulator of nitrate assimilation in Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.algal.2023.102998openalex-snapshot

Instability of extrachromosomal DNA transformed into the diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.algal.2023.103131openalex-snapshot

Pyruvate orthophosphate dikinase is required for the acclimation to high bicarbonate concentrations in Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.algal.2023.103137openalex-snapshot

Heterotrophic modification of Phaeodactylum tricornutum Bohlin

inferred← citeshttps://doi.org/10.1016/j.algal.2023.103363openalex-snapshot

Microalgae as a source of bioavailable heme

inferred← citeshttps://doi.org/10.1016/j.bbabio.2012.08.005openalex-snapshot

Proteases are associated with a minor fucoxanthin chlorophyll a/c-binding protein from the diatom, Chaetoceros gracilis

inferred← citeshttps://doi.org/10.1016/j.bbalip.2015.12.023openalex-snapshot

Identification of a triacylglycerol lipase in the diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.biochi.2010.07.020openalex-snapshot

Unraveling algal lipid metabolism: Recent advances in gene identification

inferred← citeshttps://doi.org/10.1016/j.biortech.2021.124708openalex-snapshot

New paradigm in diatom omics and genetic manipulation

inferred← citeshttps://doi.org/10.1016/j.biotechadv.2012.05.004openalex-snapshot

Advances in genetic engineering of marine algae

inferred← citeshttps://doi.org/10.1016/j.biotechadv.2015.01.009openalex-snapshot

Improving microalgae for biotechnology — From genetics to synthetic biology

inferred← citeshttps://doi.org/10.1016/j.biotechadv.2019.107417openalex-snapshot

Diatom isoprenoids: Advances and biotechnological potential

inferred← citeshttps://doi.org/10.1016/j.biotechadv.2021.107885openalex-snapshot

Improving microalgae for biotechnology — From genetics to synthetic biology – Moving forward but not there yet

inferred← citeshttps://doi.org/10.1016/j.cbpa.2013.03.038openalex-snapshot

Advances in microalgae engineering and synthetic biology applications for biofuel production

inferred← citeshttps://doi.org/10.1016/j.chemosphere.2022.133513openalex-snapshot

Recent biotechnological developments in reshaping the microalgal genome: A signal for green recovery in biorefinery practices

inferred← citeshttps://doi.org/10.1016/j.cropro.2016.04.005openalex-snapshot

Short hairpin RNA engineering: In planta gene silencing of potato virus Y

inferred← citeshttps://doi.org/10.1016/j.cub.2014.12.004openalex-snapshot

A Novel Protein, Ubiquitous in Marine Phytoplankton, Concentrates Iron at the Cell Surface and Facilitates Uptake

inferred← citeshttps://doi.org/10.1016/j.enconman.2016.01.050openalex-snapshot

Progress toward isolation of strains and genetically engineered strains of microalgae for production of biofuel and other value added chemicals: A review

inferred← citeshttps://doi.org/10.1016/j.envexpbot.2014.07.007openalex-snapshot

Light signaling in photosynthetic eukaryotes with ‘green’ and ‘red’ chloroplasts

inferred← citeshttps://doi.org/10.1016/j.foodchem.2019.06.004openalex-snapshot

Phaeodactylum tricornutum microalgae as a rich source of omega-3 oil: Progress in lipid induction techniques towards industry adoption

inferred← citeshttps://doi.org/10.1016/j.fuel.2021.122738openalex-snapshot

Latest trends and developments in microalgae as potential source for biofuels: The case of diatoms

inferred← citeshttps://doi.org/10.1016/j.gene.2020.144929openalex-snapshot

Sexual reproduction potential implied by functional analysis of SPO11 in Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.hal.2018.11.014openalex-snapshot

Initial evidence of functional siRNA machinery in dinoflagellates

inferred← citeshttps://doi.org/10.1016/j.jbiotec.2014.08.021openalex-snapshot

Improving the sunlight-to-biomass conversion efficiency in microalgal biofactories

inferred← citeshttps://doi.org/10.1016/j.jclepro.2019.119509openalex-snapshot

Strategies for enhanced lipid production of Desmodesmus sp. mutated by atmospheric and room temperature plasma with a new efficient screening method

inferred← citeshttps://doi.org/10.1016/j.jplph.2017.06.010openalex-snapshot

An update on aureochromes: Phylogeny – mechanism – function

inferred← citeshttps://doi.org/10.1016/j.jplph.2017.07.005openalex-snapshot

Structural and evolutionary aspects of algal blue light receptors of the cryptochrome and aureochrome type

inferred← citeshttps://doi.org/10.1016/j.margen.2013.11.006openalex-snapshot

Histone extraction protocol from the two model diatoms Phaeodactylum tricornutum and Thalassiosira pseudonana

inferred← citeshttps://doi.org/10.1016/j.margen.2014.05.003openalex-snapshot

Re-print of "Histone extraction protocol from the two model diatoms Phaeodactylum tricornutum and Thalassiosira pseudonana"

inferred← citeshttps://doi.org/10.1016/j.margen.2014.07.002openalex-snapshot

The molecular life of diatoms

inferred← citeshttps://doi.org/10.1016/j.margen.2015.05.018openalex-snapshot

The diatom molecular toolkit to handle nitrogen uptake

inferred← citeshttps://doi.org/10.1016/j.margen.2015.06.010openalex-snapshot

The upstream regulatory sequence of the light harvesting complex Lhcf2 gene of the marine diatom Phaeodactylum tricornutum enhances transcription in an orientation- and distance-independent fashion

inferred← citeshttps://doi.org/10.1016/j.margen.2017.07.001openalex-snapshot

Diatom Frustule Morphogenesis and Function: a Multidisciplinary Survey

inferred← citeshttps://doi.org/10.1016/j.mib.2010.08.001openalex-snapshot

The voyage of the microbial eukaryote

inferred← citeshttps://doi.org/10.1016/j.nbt.2015.06.003openalex-snapshot

Silencing UDP-glucose pyrophosphorylase gene in Phaeodactylum tricornutum affects carbon allocation

inferred← citeshttps://doi.org/10.1016/j.pbi.2010.09.014openalex-snapshot

Diatom cell division in an environmental context

inferred← citeshttps://doi.org/10.1016/j.pbi.2016.03.013openalex-snapshot

The physiology and genetics of CO2 concentrating mechanisms in model diatoms

inferred← citeshttps://doi.org/10.1016/j.pbi.2017.02.001openalex-snapshot

Recent progress in diatom genomics and epigenomics

inferred← citeshttps://doi.org/10.1016/j.plipres.2018.03.001openalex-snapshot

Current trends to comprehend lipid metabolism in diatoms

inferred← citeshttps://doi.org/10.1016/j.plipres.2019.01.003openalex-snapshot

The lipid biochemistry of eukaryotic algae

inferred← citeshttps://doi.org/10.1016/j.protis.2011.02.002openalex-snapshot

Physiological and Molecular Evidence that Environmental Changes Elicit Morphological Interconversion in the Model Diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.protis.2015.01.003openalex-snapshot

In vivo Localization Studies in the Stramenopile Alga Nannochloropsis oceanica

inferred← citeshttps://doi.org/10.1016/j.protis.2015.07.005openalex-snapshot

Ultrastructure and Membrane Traffic During Cell Division in the Marine Pennate Diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.protis.2016.04.001openalex-snapshot

Ultrastructure of the Periplastidial Compartment of the Diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.semcdb.2015.06.007openalex-snapshot

Diatom silica biomineralization: Parallel development of approaches and understanding

inferred← citeshttps://doi.org/10.1016/j.tibtech.2014.01.004openalex-snapshot

Diatoms: a fossil fuel of the future

inferred← citeshttps://doi.org/10.1016/j.tplants.2012.02.005openalex-snapshot

Leveraging metabolomics for functional investigations in sequenced marine diatoms

inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101519openalex-snapshot

The marine diatom Phaeodactylum tricornutum as a versatile bioproduction chassis: Current progress, challenges, and perspectives

inferred← citeshttps://doi.org/10.1016/j.ymben.2010.10.003openalex-snapshot

Genetic engineering of fatty acid chain length in Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1016/j.ymben.2019.03.004openalex-snapshot

Knockdown of carbonate anhydrase elevates Nannochloropsis productivity at high CO2 level

inferred← citeshttps://doi.org/10.1021/acssynbio.1c00367openalex-snapshot

Episome-Based Gene Expression Modulation Platform in the Model Diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1021/acssynbio.3c00163openalex-snapshot

Validating a Promoter Library for Application in Plasmid-Based Diatom Genetic Engineering

inferred← citeshttps://doi.org/10.1021/acssynbio.8b00234openalex-snapshot

Knock-Down of a ligIV Homologue Enables DNA Integration via Homologous Recombination in the Marine Diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1021/bi3013565openalex-snapshot

Red/Green Cyanobacteriochromes: Sensors of Color and Power

inferred← citeshttps://doi.org/10.1021/bi501548topenalex-snapshot

Characterization of Red/Green Cyanobacteriochrome NpR6012g4 by Solution Nuclear Magnetic Resonance Spectroscopy: A Protonated Bilin Ring System in Both Photostates

inferred← citeshttps://doi.org/10.1021/jp302637uopenalex-snapshot

Chemical Inhomogeneity in the Ultrafast Dynamics of the DXCF Cyanobacteriochrome Tlr0924

inferred← citeshttps://doi.org/10.1021/jz500378nopenalex-snapshot

Optically Guided Photoactivity: Coordinating Tautomerization, Photoisomerization, Inhomogeneity, and Reactive Intermediates within the RcaE Cyanobacteriochrome

inferred← citeshttps://doi.org/10.1021/pr401290uopenalex-snapshot

Phosphoproteomic Analysis Provides Novel Insights into Stress Responses in Phaeodactylum tricornutum, a Model Diatom

inferred← citeshttps://doi.org/10.1038/ismej.2017.100openalex-snapshot

A role for the cell-wall protein silacidin in cell size of the diatom Thalassiosira pseudonana

inferred← citeshttps://doi.org/10.1038/nature10074openalex-snapshot

Evolution and metabolic significance of the urea cycle in photosynthetic diatoms

inferred← citeshttps://doi.org/10.1038/nature14599openalex-snapshot

Energetic coupling between plastids and mitochondria drives CO2 assimilation in diatoms

inferred← citeshttps://doi.org/10.1038/ncomms3091openalex-snapshot

Insights into the role of DNA methylation in diatoms by genome-wide profiling in Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1038/ncomms4831openalex-snapshot

Genome engineering empowers the diatom Phaeodactylum tricornutum for biotechnology

inferred← citeshttps://doi.org/10.1038/s41396-019-0528-3openalex-snapshot

A genomics approach reveals the global genetic polymorphism, structure, and functional diversity of ten accessions of the marine model diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1038/s41564-018-0305-5openalex-snapshot

A widespread alternative squalene epoxidase participates in eukaryote steroid biosynthesis

inferred← citeshttps://doi.org/10.1038/s41586-024-08301-3openalex-snapshot

Diatom phytochromes integrate the underwater light spectrum to sense depth

inferred← citeshttps://doi.org/10.1038/s41598-019-44710-5openalex-snapshot

A novel endogenous selection marker for the diatom Phaeodactylum tricornutum based on a unique mutation in phytoene desaturase 1

inferred← citeshttps://doi.org/10.1038/s41598-019-45786-9openalex-snapshot

Identification and characterisation of the novel endogenous promoter HASP1 and its signal peptide from Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1038/s41598-020-71002-0openalex-snapshot

Global identification of a marine diatom long noncoding natural antisense transcripts (NATs) and their response to phosphate fluctuations

inferred← citeshttps://doi.org/10.1038/s41598-021-00565-3openalex-snapshot

The genome of the diatom Chaetoceros tenuissimus carries an ancient integrated fragment of an extant virus

inferred← citeshttps://doi.org/10.1038/s41598-021-95106-3openalex-snapshot

Diploid genomic architecture of Nitzschia inconspicua, an elite biomass production diatom

inferred← citeshttps://doi.org/10.1038/srep27810openalex-snapshot

CRISPR/Cas9-induced knockout and knock-in mutations in Chlamydomonas reinhardtii

inferred← citeshttps://doi.org/10.1039/9781839169717-00190openalex-snapshot

Biogenic Silica for Drug Delivery and Gene Therapy

inferred← citeshttps://doi.org/10.1039/c0ee00593bopenalex-snapshot

Metabolic engineering of algae for fourth generation biofuels production

inferred← citeshttps://doi.org/10.1039/c9pp00295bopenalex-snapshot

Conservation and diversity in the secondary forward photodynamics of red/green cyanobacteriochromes†

inferred← citeshttps://doi.org/10.1042/bst20160061openalex-snapshot

Towards developing algal synthetic biology

inferred← citeshttps://doi.org/10.1051/ocl/2013031openalex-snapshot

Third-generation biofuels: current and future research on microalgal lipid biotechnology

inferred← citeshttps://doi.org/10.1073/pnas.1007703107openalex-snapshot

An atypical member of the light-harvesting complex stress-related protein family modulates diatom responses to light

inferred← citeshttps://doi.org/10.1073/pnas.1309299110openalex-snapshot

Metabolic engineering of lipid catabolism increases microalgal lipid accumulation without compromising growth

inferred← citeshttps://doi.org/10.1073/pnas.1419818112openalex-snapshot

Remodeling of intermediate metabolism in the diatom Phaeodactylum tricornutum under nitrogen stress

inferred← citeshttps://doi.org/10.1079/9781800621954.0001openalex-snapshot

Engineering Microalgae: Transition from Empirical Design to Programmable Cells

inferred← citeshttps://doi.org/10.1080/07388551.2021.1917507openalex-snapshot

Engineering microalgae: transition from empirical design to programmable cells

inferred← citeshttps://doi.org/10.1080/07388551.2023.2208284openalex-snapshot

Molecular approaches to enhance astaxanthin biosynthesis; future outlook: engineering of transcription factors in Haematococcus pluvialis

inferred← citeshttps://doi.org/10.1080/08927014.2017.1319473openalex-snapshot

Surface sensing and stress-signalling inUlvaand fouling diatoms – potential targets for antifouling: a review

inferred← citeshttps://doi.org/10.1080/09670262.2017.1358827openalex-snapshot

Random mutagenesis and precise gene editing technologies: applications in algal crop improvement and functional genomics

inferred← citeshttps://doi.org/10.1080/10408398.2019.1680525openalex-snapshot

Transgenic microalgae as bioreactors

inferred← citeshttps://doi.org/10.1080/14756366.2018.1559840openalex-snapshot

Phaeodactylum tricornutum as a model organism for testing the membrane penetrability of sulphonamide carbonic anhydrase inhibitors

inferred← citeshttps://doi.org/10.1089/ind.2013.0039openalex-snapshot

Advances in the Production of High-Value Products by Microalgae

inferred← citeshttps://doi.org/10.1093/bioinformatics/btq329openalex-snapshot

MIReNA: finding microRNAs with high accuracy and no learning at genome scale and from deep sequencing data

inferred← citeshttps://doi.org/10.1093/jxb/erab026openalex-snapshot

Hydrolysis of organophosphorus by diatom purple acid phosphatase and sequential regulation of cell metabolism

inferred← citeshttps://doi.org/10.1093/jxb/err117openalex-snapshot

Algal models in plant biology

inferred← citeshttps://doi.org/10.1093/jxb/ers005openalex-snapshot

Exploring the molecular basis of responses to light in marine diatoms

inferred← citeshttps://doi.org/10.1093/jxb/erw198openalex-snapshot

Multisignal control of expression of the LHCX protein family in the marine diatomPhaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1093/plcell/koae275openalex-snapshot

Monogalactosyldiacylglycerol synthase isoforms play diverse roles inside and outside the diatom plastid

inferred← citeshttps://doi.org/10.1093/synbio/ysaa001openalex-snapshot

Universal loop assembly: open, efficient and cross-kingdom DNA fabrication

inferred← citeshttps://doi.org/10.1098/rstb.2016.0402openalex-snapshot

Intracellular metabolic pathway distribution in diatoms and tools for genome-enabled experimental diatom research

inferred← citeshttps://doi.org/10.1098/rstb.2016.0407openalex-snapshot

Modulation of lipid biosynthesis by stress in diatoms

inferred← citeshttps://doi.org/10.1098/rstb.2016.0409openalex-snapshot

3-Hydroxyisobutyryl-CoA hydrolase involved in isoleucine catabolism regulates triacylglycerol accumulation in Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1098/rstb.2016.0411openalex-snapshot

Genetic and metabolic engineering in diatoms

inferred← citeshttps://doi.org/10.1098/rstb.2019.0196openalex-snapshot

Identification of proteins in the adhesive trails of the diatom Amphora coffeaeformis

inferred← citeshttps://doi.org/10.1101/176008openalex-snapshot

Continuous gene flow contributes to low global species abundance and distribution of a marine model diatom

inferred← citeshttps://doi.org/10.1101/2020.10.01.322594openalex-snapshot

The Phaeodactylum tricornutum Diaminopimelate Decarboxylase was Acquired via Horizontal Gene Transfer from Bacteria and Displays Substrate Promiscuity

inferred← citeshttps://doi.org/10.1101/2023.01.25.525482openalex-snapshot

Diatom phytochromes integrate the entire visible light spectra for photosensing in marine environments

inferred← citeshttps://doi.org/10.1101/744854openalex-snapshot

Universal Loop assembly (uLoop): open, efficient, and species-agnostic DNA fabrication

inferred← citeshttps://doi.org/10.1103/physreve.94.022418openalex-snapshot

Regulation of chain length in two diatoms as a growth-fragmentation process

inferred← citeshttps://doi.org/10.1104/pp.110.169631openalex-snapshot

Identification of the UMP Synthase Gene by Establishment of Uracil Auxotrophic Mutants and the Phenotypic Complementation System in the Marine DiatomPhaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1104/pp.17.01042openalex-snapshot

Nitric Oxide Mediates Nitrite-Sensing and Acclimation and Triggers a Remodeling of Lipids

inferred← citeshttps://doi.org/10.1104/pp.17.01804openalex-snapshot

Screening for Biologically Annotated Drugs That Trigger Triacylglycerol Accumulation in the Diatom Phaeodactylum

inferred← citeshttps://doi.org/10.1105/tpc.112.106377openalex-snapshot

AUREOCHROME1a-Mediated Induction of the Diatom-Specific Cyclin dsCYC2 Controls the Onset of Cell Division in Diatoms (Phaeodactylum tricornutum)

inferred← citeshttps://doi.org/10.1105/tpc.113.109256openalex-snapshot

Small Interfering RNA–Mediated Translation Repression Alters Ribosome Sensitivity to Inhibition by Cycloheximide inChlamydomonas reinhardtii

inferred← citeshttps://doi.org/10.1105/tpc.114.124982openalex-snapshot

Methylcrotonyl-CoA Carboxylase Regulates Triacylglycerol Accumulation in the Model Diatom Phaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1105/tpc.15.00928openalex-snapshot

Diatom Phytochromes Reveal the Existence of Far-Red-Light-Based Sensing in the Ocean

inferred← citeshttps://doi.org/10.1105/tpc.17.00651openalex-snapshot

An Emerging Model Diatom to Study Nitrogen Metabolism

inferred← citeshttps://doi.org/10.1105/tpc.19.00158openalex-snapshot

Diatom Molecular Research Comes of Age: Model Species for Studying Phytoplankton Biology and Diversity

inferred← citeshttps://doi.org/10.1111/1462-2920.13830openalex-snapshot

Toward establishing model organisms for marine protists: Successful transfection protocols for Parabodo caudatus (Kinetoplastida: Excavata)

inferred← citeshttps://doi.org/10.1111/1462-2920.14428openalex-snapshot

Functional CTR‐type Cu(I) transporters in an oceanic diatom

inferred← citeshttps://doi.org/10.1111/1462-2920.16135openalex-snapshot

Responses of dinoflagellate cells to ultraviolet‐C irradiation

inferred← citeshttps://doi.org/10.1111/febs.12781openalex-snapshot

A knot in the protein structure – probing the near‐infrared fluorescent protein i RFP designed from a bacterial phytochrome

inferred← citeshttps://doi.org/10.1111/j.1365-313x.2011.04540.xopenalex-snapshot

Decoding algal genomes: tracing back the history of photosynthetic life on Earth

inferred← citeshttps://doi.org/10.1111/j.1469-8137.2012.04375.xopenalex-snapshot

The role of C 4 metabolism in the marine diatom P haeodactylum tricornutum

inferred← citeshttps://doi.org/10.1111/j.1574-6976.2011.00304.xopenalex-snapshot

Microalgae in the postgenomic era: a blooming reservoir for new natural products

inferred← citeshttps://doi.org/10.1111/jam.13020openalex-snapshot

Metabolic flux ratio analysis and cell staining suggest the existence of C4photosynthesis inPhaeodactylum tricornutum

inferred← citeshttps://doi.org/10.1111/jeu.12298openalex-snapshot

Diatom Vacuolar 1,6‐β‐Transglycosylases can Functionally Complement the Respective Yeast Mutants

inferred← citeshttps://doi.org/10.1111/jpy.12096openalex-snapshot

Gene silencing in F ucusembryos: developmental consequences of RNA i‐mediated cytoskeletal disruption

inferred← citeshttps://doi.org/10.1111/jpy.13073openalex-snapshot

Co‐suppression in Pyropia yezoensis (Rhodophyta) Reveals the Role of PyLHCI in Light Harvesting and Generation Switch

inferred← citeshttps://doi.org/10.1111/jpy.13325openalex-snapshot

The diatom Fragilariopsis cylindrus: A model alga to understand cold‐adapted life

inferred← citeshttps://doi.org/10.1111/jpy.13400openalex-snapshot

Phaeodactylum tricornutum : An established model species for diatom molecular research and an emerging chassis for algal synthetic biology

inferred← citeshttps://doi.org/10.1111/mec.12000openalex-snapshot

Ecological and evolutionary genomics of marine photosynthetic organisms

inferred← citeshttps://doi.org/10.1111/nph.12917openalex-snapshot

Tracking the sterol biosynthesis pathway of the diatom P haeodactylum tricornutum

inferred← citeshttps://doi.org/10.1111/nph.13787openalex-snapshot

Noncoding and coding transcriptome responses of a marine diatom to phosphate fluctuations

inferred← citeshttps://doi.org/10.1111/nph.13946openalex-snapshot

Phytophthora infestansArgonaute 1 binds micro RNA and small RNA s from effector genes and transposable elements

inferred← citeshttps://doi.org/10.1111/nph.17739openalex-snapshot

Silencing of a Pseudo‐nitzschia arenysensis lipoxygenase transcript leads to reduced oxylipin production and impaired growth

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