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Gene silencing in Neurospora crassa requires a protein homologous to RNA-dependent RNA polymerase
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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.1460-2075.1996.tb00678.xopenalex-snapshot
Transgene silencing of the al‐1 gene in vegetative cells of Neurospora is mediated by a cytoplasmic effector and does not depend on DNA‐DNA interactions or DNA methylation.
inferredcites →https://doi.org/10.1006/anbo.1996.0295openalex-snapshot
Review Article: The Silence of Genes in Transgenic Plants
inferredcites →https://doi.org/10.1007/bf00028978openalex-snapshot
Epigenetic repeat-induced gene silencing (RIGS) inArabidopsis
inferredcites →https://doi.org/10.1007/bf00039378openalex-snapshot
RNA as a target and an initiator of post-transcriptional gene silencing in trangenic plants
inferredcites →https://doi.org/10.1016/0076-6879(71)17168-6openalex-snapshot
[4] Genetic and microbiological research techniques for Neurospora crassa
inferredcites →https://doi.org/10.1016/0076-6879(93)14085-wopenalex-snapshot
[38] Photoregulated carotenoid biosynthetic genes of Neurospora crassa
inferredcites →https://doi.org/10.1016/0307-4412(83)90068-7openalex-snapshot
Molecular Cloning. A Laboratory Manual
inferredcites →https://doi.org/10.1016/s0092-8674(00)80496-1openalex-snapshot
Cosuppression Comes to the Animals
inferredcites →https://doi.org/10.1016/s0092-8674(00)81614-1openalex-snapshot
A Counterdefensive Strategy of Plant Viruses
inferredcites →https://doi.org/10.1016/s0092-8674(00)81749-3openalex-snapshot
Systemic Spread of Sequence-Specific Transgene RNA Degradation in Plants Is Initiated by Localized Introduction of Ectopic Promoterless DNA
inferredcites →https://doi.org/10.1016/s0092-8674(00)81930-3openalex-snapshot
RNA-Mediated RNA Degradation and Chalcone Synthase A Silencing in Petunia
inferredcites →https://doi.org/10.1016/s0168-9525(98)01510-8openalex-snapshot
Double-stranded RNA as a mediator in sequence-specific genetic silencing and co-suppression
inferredcites →https://doi.org/10.1016/s0955-0674(97)80010-5openalex-snapshot
Post-transcriptional gene silencing in plants
inferredcites →https://doi.org/10.1016/s1360-1385(96)80313-xopenalex-snapshot
Paramutation and transgene silencing: a common response to invasive DNA?
inferredcites →https://doi.org/10.1016/s1360-1385(97)90028-5openalex-snapshot
Conservation of transgene-induced post-transcriptional gene silencing in plants and fungi
inferredcites →https://doi.org/10.1023/a:1005946720438openalex-snapshot
A model for RNA-mediated gene silencing in higher plants
inferredcites →https://doi.org/10.1038/27579openalex-snapshot
Specific interference by ingested dsRNA
inferredcites →https://doi.org/10.1038/35888openalex-snapshot
Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans
inferredcites →https://doi.org/10.1073/pnas.83.13.4869openalex-snapshot
Efficient cloning of genes of Neurospora crassa
inferredcites →https://doi.org/10.1073/pnas.91.9.3490openalex-snapshot
Inactivation of gene expression in plants as a consequence of specific sequence duplication.
inferredcites →https://doi.org/10.1073/pnas.94.19.10233openalex-snapshot
Isolation of quelling-defective ( qde ) mutants impaired in posttranscriptional transgene-induced gene silencing in Neurospora crassa
inferredcites →https://doi.org/10.1093/emboj/16.15.4738openalex-snapshot
Systemic acquired silencing: transgene‐specific post‐transcriptional silencing is transmitted by grafting from silenced stocks to non‐silenced scions
inferredcites →https://doi.org/10.1105/tpc.10.12.2087openalex-snapshot
Isolation of an RNA-Directed RNA Polymerase–Specific cDNA Clone from Tomato
inferredcites →https://doi.org/10.1105/tpc.5.12.1749openalex-snapshot
Induction of a Highly Specific Antiviral State in Transgenic Plants: Implications for Regulation of Gene Expression and Virus Resistance.
inferredcites →https://doi.org/10.1111/j.1365-2958.1992.tb02202.xopenalex-snapshot
Quelling: transient inactivation of gene expression in Neurospora crassa by transformation with homologous sequences
inferredcites →https://doi.org/10.1126/science.276.5318.1558openalex-snapshot
A Similarity Between Viral Defense and Gene Silencing in Plants
inferredcites →https://doi.org/10.1128/mcb.10.10.5064openalex-snapshot
Cloning, Sequence, and Photoregulation of al-1, a Carotenoid Biosynthetic Gene of Neurospora crassa
inferredcites →https://doi.org/10.4148/1941-4765.1449openalex-snapshot
CBM1, a Neurospora crassa genomic cosmid library in pAC3 and its use for walking on the right arm of linkage group VII
inferredcites →https://doi.org/10.4148/1941-4765.1519openalex-snapshot
Use of a bacterial hygromycin B resistance gene as a dominant selectable marker in Neurospora crassa transformation
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Gene silencing with RNA interference in the human pathogenic fungus
inferred← citeshttps://doi.org/10.1016/j.fgb.2004.08.002openalex-snapshot
Efficient gene silencing by expression of double stranded RNA in Neurospora crassa
inferred← citeshttps://doi.org/10.1016/j.fgb.2005.01.002openalex-snapshot
RNA silencing as a tool for exploring gene function in ascomycete fungi
inferred← citeshttps://doi.org/10.1016/j.fgb.2009.06.012openalex-snapshot
dsRNA-induced gene silencing in Moniliophthora perniciosa, the causal agent of witches’ broom disease of cacao
inferred← citeshttps://doi.org/10.1016/j.fgb.2010.10.005openalex-snapshot
Characterizing the role of RNA silencing components in Cryptococcus neoformans
inferred← citeshttps://doi.org/10.1016/j.fgb.2012.01.011openalex-snapshot
Vector-initiated transitive RNA interference in the filamentous fungus Aspergillus oryzae
inferred← citeshttps://doi.org/10.1016/j.fgb.2015.11.006openalex-snapshot
RNAi pathways in Mucor: A tale of proteins, small RNAs and functional diversity
inferred← citeshttps://doi.org/10.1016/j.fgb.2020.103488openalex-snapshot
Biochemical characterization of the dicing activity of Dicer-like 2 in the model filamentous fungus Neurospora crassa
inferred← citeshttps://doi.org/10.1016/j.gene.2009.07.004openalex-snapshot
Evolution of the RNA-dependent RNA polymerase (RdRP) genes: Duplications and possible losses before and after the divergence of major eukaryotic groups
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.05.017openalex-snapshot
The Extended “Two-Barrel” Polymerases Superfamily: Structure, Function and Evolution
inferred← citeshttps://doi.org/10.1016/j.jtbi.2006.10.026openalex-snapshot
Coupling of transcription termination to RNAi
inferred← citeshttps://doi.org/10.1016/j.mib.2007.03.016openalex-snapshot
Quelling: post-transcriptional gene silencing guided by small RNAs in Neurospora crassa
inferred← citeshttps://doi.org/10.1016/j.micres.2018.10.005openalex-snapshot
The histidine kinase slnCl1 of Colletotrichum lindemuthianum as a pathogenicity factor against Phaseolus vulgaris L
inferred← citeshttps://doi.org/10.1016/j.molbiopara.2009.01.007openalex-snapshot
Gene silencing of nfa1 affects the in vitro cytotoxicity of Naegleria fowleri in murine macrophages
inferred← citeshttps://doi.org/10.1016/j.molcel.2010.01.012openalex-snapshot
Distinct Phases of siRNA Synthesis in an Endogenous RNAi Pathway in C. elegans Soma
inferred← citeshttps://doi.org/10.1016/j.molcel.2010.04.005openalex-snapshot
Diverse Pathways Generate MicroRNA-like RNAs and Dicer-Independent Small Interfering RNAs in Fungi
inferred← citeshttps://doi.org/10.1016/j.molcel.2012.03.019openalex-snapshot
Reconstitution of an Argonaute-Dependent Small RNA Biogenesis Pathway Reveals a Handover Mechanism Involving the RNA Exosome and the Exonuclease QIP
inferred← citeshttps://doi.org/10.1016/j.molcel.2018.10.038openalex-snapshot
Maelstrom Represses Canonical Polymerase II Transcription within Bi-directional piRNA Clusters in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.pestbp.2021.104872openalex-snapshot
Transcript level is a key factor affecting RNAi efficiency
inferred← citeshttps://doi.org/10.1016/j.pestbp.2025.106331openalex-snapshot
A sprayable long hairpin dsRNA formulated with layered double hydroxide against the western flower thrips, Frankliniella occidentalis: Control efficacy in a greenhouse and influence on beneficial insects
inferred← citeshttps://doi.org/10.1016/j.pmpp.2026.103161openalex-snapshot
Functional RNAi response in Colletotrichum graminicola reveals potential for host-induced gene silencing against maize anthracnose
inferred← citeshttps://doi.org/10.1016/j.tcb.2005.03.006openalex-snapshot
RNA silencing and genome regulation
inferred← citeshttps://doi.org/10.1016/j.tcb.2013.10.003openalex-snapshot
Guest list or black list: heritable small RNAs as immunogenic memories
inferred← citeshttps://doi.org/10.1016/j.tig.2004.07.007openalex-snapshot
RIP: the evolutionary cost of genome defense
inferred← citeshttps://doi.org/10.1016/j.tplants.2006.01.003openalex-snapshot
Nomenclature and functions of RNA-directed RNA polymerases
inferred← citeshttps://doi.org/10.1016/j.virol.2014.09.024openalex-snapshot
The chestnut blight fungus for studies on virus/host and virus/virus interactions: From a natural to a model host
inferred← citeshttps://doi.org/10.1016/j.virusres.2004.01.016openalex-snapshot
RNA interference against retroviruses
inferred← citeshttps://doi.org/10.1016/s0006-291x(03)01124-0openalex-snapshot
RNA interference-mediated reduction in GLUT1 inhibits serum-induced glucose transport in primary human skeletal muscle cells
inferred← citeshttps://doi.org/10.1016/s0027-5107(01)00098-7openalex-snapshot
Evidence for gene silencing in Haemophilus influenzae
inferred← citeshttps://doi.org/10.1016/s0065-2296(09)51002-6openalex-snapshot
Chapter 2 Plant Pathogens as Suppressors of Host Defense
inferred← citeshttps://doi.org/10.1016/s0065-2660(02)46009-9openalex-snapshot
8 Homology-dependent gene silencing and host defense in plants
inferred← citeshttps://doi.org/10.1016/s0065-2660(02)46010-5openalex-snapshot
9 Quelling in Neurospora crassa
inferred← citeshttps://doi.org/10.1016/s0065-2660(02)46012-9openalex-snapshot
11 RNAi (nematodes: Caenorhabditis elegans)
inferred← citeshttps://doi.org/10.1016/s0065-3527(10)76003-6openalex-snapshot
Signaling in Induced Resistance
inferred← citeshttps://doi.org/10.1016/s0065-7743(03)38027-3openalex-snapshot
Chapter 26. RNAi: When interfering is a plus
inferred← citeshttps://doi.org/10.1016/s0076-6879(04)92021-6openalex-snapshot
Analysis of Short Interfering RNA Function in RNA Interference by Using Drosophila Embryo Extracts and Schneider Cells
inferred← citeshttps://doi.org/10.1016/s0092-8674(00)80863-6openalex-snapshot
Arabidopsis SGS2 and SGS3 Genes Are Required for Posttranscriptional Gene Silencing and Natural Virus Resistance
inferred← citeshttps://doi.org/10.1016/s0092-8674(00)80864-8openalex-snapshot
An RNA-Dependent RNA Polymerase Gene in Arabidopsis Is Required for Posttranscriptional Gene Silencing Mediated by a Transgene but Not by a Virus
inferred← citeshttps://doi.org/10.1016/s0092-8674(00)81644-xopenalex-snapshot
The rde-1 Gene, RNA Interference, and Transposon Silencing in C. elegans
inferred← citeshttps://doi.org/10.1016/s0092-8674(00)81645-1openalex-snapshot
mut-7 of C. elegans, Required for Transposon Silencing and RNA Interference, Is a Homolog of Werner Syndrome Helicase and RNaseD
inferred← citeshttps://doi.org/10.1016/s0092-8674(01)00537-2openalex-snapshot
RNAi as Random Degradative PCR
inferred← citeshttps://doi.org/10.1016/s0092-8674(01)00576-1openalex-snapshot
On the Role of RNA Amplification in dsRNA-Triggered Gene Silencing
inferred← citeshttps://doi.org/10.1016/s0092-8674(01)00609-2openalex-snapshot
Meiotic Silencing by Unpaired DNA
inferred← citeshttps://doi.org/10.1016/s0092-8674(02)00793-6openalex-snapshot
The dsRNA Binding Protein RDE-4 Interacts with RDE-1, DCR-1, and a DExH-Box Helicase to Direct RNAi in C. elegans
inferred← citeshttps://doi.org/10.1016/s0092-8674(02)71133-1openalex-snapshot
Double-Stranded RNA as a Template for Gene Silencing
inferred← citeshttps://doi.org/10.1016/s0092-8674(03)00157-0openalex-snapshot
Polycomb, Epigenomes, and Control of Cell Identity
inferred← citeshttps://doi.org/10.1016/s0166-6851(03)00071-9openalex-snapshot
Efficiency and specificity of RNA interference generated by intra- and intermolecular double stranded RNA in Trypanosoma brucei
inferred← citeshttps://doi.org/10.1016/s0167-4781(02)00280-4openalex-snapshot
Antisense-RNA regulation and RNA interference
inferred← citeshttps://doi.org/10.1016/s0167-7799(01)01883-2openalex-snapshot
Genes, technology and public dialogue in Tartu, Estonia
inferred← citeshttps://doi.org/10.1016/s0167-7799(01)01900-xopenalex-snapshot
A new approach to the inhibition of gene expression
inferred← citeshttps://doi.org/10.1016/s0168-7972(00)80102-4openalex-snapshot
Post-Transcriptional Gene Silencing In Plants: Pain Or Delight In Transgene Research?
inferred← citeshttps://doi.org/10.1016/s0168-7972(00)80130-9openalex-snapshot
Toward The Identification Of The Genes For The Synthesis Of Condensed Tannins In Forage Legumes
inferred← citeshttps://doi.org/10.1016/s0168-9525(01)02367-8openalex-snapshot
RNA silencing as a plant immune system against viruses
inferred← citeshttps://doi.org/10.1016/s0168-9525(01)02479-9openalex-snapshot
Stop making nonSense: the C. elegans smg genes
inferred← citeshttps://doi.org/10.1016/s0168-9525(99)01818-1openalex-snapshot
RNA-triggered gene silencing
inferred← citeshttps://doi.org/10.1016/s0378-1119(00)00224-9openalex-snapshot
dsRNA-mediated gene silencing in cultured Drosophila cells: a tissue culture model for the analysis of RNA interference
inferred← citeshttps://doi.org/10.1016/s0764-4469(01)01369-5openalex-snapshot
Plant viruses and the recent discovery of unforeseen basic cellular processes
inferred← citeshttps://doi.org/10.1016/s0923-2508(01)01182-2openalex-snapshot
Genetic interference in protozoa
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