On the public citation graph

Insights from CRISPR/Cas9-mediated gene editing of centromeric histone H3 (CENH3) in carrot ( Daucus carota subsp. sativus )

https://doi.org/10.1101/2022.09.19.508489
0 signed · 45 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/1873-3468.13073openalex-snapshot
Transforming plant biology and breeding with CRISPR /Cas9, Cas12 and Cas13
inferredcites →https://doi.org/10.1007/s00122-018-3261-9openalex-snapshot
State-of-the-art and novel developments of in vivo haploid technologies
inferredcites →https://doi.org/10.1007/s00299-004-0776-0openalex-snapshot
TheCaMV 35S promoter is highly active on floral organs and pollen of transgenic strawberry plants
inferredcites →https://doi.org/10.1007/s11103-010-9723-3openalex-snapshot
Recognition of A. thaliana centromeres by heterologous CENH3 requires high similarity to the endogenous protein
inferredcites →https://doi.org/10.1007/s11240-019-01665-9openalex-snapshot
Deep sequencing analysis of CRISPR/Cas9 induced mutations by two delivery methods in target model genes and the CENH3 region of red cabbage (Brassica oleracea var. capitata f. rubra)
inferredcites →https://doi.org/10.1007/s11816-018-0508-5openalex-snapshot
Segregation of genetic chimeras generated by CRISPR/Cas9 system in rice
inferredcites →https://doi.org/10.1016/j.hpj.2022.01.005openalex-snapshot
Efficient generation of targeted point mutations in the Brassica oleracea var. botrytis genome via a modified CRISPR/Cas9 system
inferredcites →https://doi.org/10.1016/j.tplants.2003.10.011openalex-snapshot
A molecular view of plant centromeres
inferredcites →https://doi.org/10.1038/hortres.2014.47openalex-snapshot
Temporal and spatial control of gene expression in horticultural crops
inferredcites →https://doi.org/10.1038/nature08842openalex-snapshot
Haploid plants produced by centromere-mediated genome elimination
inferredcites →https://doi.org/10.1038/nbt.3389openalex-snapshot
DNA-free genome editing in plants with preassembled CRISPR-Cas9 ribonucleoproteins
inferredcites →https://doi.org/10.1038/ncomms6334openalex-snapshot
A haploid genetics toolbox for Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/ng.3565openalex-snapshot
A high-quality carrot genome assembly provides new insights into carotenoid accumulation and asterid genome evolution
inferredcites →https://doi.org/10.1038/s41438-020-0258-8openalex-snapshot
Perspectives of CRISPR/Cas-mediated cis-engineering in horticulture: unlocking the neglected potential for crop improvement
inferredcites →https://doi.org/10.1038/s41587-019-0038-xopenalex-snapshot
One-step genome editing of elite crop germplasm during haploid induction
inferredcites →https://doi.org/10.1038/s41587-020-0728-4openalex-snapshot
Generation of paternal haploids in wheat by genome editing of the centromeric histone CENH3
inferredcites →https://doi.org/10.1038/s42003-020-01507-xopenalex-snapshot
Unequal contribution of two paralogous CENH3 variants in cowpea centromere function
inferredcites →https://doi.org/10.1073/pnas.1103190108openalex-snapshot
Loss of centromeric histone H3 (CENH3) from centromeres precedes uniparental chromosome elimination in interspecific barley hybrids
inferredcites →https://doi.org/10.1073/pnas.1504333112openalex-snapshot
Point mutation impairs centromeric CENH3 loading and induces haploid plants
inferredcites →https://doi.org/10.1093/molbev/msp208openalex-snapshot
Lineage-Specific Adaptive Evolution of the Centromeric Protein CENH3 in Diploid and Allotetraploid Oryza Species
inferredcites →https://doi.org/10.1093/molbev/msv070openalex-snapshot
Centromeres Off the Hook: Massive Changes in Centromere Size and Structure Following Duplication ofCenH3Gene inFabeaeSpecies
inferredcites →https://doi.org/10.1093/nar/27.1.295openalex-snapshot
PlantCARE, a plant cis-acting regulatory element database
inferredcites →https://doi.org/10.1093/nar/gkr944openalex-snapshot
Phytozome: a comparative platform for green plant genomics
inferredcites →https://doi.org/10.1093/plphys/kiac032openalex-snapshot
Updates on gene editing and its applications
inferredcites →https://doi.org/10.1111/nph.14702openalex-snapshot
Towards CRISPR /Cas crops – bringing together genomics and genome editing
inferredcites →https://doi.org/10.1111/pbi.13365openalex-snapshot
A variety of changes, including CRISPR/Cas9‐mediated deletions, in CENH3 lead to haploid induction on outcrossing
inferredcites →https://doi.org/10.1111/tpj.12554openalex-snapshot
Both CRISPR / C as‐based nucleases and nickases can be used efficiently for genome engineering in A rabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.12704openalex-snapshot
The CRISPR / C as system can be used as nuclease for in planta gene targeting and as paired nickases for directed mutagenesis in A rabidopsis resulting in heritable progeny
inferredcites →https://doi.org/10.1126/sciadv.abe2299openalex-snapshot
Haploid induction by a maize cenh3 null mutant
inferredcites →https://doi.org/10.1128/jb.116.1.378-383.1973openalex-snapshot
Utilization of Octopine and Nopaline by Agrobacterium
inferredcites →https://doi.org/10.1186/1471-2164-14-245openalex-snapshot
Transcriptome analysis reveals ginsenosides biosynthetic genes, microRNAs and simple sequence repeats in Panax ginsengC. A. Meyer
inferredcites →https://doi.org/10.1186/s12870-015-0700-5openalex-snapshot
CENH3-GFP: a visual marker for gametophytic and somatic ploidy determination in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pgen.1002777openalex-snapshot
Stretching the Rules: Monocentric Chromosomes with Multiple Centromere Domains
inferredcites →https://doi.org/10.1371/journal.pgen.1004970openalex-snapshot
Naturally Occurring Differences in CENH3 Affect Chromosome Segregation in Zygotic Mitosis of Hybrids
inferredcites →https://doi.org/10.1371/journal.pgen.1005494openalex-snapshot
Point Mutations in Centromeric Histone Induce Post-zygotic Incompatibility and Uniparental Inheritance
inferredcites →https://doi.org/10.1371/journal.pone.0098504openalex-snapshot
Characterization of Centromeric Histone H3 (CENH3) Variants in Cultivated and Wild Carrots (Daucus sp.)
inferredcites →https://doi.org/10.3389/fpls.2016.00414openalex-snapshot
Maternal Haploids Are Preferentially Induced by CENH3-tailswap Transgenic Complementation in Maize
inferredcites →https://doi.org/10.3389/fpls.2016.01995openalex-snapshot
RNA-Guided Cas9-Induced Mutagenesis in Tobacco Followed by Efficient Genetic Fixation in Doubled Haploid Plants
inferredcites →https://doi.org/10.3390/plants10102043openalex-snapshot
Expression of Two Rye CENH3 Variants and Their Loading into Centromeres
inferredcites →https://doi.org/10.5073/20180910-125444openalex-snapshot
Using CRISPR/Cas9 to produce haploid inducers of carrot through targeted mutations of centromerichistone H3 (CENH3)

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s44279-025-00361-xopenalex-snapshot
Role of omics and gene editing tools in development of abiotic stress tolerant carrots (Daucus carota L.)
inferred← citeshttps://doi.org/10.17660/actahortic.2024.1393.22openalex-snapshot
Exploring modification of centromeric histone H3 (CENH3) as a strategy for haploid induction in carrot (Daucus carota)
inferred← citeshttps://doi.org/10.3389/fpls.2023.1294551openalex-snapshot
Chromosome-level changes and genome elimination by manipulation of CENH3 in carrot (Daucus carota)
inferred← citeshttps://doi.org/10.3390/agronomy13030676openalex-snapshot
History and Current Status of Haploidization in Carrot (Daucus carota L.)
inferred← citeshttps://doi.org/10.3390/plants12030485openalex-snapshot
Accelerated Breeding for Helianthus annuus (Sunflower) through Doubled Haploidy: An Insight on Past and Future Prospects in the Era of Genome Editing
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.