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Chromosomal localization of a novel repetitive sequence in theChenopodium quinoa genome

https://doi.org/10.1007/bf03195629

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What this work says

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

inferredcites →https://doi.org/10.1006/anbo.1998.0779openalex-snapshot

Repetitive DNA Elements as a Major Component of Plant Genomes

inferredcites →https://doi.org/10.1007/bf00019545openalex-snapshot

High-resolution mapping of repetitive DNA by in situ hybridization: molecular and chromosomal features of prominent dispersed and discretely localized DNA families from the wild beet species Beta procumbens

inferredcites →https://doi.org/10.1007/bf00710014openalex-snapshot

Analysis and chromosomal localization of retrotransposons in sugar beet (Beta vulgaris L.): LINEs andTy1-copia-like elements as major components of the genome

inferredcites →https://doi.org/10.1007/bf02134133openalex-snapshot

Insertion of an intermediate repetitive sequence into a sea urchin histone-gene spacer

inferredcites →https://doi.org/10.1007/bf02860478openalex-snapshot

Quinua and Relatives (Chenopodium sect.Chenopodium subsect.Celluloid)

inferredcites →https://doi.org/10.1007/s00122-004-1730-9openalex-snapshot

A genetic linkage map of quinoa (Chenopodium quinoa) based on AFLP, RAPD, and SSR markers

inferredcites →https://doi.org/10.1007/s001220050945openalex-snapshot

Molecular and chromosomal organization of two repetitive DNA sequences with intercalary locations in sugar beet and other Beta species

inferredcites →https://doi.org/10.1007/s001220100653openalex-snapshot

Ribosomal DNA is an effective marker of Brassica chromosomes

inferredcites →https://doi.org/10.1007/s004120050224openalex-snapshot

Genomic organization and phylogenetic relationships in the genus Dasypyrum analysed by Southern and in situ hybridization of total genomic and cloned DNA probes

inferredcites →https://doi.org/10.1007/s004120050383openalex-snapshot

A family of dispersed repeats in the genome of Vicia faba : structure, chromosomal organization, redundancy modulation, and evolution

inferredcites →https://doi.org/10.1007/s00606-002-0224-yopenalex-snapshot

inferredcites →https://doi.org/10.1007/s00606-003-0026-xopenalex-snapshot

Karyotype evolution in South American species of Hypochaeris (Asteraceae, Lactuceae)

inferredcites →https://doi.org/10.1016/0031-9422(80)85004-7openalex-snapshot

Deviations from michaelis-menten behaviour of plant glutamate dehydrogenase with ammonium as variable substrate

inferredcites →https://doi.org/10.1016/s1369-5266(98)80010-1openalex-snapshot

The structure and evolution of angiosperm nuclear genomes

inferredcites →https://doi.org/10.1023/a:1003480414735openalex-snapshot

Genetic relationship among 19 accessions of six species of Chenopodium L., by Random Amplified Polymorphic DNA fragments (RAPD)

inferredcites →https://doi.org/10.1023/a:1004070517808openalex-snapshot

Allotetraploid segregation for single-gene morphological characters in quinoa (Chenopodium quinoa} Willd.)

inferredcites →https://doi.org/10.1023/a:1005797222148openalex-snapshot

Comparative analysis of the chromosomal and genomic organization of Ty1-copia-like retrotransposons in pteridophytes, gymnosperms and angiosperms

inferredcites →https://doi.org/10.1023/a:1022005514470openalex-snapshot

Divergence of satellite DNA and interspersion of dispersed repeats in the genome of the wild beet Beta procumbens

inferredcites →https://doi.org/10.1023/a:1025472709537openalex-snapshot

Abundance of plastid DNA insertions in nuclear genomes of rice and Arabidopsis

inferredcites →https://doi.org/10.1046/j.1365-313x.1996.09030421.xopenalex-snapshot

High‐resolution physical mapping in Arabidopsis thaliana and tomato by fluorescence in situ hybridization to extended DNA fibres

inferredcites →https://doi.org/10.1093/nar/18.13.4011openalex-snapshot

Nucleotide sequence of the 5.8S and 25S rRNA genes and of the internal transcribed spacers fromArabidopsis thaliana

inferredcites →https://doi.org/10.1093/nar/8.21.4851openalex-snapshot

Sequence organization of the repeating units in the nucleus of wheat which contain 5S rRNA genes

inferredcites →https://doi.org/10.1101/gr.8.5.479openalex-snapshot

Dispersed Repetitive DNA Has Spread to New Genomes Since Polyploid Formation in Cotton

inferredcites →https://doi.org/10.1139/g01-056openalex-snapshot

Molecular and cytogenetic analysis of repetitive DNA in pea (Pisum sativumL.)

inferredcites →https://doi.org/10.1139/g01-148openalex-snapshot

Isolation of A/D and C genome specific dispersed and clustered repetitive DNA sequences fromAvena sativa

inferredcites →https://doi.org/10.1139/g06-033openalex-snapshot

Molecular and cytological characterization of ribosomal RNA genes inChenopodium quinoaandChenopodium berlandieri

inferredcites →https://doi.org/10.1146/annurev.genet.33.1.479openalex-snapshot

Plant Retrotransposons

inferredcites →https://doi.org/10.1159/000082377openalex-snapshot

Organization and evolution of highly repeated satellite DNA sequences in plant chromosomes

inferredcites →https://doi.org/10.1159/000084941openalex-snapshot

LTR retrotransposons and flowering plant genome size: emergence of the increase/decrease model

inferredcites →https://doi.org/10.1266/ggs.76.53openalex-snapshot

Identification and Chromosomal Location of Tandemly Repeated DNA Sequences in Allium cepa.

inferredcites →https://doi.org/10.17226/1398openalex-snapshot

Lost Crops of the Incas

inferredcites →https://doi.org/10.2307/2446394openalex-snapshot

Evolution of interspersed repetitive elements in Gossypium (Malvaceae)

inferredcites →https://doi.org/10.5586/asbp.2001.011openalex-snapshot

Molecular cytogenetic studies in Chenopodium quinoa and Amaranthus caudatus

What points at this work

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

inferred← citeshttps://doi.org/10.11646/phytotaxa.392.3.1zenodo-depositor-declared

Parental origin and genome evolution of several Eurasian hexaploid species of Chenopodium (Chenopodiaceae)

inferred← citeshttps://doi.org/10.1002/9781118628041.ch7openalex-snapshot

Quinoa Cytogenetics, Molecular Genetics, and Diversity

inferred← citeshttps://doi.org/10.1007/978-3-030-65237-1_4openalex-snapshot

Quinoa Cytogenetics

inferred← citeshttps://doi.org/10.1007/978-94-007-5500-0_8openalex-snapshot

Prospects for Quinoa (Chenopodium Quinoa Willd.) Improvement Through Biotechnology

inferred← citeshttps://doi.org/10.1007/978-981-99-9175-4_7openalex-snapshot

Advancing Food Security with Genetic Resources of Amaranthus, Buckwheat, and Chenopodium

inferred← citeshttps://doi.org/10.1007/s00299-013-1468-4openalex-snapshot

Isolation and characterization of reverse transcriptase fragments of LTR retrotransposons from the genome of Chenopodium quinoa (Amaranthaceae)

inferred← citeshttps://doi.org/10.1007/s10535-015-0558-2openalex-snapshot

Precise karyotyping of carrot mitotic chromosomes using multicolour-FISH with repetitive DNA

inferred← citeshttps://doi.org/10.1007/s11032-014-0023-5openalex-snapshot

Breeding quinoa (Chenopodium quinoa Willd.): potential and perspectives

inferred← citeshttps://doi.org/10.1007/s12041-019-1079-0openalex-snapshot

Deciphering species relationships and evolution in Chenopodium through sequence variations in nuclear internal transcribed spacer region and amplified fragment-length polymorphism in nuclear DNA

inferred← citeshttps://doi.org/10.1016/j.cj.2016.06.019openalex-snapshot

Evolutionary divergence in Chenopodium and validation of SNPs in chloroplast rbcL and matk genes by allele-specific PCR for development of Chenopodium quinoa-specific markers

inferred← citeshttps://doi.org/10.1016/j.scienta.2013.09.016openalex-snapshot

Localization of ribosomal DNA and CMA3/DAPI heterochromatin in cultivated and wild Amaranthus species

inferred← citeshttps://doi.org/10.1016/j.ympev.2016.04.009openalex-snapshot

Molecular and cytogenetic evidence for an allotetraploid origin of Chenopodium quinoa and C. berlandieri (Amaranthaceae)

inferred← citeshttps://doi.org/10.1111/boj.12321openalex-snapshot

The evolution of genome size and rDNA in diploid species ofChenopodium s.l.(Amaranthaceae)

inferred← citeshttps://doi.org/10.1139/g11-035openalex-snapshot

Chromosomal localization of two novel repetitive sequences isolated from the Chenopodium quinoa Willd. genome

inferred← citeshttps://doi.org/10.1139/gen-2018-0044openalex-snapshot

Organization and evolution of two repetitive sequences, 18-24J and 12-13P, in the genome of Chenopodium (Amaranthaceae)

inferred← citeshttps://doi.org/10.1186/s12870-023-04450-1openalex-snapshot

Multi-omics insights into the positive role of strigolactone perception in barley drought response

inferred← citeshttps://doi.org/10.3389/fpls.2022.1024555openalex-snapshot

Genetic variation of Amaranthus retroflexus L. and Chenopodium album L. (Amaranthaceae) suggests multiple independent introductions into Iran

inferred← citeshttps://doi.org/10.3389/fpls.2025.1636565openalex-snapshot

Can quinoa (Chenopodium quinoa) replace traditional cereals under current climate scenarios?

inferred← citeshttps://doi.org/10.6084/m9.figshare.24180947openalex-snapshot

Additional file 1 of Multi-omics insights into the positive role of strigolactone perception in barley drought response

inferred← citeshttps://doi.org/10.6084/m9.figshare.24180950openalex-snapshot

Additional file 2 of Multi-omics insights into the positive role of strigolactone perception in barley drought response

inferred← citeshttps://doi.org/10.6084/m9.figshare.24180953openalex-snapshot

Additional file 3 of Multi-omics insights into the positive role of strigolactone perception in barley drought response

inferred← citeshttps://doi.org/10.6084/m9.figshare.24180956openalex-snapshot

Additional file 4 of Multi-omics insights into the positive role of strigolactone perception in barley drought response

inferred← citeshttps://doi.org/10.6084/m9.figshare.24180959openalex-snapshot

Additional file 5 of Multi-omics insights into the positive role of strigolactone perception in barley drought response

inferred← citeshttps://doi.org/10.6084/m9.figshare.24180962openalex-snapshot

Additional file 6 of Multi-omics insights into the positive role of strigolactone perception in barley drought response

inferred← citeshttps://doi.org/10.6084/m9.figshare.24180965openalex-snapshot

Additional file 7 of Multi-omics insights into the positive role of strigolactone perception in barley drought response

inferred← citeshttps://doi.org/10.6084/m9.figshare.24180968openalex-snapshot

Additional file 8 of Multi-omics insights into the positive role of strigolactone perception in barley drought response

inferred← citeshttps://doi.org/10.6084/m9.figshare.24180971openalex-snapshot

Additional file 9 of Multi-omics insights into the positive role of strigolactone perception in barley drought response

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