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Structural characterization of ITS2 and CBC species concept applications in the tribe Coluteocarpeae (Brassicaceae)
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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/fedr.4910840503openalex-snapshot
Conspectus der „Thlaspi”-Arten Europas, Afrikas und Vorderasiens
inferredcites →https://doi.org/10.1002/tax.615002openalex-snapshot
A generic and tribal synopsis of the Brassicaceae (Cruciferae)
inferredcites →https://doi.org/10.1006/jmbi.1999.2700openalex-snapshot
Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure
inferredcites →https://doi.org/10.1007/pl00006143openalex-snapshot
The Internal Transcribed Spacer 2 Exhibits a Common Secondary Structure in Green Algae and Flowering Plants
inferredcites →https://doi.org/10.1007/pl00006398openalex-snapshot
Trematode and Monogenean rRNA ITS2 Secondary Structures Support a Four-Domain Model
inferredcites →https://doi.org/10.1007/s00239-001-0006-0openalex-snapshot
Exploring the Phylogenetic Utility of ITS Sequences for Animals: A Test Case for Abalone (Haliotis)
inferredcites →https://doi.org/10.1007/s00606-006-0415-zopenalex-snapshot
Systematics and phylogeny of the Brassicaceae (Cruciferae): an overview
inferredcites →https://doi.org/10.1007/s00606-009-0213-5openalex-snapshot
Contribution to ITS phylogeny of the Brassicaceae, with special reference to some Asian taxa
inferredcites →https://doi.org/10.1007/s00606-010-0271-8openalex-snapshot
Closing the gaps: phylogenetic relationships in the Brassicaceae based on DNA sequence data of nuclear ribosomal ITS region
inferredcites →https://doi.org/10.1016/b978-0-12-372180-8.50042-1openalex-snapshot
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
inferredcites →https://doi.org/10.1016/j.bse.2009.01.010openalex-snapshot
Phylogenetic relationships of Old World Brassicaceae from Iran based on nuclear ribosomal DNA sequences
inferredcites →https://doi.org/10.1016/j.bse.2016.03.008openalex-snapshot
The characterisation and taxonomic utility of ITS2 in Tenthredopsis Costa, 1859 (Tenthredinidae: Hymenoptera) with some new records from Turkey
inferredcites →https://doi.org/10.1016/j.fgb.2009.08.001openalex-snapshot
Evolution of rDNA ITS1 and ITS2 sequences and RNA secondary structures within members of the fungal genera Grosmannia and Leptographium
inferredcites →https://doi.org/10.1016/j.flora.2016.09.008openalex-snapshot
Microthlaspi erraticum (Jord.) T. Ali et Thines has a wide distribution, ranging from the Alps to the Tien Shan
inferredcites →https://doi.org/10.1016/j.gene.2014.05.065openalex-snapshot
ITS2, 18S, 16S or any other RNA — simply aligning sequences and their individual secondary structures simultaneously by an automatic approach
inferredcites →https://doi.org/10.1016/j.ympev.2008.10.008openalex-snapshot
Is there a molecular key to the level of “biological species” in eukaryotes? A DNA guide
inferredcites →https://doi.org/10.1016/j.ympev.2012.01.026openalex-snapshot
ITS2 Database IV: Interactive taxon sampling for internal transcribed spacer 2 based phylogenies
inferredcites →https://doi.org/10.1016/j.ympev.2014.06.015openalex-snapshot
Gorgonia mariae and Antillogorgia bipinnata populations inferred from compensatory base change analysis of the internal transcribed spacer 2
inferredcites →https://doi.org/10.1080/01916122.2018.1463571openalex-snapshot
Pollen morphology of some taxa of Thlaspi L. sensu lato (Brassicaceae) from Turkey, and its taxonomical importance
inferredcites →https://doi.org/10.1086/314194openalex-snapshot
Evolutionary Changes in Floral Structure withinLepidiumL. (Brassicaceae)
inferredcites →https://doi.org/10.1093/bioinformatics/btm404openalex-snapshot
Clustal W and Clustal X version 2.0
inferredcites →https://doi.org/10.1093/bioinformatics/btp250openalex-snapshot
VARNA: Interactive drawing and editing of the RNA secondary structure
inferredcites →https://doi.org/10.1093/bioinformatics/btq706openalex-snapshot
phangorn: phylogenetic analysis in R
inferredcites →https://doi.org/10.1093/molbev/msp202openalex-snapshot
Molecular Phylogenetics, Temporal Diversification, and Principles of Evolution in the Mustard Family (Brassicaceae)
inferredcites →https://doi.org/10.1093/molbev/msv174openalex-snapshot
ITS2 Database V: Twice as Much: Table 1.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040480openalex-snapshot
Paired sequence difference in ribosomal RNAs: evolutionary and phylogenetic implications.
inferredcites →https://doi.org/10.1111/j.1095-8339.1997.tb02253.xopenalex-snapshot
Molecular data reveal convergence in fruit characters used in the classification of Thlaspi s. l. (Brassicaceae)
inferredcites →https://doi.org/10.1111/j.1095-8339.2006.00472.xopenalex-snapshot
A new species of Noccaea (Brassicaceae) from South Anatolia, Turkey
inferredcites →https://doi.org/10.1111/j.1438-8677.1995.tb00520.xopenalex-snapshot
Allopolyploid Origin of Arabidopsis suecica (Fries) Norrlin: Evidence from Chloroplast and Nuclear Genome Markers
inferredcites →https://doi.org/10.1111/j.1759-6831.2009.00022.xopenalex-snapshot
Notes on the family Brassicaceae in China
inferredcites →https://doi.org/10.1111/jse.12221openalex-snapshot
Ribosomal DNA ITS1, 5.8S and ITS2 secondary structure, nuclear DNA content and phytochemical analyses reveal distinctive characteristics of four subclades of Protasparagus
inferredcites →https://doi.org/10.1139/b97-051openalex-snapshot
Molecular phylogenetics ofThlaspis.l. (Brassicaceae) based on chloroplast DNA restriction site variation and sequences of the internal transcribed spacers of nuclear ribosomal DNA
inferredcites →https://doi.org/10.1146/annurev.genet.33.1.261openalex-snapshot
Ribosome Synthesis in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.11646/phytotaxa.178.4.2openalex-snapshot
Phylogenetic position and taxonomic assignment of Thlaspi aghricum P.H.Davis & K.Tan (Brassicaceae)
inferredcites →https://doi.org/10.11646/phytotaxa.297.3.12openalex-snapshot
What is Cochlearia venusta (Cruciferae)?
inferredcites →https://doi.org/10.11646/phytotaxa.336.3.2openalex-snapshot
A new perennial Erysimum species from Turkey, E. nemrutdaghense (Brassicaceae)
inferredcites →https://doi.org/10.11646/phytotaxa.344.2.5openalex-snapshot
Phylogenetic position, taxonomy, distribution, and conservation status of the rare and poorly-known Noccaea rosularis, the generic type of Masmenia (Brassicaceae)
inferredcites →https://doi.org/10.11646/phytotaxa.345.1.7openalex-snapshot
Noccaea birolmutlui, a New Crucifer Species from South West Anatolia, Turkey
inferredcites →https://doi.org/10.11646/phytotaxa.346.3.4openalex-snapshot
Contributions to Turkish Flora: Taxonomic and distributional notes on the poorly known Noccaea (Brassicaceae) species
inferredcites →https://doi.org/10.11646/phytotaxa.383.1.6openalex-snapshot
Taxonomic remarks on Pseudosempervivum (Brassicaceae)
inferredcites →https://doi.org/10.11646/phytotaxa.432.1.8openalex-snapshot
A new species of Noccaea (Brassicaceae) from central Anatolia
inferredcites →https://doi.org/10.1186/1471-2105-7-498openalex-snapshot
4SALE – A tool for synchronous RNA sequence and secondary structure alignment and editing
inferredcites →https://doi.org/10.1186/1745-6150-5-4openalex-snapshot
Including RNA secondary structures improves accuracy and robustness in reconstruction of phylogenetic trees
inferredcites →https://doi.org/10.1261/rna.7204505openalex-snapshot
A common core of secondary structure of the internal transcribed spacer 2 (ITS2) throughout the Eukaryota
inferredcites →https://doi.org/10.12705/651.6openalex-snapshot
Morphology, phylogeny, and taxonomy of Microthlaspi (Brassicaceae: Coluteocarpeae) and related genera
inferredcites →https://doi.org/10.1371/journal.pone.0066726openalex-snapshot
Compensatory Base Changes in ITS2 Secondary Structures Correlate with the Biological Species Concept Despite Intragenomic Variability in ITS2 Sequences – A Proof of Concept
inferredcites →https://doi.org/10.1371/journal.pone.0101341openalex-snapshot
Secondary Structure Analyses of the Nuclear rRNA Internal Transcribed Spacers and Assessment of Its Phylogenetic Utility across the Brassicaceae (Mustards)
inferredcites →https://doi.org/10.1600/036364404774195566openalex-snapshot
Taxonomic and Phylogenetic Evaluation of the American "Thlaspi" Species: Identity and Relationship to the Eurasian Genus Noccaea (Brassicaceae)
inferredcites →https://doi.org/10.2307/1223220openalex-snapshot
Should Thlaspi (Brassicaceae) be split? Preliminary evidence from isoelectric focusing analysis of Rubisco
inferredcites →https://doi.org/10.2307/3298580openalex-snapshot
Molecular Systematics, Evolution, and Population Biology in the Mustard Family (Brassicaceae)
inferredcites →https://doi.org/10.2307/3558431openalex-snapshot
Chloroplast DNA phylogeny and biogeography of Lepidium (Brassicaceae)
inferredcites →https://doi.org/10.3100/hpib.v19iss1.2014.n3openalex-snapshot
A Synopsis of the Genus Noccaea (coluteocarpeae, Brassicaceae)
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3417/2019347openalex-snapshot
Phylogeny of the Genus Noccaea (Brassicaceae) and a Critical Review of its Generic Circumscription
inferredcites →https://doi.org/10.3732/ajb.91.2.254openalex-snapshot
Molecular evidence for bicontinental hybridogenous genomic constitution in Lepidium sensu stricto (Brassicaceae) species from Australia and New Zealand
inferredcites →https://doi.org/10.3906/bot-1006-40openalex-snapshot
Phylogenetic relationships between Malcolmia, Strigosella, Zuvanda, and some closely related genera (Brassicaceae) from Turkey revealed by inter-simple sequence repeat amplification
inferredcites →https://doi.org/10.3906/bot-1709-28openalex-snapshot
Seed structure and its taxonomic implications for genus Thlaspi sensu lato sections Nomisma , Thlaspi , and Pterotropis (Brassicaceae
inferredcites →https://doi.org/10.3906/bot-1712-52openalex-snapshot
Resolving the position of Astragalus borysthenicus Klokov within the Astragalus L. species
inferredcites →https://doi.org/10.3906/bot-1805-40openalex-snapshot
Noccaea ali-atahanii (Brassicaceae): a new species from southern Anatolia
inferredcites →https://doi.org/10.5507/fot.2016.010openalex-snapshot
Selenastraceae (Sphaeropleales, Chlorophyceae): rbcL, 18S rDNA and ITS-2 secondary structure enlightens traditional taxonomy, with description of two new genera, Messastrum gen. nov. and Curvastrum gen. nov.
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.555.2.11zenodo-depositor-declared
Noccaea klimesii (Coluteocarpeae; Brassicaceae), a new species from Ladakh, India
inferred← citeshttps://doi.org/10.1002/tax.13329openalex-snapshot
Diversity, taxonomic delimitation, and character evolution of the subfamily Makinoelloideae (Oocystaceae, Trebouxiophyceae, Chlorophyta)
inferred← citeshttps://doi.org/10.1080/00318884.2026.2695359openalex-snapshot
Morphological and molecular characterization of Apatococcus echinosporus sp. nov . (Trebouxiophyceae, Chlorophyta) isolated from rainwater
inferred← citeshttps://doi.org/10.1139/cjb-2020-0184openalex-snapshot
Species delimitation in Noccaea densiflora species complex (Brassicaceae) based on morphological and molecular data
inferred← citeshttps://doi.org/10.1371/journal.pone.0283847openalex-snapshot
Characterizing nrDNA ITS1, 5.8S and ITS2 secondary structures and their phylogenetic utility in the legume tribe Hedysareae with special reference to Hedysarum
inferred← citeshttps://doi.org/10.1590/1983-40632024v5478330openalex-snapshot
Genetic diversity of cultivated mangosteen and its wild relatives (Garcinia spp.) based on leaf morphology and molecular markers1
inferred← citeshttps://doi.org/10.53447/communc.820287openalex-snapshot
CHARACTERIZATION OF ITS1 SECONDARY STRUCTURE IN TEN SPECIES OF COLUTEOCARPEAE (BRASSICACEAE) AND ITS TAXONOMICAL UTILITY
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