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Revisiting phylogenetic relationships in Phoradendreae (Viscaceae): utility of the trnL-F region of chloroplast DNA and presence of a homoplasious inversion in the intergenic spacer

https://doi.org/10.1139/cjb-2016-0241

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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/evan.1360030112openalex-snapshot

Cladistics, computers, and character analysis. MacClade, version 3, Analysis of Phylogeny and Character Evolution. Wayne P. Maddison and David R. Maddison (1992). Sunderland, MA: Sinauer Associates, Inc., Publishers, 398 pp. ISBN 0‐87893‐490‐1

inferredcites →https://doi.org/10.1002/tax.592019openalex-snapshot

A revised classification of Santalales

inferredcites →https://doi.org/10.1007/bf00037152openalex-snapshot

Universal primers for amplification of three non-coding regions of chloroplast DNA

inferredcites →https://doi.org/10.1007/bf02669253openalex-snapshot

The complete nucleotide sequence of the tobacco chloroplast genome

inferredcites →https://doi.org/10.1007/s00239-003-2554-yopenalex-snapshot

Extensive Intraindividual Variation in Plastid rDNA Sequences from the Holoparasite Cynomorium coccineum (Cynomoriaceae)

inferredcites →https://doi.org/10.1007/s00239-009-9224-7openalex-snapshot

On the Brink of Holoparasitism: Plastome Evolution in Dwarf Mistletoes (Arceuthobium, Viscaceae)

inferredcites →https://doi.org/10.1007/s002940050130openalex-snapshot

Hairpins create minute inversions in non-coding regions of chloroplast DNA

inferredcites →https://doi.org/10.1007/s00606-007-0582-6openalex-snapshot

The architecture of the chloroplast psbA-trnH non-coding region in angiosperms

inferredcites →https://doi.org/10.1016/s0022-5193(05)80104-3openalex-snapshot

The general stochastic model of nucleotide substitution

inferredcites →https://doi.org/10.1086/317583openalex-snapshot

Microstructural Changes in Noncoding Chloroplast DNA: Interpretation, Evolution, and Utility of Indels and Inversions in Basal Angiosperm Phylogenetic Inference

inferredcites →https://doi.org/10.1093/genetics/158.2.527openalex-snapshot

Evidence for Two Mechanisms of Palindrome-Stimulated Deletion in Escherichia coli: Single-Strand Annealing and Replication Slipped Mispairing

inferredcites →https://doi.org/10.1093/nar/17.18.7513openalex-snapshot

Nucleotide sequence of the 18S rRNA gene fromArabidopsis thalianaCol0

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/gkg595openalex-snapshot

Mfold web server for nucleic acid folding and hybridization prediction

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025922openalex-snapshot

The phylogenetic potential of entire 26S rDNA sequences in plants

inferredcites →https://doi.org/10.1093/sysbio/42.2.182openalex-snapshot

An Empirical Test of Bootstrapping as a Method for Assessing Confidence in Phylogenetic Analysis

inferredcites →https://doi.org/10.1093/sysbio/sys029openalex-snapshot

MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model Space

inferredcites →https://doi.org/10.1111/boj.12385openalex-snapshot

An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV

inferredcites →https://doi.org/10.1111/j.1096-0031.1989.tb00573.xopenalex-snapshot

THE RETENTION INDEX AND THE RESCALED CONSISTENCY INDEX

inferredcites →https://doi.org/10.1111/j.1438-8677.1961.tb00009.xopenalex-snapshot

A REVISION OF DENDROPHTHORA (LORANTHACEAE)

inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot

CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP

inferredcites →https://doi.org/10.1111/j.1558-5646.1988.tb02497.xopenalex-snapshot

THE LIMITS OF AMINO ACID SEQUENCE DATA IN ANGIOSPERM PHYLOGENETIC RECONSTRUCTION

inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb02626.xopenalex-snapshot

PATTERNS OF VARIATION IN LEVELS OF HOMOPLASY

inferredcites →https://doi.org/10.12705/643.2openalex-snapshot

Phylogenetic relationships of Santalales with insights into the origins of holoparasitic Balanophoraceae

inferredcites →https://doi.org/10.1371/journal.pone.0011533openalex-snapshot

Intraspecific Inversions Pose a Challenge for the trnH-psbA Plant DNA Barcode

inferredcites →https://doi.org/10.1600/036364408783887438openalex-snapshot

A Molecular Phylogeny of Santalaceae (Santalales)

inferredcites →https://doi.org/10.2307/2399772openalex-snapshot

Phylogenetic Relationships of Dipsacales Based on rbcL Sequences

inferredcites →https://doi.org/10.2307/2399875openalex-snapshot

Phylogenetic Inference in Saxifragaceae Sensu Stricto and Gilia (Polemoniaceae) Using matK Sequences

inferredcites →https://doi.org/10.2307/2412407openalex-snapshot

Quantitative Phyletics and the Evolution of Anurans

inferredcites →https://doi.org/10.2307/2445477openalex-snapshot

A Molecular Phylogeny of Arceuthobium (Viscaceae) Based on Nuclear Ribosomal DNA Internal Transcribed Spacer Sequences

inferredcites →https://doi.org/10.2307/25011253openalex-snapshot

Monograph of Phoradendron (Viscaceae)

inferredcites →https://doi.org/10.2307/2656940openalex-snapshot

Phylogenetic relationships within Korthalsella (Viscaceae) based on nuclear ITS and plastid trnL‐F sequence data

inferredcites →https://doi.org/10.2307/2666142openalex-snapshot

The Evolution of Non-Coding Chloroplast DNA and Its Application in Plant Systematics

inferredcites →https://doi.org/10.2307/2666647openalex-snapshot

Phylogenetic Relationships in Phoradendreae (Viscaceae) Inferred from Three Regions of the Nuclear Ribosomal Cistron. I. Major Lineages and Paraphyly of Phoradendron

inferredcites →https://doi.org/10.2307/2805182openalex-snapshot

Revision of the Acataphyllous Species of Phoradendron

inferredcites →https://doi.org/10.2307/2807679openalex-snapshot

Phoradendron olae Kuijt, a New Species from Mexico Pivotal in the Taxonomy of the Genus, with Comments on P. Californicum Nutt.

inferredcites →https://doi.org/10.2307/2992540openalex-snapshot

An Empirical Test of Bootstrapping as a Method for Assessing Confidence in Phylogenetic Analysis

inferredcites →https://doi.org/10.3732/ajb.1400398openalex-snapshot

Chloroplast DNA sequence utility for the lowest phylogenetic and phylogeographic inferences in angiosperms: The tortoise and the hare IV

inferredcites →https://doi.org/10.3732/ajb.91.1.125openalex-snapshot

A phylogeny of all species of Arceuthobium (Viscaceae) using nuclear and chloroplast DNA sequences

inferredcites →https://doi.org/10.3732/ajb.92.1.142openalex-snapshot

The tortoise and the hare II: relative utility of 21 noncoding chloroplast DNA sequences for phylogenetic analysis

inferredcites →https://doi.org/10.3732/ajb.94.3.275openalex-snapshot

Comparison of whole chloroplast genome sequences to choose noncoding regions for phylogenetic studies in angiosperms: the tortoise and the hare III

inferredcites →https://doi.org/10.5642/aliso.20001901.05openalex-snapshot

Phylogenetic Relationships in Phoradendreae (Viscaceae) Inferred from Three Regions of the Nuclear Ribosomal Cistron. II. The North American Species of Phoradendron

inferredcites →https://doi.org/10.5962/bhl.title.23openalex-snapshot

The genus Phoradendron :a monographic revision

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.490.3.7zenodo-depositor-declared

Novelties in Phoradendron killipii (Viscaceae): an endemic and rare species from Colombia

inferred← citeshttps://doi.org/10.1007/s00709-026-02213-xopenalex-snapshot

Flower development and morphoanatomy of Dendrophthora costaricensis Urb. (Viscaceae) and its implications in the taxonomy of Phoradendreae

inferred← citeshttps://doi.org/10.15666/aeer/1504_20352044openalex-snapshot

THE COMPARISON OF TOTAL PHENOLIC CONTENT, ANTIOXIDANT CAPACITY AND MOLECULAR ANALYSIS OF SOME SELECTED TURKISH APPLE (MALUS SPP.) GENOTYPES

inferred← citeshttps://doi.org/10.1590/2175-7860201768348openalex-snapshot

Flora das cangas da Serra dos Carajás, Pará, Brasil: Santalaceae

inferred← citeshttps://doi.org/10.1590/2175-7860202172132openalex-snapshot

Synopsis of Dendrophthora and Phoradendron (Santalaceae) in Brazil

inferred← citeshttps://doi.org/10.3120/0024-9637-250033openalex-snapshot

PHORADENDRON TYPE MATERIAL IN THE UNIVERSITY AND JEPSON HERBARIA AT THE UNIVERSITY OF CALIFORNIA, BERKELEY

inferred← citeshttps://doi.org/10.3389/fpls.2023.1179009openalex-snapshot

Comparative analysis of chloroplast genomes of 29 tomato germplasms: genome structures, phylogenetic relationships, and adaptive evolution

inferred← citeshttps://doi.org/10.3389/fpls.2024.1498543openalex-snapshot

Complete chloroplast genome data reveal the existence of the Solidago canadensis L. complex and its potential introduction pathways into China

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