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FabElm_BarcodeDb: matK barcode database of legumes
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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.1537-2197.1994.tb15615.xopenalex-snapshot
Chloroplast DNA Systematics: A Review of Methods and Data Analysis
inferredcites →https://doi.org/10.1006/bojl.2000.0380openalex-snapshot
Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences
inferredcites →https://doi.org/10.1007/bf00355398openalex-snapshot
The chloroplast tRNALys(UUU) gene from mustard (Sinapis alba) contains a class II intron potentially coding for a maturase-related polypeptide
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/j.mito.2014.05.008openalex-snapshot
Comparative analysis of 11 Brassicales mitochondrial genomes and the mitochondrial transcriptome of Brassica oleracea
inferredcites →https://doi.org/10.1016/j.ympev.2006.06.017openalex-snapshot
Phylogenetic utility of rapidly evolving DNA at high taxonomical levels: Contrasting matK, trnT-F, and rbcL in basal angiosperms
inferredcites →https://doi.org/10.1043/0363-6445-26.3.515openalex-snapshot
rbcL and Legume Phylogeny, with Particular Reference to Phaseoleae, Millettieae, and Allies
inferredcites →https://doi.org/10.1073/pnas.042694899openalex-snapshot
Punctuated evolution of mitochondrial gene content: High and variable rates of mitochondrial gene loss and transfer to the nucleus during angiosperm evolution
inferredcites →https://doi.org/10.1073/pnas.0905845106openalex-snapshot
A DNA barcode for land plants
inferredcites →https://doi.org/10.1073/pnas.89.22.10648openalex-snapshot
Function and evolution of a minimal plastid genome from a nonphotosynthetic parasitic plant.
inferredcites →https://doi.org/10.1073/pnas.92.7.2647openalex-snapshot
Chloroplast gene sequence data suggest a single origin of the predisposition for symbiotic nitrogen fixation in angiosperms.
inferredcites →https://doi.org/10.1093/aob/mch042openalex-snapshot
Phylogeny of Valerianaceae based on matK and ITS markers, with reference to matK individual polymorphism
inferredcites →https://doi.org/10.1093/molbev/msk018openalex-snapshot
The Chloroplast Genome Sequence of Chara vulgaris Sheds New Light into the Closest Green Algal Relatives of Land Plants
inferredcites →https://doi.org/10.1093/molbev/msr028openalex-snapshot
Rampant Gene Loss in the Underground Orchid Rhizanthella gardneri Highlights Evolutionary Constraints on Plastid Genomes
inferredcites →https://doi.org/10.1093/molbev/mst197openalex-snapshot
MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0
inferredcites →https://doi.org/10.1093/molbev/msw054openalex-snapshot
MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets
inferredcites →https://doi.org/10.1093/nar/gkg155openalex-snapshot
The complete nucleotide sequence of the hornwort (Anthoceros formosae) chloroplast genome: insight into the earliest land plants
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/nar/gkr319openalex-snapshot
psRNATarget: a plant small RNA target analysis server
inferredcites →https://doi.org/10.1093/sysbio/46.3.537openalex-snapshot
Trees within Trees: Genes and Species, Molecules and Morphology
inferredcites →https://doi.org/10.1104/pp.106.079855openalex-snapshot
Plastid Cues Posttranscriptionally Regulate the Accumulation of Key Enzymes of the Methylerythritol Phosphate Pathway in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.034454openalex-snapshot
RNA Immunoprecipitation and Microarray Analysis Show a Chloroplast Pentatricopeptide Repeat Protein to Be Associated with the 5′ Region of mRNAs Whose Translation It Activates
inferredcites →https://doi.org/10.1105/tpc.16.00398openalex-snapshot
The Reverse Transcriptase/RNA Maturase Protein MatR Is Required for the Splicing of Various Group II Introns in Brassicaceae Mitochondria
inferredcites →https://doi.org/10.1139/b96-017openalex-snapshot
Application of the matK gene sequences to grass systematics
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112242openalex-snapshot
Chloroplast RNA Metabolism
inferredcites →https://doi.org/10.1186/1471-2229-7-45openalex-snapshot
Complete DNA sequences of the plastid genomes of two parasitic flowering plant species, Cuscuta reflexa and Cuscuta gronovii
inferredcites →https://doi.org/10.1261/rna.032623.112openalex-snapshot
A short PPR protein required for the splicing of specific group II introns in angiosperm chloroplasts
inferredcites →https://doi.org/10.1371/journal.pone.0005982openalex-snapshot
Parallel Loss of Plastid Introns and Their Maturase in the Genus Cuscuta
inferredcites →https://doi.org/10.21921/jas.v3i2.11277openalex-snapshot
Smart Way to Nutritional Security in India
inferredcites →https://doi.org/10.2307/1223706openalex-snapshot
Phylogenetic relationships in Polygalaceae based on plastid DNA sequences from the trnL‐F region
inferredcites →https://doi.org/10.2307/2399846openalex-snapshot
Phylogenetics of Seed Plants: An Analysis of Nucleotide Sequences from the Plastid Gene rbcL
inferredcites →https://doi.org/10.2307/2419717openalex-snapshot
Phylogenetic Analyses of Polemoniaceae Using Nucleotide Sequences of the Plastid Gene matK
inferredcites →https://doi.org/10.2307/2419718openalex-snapshot
matK DNA Sequences and Phylogenetic Reconstruction in Saxifragaceae s. str.
inferredcites →https://doi.org/10.2307/2656837openalex-snapshot
Subtribal and generic relationships of Maxillarieae (Orchidaceae) with emphasis on Stanhopeinae: combined molecular evidence
inferredcites →https://doi.org/10.2307/4119796openalex-snapshot
Phytochemical Ecology, Phytochemical Society Symposia Series no. 8
inferredcites →https://doi.org/10.3732/ajb.90.12.1758openalex-snapshot
Angiosperm phylogeny based on <011>mat K sequence information
inferredcites →https://doi.org/10.3732/ajb.91.11.1846openalex-snapshot
A phylogeny of legumes (Leguminosae) based on analysis of the plastid mat K gene resolves many well‐supported subclades within the family
inferredcites →https://doi.org/10.3732/ajb.91.5.707openalex-snapshot
Molecular and cytological examination of Calopogon (Orchidaceae, Epidendroideae): circumscription, phylogeny, polyploidy, and possible hybrid speciation
inferredcites →https://doi.org/10.3732/ajb.91.6.997openalex-snapshot
Amborella not a “basal angiosperm”? Not so fast
inferredcites →https://doi.org/10.3732/ajb.94.8.1402openalex-snapshot
Expression of matK: functional and evolutionary implications
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s00425-022-03923-1openalex-snapshot
Orphan legumes: harnessing their potential for food, nutritional and health security through genetic approaches
inferred← citeshttps://doi.org/10.1007/s00425-024-04420-3openalex-snapshot
Mfind: a tool for DNA barcode analysis in angiosperms and its relationship with microsatellites using a sliding window algorithm
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