| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1014502603 |
| P356 | DOI | 10.1007/S11103-012-9884-3 |
| P698 | PubMed publication ID | 22442035 |
| P5875 | ResearchGate publication ID | 221970800 |
| P50 | author | Thomas Braukmann | Q83732544 |
| P2093 | author name string | Saša Stefanović | |
| P2860 | cites work | Mitochondrial DNA suggests at least 11 origins of parasitism in angiosperms and reveals genomic chimerism in parasitic plants | Q21283920 |
| Phylogenetic inference in Rafflesiales: the influence of rate heterogeneity and horizontal gene transfer | Q21283977 | ||
| Complete plastid genome sequences suggest strong selection for retention of photosynthetic genes in the parasitic plant genus Cuscuta | Q22065303 | ||
| Complete DNA sequences of the plastid genomes of two parasitic flowering plant species, Cuscuta reflexa and Cuscuta gronovii | Q22065304 | ||
| Functional Gene Losses Occur with Minimal Size Reduction in the Plastid Genome of the Parasitic Liverwort Aneura mirabilis | Q22066009 | ||
| Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns | Q22066341 | ||
| Evolution of the angiosperms: calibrating the family tree | Q24522462 | ||
| The complete nucleotide sequence of the tobacco chloroplast genome: its gene organization and expression. | Q24531822 | ||
| The chloroplast ycf3 and ycf4 open reading frames of Chlamydomonas reinhardtii are required for the accumulation of the photosystem I complex | Q24536010 | ||
| Confidence Limits on Phylogenies: an Approach using the Bootstrap | Q26778379 | ||
| MODELTEST: testing the model of DNA substitution | Q26778437 | ||
| Evolutionary trees from DNA sequences: A maximum likelihood approach | Q27860898 | ||
| Likelihood-based tests of topologies in phylogenetics | Q28214588 | ||
| Rampant gene loss in the underground orchid Rhizanthella gardneri highlights evolutionary constraints on plastid genomes | Q28743740 | ||
| The rbcL gene from the non-photosynthetic parasite Lathraea clandestina is not transcribed by a plastid-encoded RNA polymerase | Q77323784 | ||
| Evolution of mycoheterotrophy in plants: a phylogenetic perspective | Q83962304 | ||
| Delimitation of major lineages within Cuscuta subgenus Grammica (Convolvulaceae) using plastid and nuclear DNA sequences | Q84258981 | ||
| Rates of nucleotide substitution vary greatly among plant mitochondrial, chloroplast, and nuclear DNAs | Q28776549 | ||
| Floral Gigantism in Rafflesiaceae | Q29029752 | ||
| The evolutionary ecology of myco-heterotrophy | Q29544657 | ||
| CONSEL: for assessing the confidence of phylogenetic tree selection | Q29547244 | ||
| An approximately unbiased test of phylogenetic tree selection | Q29547508 | ||
| A new method for calculating evolutionary substitution rates | Q29615058 | ||
| Testing the phylogenetic position of a parasitic plant (Cuscuta, Convolvulaceae, asteridae): Bayesian inference and the parametric bootstrap on data drawn from three genomes | Q30972401 | ||
| Systematics and plastid genome evolution of the cryptically photosynthetic parasitic plant genus Cuscuta (Convolvulaceae). | Q33310212 | ||
| Complete chloroplast genome of Oncidium Gower Ramsey and evaluation of molecular markers for identification and breeding in Oncidiinae | Q33557740 | ||
| Phylogeny of Pyroleae (Ericaceae): implications for character evolution | Q33700714 | ||
| Contrasting modes and tempos of genome evolution in land plant organelles | Q33822384 | ||
| Brassicaceae phylogeny inferred from phytochrome A and ndhF sequence data: tribes and trichomes revisited | Q33919371 | ||
| Phylogeny of the parasitic plant family Orobanchaceae inferred from phytochrome A. | Q33923095 | ||
| Green plants that feed on fungi: facts and questions about mixotrophy | Q34015751 | ||
| Why do chloroplasts and mitochondria contain so many copies of their genome? | Q34050314 | ||
| The distribution and phylogenetic significance of a 50-kb chloroplast DNA inversion in the flowering plant family Leguminosae | Q34390386 | ||
| Why are plastid genomes retained in non-photosynthetic organisms? | Q34483447 | ||
| From chloroplasts to "cryptic" plastids: evolution of plastid genomes in parasitic plants. | Q34807488 | ||
| Loss of all plastid ndh genes in Gnetales and conifers: extent and evolutionary significance for the seed plant phylogeny. | Q34981489 | ||
| Rate accelerations in nuclear 18S rDNA of mycoheterotrophic and parasitic angiosperms | Q35175622 | ||
| Photosynthetic evolution in parasitic plants: insight from the chloroplast genome | Q35677635 | ||
| Protein transport in organelles: Dual targeting of proteins to mitochondria and chloroplasts | Q37383481 | ||
| Evolution of chlorophyll and bacteriochlorophyll: the problem of invariant sites in sequence analysis | Q37705639 | ||
| Plastid ndh genes in plant evolution | Q37759607 | ||
| The evolution of the plastid chromosome in land plants: gene content, gene order, gene function | Q37855690 | ||
| Alternate paths of evolution for the photosynthetic gene rbcL in four nonphotosynthetic species of Orobanche | Q42656340 | ||
| Substitution of the gene for chloroplast RPS16 was assisted by generation of a dual targeting signal. | Q45177774 | ||
| Extreme specificity in epiparasitic Monotropoideae (Ericaceae): widespread phylogenetic and geographical structure | Q46586213 | ||
| Recent loss of plastid-encoded ndh genes within Erodium (Geraniaceae). | Q47320795 | ||
| The effect of relaxed functional constraints on the photosynthetic gene rbcL in photosynthetic and nonphotosynthetic parasitic plants | Q48013990 | ||
| Structural analyses of plastid-derived 16S rRNAs in holoparasitic angiosperms | Q48047549 | ||
| Do nonasterid holoparasitic flowering plants have plastid genomes? | Q48047552 | ||
| The phytochrome gene family in grasses (Poaceae): a phylogeny and evidence that grasses have a subset of the loci found in dicot angiosperms | Q48059676 | ||
| Rapid evolution of the plastid translational apparatus in a nonphotosynthetic plant: loss or accelerated sequence evolution of tRNA and ribosomal protein genes | Q48154895 | ||
| The obligate root parasite Orobanche cumana exhibits several rbcL sequences | Q48277892 | ||
| Molecular evolution of rbcL in the mycoheterotrophic coralroot orchids (Corallorhiza Gagnebin, Orchidaceae). | Q50640559 | ||
| Toward Defining the Course of Evolution: Minimum Change for a Specific Tree Topology | Q56059375 | ||
| The Utility of atpB Gene Sequences in Resolving Phylogenetic Relationships: Comparison with rbcL and 18S Ribosomal DNA Sequences in the Lardizabalaceae | Q56191259 | ||
| Utility of 17 chloroplast genes for inferring the phylogeny of the basal angiosperms | Q73194415 | ||
| Stamen development in the Ericaceae. I. Anther wall, microsporogenesis, inversion, and appendages | Q74013679 | ||
| P433 | issue | 1-2 | |
| P921 | main subject | Myco-heterotrophy | Q2420488 |
| Ericaceae | Q975872 | ||
| P1104 | number of pages | 16 | |
| P304 | page(s) | 5-20 | |
| P577 | publication date | 2012-03-23 | |
| P1433 | published in | Plant Molecular Biology | Q15761850 |
| P1476 | title | Plastid genome evolution in mycoheterotrophic Ericaceae | |
| P478 | volume | 79 |
| Q42407141 | Comparative analysis of plastid genomes of non-photosynthetic Ericaceae and their photosynthetic relatives. |
| Q58692363 | Convergent Plastome Evolution and Gene Loss in Holoparasitic Lennoaceae |
| Q28603252 | Detecting and Characterizing the Highly Divergent Plastid Genome of the Nonphotosynthetic Parasitic Plant Hydnora visseri (Hydnoraceae) |
| Q46958771 | Disproportional plastome-wide increase of substitution rates and relaxed purifying selection in genes of carnivorous Lentibulariaceae |
| Q57898861 | Evolutionary reversion of editing sites of ndh genes suggests their origin in the Permian-Triassic, before the increase of atmospheric CO2 |
| Q64229848 | Extensive Losses of Photosynthesis Genes in the Plastome of a Mycoheterotrophic Orchid, Cyrtosia septentrionalis (Vanilloideae: Orchidaceae) |
| Q91811459 | Intraspecific Variation within the Utricularia amethystina Species Morphotypes Based on Chloroplast Genomes |
| Q35235397 | Investigating the path of plastid genome degradation in an early-transitional clade of heterotrophic orchids, and implications for heterotrophic angiosperms |
| Q35869681 | Massive intracellular gene transfer during plastid genome reduction in nongreen Orobanchaceae |
| Q34379074 | Mechanisms of functional and physical genome reduction in photosynthetic and nonphotosynthetic parasitic plants of the broomrape family |
| Q64065839 | Mitochondrial genome evolution in parasitic plants |
| Q36391156 | Mixotrophy in Pyroleae (Ericaceae) from Estonian boreal forests does not vary with light or tissue age. |
| Q46332750 | On the brink: the highly reduced plastomes of nonphotosynthetic Ericaceae. |
| Q34351963 | Parasitic plants have increased rates of molecular evolution across all three genomes |
| Q42168424 | Plastid genome evolution across the genus Cuscuta (Convolvulaceae): two clades within subgenus Grammica exhibit extensive gene loss |
| Q91421741 | Plastid phylogenomic insights into the evolution of Caryophyllales |
| Q52707926 | Plastid phylogenomics resolves infrafamilial relationships of the Styracaceae and sheds light on the backbone relationships of the Ericales. |
| Q34491497 | Plastome Evolution in Hemiparasitic Mistletoes |
| Q34399816 | Possible loss of the chloroplast genome in the parasitic flowering plant Rafflesia lagascae (Rafflesiaceae) |
| Q110445029 | Resurrection of the East Asian genusEremotropa(Monotropoideae, Ericaceae), based on molecular and morphological data |
| Q35838570 | Seven New Complete Plastome Sequences Reveal Rampant Independent Loss of the ndh Gene Family across Orchids and Associated Instability of the Inverted Repeat/Small Single-Copy Region Boundaries |
| Q47865630 | The elusive predisposition to mycoheterotrophy in Ericaceae |
| Q34549742 | The loss of photosynthetic pathways in the plastid and nuclear genomes of the non-photosynthetic mycoheterotrophic eudicot Monotropa hypopitys |
| Q41989922 | The rise of the photosynthetic rate when light intensity increases is delayed in ndh gene-defective tobacco at high but not at low CO2 concentrations |
| Q34534863 | Understanding the evolution of holoparasitic plants: the complete plastid genome of the holoparasite Cytinus hypocistis (Cytinaceae) |
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