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1 in the green lineage and FtsZA and FtsZB in red algae.
2 ations that characterize these multicellular red algae.
3 be regulated in mesophilic and thermophilic red algae.
4 the protein-bound form in cyanobacteria and red algae.
5 rters or their evolutionary histories in the red algae.
6 nd kelps, that possess plastids derived from red algae.
7 acteria, archaea, mitochondria of plants and red algae.
8 arvesting pigments in most cyanobacteria and red algae.
9 ondary metabolites of some edible species of red algae.
10 stem II (PS II) complex of cyanobacteria and red algae.
11 o been isolated from other species of marine red algae.
12 g complexes of cyanobacteria, cyanelles, and red algae.
13 ssible relationship between green plants and red algae.
14 ontain fossils of well-preserved bangiophyte red algae.
15 lutionary history of plasmid-derived DNAs in red algae.
16 argest subunit of RNA polymerase II from two red algae, a green alga and a relatively derived amoeboi
17 f the expected molecular weight in six other red algae (Achrochaetium, Bangia, Callithamnion, Cyanidi
18 urpureum suggests that ancestral lineages of red algae acted as mediators of horizontal gene transfer
19 a: 6 land plants, 2 green algae, a diatom, 2 red algae and a cryptophyte, the cyanelle of the glaucoc
20 gives insights into the metabolism of marine red algae and adaptations to the marine environment, inc
22 hosts feeding predominantly on polysiphonous red algae and brown Turbinaria algae, which contain diff
24 amples of transfer events to the ancestor of red algae and green plants that support a common origin
26 and land plants, inverted repeat regions in red algae and in Cyanophora show abundant differences am
27 peats in quite diverse proteins of green and red algae and in the cyanobacterium Microcoleus sp PCC 7
28 analyzing mitogenomes from type specimens of red algae and other morphologically simple organisms for
29 s elucidate the evolution of plasmid DNAs in red algae and suggest that they spread as parasitic gene
30 nt loss among green algae, as well as in the red algae and their secondary plastid derivatives (excep
31 utionary history of these traits, given that red algae and vascular plants probably diverged more tha
33 light-harvesting proteins in cyanobacteria, red algae, and cryptomonads, and the globins that functi
35 uman pathways and to the proteomes of yeast, red algae, and malaria reveals unanticipated evolutionar
36 se of a liverwort, a moss, several green and red algae, and Reclinomonas americana, an early-branchin
37 us of such organisms, including amoebozoans, red algae, and stramenopiles, seems preserved in a near-
38 ars are abundant polysaccharides from marine red algae, and their chemical structure consists of alte
39 ast genomes of diatoms, dinoflagellates, and red algae; and in the nuclear genome of Arabidopsis thal
41 her "crown" group in the eukaryote tree, (2) red algae are the closest relatives of animals, true fun
42 s, whereas parsimony puts them as sisters to red algae, but there is no reason to think that either p
44 t limited complete genome data available for red algae, currently only the highly reduced genome of C
45 ed by the nuclear and plastid genomes of the red algae Cyanidioschyzon merolae are nonfunctional in i
46 esponds to the polysaccharide porphyran from red algae, enabling growth on this carbohydrate but not
48 trate that this protein in the extremophilic red algae Galdieria sulphuraria and Cyanidioschyzon mero
49 structures of nitrosylated RuBisCO from the red algae Galdieria sulphuraria with O(2) and CO(2) boun
50 obiliproteins are employed by cyanobacteria, red algae, glaucophytes, and cryptophytes for light-harv
51 Archaeplastida, consisting of glaucophytes, red algae, green algae, and land plants, share a common
54 important regulatory function in mesophilic red algae; however, in thermophilic red algae, this proc
55 These findings place fungi, protozoa, and red algae in a common lineage distinct from that of meta
56 , a pattern taken to an extreme in fungi and red algae, in which the CTD has undergone dramatic to co
61 common CCA genera and a crustose calcifying red algae, Peyssonnelia (collectively CCRA) from Califor
62 ta apo-subunit genes of R-phycoerythrin from red algae Polisiphonia boldii were cloned in plasmid pET
64 d 15 mitochondrial genomes attributed to the red algae Pyropia perforata, Py. fucicola, and Py. kanak
65 The finding of secondary walls and lignin in red algae raises many questions about the convergent or
70 romoperoxidase (V-BrPO) isolated from marine red algae (species of Laurencia, Plocamium, Corallina) c
71 nery that divides chloroplasts in plants and red algae, suggesting that these mechanisms are unique.
72 1,4-galactans found in the cell wall of some red algae that are practically valuable for their gelati
73 sophilic red algae; however, in thermophilic red algae, this process is replaced by nonphotochemical
74 A genes), we generated a robust phylogeny of red algae to provide an evolutionary timeline for florid
75 e majority of plasmid DNAs originated within red algae, whereas others were derived from cyanobacteri
76 onate nodules accreted by crustose coralline red algae which recently have been identified as useful
77 thrin is a major light-harvesting pigment of red algae, which could be used as a natural dye in foods
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