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1 ionship between the alveolate ancestor and a red alga.
2 ate macrolides previously isolated from this red alga.
3 ars ago) secondary endosymbiosis involving a red alga.
4 ed from a putative host cell that engulfed a red alga.
5 ity in this phylogenetically distinct marine red alga.
6     These protists evolved from a progenitor red alga and synthesize an insoluble carbohydrate whose
7  fungal flavohemoglobins in many bacteria, a red alga, and a diatom.
8 , 2C, and 2D originated from the green alga, red alga, and eukaryotic host ancestral participants of
9 this work, low MW fractions derived from the red alga Botryocladia occidentalis sulfated galactan (Bo
10 osymbioses, beginning with the adoption of a red alga by cryptophytes, then a cryptophyte by the ance
11 l contain plastids derived from an ancestral red alga by secondary symbiosis.
12                       In this diatom and the red alga C. merolae, a greater proportion of TEs than ge
13 ls and lignin within cells of the intertidal red alga Calliarthron cheilosporioides.
14 8) were isolated from extracts of the Fijian red alga Callophycus serratus and identified with 1D and
15 0) were isolated from extracts of the Fijian red alga Callophycus serratus, and identified by NMR, X-
16 ls A-D (2-5) were discovered from the Fijian red alga Callophycus sp.
17 dy we examine the cuticular structure of the red alga Chondrus crispus (Irish Moss) using anatomical
18                          The carrageenophyte red alga Chondrus crispus produces three family 16 glyco
19          The photosynthetic apparatus of the red alga Cyanidioschyzon merolae represents an intermedi
20 SI-LHCI) supercomplex from the extremophilic red alga Cyanidioschyzon merolae represents an intermedi
21 haracterized the splicing machinery from the red alga Cyanidioschyzon merolae, which has been reporte
22 l characterization of glycoproteins from the red alga Cyanidioschyzon merolae.
23 f the unicellular, obligate photoautotrophic red alga Cyanidioschyzon merolae.
24  separate guanylyltransferase encoded by the red alga Cyanidioschyzon merolae.
25 itis elegans, Drosophila melanogaster, and a red alga (Cyanidioschyzon merolae 10D) did not reveal th
26 o phycobilisome mobility in the thermophilic red alga Cyanidium caldarium that was not caused by a de
27 n the nuclear genomes of both a diatom and a red alga encoding a signal for import into the plastid,
28 containing pigments from a Jurassic putative red alga, from samples of less than 50 mug using microcr
29 cation of two loliolide derivatives from the red alga Galaxaura filamentosa and two acetylated diterp
30           The thermo-acidophilic unicellular red alga Galdieria sulphuraria represents a particularly
31 HCI) was isolated from the thermoacidophilic red alga Galdieria sulphuraria, and its structure, compo
32 robial eukaryotes, such as the extremophilic red alga Galdieria sulphuraria, live in hot, toxic metal
33  decreased by 75% in plasma membranes of the red alga Galdieria sulphuraria.
34 l characterization of two proteases from the red alga Gracilaria edulis.
35  was isolated from an aqueous extract of the red alga Griffithsia sp.
36 e from a single secondary endosymbiosis of a red alga in the "chromalveloate" hypothesis.
37 ided fractionation of extracts from a Fijian red alga in the genus Callophycus resulted in the isolat
38 with potential bioactive compounds from this red alga, increasing the efficiency of this drying metho
39 lso purified from a second benthic Antarctic red alga, Iridaea cordata.
40 olyether triterpenes) were isolated from the red alga Laurencia viridis.
41 a-porphyranase activity in a carrageenophyte red alga may provide defense against red algal pathogens
42  in Cyanidioschizon merolae-an extremophilic red alga of increasing importance as a new model organis
43  enzymatic digestion of the cell wall of the red alga P. umbilicalis.
44 pane ring have been isolated from the marine red alga Peyssonnelia sp. Combination of a wide array of
45  from the brown alga Odontella sinensis, the red alga Porphyra purpurea, and the cyanobacterium Synec
46 he cyanobacterium Synechocystis spp. and the red alga Porphyra purpurea, which together define a new
47  membranes from the phycobilisome-containing red alga Porphyridium cruentum were isolated from cells
48 mproved genome assembly from the unicellular red alga Porphyridium purpureum with a diverse collectio
49 le light-harvesting protein (LHCaR1), from a red alga (Porphyridium cruentum), that normally has eigh
50 nome sequence from a mesophilic, unicellular red alga, Porphyridium purpureum.
51 gen-swapped isomer iso-halomon (1b) from the red alga, Portieria hornemannii, and callophycols A (3)
52                         Gracilaria edulis, a red alga present in southeast coast of India was evaluat
53         Chemical investigation of the marine red alga (Rhodophyta) Ceratodictyon spongiosum containin
54 nalysis of phycobilisome dynamics in several red alga strains and compared these results with the pre
55 ycobilisome mobility in two model mesophilic red alga strains, Porphyridium cruentum and Rhodella vio
56 ts niche deeper in the water column than the red alga that has the typical R-phycoerythrin.
57 evolutionary scenario involving an ancestral red alga that was driven by early ecological forces to l
58                                         This red alga thrives autotrophically as well as heterotrophi
59                 Chondrus crispus is a marine red alga with sulfated galactans, called carrageenans, i
60 ve successfully transformed an exthemophilic red alga with the chloramphenicol acetyltransferase gene
61 ve successfully transformed an exthemophilic red alga with the chloramphenicol acetyltransferase gene