1999
DOI: 10.2216/i0031-8884-38-6-496.1
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Phylogeny of the order Scytosiphonales (Phaeophyceae) based on DNA sequences of rbcL, partial rbcS, and partial LSU nrDNA

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Cited by 117 publications
(110 citation statements)
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“…still differs by only two bp from Korean P. latifolia. The two bp difference (-0.14%) can be due to isolation by distance and falls well within the intraspecific variation for this gene in brown algae (Kogame et al 1999, Cho et al 2003, Cho and Boo 2006. P. plantaginea (Roth) Greville (AF055410, Greenland) differs by 28 bp (1.91%) from both Hecatonema.…”
Section: Claveiformis Is Probablysupporting
confidence: 77%
“…still differs by only two bp from Korean P. latifolia. The two bp difference (-0.14%) can be due to isolation by distance and falls well within the intraspecific variation for this gene in brown algae (Kogame et al 1999, Cho et al 2003, Cho and Boo 2006. P. plantaginea (Roth) Greville (AF055410, Greenland) differs by 28 bp (1.91%) from both Hecatonema.…”
Section: Claveiformis Is Probablysupporting
confidence: 77%
“…The purified DNA was used as template DNA in a polymerase chain reaction (PCR) to amplify the ITS2 region, the partial rbcL-spacer-partial rbcS (rbcL-sp-S) region and the mitochondrion-encoded cox3 (cytochrome oxidase subunit 3) gene. Kogame et al, 1999; for reverse) for the rbcLsp-S region; CAF4A (5 0 -ATGTTTACTTGGTGRA GRGA-3 0 ; this study; for forward) and CAR4A (5 0 -CCCCACCARTAWATNGTNAG-3 0 ; this study; for reverse) for the cox3 gene. PCR and sequencing were carried out as described by Kogame et al (1999) except that the annealing temperature was 45 C for PCR of the cox3.…”
mentioning
confidence: 80%
“…Kogame et al, 1999; for reverse) for the rbcLsp-S region; CAF4A (5 0 -ATGTTTACTTGGTGRA GRGA-3 0 ; this study; for forward) and CAR4A (5 0 -CCCCACCARTAWATNGTNAG-3 0 ; this study; for reverse) for the cox3 gene. PCR and sequencing were carried out as described by Kogame et al (1999) except that the annealing temperature was 45 C for PCR of the cox3.…”
mentioning
confidence: 80%
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“…Culture conditions used were 5°C SD (short day, 8:16 h light:dark regime), 10°C SD, 10°C LD (long day, 16:8 h light:dark regime), 15°C SD, 15°C LD, 20°C SD, 20°C LD and 25°C LD, under 30-50 μmol m -2 s -1 . Total genomic DNA was extracted from cultured thalli and purified as previously described by Kogame et al (1999). The purified DNA was used as template DNA for PCR to amplify the rbcL and cox1 genes.…”
Section: Methodsmentioning
confidence: 99%