1993
DOI: 10.1016/0001-706x(93)90079-q
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Nuclear and mitochondrial genetic markers highly conserved between Chinese and Philippine Schistosoma japonicum

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Cited by 213 publications
(125 citation statements)
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“…cox1 Sequences have been widely used to define species limits and phylogenetic affinities in the platyhelminthes (Bowles et al 1993(Bowles et al , 1995Bowles and McManus 1994;Iwagami et al 2000Iwagami et al , 2003Morgan et al 2003;Razo-Mendivil et al 2004; nevertheless, most of those studies used a region of the cox1 that overlaps only in a short fragment at the 5 0 end of the standard barcode. The generation of primers that amplify the standard barcode region for a wide variety of platyhelminth groups has been a challenge (Moszczynska et al 2009), and is still at the experimental stage.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…cox1 Sequences have been widely used to define species limits and phylogenetic affinities in the platyhelminthes (Bowles et al 1993(Bowles et al , 1995Bowles and McManus 1994;Iwagami et al 2000Iwagami et al , 2003Morgan et al 2003;Razo-Mendivil et al 2004; nevertheless, most of those studies used a region of the cox1 that overlaps only in a short fragment at the 5 0 end of the standard barcode. The generation of primers that amplify the standard barcode region for a wide variety of platyhelminth groups has been a challenge (Moszczynska et al 2009), and is still at the experimental stage.…”
Section: Discussionmentioning
confidence: 99%
“…Amplification and sequencing were performed using the primers JB3 5 0 -TTTTT-TGGG CATCCTGAGGTTTAT-3 0 (forward) and JB4.5 5 0 -TAAAGAAAGAACATAATG AAAATG-3 0 (reverse) (Bowles et al 1993 Note: Minimum and maximum values are shown for groups with multiple sequences and intraspecific variation. O, Oaxaca; V, Veracruz; C, Colima; P, Puebla; and JO, Jalisco-Oaxaca.…”
Section: Laboratory Methodsmentioning
confidence: 99%
“…The cytochrome oxidase subunit 1 gene, or COI gene, of each individual was amplified using the JB3 (S'-TTTTTTGGGCATCCTGAGGTTTAT-3') of Bowles et al (1993) as the forward primer. The reverse primer used was trem.coxl.rrnl (S'AATCATGATGCAAAAGGTA-S') of Králová-Hromadová et al (2001).…”
Section: Methodsmentioning
confidence: 99%
“…For PCR-amplification we used three rDNA marker gene regions: 18S, 28S and internal transcribed spacer 2 (ITS2) and the mitochondrial cytochrome oxidase subunit 1 (CO1) region. Primers used for the respective gene region are detailed as follows: ITS2: 3S (Forward)/ A28 (Reverse) (Bowles et al, 1995) 18S: EukA (Forward)/ EukB (Reverse) (Diez et al, 2001) 28S: dig12 (Forward)/ 1500R (Reverse) (Tkach et al, 2000) mtCO1: JB3 (Forward)/ JB4.5 (Reverse) (Bowles et al, 1993). The thermal gradient of these marker regions started with an initial denaturation at 94 ºC (5min), annealing -for 18S at 58 ºC (1.10 min), 28S at 57 ºC (1 min), ITS2 at 57 ºC (1.10 min) and CO1 at 56 ºC (1.10 min), and final extension at 72 ºC (10 min).…”
Section: Molecular Studymentioning
confidence: 99%