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2011
DOI: 10.1016/j.ijpara.2011.03.008
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Phylogenetic and phylogeographic relationships in Ixodes holocyclus and Ixodes cornuatus (Acari: Ixodidae) inferred from COX1 and ITS2 sequences

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Cited by 65 publications
(57 citation statements)
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References 39 publications
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“…Sanger sequencing was performed in a 48 well plate with robotic instrumentation using T7 Transcription Start (5'-CTAATACGACTCACTATAGGG-3') universal sequencing primer (Promega, Madison, WI-USA). Samples were sequenced using an Applied Biosystems TM ABI 3730 DNA Analyzer and the conditions described by Song et al (2011). The sequencing reactions were done using the Big Dye  Terminator v3.1 cycle sequencing kit.…”
Section: Genetic Analysismentioning
confidence: 99%
See 1 more Smart Citation
“…Sanger sequencing was performed in a 48 well plate with robotic instrumentation using T7 Transcription Start (5'-CTAATACGACTCACTATAGGG-3') universal sequencing primer (Promega, Madison, WI-USA). Samples were sequenced using an Applied Biosystems TM ABI 3730 DNA Analyzer and the conditions described by Song et al (2011). The sequencing reactions were done using the Big Dye  Terminator v3.1 cycle sequencing kit.…”
Section: Genetic Analysismentioning
confidence: 99%
“…The internal transcribed spacer 2 (ITS-2) is located between the 5.8S and 28S ribosomal subunits of rDNA (CRUICKSHANK, 2002). These genes are arranged in repeated units known as ribosomal cistrons, which have repeated copies and have been used to study phylogenetic relationships (CAMPBELL et al, 1993;SONG et al, 2011;BURGER et al, 2014).…”
Section: Introductionmentioning
confidence: 99%
“…These include the second internal transcribed spacer region (ITS2) of the nuclear ribosomal gene cluster. Since the ITS2 region does not encode for proteins it is thought that it is under minimal selection pressure, which in turn allows for the accumulation of nucleotide substitutions (Barker, 1998;Coleman, 2003;Song et al, 2011). Thus, the genetic variation in this region may allow for the elucidation of evolutionary relationships within and between species.…”
Section: Introductionmentioning
confidence: 99%
“…The traditional morphology based identification is sometimes problematic due to variations caused by blood meal [17] and chances of geographical strains of tick species having different vectorial capacity [18][19][20], genetic introgression, fertile hybrids [21][22], and resistance to acaricides [23] are always there. During the past two decades several molecular markers have been used to resolve relationships and solve problems facing systematics of hard ticks in the family Ixodidae [24][25][26][27][28][29][30][31][32][33][34][35][36][37][38][39][40]. In this context, there is lack of any study on molecular analysis of hard ticks from the India [2,41].…”
Section: Introductionmentioning
confidence: 99%