2002
DOI: 10.1642/0004-8038(2002)119[1114:amattc]2.0.co;2
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A Multifaceted Approach to the Characterization of an Intergeneric Hybrid Manakin (Pipridae) from Brazil

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Cited by 42 publications
(14 citation statements)
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“…The mitochondrial encoded cytochrome b and NADH dehydrogenase subunit 2 (ND2) were amplified for all ingroup and outgroup samples across all taxa and the mitochondrial encoded NADH dehydrogenase subunit 3 (ND3) gene was amplified from all ingroup and outgroup samples except for L. bugunorum. Conserved autosomal nuclear intron loci including introns from a magmas-like protein (12630), phosphotyrosyl phosphatase (14572), and myeloid leukemia factor 2 (23361) described in Backström et al [34], intron 5 from transforming growth factor β2 (TGFB2, [35]) and intron 5 from β-fibrinogen (Fib5, [36]) were also amplified. In cases where primers derived from the available literature failed to amplify all samples we constructed Liocichlaspecific internal primers based on sequence alignments from Liocichla and outgroup sequences.…”
Section: Sampling and Laboratory Methodsmentioning
confidence: 99%
“…The mitochondrial encoded cytochrome b and NADH dehydrogenase subunit 2 (ND2) were amplified for all ingroup and outgroup samples across all taxa and the mitochondrial encoded NADH dehydrogenase subunit 3 (ND3) gene was amplified from all ingroup and outgroup samples except for L. bugunorum. Conserved autosomal nuclear intron loci including introns from a magmas-like protein (12630), phosphotyrosyl phosphatase (14572), and myeloid leukemia factor 2 (23361) described in Backström et al [34], intron 5 from transforming growth factor β2 (TGFB2, [35]) and intron 5 from β-fibrinogen (Fib5, [36]) were also amplified. In cases where primers derived from the available literature failed to amplify all samples we constructed Liocichlaspecific internal primers based on sequence alignments from Liocichla and outgroup sequences.…”
Section: Sampling and Laboratory Methodsmentioning
confidence: 99%
“…H4a (Harshman, 1994), and nuclear intron β-fibrinogen 5 using primers FGB5 and FGB6 (Marini & Hackett, 2002) on an Applied Biosystems Thermal Cycler (model 2720) and resulting bands were visualized by gel electrophoresis on a 1% agarose/TAE gel. Cytochrome b and βfibrinogen intron 5 were sequenced from 64 samples we collected in the field, two samples from Mozambique, obtained from the Muséum National d'Histoire Naturelle (MNHN), and one sample from Mafia Island, Tanzania, obtained from ZMUC.…”
Section: Genetic Sampling and Analysismentioning
confidence: 99%
“…were used to amplify approximately half of the ND2 gene using primers L5758 and H6313 (Sorenson et al . 1999), and the complete β -fib5 with primers FIB5 and FIB6 (Marini & Hackett 2002). PCR products were purified using a QIAQuick PCR kit (Qiagen), and in the case of the mitochondrial product, used as template for direct sequencing using the same primers employed for amplification.…”
Section: Molecular Geneticsmentioning
confidence: 99%