1999
DOI: 10.1520/jfs14551j
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A Time Course Study on STR Profiles Derived from Human Bone, Muscle and Bone Marrow

Abstract: The use of the polymerase chain reaction (PCR) to define deoxyribonucleic acid (DNA) types at several loci was investigated. PCR was used to amplify nine short tandem repeat (STR) loci along with the amelogenin locus on the X and Y chromosomes using the AmpF/STR Profiler Plus PCR amplification kit (Perkin Elmer). Rib bones were collected from 12 individuals. Five cm portions were buried at a depth of approximately 30 cm and 5 cm portions were left on the surface of the ground. Samples were exposed to the envir… Show more

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Cited by 3 publications
(3 citation statements)
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“…A differential extraction procedure (23) was used to isolate epithelial cell DNA and sperm cell DNA for these amplifications. Consistent with studies of different tissue types (24), no differences were noted between blood standard DNA profiles and the corresponding epithelial cell DNA profile defined by the AmpFᐉSTR Profiler Plus PCR Amplification Kit.…”
Section: Discussionsupporting
confidence: 80%
“…A differential extraction procedure (23) was used to isolate epithelial cell DNA and sperm cell DNA for these amplifications. Consistent with studies of different tissue types (24), no differences were noted between blood standard DNA profiles and the corresponding epithelial cell DNA profile defined by the AmpFᐉSTR Profiler Plus PCR Amplification Kit.…”
Section: Discussionsupporting
confidence: 80%
“…Polymerase chain reaction analysis of STR loci is a simple and accurate way to genotype individuals using a limited amount of DNA, 7,12,13 and laser‐based microdissection efficiently procures a pure target cell population 14 . Therefore, we were able to isolate neutrophils from histological sections of the placenta and successfully perform the genotypical analysis of those neutrophils from different anatomical compartments of the placenta.…”
Section: Discussionmentioning
confidence: 99%
“…BM may therefore be a relevant alternative tissue, especially when remains are skeletonized, bloodless or in extreme putrefaction. BM is already used in forensic science for genetic analysis [4], to estimate postmortem interval [5][6][7][8], in the diatom test for diagnosis of drowning [9,10] and in histopathology to establish certain malignancies postmortem [11][12][13]. In forensic toxicology, the first report of BM analysis was in 1943, to document the kinetics of alcohol [14].…”
Section: Introductionmentioning
confidence: 99%