Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Ines Plate"'
Autor:
Jeanett Edelmann, Ines Plate, Sandra Hering, Reinhard Szibor, Tanja Hundertmark, Christa Augustin
Publikováno v:
International Journal of Legal Medicine. 122:489-492
The evaluation of four pairs of tightly linked chromosome X (ChrX) short tandem repeat (STR)s at Xp22, Xq12, Xq26 and Xq28 led to the creation of the Argus X 8 multiplex amplification kit. These eight STRs are distributed as four closely linked pairs
Autor:
Jeanett Edelmann, Susanne Demberger, Ines Plate, Eberhard Kuhlisch, Michael Krawczak, Reinhard Szibor, Sandra Hering
Publikováno v:
International Journal of Legal Medicine. 119:363-369
Short tandem repeat (STR) markers DXS6801 (GATA41B11), DXS6809 (GATA69B129) and DXS6789 (GATA31F01) are located in a 3-Mb region on human chromosome Xq21, spanning approximately 3-6 cM. Theoretically, this cluster could give rise to 1,144 different h
Autor:
Peter Wiegand, Jeanett Edelmann, Lutz Roewer, Matthias Michael, H. Wittig, Ines Plate, Valentino Romano, Reinhard Szibor, Sandra Hering, Francesco Calì
Publikováno v:
Forensic Science International. 138:37-43
The incorporation of reference DNA is crucial to the validation of any DNA typing protocol. This paper aims to provide a panel of reference DNAs for actual forensic profiling strategies, i.e. autosomal and gonosomal STR typing as well as mtDNA sequen
Autor:
Reinhard Szibor, Sandra Hering, Matthias Michael, D. Krause, Jeanett Edelmann, Ines Plate, Eberhard Kuhlisch
Publikováno v:
International Congress Series. 1239:815-820
This paper presents an example of deficiency paternity testing by using 15 chromosome X (ChrX) markers. The special power of ChrX typing in deficiency kinship testing is demonstrated. In the case of investigation, ChrX haplotyping confirmed the claim
Autor:
Matthias Michael, Edelman J, Sandra Hering, Rüdiger Lessig, Reinhard Szibor, Deischel D, Meier-Sundhausen G, Lutz Roewer, Ines Plate
Publikováno v:
Forensic Science International. 124:215-218
Allele frequencies for 16 X-linked STRs, suitable for forensic purposes, were obtained from a sample of unrelated German individuals (male and female), The presented data show also repeat sequence structures and statistic parameters describing there
Publikováno v:
Forensic Science International. 113:71-78
The paper presents results of forensic mitochondrial DNA analyses which were aimed at typing the traces caused by touching or abrasion of skin cells. Five cases of strangulation tool investigation are summarised. Two cases of homicide could be cleare
Publikováno v:
International journal of legal medicine. 120(6)
At the forensic autopsy of a sexual murder victim, some trace hairs, possibly belonging to the perpetrator, were saved. Initially, the analysis of a pubic hair shaft only revealed the presence of the mitochondrial (mt) DNA haplotype profile consistin
Autor:
Ines Plate, H. Wittig, Mathias Michael, Reinhard Szibor, Marielle Heinrich, Sabine Lutz-Bonengel, R. Schöning
Publikováno v:
International journal of legal medicine. 121(3)
Sequence analysis of the human mitochondrial genome (mtDNA) has proven to be a valuable tool in forensic identity testing and the analysis of crime scene stains. In contrast to the very expensive sequencing technique, typing of different length varia
Autor:
Reinhard Szibor, Sandra Hering, Nicola Brundirs, Pham Hung Van, Matthias Michael, Jeanett Edelmann, Mark Benecke, Eberhard Kuhlisch, Ines Plate
Publikováno v:
International journal of legal medicine. 118(6)
The hypervariable tetranucleotide STR polymorphism DXS10011 is a powerful marker for forensic purposes. Investigation of this STR led to an allele nomenclature which is in consensus with the ISFG recommendations. DXS10011 is located at Xq28 and genet
Publikováno v:
International journal of legal medicine. 117(4)
This paper presents sequence and population genetic data of the microsatellite marker DXS6809 (GDB 365492) obtained from a German population sample ( n=725 chromosomes). DXS6809 is a highly polymorphic X-linked tetranucleotide polymorphism presenting