Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Marielle Heinrich"'
Autor:
Sabine Lutz-Bonengel, Timo Sänger, Marielle Heinrich, Ulrike Schmidt, Tina Braun, Pekka Saukko
Publikováno v:
International Journal of Legal Medicine. 123:413-418
Single-nucleotide extension is a widespread method for typing Y-chromosomal single-nucleotide polymorphisms. In our study, we validated a multiplex minisequencing assay in a reduced-volume and in a low-volume approach. A four-plex assay was performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7eab6925132285feae7fcad24bc1fff0
https://doi.org/10.1007/s00414-009-0358-3
https://doi.org/10.1007/s00414-009-0358-3
Publikováno v:
International Journal of Legal Medicine. 123:521-525
The aim of the present study was to examine an ultrasound-accelerated fixation technique that reduces the exposure time of the tissue to formaldehyde with respect to the analysis of nucleic acids. We extracted and analysed DNA and RNA from three seri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a386a68ee2d3b6e6216842224511573
https://doi.org/10.1007/s00414-009-0368-1
https://doi.org/10.1007/s00414-009-0368-1
Autor:
Stefan Pollak, Timo Sänger, Ulrike Schmidt, Sabine Lutz-Bonengel, Marielle Heinrich, Peter M. Schneider
Publikováno v:
International Journal of Legal Medicine. 122:315-321
The segregation of mitochondrial genomes and the inheritance of mitochondrial DNA are constant matters of debate. To obtain more information about this issue and to answer the question whether or not it is possible to distinguish mitochondrial DNA (m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23594250bea0285656dd108eff3cf4c7
https://doi.org/10.1007/s00414-008-0240-8
https://doi.org/10.1007/s00414-008-0240-8
Autor:
Sabine Lutz-Bonengel, Harald Niederstätter, Timo Sänger, Helena Müller, Marielle Heinrich, Walther Parson, Marie Follo, Joachim W. Ellwart, Ulrike Schmidt, Bernhard Bonengel
Publikováno v:
International Journal of Legal Medicine. 122:189-197
The nature of mitochondrial DNA heteroplasmy is still unclear. It could either be caused by two mitochondrial DNA (mtDNA) haplotypes coexisting within a single cell or by an admixture of homoplasmic cells, each of which contains only one type of mtDN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::618ab4355faec48d92cb177ed7c5ea50
https://doi.org/10.1007/s00414-007-0190-6
https://doi.org/10.1007/s00414-007-0190-6
Publikováno v:
Forensic Science International: Genetics. 1:163-169
Relative quantification of mRNA using quantitative real-time reverse transcription (RT)-PCR is a commonly used method for analysis and comparison of gene expression levels. This method requires a normalisation of data against expression levels of a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0837d350e8026814307959c43e85383f
https://doi.org/10.1016/j.fsigen.2007.01.002
https://doi.org/10.1016/j.fsigen.2007.01.002
Publikováno v:
International Journal of Legal Medicine. 121:136-142
Recently, several authors described the observation that RNA degradation does not correlate with the postmortem interval (PMI), but rather with other parameters like environmental impact and the circumstances of death. Therefore, the question arose i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b75ae89d3578966c9414ebf0f616007
https://doi.org/10.1007/s00414-006-0131-9
https://doi.org/10.1007/s00414-006-0131-9
Publikováno v:
International Journal of Legal Medicine. 121:68-73
Low volume (LV) amplification (1 microL) of nuclear DNA (nucDNA) on a chemically structured chip is an appropriate and highly sensitive method to simultaneously amplify amelogenin and 15 forensically relevant short tandem repeats (STR). In this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76a0429ba164322dff2fd77e0ea22f99
https://doi.org/10.1007/s00414-006-0125-7
https://doi.org/10.1007/s00414-006-0125-7
Autor:
Juan J. Sanchez, Bertrand Ludes, Bernardette Hoste, Conceiçao Vide, B. Mevåg, Berit Myhre Dupuy, Nathalie Siebert, Harald Niederstätter, Maria Brion, Niels Morling, Walther Parson, Carsten Hohoff, C.R. Thacker, Klaus Bender, Marielle Heinrich, Angel Carracedo
Publikováno v:
Forensic Science International. 153:103-108
A collaborative study was carried out by the European DNA Profiling Group (EDNAP) in order to evaluate the performance of Y-chromosome binary polymorphism analysis in different European laboratories. Four blood samples were sent to the laboratories,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::902f06c9be56c5f6a8e8e5da8564321e
https://doi.org/10.1016/j.forsciint.2005.06.002
https://doi.org/10.1016/j.forsciint.2005.06.002
Autor:
Sahar Elias, Carsten Hohoff, Micaela Poetsch, Sławomir Lewicki, Katja Anslinger, Tadeusz Dobosz, Manfred Kayser, Oscar Lao, R. Wegener, Beate Stradmann-Bellinghausen, Rüdiger Lessig, Agnieszka Maciejewska, Grazyna Bargel, Piotr Kuzniar, Lotte Henke, Arleta Lebioda, Jeanett Edelmann, Marielle Heinrich, Dorota Monies, Christa Augustin, Anna Jonkisz, Magdalena Zoledziewska, Rafał Płoski, Jürgen Henke, Ulrike Schmidt, Marcin Wozniak, Dagmar Schmid, Reinhard Szibor, Anett Illing, Lutz Roewer, Peter M. Schneider, Ryszard Pawłowski
Publikováno v:
Human Genetics, 117(5), 428-443. Springer-Verlag
To test for human population substructure and to investigate human population history we have analysed Y-chromosome diversity using seven microsatellites (Y-STRs) and ten binary markers (Y-SNPs) in samples from eight regionally distributed population
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aa3afdc7b135aafea374ce49db2d68a
https://doi.org/10.1007/s00439-005-1333-9
https://doi.org/10.1007/s00439-005-1333-9
Autor:
Marielle Heinrich, Benedikt Vennemann, T. Fracasso, Antje Koppelkamm, Ulrike Schmidt, Sabine Lutz-Bonengel
Publikováno v:
International journal of legal medicine. 124(5)
Gene expression analyses based on messenger RNA (mRNA) profiling require accurate data normalisation. When using endogenous reference genes, these have to be validated carefully. Therefore, we examined the transcript stability of 10 potential referen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::687509da0553603e847db9b91233775b
https://pubmed.ncbi.nlm.nih.gov/20300940
https://pubmed.ncbi.nlm.nih.gov/20300940