Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Timo Sänger"'
Autor:
Walther Parson, Christina Amory, Turi King, Michaela Preick, Cordula Berger, Anna König, Gabriela Huber, Katja Anslinger, Birgit Bayer, Gottfried Weichhold, Timo Sänger, Sabine Lutz-Bonengel, Heidi Pfeiffer, Michael Hofreiter, Dietmar Pfründer, Carsten Hohoff, Bernd Brinkmann
Publikováno v:
iScience, Vol 27, Iss 9, Pp 110539- (2024)
Summary: Kaspar Hauser’s parentage has been the subject of research and debate for nearly 200 years. As for his possible aristocratic descent through the House of Baden, there is suspicion that he was swapped as a baby, kidnapped, and kept in isola
Externí odkaz:
https://doaj.org/article/e1f47a2019ef40049b9968848d7ba746
Autor:
Alexander Behnke, Anja Maria Gumpp, Roberto Rojas, Timo Sänger, Sabine Lutz-Bonengel, Dirk Moser, Gustav Schelling, Aniko Krumbholz, Iris-Tatjana Kolassa
Publikováno v:
The World Journal of Biological Psychiatry. 24:58-69
Major depressive disorder (MDD) involves peripheral low-grade pro-inflammatory activity. This multi-biomarker case-control study characterises the proinflammatory status in MDD beyond C-reactive protein (CRP) and Interleukin (IL)-6 levels through inv
Autor:
Matthias Schmuth, Sandra Carina Weiß, Thomas Liehr, Jana Naue, Stefan Pollak, Timo Sänger, Fengtang Yang, Jodi A. Irwin, Peter Lichter, Cordula Berger, Pidder Jansen-Dürr, Erica L. Romsos, Marianne Volleth, Thomas J. Parsons, René Pflugradt, Rafal Koziel, Christina Strobl, Sabine Lutz-Bonengel, Catarina Xavier, Gabriela Huber, Peter M. Vallone, Walther Parson, Harald Niederstätter, Gudrun Ratzinger
Publikováno v:
Nucleic Acids Research
The maternal mode of mitochondrial DNA (mtDNA) inheritance is central to human genetics. Recently, evidence for bi-parental inheritance of mtDNA was claimed for individuals of three pedigrees that suffered mitochondrial disorders. We sequenced mtDNA
Autor:
Sabine Lutz-Bonengel, Pernette J. Verschure, Timo Sänger, Jana Naue, Ate D. Kloosterman, Huub C. J. Hoefsloot
Publikováno v:
Forensic Science International. Genetics, 36, 152-159. Elsevier
The use of DNA methylation (DNAm) for chronological age determination has been widely investigated within the last few years for its application within the field of forensic genetics. The majority of forensic studies are based on blood, saliva, and b
Publikováno v:
Forensic science international. Genetics. 45
The analysis of hair samples is a common task in forensic investigations. Material transferred to the surface of a hair during a crime challenges the analysis as it has to be removed efficiently. However, the removal of the stain can also lead to a l
Publikováno v:
Forensic Science International: Genetics. 19:252-254
The "Dark Counts" were a mysterious couple that appeared in the Thuringian village Eishausen in 1807. After living in self imposed solitude for 30 years the woman died and was buried under the name Sophia Botta. Her companion, who presented himself a
Publikováno v:
Rechtsmedizin. 22:237-243
Eine erfolgreiche „Multiplex-short-tandem-repeat“(Multiplex-STR)-Typisierung wird durch den optimalen Einsatz an „Template“-DNA erleichtert. Die DNA-Konzentration kann mithilfe verschiedener Methoden bestimmt werden. In der vorgestellten Stud
Autor:
Timo Sänger, Wolf Rupp, Annette Thierauf, Markus Grosse Perdekamp, Susanne Vogt, Sabine Lutz-Bonengel
Publikováno v:
Forensic Science International. 214:e47-e50
Apart from collisions with road or rail vehicles and falls from height, self inflicted blunt force is a rare suicide method and mainly seen in psychiatric patients. The paper presents a rare case of suicide by active blunt force. A 68-year-old man co
Publikováno v:
International Journal of Legal Medicine. 125:427-436
Mitochondrial DNA analysis plays an important role in forensic science as well as in the diagnosis of mitochondrial diseases. The occurrence of two different nucleotides at the same sequence position can be caused either by heteroplasmy or by a mix o
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