Zobrazeno 1 - 4
of 4
pro vyhledávání: '"René Pflugradt"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6883cbb0124ea728d7a8a3e9100f1f51
https://doi.org/10.1093/nar/gkaa1271
https://doi.org/10.1093/nar/gkaa1271
Autor:
Elizabeth Barrett, Bernd Brinkmann, Peter Forster, Susan M. R. Gurney, Sandra Schneider, Thomas Jansen, Anna Catharina Forster, René Pflugradt
Publikováno v:
International Journal of Legal Medicine. 124:617-622
Horse mtDNA profiling can be useful in forensic work investigating degraded samples, hair shafts or highly dilute samples. Degraded DNA often does not allow sequencing of fragments longer than 200 nucleotides. In this study we therefore search for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0ca4262ca4c9f962310dc88625c14b2
https://doi.org/10.1007/s00414-010-0506-9
https://doi.org/10.1007/s00414-010-0506-9
Publikováno v:
Mitochondrion. 11(2)
To investigate the set of mtDNA molecules contained in small biological structures, powerful techniques for separation are required. We tested flow cytometry (FCM 1 ), laser capture microdissection (LCM 2 ) and a method using optical tweezers (OT 3 )
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c22376d9cce27a905fec995061edc06
https://pubmed.ncbi.nlm.nih.gov/21147269
https://pubmed.ncbi.nlm.nih.gov/21147269
Autor:
Takaki Ishikawa, Michael Bohnert, Annette Thierauf, Hitoshi Maeda, René Pflugradt, Markus Grosse Perdekamp, Stefan Pollak
Publikováno v:
International journal of legal medicine. 124(5)
A sudden death due to hemothorax caused by spontaneous rupture of a congenital pulmonary arteriovenous malformation (AVM) is reported. A 44-year-old woman died unexpectedly with chest pain and dyspnea. The post-mortem examination revealed a massive r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91d37e2b9672e3897adb9224f62d7411
https://pubmed.ncbi.nlm.nih.gov/20039052
https://pubmed.ncbi.nlm.nih.gov/20039052