Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Beate Stradmann-Bellinghausen"'
„Es ist schon eine Crux mit den Medizindoktoranden. Da kommen sie in Deine Sprechstunde, machen Dir schöne Augen - und wollen doch nur später mal das Dr. med. auf ihrem Praxisschild. Was hat das mit Wissenschaft zu tun? Gar nichts.“ Schreibt Pr
Autor:
Helle Smidt Mogensen, M. Briōn, Denise Syndercombe-Court, Jodi A. Irwin, J. N. Butler, Angel Carracedo, Klaus Bender, H. Schmitter, Thomas J. Parsons, E. Ramos-Luis, L.A. Dixon, E. Petkovski, Paula Sánchez-Diz, A.E. Dobbins, Peter M. Vallone, Peter Gill, Walther Parson, Burkhard Berger, H.K. Pulker, Beate Stradmann-Bellinghausen, Kristian Nielsen, Niels Morling, Rebecca S. Just, Odile Loreille, Michael D. Coble, Juan J. Sanchez, Petra Grubwieser
Publikováno v:
Forensic Science International. 164:33-44
Recently, there has been much debate about what kinds of genetic markers should be implemented as new core loci that constitute national DNA databases. The choices lie between conventional STRs, ranging in size from 100 to 450 bp; mini-STRs, with amp
Autor:
Alejandro Blanco-Verea, Beate Stradmann-Bellinghausen, Juan J. Sanchez, Kinga Balogh, Maria Brion, Claus Børsting, Niels Morling, Peter M. Schneider, Denise Syndercombe-Court, Angel Carracedo, C.R. Thacker, Magdalena Bogus
Publikováno v:
ELECTROPHORESIS. 26:4411-4420
The European Consortium "High-throughput analysis of single nucleotide polymorphisms for the forensic identification of persons--SNPforID", has performed a selection of candidate Y-chromosome single nucleotide polymorphisms (SNPs) for making inferenc
Autor:
Peter M. Schneider, Liza P. Faustino, Beate Stradmann-Bellinghausen, Maria Corazon A. De Ungria, Kristina A. Tabbada, Despina Athanasiadou
Publikováno v:
Forensic Science International. 154:173-180
Quadruplex and pentaplex systems for polymerase chain reaction amplification of X-chromosomal short tandem repeats DXS101, HPRTB, DXS8377, DXS981 (STRX1) and DXS6789 were developed for automated profiling of liquid and membrane-bound DNA samples. Chi
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
Autor:
N. Winkelmann, J. Lummer, Peter M. Schneider, Sebastian Kreiter, G. Derigs, Ch. Rittner, Karin Kolbe, Beate Stradmann-Bellinghausen
Publikováno v:
International Congress Series. 1239:653-656
1. IntroductionEngraftment of donor stem cells after allogeneic bone marrow transplantation can begenetically monitored by PCR typing of DNA polymorphisms [1]. Successful engraftmentwith complete chimerism and presence of the donor’s genotype in th
Publikováno v:
International Congress Series. 1239:283-286
1. IntroductionThe study of Y chromosomal haplotypes and their relationship to human evolution andvariation is increasing rapidly in the fields of anthropology and forensic genetics.Although autosomal STRs are commonly used and very informative for p
Publikováno v:
International Congress Series. 1239:311-314
Short tandem repeat systems on the X chromosome are the natural counterpart to the well-established Y-chromosomal STR loci. The X-linked systems are inherited as a single haplotype only in males, whereas in females, the X chromosomes recombine and ex
Autor:
Christian Rittner, Roland Sänger, Roland Starke, Thomas Höhler, Anja Victor, Beate Stradmann-Bellinghausen, Peter M. Schneider
Publikováno v:
Journal of Hepatology. 37:387-392
Hepatitis B vaccination failure has been linked to the presence of certain human leukocyte antigen class II alleles. However, the functional background of these associations has remained unclear. Complement component C 4 is encoded within the major h
Autor:
Beate Stradmann-Bellinghausen, Constanze Steinhauer, K. Witzel-Schlömp, Peter M. Schneider, Christian Rittner
Publikováno v:
Experimental and Clinical Immunogenetics. 18:130-134
The fourth component of complement (C4) is coded for by two tandem-duplicated genes located in the class III region of the MHC of humans as well as a number of primates. A C4 gene size polymorphism giving rise to two gene variants of 16 and 22.3 kb l