Search Results - "Petershofen, Eduard K"

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    In-frame triplet deletions in RHD alter the D antigen phenotype by Flegel, Willy A., Eicher, Nicole I., Doescher, Andrea, Hustinx, Hein, Gowland, Peter, Mansouri Taleghani, Behrouz, Petershofen, EduardK., Bauerfeind, Ursula, Ernst, Manfred, Von Zabern, Ingeborg, Schrezenmeier, Hubert, Wagner, Franz F.

    Published in Transfusion (Philadelphia, Pa.) (01-12-2006)
    “…BACKGROUND: The deletion of three adjacent nucleotides in an exon may cause the lack of a single amino acid, while the protein sequence remains otherwise…”
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    Journal Article
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    Platelet engraftment after allogenic stem cell transplantation is monitored by digital polymerase chain reaction without interference by platelet support by Doescher, Andrea, Casper, Jochen, Kraemer, Doris, Kapels, Hans-Hermann, Petershofen, Eduard K., Müller, Thomas H.

    Published in Experimental hematology (01-12-2018)
    “…•Cutoff value for quantification of platelets with digital polymerase chain reaction (ddPCR) was 1 platelet/nL.•Engraftment as determined by ddPCR was earlier…”
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    Evaluation of single-nucleotide polymorphisms as internal controls in prenatal diagnosis of fetal blood groups by Doescher, Andrea, Petershofen, Eduard K., Wagner, Franz F., Schunter, Markus, Müller, Thomas H.

    Published in Transfusion (Philadelphia, Pa.) (01-02-2013)
    “…BACKGROUND: Determination of fetal blood groups in maternal plasma samples critically depends on adequate amplification of fetal DNA. We evaluated the routine…”
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    Platelet recovery and survival measured in patients by quantitative polymerase chain reaction of mitochondrial DNA by Doescher, Andrea, Petershofen, Eduard K., Hertenstein, Bernd, Kraemer, Doris, Casper, Jochen, Schmidt, Jörg-Peter, Müller, Thomas H.

    Published in Transfusion (Philadelphia, Pa.) (01-01-2015)
    “…Background Mitochondrial (mt) DNA markers have been identified as potential targets for the quantification of endogenous and allogeneic platelets (PLTs) in the…”
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    Journal Article
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    Cost-efficient sequence-specific priming-polymerase chain reaction screening for blood donors with rare phenotypes by Wagner, Franz F., Bittner, Rita, Petershofen, Eduard K., Doescher, Andrea, Müller, Thomas H.

    Published in Transfusion (Philadelphia, Pa.) (01-06-2008)
    “…BACKGROUND: Transfusion support for patients with irregular antibodies to red blood cell (RBC) antigens of high frequency may be hampered by lack of…”
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    The Glass Slide Extraction System Snap Card Improves Non-Invasive Prenatal Genotyping in Pregnancies with Antibodies by Adamczyk, Thomasz, Doescher, Andrea, Haydock, Paul V., Aldrich, Russ, Petershofen, Eduard K., Müller, Thomas H.

    Published in Transfusion medicine and hemotherapy (01-11-2015)
    “…Background: Determination of fetal blood groups in maternal plasma samples critically depends on adequate pre-analytical steps for optimal amplification of…”
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    Journal Article
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    RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany by Döscher, Andrea, Vogt, Claudia, Bittner, Rita, Gerdes, Ingrid, Petershofen, Eduard K., Wagner, Franz F.

    Published in Transfusion (Philadelphia, Pa.) (01-09-2009)
    “…BACKGROUND: More than 170 weak or partial RHD alleles are currently known. A similar heterogeneity of RHCE alleles may be anticipated, but a large‐scale…”
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    Weak D type 1.1 exemplifies another complexity in weak D genotyping by Doescher, Andrea, Flegel, Willy A., Petershofen, Eduard K., Bauerfeind, Ursula, Wagner, Franz F.

    Published in Transfusion (Philadelphia, Pa.) (01-10-2005)
    “…BACKGROUND: Weak D expression is caused by a large number of RHD alleles. Increasingly recommendations for D+ or D– transfusions are based on polymerase chain…”
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    Journal Article
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