Search Results - "Wagner, Annett"

G-CSF and repeated spontaneous abortions: comparability of inclusion and exclusion criteria in existing RCT-studies by Santjohanser, Claudia, Wagner, Annett, Hirv, Kaimo

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Limited sensitivity of NGS-based detection of unbalanced products from reciprocal translocations inpolar bodies and blastocysts by Osetek, Katarzyna, Kotanidou, Alexandra, Harasim, Thomas, Wagner, Annett, Rost, Imma, Klein, Hanns-Georg

“…Numerous publications have demonstrated that preimplantation genetic diagnosis (PGD) increases the implantation rate and percentage of healthy newborns or at…”
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P-57 - Prenatalis® NIPT: accredited high resolution non-invasive prenatal testing by using massive parallel ultra- deep sequencing by Harasim, Thomas, Wagner, Annett, Rath, Sabine, Benhaqi, Petra, Kotanidou, Alexandra, Rost, Imma, Klein, Hanns-Georg

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Prenatalis® NIPT: accredited high resolution non-invasive prenatal testing by using massive parallel ultra- deep sequencing by Harasim, Thomas, Wagner, Annett, Rath, Sabine, Benhaqi, Petra, Kotanidou, Alexandra, Rost, Imma, Klein, Hanns-Georg

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Challenge-confirmed peanut allergy in older patients: Performance of skin tests, specific immunoglobulin E, and ara h 2 by Li, Philip H., Rutkowski, Krzysztof, Kennard, Lucinda, Sellaturay, Priya, Watts, Timothy J., Haque, Rubaiyat, Wagner, Annette

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Lessons From the EThIGII Trial: Proper Putative Benefit Assessment of Low-Molecular-Weight Heparin Treatment in M2/ANXA5 Haplotype Carriers by Rogenhofer, Nina, Markoff, Arseni, Wagner, Annett, Klein, Hanns-Georg, Petroff, David, Schleussner, Ekkehard, Thaler, Christian J

“…This study presents sample size considerations derived from the Efficacy of Thromboprophylaxis as an Intervention during Gravidity (EThIGII) trial…”
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DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion by Bartsch, Oliver, Nemecková, Michaela, Kocárek, Eduard, Wagner, Annett, Puchmajerová, Alena, Poppe, Maja, Ounap, Katrin, Goetz, Petr

“…DiGeorge anomaly/velocardiofacial syndrome (DG/VCFS) occurs with different deletion intervals on chromosomes 22q11, while the DiGeorge anomaly (with other…”
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FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy by Bartsch, O, Wagner, A, Hinkel, G K, Krebs, P, Stumm, M, Schmalenberger, B, Böhm, S, Balci, S, Majewski, F

“…Rubinstein-Taybi syndrome (RTS) is a dominant Mendelian disorder characterised by mental retardation, a typical facies, broad thumbs and short stature…”
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Interaction of Guanosine Nucleotides and Their Analogs with Elongation Factor Tu from Thermus thermophilus by Wagner, Annett, Simon, Iris, Sprinzl, Mathias, Goody, Roger S

“…Transient kinetic experiments on the interaction of nucleotide-free EF-Tu from Thermus thermophilus with nucleotides using intrinsic protein fluorescence,…”
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Site‐Directed Mutagenesis of Thermus thermophilus Elongation Factor Tu: Replacement of His85, Asp81 and Arg300 by Zeidler, Waltraud, Egle, Christian, Ribeiro, Sofia, Wagner, Annett, Katunin, Vladimir, Kreutzer, Roland, Rodnina, Marina, Wintermeyer, Wolfgang, Sprinzl, Mathias

“…His85 in Thermus thermophilus elongation factor Tu (EF‐Tu) was replaced by glutamine, leucine and glycine residues, leading to [H85Q]EF‐Tu, [H85L] EF‐Tu and…”
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Site-directed mutagenesis of Thermus thermophilus elongation factor Tu. Replacement of His85, Asp81 and Arg300 by Zeidler, W, Egle, C, Ribeiro, S, Wagner, A, Katunin, V, Kreutzer, R, Rodnina, M, Wintermeyer, W, Sprinzl, M

“…His85 in Thermus thermophilus elongation factor Tu (EF-Tu) was replaced by glutamine, leucine and glycine residues, leading to [H85Q]EF-Tu, [H85L] EF-Tu and…”
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Site‐Directed Mutagenesis of Thermus thermophilus Elongation Factor Tu by Zeidler, Waltraud, Egle, Christian, Ribeiro, Sofia, Wagner, Annett, Katunin, Vladimir, Kreutzer, Roland, Rodnina, Marina, Wintermeyer, Wolfgang, Sprinzl, Mathias

“…His85 in Thermus thermophilus elongation factor Tu (EF‐Tu) was replaced by glutamine, leucine and glycine residues, leading to [H85Q]EF‐Tu, [H85L] EF‐Tu and…”
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No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585 by Bartsch, Oliver, Wagner, Annett, Hinkel, Georg Klaus, Lichtner, Peter, Murken, Jan, Schuffenhauer, Simone

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