Search Results - "Taralczak, Malgorzata"

Oxaloacetate decarboxylase of Vibrio cholerae: purification, characterization, and expression of the genes in Escherichia coli by DAHINDEN, Pius, AUCHLI, Yolanda, GRANJON, Thierry, TARALCZAK, Malgorzata, WILD, Markus, DIMROTH, Peter

“…The oxaloacetate decarboxylase (OAD) Na(+) pump consists of subunits alpha, beta, and gamma, which are expressed from an oadGAB gene cluster present in various…”
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Genome-wide non-invasive prenatal testing in single- and multiple-pregnancies at any risk: Identification of maternal polymorphisms to reduce the number of unnecessary invasive confirmation testing by Oneda, Beatrice, Sirleto, Pietro, Baldinger, Rosa, Taralczak, Malgorzata, Joset, Pascal, Zweier, Markus, Niedrist, Dunja, Azzarello-Burri, Silvia, Britschgi, Christian, Breymann, Christian, Ochsenbein-Kölble, Nicole, Burkhardt, Tilo, Wisser, Josef, Zimmermann, Roland, Steindl, Katharina, Rauch, Anita

“…Non-invasive prenatal testing by targeted or genome-wide copy number profiling (cnNIPT) has the potential to outperform standard NIPT targeting the common…”
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Noninvasive prenatal testing: more caution in counseling is needed in high risk pregnancies with ultrasound abnormalities by Oneda, Beatrice, Steindl, Katharina, Masood, Rahim, Reshetnikova, Irina, Krejci, Pavel, Baldinger, Rosa, Reissmann, Regina, Taralczak, Malgorzata, Guetg, Adriano, Wisser, Josef, Fauchère, Jean-Claude, Rauch, Anita

“…Abstract Objective Non-invasive prenatal testing (NIPT) is increasingly being used in prenatal aneuploidy screening. The objective of this study was to assess…”
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A novel PITX2 mutation and a polymorphism in a 5-generation family with Axenfeld-Rieger anomaly and coexisting Fuchs' endothelial dystrophy by Kniestedt, Christoph, Taralczak, Malgorzata, Thiel, Michael A, Stuermer, Joerg, Baumer, Alessandra, Gloor, Balder P

“…To investigate the clinical and genetic appearance of Axenfeld-Rieger anomaly or syndrome (ARAS) and Fuchs' endothelial dystrophy (FED) in a 5-generation…”
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Pre- and postnatal findings in trisomy 17 mosaicism by Utermann, Barbara, Riegel, Mariluce, Leistritz, Dru, Karall, Thomas, Wisser, Josef, Meisner, Lorraine, Fauth, Christine, Baldinger, Rosa, Johnson, Julie, Erdel, Martin, Taralczak, Malgorzata, Pauli, Richard M., Baumer, Alessandra, Schinzel, Albert, Kotzot, Dieter

“…Trisomy 17 mosaicism is one of the rarest autosomal trisomies in humans. Thus far, only 23 cases have been described, most of them detected prenatally. In only…”
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Oxaloacetate decarboxylase of Archaeaglobvs fulgidus: cloning of genes and expression in Escherichia coli by DAHINDEN, Pius, POS, Klaas M, TARALCZAK, Malgorzata, DIMROTH, Peter

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Oxaloacetate decarboxylase of Archaeoglobus fulgidus: cloning of genes and expression in Escherichia coli by Dahinden, Pius, Pos, Klaas M, Taralczak, Malgorzata, Dimroth, Peter

“…Archaeoglobus fulgidus harbors three consecutive and one distantly located gene with similarity to the oxaloacetate decarboxylase Na+ pump of Klebsiella…”
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