Eva Wey
University of Zurich
5 Papers
44 Citations
Eva Wey is an academic researcher from University of Zurich. The author has contributed to research in topics: POU domain & Gene. The author has an hindex of 5, co-authored 5 publications.
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Papers
A human POU domain gene, mPOU, is expressed in developing brain and specific adult tissues.
TL;DR: mPOU is shown to bind to DNA sequences containing the octamer motif and other POU factor target sites, indicating that mPOU may regulate a distinct set of genes.
34
Quantitative 1-Step DNA Methylation Analysis with Native Genomic DNA as Template
Thomas von Kanel,Dominik Gerber,André Schaller,Alessandra Baumer,Eva Wey,Christopher B. Jackson,Franziska M. Gisler,Karl Heinimann,Sabina Gallati +8 more
TL;DR: The novel DNA methylation assay reduces both the hands-on time and errors caused by handling and pipetting and allows methylation analyses to be completed within 90 min after DNA extraction, which makes the assay well suited for diagnostic procedures as well as high-throughput analyses.
Mosaic imprinting defect in a patient with an almost typical expression of the Prader–Willi syndrome
Eva Wey,Deborah Bartholdi,Mariluce Riegel,Hülya Nazlican,Bernhard Horsthemke,Albert Schinzel,Alessandra Baumer +6 more
TL;DR: It is estimated that approximately 50% of the patient's blood cells have an imprinting defect and half of the cells are normal, which means that the proband has typical features of PWS.
25
Identification of Novel DNA Binding Sites Recognized by the Transcription Factor mPOU (POU6F1)
Eva Wey,Beat W. Schäfer +1 more
TL;DR: Novel DNA binding sites for the POU protein mPOU (POU6F1) are identified which contain two TAAT motifs either as palindromes or as direct repeats.
13
Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18
Ariana Kariminejad,Roxana Kariminejad,Azadeh Moshtagh,Maryam Zanganeh,Mohammad Hassan Kariminejad,Stefan Neuenschwander,Michal J. Okoniewski,Eva Wey,Albert Schinzel,Alessandra Baumer +9 more
TL;DR: It seems to be the first reported case with two opposite recombinant chromosomes that compensate each other and lead to segmental uniparental disomy for two segments on the chromosome, one maternal and the other paternal.