Fraunhofer-Gesellschaft

Publica

Hier finden Sie wissenschaftliche Publikationen aus den Fraunhofer-Instituten.
2019Adverse effects of long and straight multiwalled carbon nanotubes on cytoskeleton, nuclear lamina, and genome-wide transcriptome of primary human mesothelial cells
Reamon-Buettner, S.M.; Voepel, I.; Hiemisch, A.; Eckert, V.; Schaudien, D.; Ziemann, C.
Abstract
2019Transcriptomic Analysis Reveals Priming of The Host Antiviral Interferon Signaling Pathway by Bronchobini® Resulting in Balanced Immune Response to Rhinovirus Infection in Mouse Lung Tissue Slices
Reamon-Buettner, S.M.; Niehof, M.; Hirth, N.; Danov, O.; Obernolte, H.; Braun, A.; Warnecke, J.; Sewald, K.; Wronski, S.
Journal Article
2010Commentary on "Investigations of somatic NKX2-5 mutations in congenital heart disease (CHD)"
Reamon-Buettner, S.M.; Borlak, J.
Journal Article
2010NKX2-5: An update on this hypermutable homeodomain protein and its role in human congenital heart disease (CHD)
Reamon-Büttner, S.M.; Borlak, J.
Journal Article
2009A functional genetic study identifies HAND1 mutations in septation defects of the human heart
Reamon-Buettner, S.M.; Ciribilli, Y.; Traverso, I.; Kuhls, B.; Inga, A.; Borlak, J.
Journal Article
2008Epigenetic silencing of cell adhesion molecule 1 in different cancer progenitor cells of transgenic c-Myc and c-Raf mouse lung tumors
Reamon-Büttner, S.M.; Borlak, J.
Journal Article
2008A loss-of-function mutation in the binding domain of HAND1 predicts hypoplasia of the human hearts
Reamon-Büttner, S.M.; Ciribilli, Y.; Inga, A.; Borlak, J.
Journal Article
2008The next innovation cycle in toxicogenomics
Reamon-Büttner, S.M.; Mutschler, V.; Borlak, J.
Journal Article, Conference Paper
2007Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD)
Reamon-Buettner, S.M.; Cho, S.H.; Borlak, J.
Journal Article
2007A new paradigm in toxicology and teratology: Altering gene activity in the absence of DNA sequence variation
Reamon-Buettner, S.M.; Borlak, J.
Journal Article, Conference Paper
2006Bridging the gap between anatomy and molecular genetics for an improved understanding of congenital heart disease
Reamon-Buettner, S.M.; Spanel-Borowski, K.; Borlak, J.
Journal Article
2006HEY2 mutations in malformed hearts
Reamon-Buettner, S.M.; Borlak, J.
Journal Article
2006N-acetyltransferase 2 (NAT2) gene polymorphisms in Parkinson's disease
Borlak, J.; Reamon-Büttner, S.M.
Journal Article
2006Somatic mutations in cardiac malformations
Reamon-Büttner, S.M.; Borlak, J.
Journal Article
2005Functional dissection of sequence-specific NKX2-5 DNA binding domain mutations associated with human heart septation defects using a yeast-based system
Inga, A.; Reamon-Büttner, S.M.; Borlak, J.; Resnick, M.A.
Journal Article
2005GATA4 zinc finger mutations as a molecular rationale for septation defects of the human heart
Reamon-Buettner, S.M.; Borlak, J.
Journal Article
2005GATA4 zinc finger mutations as a molecular rationale for septation defects of the human heart.
Reamon-Buettner, S.M.; Borlak, J.
Journal Article
2005Genetic analysis of cardiac-specific transcription factors reveals novel insights into molecular causes of congenital heart disease
Reamon-Buettner, S.M.; Borlak, J.
Journal Article
2005Physical map of the Azoarcus sp. strain BH72 genome based on a bacterial artificial chromosome library as a platform for genome sequencing and functional analysis
Battistoni, F.; Bartels, D.; Kaiser, O.; Reamon-Buettner, S.M.; Hurek, T.; Reinhold-Hurek, B.
Journal Article
2004BAC-derived diagnostic markers for sex determination in asparagus
Jamsari, A.; Nitz, I.; Reamon-Büttner, S.M.; Jung, C.
Journal Article
2004Breakdown of transcription factor crosstalk in congenital heart disease
Borlak, J.; Reamon-Büttner, S.M.
Abstract
2004Genetic analysis of cardiac-specific transcription factors reveals insight into congenital heart disease
Reamon-Büttner, S.M.; Borlak, J.
Journal Article
2004Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations
Reamon-Büttner, S.M.; Hecker, H.; Spanel-Borowski, K.; Craatz, S.; Kuenzel, E.; Borlak, J.
Journal Article
2004Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease
Reamon-Büttner, S.M.; Borlak, J.
Journal Article
2004TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed heart
Reamon-Büttner, S.M.; Borlak, J.
Abstract