GATA4 zinc finger mutations as a molecular rationale for septation defects of the human heart

Por Reamon-Buettner, S, Borlak, J
Publicado em 2005

Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease

Por Reamon-Buettner, S, Borlak, J
Publicado em 2004

Somatic mutations in cardiac malformations

Por Reamon‐Buettner, S M, Borlak, J
Publicado em 2006

N-acetyltransferase 2 (NAT2) gene polymorphisms in Parkinson's disease

Por Borlak, Juergen, Reamon-Buettner, Stella Marie
Publicado em 2006

N-acetyltransferase 2 (NAT2) gene polymorphisms in colon and lung cancer patients

Por Borlak, Juergen, Reamon-Buettner, Stella Marie
Publicado em 2006

Dissecting Epigenetic Silencing Complexity in the Mouse Lung Cancer Suppressor Gene Cadm1

Por Reamon-Buettner, Stella Marie, Borlak, Juergen
Publicado em 2012

Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD)

Por Reamon-Buettner, Stella Marie, Cho, Si-Hyen, Borlak, Juergen
Publicado em 2007

Mechanisms underlying epigenetic and transcriptional heterogeneity in Chinese hamster ovary (CHO) cell lines

Por Veith, Nathalie, Ziehr, Holger, MacLeod, Roderick A. F., Reamon-Buettner, Stella Marie
Publicado no BMC Biotechnol (2016)

Transcriptional Defect of an Inherited NKX2-5 Haplotype Comprising a SNP, a Nonsynonymous and a Synonymous Mutation, Associated with Human Congenital Heart Disease

Por Reamon-Buettner, Stella Marie, Sattlegger, Evelyn, Ciribilli, Yari, Inga, Alberto, Wessel, Armin, Borlak, Jürgen
Publicado em 2013

Novel NKX2–5 Mutations in Diseased Heart Tissues of Patients with Cardiac Malformations

Por Reamon-Buettner, Stella Marie, Hecker, Hartmut, Spanel-Borowski, Katharina, Craatz, Steffen, Kuenzel, Eberhard, Borlak, Juergen
Publicado em 2004