Maternal microchimeric cell trafficking and its biological consequences depend on the onset of inflammation at the feto-maternal interface
Emiel Slaats(Medical University of Graz), Thomas Kroneis(Medical University of Graz), Katja Sallinger(Medical University of Graz), Rachel C. Quilang(University of Leeds), Michael Eikmans(Leiden University Medical Center), Kristine J. Chua(University of Notre Dame), Bernadette Bramreiter(Medical University of Graz)
Cited by 3
Related Papers
In Situ Detection and Quantification of AR-V7, AR-FL, PSA, and KRAS Point Mutations in Circulating Tumor Cells
|Clinical Chemistry|2018|81
Multiplex Gene Expression Profiling of In Vivo Isolated Circulating Tumor Cells in High-Risk Prostate Cancer Patients
|Clinical Chemistry|2017|76
Are morphological criteria sufficient for the identification of circulating tumor cells in renal cancer?
|Journal of Translational Medicine|2013|62
Non-coding Natural Antisense Transcripts: Analysis and Application
|Journal of Biotechnology|2021|52