المؤلفون: Ankie Poutsma, Marjan M. Weiss, Marie van Dijk, Rob Janssen, Erik A. Sistermans, Omar J. Michel, Danny Incarnato, Gunilla Kleiverda, Cees B.M. Oudejans, Rob Habets, Salvatore Oliviero, Reynir Arngrímsson

المساهمون: Physiology, Human genetics, Clinical chemistry, ICaR - Ischemia and repair

المصدر: Oudejans, C B M, Michel, O J, Janssen, R, Habets, R, Poutsma, A, Sistermans, E A, Weiss, M M, Incarnato, D, Oliviero, S, Kleiverda, G, van Dijk, M & Arngrimsson, R 2015, ' Susceptibility allele-specific loss of miR-1324-mediated silencing of the INO80B chromatin-assembly complex gene in pre-eclampsia ', Human Molecular Genetics, vol. 24, no. 1, pp. 118-127 . https://doi.org/10.1093/hmg/ddu423
Human Molecular Genetics, 24(1), 118-127. Oxford University Press

مصطلحات موضوعية: Candidate gene, Placenta, DNA Mutational Analysis, Iceland, Cell Cycle Proteins, Biology, medicine.disease_cause, Polymorphism, Single Nucleotide, Exon, Pre-Eclampsia, Pregnancy, microRNA, Genetics, medicine, Gene silencing, Humans, Genetic Predisposition to Disease, Allele, Molecular Biology, Gene, Genetics (clinical), Genetic Association Studies, Mutation, Intracellular Signaling Peptides and Proteins, Nuclear Proteins, General Medicine, Chromatin, MicroRNAs, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3525953b19ca67512f46c684413685e
https://research.vumc.nl/en/publications/44f793d4-cc9d-4491-a8ed-3809ff40a527