97 results on '"Oudejans, Cees B.M."'
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2. Supplementary Appendix and Figure 1 from Expression Microarray Analysis and Oligo Array Comparative Genomic Hybridization of Acquired Gemcitabine Resistance in Mouse Colon Reveals Selection for Chromosomal Aberrations
3. Maternal plasma RNA sequencing
4. MicroRNA transcriptome profiling in cardiac tissue of hypertrophic cardiomyopathy patients with MYBPC3 mutations
5. Maternal Plasma DNA and RNA Sequencing for Prenatal Testing
6. Mutations within the LINC-HELLP non-coding RNA differentially bind ribosomal and RNA splicing complexes and negatively affect trophoblast differentiation
7. Susceptibility allele-specific loss of miR-1324-mediated silencing of the INO80B chromatin-assembly complex gene in pre-eclampsia
8. Detection of the placental epigenetic signature of the maspin gene in maternal plasma
9. Cardiac Expression of Deiodinase type 3 (Dio3) Following Myocardial Infarction Is Associated With the Induction of a Pluripotency microRNA Signature from the Dlk1-Dio3 Genomic Region
10. Novel biomarkers in preeclampsia
11. HELLP babies link a novel lincRNA to the trophoblast cell cycle
12. Non-invasive aneuploidy detection using free fetal DNA and RNA in maternal plasma: recent progress and future possibilities
13. The STOX1 genotype associated with pre-eclampsia leads to a reduction of trophoblast invasion by α-T-catenin upregulation
14. The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27
15. The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas
16. HLA-G expression in trophoblast cells circulating in maternal peripheral blood during early pregnancy
17. HLA-G expression in trophoblast cells circulating in maternal peripheral blood during early pregnancy
18. Enrichment of fetal trophoblast cells from the maternal peripheral blood followed by detection of fetal deoxyribonucleic acid with a nested X/Y polymerase chain reaction
19. Enrichment of fetal trophoblast cells from the maternal peripheral blood followed by detection of fetal deoxyribonucleic acid with a nested X/Y polymerase chain reaction
20. Plasma placenta growth factor levels in midtrimester pregnancies
21. Response to letter to the editor PD-17-0390, a comment on “Comparing methods for fetal fraction determination and quality control of NIPT samples”
22. Comparing methods for fetal fraction determination and quality control of NIPT samples
23. Response to letter to the editor PD-17-0390, a comment on “Comparing methods for fetal fraction determination and quality control of NIPT samples”
24. Calculating the fetal fraction for noninvasive prenatal testing based on genome-wide nucleosome profiles
25. Cover Image, Volume 36, Issue 7
26. Circulating Nucleic Acids Special Issue
27. Mutations within theLINC-HELLPnon-coding RNA differentially bind ribosomal and RNA splicing complexes and negatively affect trophoblast differentiation
28. Differential Expression of microRNA in Cerebrospinal Fluid as a Potential Novel Biomarker for Alzheimer’s Disease
29. Épigénétique de la prééclampsie
30. Reply to STOX1 is not imprinted and is not likely to be involved in preeclampsia [2]
31. Susceptibility allele-specific loss of miR-1324-mediated silencing of the INO80B chromatin-assembly complex gene in pre-eclampsia
32. Mutations of MLC1 (KIAA0027), Encording a Putative Membrane Protein, Cause Megalencephalic Leucoencephalopathy with Subcortical Cysts
33. STOX1A induces phosphorylation of tau proteins at epitopes hyperphosphorylated in Alzheimer's disease
34. Direct Downregulation of CNTNAP2 by STOX1A is Associated with Alzheimer's Disease
35. Differential methylation of STOX1 in human placenta
36. P1-055: A genome-wide search for STOX1 target genes, a transcription factor associated with Alzheimer's disease
37. Expression Microarray Analysis and Oligo Array Comparative Genomic Hybridization of Acquired Gemcitabine Resistance in Mouse Colon Reveals Selection for Chromosomal Aberrations
38. C2360, a nuclear protein expressed in human proliferative cytotrophoblasts, is a representative member of a novel protein family with a conserved coiled coil–helix–coiled coil–helix domain
39. Markers for Presymptomatic Prediction of Preeclampsia and Intrauterine Growth Restriction
40. NEUROD1 acts in vitro as an upstream regulator of NEUROD2 in trophoblast cells
41. The cellular Pax–Hox–Helix connection
42. Plasma hepatocyte growth factor as a marker for small-for-gestational age fetuses
43. The proneural genes NEUROD1 and NEUROD2 are expressed during human trophoblast invasion
44. Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter
45. Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter
46. Allelic IGF2R Repression Does Not Correlate with Expression of Antisense RNA in Human Extraembryonic Tissues
47. Mutations of MLC1 (KIAA0027), Encoding a Putative Membrane Protein, Cause Megalencephalic Leukoencephalopathy with Subcortical Cysts
48. Identification of hash2-positive extravillus trophoblast cells in the peripheral blood of pregnant women
49. Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter.
50. A genome-wide search for STOX1 target genes, a transcription factor associated with Alzheimer's disease
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