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Cov2MS
Cov-MS
Activin A-derived human embryonic stem cells show increased competence to differentiate into primordial germ cell-like cells
WNT Inhibition and Increased Fibroblast Growth Factor Signaling Promotes Derivation of Less Heterogeneous Primed Human Embryonic Stem Cells, Compatible with Differentiation
Integrative Proteomic Profiling Reveals PRC2-Dependent Epigenetic Crosstalk Maintains Ground-State Pluripotency
Transcriptional landscape changes during human embryonic stem cell derivation
Comparative analysis of naive, primed and ground state pluripotency in mouse embryonic stem cells originating from the same genetic background
Origins of Human Embryonic Stem Cell Fate: Role of the Post Inner Cell Mass Intermediate
Direct comparison of distinct naive pluripotent states in human embryonic stem cells
BMP-SMAD Signaling Regulates Lineage Priming, but Is Dispensable for Self-Renewal in Mouse Embryonic Stem Cells
Alternative Routes to Induce Naive Pluripotency in Human Embryonic Stem Cells
Comparative analysis of different culture conditions inducing naive pluripotency in human embryonic stem cells
Application Of Small Molecules Favoring Naive Pluripotency during Human Embryonic Stem Cell Derivation
Exogenous supplementation of Activin A enhances germ cell differentiation of human embryonic stem cells
BMP-SMAD Signaling Regulates Lineage Priming, but Is Dispensable for Self-Renewal in Mouse Embryonic Stem Cells
Treatment of human embryos with the TGF beta inhibitor SB431542 increases epiblast proliferation and permits successful human embryonic stem cell derivation
Influence of Activin A Supplementation During Human Embryonic Stem Cell Derivation on Germ Cell Differentiation Potential
The Combination of Inhibitors of FGF/MEK/Erk and GSK3 beta Signaling Increases the Number of OCT3/4-and NANOG-Positive Cells in the Human Inner Cell Mass, But Does Not Improve Stem Cell Derivation
The TGF beta pathway plays a pivotal role in early embryo lineage segregation in both mouse and human
Tracking the progression of the human inner cell mass during embryonic stem cell derivation

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