Figure S5. The MAP of the reprogramming process in the WT model. The MAP (white curve) starting from the ME differentiated state (the blue point) to the pluripotent state (the green point) is different from that of differentiation process (Fig. 3A). The green dotted line is the ODE trajectory to compare with the MAP. (PDF 3338 kb
Diagrams of the apparatus for MET stimulation and differentiation flow of ES cells on M15 feeder cel...
is Figure S1 showing differentiation of hiPSCs into NPCs using commercial reagents. Two hiPSC lines ...
Figure S7. In vitro characterization of iPSCs. (A) qRT-PCR measurements of Esrp1/2 expression 4 days...
Figure S2. The simplified two-dimensional Oct4-Nanog model on the phase plate and the distribution o...
Table S2. Parameters used in Eq. (2) for the simplified Oct4-Nanog model. (DOCX 42Â kb
Figure S3. Parameter sensitivity analysis for the model. Illustration of the relative changes of the...
Figure S6. Three different strategies of reprogramming demonstrate additional Nanog activation is ne...
<p>The sizes of nodes and edges are proportional to the occurrence probability of the corresponding ...
BackgroundHeterogeneous gene expressions of cells are widely observed in self-renewing pluripotent s...
Generation and characterization of induced pluripotent stem cell (iPSC) clones derived from wildtype...
In vitro differentiation analysis and karyotyping of LiPSC. (A) Representative karyotype of the esta...
Figure S1. Quality control of the dataset. Figure S2. Surface marker analysis and GO enrichment anal...
(A) Trajectories of five randomly selected stem cells after reduction in LIF concentration (L = 0), ...
Figure S1. Schematic diagram of the TranswellÂŽ system. DRGs were seeded in the lower chambers of th...
lineage. Also, under/over-expression studies of the master regulator Oct4 have revealed that some s...
Diagrams of the apparatus for MET stimulation and differentiation flow of ES cells on M15 feeder cel...
is Figure S1 showing differentiation of hiPSCs into NPCs using commercial reagents. Two hiPSC lines ...
Figure S7. In vitro characterization of iPSCs. (A) qRT-PCR measurements of Esrp1/2 expression 4 days...
Figure S2. The simplified two-dimensional Oct4-Nanog model on the phase plate and the distribution o...
Table S2. Parameters used in Eq. (2) for the simplified Oct4-Nanog model. (DOCX 42Â kb
Figure S3. Parameter sensitivity analysis for the model. Illustration of the relative changes of the...
Figure S6. Three different strategies of reprogramming demonstrate additional Nanog activation is ne...
<p>The sizes of nodes and edges are proportional to the occurrence probability of the corresponding ...
BackgroundHeterogeneous gene expressions of cells are widely observed in self-renewing pluripotent s...
Generation and characterization of induced pluripotent stem cell (iPSC) clones derived from wildtype...
In vitro differentiation analysis and karyotyping of LiPSC. (A) Representative karyotype of the esta...
Figure S1. Quality control of the dataset. Figure S2. Surface marker analysis and GO enrichment anal...
(A) Trajectories of five randomly selected stem cells after reduction in LIF concentration (L = 0), ...
Figure S1. Schematic diagram of the TranswellÂŽ system. DRGs were seeded in the lower chambers of th...
lineage. Also, under/over-expression studies of the master regulator Oct4 have revealed that some s...
Diagrams of the apparatus for MET stimulation and differentiation flow of ES cells on M15 feeder cel...
is Figure S1 showing differentiation of hiPSCs into NPCs using commercial reagents. Two hiPSC lines ...
Figure S7. In vitro characterization of iPSCs. (A) qRT-PCR measurements of Esrp1/2 expression 4 days...