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Journal Article
PLoS Genetics, ISSN 1553-7390, 03/2017, Volume 13, Issue 3, p. e1006682
Understanding the mechanisms regulating cell cycle, proliferation and potency of pluripotent stem cells guarantees their safe use in the clinic. Embryonic stem... 
TRANSCRIPTION FACTORS | REPRESSION | GENETICS & HEREDITY | SELF-RENEWAL | TUMOR-SUPPRESSOR | REGULATORY CIRCUITRY | PLURIPOTENCY | DIFFERENTIATION | TCF3 | BETA-CATENIN | ENRICHMENT ANALYSIS | Cell Cycle - genetics | Cell Proliferation - genetics | Hepatocyte Nuclear Factor 1-alpha - genetics | Humans | Cells, Cultured | Gene Expression Regulation | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Mice, Transgenic | Hepatocyte Nuclear Factor 1-alpha - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Promoter Regions, Genetic - genetics | Blotting, Western | Mouse Embryonic Stem Cells - metabolism | Gene Knockdown Techniques | Animals | Wnt Signaling Pathway - genetics | Cyclin-Dependent Kinase Inhibitor p15 - genetics | Base Sequence | HEK293 Cells | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Mice | Cyclin-Dependent Kinase Inhibitor p15 - metabolism | Research | Embryonic stem cells | Wnt proteins | Gene expression | Cell cycle | Cell culture | Transcription factors | High resolution | Target recognition | Genomics | Diapause | Embryo cells | c-Myc protein | Mimicry | Proteins | Signal transduction | Cell activation | Deoxyribonucleic acid--DNA | Data acquisition | Melanoma | RNA polymerase | Nucleic acids | Ablation | Adenomatous polyposis coli | Gene silencing | Antigen-presenting cells | Stem cells | Ligands | Nuclei (cytology) | Cell proliferation | Destruction | Laboratories | Genes | Homeostasis | Antibodies | Genomes | Activation | Malignancy | CCAAT/enhancer-binding protein | Kinases | Regeneration (physiology) | β-catenin | Adipogenesis | Deactivation | Drosophila | Decision analysis | Urban regeneration | Effectors | Tumor suppressor genes | Differentiation | Pluripotency | Tumors | Cancer | Cloning | Cell cycle inhibitors | Cell division | Cell staining | Gene expression regulation | G1 phase | Deoxyribonucleic acid | DNA
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2008, Volume 105, Issue 47, pp. 18331 - 18336
Journal Article
Journal of Tissue Engineering and Regenerative Medicine, ISSN 1932-6254, 04/2019, Volume 13, Issue 4, pp. 612 - 624
Journal Article
Physical Biology, ISSN 1478-3967, 05/2017, Volume 14, Issue 3, p. 036001
Accessing gene expression at a single-cell level has unraveled often large heterogeneity among seemingly homogeneous cells, which remains obscured when using... 
computational biology | single cell gene expression | cell growth | BIOCHEMISTRY & MOLECULAR BIOLOGY | RESOLUTION | NOISE | NETWORKS | STEM | STOCHASTIC GENE-EXPRESSION | BIOPHYSICS | RNA-SEQ | PCR | CYCLE | Gene Expression | Computational Biology | Cell Size | Gene Expression Profiling - methods | Models, Genetic | Cell Enlargement | RNA, Messenger - metabolism
Journal Article
Nature Reviews Molecular Cell Biology, ISSN 1471-0072, 2017, Volume 18, Issue 11, pp. 685 - 701
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 04/2010, Volume 14, Issue 4, pp. 729 - 740
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2016, Volume 55, Issue 33, pp. 9620 - 9624
The LacZ gene, which encodes Escherichia coli β‐galactosidase, is widely used as a marker for cells with targeted gene expression or disruption. However, it... 
single-cell resolution | β-galactosidase | quinone methide intermediates | fluorescent probes | lacZ | FLUORESCENCE PROBE | ACID | beta-galactosidase | MICE | SELECTION | CHEMISTRY, MULTIDISCIPLINARY | Fluorescence | Enzymes | Gene expression | Quinone | Escherichia coli | Proteins | Cell culture | Receptors | E coli | Galactosidase | LacZ gene | Disruption | Tissues | Anchoring
Journal Article
Allergy, ISSN 0105-4538, 10/2012, Volume 67, Issue 10, pp. 1215 - 1222
Journal Article
Cell, ISSN 0092-8674, 04/2014, Volume 157, Issue 2, pp. 407 - 419
Journal Article