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Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2014, Volume 111, Issue 34, pp. 12426 - 12431
Pluripotency can be induced in somatic cells by overexpressing transcription factors, including POU class 5 homeobox 1 (OCT3/4), sex determining region Y-box 2... 
Phenotypes | Induced pluripotent stem cells | Somatic cells | Stem cells | Retroviridae | Embryonic stem cells | Pluripotent stem cells | Cellular differentiation | Cells | Mesenchymal stem cells | Epigenetics | Retrotransposon | Evolution | NONCODING RNA-ROR | ROADBLOCK | DNA METHYLATION | MULTIDISCIPLINARY SCIENCES | TRANSPOSABLE ELEMENTS | evolution | INDUCTION | epigenetics | IPS CELLS | PLURIPOTENT STEM-CELLS | PATHWAY | HUMAN FIBROBLASTS | retrotransposon | EXPRESSION | Octamer Transcription Factor-3 - physiology | Endogenous Retroviruses - physiology | Embryonic Stem Cells - cytology | Epigenesis, Genetic | Humans | Endogenous Retroviruses - genetics | Pluripotent Stem Cells - virology | Gene Knockdown Techniques | Octamer Transcription Factor-3 - genetics | Cell Differentiation - genetics | RNA, Viral - antagonists & inhibitors | RNA, Viral - genetics | SOXB1 Transcription Factors - genetics | Embryonic Stem Cells - virology | SOXB1 Transcription Factors - physiology | Induced Pluripotent Stem Cells - cytology | Cell Differentiation - physiology | Cellular Reprogramming - genetics | Gene Expression | Pluripotent Stem Cells - cytology | Induced Pluripotent Stem Cells - physiology | Induced Pluripotent Stem Cells - virology | Pluripotent Stem Cells - physiology | Kruppel-Like Transcription Factors - physiology | RNA, Long Noncoding - genetics | Embryonic Stem Cells - physiology | RNA, Long Noncoding - antagonists & inhibitors | Kruppel-Like Transcription Factors - genetics | Cellular Reprogramming - physiology | Epigenetic inheritance | Transcription factors | Retroviruses | Physiological aspects | Genetic research | Genetic aspects | Research | Cell differentiation | Gene expression | Virus research | Biological Sciences
Journal Article
Nature structural & molecular biology, ISSN 1545-9985, 2013, Volume 20, Issue 7, pp. 851 - 858
Many Saccharomyces cerevisiae genes encode antisense transcripts, some of which are unstable and degraded by the exosome component Rrp6. Loss of Rrp6 results... 
CRYPTIC UNSTABLE TRANSCRIPTS | PERVASIVE TRANSCRIPTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | INTERGENIC TRANSCRIPTION | SACCHAROMYCES-CEREVISIAE | CELL BIOLOGY | BIOPHYSICS | BINDING PROTEINS NRD1 | GENE-EXPRESSION | POLY(A) POLYMERASE | POLYMERASE-II TRANSCRIPTS | BIDIRECTIONAL PROMOTERS | RNA DEGRADATION | Saccharomyces cerevisiae - genetics | Multiprotein Complexes | Saccharomyces cerevisiae Proteins - biosynthesis | RNA, Messenger - metabolism | Promoter Regions, Genetic - genetics | RNA, Messenger - biosynthesis | RNA Helicases - physiology | Transcription, Genetic | RNA, Fungal - genetics | Gene Expression Regulation, Fungal | RNA-Binding Proteins - physiology | In Situ Hybridization, Fluorescence | Exosome Multienzyme Ribonuclease Complex - physiology | Saccharomyces cerevisiae Proteins - genetics | RNA, Fungal - metabolism | Polynucleotide Adenylyltransferase - physiology | Proton-Phosphate Symporters - genetics | RNA, Antisense - metabolism | Polyadenylation | Metalloendopeptidases - physiology | Models, Genetic | Nuclear Proteins - physiology | Saccharomyces cerevisiae Proteins - physiology | Histone Deacetylases - physiology | Proton-Phosphate Symporters - biosynthesis | Histone-Lysine N-Methyltransferase - physiology | DNA Helicases - physiology | RNA, Antisense - genetics | Cytogenetics | Research | Genetic transcription | DNA methylation | Gene expression | Molecular biology | Ribonucleic acid--RNA | Rrp6 | Nrd1-Nab3-Sen1 | transcription termination | PHO84 regulation | antisense RNA | yeast | single molecule FISH | antisense 3′ end processing
Journal Article
Molecular and cellular biology, ISSN 0270-7306, 2008, Volume 28, Issue 7, pp. 2426 - 2436
Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley... 
INACTIVATION | APOPTOSIS | PROTEIN | SIGNALING PATHWAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | YAP | SIZE-CONTROL | DIFFERENTIATION | DROSOPHILA | TUMOR-SUPPRESSOR PATHWAY | CELL BIOLOGY | 14-3-3 Proteins - physiology | Phosphorylation | Transferases (Other Substituted Phosphate Groups) - genetics | Humans | Receptor Protein-Tyrosine Kinases - physiology | Recombinant Fusion Proteins - physiology | Transferases (Other Substituted Phosphate Groups) - physiology | Mesoderm - cytology | Drosophila Proteins - physiology | Cell Transdifferentiation - physiology | Membrane Proteins - physiology | Cell Division | c-Mer Tyrosine Kinase | Cell Cycle Proteins - genetics | Conserved Sequence | Transcription, Genetic | Epithelial Cells - cytology | Proteins - physiology | Nerve Tissue Proteins - physiology | Transcription Factors - physiology | Membrane Proteins - genetics | Protein-Serine-Threonine Kinases - physiology | Protein-Serine-Threonine Kinases - genetics | Proto-Oncogene Proteins - genetics | Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Protein Processing, Post-Translational - physiology | Amino Acid Motifs | Proteins - genetics | Receptor Protein-Tyrosine Kinases - genetics | Cell Transformation, Neoplastic | Proto-Oncogene Proteins - physiology | Cell Line, Tumor | Nuclear Proteins - physiology | Drosophila Proteins - genetics | Cell Cycle Proteins - physiology | Cell Movement
Journal Article
by Beaumont, Robin N and Warrington, Nicole M and Cavadino, Alana and Tyrrell, Jessica and Nodzenski, Michael and Horikoshi, Momoko and Geller, Frank and Myhre, Ronny and Richmond, Rebecca C and Paternoster, Lavinia and Bradfield, Jonathan P and Kreiner-Møller, Eskil and Huikari, Ville and Metrustry, Sarah and Lunetta, Kathryn L and Painter, Jodie N and Hottenga, Jouke-Jan and Allard, Catherine and Barton, Sheila J and Espinosa, Ana and Marsh, Julie A and Potter, Catherine and Zhang, Ge and Ang, Wei and Berry, Diane J and Bouchard, Luigi and Das, Shikta and Hakonarson, Hakon and Heikkinen, Jani and Helgeland, Øyvind and Hocher, Berthold and Hofman, Albert and Inskip, Hazel M and Jones, Samuel E and Kogevinas, Manolis and Lind, Penelope A and Marullo, Letizia and Medland, Sarah E and Murray, Anna and Murray, Jeffrey C and Njølstad, Pål R and Nohr, Ellen A and Reichetzeder, Christoph and Ring, Susan M and Ruth, Katherine S and Santa-Marina, Loreto and Scholtens, Denise M and Sebert, Sylvain and Sengpiel, Verena and Tuke, Marcus A and Vaudel, Marc and Weedon, Michael N and Willemsen, Gonneke and Wood, Andrew R and Yaghootkar, Hanieh and Muglia, Louis J and Bartels, Meike and Relton, Caroline L and Pennell, Craig E and Chatzi, Leda and Estivill, Xavier and Holloway, John W and Boomsma, Dorret I and Montgomery, Grant W and Murabito, Joanne M and Spector, Tim D and Power, Christine and Järvelin, Marjo-Ritta and Bisgaard, Hans and Grant, Struan F A and Sørensen, Thorkild I A and Jaddoe, Vincent W and Jacobsson, Bo and Melbye, Mads and McCarthy, Mark I and Hattersley, Andrew T and Hayes, M Geoffrey and Frayling, Timothy M and Hivert, Marie-France and Felix, Janine F and Hyppönen, Elina and Lowe, William L and Evans, David M and Lawlor, Debbie A and Feenstra, Bjarke and Freathy, Rachel M and Early Growth Genetics (EGG) Consortium and Early Growth Genetics EGG and Institutionen för kliniska vetenskaper, Avdelningen för obstetrik och gynekologi and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Institute of Clinical Sciences, Department of Obstetrics and Gynecology and Sahlgrenska Academy
Human molecular genetics, ISSN 1460-2083, 2018, Volume 27, Issue 4, pp. 742 - 756
Journal Article
Journal Article
Nature Biotechnology, ISSN 1087-0156, 06/2004, Volume 22, Issue 6, pp. 707 - 716
Human embryonic stem (hES) cells hold promise for generating an unlimited supply of cells for replacement therapies. To characterize hES cells at the molecular... 
DATABASE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | EMBRYONIC STEM-CELLS | ENHANCER | PATTERNS | GENERATION | IDENTIFICATION | EXPRESSION | CULTURE | LINES | MURINE | Humans | Fibroblast Growth Factors - genetics | Dimethyl Sulfoxide - pharmacology | Gene Expression Profiling | Wnt Proteins | Antigens, CD - genetics | Membrane Glycoproteins - physiology | Expressed Sequence Tags | Fibroblast Growth Factors - physiology | Receptors, G-Protein-Coupled - physiology | Tretinoin - pharmacology | Cytokine Receptor gp130 | Signal Transduction - genetics | Reverse Transcriptase Polymerase Chain Reaction | Sequence Analysis, DNA | Cell Division - drug effects | Down-Regulation - genetics | Cell Division - physiology | Embryo, Mammalian - cytology | Growth Substances - pharmacology | Antigens, CD - physiology | Receptors, G-Protein-Coupled - genetics | Transcription, Genetic - genetics | Nodal Protein | Gene Expression - drug effects | Stem Cells - cytology | Stem Cells - metabolism | Intercellular Signaling Peptides and Proteins - physiology | Interleukin-6 | RNA - genetics | Cell Differentiation - genetics | RNA - isolation & purification | Receptors, Fibroblast Growth Factor - genetics | Cell Differentiation - physiology | Leukemia Inhibitory Factor | Cell Division - genetics | Cell Line | Proteins - physiology | Transcription Factors - physiology | Gene Library | Intercellular Signaling Peptides and Proteins - genetics | Transforming Growth Factor beta - physiology | Proto-Oncogene Proteins - genetics | Up-Regulation - genetics | Transcription Factors - genetics | Down-Regulation - drug effects | Membrane Glycoproteins - genetics | Proteins - genetics | Up-Regulation - drug effects | Transforming Growth Factor beta - genetics | Cell Differentiation - drug effects | Proto-Oncogene Proteins - physiology | Signal Transduction - physiology | Receptors, Fibroblast Growth Factor - physiology
Journal Article
Nature reviews. Molecular cell biology, ISSN 1471-0080, 2017, Volume 18, Issue 12, pp. 758 - 770
... (for example, inside of a tumour lump), is central to our understanding of physiology and disease pathogenesis... 
YES-ASSOCIATED PROTEIN | BREAST-CANCER | TRANSCRIPTION FACTORS | NUCLEAR-LOCALIZATION | F-ACTIN | BETA-CATENIN ACTIVATION | PULMONARY-HYPERTENSION | HIPPO SIGNALING PATHWAY | INTESTINAL REGENERATION | MESENCHYMAL STEM-CELLS | CELL BIOLOGY | Neoplasms - metabolism | Atherosclerosis - genetics | Humans | Extracellular Matrix - metabolism | Muscular Dystrophies - genetics | Phosphoproteins - metabolism | Extracellular Matrix - genetics | Neoplasms - genetics | Cell Shape | Transcription, Genetic | Atherosclerosis - pathology | Shear Strength | Muscular Dystrophies - metabolism | Hypertension, Pulmonary - genetics | Hypertension, Pulmonary - metabolism | Phosphoproteins - genetics | Transcription Factors - genetics | Muscular Dystrophies - pathology | Atherosclerosis - metabolism | Transcription Factors - metabolism | Mechanotransduction, Cellular | Animals | Adaptor Proteins, Signal Transducing - genetics | Fibrosis | Adaptor Proteins, Signal Transducing - metabolism | Extracellular Matrix - pathology | Hypertension, Pulmonary - pathology | Transcription factors | Genetic aspects | Disease susceptibility | Health aspects | Cellular control mechanisms | Regulators | Pathogenesis | Rigidity | Muscular dystrophy | Atherosclerosis | Extracellular matrix | Physiology | Gravity | Hypertension | Cues | Gravitation | Lung diseases | Muscles | Gene expression | Muscle contraction | Blood flow | Yes-associated protein | Regeneration | Arteriosclerosis | Stem cells | Shear stress | Mechanotransduction | Dystrophy | Mechanical stimuli | Cell size | Aberration | Cancer | Tumors
Journal Article
Cerebral cortex (New York, N.Y. 1991), ISSN 1460-2199, 2014, Volume 24, Issue 1, pp. 186 - 198
Journal Article