Source:http://linkedlifedata.com/resource/pubmed/id/16227977
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2005-11-1
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pubmed:abstractText |
Mammalian development requires the specification of over 200 cell types from a single totipotent cell. Investigation of the regulatory networks that are responsible for pluripotency in embryo-derived stem cells is fundamental to understanding mammalian development and realizing therapeutic potential. Extracellular signals and second messengers modulate cell-autonomous regulators such as OCT4, SOX2 and Nanog in a combinatorial complexity. Knowledge of this circuitry might reveal how to achieve phenotypic changes without the genetic manipulation of Oct4, Nanog and other toti/pluripotency-associated genes.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1471-0072
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
872-84
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:16227977-Animals,
pubmed-meshheading:16227977-Cell Nucleus,
pubmed-meshheading:16227977-Embryo, Mammalian,
pubmed-meshheading:16227977-Mice,
pubmed-meshheading:16227977-Pluripotent Stem Cells,
pubmed-meshheading:16227977-Signal Transduction,
pubmed-meshheading:16227977-Transcription Factors
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pubmed:year |
2005
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pubmed:articleTitle |
Regulatory networks in embryo-derived pluripotent stem cells.
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pubmed:affiliation |
Max-Planck Institute for Molecular Biomedicine, Department of Cell and Developmental Biology, Mendelstrasse 7/Von-Esmarch Strasse 56, 48149 Münster, Germany.
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pubmed:publicationType |
Journal Article,
Review,
Research Support, Non-U.S. Gov't
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