lin-28 Controls the Succession of Cell Fate Choices via Two Distinct Activities
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Title
lin-28 Controls the Succession of Cell Fate Choices via Two Distinct Activities
Authors
Keywords
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Journal
PLoS Genetics
Volume 8, Issue 3, Pages e1002588
Publisher
Public Library of Science (PLoS)
Online
2012-03-23
DOI
10.1371/journal.pgen.1002588
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Note: Only part of the references are listed.- The let-7 microRNA target gene, Mlin41/Trim71 is required for mouse embryonic survival and neural tube closure
- (2011) Betsy R. Maller Schulman et al. CELL CYCLE
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- (2011) Priscilla M Van Wynsberghe et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Genome-Wide Studies Reveal That Lin28 Enhances the Translation of Genes Important for Growth and Survival of Human Embryonic Stem Cells
- (2011) Shuping Peng et al. STEM CELLS
- LIN28 alters cell fate succession and acts independently of the let-7 microRNA during neurogliogenesis in vitro
- (2010) E. Balzer et al. DEVELOPMENT
- Lin28a transgenic mice manifest size and puberty phenotypes identified in human genetic association studies
- (2010) Hao Zhu et al. NATURE GENETICS
- TUT4 in Concert with Lin28 Suppresses MicroRNA Biogenesis through Pre-MicroRNA Uridylation
- (2009) Inha Heo et al. CELL
- Lin28 promotes transformation and is associated with advanced human malignancies
- (2009) Srinivas R Viswanathan et al. NATURE GENETICS
- Lin28 recruits the TUTase Zcchc11 to inhibit let-7 maturation in mouse embryonic stem cells
- (2009) John P Hagan et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- LIN-28 and the poly(U) polymerase PUP-2 regulate let-7 microRNA processing in Caenorhabditis elegans
- (2009) Nicolas J Lehrbach et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Histone H2a mRNA interacts with Lin28 and contains a Lin28-dependent posttranscriptional regulatory element
- (2009) Bingsen Xu et al. NUCLEIC ACIDS RESEARCH
- Lin28-mediated post-transcriptional regulation of Oct4 expression in human embryonic stem cells
- (2009) Caihong Qiu et al. NUCLEIC ACIDS RESEARCH
- A feedback circuit involving let-7-family miRNAs and DAF-12 integrates environmental signals and developmental timing in Caenorhabditis elegans
- (2009) C. M. Hammell et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Lin28 modulates cell growth and associates with a subset of cell cycle regulator mRNAs in mouse embryonic stem cells
- (2009) B. Xu et al. RNA
- Floral organ identity: 20 years of ABCs
- (2009) Barry Causier et al. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
- Temporal Regulation of Metamorphic Processes in Drosophila by the let-7 and miR-125 Heterochronic MicroRNAs
- (2008) Elizabeth E. Caygill et al. CURRENT BIOLOGY
- Drosophila let-7 microRNA is required for remodeling of the neuromusculature during metamorphosis
- (2008) N. S. Sokol et al. GENES & DEVELOPMENT
- Determinants of MicroRNA Processing Inhibition by the Developmentally Regulated RNA-binding Protein Lin28
- (2008) Elena Piskounova et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Lin28 Mediates the Terminal Uridylation of let-7 Precursor MicroRNA
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- Lin-28 interaction with the Let-7 precursor loop mediates regulated microRNA processing
- (2008) M. A. Newman et al. RNA
- Selective Blockade of MicroRNA Processing by Lin28
- (2008) S. R. Viswanathan et al. SCIENCE
- The let-7 family of microRNAs
- (2008) Sarah Roush et al. TRENDS IN CELL BIOLOGY
- let-7 microRNAs in development, stem cells and cancer
- (2008) Ingo Büssing et al. TRENDS IN MOLECULAR MEDICINE
- Dynamic gene expression of Lin-28 during embryonic development in mouse and chicken
- (2007) Shigetoshi Yokoyama et al. GENE EXPRESSION PATTERNS
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