Literature DB >> 11840324

Id proteins in cell cycle control and cellular senescence.

Z Zebedee1, E Hara.   

Abstract

The Id family of helix-loop-helix (HLH) proteins are thought to affect the balance between cell growth and differentiation by negatively regulating the function of basic-helix-loop-helix (bHLH) transcription factors. Although it has been suggested for some time that Id is involved in cell cycle regulation, little is known about the molecular mechanism of this control. Recent studies, however, have revealed that Id binds to important cell cycle regulatory proteins other than bHLH proteins. Two such proteins, pRB (retinoblastoma tumour suppressor protein) family proteins and Ets-family transcription factors are known to play key roles in cell cycle regulation, transformation and tumour suppression. Through the characterization of these pathways we will begin to understand the mechanisms by which Id controls normal and abnormal cell cycle progression.

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Year:  2001        PMID: 11840324     DOI: 10.1038/sj.onc.1205092

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  90 in total

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4.  Physical and functional interaction between the ID1 and p65 for activation of NF-κB.

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6.  Neural differentiation arrest in embryonal carcinoma cells with forced expression of EWS-FLI1.

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7.  Crystallization and preliminary X-ray diffraction analysis of GCIP/HHM transcriptional regulator.

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8.  SHIP1 regulates MSC numbers and their osteolineage commitment by limiting induction of the PI3K/Akt/β-catenin/Id2 axis.

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9.  Inhibitor of differentiation 1 promotes endothelial survival in a bleomycin model of lung injury in mice.

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10.  Defects in the cerebella of conditional Neurod1 null mice correlate with effective Tg(Atoh1-cre) recombination and granule cell requirements for Neurod1 for differentiation.

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Journal:  Cell Tissue Res       Date:  2009-07-17       Impact factor: 5.249

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