Multiple niches for Notch in cancer: context is everything.

No abstract is available for this paper.

• Publication year

  2004

• Venue

  Current Opinion in Genetics and Development

• Publication date

  2004-02-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/J.GDE.2003.11.004PMID 15108805
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• p300 and PCAF Act Cooperatively To Mediate Transcriptional Activation from Chromatin Templates by Notch Intracellular Domains In Vitro

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• Mastermind mediates chromatin-specific transcription and turnover of the Notch enhancer complex.

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• An Epstein-Barr Virus Protein Interacts with Notch

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• Embryonic lethality in mice homozygous for a processing-deficient allele of Notch1

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• MAML1, a human homologue of Drosophila Mastermind, is a transcriptional co-activator for NOTCH receptors

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• Cell Cycle Arrest and Apoptosis Induced by Notch1 in B Cells*

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• Essential Roles for Ankyrin Repeat and Transactivation Domains in Induction of T-Cell Leukemia by Notch1

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• Neurogenic phenotypes and altered Notch processing in Drosophila Presenilin mutants

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• Notch Signaling : Cell Fate Control and Signal Integration in Development

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• Notch1 expression in early lymphopoiesis influences B versus T lineage determination.

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• Notch signaling: cell fate control and signal integration in development.

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• Presenilin is required for activity and nuclear access of Notch in Drosophila

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• A presenilin-1-dependent γ-secretase-like protease mediates release of Notch intracellular domain

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• Deficient T cell fate specification in mice with an induced inactivation of Notch1.

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