(Q57675158)

6

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author name string

Jane M. Owens

2

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Martin Tonko

3

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Candace Elliott

4

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Timothy J. Chambers

https://scigraph.springernature.com/pub.10.1038/72855

5

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language of work or name

English

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publication date

February 2000

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published in

Nature Genetics

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volume

24

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page(s)

184-187

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issue

2

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exact match

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cites work

Transformation by Fos proteins requires a C-terminal transactivation domain

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A novel, transformation-relevant activation domain in Fos proteins

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Transcriptional activation of the fra-1 gene by AP-1 is mediated by regulatory sequences in the first intron

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TRANCE (tumor necrosis factor [TNF]-related activation-induced cytokine), a new TNF family member predominantly expressed in T cells, is a dendritic cell-specific survival factor

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A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function

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Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis-inhibitory factor and is identical to TRANCE/RANKL

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Osteoprotegerin ligand is a cytokine that regulates osteoclast differentiation and activation

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Fra-1 induces morphological transformation and increases in vitro invasiveness and motility of epithelioid adenocarcinoma cells

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Osteoblasts are target cells for transformation in c-fos transgenic mice

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Conserved motifs in Fos and Jun define a new class of activation domain

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c-Fos-induced activation of a TATA-box-containing promoter involves direct contact with TATA-box-binding protein

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Transformation by FosB requires a trans-activation domain missing in FosB2 that can be substituted by heterologous activation domains

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Direct transcriptional stimulation of the ornithine decarboxylase gene by Fos in PC12 cells but not in fibroblasts

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Fra-1 potentiates osteoclastic differentiation in osteoclast-macrophage precursor cell lines

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Tumor necrosis factor receptor family member RANK mediates osteoclast differentiation and activation induced by osteoprotegerin ligand

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Bisphosphonates: from the laboratory to the clinic and back again

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Structure and chromosomal assignment of the mouse fra-1 gene, and its exclusion as a candidate gene for oc (osteosclerosis)

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OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis

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A C-terminal domain in FosB, absent in FosB/SF and Fra-1, which is able to interact with the TATA binding protein, is required for altered cell growth.

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Yeast GCN4 as a probe for oncogenesis by AP-1 transcription factors: transcriptional activation through AP-1 sites is not sufficient for cellular transformation

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An inhibitor domain in c-Fos regulates activation domains containing the HOB1 motif.

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