Phosphorylation of the C terminus of Fos protein is required for transcriptional transrepression of the c-fos promoter.

The ribosomal protein rpl26 promoter is required for its 3' sense terminus ncRNA transcription in Schizosaccharomyces pombe, implicating a new transcriptional mechanism for ncRNAs.

The N-terminus of the prion protein is a toxic effector regulated by the C-terminus.

Mutual transrepression of Fos and the glucocorticoid receptor: involvement of a functional domain in Fos which is absent in FosB.

Tyrosine protein phosphorylation is required for protein kinase C-mediated proliferation in T cells.

The N-terminus of murine leukaemia virus p12 protein is required for mature core stability.

The TAF9 C-terminal conserved region domain is required for SAGA and TFIID promoter occupancy to promote transcriptional activation.

A site of tyrosine phosphorylation in the C terminus of the epidermal growth factor receptor is required to activate phospholipase C.

Heat shock induces the transcriptional activation of c-fos protooncogene.

The extreme Albino3 (Alb3) C terminus is required for Alb3 stability and function in Arabidopsis thaliana.

Nerve growth factor transcriptional control of c-fos promoter transfected in cultured spinal sensory neurons.

The C-terminus SH3-binding domain of Kv1.3 is required for the actin-mediated immobilization of the channel via cortactin.

Phosphorylation of transcription factor p62TCF by MAP kinase stimulates ternary complex formation at c-fos promoter.

Cell-type specific multiprotein complex formation over the c-fos serum response element in vivo: ternary complex formation is not required for the induction of c-fos.

Inhibitory effect of myristylation on transrepression by FBR (Gag-Fos) protein.

Phosphorylation of Atg31 is required for autophagy.

Phosphorylation of the Retinoblastoma protein (Rb) on serine-807 is required for association with Bax.

Characterization of the bacteriophage lambda excisionase (Xis) protein: the C-terminus is required for Xis-integrase cooperativity but not for DNA binding.

The C-Terminus of Epstein-Barr Virus BRRF2 Is Required for its Proper Localization and Efficient Virus Production.

Alteration of a cyclic AMP-dependent protein kinase phosphorylation site in the c-Fos protein augments its transforming potential.

Protein truncation is required for the activation of the c-myb proto-oncogene.

Human X-box-binding protein 1 is required for the transcription of a subset of human class II major histocompatibility genes and forms a heterodimer with c-fos.

The expression of c-fos protein in human breast.

Adenovirus E4orf4 protein reduces phosphorylation of c-Fos and E1A proteins while simultaneously reducing the level of AP-1.

A DNA binding domain is contained in the C-terminus of wild type p53 protein.

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The ribosomal protein rpl26 promoter is required for its 3' sense terminus ncRNA transcription in Schizosaccharomyces pombe, implicating a new transcriptional mechanism for ncRNAs.

The N-terminus of the prion protein is a toxic effector regulated by the C-terminus.

Mutual transrepression of Fos and the glucocorticoid receptor: involvement of a functional domain in Fos which is absent in FosB.

Tyrosine protein phosphorylation is required for protein kinase C-mediated proliferation in T cells.

The N-terminus of murine leukaemia virus p12 protein is required for mature core stability.

The TAF9 C-terminal conserved region domain is required for SAGA and TFIID promoter occupancy to promote transcriptional activation.

A site of tyrosine phosphorylation in the C terminus of the epidermal growth factor receptor is required to activate phospholipase C.

Heat shock induces the transcriptional activation of c-fos protooncogene.

The extreme Albino3 (Alb3) C terminus is required for Alb3 stability and function in Arabidopsis thaliana.

Nerve growth factor transcriptional control of c-fos promoter transfected in cultured spinal sensory neurons.

The C-terminus SH3-binding domain of Kv1.3 is required for the actin-mediated immobilization of the channel via cortactin.

Phosphorylation of transcription factor p62TCF by MAP kinase stimulates ternary complex formation at c-fos promoter.

Cell-type specific multiprotein complex formation over the c-fos serum response element in vivo: ternary complex formation is not required for the induction of c-fos.

Inhibitory effect of myristylation on transrepression by FBR (Gag-Fos) protein.

Phosphorylation of Atg31 is required for autophagy.

Phosphorylation of the Retinoblastoma protein (Rb) on serine-807 is required for association with Bax.

Characterization of the bacteriophage lambda excisionase (Xis) protein: the C-terminus is required for Xis-integrase cooperativity but not for DNA binding.

The C-Terminus of Epstein-Barr Virus BRRF2 Is Required for its Proper Localization and Efficient Virus Production.

Alteration of a cyclic AMP-dependent protein kinase phosphorylation site in the c-Fos protein augments its transforming potential.

Protein truncation is required for the activation of the c-myb proto-oncogene.

Human X-box-binding protein 1 is required for the transcription of a subset of human class II major histocompatibility genes and forms a heterodimer with c-fos.

The expression of c-fos protein in human breast.

Adenovirus E4orf4 protein reduces phosphorylation of c-Fos and E1A proteins while simultaneously reducing the level of AP-1.

A DNA binding domain is contained in the C-terminus of wild type p53 protein.

Phosphorylation of the C terminus of Fos protein is required for transcriptional transrepression of the c-fos promoter.

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