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Pde4b  -  phosphodiesterase 4B, cAMP specific

Mus musculus

Synonyms: Dpde4, R74983, dunce
 
 
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Disease relevance of Pde4b

  • Analyses of TCRB rearrangements substantiate a profound deficit in recombination signal sequence joining in SCID foals: implications for the role of DNA-dependent protein kinase in V(D)J recombination [1].
  • A profound alteration of blood TCRB repertoire allows prediction of cerebral malaria [2].
 

High impact information on Pde4b

  • Pre-TCR expression on developing thymocytes allows cells with productive TCRB gene rearrangements to further differentiate [3].
  • After establishing a short-term T cell line, cells were 1) stained with mAbs for flow cytometric analysis, 2) analyzed for TCRB chain transcript expression, and 3) used as effector cells for cytotoxicity and proliferation [4].
  • In one case, two expanded TCRB clones could be identified that were persistent in the bile duct over a 1-yr period [4].
 

Analytical, diagnostic and therapeutic context of Pde4b

  • This was confirmed by cloning and random sequencing of PCR amplification products using TCRBV region family-specific primers; TCRB chain sequences were reiterated in all transcripts analyzed [4].

References

  1. Analyses of TCRB rearrangements substantiate a profound deficit in recombination signal sequence joining in SCID foals: implications for the role of DNA-dependent protein kinase in V(D)J recombination. Shin, E.K., Rijkers, T., Pastink, A., Meek, K. J. Immunol. (2000) [Pubmed]
  2. A profound alteration of blood TCRB repertoire allows prediction of cerebral malaria. Collette, A., Bagot, S., Ferrandiz, M.E., Cazenave, P.A., Six, A., Pied, S. J. Immunol. (2004) [Pubmed]
  3. TCR alpha-chain repertoire in pTalpha-deficient mice is diverse and developmentally regulated: implications for pre-TCR functions and TCRA gene rearrangement. Mancini, S., Candéias, S.M., Fehling, H.J., von Boehmer, H., Jouvin-Marche, E., Marche, P.N. J. Immunol. (1999) [Pubmed]
  4. Analysis of human common bile duct-associated T cells: evidence for oligoclonality, T cell clonal persistence, and epithelial cell recognition. Probert, C.S., Christ, A.D., Saubermann, L.J., Turner, J.R., Chott, A., Carr-Locke, D., Balk, S.P., Blumberg, R.S. J. Immunol. (1997) [Pubmed]
 
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