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CD34  -  CD34 molecule

Canis lupus familiaris

 
 
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Disease relevance of CD34

  • Highly efficient retroviral gene transfer into immortalized CD34(-) cells and organ distribution after transplantation into NOD/SCID mice [1].
  • CD34 expression was common in acute, non-LGL leukemias of dogs, both myeloid and lymphoid [2].
 

High impact information on CD34

  • METHODS: We used multiparameter flow cytometry to examine expression of cell-surface determinants associated with hematopoietic precursors (c-kit, CD34, CD133, CD45) or with lineage-committed cells (CD3, CD11b, CD14, CD21, CD105, CD146, alphavbeta3-integrin) in HSA cell lines and in blood samples from healthy dogs or dogs with HSA [3].
  • A CD34-negative haematopoietic progenitor cell line, D064, derived from canine bone marrow stromal cells is able to differentiate into haematopoietic progenitors under the influence of growth factor-mediated signalling [4].
  • Three B-cell cases also expressed the stem cell antigen, CD34 [5].
  • BACKGROUND: CD34(-) stem cells are apparently the earliest progenitors of hematopoiesis and mesenchymal tissues [1].
  • In standard colony assays, CD34(-), fibroblast-like cells produce a significant number of colony-forming-units (CFUs), mainly CFU-F (fibroblast) [1].
 

Biological context of CD34

  • One week after MI, the circulating CD34-positive mononuclear cell numbers in both the EPO(0) and the EPO(6h) groups were significantly higher than in the control group [6].
 

Anatomical context of CD34

  • DISCUSSION: CD34(-), fibroblast-like progenitor cells can give rise to hematopoietic progeny, but also home to mesenchymal organ sites in recipient animals [1].
  • A strong expression of CD34 mRNA and glycoprotein was observed in a well-defined area of the hair follicle isthmic region and appeared uniformly concentrated at the level of the basal layer of the outer root sheath [7].
  • These findings provide compelling support to the hypothesis that in dogs, a subpopulation of basal keratinocytes located in the hair follicle isthmic region and characterized by the selective expression of CD34 is potentially associated with the stem cell compartment of this skin appendage [7].
 

Analytical, diagnostic and therapeutic context of CD34

References

  1. Highly efficient retroviral gene transfer into immortalized CD34(-) cells and organ distribution after transplantation into NOD/SCID mice. Thalmeier, K., Huss, R. Cytotherapy. (2001) [Pubmed]
  2. An immunophenotypic study of canine leukemias and preliminary assessment of clonality by polymerase chain reaction. Vernau, W., Moore, P.F. Vet. Immunol. Immunopathol. (1999) [Pubmed]
  3. Canine hemangiosarcoma originates from hematopoietic precursors with potential for endothelial differentiation. Lamerato-Kozicki, A.R., Helm, K.M., Jubala, C.M., Cutter, G.C., Modiano, J.F. Exp. Hematol. (2006) [Pubmed]
  4. CDK-inhibitor independent cell cycle progression in an experimental haematopoietic stem cell leukaemia despite unaltered Rb-phosphorylation. Huss, R., Theis, S., Deeg, H.J. Br. J. Cancer (1999) [Pubmed]
  5. Lineage differentiation of canine lymphoma/leukemias and aberrant expression of CD molecules. Wilkerson, M.J., Dolce, K., Koopman, T., Shuman, W., Chun, R., Garrett, L., Barber, L., Avery, A. Vet. Immunol. Immunopathol. (2005) [Pubmed]
  6. Erythropoietin enhances neovascularization of ischemic myocardium and improves left ventricular dysfunction after myocardial infarction in dogs. Hirata, A., Minamino, T., Asanuma, H., Fujita, M., Wakeno, M., Myoishi, M., Tsukamoto, O., Okada, K., Koyama, H., Komamura, K., Takashima, S., Shinozaki, Y., Mori, H., Shiraga, M., Kitakaze, M., Hori, M. J. Am. Coll. Cardiol. (2006) [Pubmed]
  7. CD34 glycoprotein identifies putative stem cells located in the isthmic region of canine hair follicles. Pascucci, L., Mercati, F., Gargiulo, A.M., Pedini, V., Sorbolini, S., Ceccarelli, P. Vet. Dermatol. (2006) [Pubmed]
  8. Purified canine CD34+Lin- marrow cells transduced with retroviral vectors give rise to long-term multi-lineage hematopoiesis. Bruno, B., Goerner, M.A., Nash, R.A., Storb, R., Kiem, H.P., McSweeney, P.A. Biol. Blood Marrow Transplant. (2001) [Pubmed]
 
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