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  • Recombinant human erythropoietin  (1)
  • hypoxic neonates (neonates with transposition of the major arteries)  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 66 (1988), S. 236-240 
    ISSN: 1432-1440
    Keywords: Recombinant human erythropoietin ; Stem cells ; Megakaryopoiesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Recombinant human erythropoietin (rhEpo), now available, might become increasingly more important for clinical use, e.g., in the treatment of anemia of chronic renal failure. As a prerequisite of clinical trials, we analyzed the stimulatory and suppressive effects of rhEpo on human hemopoiesis by adding rhEpo to in vitro cultures of nonadherent low-density bone marrow cells obtained from normal persons and from patients undergoing hemodialysis for chronic renal failure. rhEpo was shown to be an effective stimulus for erythroid and multilineage colony formation. The dose-response curve was similar for erythroid progenitors BFU-E from normal controls and patients with chronic renal failure. rhEpo had no effect on megakaryocytic colony formation nor on the megakaryocytic differentiation of multilineage stem cells. Because of a good stimulatory activity on erythroid and multilineage stem cells and lack of toxic effects, rhEpo might be useful in the treatment of certain kinds of anemia.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of experimental biology and medicine 86 (1978), S. 1007-1010 
    ISSN: 1573-8221
    Keywords: erythropoietin ; erythropoiesis inhibitor ; hypoxic neonates (neonates with transposition of the major arteries) ; polycythemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Erythropoietin and erythropoiesis inhibitor were studied in 22 healthy neonates and 31 neonates with transposition of the major arteries (TMA) using polycythemic mice as the model. Erythropoietin could not be detected in the plasma or urine of healthy neonates aged 5–7 days, but erythropoiesis inhibitor was found during this period. The erythropoietin level was raised in neonates with TMA until the 14th day, and lowered from the 14th to the 56th day. In concentrates of the 24-hourly urine sample from neonates with hypoxia aged 3–4 weeks erythropoiesis inhibitor also was found. The role of erythropoiesis inhibitor as a physiological regulator appearing in the blood of healthy neonates and neonates with hypoxia in the normalization of erythropoiesis during the first weeks after birth is discussed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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