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Bernhard Kubanek

Researcher at Tufts University

Publications -  6
Citations -  175

Bernhard Kubanek is an academic researcher from Tufts University. The author has contributed to research in topics: Erythropoiesis & Erythropoietin. The author has an hindex of 5, co-authored 6 publications receiving 175 citations. Previous affiliations of Bernhard Kubanek include University of Massachusetts Lowell & St. Elizabeth's Medical Center.

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Journal ArticleDOI

Regulation of Erythropoiesis: XXIII. Dissociation between Stem Cell and Erythroid Response to Hypoxia

TL;DR: It is suggested that the dissociation between erythroid response and changes in the CFU reflect a secondary effect of hypoxia not directly related to the erythropoietin-induced increase in red cell production.
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Regulation of erythropoiesis. XXI. The effect of erythropoietin on the stem cell.

TL;DR: It is concluded that the stem cell participates in the physiologic response to erythropoietin but without depletion of this compartment and the splenic CFU began to increase within 24 hours after the beginning of treatment and reached levels of 5-fold those of controls between days 8 and 16.
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The pattern of stem cell repopulation in heavily irradiated mice receiving transplants of fetal liver.

TL;DR: Pluripotential cells derived from fetal liver had a lower plating efficiency than adult marrow cells, but estimates of the generation time derived from the growth curve are significantly shorter and may account for the earlier erythroid population.
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Regulation of erythropoiesis (XXIV). Studies on the post-hypoxic "rebound" phase.

TL;DR: Findings might best be explained by a migration of stem cells during the post-hypoxic interval, which decreased during hypoxia and rose gradually there-after following, rather than preceeding, the increase in bone marrow CFU’s.
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Erythroid Differentiation of Fetal, Newborn and Adult Haemopoietic Stem Cells

TL;DR: The data reported herein suggest that the differences in erythroid regeneration evoked by transplants of fetal liver, neonatal marrow or adult marrow, are not solely attributed to the degree of proliferation in the pluripotential stem cell compartment, and may suggest a shorter doubling time for cells comprising the fetal and newborn committed erythyroid compartments.