α1-adrenergic drugs exhibit affinity to a thapsigargin-sensitive binding site and interfere with the intracellular Ca2+ homeostasis in human erythroleukemia cells

Robert Fuchs, Elisabeth Schraml, Gerd Leitinger, Ilse Letofsky-Papst, Ingeborg Stelzer, Helga Susanne Haas, Konrad Schauenstein, Anton Sadjak

Research output: Contribution to journalArticleResearchpeer-review

Original languageEnglish
Pages (from-to)2969-2980
JournalExperimental cell research
Volume317
Issue number30
DOIs
Publication statusPublished - 2011

Fields of Expertise

  • Advanced Materials Science

Treatment code (Nähere Zuordnung)

  • Basic - Fundamental (Grundlagenforschung)

Cite this

α1-adrenergic drugs exhibit affinity to a thapsigargin-sensitive binding site and interfere with the intracellular Ca2+ homeostasis in human erythroleukemia cells. / Fuchs, Robert; Schraml, Elisabeth; Leitinger, Gerd; Letofsky-Papst, Ilse; Stelzer, Ingeborg; Haas, Helga Susanne; Schauenstein, Konrad; Sadjak, Anton.

In: Experimental cell research, Vol. 317, No. 30, 2011, p. 2969-2980.

Research output: Contribution to journalArticleResearchpeer-review

Fuchs, Robert ; Schraml, Elisabeth ; Leitinger, Gerd ; Letofsky-Papst, Ilse ; Stelzer, Ingeborg ; Haas, Helga Susanne ; Schauenstein, Konrad ; Sadjak, Anton. / α1-adrenergic drugs exhibit affinity to a thapsigargin-sensitive binding site and interfere with the intracellular Ca2+ homeostasis in human erythroleukemia cells. In: Experimental cell research. 2011 ; Vol. 317, No. 30. pp. 2969-2980.
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AU - Fuchs, Robert

AU - Schraml, Elisabeth

AU - Leitinger, Gerd

AU - Letofsky-Papst, Ilse

AU - Stelzer, Ingeborg

AU - Haas, Helga Susanne

AU - Schauenstein, Konrad

AU - Sadjak, Anton

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