Extracellular metabolism of ATP and other nucleotides
By H. Zimmermann. Naunyn-Schmiedeberg's Archives of Pharmacology, 2000
1,025 citations recorded by the source corpus.
Subfields: Genetics, Physiology, Surgery
View Paper: https://www.semanticscholar.org/paper/d15c30d7b5b333490597773f5d6be3e19a685056
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In Genetics
In Physiology
- W. Junger
- H. Zimmermann
- Kenneth A. Jacobson
- Zhang-Guo Gao
- Maria P. Abbracchio
- G. Knight
- G. Burnstock
In Surgery
Citations in the corpus
- International Union of Pharmacology. XXV. Nomenclature and classification of adenosine receptors. (2001, neutral): “Ectonucleotidases include ectonucleoside triphosphate diphosphohydrolases, including CD39, which can hydrolyze ATP or ADP, ectonucleotide pyrophosphatase/ phosphodiesterases, alkaline phosphatases and 5 nucleotidases such as CD73 (Zimmermann, 2000).”
- Mesenchymal stem cell-derived exosomes increase ATP levels, decrease oxidative stress and activate PI3K/Akt pathway to enhance myocardial viability and prevent adverse remodeling after myocardial ischemia/reperfusion injury. (2013, background): “More importantly, CD73 has been shown to be the major enzyme responsible for the formation of extracellular adenosine from released adenine nucleotides (Zimmermann, 2000).”
- The E-NTPDase family of ectonucleotidases: Structure function relationships and pathophysiological significance (2006, neutral): “The literature on the molecular and functional characterization of the E-NTPDase family has been intensively reviewed [18–22, 31–36] and will not be 410 Purinergic Signalling (2006) 2:409–430”
- Ectonucleotidases: Some recent developments and a note on nomenclature (2001, background): “Apparent Km-values are thus similar to those of E-NTPDase family members [references in Goding et al., 1998; Goding, 2000; Sano and Piao, 2000; Zimmermann, 2000, 2001].”
- Immune cell regulation by autocrine purinergic signalling (2011, background): “In addition, several families of ectonucleotidases that hydrolyse ATP to ADP, AMP and adenosine have been foun”
- International Union of Pharmacology LVIII: Update on the P2Y G Protein-Coupled Nucleotide Receptors: From Molecular Mechanisms and Pathophysiology to Therapy (2006, background): “All members of this family share five highly conserved sequence domains, known as apyrase conserved domains that are essential for the catalytic activity (Handa and Guidotti, 1996; Vasconcelos et al., 1996; Zimmermann, 2000).”
- Adenosine receptors as therapeutic targets (2006, background): “, or nucleotidase-mediated hydrolysis of extracellular adenine nucleotide”