Characterization of recombinant human P2X4 receptor reveals pharmacological differences to the rat homologue

Molecular Pharmacology

Volumn 51, Issue 1, 1997, Pages 109-118

  Garcia Guzman, Miguel ^a   Soto, Florentina ^a   Gomez Hernandez, Juan Manuel ^a   Lund, Per Eric ^a   Stühmer, Walter ^a  

^a MAX PLANCK INSTITUTE OF EXPERIMENTAL MEDICINE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

2 METHYLTHIOADENOSINE TRIPHOSPHATE; ADENOSINE TRIPHOSPHATE; ALPHA,BETA METHYLENEADENOSINE TRIPHOSPHATE; BROMOPHENOL BLUE; CALCIUM ION; COMPLEMENTARY DNA; CYTIDINE TRIPHOSPHATE; DEOXYADENOSINE TRIPHOSPHATE; DIVALENT CATION; FURA 2; MESSENGER RNA; PURINE P2X RECEPTOR; PURINERGIC RECEPTOR BLOCKING AGENT; PURINERGIC RECEPTOR STIMULATING AGENT; PYRIDOXAL 5 PHOSPHATE; SULFONIC ACID DERIVATIVE; SURAMIN; ZINC;

ANIMAL CELL; ARTICLE; CALCIUM TRANSPORT; CELL MEMBRANE PERMEABILITY; CONTROLLED STUDY; DRUG POTENCY; DRUG RECEPTOR BINDING; DRUG SENSITIVITY; EMBRYO; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; HUMAN; HUMAN CELL; MOLECULAR CLONING; NONHUMAN; POINT MUTATION; PRIORITY JOURNAL; RECOMBINANT DNA TECHNOLOGY; SEQUENCE HOMOLOGY; XENOPUS LAEVIS;

EID: 0031033013     PISSN: 0026895X     EISSN: None     Source Type: Journal    
DOI: 10.1124/mol.51.1.109     Document Type: Article

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