The role of histidine residues in modulation of the rat P2X2 purinoceptor by zinc and pH

Journal of Physiology

Volumn 539, Issue 2, 2002, Pages 347-359

  Clyne, J Dylan ^a   LaPointe, Lisa D ^a   Hume, Richard I ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; ALANINE; CATION CHANNEL; HISTIDINE; LYSINE; MUTANT PROTEIN; PROTON; PURINE P2X RECEPTOR; ZINC; PURINERGIC P2X2 RECEPTOR;

ACIDITY; ALKALINITY; AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; CELL MEMBRANE POTENTIAL; CELL PH; CONCENTRATION RESPONSE; CONTROLLED STUDY; DISSOCIATION CONSTANT; MUTATION; NONHUMAN; OOCYTE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN CONFORMATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; RAT; VOLTAGE CLAMP; WILD TYPE; XENOPUS; EC50; FEMALE; RECEPTOR UPREGULATION; VOLTAGE CLAMP TECHNIQUE;

ADENOSINE TRIPHOSPHATE; ANIMALS; DNA PRIMERS; ELECTROPHYSIOLOGY; HISTIDINE; HYDROGEN-ION CONCENTRATION; KINETICS; MUTAGENESIS; OOCYTES; PATCH-CLAMP TECHNIQUES; RATS; RECEPTORS, PURINERGIC P2; XENOPUS LAEVIS; ZINC;

EID: 0036521874     PISSN: 00223751     EISSN: None     Source Type: Journal    
DOI: 10.1113/jphysiol.2001.013244     Document Type: Article

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