Loss of function of transient receptor potential vanilloid 1 (TRPV1) genetic variant is associated with lower risk of active childhood asthma

Journal of Biological Chemistry

Volumn 285, Issue 36, 2010, Pages 27532-27535

  Cantero Recasens, Gerard ^a   Gonzalez, Juan R ^b   Fandos, César ^a   Duran Tauleria, Enric ^c,f   Smit, Lidwien A M ^e   Kauffmann, Francine ^f   Antó, Josep M ^a,b,d   Valverde, Miguel A ^a  

^a UNIVERSITAT POMPEU FABRA   (Spain)

^b CENTRE FOR RESEARCH IN ENVIRONMENTAL EPIDEMIOLOGY CREAL   (Spain)

^c PAMEM Institut de Prestacions d'Assistència Mèdica Al Personal Municipal   (Spain)

^d INST MUNIC D INVESTIGACIO MEDICA   (Spain)

^e UTRECHT UNIVERSITY   (Netherlands)

^f CENTRE FOR RESEARCH IN EPIDEMIOLOGY AND POPULATION HEALTH   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM; RESPIRATORY SYSTEM;

CATION CHANNELS; CHANNEL ACTIVITY; CHANNEL FUNCTIONS; CHRONIC OBSTRUCTIVE PULMONARY DISEASE; GENETIC IMPACT; GENETIC VARIANTS; INTRACELLULAR CA; ODDS RATIOS; PATHOPHYSIOLOGICAL; PATHOPHYSIOLOGY; RESPIRATORY SYMPTOMS; SINGLE-NUCLEOTIDE POLYMORPHISMS; TRANSIENT RECEPTOR POTENTIAL VANILLOID; TRANSIENT RECEPTOR POTENTIALS;

DISEASES;

VANILLOID RECEPTOR 1; VANILLOID RECEPTOR 4; TRPV1 PROTEIN, HUMAN; VANILLOID RECEPTOR;

ARTICLE; ASTHMA; CHILD; CONTROLLED STUDY; FORCED EXPIRATORY VOLUME; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; LOSS OF FUNCTION MUTATION; LUNG FUNCTION; MAJOR CLINICAL STUDY; PATHOGENESIS; PLASMID; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; WHEEZING; GENETIC PREDISPOSITION; GENETICS; HELA CELL LINE; METABOLISM; PATHOPHYSIOLOGY;

ASTHMA; CHILD; GENETIC PREDISPOSITION TO DISEASE; HELA CELLS; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; TRPV CATION CHANNELS;

EID: 77956235414     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.C110.159491     Document Type: Article

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