Importin-13 genetic variation is associated with improved airway responsiveness in childhood asthma

Respiratory Research

Volumn 10, Issue , 2009, Pages

  Raby, Benjamin A ^a,b   Van Steen, Kristel ^c   Lasky Su, Jessica ^a   Tantisira, Kelan ^a,b   Kaplan, Feige ^d   Weiss, Scott T ^a,b  

^a BRIGHAM AND WOMEN S HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c GHENT UNIVERSITY   (Belgium)

^d MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

BUDESONIDE; IMPORTIN 13; KARYOPHERIN; METHACHOLINE; NEDOCROMIL; PLACEBO; UNCLASSIFIED DRUG; ANTIASTHMATIC AGENT; IMPORTIN 13, HUMAN;

ANTIINFLAMMATORY ACTIVITY; ARTICLE; ASTHMA; CHILD; CHILDHOOD DISEASE; DOUBLE BLIND PROCEDURE; FEMALE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; LONG TERM CARE; MAJOR CLINICAL STUDY; MALE; MULTICENTER STUDY; PRESCHOOL CHILD; PROTEIN FUNCTION; RANDOMIZED CONTROLLED TRIAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; BRONCHUS HYPERREACTIVITY; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; GENE LINKAGE DISEQUILIBRIUM; GENETIC POLYMORPHISM; GENETICS; PATHOPHYSIOLOGY;

ANTI-ASTHMATIC AGENTS; ASTHMA; BRONCHIAL HYPERREACTIVITY; BUDESONIDE; CHILD; DOUBLE-BLIND METHOD; GENETIC VARIATION; GENOTYPE; HAPLOTYPES; HUMANS; KARYOPHERINS; LINKAGE DISEQUILIBRIUM; NEDOCROMIL; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 70249091813     PISSN: 14659921     EISSN: 1465993X     Source Type: Journal    
DOI: 10.1186/1465-9921-10-67     Document Type: Article

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