Lack of association of TIM3 polymorphisms and allergic phenotypes

BMC Medical Genetics

Volumn 10, Issue , 2009, Pages

  Zhang, Jian ^a   Daley, Denise ^a   Akhabir, Loubna ^a   Stefanowicz, Dorota ^a   Chan Yeung, Moira ^b   Becker, Allan B ^c   Laprise, Catherine ^d   Paré, Peter D ^a   Sandford, Andrew J ^a  

^a ST PAUL S HOSPITAL   (Canada)

^b UNIVERSITY OF HONG KONG   (Hong Kong)

^c UNIVERSITY OF MANITOBA   (Canada)

^d UNIVERSITÉ DU QUÉBEC À CHICOUTIMI   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; GENE PRODUCT; MUCIN 3; T CELL IMMUNOGLOBULIN MUCIN 3; UNCLASSIFIED DRUG; HAVCR2 PROTEIN, HUMAN; MEMBRANE PROTEIN;

ALLERGY; ARTICLE; ASTHMA; ATOPY; CONTROLLED STUDY; GENE DELETION; GENE EXPRESSION; GENE LOCATION; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; GENOTYPE; HUMAN; HUMAN CELL; HUMAN TISSUE; IN VITRO STUDY; KIDNEY; LEUKOCYTE; LUNG; PHENOTYPE; PLACENTA; PROMOTER REGION; REPORTER GENE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SINGLE NUCLEOTIDE POLYMORPHISM; SPLEEN; TRANSCRIPTION INITIATION; ALLELE; CANADA; CAUCASIAN; CHILD; COHORT ANALYSIS; DNA FLANKING REGION; FEMALE; GENE FREQUENCY; GENETIC SCREENING; GENETICS; INFANT; MALE; NEGRO; PRESCHOOL CHILD;

5' FLANKING REGION; AFRICAN CONTINENTAL ANCESTRY GROUP; ALLELES; ASTHMA; CANADA; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; GENETIC SCREENING; GENOTYPE; HUMANS; INFANT; MALE; MEMBRANE PROTEINS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS, GENETIC;

EID: 67650727928     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-10-62     Document Type: Article

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