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Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma.
Genome-wide search for atopy susceptibility genes in Dutch families with asthma.
Mapping susceptibility genes for allergic diseases.
Association of autoimmune thyroid disease with a microsatellite marker for the thyrotropin receptor gene and CTLA-4 in a Japanese population.
Major genes regulating total serum immunoglobulin E levels in families with asthma.
Major recessive gene(s) with considerable residual polygenic effect regulating adult height: confirmation of genomewide scan results for chromosomes 6, 9, and 12.
Fine mapping of an IgE-controlling gene on chromosome 2q: Analysis of CTLA4 and CD28.
Identification of polymorphisms in the human glucocorticoid receptor gene (NR3C1) in a multi-racial asthma case and control screening panel.
Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21.
Identification of PCDH1 as a novel susceptibility gene for bronchial hyperresponsiveness.
Physical and genetic mapping of the muscle phosphofructokinase gene (PFKM): reassignment to human chromosome 12q.
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome.
A physical map of the 20q12-q13.1 region associated with type 2 diabetes.
Mapping susceptibility genes for asthma and allergy.
Physical Chromosome Mapping
Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons.