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14-3-3 protein eta chain gene (YWHAH) polymorphism and its genetic association with schizophrenia.
Recent genetic analyses have suggested a linkage between schizophrenia and the chromosomal region 22q12-q13. 14-3-3 protein, abundant in the brain, mediates interactions between diverse molecules ofExpand
Sisters homozygous for the spinocerebellar ataxia type 6 (SCA6)/CACNA1A gene associated with different clinical phenotypes
Spinocerebellar ataxia type 6 (SCA6) is a neurodegenerative disease caused by a CAG repeat expansion in the CACNA1A gene. The neurodegeneration that occurs in CAG repeat diseases is considered toExpand
Functional variants in the thromboxane A2 receptor gene are associated with lung function in childhood‐onset asthma
The thromboxane A2 receptor (TBXA2R) gene is associated with asthma, but no functional genetic variations are known to associate with the disease or its related phenotypes.
Increased coating efficiency of antigens and preservation of original antigenic structure after coating in ELISA.
Three monoclonal antibodies (MAbs) to recombinant interferon-gamma (rIFN-gamma) did not react well with rIFN-gamma immobilized on the ELISA plate surface. However, binding of the MAbs to immobilizedExpand
Chemically humanized murine monoclonal antibody against a cell nuclear antigen: Usefulness in autoimmune diagnostics
The cellular nuclear antigen SS‐B/La is known to be a major antigenic target to an autoantibody in patients with Sjogren's syndrome and systemic lupus erythematosus. It is useful to detect anExpand
The detection of influenza A virus antigens in cultured cells by enzyme-linked immunosorbent assay
SummaryAn enzyme-linked immunosorbent assay (ELISA) was employed to investigate the expression of influenza A/Hong Kong/68 (H3N2) virus structural proteins on the surface of infected MDCK cells, andExpand