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Author Report for: Emi M

No contact information in database for Emi M

    Title: Association of an intronic haplotype of the LIPC gene with hyperalphalipoproteinemia in two independent populations
    Iijima H, Emi M, Wada M, Daimon M, Toriyama S, Koyano S, Sato H, Hopkins PN, Hunt SC and Kato T <2 more author(s)>
    Ref: J Hum Genet, 53:193, 2008 : PubMed


    Title: Common null variant, Arg192Stop, in a G-protein coupled receptor, olfactory receptor 1B1, associated with decreased serum cholinesterase activity
    Koyano S, Emi M, Saito T, Makino N, Toriyama S, Ishii M, Kubota I, Kato T, Kawata S
    Ref: Hepatol Res, 38:696, 2008 : PubMed


    Title: Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients
    Ishihara M, Iwasaki T, Nagano M, Ishii J, Takano M, Kujiraoka T, Tsuji M, Hattori H, Emi M
    Ref: J Hum Genet, 49:302, 2004 : PubMed


    Title: Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: intrafamilial association study in an eight-generation hyperlipidemic kindred
    Sato K, Emi M, Ezura Y, Fujita Y, Takada D, Ishigami T, Umemura S, Xin Y, Wu LL and Hopkins PN <3 more author(s)>
    Ref: J Hum Genet, 49:29, 2004 : PubMed


    Title: Overestimated frequency of a possible emphysema-susceptibility allele when microsomal epoxide hydrolase is genotyped by the conventional polymerase chain reaction-based method
    Keicho N, Emi M, Kajita M, Matsushita I, Nakata K, Azuma A, Ohishi N, Kudoh S
    Ref: J Hum Genet, 46:96, 2001 : PubMed


    Title: Structure, organization, and chromosomal mapping of the human macrophage scavenger receptor gene
    Emi M, Asaoka H, Matsumoto A, Itakura H, Kurihara Y, Wada Y, Kanamori H, Yazaki Y, Takahashi E and Mukai T <3 more author(s)>
    Ref: Journal of Biological Chemistry, 268:2120, 1993 : PubMed


    Title: Binding of lipoprotein lipase to heparin. Identification of five critical residues in two distinct segments of the amino-terminal domain
    Hata A, Ridinger DN, Sutherland S, Emi M, Shuhua Z, Myers RL, Ren K, Cheng T, Inoue I and et al. <1 more author(s)>
    Ref: Journal of Biological Chemistry, 268:8447, 1993 : PubMed


    Title: Missense mutations in exon 5 of the human lipoprotein lipase gene. Inactivation correlates with loss of dimerization
    Hata A, Ridinger DN, Sutherland SD, Emi M, Kwong LK, Shuhua J, Lubbers A, Guy-Grand B, Basdevant A and et al. <1 more author(s)>
    Ref: Journal of Biological Chemistry, 267:20132, 1992 : PubMed


    Title: Lipoprotein lipase deficiency resulting from a nonsense mutation in exon 3 of the lipoprotein lipase gene
    Emi M, Hata A, Robertson M, Iverius PH, Hegele R, Lalouel JM
    Ref: American Journal of Human Genetics, 47:107, 1990 : PubMed


    Title: Missense mutation (Gly----Glu188) of human lipoprotein lipase imparting functional deficiency
    Emi M, Wilson DE, Iverius PH, Wu L, Hata A, Hegele R, Williams RR, Lalouel JM
    Ref: Journal of Biological Chemistry, 265:5910, 1990 : PubMed


    Title: Compound heterozygote for lipoprotein lipase deficiency: Ser----Thr244 and transition in 3' splice site of intron 2 (AG----AA) in the lipoprotein lipase gene
    Hata A, Emi M, Luc G, Basdevant A, Gambert P, Iverius PH, Lalouel JM
    Ref: American Journal of Human Genetics, 47:721, 1990 : PubMed


    Title: Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene
    Hata A, Robertson M, Emi M, Lalouel JM
    Ref: Nucleic Acids Research, 18:5407, 1990 : PubMed


    Title: Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation
    Wilson DE, Emi M, Iverius PH, Hata A, Wu LL, Hillas E, Williams RR, Lalouel JM
    Ref: J Clinical Investigation, 86:735, 1990 : PubMed


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Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
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