Iijima H, Emi M, Wada M, Daimon M, Toriyama S, Koyano S, Sato H, Hopkins PN, Hunt SC, Kubota I, Kawata S, Kato T (2008) <br />Association of an intronic haplotype of the LIPC gene with hyperalphalipoproteinemia in two independent populations<br /><i>J Hum Genet</i> <b>53</b>: 193<br /><br />Koyano S, Emi M, Saito T, Makino N, Toriyama S, Ishii M, Kubota I, Kato T, Kawata S (2008) <br />Common null variant, Arg192Stop, in a G-protein coupled receptor, olfactory receptor 1B1, associated with decreased serum cholinesterase activity<br /><i>Hepatol Res</i> <b>38</b>: 696<br /><br />Ishihara M, Iwasaki T, Nagano M, Ishii J, Takano M, Kujiraoka T, Tsuji M, Hattori H, Emi M (2004) <br />Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients<br /><i>J Hum Genet</i> <b>49</b>: 302<br /><br />Sato K, Emi M, Ezura Y, Fujita Y, Takada D, Ishigami T, Umemura S, Xin Y, Wu LL, Larrinaga-Shum S, Stephenson SH, Hunt SC, Hopkins PN (2004) <br />Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: intrafamilial association study in an eight-generation hyperlipidemic kindred<br /><i>J Hum Genet</i> <b>49</b>: 29<br /><br />Keicho N, Emi M, Kajita M, Matsushita I, Nakata K, Azuma A, Ohishi N, Kudoh S (2001) <br />Overestimated frequency of a possible emphysema-susceptibility allele when microsomal epoxide hydrolase is genotyped by the conventional polymerase chain reaction-based method<br /><i>J Hum Genet</i> <b>46</b>: 96<br /><br />Emi M, Asaoka H, Matsumoto A, Itakura H, Kurihara Y, Wada Y, Kanamori H, Yazaki Y, Takahashi E, Lepert M, Jean-Marc Lalouel JM, Kodama T, Mukai T (1993) <br />Structure, organization, and chromosomal mapping of the human macrophage scavenger receptor gene<br /><i>Journal of Biological Chemistry</i> <b>268</b>: 2120<br /><br />Hata A, Ridinger DN, Sutherland S, Emi M, Shuhua Z, Myers RL, Ren K, Cheng T, Inoue I, Wilson DE, et al. (1993) <br />Binding of lipoprotein lipase to heparin. Identification of five critical residues in two distinct segments of the amino-terminal domain<br /><i>Journal of Biological Chemistry</i> <b>268</b>: 8447<br /><br />Hata A, Ridinger DN, Sutherland SD, Emi M, Kwong LK, Shuhua J, Lubbers A, Guy-Grand B, Basdevant A, Iverius PH, et al. (1992) <br />Missense mutations in exon 5 of the human lipoprotein lipase gene. Inactivation correlates with loss of dimerization<br /><i>Journal of Biological Chemistry</i> <b>267</b>: 20132<br /><br />Emi M, Hata A, Robertson M, Iverius PH, Hegele R, Lalouel JM (1990) <br />Lipoprotein lipase deficiency resulting from a nonsense mutation in exon 3 of the lipoprotein lipase gene<br /><i>American Journal of Human Genetics</i> <b>47</b>: 107<br /><br />Emi M, Wilson DE, Iverius PH, Wu L, Hata A, Hegele R, Williams RR, Lalouel JM (1990) <br />Missense mutation (Gly----Glu188) of human lipoprotein lipase imparting functional deficiency<br /><i>Journal of Biological Chemistry</i> <b>265</b>: 5910<br /><br />Hata A, Emi M, Luc G, Basdevant A, Gambert P, Iverius PH, Lalouel JM (1990) <br />Compound heterozygote for lipoprotein lipase deficiency: Ser----Thr244 and transition in 3' splice site of intron 2 (AG----AA) in the lipoprotein lipase gene<br /><i>American Journal of Human Genetics</i> <b>47</b>: 721<br /><br />Hata A, Robertson M, Emi M, Lalouel JM (1990) <br />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<br /><i>Nucleic Acids Research</i> <b>18</b>: 5407<br /><br />Wilson DE, Emi M, Iverius PH, Hata A, Wu LL, Hillas E, Williams RR, Lalouel JM (1990) <br />Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation<br /><i>J Clinical Investigation</i> <b>86</b>: 735<br /><br />