4 results for author:"Iverius P.-H." in Literature citations
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| Mutations in exon 3 of the lipoprotein lipase gene segregating in a family with hypertriglyceridemia, pancreatitis, and non-insulin-dependent diabetes. Wilson D.E., Hata A., Kwong L.K., Lingam A., Shuhua J., Ridinger D.N., Yeager C., Kaltenborn K.C., Iverius P.-H., Lalouel J.-M. J. Clin. Invest. 92:203-211(1993) · UniProtKB (1) |
| 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 P.-H., Lalouel J.-M. Am. J. Hum. Genet. 47:721-726(1990) · UniProtKB (1) |
| Missense mutation (Gly-->Glu188) of human lipoprotein lipase imparting functional deficiency. Emi M., Wilson D.E., Iverius P.H., Wiu L., Hata A., Hegele R., Williams R.R., Lalouel J.-M. J. Biol. Chem. 265:5910-5916(1990) · UniProtKB (1) |
| Missense mutations in exon 5 of the human lipoprotein lipase gene. Inactivation correlates with loss of dimerization. Hata A., Ridinger D.N., Sutherland S.D., Emi M., Kwong L.K., Shuhua J., Lubbers A., Guy-Grand B., Basdevant A., Iverius P.H. et al. J. Biol. Chem. 267:20132-20139(1992) · UniProtKB (1) |