1MADSEN HO,GARRED P,KURTZHALS JA,et al.A new frequent allele is the missing link in the structueal poly morphism of the human mannan-binding protein.Immunogenetics,1994,40(1):37-44.
2LAU YL,CHAN SY,TURNER MW.Mannose-binding protein in preterm infants:Develop mental profile and clinical significance.Clin Exp Immunol,1995,102(3):649-654.
3TURNER MW.Mannose binding lectin:The pluripotent molecule of the innate immune system.Immunol Today,1996,17(11):532-540.
1Madsen HO, Garred P, Kurtzhals JA, et al. A new frequent allele is the missing link in the structural polymorphism of the human mannan binding protein[J]. Immunogenetics, 1994, 40: 37-44.
2Ezekowitz RA. Role of the mannose-binding lectin in innate immunity[J]. J Infect Dis, 2003, 187( Suppl 2): 335-339.
3Ipscombe RJ, Lau YL, Levinsky RJ, et al. Identical point mutation leading to low levels of mannose binding protein and poor C3b mediated opsonisation in Chinese and Caucasian populations[J]. Immunol Lett, 1992, 32: 253-258.
7Juliger S, Kremsner PG, AlpersMP, et al. Restricted polymorphisms of the mannose-binding lectin gene in a population of Papua New Guinea[J]. Mutation Res, 2002, 505: 87-91.
8Sumiya M, Super M, Tabona P, et al. Molecular basis of opsonic defect in immunodeficient children[J]. Lancet, 1991, 337: 1569-1570.
9Lipscombe RJ, Sumiya M, Hill AV, et al. High frequencies in African and non-African populations of independent muta- tions in the mannose binding protein gene[J]. Hum Mol Genet, 1992, 1: 709-715.
10Perterson SV, Thiel S, Jensenius JC. The mannan-binding lectin pathway of complement activation: biology and disease association[J]. Mol Immunol, 2001, 38: 133-149.