Mannose-binding lectin variant associated with severe malaria in young African children.
about
Genetic polymorphisms linked to susceptibility to malariaInfections of People with Complement Deficiencies and Patients Who Have Undergone SplenectomyMutations of complement lectin pathway genes MBL2 and MASP2 associated with placental malariaGenetic polymorphisms of mannose-binding lectin do not influence placental malaria but are associated with preterm deliveries.Haplotype specific-sequencing reveals MBL2 association with asymptomatic Plasmodium falciparum infection.MBL2 variations and malaria susceptibility in Indian populations.Polymorphisms of innate immunity receptors in infection by parasites.Mannose-binding lectin and susceptibility to schistosomiasis.Polymorphisms in host genes encoding NOSII, C-reactive protein, and adhesion molecules thrombospondin and E-selectin are risk factors for Plasmodium falciparum malaria in India.No Evidence that Knops Blood Group Polymorphisms Affect Complement Receptor 1 Clustering on Erythrocytes.The emerging role of complement lectin pathway in trypanosomatids: molecular bases in activation, genetic deficiencies, susceptibility to infection, and complement system-based therapeutics.
P2860
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P2860
Mannose-binding lectin variant associated with severe malaria in young African children.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh
2007年學術文章
@zh-hant
name
Mannose-binding lectin variant associated with severe malaria in young African children.
@en
type
label
Mannose-binding lectin variant associated with severe malaria in young African children.
@en
prefLabel
Mannose-binding lectin variant associated with severe malaria in young African children.
@en
P2093
P1476
Mannose-binding lectin variant associated with severe malaria in young African children.
@en
P2093
Ekkehart Dietz
Friederike Schuster
J Chantale Sagarriga Visconti
Sylvester D Anemana
Ulrich Bienzle
P304
P356
10.1016/J.MICINF.2007.12.008
P577
2007-12-28T00:00:00Z