Literature DB >> 11796577

Association of a determinant on mouse chromosome 18 with experimental severe Plasmodium berghei malaria.

Eiji Nagayasu1, Koichi Nagakura, Mayumi Akaki, Gen Tamiya, Satoshi Makino, Yamaji Nakano, Minoru Kimura, Masamichi Aikawa.   

Abstract

Experimental severe malaria (ESM; also known as experimental cerebral malaria) is an acute lethal syndrome caused by infection with Plasmodium berghei ANKA and associated with coma and other neurological manifestations in mice. Various inbred strains of mice exhibit differences in susceptibility to the development of ESM. For example, C57BL/6 mice are highly susceptible and DBA/2 mice are relatively resistant. We report here the results of a genomewide scan for host genomic regions that control resistance to ESM in DBA/2 mice using an F(2) intercross population of susceptible and resistant strains. A region of mid-chromosome 18 was found to be a major determinant of resistance to ESM.

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Year:  2002        PMID: 11796577      PMCID: PMC127666          DOI: 10.1128/IAI.70.2.512-516.2002

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  23 in total

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5.  Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results.

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6.  Cytokine profile suggesting that murine cerebral malaria is an encephalitis.

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  14 in total

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Review 5.  Genetic mapping of determinants in drug resistance, virulence, disease susceptibility, and interaction of host-rodent malaria parasites.

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8.  Common strategies to prevent and modulate experimental cerebral malaria in mouse strains with different susceptibilities.

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9.  Identification of two cerebral malaria resistance loci using an inbred wild-derived mouse strain.

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10.  Malaria liver stage susceptibility locus identified on mouse chromosome 17 by congenic mapping.

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