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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1981-2-19
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pubmed:abstractText |
Earlier studies showed that genetic resistance of adult, inbred strains of mice to Herpes Simplex Virus-type 1 (HSV-1) is a dominant genetic trait. The present studies were undertaken to determine the number of genetic loci involved and whether they were found within the major histocompatibility complex, H-2, of the mouse. Challenge with HSV-1 of progeny of mice backcrossed to moderately susceptible BALB/c mice, of progeny of mice backcrossed to very susceptible A/J strain mice, and of progeny of the F-2 cross using (C57BL/6 x A/J)F1 mice indicated that two major loci were responsible for resistance. The backcrosses to BALB/c mice suggested that additional genes on this background enhanced resistance, while further backcrosses with the A/J mice indicated that other genes on the A/J background (or the lack thereof) reduced resistance. Studies with congenic mice showed that genes within the H-2 did not influence resistance or susceptibility.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0093-7711
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
87-92
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:6254873-Animals,
pubmed-meshheading:6254873-Chromosome Mapping,
pubmed-meshheading:6254873-Crosses, Genetic,
pubmed-meshheading:6254873-Female,
pubmed-meshheading:6254873-Genes,
pubmed-meshheading:6254873-Genetic Linkage,
pubmed-meshheading:6254873-H-2 Antigens,
pubmed-meshheading:6254873-Herpes Simplex,
pubmed-meshheading:6254873-Immunity, Innate,
pubmed-meshheading:6254873-Male,
pubmed-meshheading:6254873-Mice,
pubmed-meshheading:6254873-Mice, Inbred Strains,
pubmed-meshheading:6254873-Simplexvirus
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pubmed:year |
1980
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pubmed:articleTitle |
Resistance to HSV-1 in the mouse is governed by two major, independently segregating, non-H-2 loci.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|