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The transfer of F1 spleen cells into the low responder parent demonstrated that ability to respond was a property of immunocompetent cells (spleen cells), not of the recipient's background genes.
Although much of the information itself may be considered harmless, this does not necessarily mean that the effects cannot be harmful, as the utility of health information depends on the recipient's background knowledge that is necessary to evaluate the information adequately [ 44].
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On condition that a recipient's genetic background and major histocompatibility are coincident with the donor's, the immunological response of hosts depends mainly on the structure and the dose of exogenous protein, the route of entry, the type of cells expressing the transgene as well as the viral vector system [ 16, 33, 34].
At week 24 of gestation, donor HLA class II alleles were detected at a low level in the background of the recipient's fetal HLA genotype.
The second reason is the quantitative nature of multiple gene/QTL may partially regulated by recipient genetic background of CholSub1 donor and the 'PinK3', the highly susceptible recipient.
Successful quantitative trait locus (QTL) introgression depends on the optimized expression of newly introgressed QTLs in the recipient genome background, with the aim of maximizing productivity.
Measure recipient's wrist.
Recipient's Name.
We identified BC3F3 qGnear-isogenicgenic lines (NILs) with 92.0 98.0% similarity to the respective recipient parent by background analysis using a 50 K rice SNP genotyping chip.
In the initial step, one round of backcrossing is conducted to donate the favorable QTL allele to the recipient background using marker-assisted backcrossing (MAB).
2×10 spleen cells (recipient background) were co-injected to promote short-term survival.
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