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Size-exclusion chromatography and heteronuclear NMR-based chemical shift mapping studies indicate that the helical face of the dockerin module recognizes the CpGH84C X82 module.
Structural modeling of one DBL2X variant combined with ligand binding and antibody epitope mapping studies indicate that this dimorphic sequence is surface exposed on the VAR2CSA antigen, binds the glycosaminoglycan ligand CSA and is also a binding site for IgG antibodies from women who had suffered pregnancy associated malaria [58].
Results of QTL mapping studies indicate β-defensin gene clusters as candidate regions influencing the number of somatic cells in milk [ 15, 16].
Our mapping studies indicate that the two subgenomes of allotetraploid cottons are equivalent in recombination frequencies despite the extra repetitive DNA in the At subgenome (Zhao et al. 1998).
Epitope mapping studies indicate that BP autoantibodies of IgE and IgG isotypes and IgG1 and IgG4 subclasses recognize multiple epitopes that cluster within BP180 NC16A [ 3, 11, 16, 26, 63].
In fact, our mapping studies indicate that more than one gene likely underlies the insulin locus (Solberg Woods et al. 2012), and it is reasonable to expect that Tpcn2 may interact with one or more genes within this region.
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B cell mapping studies indicated that sera from all of the haplotype mice vaccinated with any of the ABeta42 peptides reacted specifically to the first 10 amino acids of ABeta42 with the ABeta42 mutants eliciting higher immune responses.
‡Deletion mapping studies indicates that the plcC gene of the Oryx bacilli is present [ 23].
Our fate-mapping studies indicate that Reck-positive cells are abundant in the anterior meshenchyme (AM) in the limb bud of mid-gestation embryos (Fig. 3).
Recent genetic 'fate-mapping' studies indicate that epithelial cells are unable to migrate from the endothelial compartment, and instead, they implicate pericytes as the myofibroblast progenitor (Lin et al. 2008, Humphreys et al. 2010).
Epitope mapping study indicated that a cluster of overlapping peptides located in the C-terminal region (amino acids [aa] 331 to 362) of N protein contained at least two different T-cell epitopes.
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