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For example, the dynamic association between glucocorticoid receptor and cognate binding sites is refractory to formaldehyde crosslinking [11].
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Supporting this supposition, the oxime formed by reaction of methoxyamine with Ap sites is refractory to processing by APE.
One method to reduce the presence of these information-poor binding sites is to apply stricter binding site conservation criteria.
Twelve binding sites are present within the dodecameric channel.
[3H]nicotine binding sites are associated with mammalian optic nerve terminals.
Potential binding sites were elucidated by docking.
Residues defining the binding sites were selected for site-directed mutagenesis.
Here, these binding sites are not discussed one by one.
These binding sites are highly charged.
Common major Atf1/Pcr1 binding sites are overlapping major Atf1 and major Pcr1 binding sites.
Noteworthy, these binding sites are juxtaposed to GATA3-binding sites.
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