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How do I apply for mutation of property online in AP? 

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Open accessJournal ArticleDOI
B. J. F. Rossiter, Charles T. Caskey 
75 Citations
The existence of different types of mutation therefore means that diverse ap- proaches to mutation detection are required.
Open accessJournal ArticleDOI
B. J. F. Rossiter, Charles T. Caskey 
75 Citations
Mutation detection procedures can thus be tailored to the partic- ular gene of interest if such a predisposition exists or designed to detect virtually all types of mutation for a more universal ap- proach.
The AP site-induced mutation spectrum supports evidence for the 'A-rule' and is also consistent with the use of the 5' neighbouring base to instruct nucleotide incorporation (5'-rule).
Nonetheless, under sufficient selection, AP is often resolvable through regulatory evolution, primarily by trans-acting changes, although in one case we also detected a cis-acting change and localized its causal mutation.
Our data point to two independent and additive effects of FLG mutations: i) carrying a mutation and ii) having a mutation carrier mother.
The search for mutation is also useful for the identification of the family members who do not carry the mutation and can avoid unnecessary biochemical and instrumental evaluations.
In this method, experimental conditions do not need to be altered depending on mutation sites, and it should be the alternative method for mutation screening.
Open accessJournal ArticleDOI
13 Sep 2018-Evolution
30 Citations
In particular, antagonistic pleiotropy (“AP”: when a mutation has opposite fitness effects in different environments) generates tradeoffs, which may constrain adaptation.
We conclude this nucleotide site is not a mutation hot spot even after accounting for possible Luria–Delbruck “mutation jackpots.” An alternative explanation for such foci involving positive selection acting on adult self-renewing Ap spermatogonia experiencing the rare mutation could not be rejected.
In vitro assays suggest that this mutation causes a “gain of function” in the transcriptional activation of AP-2α.