Sentence examples for mutation that eliminates from inspiring English sources
Males carrying a mutation that eliminates GABA synthesis, unc-25, show decreased dorsal and ventral tail curling in response to increased levels of acetylcholine.
By analyzing mice with a Dido3-specific mutation that eliminates almost 50% of the Dido3 C-terminal sequence, we show that Dido3 is essential for early embryonic development.
Conversely, if a HisMBP-TEV-Sna3C with a K125A mutation that eliminates Sna3 ubiquitination but still retains its Rsp5-binding PPXY motif is used, Ub is ligated to both HisMBP and Rsp5WW1-3-HECT.
The dat-1 (ok157 )III strain was a gift of J. Duerr and J. Rand (Oklahoma Medical Research Foundation, Oklahoma City) and is a complete loss-of-function mutation that eliminates the majority of the DAT-1 coding sequence.
One of these introduces a premature stop codon into the third exon of gene mel-32 C05D11.11, and the other is a splice junction mutation that eliminates the splice donor site of first intron of the gene cki-2 T05A6.2.
We showed that a mutation that eliminates the CP 1 6 motor neurons does not significantly decrease aldicarb-induced ventral tail curling suggesting that there are cholinergic neurons that act, in part, in parallel to the CP motor neurons to regulate ventral tail curling.
Only 7 out of the 12 populations studied showed changes in their genomic sequence, which included four reversions (17% of the changes), one mutation that eliminated a stop codon in nef coding region of virus H (Table 1) and a common mutation in the 5'LTR in three viruses, as described [4].
A new construct was designed encoding an engineered gelatin, FG-5009, with point mutations that eliminated the charge heterogeneity.
In addition, a defective transposable element family from Phytophthora infestans was named DodoPi as it contained mutations that eliminated the element's ability to jump to new locations in a chromosome.
Further, mutations that eliminate the microtubule-binding domain of APC result in defective chromosomal segregation [46].
It is possible to address CTCF function in intact animals using mutations that eliminate detectable CTCF protein.
