Exact(3)
Loss of both eiger copies strongly suppressed apoptosis, invasion and overgrowth of Vha44-expressing cells (Fig. 6I,J).
The signatures of CpG to TpG mutations found in some TE copies strongly suggest a mechanism of methyl-cytosine deamination following de novo methylation induced by a process similar to MIP.
The high degree of sequence similarity shared by these different copies strongly suggests that they belong to a paralogous gene family, originated from an ancestral ceoB-like sequence that underwent many duplication events and existing long before the appearance of the ancestor of Burkholderia.
Similar(56)
In fact, we found that reducing the dose of the dl gene from 2 to 1 wild type copy strongly suppresses the neuropathological effects of the Aβ42 polypeptide.
Disruption of the rpf gene was not possible in M. luteus in the absence of a second functional copy, strongly suggesting essentiality of this protein for normal growth [ 17].
Therefore, the regain of egfr copies might strongly contribute to the survival and outgrowth of disseminated cancer cells at the metastatic site [ 31].
Bootstrap values are not strong for internal nodes, certainly because of the weak phylogenetic signal for these sequences (Table 2), but terminal nodes grouping the paralogous copies are strongly supported.
The degeneration of PMM-2 genes and the comparatively high mean evolutionary rate of these members indicate the occurrence of relaxed purifying selection in the evolution of PMM gene family in wheat and relatives, which may have affected PMM-2 copies more strongly than PMM-1 paralogs.
Reversely, embryonic lethality correlated with a higher transgene copy number, strongly suggesting that when the Cre is partly efficient, the GFP cassette is excised from multiple transgene copies, resulting in a tiar transgene expression above the threshold level compatible with embryonic survival.
Our results reveal a complex genomic architecture in the i(17q) breakpoint cluster region, characterized by large (∼38 49-kb ∼38 49-kbomic, low-copalindromic strongly suggesting that somatic rearrangements are not random events but rather reflect susceptibilities due to the genomic strepeats.
Hence, even though non-binomial distributions were rare in the three cell lines, they were sufficiently frequent to generate cells with a DM copy-number strongly deviating from the modal value of the cell population.
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com