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Our results also show an association between tumour site and D-Loop mutation, demonstrating that hypopharyngeal tumours were significantly more frequent in the group of mutated tumours compared to that of nonmutated tumours.
However the ATRT also bore somatic loss of 22q and an inactivating SMARCB1 mutation, demonstrating that germ-line inactivation of CDKN1C was not sufficient to cause ATRT.
Only one case presented a BRAF mutation, demonstrating that is a rare alteration in EAL.
DCs sorted from the ITD+ AML samples contained the ITD mutation, demonstrating that they originated from leukemic blasts (Fig. 4).
The M. tuberculosis strain C, which possesses the RvD7 deletion, also shows this mutation, demonstrating that PPE38, rather than PPE71, has been deleted in this case.
No PIP3 was produced in age-1 mg44) age-1 mg44ts that were made viable by the daf-16(m27) loss-of-funullon mutantsn, demonsthating that PIP3 generation requires the AGE-1 Class IA PI3K.
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Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development.
Functional characterization of the F139WfsX24 mutation demonstrated that it causes a complete loss of TRESK function and that the mutant subunit suppresses the wild-type channel function through a dominant-negative effect.
In vivo functional characterization of the endogenous heterozygous nonsense mutation demonstrated that the molecular mechanism underlying glucocorticoid insensitivity in this kindred involves GR haploinsufficiency and nonsense-mediated mRNA Decay (NMD) [17].
Serial deletion mutation demonstrated that OsSec18 binds to the Os60sP0p in a head/tail to head manner.
One "conventional" knock-in model of NPM1 mutation demonstrated that NPM1 mutation can result in myeloproliferative disease but is insufficient for leukemogenesis [ 13].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com