Sentence examples for attributable to deletion from inspiring English sources

Suggestions(1)

The phrase "attributable to deletion" is correct and usable in written English.
It can be used when discussing the cause or reason for something being lost or removed, particularly in contexts like data management or analysis.
Example: "The missing files were found to be attributable to deletion during the system update."
Alternatives: "due to removal" or "resulting from deletion".

Exact(2)

Our findings show that CDKN1C silencing is common in RT, suggest that CDKN1C is an important regulator of RT cell growth, and that RT cell proliferation is mediated in part via suppression of CDKN1C expression attributable to deletion of SMARCB1.

This failure is likely attributable to deletion of HHF2, which results in reduced starvation resistance (Davey et al., 2012) and is associated with reduced lifespan (Feser et al., 2010).

Similar(58)

Although relatively rare, clear examples of maternally inherited diabetes attributable to deletions or mutations in the mitochondrial genome have been documented [ 4- 6], are often accompanied by deafness, and may account for as much as 1% of the overall diabetes burden [ 7].

We set out to derive an ES cell line in which the gene encoding Dicer can be deleted conditionally using CRE/loxP, allowing us to discriminate between primary effects attributable to Dicer deletion and secondary effects resulting from derivation and long-term culture of ES cells deficient for this essential factor.

It is thus possible that the 10 instances of observed fragment loss are attributable to fragment deletion caused possibly by ectopic or unequal recombination rather than homeologous recombination.

Such outcomes could be attributable to spontaneous deletion of an rDNA-containing fragment from the short arm of the chromosome(s) [ 33], or to unequal crossing over, which could lead to a loss (and/or gain) of repeats from different sites [ 34].

These results suggest that the observed phenotypes are attributable to the deletions and not to linked mutations.

However, the present work provides evidence that only a small fraction of the unexplained familial risk of CMM is attributable to large deletions of CDKN2A locus.

However, the diversity was mostly attributable to the entire deletion of exon 2 or exon 3 or to variations in the length of the neck region (exon 4) of DC-SIGNR.

All inconsistencies were attributable to a deleted region from chromosome 1 in a proband which may be caused by a bona fide de novo micro-deletion event or an artifact of the DNA derived from the EBV-immortalised cell-lines.

Molecular complementation verified that the asl1 mutant phenotype is attributable to the 2-bp deletion in ASL1 encoding PRPS20, a protein belonging to the PRP family.

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