Exact(8)
This finding suggests the deregulation epigenetic components at the kinetochore complex could lead to chromosome defects and the development of chromosomal instability.
The selection of a key thiolase (bktB) and thioesterase (ydiI) in combination with previously established core β-oxidation reversal enzymes, as well as the development of chromosomal expression systems for the independent control of pathway enzymes, enabled the generation of C6 C10 carboxylic acids and provided a platform for vector based independent expression of ω-functionalization enzymes.
Our studies using these cells indicate that polyploidy induced by Pim-1 can promote the development of chromosomal abnormalities and tumorigenicity in human prostate and mammary epithelial cells.
Disorders of sex development (DSD) comprise a large number of cases in which development of chromosomal, gonadal or anatomical sex is atypical [1].
It is noteworthy that non-homologous-mediated end joining of DNA DSB was proposed to reverse apoptosis, albeit at low frequency, leading to the development of chromosomal translocations, particularly those linked to t-AML [53], [54].
Binding of HR-E6 to MCM7 leads to the development of chromosomal abnormalities which promote DNA damage.
The precise roles of these factors in the development of chromosomal instability and retro-transposition require further study.
Unrepaired DNA ends might contribute to the development of chromosomal translocations by acting as transposable elements (Hall, 2006a).
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