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In cancer cells, levels of misfolded proteins and ER stress are often increased because of gene mutations and stressful microenvironment.
In contrast with high EpCAM levels, absence of EpCAM because of gene mutations results in CTE (congenital tufting enteropathy), a rare disease causing severe diarrhea in newborns due to abnormal development of the intestinal epithelium [ 8].
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For example, during metastasis, cancer cells frequently have reduced expression of tumor suppressors probably because of gene mutation or epigenetic inactivation.
This may be a better strategy to study PC because of the multiplicity of gene mutations and pathway deregulations that underlie its aggressiveness and resistance to therapy (Sarkar et al, 2010; Wang et al, 2010).
Because miRNAs can regulate hundreds of genes, mutations in target gene binding sites ought to confer less pleiotropic effects than mutations to the trans-acting miRNA.
Podocytes have become the focus of attention in recent years because of other gene mutations that have been identified which encode proteins at, or in association with the podocyte slit diaphragm and cause hereditary nephrotic syndrome, such as NPHS1 (nephrin) [22], ACTN4 (α actinin-4) [42] and NPHS2 (podocin) [43], of which TRPC6 is the latest addition.
The vast majority of these mobile elements have deleterious effects on the host genome, because of the gene mutations and chromosomal rearrangements they promote, and usually they are efficiently eliminated by selection [2].
Considering that p53 protein accumulation was correlated with poorly-differentiation and T2, T3 and T4 TNM stage of GC, we concluded that p53 protein accumulation in this study may lead to the loss of cell proliferation control and inhibition for iNOS and VEGF, possibly because of p53 gene mutation.
In conventional breeding, large sizes of breeding populations are required, especially for the selection of recessive traits, because single gene mutations often do not confer phenotypic variation in peanut due to functional complementation by homoeologous genes.
Because of two founder gene mutations found in two ethnic populations, one mitochondrial DNA (mtDNA -encoded mtDNA -encodedng to the disease occurs in 1 in 2,000 births in an isolated population near Quebec, Canada, and another nuclear-encoded mutation with an estimated homozygote frequency of 1:2,500 occurs in the Faroese populeading
Genotoxic effects on germ cells are of crucial importance because gene mutations or chromosome damage may be transferred to the offspring and future generations.
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