Sentence examples for mutations codify for from inspiring English sources

There is still no evidence concerning PTCH1 associated transcriptome for nonsense PTCH1 mutations, but we can speculate that such mutations codify for decay mRNA linked to soluble cytosolic PTCH1 variants, instead of transmembranous proteins.

A number of authors agree that mutations, codifying for stop codons within the open reading frame, could target mutant WRN mRNA for non-sense mediated decay.

Mutations in COL4A3 or COL4A4, the genes that codify for α-3 and α-4 chains of type IV collagen are the cause of the disease and such mutations are similar to those reported in autosomal recessive Alport syndrome [ 6– 8].

The top genes which appeared most significantly overexpressed in the PH areas codify for cytokines, chemokines, coagulation factors, cell growth and proliferation factors while the underexpressed codify for proteins involved in cell cycle or neurotrophins.

Along these lines, we found that other Ty3/Gypsy clades codify for LTRCAPs bearing this variant.

They codify for proteins involved in cellular growth and proliferation and/or in cellular organization, morphology and migration.

Therefore, we analysed the expression of CAT, GPX1, and GPX4 genes (which codify for the most active glutathione peroxidases).

They are small, non-autonomous elements (~100-500 bp) that contain TIRs but do not codify for any protein.

CTNNB1 and GSK3B genes codify for protein β-catenin and its repressor, Glycogen Synthase Kinase 3- β, respectively.

The S. exigua ABCC2 and ABBC3 genes codify for a 12-transmembrane domain protein [see Additional file 4: Figure S1].

The gene amoA, together with the genes amoC and amoB, codify for the different subunits of the ammonia monooxygenase (AMO).