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As they report in the journal Development, that mutation led to some mouse embryos' developing a mirror-image anatomy.
A genetic mutation led to lighter fur, and the sandhills mice lucky enough to be born mutants were more likely to survive and breed.
The marR109 mutation led to the truncation of 35 C-terminal amino acids in MarR.
First, the W71V mutation led to a change in the relative proportion of the two Fe-based EPR signals.
The mutation led to a one-amino-acid change within E1, a protein sitting on the viral coat.
These observations indicated that mutations of XP genes resulted in compromised NER or TLS abilities, and XPA mutation led to most severe DNA repair defects in NSCs.
The mutation led to a 50% reduction of FERMT1 mRNA and 90% reduction of kindlin-1 protein in keratinocytes derived from the patient, as compared with control cells.
To further investigate the molecular mechanism by which NR5A1/SF-1 mutation led to gonadal dysgenesis with predominant Sertoli cell defect.
Changes in starch structure induced by the r mutation led to clear differences in starch digestion kinetics for purified starches and pea flours.
The dystrophin exon 16 donor splice mutation led to the retention of ∼20,370 bases, the entire intron 16 in the mature mRNA, accounting for the inability to amplify across dystrophin exons 15 18 in RNA extracted from this patient.
However, the E2-I211T mutation led to no apparent effect on CHIKV infectivity for Ae. albopictus.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com