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It is possible that the Fto mutant mice suffer some degrees of GH deficiency.
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Similar as observed in patients suffering from NLSDI, newborn CGI-58-deficient mice suffer from an ichthyosiform skin defect.
Although the mutant mice suffer severe growth retardation at 2 4 weeks of age, some of them survived when they were provided with water gel and food at the bottom of the cages.
They've found that mice suffer similar changes in their behavior if their mothers are exposed to viral proteins.
The results demonstrate that STX-T-deficiency mice suffer from iron deficiency anemia.
The experimental mice suffer sever spinal cord injury similar to human extremely sever damage caused by traffic accident.
Nevertheless, most preclinical studies in mice suffer from insufficient predictive value when compared with cancer biology and therapy response of human patients.
Earlier results had shown, for example, that the healthy tissues of normal mice suffer more from gamma irradiation than do the healthy tissues of p53-deficient mice.
Normally, these mice suffer from the degeneration of Purkinje cells in the cerebellum, a part of the brain important for balance and movement.
Homozygous Mariusz mice suffer from a profound muscle weakness and fusion of hind paw digits.
These mice suffer severe postnatal growth retardation, and 80% die before weaning.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com