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The DNA molecules in human chromosomes range from 40 million to 250 million units in length, presenting a different scale of difficulty.
Most hemoglobin molecules in human blood consist of two alpha chains and two beta chains, but in 10 percent of the blood, delta chains substitute for the betas.
The existence of several non-antibody protein fragments in clinical studies certainly points to the promise of these molecules in human therapy.
Hoping for a clear answer, a team led by cell biologist Nissim Benvenisty of the Hebrew University of Jerusalem looked for MHC molecules in human ES cell lines.
The purpose of this study was to investigate the effects of N15 on the expression of adhesion molecules in human umbilical vein endothelial cells (HUVECs).
The present study investigated the effect of OPA on the expression of adhesion molecules in human umbilical vein endothelial cells (HUVEC).
Research during the past three decades has revealed that three small "toxic" molecules namely nitric oxide (NO), carbon monoxide (CO) and hydrogen sulfide (H2S) act as important signaling molecules in human physiology and pathology at submicromolar to micromolar levels.
Despite of the inevitable input of laboratory animal trials, recent studies have shown that animal pain models have repeatedly failed to predict clinical analgesic efficacy and adverse side effects of potential drug molecules in human pain patients.
To validate the results of our in vitro model in vivo, we analyzed the expression of these adhesion molecules in human endometrium throughout the menstrual cycle.
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The roles of these molecules in humans and in rodents are considered against a set of criteria established in classical endocrinology for establishing physiological endocrine action.
In a recent study, Khan and collaborators built a mathematical model to predict the hedonic valence of molecules in humans on the basis of their physicochemical properties.
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