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A better understanding of the biology of differentiation of secretory cells known to harbor azadirachtin and other triterpenoids [ 14] may permit development of varieties with higher percentage of these cells in the cotyledons.
Student providers were thought to have more time to listen and educate patients than physicians – this time may permit development of more empathetic relationships than possible in a typical brief patient-physician encounter.
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Thus cell surface presentation of glycosylated mammalian antigens may now permit development of novel and inexpensive vaccine platforms.
The increased speed of this algorithm may permit the development of more flexible monitoring guidelines for multiple endpoints for clinical trials.
This new knowledge may permit the development of screens for tumour response to crosslinking agents, and should also aid the design of more effective crosslinking agents that evade DNA repair.
Accordingly, disruption of the interaction between TR3 and the TSC may be a novel approach for the prevention of cardiac hypertrophy and may permit the development of a new class of therapeutic drugs for hypertrophic ablation.
Furthermore, elucidation of common pathway alterations across different classes of RC dysfunction may permit the development of pathway-targeted therapies for the difficult to treat class of primary mitochondrial disorders (Parikh et al, 2009).
Thus, the capacity of SGTP1/4 to transport glucose may have evolved independently, while SGTP2/3 apparently lost this capacity after the divergence from the last common ancestor with the other glucose transporters of class I. Overall, these observations may permit the development of specific inhibitors for S. mansoni glucose transporters.
Therefore, the adsorption behavior is characteristic for each singular protein, and computer-based simulation may permit recommending trends or development directions [28].
miRNA editing increases during brain development and may permit the emergence of new biological functions (e.g., a novel translational control of the development of nerve cell extensions [i.e., dendritogenesis]) (Ekdahl et al. 2012).
They can be subject to genetic alteration, associating with tumourigenesis for inherited (for example, BRCA proteins) and for sporadic (for example, Aurora A: 30% to 60% overexpression) breast cancer because they cause genetic instability that may permit secondary alteration, accelerating the development of cancer.
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