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With the international research collaboration and advances in genome sequencing techniques, understanding of human genome and disease pathogenesis has dramatically increased.
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From the development of molecular cytogenetic techniques, understanding the organization of genomes had a large impact on taxonomic and evolutionary studies (Fedak and Kim [2008]; Figueroa and Bass [2010]), in breeding and genetic engineering (Seijo et al. [2010]).
Collecting and analyzing such data through quantitative and qualitative techniques enhances understanding of the validity of the assumptions and the relevance of key program processes.
With TEM and related techniques, fundamental understanding of how the microstructures affect the properties of the TMC nanostructured anodes can be improved.
With the refining of EM techniques, our understanding of the endo-lysosomal system has equally evolved.
Using these techniques, our understanding of the functional mechanism of proteins has made significant steps forward.
With the rapid development of various molecular biology techniques, our understanding of bone atrophy-related diseases, including PMOP, has greatly expanded.
Using established EBV-negative NPC cell lines and advanced molecular biology techniques, our understanding of molecular alternations in these cells has been tremendously improved [ 40– 40].
Through these observations, supplemented more recently by investigative techniques, an understanding of how symptoms and signs are generated by disease has developed.
However, ongoing refinements in technology, development of minimally invasive techniques, better understanding of the physiological impact of the ECLS circuit (for example, altered pharmacokinetics of vital drugs [ 62]) and improved clinical delivery may improve patient outcomes.
With the availability of novel optical techniques, our understanding of the biochemical environment of tumours (e.g. hypoxia, low pH) has increased dramatically in recent years (Carmeliet and Jain, 2000; Helmlinger et al, 1997b, 2000).
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