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Combined with ongoing efforts to map chromatin binding proteins and long distance interactions by 3C techniques genome-wide, mapping of chromosomal attachments to a nuclear substructure may lead to a better understanding of gene regulation and the identification new gene regulatory elements.
This approach, termed 'serologic identification of antigens by recombinant expression cloning' (SEREX), is based on the observation that cancer patients exhibit circulating antibodies directed towards tumor antigens, and that these antibodies may provide a useful reagent for the identification new tumor antigens [ 45, 46].
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The identification of new themes suggested new facets.
Those inputs are specific for the target relation, thus, the identification of new relations requires identification of new extraction patterns or the definition of new examples for training, both to be executed manually.
Our clustering resulted in the identification of new protein groups and novel members of existing families.
The identification of new contaminants is critical in the development of new medicinal products.
Clearly, identification of new molecules involved in osteolytic bone metastasis will provide new therapeutics possibilities.
We describe here a novel proteome-wide approach for the identification of new PKMT substrates.
We describe a novel proteome-wide methodology for the identification of new PKMT substrates.
The identification of new species has become commonplace.
Mining these data leads to scientific discoveries and to the identification of new clinical applications.
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CEO of Professional Science Editing for Scientists @ prosciediting.com