The phrase "ability to generate both" is correct and usable in written English.
It can be used when discussing the capacity to produce two different outcomes, results, or items in a specific context.
Example: "The software's ability to generate both reports and visualizations makes it a valuable tool for data analysis."
Alternatives: "capacity to produce both" or "capability to create both".
The pikromycin polyketide synthase (PKS) is unique in its ability to generate both 12 and 14 membered ring macrolactones.
Totipotency – the unbiased ability to generate both embryonic and extraembryonic cell types - has only unequivocally been shown to exist during the first few cell divisions of early mouse development.
"Economic growth is the key to avoiding the kind of painful austerity that would limit our ability to generate both hard and soft power," Mr. Ryan said in a speech to the Alexander Hamilton Society last summer.
The adult rat hippocampus contains fibroblast growth factor 2-responsive stem cells that are self-renewing and have the ability to generate both neurons and glia in vitro, but little is known about the molecular events that regulate stem cell differentiation.
A comparison of the two subtypes indicated that the ability to generate both CD44+ and CD44- progeny was significantly associated with the SCP phenotype (P = 0.0046).
Like normal tissue-resident stem cells that support the cellular hierarchy comprising a particular tissue over the lifespan of an individual, cancer stem cells (CSC) are defined by their ability to self-renew indefinitely, while maintaining their ability to generate both tumorigenic (TG) and non-tumorigenic (NTG) cells [1].
The ability of CD44+CD24low+ to generate both cell types, while CD44+CD24neg cells generated only like progeny was also observed in two independent primary dissociated tumour cultures, DT-22 and DT-25 (Supporting Information Fig S3).
The ability of a fertilized egg to generate both embryonic and extra-embryonic tissues is referred to as "totipotency," an ultimate stem cell state seen only during the earliest stages of embryonic development.
We thus aimed to assess the ability of single NMP cells to generate both neural and mesodermal derivatives at the same time using conditions promoting the simultaneous emergence of both lineages (i.e. FGF/CHIR treatment).
Strikingly, the ability of Dicer-null NS cells to generate both neurons and glia is restored by the acute reintroduction of Dicer, demonstrating that these cells are not irreversibly transformed despite the absence of Dicer and microRNAs.
Following a study on the differentiation of dual-fated Neuromesodermal Progenitors (NMPs) at the population level, Tsakiridis and Wilson describe here the ability of a single NMP cell to generate both neural and mesodermal derivatives.
