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Going into the development of an ad with this thinking and testing was invaluable and saved time.
Interestingly, Elan and Wyeth used a similar strategy for the development of an AD protein vaccine (ACC-001), in which an N-terminal sequence of Aβ is conjugated to diphtheria toxin that should provide foreign Th epitope/s.
The development of an ad hoc scaffold for effective tissue engineering applications plays a pivotal role in promoting and support the healing process.
Because vaccinations may cause brain inflammation that leads to meningoencephalitis, minimizing the risk of such inflammation and meningoencephalitis has to be a major goal in the development of an AD vaccine.
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Postnatal skin-specific inactivation of both RXRα and RXRβ (RXRs) leads to the development of an AD-like disease characterized by partial hair loss, Th2 inflammation, eosinophilia, elevated TSLP epidermal secretion, and high TSLP serum levels [24].
Histological analysis of the skin of control, RBP-JK5 and RBP-JK5/G-CSF+/− mice showed the development of an AD-like disease in both mutant mice, implying that reduced G-CSF serum levels did not ameliorate the skin phenotype (Figure 6C), which is expected as TSLP serum levels are still elevated in the RBPJ-K5/G-CSF+/− mice (Figure 6D).
Nevertheless, due to the lack of direct evidence of neurofibrillary tangle (NFT) deposition in the brain, we do not know whether hyperphosphorylated tau plays a role in promoting the development of an AD-like syndrome in experimental CT.
The funds will also be used to provide the vaccine and over 500 million auto-disable (AD) syringes and safety boxes to ensure safe injection practices and foster the development of a local AD syringe industry in China.
Here, we focus on the development of a CAT for the AD sub-scale, which contains 22 items.
The ablation of canonical Notch signaling in keratinocytes by simultaneous deletion of both Notch1 and Notch2 or RBP-J resulted in defective skin barrier function and increased expression of TSLP, leading to the development of a severe AD-like skin phenotype in mice (Demehri et al., 2008; Dumortier et al., 2010).
Although 'A β cascade theory' is one of the most accredited hypothesis to explain the development of AD, a growing body of evidence support a role of oxidative stress, as well as inflammation mechanisms in the pathogenesis of the disease.
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