(LOT OF DX-124-12A VAC 105-305 Control Photoelectric Outdoor DARK-TO-LIGHT 5) Other Sensors


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(LOT OF 5) DARK-TO-LIGHT Outdoor Photoelectric Control 105-305 VAC DX-124-12A
Condition: New: A brand-new, unused, unopened, undamaged item in its original packaging (where packaging is Country/Region of Manufacture: Mexico
Model:

DX-124-12A

Current Type: AC
MPN:

DX-124-12A

Sensor Type: Photoelectric
Brand:

DTL

UPC:

na

published on tue nov 09 2021

(LOT OF DX-124-12A VAC 105-305 Control Photoelectric Outdoor DARK-TO-LIGHT 5) Other Sensors

gandhi, s., klein, j., robertson, a., pena-hernandez, m. a.,

(LOT OF DX-124-12A VAC 105-305 Control Photoelectric Outdoor DARK-TO-LIGHT 5) Other Sensors

lin, m. j., roychoudhury, p., lu, p., fournier, j., ferguson, d., mohamed bakhash, s. a., muenker, m. c., srivathsan, a., wunder, e. a., kerantzas, n., wang, w., pyle, a., wilen, c. b., ogbuagu, o., greninger ,, a. l., iwasaki, a., schulz, w. l., ko, a. i.

sars-cov-2 remdesivir resistance mutations have been generated in vitro but have not been reported in patients receiving treatment with the antiviral agent. we present a case of an immunocompromised patient with acquired b-cell deficiency who developed an indolent, protracted course of sars-cov-2 infection. remdesivir therapy alleviated symptoms and produced a transient virologic response, but her course was complicated by recrudescence of high-grade viral shedding. whole genome sequencing identified a mutation, e802d, in the nsp12 rna-dependent rna polymerase which was not present in pre-treatment specimens. in vitro experiments demonstrated that the mutation conferred a ~6-fold increase in remdesivir ic50 but resulted in a fitness cost in the absence of remdesivir. sustained clinical and virologic response was achieved after treatment with casirivimab-imdevimab. although the fitness cost observed in vitro may limit the risk posed by e802d,

, this case illustrates the importance of monitoring for remdesivir resistance and the potential benefit of combinatorial therapies in immunocompromised patients with sars-cov-2 infection.

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