Scale 1/43 NIB Diecast K-Line & MTH,Lionel for "WOODY" FORD 1948 Burgundy Other O Scale


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NIB 1/43 Scale Diecast Burgundy 1948  FORD  "WOODY"  for  MTH,Lionel & K-Line
Condition: New: A brand-new, unused, unopened, undamaged item (including handmade items). See the seller's Scale: 1:43
Color:

Burgundy

Vehicle Make: Ford
MPN:

94243

Modified Item: No
Brand:

Road Signature

Material: DieCast
Non-Domestic Product: No Type: Cars
Grading: C-10 Mint - Brand New UPC:

047816942438



published on tue nov 09 2021

Scale 1/43 NIB Diecast K-Line & MTH,Lionel for "WOODY" FORD 1948 Burgundy Other O Scale

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

Scale 1/43 NIB Diecast K-Line & MTH,Lionel for "WOODY" FORD 1948 Burgundy Other O Scale

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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