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Carol Mackie produced its own genetic mutation with reverse variegation (white leaves edged in green).
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A dramatic fluctuation of CD4+ T cell count around 100 days p/s (Figure 3A) coincided with dynamic changes in the spectrum of viral quasispecies associated with reverse mutations to the wild type (Figure 3B; amino acid positions 215, 389, and 453) and escape mutations from the wild type (Figure 3C; amino acid positions 35, 142, 146, 370, and 428).
Samples with resistance mutations were obtained from 51 individuals with protease L90M, and those with reverse transcriptase mutations included 78 subjects with M41L, 26 with K65R, 59 with K70R, 81 with K103N, 28 with Y181C, 67 with M184V, 44 with T215Y, and 35 with T215F.
41 Dual ritonavir-boosted PI (PI/r) regimens represent an option for salvage or maintenance therapy for patients with reverse transcriptase mutations or intolerance.
It is now clear that adult-onset obesity is associated with region-specific upregulation of astrocytic ObR, shown in both agouti viable yellow (Avy) mice that have a genetic mutation with constitutive production of a reverse melanocortin receptor antagonist and reduced apparent influx of leptin from blood to the brain, 22, 53 and in control C57 mice with adult-onset obesity.
Primers 15 and 16 amplify the region encompassing the mutation; the reverse primer is marked with 5'HEX.
One participant receiving DTG 10 mg developed virus with the mutation M184M/V in reverse transcriptase.
MglB+ YFP does not fully complement a Δ mglB mutation and cells reverse with an average period of 8.2 min. We therefore analysed the M. xanthus MglBA64/G68R mutant that corresponds to the T.t.MglBA68/72R mutant, which is unable to stimulate MglA GTPase activity, without YFP in Δ mglB+ cells.
Its mutation or reverse mutation variants had no activities.
Encourage experimentation with reverse psychology.
In our previous study of >10,000 samples from patients with suspected MPNs tested for JAK2 mutations by reverse transcription-PCR (RT-PCR) with direct sequencing, complete deletion of exon 14 (Δexon14) constituted <1% of JAK2 mutations.
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