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We obtained different read-through efficacies of the applied TRIDs on the USH1C p.R31X mutation at diverse systemic levels including cell culture, retinal explants and in vivo.
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These mutations might be at diverse loci, but they all finally led to a "convergent developmental feature", i.e. a restricted pattern of RhAG expression leading to double flower formation.
Mutations at various positions within the loop had diverse effects on the expression of different genes containing different GR-response elements.
Patients with resistant mutations at baseline showed diverse outcomes from SVR to NR suggesting no correlation between baseline profile and outcome.
The clinical consequences of the R281T mutation were diverse.
In addition, genotype Ia was associated with diverse mutations at VP1 loops and sites under positive selection outside loops, which were totally absent in Ib1.
New sequencing technology promises to facilitate identification of mutations in diverse species.
Patients with SCN harbor mutations in diverse genes.
We suggest further research into the presence of mutations in diverse cohorts from varied populations.
The mutations observed were diverse and few recurrent mutations were detected.
Protein kinase resequencing at the Sanger Institute has culminated in the identification of 921 base substitution somatic mutations in 210 diverse human cancers types [12].
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