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The three-dimensional solution space reveals a point where a specific rotation period and discount rate maximise SEV.
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The elucidation of the cDNA clone of violacin A revealed a point mutation that introduces a stop codon, which inhibits the translation of a key Asn residue that is thought to be required for cyclization.
Genome re-sequencing of the evolved strain (SOS4) revealed a point mutation (A81P) in MTH1 coding for a transcriptional regulator involved in glucose sensing, unlike the previously reported Pdc-deficient mutant which had internal deletion in MTH1.
Chandra observations have also revealed a point source at the position of the central star.
This analysis revealed a point mutation in ropB, leading to truncation of RopB at amino acid 170 of the 280 amino acid protein (Fig. 1A).
The SLC39A13 gene was contained in a single region of homozygosity on chromosome 11, and mutation analysis revealed a point mutation predicting the substitution of a highly conserved amino acid (G74D) in the second transmembrane domain (Figures 4I and 4J).
Sequencing candidate genes revealed a point mutation in the poorly characterized WDR72 gene.
Exome sequencing revealed a point mutation c.1438C>T, p.R480W in SPTBN2 in this patient.
DNA sequencing revealed a point mutation at position 2709 C>T in this exon.
Sequence analysis revealed a point mutation in both patients nearly midway in intron 44i (c.4886+1249 (G>T) (Fig. 4A).
Sequence analysis revealed a point mutation at codon 972 of CaSR gene (chromosome 3q), located within cytoplasmic domain of the CaSR, that changes Threonine with Methionine.
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