Sentence examples for mutation that corresponds from inspiring English sources

However, a few agents comment on articles because of the mutation that corresponds to the vagaries of users.

These knock-in mice have a mutation that corresponds to the p53 R175hotot spot in human cancers.

R181L, a mutation that corresponds to a substitution in human patients exhibiting lipoid CAH, affects the charge of a highly-conserved residue within β6 of the START domain that contains other residues implicated in direct ligand contact.

mtDNA sequencing revealed a novel mutation that corresponds to an insertion of one or two cytosine residues in the coding region of the MT-ND6 gene (m.14535_14536insC or CC), leading to premature stop codons.

This residue has previously been found mutated in viral escape mutants resistant to a mAb-targeting antigenic site I (34), so we prepared CVS11 pseudotype virus harboring a G229E point mutation that corresponds to the escape mutant previously described (34).

Although, a similar extended isoform of the related C/EBPβ exists that is translated from an upstream AUG-codon, it does not have a NoLS, and we did not observe localization of extended-C/EBPβ in the nucleolus whether it harbours an S239D mutation that corresponds to the S299D mutation in C/EBPα or not (data not shown).

Microfluidics platforms are currently being used to detect genetic mutations that correspond to breast cancer, including DNA and miRNA mutations [106, 107, 108, 109, 110, 111].

Of special interest is a spectrum of EGFR, ABL, MET, FLT3 and KIT cancer mutations that correspond to the same structurally conserved position in the activation loop, which appeared to be mutated in at least 8 different kinases (Figure 6A, Table S1).

When the Caton et al. escape mutants are mapped onto the 1RVX structure, there are clusters of mutations that correspond to each antigenic site.

Two mutations encoded premature stop codons (Y262X, L265X) and resulted in a deletion of the C-terminus, whereas the third encoded a point mutation (G264D) that corresponded to a human mutation associated with a severe form of SMA.

The Deletor mouse carries a dominant pathogenic mutation in the major mitochondrial DNA (mtDNA) replicative helicase, Twinkle, that corresponds to a mutation found in patients (Tyynismaa et al, 2005).