Sentence examples for for this nucleotide from inspiring English sources

A polymerase chain reaction-restriction fragment length polymorphism-method was established as a DNA-based test for this nucleotide substitution.

The GenBank access number for this nucleotide sequence is KY315817.

We next statistically normalized for this nucleotide bias, by weighting each read based on the relative frequency of reads starting with the nucleotide at its first position (see Materials and Methods).

Children of Amish origin with extended-family members known to carry the 923G>T (G308V) "Byler mutation" in ATP8B1 [ 18] were assessed for homozygosity for this nucleotide substitution.

The T H1′→X H2 NOE (the imidazole proton of 1, N-ϵdG; note the modified numbering scheme for this nucleotide) was missing, interrupting the NOE connectivity.

However, the T H1′ → X H2 NOE (the imidazole proton of 1, N-εdG; note the modified numbering scheme for this nucleotide) was weak compared to the corresponding NOEs.

We previously replaced the 3′-loop adenine of SLIV with 2-aminopurine (2AP) and showed that it does not affect the RNA binding affinity of SLIV for SNF; this nucleotide is stacked with its neighboring bases in the free RNA but becomes flipped out of the stack upon binding to SNF.

Carboxyl and hydroxyl groups of side radicals of dicarbonic and hydroxy Aa's do not have sufficient opportunity for interaction with this nucleotide.

Although paired normal DNA is not available for this cell line this nucleotide change is not listed as a known SNP (single nucleotide polymorphism) in the Entrez SNP database (Build 129).

During electrophoresis some of the actin molecules loose their bound ATP (originating from the transcription/translation reaction) and since actin needs this nucleotide for its stability (30), this part of the population denatures.

The relative mutant load for this new nucleotide variant was measured by PCR-RFLP analysis in blood (not shown), muscle and fibroblasts of the patient (Figure 1B), and showed homoplasmic levels of the mutation in all tissues.