Sentence examples for mutation were examined from inspiring English sources

Family members of the Danish and of the Czech probands carrying the GHSR -151 C/T promoter mutation were examined for the presence of this variant using sequencing.

The dynamics effects of the S14A mutation were examined for [S14A,P18A]-TC16b.

Chimeric receptors harboring an intact unmodified tail (WT) versus a cytoplasmic FFF mutation were examined after BCR ligation or co-ligation by immunoblotting whole-cell lysates.

Differences in the incidences of tumours with CTNNB1 mutation were examined between any two of three groups of tumours classified on the basis of the IGF2 status by the χ test.

Methods: Using a cross-sectional design in this study, the relationship between arteriovenous fistula (AVF) obstruction and the MTHFR C677T point mutation was examined in 337 HD patients.

The daughter (H2630) who did not carry the p.Arg423His mutation was examined at age 15 and had no abnormal neurological findings.

Due to the established functionality of the -151T GHSR mutation the physiological and biochemical profile of carriers of the -151T transcription-activating mutation was examined in the Danish and Czech families.

In a subgroup of patients, the influence of EGFR mutation was examined.

EGFR exon 20 mutation was examined using direct sequencing as previously reported.

IDH1 mutation was examined by immunohistochemistry in formalin-fixed and paraffin-embedded tumor samples.

In this study, SF3B1 mutation was examined in nine cases of CSA; however, its mutation was not detectable in CSA.