Sentence examples for mutations characteristic of from inspiring English sources

Consistent with a unique origin for pediatric low-grade glioma, third ventricle, but not lateral ventricle, NSCs hyperproliferate in response to mutations characteristic of childhood glioma.

High throughput sequencing approaches have facilitated genome-wide discovery of mutations characteristic of various disease statuses [1].

In this biologically relevant application, we found that the array correctly identified mutations characteristic of ribavirin's mode of action and detected drug resistant variants at an early stage.

This shift in SpeA and SpeB expression levels is a hallmark reflection of covS mutations characteristic of many invasive M1T1 isolates and is reproduced upon experimental animal passage of M1T1 isolates [36], [37].

As shown in Fig. 2, the primary constituent of NDsq0168 comprises most of the mutations characteristic of haplogroup M7a2 (except C12705T and G12771A), whereas the secondary constituent of the sample encompasses five seemingly "private" variants (viz. G12406A, C12882T, G13759A, G13928C, and A14002G) which clearly point to haplogroup F1a1b.

Namely, the primary constituent of NDsq0167 encompasses most of the mutations characteristic of haplogroup F1a1b (with the exception of G12406A, C12882T, G13759A, G13928C, and A14002G), whereas the secondary constituent of the sample consists of two "homoplasious" mutations, C12705T and G12771A (score 4.0), which occur on the pathway to haplogroup M7a.

METHODS: A total of 50 patients 19 years of age or younger who were consecutively identified through a genetic screening program as carriers of a RET mutation characteristic of MEN-2A underwent total thyroidectomy.

CONCLUSIONS: In this study, young patients identified by direct DNA analysis as carriers of a RET mutation characteristic of MEN-2A had no evidence of persistent or recurrent medullary thyroid carcinoma five or more years after total thyroidectomy.

The only exception are the primers surrounding the V2697F mutation, characteristic of the AS-ATN clone [29].

A subset of six subjects tested positive for the PHOX2B mutation characteristic of the syndrome [18], and two were inconclusive; the other subjects had not been evaluated.

However, none of these pandemic strains possessed the HA cleavage site mutation characteristic of HPAI viruses (3 ).