Sentence examples for variant was provided from inspiring English sources

MAGp72_pXM plasmid containing full-length rat L-MAG was a kind gift from Rainer Hillenbrand, Basel, Novartis Institutes for BioMedical Research [28], MOG_pCMV containing full-length human MOG alpha variant was provided by Markus Reindl, Innsbruck Medical University and N-CAM_pBK-CMV containing full-length chicken N-CAM180 was given to us from Jozsef Kiss, Geneva, University Medical Center.

An online tool reporting the AACDS score for any variant is provided at the authors' website.

An online tool for computing the AACDS scores for any variant is provided at http://www.cig.gatech.edu/Tools.edu/Tools

The associations with each coding variant by race-ethnicity and the genotype counts for each variant are provided (see Additional file 1, Supplementary tables 1 and 3). a Minor allele frequency among controls across populations.

The 44 subjects presenting with an ONCOblot® Tissue of Origin Test with evidence for an ENOX2 transcript variant, were provided with successive 3 month supplies of Capsol-T® and retested at the interval shown.

Another example of a modifying 3′UTR variant is provided by the G>A polymorphism (rs1799963) at position 20210 in the prothrombin (F2) gene, which increases the risk of venous thrombosis by enhancing F2 mRNA 3′ end formation efficiency, thereby boosting thrombin formation (Gehring et al. 2001).

In order to classify UVs via co-segregation, a simple Bayesian method to assess causality of rare sequence variants was provided by Petersen et al. [ 10].

A brief background of the motivation behind the creation of the above variants is provided.

An overview and critical evaluation of the h-index and its variants are provided by Froghi et al.

The nomenclature and short description of the recombinant NYVAC variants is provided in table 1. Virological and pathogenic characterization of these vectors in cultured cells and in mice is described (Kibler et al., submitted for publication).

The APEX microarray (Asper Biotech) includes 198 mutations selected from six nuclear genes (GJB2, GJB6, GJB3, GJA1, SLC26A4 and SLC26A5) and two mitochondrial genes (MTRNR1 and MTTS1); a detailed list of sequence variants is provided in Table S1.