When the gene was sequenced in 200 control patients, none had the mutation.
A 5-kb DNA fragment containing the CYP102A1 gene was sequenced.
The TGFBR2 gene was sequenced in three of the cancers from patients with HNPCC, and all of these harbored inactivating mutations.
For 209 randomly chosen strains (about 11 per sample), the cts gene was sequenced and then strains were classified as described previously (Morris et al., 2010; Monteil et al., 2012) to characterize the genetic structure of the P. syringae population.
Furthermore, the EG gene was sequenced.
On the basis of neuroradiological findings, SLC20A2 gene was sequenced.
The mutated gene was sequenced to confirm that only the desired mutations were inserted.
The amplified 16S rRNA gene was sequenced using ABI 3730xl DNA Analyzer (Applied Biosystems, USA).
The enzyme was then purified from the thermophile and characterized as a thermostable meso-DAPDH, and the gene was sequenced.
We sought to determine the overall frequency and clinical relevance of MSH6 alterations in glioblastomas.The MSH6 gene was sequenced in 54 glioblastomas.
The cloned EG gene was sequenced by Sangon Biotech (Shanghai) Co., Ltd and the EG gene nucleotide sequence was deposited in GenBank® database with an accession number KX931112.
