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1 AD(65) as shown by gel mobility shift in non-denaturing gradient gel electrophoresis.
2 apo E locus were identified by the method of denaturing gradient-gel electrophoresis.
3 VH4 families in each tube were identified by denaturing gradient gel electrophoresis after PCR amplif
6 ion, analysis of PTEN using a combination of denaturing gradient gel electrophoresis and direct seque
7 viral quasispecies by using a combination of denaturing gradient gel electrophoresis and DNA heterodu
8 submitted to polymerase chain reaction(PCR)-denaturing gradient gel electrophoresis and real-time qu
9 C gene were screened for mutations either by denaturing gradient gel electrophoresis and single-stran
10 ibosomal DNA polymerase chain reaction (PCR)-denaturing gradient gel electrophoresis and with a PCR-b
11 ic sequence of the CFTR gene was analyzed by denaturing gradient-gel electrophoresis and sequencing i
12 s of the biocides applied, by using cloning, denaturing gradient gel electrophoresis, and culture-dep
14 d-dimension electrophoretic separation step--denaturing gradient gel electrophoresis--and the current
15 he following polymorphisms in our sample via denaturing gradient gel electrophoresis, database compar
16 her direct nucleotide sequencing (28 cases), denaturing gradient gel electrophoresis (DGGE) (34 cases
18 munities and T. versicolor was studied using denaturing gradient gel electrophoresis (DGGE) and the c
20 hism (SSCP) for p53 mutations and by PCR and denaturing gradient gel electrophoresis (DGGE) for K-ras
21 ntial isolation and eubacterium-specific PCR-denaturing gradient gel electrophoresis (DGGE) in conjun
24 t bacterial community structure derived from denaturing gradient gel electrophoresis (DGGE) shifted m
25 uence the mutational spectra, we applied the denaturing gradient gel electrophoresis (DGGE) system co
34 individuals were examined using a sensitive denaturing gradient-gel electrophoresis (DGGE) system.
35 alyzed by the polymerase chain reaction with denaturing gradient gel electrophoresis for exons 5-8 of
36 cation test (PTT) for exon 11 of BRCA1, with denaturing gradient gel electrophoresis for the remainde
37 re identified by a combination of screening (denaturing gradient gel electrophoresis, heteroduplex an
38 e coding sequences and promoter sequences by denaturing gradient gel electrophoresis in unrelated ind
40 ently established mutant allele enrichment + denaturing gradient gel electrophoresis method, which ca
42 from individual cultured isolates by PCR and denaturing gradient gel electrophoresis (PCR-DGGE), allo
43 etermined by principal component analysis of denaturing gradient gel electrophoresis profiles was evi
45 dant with ITS lineage membership (defined by denaturing gradient gel electrophoresis screening), yet
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