| Literature DB >> 30425743 |
Vinodh Kumar Radhakrishnan1, Lorraine Christine Hernandez1, Kendra Anderson1, Qianwei Tan1, Marino De León1, Daisy D De León1.
Abstract
[This corrects the article DOI: 10.1155/2015/401851.].Entities:
Year: 2018 PMID: 30425743 PMCID: PMC6218738 DOI: 10.1155/2018/8434297
Source DB: PubMed Journal: Int J Endocrinol ISSN: 1687-8337 Impact factor: 3.257
Figure 1ApaI digestion of the 292 bp nested PCR (QPCR) fragment generated from the fragment of 1.12 RT-PCR reactions. Biallelic expression was identifiable by the presence of each of the 292, 227, and 63 bp restriction fragments. The first lane shows Fisher's exACTGene 100 bp DNA Ladder, showing the 500 bp–25 bp respective molecular weight size markers. ∗ denotes paired breast samples from the same patient (normal, malignant).
Figure 2((a), (b), and (c)) Western blot of paired normal/malignant TNBC samples (1–48). The total number of samples (n) analyzed per group was as follows: Heterozygous (Het; n = 27), Homozygous with SNP (Hom SNP; n = 11), and Homozygous (Hom; n = 10). Bar graphs (a–c) of free proIGF-II (17.5 kDa) and Survivin (16.5 kDa). Ponceau red staining was used to normalize for sample loading. Bars represent the mean ± SE of all normalized samples per group. Asterisks indicate values statistically significant ∗(p < 0.05) using the Wilcoxon paired 𝑡-test.