Searching journal content for articles similar to Graim et al..

Displaying results 1-10 of 5422
For checked items
  1. ...a normal to a breast cancer malignant state remains unknown. To address this, we have conducted an analysis combining Hi-C data with lamina-associated domains (LADs), epigenomic marks, and gene expression in an in vitro model of breast cancer progression. Our results reveal that although the fundamental...
  2. ...trait. We characterize coding variation across 2291 canine s from over 200 phylogenetically informed breeds/subpopulations and develop a canine-specific mutation model to determine whether gene/site constraint metrics are predictive of variant fitness consequences. From this, we identify breed...
  3. ..., promoting tumor cell proliferation and survival (Yarden and Sliwkowski 2001). The HER2-positive breast cancer subtype is associated with aggressive tumor behavior and poor prognosis in the absence of anti-HER2-targeted therapy (Slamon et al. 1987).The advent of HER2-targeted therapies has significantly...
  4. ...on TE silencing and the functional consequences of this have remained unclear. To assess the epigenetic regulation of TEs in aging, we profiled DNA methylation in human mammary luminal epithelial cells (LEps)—a key cell lineage implicated in age-related breast cancers—from younger and older women. We...
  5. ....zwart@nki.nlAbstractEstrogen Receptor 1 (ESR1; also known as ERα, encoded by ESR1 gene) is the main driver and prime drug target in luminal breast cancer. ESR1 chromatin binding is extensively studied in cell lines and a limited number of human tumors, using consensi of peaks shared among samples. However, little is known about inter-tumor...
  6. .... These findings are confirmed by genomic data in situ, indicating that enhancer activation within a chromatinized context is robustly captured in a plasmid-based reporter assay. In silico integration of our findings with publicly available functional genomics data sets from breast cancer cell lines and tumor...
  7. ...@illinois.eduAbstractCancer results from an evolutionary process that typically yields multiple clones with varying sets of mutations within the same tumor. Accurately modeling this process is key to understanding and predicting cancer evolution. Here, we introduce clone to mutation (CloMu), a flexible and low-parameter tree...
  8. ...Peng Xu1,2,3 and Bin Zhang1,2,3,4 1Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA; 2Mount Sinai Center for Transformative Disease Modeling, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA; 3Icahn Institute...
  9. ...cell renal cell carcinoma (ccRCC) tumors (P = 0.011) (Fig. 3A), EWS894 Ewing sarcoma tumors (P = 0.044) (Fig. 3B), and MDA-MB-231 basal breast tumors (P = 0.008) (Fig. 3C).View larger version: In this window In a new window Figure 3. Nanodroplets facilitate the extraction of chromatin from archival...
  10. ...questioned (Thompson et al. 2015). On the other hand, SMARCA4 is essential, as SMARCA4 mice are embryonic lethal, and SMARCA4 heterozygous mice show developmental defects and are prone to mammary tumor formation (Bultman et al. 2000, 2008). SMARCA4 has been shown to be involved in many developmental...
For checked items

Preprint Server