Integrative analyses of triple negative dysregulated transcripts compared with non‐triple negative tumors and their functional and molecular interactions-Reference-Cited by-同舟云学术

Integrative analyses of triple negative dysregulated transcripts compared with non‐triple negative tumors and their functional and molecular interactions

Published:2019-05-12 Issue:12 Volume:234 Page:22386-22399
ISSN:0021-9541
Container-title:Journal of Cellular Physiology
language:en
Short-container-title:J Cell Physiol

Author:

Darbeheshti Farzaneh¹²^ORCID,Rezaei Nima³⁴⁵,Amoli Mahsa M.⁶,Mansoori Yaser⁷⁸,Tavakkoly Bazzaz Javad¹

Affiliation:

1. Department of Medical Genetics School of Medicine, Tehran University of Medical Sciences Tehran Iran

2. Breast Cancer Association (BrCA) Universal Scientific Education and Research Network (USERN) Tehran Iran

3. Research Center for Immunodeficiencies Children's Medical Center, Tehran University of Medical Sciences Tehran Iran

4. Department of Immunology, School of Medicine Tehran University of Medical Sciences Tehran Iran

5. Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA) Universal Scientific Education and Research Network (USERN) Tehran Iran

6. Metabolic Disorders Research Center Endocrinology and Metabolism Molecular ‐Cellular Sciences Institute, Tehran University of Medical Sciences Tehran Iran

7. Noncommunicable Disease Research Center Fasa University of Medical Sciences Fasa Iran

8. Department of Medical Genetics Fasa University of Medical Sciences Fasa Iran

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcp.28804

Reference63 articles.

1. Competing endogenous RNA (ceRNA) cross talk and language in ceRNA regulatory networks: A new look at hallmarks of breast cancer

2. A nuclear export signal and oxidative stress regulate ShcD subcellular localisation: A potential role for ShcD in the nucleus

3. FOXA1 Induces E-Cadherin Expression at the Protein Level via Suppression of Slug in Epithelial Breast Cancer Cells